USE OF MARKERS INCLUDING FILAMIN A IN THE DIAGNOSIS AND TREATMENT OF PROSTATE CANCER

Abstract

Methods for diagnosing the presence of prostate cancer in a subject are provided, such methods including the detection of levels of variety of biomarkers diagnostic of prostate cancer, including filamin A alone, or in combination with one or more additional biomarkers of prostate cancer, including, PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, and LY9. Additionally, age can be used as a predictor variable. The invention also provides methods of treating prostate cancer which rely on diagnostic information obtained based on the detection of biomarkers of prostate cancer, including filamin A alone, or in combination with one or more additional biomarkers of prostate cancer, including, PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, LY9, and/or age. Compositions in the form of kits and panels of reagents for detecting the biomarkers of the invention are also provided.

Description

RELATED APPLICATIONS

[0001] This application is a Continuation of U.S. patent application Ser. No. 14/962,966, filed on Dec. 8, 2015, which, in turn, claims priority to U.S. Provisional Application No. 62/088,931, filed on Dec. 8, 2014; U.S. Provisional Application No. 62/134,956, filed on Mar. 18, 2015; and U.S. Provisional Application No. 62/148,294, filed on Apr. 16, 2015, the entire contents of each of which are expressly incorporated herein by reference.

SEQUENCE LISTING

[0002] This specification incorporates by reference the Sequence Listing submitted via EFS web on Nov. 19, 2019 identified as 119992_10806, which is 527 kb, and was created on Nov. 18, 2019. The Sequence Listing, electronically filed, does not extend beyond the scope of the specification and does not contain new matter.

INCORPORATION BY REFERENCE

[0003] All documents cited or referenced herein and all documents cited or referenced in the herein cited documents, together with any manufacturer's instructions, descriptions, product specifications, and product sheets for any products mentioned herein or in any document incorporated by reference herein, are hereby incorporated by reference, and may be employed in the practice of the invention.

BACKGROUND

A. Field of the Invention

[0004] The invention generally relates to novel biomarkers and combinations of biomarkers which can be used to detect and monitor prostate cancer. The invention also generally relates to methods for diagnosing, monitoring, and treating prostate cancer involving the detection of biomarkers of the invention.

B. Background of the Invention

[0005] Prostate cancer is a leading cause of male cancer-related deaths--second only to lung cancer--and afflicts one out of nine men over the age of 65. According to the American Cancer Society, 241,000 new cases of prostate cancer were reported with about 30,000 prostate cancer-related deaths that same year. Although the disease is typically diagnosed in men over the age of 65, its impact is still significant in that the average life span of a man who dies from prostate cancer is reduced by nearly a decade on average. However, if prostate cancer is discovered early, 90% of the cases may be cured with surgery. Once the tumor spreads outside the area of the prostate gland and forms distant metastases, the disease is more difficult to treat. Therefore, early detection is of critical importance to the success of interventional therapies, and for reducing the mortality rate associated with prostate cancer.

[0006] Prostate cancer typically develops in the various tissues of the prostate, a gland in the male reproductive system. Most prostate cancers are slow growing. However, there are also a significant number of cases per year of aggressive prostate cancers, in which the cancer cells may metastasize from the prostate to other parts of the body, particularly to the bones and lymph nodes. Prostate cancer may cause pain, difficulty in urinating, problems during sexual intercourse, or erectile dysfunction. Other symptoms can potentially develop during later stages of the disease.

[0007] Currently, prostate cancer is screened using only a limited number of detection means, including the digital rectal exam (DRE) and/or the measurement of the levels of prostate specific antigen (PSA). However, these approaches have an unacceptably high rate of false-positives. Indeed, most men (75%) with an elevated PSA level turn out not to have prostate cancer as determined by subsequent confirmatory prostate biopsies.

[0008] As such, the current screening tests are not specific enough to robustly screen for prostate cancer. Each year, based on the results of the DRE and PSA screens, about one million prostate biopsies are performed in the U.S. alone. Only 25% of these biopsies confirm the presence of cancer. PSA is secreted from epithelial cells of the prostate gland and is higher in blood due to increased number of prostate epithelial cells. When prostate cancers develop, PSA levels in the blood can start to climb. In the United States, the FDA has approved the PSA test for annual screening of prostate cancer in men of age 50 and older. PSA levels between 4 and 10 ng/mL are considered to be suspicious and consideration should be given to confirming the abnormal PSA with a repeat test. If indicated, a prostate biopsy is performed to obtain a tissue sample for histopathological analysis. Complications--such as infection, internal bleeding, allergic reactions, impotence, and urinary incontinence--induced by needless biopsies and treatments injure many more men than are potentially helped by early detection of cancers.

[0009] Indeed, the U.S. Preventative Services Task Force (USPSTF) estimates that about 90% of diagnosed men are treated and 2 in 1000 men will develop serious cardiovascular events, 1 in 1000 men will develop deep venous thrombosis, 29 in 1000 men will develop erectile dysfunction, 18 in 1000 men will develop urinary incontinence, and 1 in 1000 men will die due to treatment. A large majority of these men would have have remained asymptomatic for life if left untreated. As such, most cancers found through PSA tests are not, in fact, dangerous. Nevertheless, given the lack of more effective predictors of prostate cancer, the field takes a more conservative approach in the use of biopsies and treatment, erring on the side of precaution but risking significant harm to otherwise healthy men.

[0010] Despite the current drawbacks in prostate cancer detection, the USPSTF estimates that one life will be saved for every 1,000 men screened every 1-4 years over a 10-year period. This overall outlook can be further improved by limiting unnecessary biopsies with the use of improved pre-biopsy screening methods that are associated with fewer false-positive results. With fewer unnecessary biopsies, fewer men will suffer the associated biopsy complications. In addition, fewer complications will also lead to an overall cost reduction to the healthcare system in the management of prostate cancer.

[0011] Accordingly, there is an unmet need for improved prostate cancer screening tools that improve the accuracy of prostate cancer detection. Molecular-based biomarkers may address this need.

SUMMARY OF THE INVENTION

[0012] In view of the fact that prostate cancer remains a life threatening disease reaching a significant portion of the male population, there remains a need for efficient, accurate, and rapid molecular diagnosis means, particularly which do not suffer from a high proportion of false results. The development of molecular tests for the accurate detection of prostate cancer will also lead to improved management of appropriate therapies, and an overall improved survival rate. Thus, there remains a need to provide an improved diagnostic test for the detection of prostate cancer which is more reliable and accurate than PSA and other current screening tests. The present invention addresses this need by providing the use of a new biomarker, filamin A, either used alone or in combination with other markers, for the accurate and reliable detection of prostate cancer.

[0013] The present invention is based, at least in part, on the discovery that filamin A is differentially regulated in prostate cancer cells. In particular, the invention is based on the surprising discovery that filamin A levels are significantly elevated in the serum of patients with prostate cancer. Accordingly, the invention provides methods for diagnosing and/or monitoring (e.g., monitoring of disease progression or treatment) an oncological disease state, e.g., prostate cancer, in a mammal. The invention also provides methods for treating or for adjusting treatment regimens based on diagnostic information relating to the levels of filamin A in the serum of a subject with an oncological disease state, e.g., prostate cancer. The invention further provides panels and kits for practicing the methods of the invention.

[0014] Accordingly, in one aspect, the present invention provides a method for diagnosing the presence of prostate cancer in a subject, comprising: (a) detecting the level of filamin A in a biological sample of the subject, and (b) comparing the level of filamin A in the biological sample with a predetermined threshold value, wherein the level filamin A above the predetermined threshold value indicates the presence of prostate cancer in the subject.

[0015] In another aspect, the invention provides a method for diagnosing the presence of prostate cancer in a subject, comprising: (a) contacting a biological sample with a reagent that selectively binds to filamin A; (b) allowing a complex to form between the reagent and filamin A; (c) detecting the level of the complex, and (d) comparing the level of the complex with a predetermined threshold value, wherein the level of the complex above the predetermined threshold value indicates the presence of prostate cancer in the subject.

[0016] In certain embodiments, the diagnostic method further comprises detecting the level of one or more additional markers of prostate cancer.

[0017] The one or more additional markers of prostate cancer can include, but is not limited to, prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, kertin 18, keratin 19, and tubulin-beta 3. In another embodiment, the one or more additional markers of prostate cancer can include age. Age can be used as a continuous predictive biomarker. For example, increased age is associated with higher risk of having prostate cancer. Lower age is associated with decreased risk of having prostate cancer.

[0018] In certain other embodiments, the one or more additional markers can include genes that have been described in the literature as being specifically expressed in the prostate. These genes can include, for example, prostate-specific membrane antigen (PSM) (Fair et al., 1997, Prostate-specific membrane antigen. Prostate 32:140-148), prostate stem cell antigen (PSCA) (Reiter et al., 1998, Prostate stem cell antigen: a cell surface marker overexpressed in prostate cancer. Proc. Natl. Acad. Sci. USA 95:1735-1740), TMPRSS2 (Lin et al., 1999. Prostate-localized and androgen-regulated expression of the membrane-bound serine protease TMPRSS2. Cancer Res. 59:4180-4184), PDEF (Oettgen et al., 2000, PDEF, a novel prostate epithelium-specific ETS transcription factor, interacts with the androgen receptor and activates prostate-specific antigen gene expression. J. Biol. Chem. 275:1216-1225), prostate-specific gene-1 (Herness, 2003. A novel human prostate-specific gene-1 (HPG-1): molecular cloning, sequencing, and its potential involvement in prostate carcinogenesis. Cancer Res. 63:329-336), and even various non-coding RNA's (ncRNA's), like PCA3 (Bussemakers et al., 1999. DD3: a new prostate-specific gene, highly overexpressed in prostate cancer, Cancer Res. 59:5975-5979), PCGEM1 (Srikantan et al., 2000. PCGEM1, a prostate-specific gene, is overexpressed in prostate cancer. Proc. Natl. Acad. Sci. USA 97:12216-12221) and the gene cluster P704P, P712P, and P775P (Stolk et al., 2004. P704P, P712P, and P775P: A genomic cluster of prostate-specific genes. Prostate 60:214-226). Only a fraction of these markers have been associated with prostate cancer prognosis, progression and/or metastatic capacity and as such, their potential as valuable biomarkers and/or therapeutic targets is largely unknown.

[0019] In one embodiment, the prostate cancer is a prostate cancer characterized by overexpression of filamin A. In another embodiment, the prostate cancer is a prostate cancer characterized by overexpression of filamin A and overexpression of one or more additional markers selected from the group consisting of filamin B, LY9, keratin 5, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, or prostate specific antigen (PSA). In another embodiment, the prostate cancer is a prostate cancer characterized by overexpression of filamin A and overexpression of one or more additional markers selected from the group consisting of filamin B, LY9, keratin 5, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, or prostate specific antigen (PSA), and increased patient age. In another embodiment, the prostate cancer is a prostate cancer characterized by overexpression of filamin A and increased patient age. In another embodiment, the prostate cancer is a prostate cancer characterized by underexpression of filamin A and overexpression of one or more additional markers selected from the group consisting of filamin B, LY9, keratin 5, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, or prostate specific antigen (PSA). In another embodiment, the prostate cancer is a prostate cancer characterized by underexpression of filamin A and overexpression of one or more additional markers selected from the group consisting of filamin B, LY9, keratin 5, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, or prostate specific antigen (PSA), and increased patient age. In another embodiment, the prostate cancer is a prostate cancer characterized by underexpression of filamin A and increased patient age.

[0020] In certain embodiments, the biological sample can be selected from the group consisting of blood, serum, urine, organ tissue, biopsy tissue, feces, skin, hair, and cheek tissue.

[0021] In various embodiments, the level of filamin A can be determined by an assay, such as an immunoassay or ELISA. Other suitable assays may be employed.

[0022] In certain embodiments, the step of determining the level of filamin A in the biological sample can comprise (i) contacting the biological sample with a reagent that selectively binds to the filamin A polypeptide to form a biomarker complex, and (ii) detecting the biomarker complex.

[0023] In some embodiments, the reagent can be an anti-filamin A antibody that selectively binds to at least one epitope of filamin A. In certain other embodiments, the anti-filamin A antibody may further comprise a detectable label. In other embodiments, the method may include a further step that contacts the anti-filamin A antibody/filamin A complex with a secondary antibody which selectively binds to the anti-filamin A antibody, and which itself carries a detectable tag or label.

[0024] In certain other embodiments, the step of determining the level of filamin A in the biological sample can be based on determining the amount of filamin A mRNA in the biological sample.

[0025] In some embodiments, an amplification reaction can be used for determining the amount of filamin A mRNA in the biological sample. The amplification reaction can include, but is not limited to, (a) a polymerase chain reaction (PCR); (b) a nucleic acid sequence-based amplification assay (NASBA); (c) a transcription mediated amplification (TMA); (d) a ligase chain reaction (LCR); or (e) a strand displacement amplification (SDA).

[0026] In still other embodiments, the step of determining the level of filamin A in the biological sample can be based on a hybridization assay, which can include using an oligonucleotide or probe that is complementary to a portion of a filamin A mRNA to hybridize thereto, wherein the oligonucleotide further comprises a detectable label or tag.

[0027] In certain embodiments, the prostate cancer is a prostatic intraepithelial neoplasia, adenocarcinoma, small cell carcinoma, or squamous cell carcinoma. In other embodiments, the prostate cancer can be an androgen-dependent prostate cancer. In still other embodiments, the prostate cancer can be an androgen-independent prostate cancer. In yet other embodiments, the prostate cancer can be an aggressive prostate cancer or a metastasized cancer. In still other embodiments, the prostate cancer can be a non-aggressive prostate cancer.

[0028] In embodiments where a diagnosis of prostate cancer is made, the invention also contemplates administering a therapeutic anti-cancer treatment, wherein the anti-cancer treatment is selected from the group consisting of (a) radiation therapy, (b) chemotherapy, (c) surgery, (d) hormone therapy, (e) antibody therapy, (f) immunotherapy, (g) cytokine therapy, (h) growth factor therapy, and (d) any combination of (a)-(h).

[0029] In various embodiments, the methods of the invention can involve first selecting a subject suspected of having or being at risk of having prostate cancer and obtaining a biological sample from that subject suspected of having or being at risk of having prostate cancer.

[0030] In still other embodiments, the diagnostic methods of the invention may further comprise comparing the level of the one or more prostate cancer related markers in the biological sample, e.g., filamin A and one or more of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, kertin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 with the level of the one or more prostate cancer related markers in a control sample selected from the group consisting of: a sample obtained from the same subject at an earlier time point than the biological sample, a sample from a subject with benign prostatic hyperplasia (BPH), a sample from a subject with non-metastatic prostate cancer, a sample from a subject with metastatic prostate cancer, a sample from a subject with androgen sensitive prostate cancer, a sample from a subject with androgen insensitive prostate cancer, a sample from a subject with aggressive prostate cancer, and a sample from a subject with non-aggressive prostate cancer.

[0031] In still other embodiments, the diagnostic methods of the invention can comprise differentiating between two prostate cancer states selected from the group consisting of: normal prostate and prostate cancer, benign prostate hyperplasia and prostate cancer, benign prostate hyperplasia and normal prostate, androgen dependent and androgen independent prostate cancer, aggressive prostate cancer and non-aggressive prostate cancer, and metastatic prostate cancer and non-metastatic prostate cancer.

[0032] In yet another aspect, the present invention provides a method for monitoring prostate cancer in a subject, the method comprising: (1) determining a level of filamin A in a first biological sample obtained at a first time from a subject having prostate cancer; (2) determining a level of filamin A in a second biological sample obtained from the subject at a second time, wherein the second time is later than the first time; and (3) comparing the level of filamin A in the second sample with the level of filamin A in the first sample, wherein a change in the level of filamin A is indicative of a change in prostate cancer status in the subject.

[0033] In certain embodiments, the determining steps (1) and (2) above further comprise determining the level of one or more additional prostate cancer related markers selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In certain embodiments, the determining steps (1) and (2) above further comprise determining the level of the patient's age.

[0034] In certain embodiments, the subject is actively treated for prostate cancer prior to obtaining the second sample. In other embodiments, the subject is not actively treated for prostate cancer prior to obtaining the second sample.

[0035] In certain embodiments relating to monitoring prostate cancer, the increased level of filamin A and/or the one or more additional prostate cancer related markers in the second biological sample as compared to the first biological sample is indicative of progression of the prostate cancer in the subject.

[0036] In certain other embodiments relating to monitoring prostate cancer, a decreased or equivalent level of filamin A and/or the one or more additional prostate cancer related markers in the second biological sample as compared to the first biological sample is indicative of non-progression of the prostate cancer in the subject.

[0037] In other embodiments relating to monitoring prostate cancer, wherein the method further comprises comparing the level of the one or more prostate cancer related markers in the first biological sample or the second biological sample with the level of the one or more prostate cancer related markers in a control sample selected from the group consisting of: a normal control sample, a sample from a subject with benign prostatic hyperplasia (BPH), a sample from a subject with non-metastatic prostate cancer, a sample from a subject with metastatic prostate cancer, a sample from a subject with androgen sensitive prostate cancer, a sample from a subject with androgen insensitive prostate cancer, a sample from a subject with aggressive prostate cancer, and a sample from a subject with non-aggressive prostate cancer.

[0038] In still other embodiments, any of the methods of the invention can include detecting the size of the prostate tumor in the subject.

[0039] In still other embodiments, any of the methods further comprise obtaining a first sample and a second sample from the subject.

[0040] In still other embodiments, the diagnostic methods of the invention further comprise the step of selecting and/or administering a different treatment regimen for the subject based on progression of the prostate cancer in the subject.

[0041] In yet other embodiments, the diagnostic methods of the invention further comprise administering a therapeutic anti-cancer based on progression of the prostate cancer in the subject, wherein the anti-cancer treatment is selected from the group consisting of (a) radiation therapy, (b) chemotherapy, (c) surgery, (d) hormone therapy, (e) antibody therapy, (f) immunotherapy, (g) cytokine therapy, (h) growth factor therapy, and (d) any combination of (a)-(h).

[0042] In still other embodiments, the methods of the invention further comprise withholding an active treatment of the prostate cancer in the subject based on non-progression of the prostate cancer in the subject.

[0043] In another aspect, the present invention provides a method of treating prostate cancer in a subject, comprising: (a) obtaining a biological sample from a subject suspected of having prostate cancer, (b) submitting the biological sample to obtain diagnostic information as to the level of filamin A, (c) administering a therapeutically effective amount of an anti-cancer therapy if the level of filamin A is above a threshold level.

[0044] In yet another aspect, the present invention provides a method of treating prostate cancer in a subject, comprising: (a) obtaining diagnostic information as to the level of filamin A in a biological sample, and (b) administering a therapeutically effective amount of an anti-cancer therapy if the level of filamin A is above a threshold level.

[0045] In still another aspect, the present invention provides a method of treating prostate cancer in a subject, comprising: (a) obtaining a biological sample from a subject suspected of having prostate cancer for use in identifying diagnostic information as to the level of filamin A, (b) measuring the level of filamin A in the biological sample, (c) recommending to a healthcare provider to administer an anti-cancer therapy if the level of filamin A is above a threshold level.

[0046] In certain embodiments, the method of the invention further comprises obtaining diagnostic information as to the level of one or more additional markers of prostate cancer.

[0047] In still other embodiments, the method of the invention further comprises obtaining diagnostic information as to the level of one or more additional markers of prostate cancer. The one or more additional markers of prostate cancer can include, but are not limited to, PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In another embodiment, the patient's age is determined. Age can be used as a continuous predictive variable. For example, increased age is associated with increased risk of prostate cancer. Conversely, decreased age is associated with decreased risk of prostate cancer.

[0048] In certain other embodiments, the method of the invention involves administering a therapeutically effective amount of an anti-cancer therapy if the level of filamin A and at least one of the additional markers of prostate cancer are above a threshold level.

[0049] In still other embodiments, the method of the invention involves recommending to a healthcare provider to administer an anti-cancer therapy if the level of filamin A and at least one of the additional markers of prostate cancer are above a threshold level.

[0050] The biological sample of any of the methods of the invention can be obtained from the blood, serum, urine, organ tissue, biopsy tissue, feces, skin, hair, or cheek tissue, or any other suitable tissue or bodily site.

[0051] In still further embodiments, the methods of treatment of the invention can measure the level of filamin A as determined by immunoassay or ELISA. In still other embodiments, the level of filamin A can be determined by (i) contacting the biological sample with a reagent that selectively binds to the filamin A to form a biomarker complex, and (ii) detecting the biomarker complex. The reagent can be an anti-filamin A antibody that selectively binds to at least one epitope of filamin A.

[0052] In certain other embodiments, the level of filamin A can be determined by measuring the amount of filamin A mRNA in the biological sample. The filamin A mRNA level can be determine by an amplification reaction, including (a) a polymerase chain reaction (PCR); (b) a nucleic acid sequence-based amplification assay (NASBA); (c) a transcription mediated amplification (TMA); (d) a ligase chain reaction (LCR); or (e) a strand displacement amplification (SDA). The level of filamin A mRNA can also be determined by a hybridization assay using an oligonucleotide that is complementary to a portion of a filamin A mRNA.

[0053] In still another aspect, the present invention relates to a kit for detecting filamin A in a biological sample comprising at least one reagent for measuring the level of filamin A in the biological sample, and a set of instructions for measuring the level of filamin A. The reagent can be an anti-filamin A antibody. The kit can also comprise a means to detect the anti-filamin A antibody, such as a detectable secondary antibody.

[0054] The kit of the invention may also include a reagent that is an oligonucleotide that is complementary to a filamin A mRNA.

[0055] The kit of the invention can also include a set of instructions which set forth an immunoassay or ELISA for detecting the filamin A level in the biological sample. The instruction may set forth an amplification or hybridization reaction for assaying the level of filamin A mRNA in the biological sample. The amplification reaction can be (a) a polymerase chain reaction (PCR); (b) a nucleic acid sequence-based amplification assay (NASBA); (c) a transcription mediated amplification (TMA); (d) a ligase chain reaction (LCR); or (e) a strand displacement amplification (SDA).

[0056] In still another aspect, the present invention provides a panel for use in a method of detecting at least two markers for prostate cancer, the panel comprising at least two detection reagents, wherein each detection reagent is specific for the detection of at least one prostate cancer marker of a set of markers, wherein the set of markers comprises filamin A and at least one other prostate cancer related marker selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0057] In yet another aspect, the present invention provides a panel for use in a method of treating prostate cancer, the panel comprising at least two detection reagents, wherein each detection reagent is specific for the detection of at least one prostate cancer marker of a set of markers, wherein the set of markers comprises filamin A and at least one other prostate cancer related marker selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0058] In still another aspect, the invention provides a panel for use in a method of monitoring the treatment of prostate cancer, the panel comprising at least two detection reagents, wherein each detection reagent is specific for the detection of at least one prostate cancer marker of a set of markers, wherein the set of markers comprises filamin A and at least one other prostate cancer related marker selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0059] In still another aspect, the present invention relates to the use of a panel comprising a plurality of detection reagents specific for detecting markers of prostate cancer in a method for diagnosing and/or treating prostate cancer, wherein at least one detection reagent of the panel is specific for detecting filamin A, and wherein the remaining one or more detection reagents are specific for detecting a prostate cancer marker selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0060] In yet another aspect, the invention provides methods for diagnosing an abnormal prostate state in a subject comprising: (1) determining a level of filamin A in combination with one or more additional prostate cancer related markers selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in a biological sample from the subject; and (2) comparing the level of the filamin A and level of the one or more prostate cancer related markers in the biological sample with the corresponding levels in a normal control sample, wherein an altered level of the filamin A and the one or more prostate cancer related markers in the biological sample relative to the normal control sample is indicative of an abnormal prostate state in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0061] In certain embodiments, the one or more prostate cancer related markers is selected from the group consisting of filamin B, LY9, and keratin 19. In certain embodiments, an increased level of filamin A and at least one or more prostate cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to a normal control sample is indicative of an abnormal prostate state in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0062] In certain embodiments, no increase in the detected level of expression of filamin A and at least one of the prostate-cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to a normal control sample is indicative of a normal prostate state in the subject. In such embodiments, levels of one, two, or all three of filamin B, LY9, and keratin 19 can be detected. In certain embodiments, none of the markers have increased levels. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0063] In certain embodiments, the method further comprises detecting the level of prostate specific antigen (PSA) in the biological sample and preferably further comprising comparing the level of PSA in the biological sample to the level of PSA in a normal control sample. In certain embodiments, an increase in the level of filamin A and at least one or more prostate cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to the normal control sample, in combination with an increase in the level of PSA in the biological sample as compared to a normal control sample has greater predictive value of the subject having an abnormal prostate state than the predictive value of a single marker alone. In certain embodiments, no increase in the detected level of expression of filamin A and in combination with the one or more prostate-cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to the normal control sample, in further combination with a decreased or normal level of PSA in the biological sample as compared to the level of PSA in the normal control sample has a greater predictive value of the subject having a normal prostate state than any single marker alone. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0064] Throughout the methods, kits, and panels of the invention, filamin A in combination with one or more of filamin B, LY9 and keratin 19 is understood filamin A in combination with any of filamin B; LY9; keratin 19; filamin B and LY9; filamin B and keratin 19; LY9 and keratin 19; or filamin B, LY9, and keratin 19. In one embodiment, the methods, kits and panels of the invention include filamin A in combination with filamin B, and Keratin 19 (KRT19). In one embodiment, the methods, kits and panels of the invention include filamin A in combination with filamin B, Keratin 19 (KRT19), and a determination of the patient's age.

[0065] Further, the invention contemplates that filamin A may be combined with any one, two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, fourteen, fifteen, sixteen, seventeen, eighteen, nineteen, twenty or more other prostate cancer related markers in any combinations, including any of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In one embodiment, the methods, kits and panels of the invention include filamin A in combination with filamin B, and Keratin 19 (KRT19).

[0066] In certain embodiments of the invention, the abnormal prostate state is prostate cancer.

[0067] In certain embodiments of the invention, the prostate cancer is androgen-dependent prostate cancer. In certain embodiments of the invention, the prostate cancer is androgen-independent prostate cancer. In certain embodiments of the invention, the prostate cancer is aggressive prostate cancer. In certain embodiments of the invention, the prostate cancer is non-aggressive prostate cancer.

[0068] In certain embodiments of the invention, the abnormal prostate state is benign prostate hyperplasia.

[0069] In another aspect, the invention provides a method for identifying a subject as being at increased risk for developing prostate cancer, the method comprising: (1) determining a level of filamin A in combination with one or more additional prostate cancer related markers selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in a biological sample from the subject; and (2) comparing the level of filamin A and the one or more prostate cancer related markers in the biological sample with the level of the markers in a normal control sample, wherein an altered level of the markers in the biological sample relative to the control sample is indicative of an increased risk for developing prostate cancer in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0070] In certain embodiments, filamin A detection is combined with detection of one or more prostate cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19. In certain embodiments, an increased level of filamin A and one or more prostate cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to the normal control sample is indicative of an increased risk for developing prostate cancer in the subject. In certain embodiments, no increase in the detected level of expression of filamin A and of each of the one or more prostate-cancer related markers selected from the group consisting of filamin B, LY9, and keratin 19 in the biological sample relative to the normal control sample is indicative of no increased risk for developing prostate cancer in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0071] In certain embodiments, the method further comprises detecting the level filamin A together with prostate specific antigen (PSA) in the biological sample. In this embodiment, the method involves comparing the levels of filamin A and PSA in the biological sample to the corresponding levels in a normal control sample. In certain embodiments, the method further comprises measuring the levels of one or more additional prostate cancer related markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the biological sample relative to the normal control sample, thereby increasing the predictive value of developing prostate cancer in the subject. In certain other embodiments, no increase in the detected level of expression of filamin A and PSA in the biological sample relative to the normal sample is indicative of having no increased risk for developing prostate cancer. In still further embodiments, no increase in the detected levels of one or more additional prostate cancer related markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 is indicative of no increased risk of prostate cancer, which has a greater predictive value of no increased risk of prostate cancer than evaluating filamin A and/or PSA alone. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0072] In certain embodiments of the diagnostic or prognostic methods of the invention, the method of diagnosis of the invention is carried out on the basis of filamin A, optionally on the additional basis of PSA, and still optionally on the basis of one or more additional prostate cancer related markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In certain embodiments, the one or more additional prostate cancer related markers is selected from the group consisting of keratin 7, keratin 8, and keratin 15. In certain other embodiments, the one or more additional prostate cancer related markers is selected from the group consisting of keratin 7 and keratin 15. In certain other embodiments, the one or more additional prostate cancer markers is selected from the group consisting of keratin 7, 15, and 19. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0073] In certain embodiments, the control sample for filamin A and PSA is the same control sample as for the one or more additional prostate cancer related markers of the invention. In certain embodiments, the control sample for the filamin A and PSA is different from the control sample used for the one or more additional prostate cancer related markers of the invention. In still other embodiments, the control sample for the filamin A is different from the control sample used for PSA, which are each also different from the control sample used to measure the one or more additional prostate cancer markers.

[0074] In certain embodiments of the diagnostic methods of the invention, wherein one or more prostate cancer related markers that are combined with filamin A is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, an increased level of one or more of the prostate cancer related markers in the biological sample relative to a normal control sample is indicative of an abnormal prostate state in the subject. In certain embodiments of the diagnostic methods of the invention, wherein one or more additional prostate cancer related markers is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, a decreased or normal level of one or more of the additional prostate cancer related markers in the biological sample relative to a normal control sample is indicative of an abnormal prostate state in the subject. In certain embodiments of the diagnostic methods of the invention, wherein one or more prostate cancer related markers is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, an increased level of one or more of the additional prostate cancer related markers in the biological sample relative to a normal control sample is indicative of a normal prostate state in the subject. In certain embodiments of the diagnostic methods of the invention, wherein one or more prostate cancer related markers is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, a decreased or normal level of one or more of the prostate cancer related markers in the biological sample relative to a normal control sample is indicative of a normal prostate state in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0075] In certain embodiments of the prognostic methods of the invention, wherein the one or more additional prostate cancer related markers that are combined with filamin A is selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, an increased level of one or more of the additional prostate cancer related markers in the biological sample relative to a normal control sample--in addition to increased filamin A--is indicative of an increased risk of developing prostate cancer in the subject. In certain embodiments of the prognostic methods of the invention, wherein one or more additional prostate cancer related markers is selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, a decreased or normal level of one or more of the additional prostate cancer related markers in the biological sample relative to a normal control sample--in addition to decreased filamin A--is indicative of a decreased risk of developing prostate cancer in the subject. In certain embodiments of the prognostic methods of the invention, wherein one or more additional prostate cancer related markers is selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, an increased level of one or more of the prostate cancer related markers in the biological sample relative to a normal control sample--in addition to increased filamin A--is indicative of increased risk of developing prostate cancer in the subject. In certain embodiments of the prognostic methods of the invention, wherein one or more additional prostate cancer related markers is selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, a decreased or normal level of one or more of the additional prostate cancer related markers in the biological sample--in addition to decreased filamin A--relative to a normal control sample is indicative of no increased risk of developing prostate cancer in the subject. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0076] In certain embodiments that involve the detection of both filamin A and PSA, the method of the invention can comprise detection of one or more additional prostate cancer related markers that are selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In certain embodiments, an increase in the level of both filamin A and PSA in combination with an increase in the level of at least one of the additional prostate cancer related markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 is indicative of an abnormal prostate state in the subject wherein the method has greater diagnostic or predictive value than the value of any of the individual markers alone. In certain other embodiments, a decrease in the level of both filamin A and PSA in combination with a decrease in the level of at least one of the additional prostate cancer related markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 is indicative of a normal prostate state in the subject wherein the method has greater diagnostic or predictive value than the value of any of the individual markers alone. In another embodiment, the patient's age is also used as a continuous predictor variable.

[0077] In various embodiments of any of the diagnostic or prognostic methods of the invention, the method may further comprise comparing the level of the one or more prostate cancer related markers in the biological sample with the level of the one or more prostate cancer related markers in a control sample selected from the group consisting of: a sample obtained from the same subject at an earlier time point than the biological sample, a sample from a subject with benign prostatic hyperplasia (BPH), a sample from a subject with non-metastatic prostate cancer, a sample from a subject with metastatic prostate cancer, a sample from a subject with androgen sensitive prostate cancer, a sample from a subject with androgen insensitive prostate cancer, a sample from a subject with aggressive prostate cancer, and a sample from a subject with non-aggressive prostate cancer. In such embodiments, comparison with one or more additional control sample can facilitate differentiating between two prostate cancer states selected from the group consisting of: normal prostate and prostate cancer, benign prostate hyperplasia and prostate cancer, benign prostate hyperplasia and normal prostate, androgen dependent and androgen independent prostate cancer, aggressive prostate cancer and non-aggressive prostate cancer, and metastatic prostate cancer and non-metastatic prostate cancer; or differentiating between any two or more of normal prostate, prostate cancer, benign prostate hyperplasia, androgen dependent prostate cancer, androgen independent prostate cancer, aggressive prostate cancer, non-aggressive prostate cancer, metastatic prostate cancer, and non-metastatic prostate cancer.

[0078] In certain embodiments of the invention, when a tumor is present, the method further comprises detecting the size of the prostate tumor in the subject.

[0079] In certain embodiments of the diagnostic and prognostic methods the invention, the method further comprises obtaining a sample from a subject.

[0080] In certain embodiments of the diagnostic and prognostic methods the invention, the method further comprises selecting a subject who has or is suspected of having prostate cancer.

[0081] In certain embodiments of the invention, the method further comprises selecting a treatment regimen for the subject based on the level of the one or more prostate cancer markers. In certain embodiments of the invention, the method further comprises treating the subject with a a treatment regimen based on the level of the one or more prostate cancer markers. In certain embodiments, a treatment regimen comprises one or more treatments selected from the group consisting of surgery, radiation, hormone therapy, antibody therapy, growth factor therapy, cytokine therapy, and chemotherapy.

[0082] Where applicable or not specifically disclaimed, any one of the embodiments described herein are contemplated to be able to combine with any other one or more embodiments, even though the embodiments are described under different aspects of the invention.

[0083] These and other embodiments are disclosed or are obvious from and encompassed by, the following Detailed Description.

BRIEF DESCRIPTION OF THE DRAWINGS

[0084] The following detailed description, given by way of example, but not intended to limit the invention solely to the specific embodiments described, may best be understood in conjunction with the accompanying drawings.

[0085] FIG. 1: Schematic representing the underlying principles of the Interrogative Platform Technology (a.k.a. Interrogative Biology.TM.) provided in WO2012119129, the entire contents of which are incorporated herein by reference.

[0086] FIG. 2A, FIG. 2B, and FIG. 2C: Causal associations of keratins, including (FIG. 2A) KRT4, KRT8, KRT15 and (FIG. 2B) KRT18 and (FIG. 2C) KRT19 in human prostate cancer cells as inferred by the Interrogative Platform Technology.

[0087] FIG. 3A, FIG. 3B, FIG. 3C, and FIG. 3D: Mechanistic insight into regulation of keratins by mitochondrial function inferred by the Interrogative Platform Technology. (FIG. 3A) KRT8-KRT15 association is abolished upon ubidecaronone treatment. Note change of direction of arrow between and positions of KRT7 and KRT15 before treatment (FIG. 3A) and after treatment (FIG. 3B). (FIG. 3C) Tubulin-beta 3 interacts with a number of proteins. (FIG. 3D) Expression levels of keratin 19 in biological samples from subjects with prostate cancer or control samples.

[0088] FIG. 4: Inference of filamin B (FLNB) as a hub of activity in prostate cancer and as a biomarker using the Interrogative Platform Technology provided in WO2012119129.

[0089] FIG. 5: Portion of an inference map showing filamin B is connected directly to LY9, which is, in turn, connected to at least one other marker.

[0090] FIG. 6A and FIG. 6B: Validation of filamin B levels in human serum samples. Levels of filamin B (FIG. 6A) and PSA (FIG. 6B) were elevated in prostate cancer samples when compared to normal serum. Data represents percent average change, with normal donors set to 100% on a log scale.

[0091] FIG. 7: Validation of LY9 levels in human serum samples. Levels of LY9 were elevated in prostate cancer samples when compared to normal serum. Data represents percent average change, with normal donors set to 100% on a log scale.

[0092] FIG. 8A, FIG. 8B, and FIG. 8C: Validation of filamin B (FIG. 8A), LY9 (FIG. 8B), and PSA (FIG. 8C) levels in human serum samples. Data are shown as ng/ml of the marker in serum.

[0093] FIG. 9A and FIG. 9B: (FIG. 9A) ROC curve analysis of sensitivity and false positive rate (FPR) of PSA, FLNB and the combination of PSA and FLNB and (FIG. 9B) area under the curve values (AUC) calculated based on the analysis. The combination of PSA and FLNB was more sensitive than either marker alone.

[0094] FIG. 10A and FIG. 10B: (FIG. 10A) ROC curve analysis of PSA, FLNB, LY9 and combinations of PSA, FLNB, and LY9 using linear and (FIG. 10B) non-linear scoring functions. The combination of PSA, LY9, and FLNB was more sensitive than any marker alone.

[0095] FIG. 11: Medical annotations for the serum samples used in connection with filamin A ELISA, as described in the Example 13.

[0096] FIG. 12: Medical annotations for the serum samples used in connection with keratin 19 ELISA, as described in the Example 13.

[0097] FIG. 13: Filamin A protein levels in serum from patients with and without prostate cancer as determined by ELISA.

[0098] FIG. 14: Keratin 19 protein levels in serum from patients with and without prostate cancer as determined by ELISA.

[0099] FIG. 15: ROC curve analysis for filamin A (FLNA) and filamin C (FLNC) and the combination (FLNA/C), as per Example 14.

[0100] FIG. 16: ROC curve analysis for keratin 18 (KRT18) and kertain 19 (KRT19) and the combination (KRT18/19), as per Example 14.

[0101] FIG. 17: AUC summary of AUC for PSA, Age, Filamin A (FLNA), Filamin B (FLNB), Keratin 19 (KRT19), and combinations thereof.

[0102] FIG. 18: PCA versus Else: Sensitivity match PSA.

[0103] FIG. 19: Predicted probability distribution for PCA versus Else.

[0104] FIG. 20: Accuracy analysis for PCA versus Else.

[0105] FIG. 21: Super High Gleason versus Else.

[0106] FIG. 22: Predicted probability distrubtion for Super High Gleason (8-10) versus Else.

[0107] FIG. 23: Acuracy Analysis for Super High Gleason (8-10) versus Else.

[0108] FIG. 24: High Gleason Versus Else.

[0109] FIG. 25: Predicted probability distrubtion for High Gleason (7 and above) versus Else.

[0110] FIG. 26: Accuracy Analysis for High Gleason (7 and above) versus Else.

[0111] FIG. 27: Prostate Cancer (PCA) versus Benign Prostatic Hyperplasia (BPH) Sensitivity.

[0112] FIG. 28: Predicted probability distribution for Prostate Cancer (PCA) versus Benign Prostatic Hyperplasia (BPH).

[0113] FIG. 29: Accuracy analysis for Prostate Cancer (PCA) versus Benign Prostatic Hyperplasia (BPH).

[0114] FIG. 30: FLNA, FLNB, and KRT19 expression in prostate cancer cells in vitro.

[0115] FIG. 31: FLNA, FLNB, and KRT19 expression in prostate cancer cells in vitro.

[0116] FIG. 32: Secretion of FLNA, FLNB, and KRT19 from prostate cancer cells in vitro.

[0117] FIG. 33: Transcriptional regulation of FLNA, FLNB, KRT19, and PSA expression by prostate-relevant stimuli of hypoxia (1% oxygen) in vitro.

[0118] FIG. 34: Transcriptional regulation of FLNA, FLNB, KRT19, and PSA expression by prostate-relevant stimuli of TNF.alpha. (10 ng/mL) in vitro.

[0119] FIG. 35: Transcriptional regulation of FLNA, FLNB, KRT19, and PSA expression by prostate-relevant stimuli of R1881 (1 nM) in vitro.

[0120] FIG. 36: Assessment of plasma FLNA and FLNB levels as biomarkers for prostate cancer.

DETAILED DESCRIPTION OF THE INVENTION

A. Overview

[0121] The identification of tumor markers or antigens associated with prostate cancer has stimulated considerable interest as promising tools for the screening, diagnosis, prognosis, clinical management and potential treatment of prostate cancer, and in particular, early detection of prostate cancer. Indeed, early detection mitigates the risk that the cancer will metastasize. Non-metastasized, local prostate tumors can often be cured by radical prostatectomy or radiation therapy, however for patients with distantly spread disease, no curative treatment is available. This emphasizes the need for new prostate (cancer) specific diagnostic tools that may improve the chances for accurate early detection.

[0122] While some prostate-specific markers are known, e.g., prostate-specific antigen and prostate stem cell antigen, very few biomarkers are in widespread or routine use as molecular diagnostics for prostate cancer. Accordingly, there remains a need for efficient, accurate, and rapid molecular diagnosis means, particularly which do not suffer from a high proportion of false results. The development of molecular tests for the accurate detection of prostate cancer will also lead to improved management of appropriate therapies, and an overall improved survival rate. Thus, there remains a need to provide an improved diagnostic test for the detection of prostate cancer which is more reliable and accurate than PSA and other current screening tests. The present invention addresses this need by providing the use of a new biomarker, filamin A, either used alone or in combination with other markers, for the accurate and reliable detection of prostate cancer.

[0123] As presently described herein, the invention at hand is based, at least in part, on the discovery that filamin A ("FLNA") is differentially regulated in prostate cancer cells and serves as a useful biomarker of prostate cancer. In one embodiment, filamin A can serve as a useful diagnostic biomarker to predict and/or detect the presence of prostate cancer in a subject. In another embodiment, filamin A can serve as a useful prognostic biomarker, serving to inform on the likely progression of prostate cancer in a subject with or without treatment. In still another embodiment, filamin A can serve as a useful predictive biomarker for helping to assess the likely response of prostate cancer to a particular treatment. Accordingly, the invention provides methods that use biomarkers, e.g., filamin A, in the diagnosis of prostate cancer (e.g., prediction of the presence of prostate cancer in a subject), in the prognosis of prostate cancer (e.g., prediction of the course or outcome of prostate cancer with or without treatment), and in the assessment of therapies intended to treat prostate cancer (i.e., filamin A as a theragnostic or predictive marker). The invention further provides compositions of matter (e.g., oligonucleotide probes specific for filamin A mRNA, antibodies specific for filamin A, therapeutic agents that target filamin A), including panels comprising binding or detection reagents specific for filamin A and optionally other biomarkers for use in the methods of the invention, as well as kits for practicing the methods of the invention.

[0124] The following is a detailed description of the invention provided to aid those skilled in the art in practicing the present invention. Those of ordinary skill in the art may make modifications and variations in the embodiments described herein without departing from the spirit or scope of the present invention. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used in the description of the invention herein is for describing particular embodiments only and is not intended to be limiting of the invention. All publications, patent applications, patents, figures and other references mentioned herein are expressly incorporated by reference in their entirety.

[0125] Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference to disclose and described the methods and/or materials in connection with which the publications are cited.

B. Definitions

[0126] Unless defined otherwise, all technical and scientific terms used herein have the meaning commonly understood by a person skilled in the art to which this invention belongs. The following references, the entire disclosures of which are incorporated herein by reference, provide one of skill with a general definition of many of the terms (unless defined otherwise herein) used in this invention: Singleton et al., Dictionary of Microbiology and Molecular Biology (2.sup.nd ed. 1994); The Cambridge Dictionary of Science and Technology (Walker ed., 1988); The Glossary of Genetics, 5.sup.th Ed., R. Rieger et al. (eds.), Springer Verlag (1991); and Hale & Marham, the Harper Collins Dictionary of Biology (1991). Generally, the procedures of molecular biology methods described or inherent herein and the like are common methods used in the art. Such standard techniques can be found in reference manuals such as for example Sambrook et al., (2000, Molecular Cloning--A Laboratory Manual, Third Edition, Cold Spring Harbor Laboratories); and Ausubel et al., (1994, Current Protocols in Molecular Biology, John Wiley & Sons, New-York).

[0127] The following terms may have meanings ascribed to them below, unless specified otherwise. However, it should be understood that other meanings that are known or understood by those having ordinary skill in the art are also possible, and within the scope of the present invention. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In the case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

[0128] As used herein, the singular forms "a", "and", and "the" include plural references unless the context clearly dictates otherwise. All technical and scientific terms used herein have the same meaning.

[0129] Unless specifically stated or obvious from context, as used herein, the term "about" is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About can be understood as within 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from context, all numerical values provided herein can be modified by the term about.

[0130] As used herein, the term "age" refers to the length of time that a subject has been alive. For example, the age of a subject is calculated from the date of birth of the subject to the current date. Age can be used as a continuous predictive variable for the presence of prostate cancer. For example, increased age is associated with increased risk of prostate cancer. Conversely, decreased age is associated with decreased risk of prostate cancer. Similarly, age can be used as a continuous predictive variable for the stage, or category, of the prostate cancer. For example, age can be used as a continuous predictive variable for the Gleason score of the prostate cancer.

[0131] As used herein, the term "amplification" refers to any known in vitro procedure for obtaining multiple copies ("amplicons") of a target nucleic acid sequence or its complement or fragments thereof. In vitro amplification refers to production of an amplified nucleic acid that may contain less than the complete target region sequence or its complement. Known in vitro amplification methods include, e.g., transcription-mediated amplification, replicase-mediated amplification, polymerase chain reaction (PCR) amplification, ligase chain reaction (LCR) amplification and strand-displacement amplification (SDA including multiple strand-displacement amplification method (MSDA)). Replicase-mediated amplification uses self-replicating RNA molecules, and a replicase such as Q-.beta.-replicase (e.g., Kramer et al., U.S. Pat. No. 4,786,600). PCR amplification is well known and uses DNA polymerase, primers and thermal cycling to synthesize multiple copies of the two complementary strands of DNA or cDNA (e.g., Mullis et al., U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159). LCR amplification uses at least four separate oligonucleotides to amplify a target and its complementary strand by using multiple cycles of hybridization, ligation, and denaturation (e.g., EP Pat. App. Pub. No. 0 320 308). SDA is a method in which a primer contains a recognition site for a restriction endonuclease that permits the endonuclease to nick one strand of a hemimodified DNA duplex that includes the target sequence, followed by amplification in a series of primer extension and strand displacement steps (e.g., Walker et al., U.S. Pat. No. 5,422,252). Two other known strand-displacement amplification methods do not require endonuclease nicking (Dattagupta et al., U.S. Pat. Nos. 6,087,133 and 6,124,120 (MSDA)). Those skilled in the art will understand that the oligonucleotide primer sequences of the present invention may be readily used in any in vitro amplification method based on primer extension by a polymerase. (see generally Kwoh et al., 1990, Am. Biotechnol. Lab. 8:14-25 and (Kwoh et al., 1989, Proc. Natl. Acad. Sci. USA 86, 1173-1177; Lizardi et al., 1988, BioTechnology 6:1197-1202; Malek et al., 1994, Methods Mol. Biol., 28:253-260; and Sambrook et al., 2000, Molecular Cloning--A Laboratory Manual, Third Edition, CSH Laboratories). As commonly known in the art, the oligos are designed to bind to a complementary sequence under selected conditions.

[0132] As used herein, the term "antigen" refers to a molecule, e.g., a peptide, polypeptide, protein, fragment, or other biological moiety, which elicits an antibody response in a subject, or is recognized and bound by an antibody.

[0133] As used herein, the term "area under the curve" or "AUC" refers to the area under the curve in a plot of sensitivity versus specificity. For example, see FIGS. 18, 21, 24, and 27. In one embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.5. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.6. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.7. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.8. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.9. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is 1.0. In specific embodiments, the AUC for a biomarker, or combination of biomarkers, of the invention is 0.5, 0.51, 0.52, 0.53, 0.54, 0.55, 0.56, 0.57, 0.58, 0.59, 0.6, 0.61, 0.62, 0.63, 0.64, 3.65, 0.66, 0.67, 0.68, 0.69, 0.7, 0.71, 0.72, 0.73, 0.74, 0.75, 0.76, 0.77, 0.78, 0.79, 0.8, 0.81, 0.82, 0.83, 0.84, 0.85, 0.86, 0.87, 0.88, 0.89, 0.9, 0.91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, 0.99 or 1.0. In one embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.5. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.6. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.7. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.8. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.9. In another embodiment, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 1.0. In specific embodiments, the AUC for a biomarker, or combination of biomarkers, of the invention is at least 0.5, 0.51, 0.52, 0.53, 0.54, 0.55, 0.56, 0.57, 0.58, 0.59, 0.6, 0.61, 0.62, 0.63, 0.64, 3.65, 0.66, 0.67, 0.68, 0.69, 0.7, 0.71, 0.72, 0.73, 0.74, 0.75, 0.76, 0.77, 0.78, 0.79, 0.8, 0.81, 0.82, 0.83, 0.84, 0.85, 0.86, 0.87, 0.88, 0.89, 0.9, 0.91, 0.92, 0.93, 0.94, 0.95, 0.96, 0.97, 0.98, 0.99 or 1.0

[0134] As used herein, the term "biomarker" is understood to mean a measurable characteristic that reflects in a quantitative or qualitative manner the physiological state of an organism. The physiological state of an organism is inclusive of any disease or non-disease state, e.g., a subject having prostate cancer or a subject who is otherwise healthy. Said another way, biomarkers are characteristics that can be objectively measured and evaluated as indicators of normal processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention. Biomarkers can be clinical parameters (e.g., age, performance status), laboratory measures (e.g., molecular biomarkers, such as prostate specific antigen), imaging-based measures, or genetic or other molecular determinants, such as phosphorylation or acetylation state of a protein marker, methylation state of nucleic acid, or any other detectable molecular modification to a biological molecule. Examples of biomarkers include, for example, polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites. Other examples of biomarkers include the age of the patient.

[0135] Preferably, a biomarker of the present invention is modulated (e.g., increased or decreased level) in a biological sample from a subject or a group of subjects having a first phenotype (e.g., having a disease) as compared to a biological sample from a subject or group of subjects having a second phenotype (e.g., not having the disease, e.g., a control). A biomarker may be differentially present at any level, but is generally present at a level that is increased relative to normal or control levels by at least 5%, by at least 10%, by at least 15%, by at least 20%, by at least 25%, by at least 30%, by at least 35%, by at least 40%, by at least 45%, by at least 50%, by at least 55%, by at least 60%, by at least 65%, by at least 70%, by at least 75%, by at least 80%, by at least 85%, by at least 90%, by at least 95%, by at least 100%, by at least 110%, by at least 120%, by at least 130%, by at least 140%, by at least 150%, or more; or is generally present at a level that is decreased relative to normal or control levels by at least 5%, by at least 10%, by at least 15%, by at least 20%, by at least 25%, by at least 30%, by at least 35%, by at least 40%, by at least 45%, by at least 50%, by at least 55%, by at least 60%, by at least 65%, by at least 70%, by at least 75%, by at least 80%, by at least 85%, by at least 90%, by at least 95%, or by 100% (i.e., absent). A biomarker is preferably differentially present at a level that is statistically significant (e.g., a p-value less than 0.05 and/or a q-value of less than 0.10 as determined using either Welch's T-test or Wilcoxon's rank-sum Test).

[0136] As used herein, the term "biopsy" or "biopsy tissue" refers to a sample of tissue (e.g., prostate tissue) that is removed from a subject for the purpose of determining if the sample contains cancerous tissue. The biopsy tissue is then examined (e.g., by microscopy) for the presence or absence of cancer.

[0137] As used herein, the term "complementary" refers to the broad concept of sequence complementarity between regions of two nucleic acid strands or between two regions of the same nucleic acid strand. It is known that an adenine residue of a first nucleic acid region is capable of forming specific hydrogen bonds ("base pairing") with a residue of a second nucleic acid region which is antiparallel to the first region if the residue is thymine or uracil. Similarly, it is known that a cytosine residue of a first nucleic acid strand is capable of base pairing with a residue of a second nucleic acid strand which is antiparallel to the first strand if the residue is guanine. A first region of a nucleic acid is complementary to a second region of the same or a different nucleic acid if, when the two regions are arranged in an antiparallel fashion, at least one nucleotide residue of the first region is capable of base pairing with a residue of the second region. Preferably, the first region comprises a first portion and the second region comprises a second portion, whereby, when the first and second portions are arranged in an antiparallel fashion, at least about 50%, and preferably at least about 75%, at least about 90%, or at least about 95% of the nucleotide residues of the first portion are capable of base pairing with nucleotide residues in the second portion. More preferably, all nucleotide residues of the first portion are capable of base pairing with nucleotide residues in the second portion.

[0138] The term "control sample," as used herein, refers to any clinically relevant comparative sample, including, for example, a sample from a healthy subject not afflicted with an oncological disorder, e.g., prostate cancer, or a sample from a subject from an earlier time point, e.g., prior to treatment, an earlier tumor assessment time point, at an earlier stage of treatment. A control sample can be a purified sample, protein, and/or nucleic acid provided with a kit. Such control samples can be diluted, for example, in a dilution series to allow for quantitative measurement of levels of analytes, e.g., markers, in test samples. A control sample may include a sample derived from one or more subjects. A control sample may also be a sample made at an earlier time point from the subject to be assessed. For example, the control sample could be a sample taken from the subject to be assessed before the onset of an oncological disorder, e.g., prostate cancer, at an earlier stage of disease, or before the administration of treatment or of a portion of treatment. The control sample may also be a sample from an animal model, or from a tissue or cell line derived from the animal model of oncological disorder, e.g., prostate cancer. The level of activity or expression of one or more markers (e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9 or more markers) in a control sample consists of a group of measurements that may be determined, e.g., based on any appropriate statistical measurement, such as, for example, measures of central tendency including average, median, or modal values. Different from a control is preferably statistically significantly different from a control.

[0139] As used herein, "changed as compared to a control" sample or subject is understood as having a level of the analyte or diagnostic or therapeutic indicator (e.g., marker) to be detected at a level that is statistically different than a sample from a normal, untreated, or abnormal state control sample. Changed as compared to control can also include a difference in the rate of change of the level of one or more markers obtained in a series of at least two subject samples obtained over time. Determination of statistical significance is within the ability of those skilled in the art and can include any acceptable means for determining and/or measuring statistical significance, such as, for example, the number of standard deviations from the mean that constitute a positive or negative result, an increase in the detected level of a biomarker in a sample (e.g., prostate cancer sample) versus a control or healthy sample, wherein the increase is above some threshold value, or a decrease in the detected level of a biomarker in a sample (e.g., prostate cancer sample) versus a control or healthy sample, wherein the decrease is below some threshold value. The threshold value can be determine by any suitable means by measuring the biomarker levels in a plurality of tissues or samples known to have a disease, e.g., prostate cancer, and comparing those levels to a normal sample and calculating a statistically significant threshold value.

[0140] The term "control level" refers to an accepted or pre-determined level of a marker in a subject sample. A control level can be a range of values. Marker levels can be compared to a single control value, to a range of control values, to the upper level of normal, or to the lower level of normal as appropriate for the assay.

[0141] In one embodiment, the control is a standardized control, such as, for example, a control which is predetermined using an average of the levels of expression of one or more markers from a population of subjects having no cancer, especially subjects having no prostate cancer. In still other embodiments of the invention, a control level of a marker is the level of the marker in a non-cancerous sample(s) derived from the subject having cancer. For example, when a biopsy or other medical procedure reveals the presence of cancer in one portion of the tissue, the control level of a marker may be determined using the non-affected portion of the tissue, and this control level may be compared with the level of the marker in an affected portion of the tissue.

[0142] In certain embodiments, the control can be from a subject, or a population of subject, having an abnormal prostate state. For example, the control can be from a subject suffering from benign prostate hyperplasia (BPH), androgen sensitive prostate cancer, androgen insensitive or resistant prostate cancer, aggressive prostate cancer, non-aggressive prostate cancer, metastatic prostate cancer, or non-metastatic prostate cancer. It is understood that not all markers will have different levels for each of the abnormal prostate states listed. It is understood that a combination of marker levels may be most useful to distinguish between abnormal prostate states, possibly in combination with other diagnostic methods. Further, marker levels in biological samples can be compared to more than one control sample (e.g., normal, abnormal, from the same subject, from a population control). Marker levels can be used in combination with other signs or symptoms of an abnormal prostate state to provide a diagnosis for the subject.

[0143] A control can also be a sample from a subject at an earlier time point, e.g., a baseline level prior to suspected presence of disease, before the diagnosis of a disease, at an earlier assessment time point during watchful waiting, before the treatment with a specific agent (e.g., chemotherapy, hormone therapy) or intervention (e.g., radiation, surgery). In certain embodiments, a change in the level of the marker in a subject can be more significant than the absolute level of a marker, e.g., as compared to control.

[0144] As used herein, "detecting", "detection", "determining", and the like are understood to refer to an assay performed for identification of filamin A and/or an additional one or more specific markers in a sample, e.g., one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9 or more) markers selected from the group consisting of PSA, filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. The amount of marker expression or activity detected in the sample can be none or below the level of detection of the assay or method.

[0145] As used herein, the term "DNA" or "RNA" molecule or sequence (as well as sometimes the term "oligonucleotide") refers to a molecule comprised generally of the deoxyribonucleotides adenine (A), guanine (G), thymine (T) and/or cytosine (C). In "RNA", T is replaced by uracil (U).

[0146] The terms "disorders", "diseases", and "abnormal state" are used inclusively and refer to any deviation from the normal structure or function of any part, organ, or system of the body (or any combination thereof). A specific disease is manifested by characteristic symptoms and signs, including biological, chemical, and physical changes, and is often associated with a variety of other factors including, but not limited to, demographic, environmental, employment, genetic, and medically historical factors. Certain characteristic signs, symptoms, and related factors can be quantitated through a variety of methods to yield important diagnostic information. As used herein the disorder, disease, or abnormal state is an abnormal prostate state, including benign prostate hyperplasia and cancer, particularly prostate cancer. The abnormal prostate state of prostate cancer can be further subdivided into stages and grades of prostate cancer as provided, for example in Prostate. In: Edge S B, Byrd D R, Compton C C, et al., eds.: AJCC Cancer Staging Manual. 7th ed. New York, N.Y.: Springer, 2010, pp 457-68 (incorporated herein by reference in its entirety). Further, abnormal prostate states can be classified as one or more of benign prostate hyperplasia (BPH), androgen sensitive prostate cancer, androgen insensitive or resistant prostate cancer, aggressive prostate cancer, non-aggressive prostate cancer, metastatic prostate cancer, and non-metastatic prostate cancer.

[0147] As used herein, a sample obtained at an "earlier time point" is a sample that was obtained at a sufficient time in the past such that clinically relevant information could be obtained in the sample from the earlier time point as compared to the later time point. In certain embodiments, an earlier time point is at least four weeks earlier. In certain embodiments, an earlier time point is at least six weeks earlier. In certain embodiments, an earlier time point is at least two months earlier. In certain embodiments, an earlier time point is at least three months earlier. In certain embodiments, an earlier time point is at least six months earlier. In certain embodiments, an earlier time point is at least nine months earlier. In certain embodiments, an earlier time point is at least one year earlier. Multiple subject samples (e.g., 3, 4, 5, 6, 7, or more) can be obtained at regular or irregular intervals over time and analyzed for trends in changes in marker levels. Appropriate intervals for testing for a particular subject can be determined by one of skill in the art based on ordinary considerations.

[0148] The term "expression" is used herein to mean the process by which a polypeptide is produced from DNA. The process involves the transcription of the gene into mRNA and the translation of this mRNA into a polypeptide. Depending on the context in which used, "expression" may refer to the production of RNA, or protein, or both.

[0149] As used herein, "greater predictive value" is understood as an assay that has significantly greater sensitivity and/or specificity, preferably greater sensitivity and specificity, than the test to which it is compared. The predictive value of a test can be determined using an ROC analysis. In an ROC analysis a test that provides perfect discrimination or accuracy between normal and disease states would have an area under the curve (AUC)=1, whereas a very poor test that provides no better discrimination than random chance would have AUC=0.5. As used herein, a test with a greater predictive value will have a statistically improved AUC as compared to another assay. The assays are preformed in an appropriate subject population.

[0150] A "higher level of expression", "higher level", and the like of a marker refers to an expression level in a test sample that is greater than the standard error of the assay employed to assess expression, and is preferably at least 25% more, at least 50% more, at least 75% more, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, or at least ten times the expression level of the marker in a control sample (e.g., sample from a healthy subject not having the marker associated disease, i.e., an abnormal prostate state) and preferably, the average expression level of the marker or markers in several control samples.

[0151] As used herein, the term "hybridization," as in "nucleic acid hybridization," refers generally to the hybridization of two single-stranded nucleic acid molecules having complementary base sequences, which under appropriate conditions will form a thermodynamically favored double-stranded structure. Examples of hybridization conditions can be found in the two laboratory manuals referred above (Sambrook et al., 2000, supra and Ausubel et al., 1994, supra, or further in Higgins and Hames (Eds.) "Nucleic acid hybridization, a practical approach" IRL Press Oxford, Washington D.C., (1985)) and are commonly known in the art. In the case of a hybridization to a nitrocellulose filter (or other such support like nylon), as for example in the well-known Southern blotting procedure, a nitrocellulose filter can be incubated overnight at a temperature representative of the desired stringency condition (60-65.degree. C. for high stringency, 50-60.degree. C. for moderate stringency and 40-45.degree. C. for low stringency conditions) with a labeled probe in a solution containing high salt (6.times.SSC or 5.times.SSPE), 5.times.Denhardt's solution, 0.5% SDS, and 100 .mu.g/ml denatured carrier DNA (e.g., salmon sperm DNA). The non-specifically binding probe can then be washed off the filter by several washes in 0.2.times.SSC/0.1% SDS at a temperature which is selected in view of the desired stringency: room temperature (low stringency), 42.degree. C. (moderate stringency) or 65.degree. C. (high stringency). The salt and SDS concentration of the washing solutions may also be adjusted to accommodate for the desired stringency. The selected temperature and salt concentration is based on the melting temperature (Tm) of the DNA hybrid. Of course, RNA-DNA hybrids can also be formed and detected. In such cases, the conditions of hybridization and washing can be adapted according to well-known methods by the person of ordinary skill Stringent conditions will be preferably used (Sambrook et al., 2000, supra). Other protocols or commercially available hybridization kits (e.g., ExpressHyb.RTM. from BD Biosciences Clonetech) using different annealing and washing solutions can also be used as well known in the art. As is well known, the length of the probe and the composition of the nucleic acid to be determined constitute further parameters of the hybridization conditions. Note that variations in the above conditions may be accomplished through the inclusion and/or substitution of alternate blocking reagents used to suppress background in hybridization experiments. Typical blocking reagents include Denhardt's reagent, BLOTTO, heparin, denatured salmon sperm DNA, and commercially available proprietary formulations. The inclusion of specific blocking reagents may require modification of the hybridization conditions described above, due to problems with compatibility. Hybridizing nucleic acid molecules also comprise fragments of the above described molecules. Furthermore, nucleic acid molecules which hybridize with any of the aforementioned nucleic acid molecules also include complementary fragments, derivatives and allelic variants of these molecules. Additionally, a hybridization complex refers to a complex between two nucleic acid sequences by virtue of the formation of hydrogen bonds between complementary G and C bases and between complementary A and T bases; these hydrogen bonds may be further stabilized by base stacking interactions. The two complementary nucleic acid sequences hydrogen bond in an antiparallel configuration. A hybridization complex may be formed in solution (e.g., Cot or Rot analysis) or between one nucleic acid sequence present in solution and another nucleic acid sequence immobilized on a solid support (e.g., membranes, filters, chips, pins or glass slides to which, e.g., cells have been fixed).

[0152] As used herein, the term "identical" or "percent identity" in the context of two or more nucleic acid or amino acid sequences, refers to two or more sequences or subsequences that are the same, or that have a specified percentage of amino acid residues or nucleotides that are the same (e.g., 60% or 65% identity, preferably, 70-95% identity, more preferably at least 95% identity), when compared and aligned for maximum correspondence over a window of comparison, or over a designated region as measured using a sequence comparison algorithm as known in the art, or by manual alignment and visual inspection. Sequences having, for example, 60% to 95% or greater sequence identity are considered to be substantially identical. Such a definition also applies to the complement of a test sequence. Preferably the described identity exists over a region that is at least about 15 to 25 amino acids or nucleotides in length, more preferably, over a region that is about 50 to 100 amino acids or nucleotides in length. Those having skill in the art will know how to determine percent identity between/among sequences using, for example, algorithms such as those based on CLUSTALW computer program (Thompson Nucl. Acids Res. 2 (1994), 4673-4680) or FASTDB (Brutlag Comp. App. Biosci. 6 (1990), 237-245), as known in the art. Although the FASTDB algorithm typically does not consider internal non-matching deletions or additions in sequences, i.e., gaps, in its calculation, this can be corrected manually to avoid an overestimation of the % identity. CLUSTALW, however, does take sequence gaps into account in its identity calculations. Also available to those having skill in this art are the BLAST and BLAST 2.0 algorithms (Altschul Nucl. Acids Res. 25 (1977), 3389-3402). The BLASTN program for nucleic acid sequences uses as defaults a word length (W) of 11, an expectation (E) of 10, M=5, N=4, and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength (W) of 3, and an expectation (E) of 10. The BLOSUM62 scoring matrix (Henikoff Proc. Natl. Acad. Sci., USA, 89, (1989), 10915) uses alignments (B) of 50, expectation (E) of 10, M=5, N=4, and a comparison of both strands. Moreover, the present invention also relates to nucleic acid molecules the sequence of which is degenerate in comparison with the sequence of an above-described hybridizing molecule. When used in accordance with the present invention the term "being degenerate as a result of the genetic code" means that due to the redundancy of the genetic code different nucleotide sequences code for the same amino acid. The present invention also relates to nucleic acid molecules which comprise one or more mutations or deletions, and to nucleic acid molecules which hybridize to one of the herein described nucleic acid molecules, which show (a) mutation(s) or (a) deletion(s).

[0153] The term "including" is used herein to mean, and is used interchangeably with, the phrase "including but not limited to."

[0154] A subject at "increased risk for developing prostate cancer" may or may not develop prostate cancer. Identification of a subject at increased risk for developing prostate cancer should be monitored for additional signs or symptoms of prostate cancer. The methods provided herein for identifying a subject with increased risk for developing prostate cancer can be used in combination with assessment of other known risk factors or signs of prostate cancer including, but not limited to decreased urinary stream, urgency, hesitancy, nocturia, incomplete bladder emptying, and age.

[0155] As used herein, the term "in vitro" refers to an artificial environment and to processes or reactions that occur within an artificial environment. In vitro environments can consist of, but are not limited to, test tubes and cell culture. The term "in vivo" refers to the natural environment (e.g., an animal or a cell) and to processes or reaction that occur within a natural environment.

[0156] As used herein, a "label" refers to a molecular moiety or compound that can be detected or can lead to a detectable signal. A label is joined, directly or indirectly, to a molecule, such as an antibody, a nucleic acid probe or the protein/antigen or nucleic acid to be detected (e.g., an amplified sequence). Direct labeling can occur through bonds or interactions that link the label to the nucleic acid (e.g., covalent bonds or non-covalent interactions), whereas indirect labeling can occur through the use of a "linker" or bridging moiety, such as oligonucleotide(s) or small molecule carbon chains, which is either directly or indirectly labeled. Bridging moieties may amplify a detectable signal. Labels can include any detectable moiety (e.g., a radionuclide, ligand such as biotin or avidin, enzyme or enzyme substrate, reactive group, chromophore such as a dye or colored particle, luminescent compound including a bioluminescent, phosphorescent or chemiluminescent compound, and fluorescent compound). Preferably, the label on a labeled probe is detectable in a homogeneous assay system, i.e., in a mixture, the bound label exhibits a detectable change compared to an unbound label.

[0157] The terms "level of expression of a gene", "gene expression level", "level of a marker", and the like refer to the level of mRNA, as well as pre-mRNA nascent transcript(s), transcript processing intermediates, mature mRNA(s) and degradation products, or the level of protein, encoded by the gene in the cell. The "level" of one of more biomarkers means the absolute or relative amount or concentration of the biomarker in the sample.

[0158] A "lower level of expression" or "lower level" of a marker refers to an expression level in a test sample that is less than 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, or 10% of the expression level of the marker in a control sample (e.g., sample from a healthy subjects not having the marker associated disease, i.e., an abnormal prostate state) and preferably, the average expression level of the marker in several control samples.

[0159] The term "modulation" refers to upregulation (i.e., activation or stimulation), down-regulation (i.e., inhibition or suppression) of a response (e.g., level of expression of a marker), or the two in combination or apart. A "modulator" is a compound or molecule that modulates, and may be, e.g., an agonist, antagonist, activator, stimulator, suppressor, or inhibitor.

[0160] As used herein, "negative fold change" refers to "down-regulation" or "decrease (of expression)" of a gene that is listed herein.

[0161] As used herein, "nucleic acid molecule" or "polynucleotides", refers to a polymer of nucleotides. Non-limiting examples thereof include DNA (e.g., genomic DNA, cDNA), RNA molecules (e.g., mRNA) and chimeras thereof. The nucleic acid molecule can be obtained by cloning techniques or synthesized. DNA can be double-stranded or single-stranded (coding strand or non-coding strand [antisense]). Conventional ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) are included in the term "nucleic acid" and polynucleotides as are analogs thereof. A nucleic acid backbone may comprise a variety of linkages known in the art, including one or more of sugar-phosphodiester linkages, peptide-nucleic acid bonds (referred to as "peptide nucleic acids" (PNA); Hydig-Hielsen et al., PCT Intl Pub. No. WO 95/32305), phosphorothioate linkages, methylphosphonate linkages or combinations thereof. Sugar moieties of the nucleic acid may be ribose or deoxyribose, or similar compounds having known substitutions, e.g., 2' methoxy substitutions (containing a 2'-O-methylribofuranosyl moiety; see PCT No. WO 98/02582) and/or 2' halide substitutions. Nitrogenous bases may be conventional bases (A, G, C, T, U), known analogs thereof (e.g., inosine or others; see The Biochemistry of the Nucleic Acids 5-36, Adams et al., ed., 11th ed., 1992), or known derivatives of purine or pyrimidine bases (see, Cook, PCT Int'l Pub. No. WO 93/13121) or "abasic" residues in which the backbone includes no nitrogenous base for one or more residues (Arnold et al., U.S. Pat. No. 5,585,481). A nucleic acid may comprise only conventional sugars, bases and linkages, as found in RNA and DNA, or may include both conventional components and substitutions (e.g., conventional bases linked via a methoxy backbone, or a nucleic acid including conventional bases and one or more base analogs). An "isolated nucleic acid molecule", as is generally understood and used herein, refers to a polymer of nucleotides, and includes, but should not limited to DNA and RNA. The "isolated" nucleic acid molecule is purified from its natural in vivo state, obtained by cloning or chemically synthesized.

[0162] As used herein, the term "obtaining" is understood herein as manufacturing, purchasing, or otherwise coming into possession of.

[0163] As used herein, "oligonucleotides" or "oligos" define a molecule having two or more nucleotides (ribo or deoxyribonucleotides). The size of the oligo will be dictated by the particular situation and ultimately on the particular use thereof and adapted accordingly by the person of ordinary skill. An oligonucleotide can be synthesized chemically or derived by cloning according to well-known methods. While they are usually in a single-stranded form, they can be in a double-stranded form and even contain a "regulatory region". They can contain natural rare or synthetic nucleotides. They can be designed to enhance a chosen criteria like stability for example. Chimeras of deoxyribonucleotides and ribonucleotides may also be within the scope of the present invention.

[0164] As used herein, "one or more" is understood as each value 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, and any value greater than 10.

[0165] The term "or" is used inclusively herein to mean, and is used interchangeably with, the term "and/or," unless context clearly indicates otherwise. For example, as used herein, filamin B or LY9 is understood to include filamin B alone, LY9 alone, and the combination of filamin B and LY9.

[0166] As used herein, "patient" or "subject" can mean either a human or non-human animal, preferably a mammal. By "subject" is meant any animal, including horses, dogs, cats, pigs, goats, rabbits, hamsters, monkeys, guinea pigs, rats, mice, lizards, snakes, sheep, cattle, fish, and birds. A human subject may be referred to as a patient. It should be noted that clinical observations described herein were made with human subjects and, in at least some embodiments, the subjects are human.

[0167] As used herein, "positive fold change" refers to "up-regulation" or "increase (of expression)" of a gene that is listed herein.

[0168] As used herein, "preventing" or "prevention" refers to a reduction in risk of acquiring a disease or disorder (i.e., causing at least one of the clinical symptoms of the disease not to develop in a patient that may be exposed to or predisposed to the disease but does not yet experience or display symptoms of the disease). Prevention does not require that the disease or condition never occurs in the subject. Prevention includes delaying the onset or severity of the disease or condition.

[0169] As used herein, a "predetermined threshold value" or "threshold value" of a biomarker refers to the level of the biomarker (e.g., the expression level or quantity (e.g., ng/ml) in a biological sample) in a corresponding control/normal sample or group of control/normal samples obtained from normal or healthy subjects, e.g., those males that do not have prostate cancer. The predetermined threshold value may be determined prior to or concurrently with measurement of marker levels in a biological sample. The control sample may be from the same subject at a previous time or from different subjects.

[0170] As used herein, a "probe" is meant to include a nucleic acid oligomer or oligonucleotide that hybridizes specifically to a target sequence in a nucleic acid or its complement, under conditions that promote hybridization, thereby allowing detection of the target sequence or its amplified nucleic acid. Detection may either be direct (i.e., resulting from a probe hybridizing directly to the target or amplified sequence) or indirect (i.e., resulting from a probe hybridizing to an intermediate molecular structure that links the probe to the target or amplified sequence). A probe's "target" generally refers to a sequence within an amplified nucleic acid sequence (i.e., a subset of the amplified sequence) that hybridizes specifically to at least a portion of the probe sequence by standard hydrogen bonding or "base pairing." Sequences that are "sufficiently complementary" allow stable hybridization of a probe sequence to a target sequence, even if the two sequences are not completely complementary. A probe may be labeled or unlabeled. A probe can be produced by molecular cloning of a specific DNA sequence or it can also be synthesized. Numerous primers and probes which can be designed and used in the context of the present invention can be readily determined by a person of ordinary skill in the art to which the present invention pertains.

[0171] As used herein, the terminology "prognosis", "staging" and "determination of aggressiveness" are defined herein as the prediction of the degree of severity of the prostate cancer and of its evolution as well as the prospect of recovery as anticipated from usual course of the disease. According to the present invention, once the aggressiveness of the prostate cancer has been determined appropriate methods of treatments can be chosen.

[0172] As used herein, "prophylactic" or "therapeutic" treatment refers to administration to the subject of one or more agents or interventions to provide the desired clinical effect. If it is administered prior to clinical manifestation of the unwanted condition (e.g., disease or other unwanted state of the host animal) then the treatment is prophylactic, i.e., it protects the host against developing at least one sign or symptom of the unwanted condition, whereas if administered after manifestation of the unwanted condition, the treatment is therapeutic (i.e., it is intended to diminish, ameliorate, or maintain at least one sign or symptom of the existing unwanted condition or side effects therefrom).

[0173] As used herein, "prostate cancer," refers to any malignant or pre-malignant form of cancer of the prostate. The term includes prostate in situ carcinomas, invasive carcinomas, metastatic carcimomas and pre-malignant conditions. The term also encompasses any stage or grade of cancer in the prostate. Where the prostate cancer is "metastatic," the cancer has spread or metastasized beyond the prostate gland to a distant site, such as a lymph node or to the bone.

[0174] As used herein, a "reference level" of a biomarker means a level of the biomarker that is indicative of a particular disease state, phenotype, or lack thereof, as well as combinations of disease states, phenotypes, or lack thereof. A "positive" reference level of a biomarker means a level that is indicative of a particular disease state or phenotype. A "negative" reference level of a biomarker means a level that is indicative of a lack of a particular disease state or phenotype. For example, a "prostate cancer-positive reference level" of a biomarker means a level of a biomarker that is indicative of a positive diagnosis of prostate cancer in a subject, and a "prostate cancer-negative reference level" of a biomarker means a level of a biomarker that is indicative of a negative diagnosis of prostate cancer in a subject. A "reference level" of a biomarker may be an absolute or relative amount or concentration of the biomarker, a presence or absence of the biomarker, a range of amount or concentration of the biomarker, a minimum and/or maximum amount or concentration of the biomarker, a mean amount or concentration of the biomarker, and/or a median amount or concentration of the biomarker; and, in addition, "reference levels" of combinations of biomarkers may also be ratios of absolute or relative amounts or concentrations of two or more biomarkers with respect to each other. Appropriate positive and negative reference levels of biomarkers for a particular disease state, phenotype, or lack thereof may be determined by measuring levels of desired biomarkers in one or more appropriate subjects, and such reference levels may be tailored to specific populations of subjects (e.g., a reference level may be age-matched so that comparisons may be made between biomarker levels in samples from subjects of a certain age and reference levels for a particular disease state, phenotype, or lack thereof in a certain age group). Such reference levels may also be tailored to specific techniques that are used to measure levels of biomarkers in biological samples (e.g., LC-MS, GC-MS, etc.), where the levels of biomarkers may differ based on the specific technique that is used.

[0175] As used herein, "sample" or "biological sample" includes a specimen or culture obtained from any source. Biological samples can be obtained from blood (including any blood product, such as whole blood, plasma, serum, or specific types of cells of the blood), urine, saliva, and the like. Biological samples also include tissue samples, such as biopsy tissues or pathological tissues that have previously been fixed (e.g., formaline snap frozen, cytological processing, etc.). In an embodiment, the biological sample is from blood. In another embodiment, the biological sample is a biopsy tissue from the prostate gland.

[0176] As use herein, the phrase "specific binding" or "specifically binding" when used in reference to the interaction of an antibody and a protein or peptide means that the interaction is dependent upon the presence of a particular structure (i.e., the antigenic determinant or epitope) on the protein; in other words the antibody is recognizing and binding to a specific protein structure rather than to proteins in general. For example, if an antibody is specific for epitope "A," the presence of a protein containing epitope A (or free, unlabeled A) in a reaction containing labeled "A" and the antibody will reduce the amount of labeled A bound to the antibody.

[0177] The phrase "specific identification" is understood as detection of a marker of interest with sufficiently low background of the assay and cross-reactivity of the reagents used such that the detection method is diagnostically useful. In certain embodiments, reagents for specific identification of a marker bind to only one isoform of the marker. In certain embodiments, reagents for specific identification of a marker bind to more than one isoform of the marker. In certain embodiments, reagents for specific identification of a marker bind to all known isoforms of the marker.

[0178] As used herein, the phrase "subject suspected of having cancer" refers to a subject that presents one or more symptoms indicative of a cancer or is being screened for a cancer (e.g., during a routine physical). A subject suspected of having cancer may also have one or more risk factors. A subject suspected of having cancer has generally not been tested for cancer. However, a "subject suspected of having cancer" encompasses an individual who has received an initial diagnosis (e.g., a CT scan showing a mass or increased PSA level) but for whom the stage of cancer is not known. The term further includes people who once had cancer (e.g., an individual in remission).

[0179] The term "such as" is used herein to mean, and is used interchangeably, with the phrase "such as but not limited to."

[0180] As used herein, the term "stage of cancer" refers to a qualitative or quantitative assessment of the level of advancement of a cancer. Criteria used to determine the stage of a cancer include, but are not limited to, the size of the tumor, whether the tumor has spread to other parts of the body and where the cancer has spread (e.g., within the same organ or region of the body or to another organ).

[0181] As used herein, the term "staging" refers to commonly used systems for grading/stating cancer, e.g., prostate cancer. In one aspect, staging can take the form of the "Gleason Score", as well known in the art, is the most commonly used system for the grading/staging and prognosis of adenocarcinoma. The system describes a score between 2 and 10, with 2 being the least aggressive and 10 being the most aggressive. The score is the sum of the two most common patterns (grade 1-5) of tumor growth found. To be counted a pattern (grade) needs to occupy more than 5% of the biopsy specimen. The scoring system requires biopsy material (core biopsy or operative specimens) in order to be accurate; cytological preparations cannot be used. The "Gleason Grade" is the most commonly used prostate cancer grading system. It involves assigning numbers to cancerous prostate tissue, ranging from 1 through 5, based on how much the arrangement of the cancer cells mimics the way normal prostate cells form glands. Two grades are assigned to the most common patterns of cells that appear; these two grades (they can be the same or different) are then added together to determine the Gleason score (a number from 1 to 10). The Gleason system is based exclusively on the architectural pattern of the glands of the prostate tumor. It evaluates how effectively the cells of any particular cancer are able to structure themselves into glands resembling those of the normal prostate. The ability of a tumor to mimic normal gland architecture is called its differentiation, and experience has shown that a tumor whose structure is nearly normal (well differentiated) will probably have a biological behavior relatively close to normal, i.e., that is not very aggressively malignant.

[0182] A Gleason grading from very well differentiated (grade 1) to very poorly differentiated (grade 5) is usually done for the most part by viewing the low magnification microscopic image of the cancer. There are important additional details which require higher magnification, and an ability to accurately grade any tumor is achieved only through much training and experience in pathology. Gleason grades 1 and 2: These two grades closely resemble normal prostate. They are the least important grades because they seldom occur in the general population and because they confer a prognostic benefit which is only slightly better than grade 3. Both of these grades are composed by mass; in grade 2 they are more loosely aggregated, and some glands wander (invade) into the surrounding muscle (stroma). Gleason grade 3 is the most common grade and is also considered well differentiated (like grades 1 and 2). This is because all three grades have a normal "gland unit" like that of a normal prostate; that is, every cell is part of a circular row which forms the lining of a central space (the lumen). The lumen contains prostatic secretion like normal prostate, and each gland unit is surrounded by prostate muscle which keeps the gland units apart. In contrast to grade 2, wandering of glands (invading) into the stroma (muscle) is very prominent and is the main defining feature. The cells are dark rather than pale and the glands often have more variable shapes.

[0183] Gleason Grade 4 is probably the most important grade because it is fairly common and because of the fact that if a lot of it is present, patient prognosis is usually (but not always) worsened by a considerable degree. Grade 4 also shows a considerable loss of architecture. For the first time, disruption and loss of the normal gland unit is observed. In fact, grade 4 is identified almost entirely by loss of the ability to form individual, separate gland units, each with its separate lumen (secretory space). This important distinction is simple in concept but complex in practice. The reason is that there are a variety of different-appearing ways in which the cancer's effort to form gland units can be distorted. Each cancer has its own partial set of tools with which it builds part of the normal structure. Grade 4 is like the branches of a large tree, reaching in a number of directions from the (well differentiated) trunk of grades 1, 2, and 3. Much experience is required for this diagnosis, and not all patterns are easily distinguished from grade 3. This is the main class of poorly differentiated prostate cancer, and its distinction from grade 3 is the most commonly important grading decision.

[0184] Gleason grade 5 is an important grade because it usually predicts another significant step towards poor prognosis. Its overall importance for the general population is reduced by the fact that it is less common than grade 4, and it is seldom seen in men whose prostate cancer is diagnosed early in its development. This grade too shows a variety of patterns, all of which demonstrate no evidence of any attempt to form gland units. This grade is often called undifferentiated, because its features are not significantly distinguishing to make it look any different from undifferentiated cancers which occur in other organs. When a pathologist looks at prostate cancer specimens under the microscope and gives them a Gleason grade, an attempt to identify two architectural patterns and assign a Gleason grade to each one is made. There may be a primary or most common pattern and then a secondary or second most common pattern which the pathologist will seek to describe for each specimen; alternatively, there may often be only a single pure grade. In developing his system, Dr. Gleason discovered that by giving a combination of the grades of the two most common patterns he could see in any particular patient's specimens, that he was better able to predict the likelihood that a particular patient would do well or badly. Therefore, although it may seem confusing, the Gleason score which a physician usually gives to a patient, is actually a combination or sum of two numbers which is accurate enough to be very widely used. These combined Gleason sums or scores may be determined as follows:

[0185] The lowest possible Gleason score is 2 (1+1), where both the primary and secondary patterns have a Gleason grade of 1 and therefore when added together their combined sum is 2.

[0186] Very typical Gleason scores might be 5 (2+3), where the primary pattern has a Gleason grade of 2 and the secondary pattern has a grade of 3, or 6 (3+3), a pure pattern.

[0187] Another typical Gleason score might be 7 (4+3), where the primary pattern has a Gleason grade of 4 and the secondary pattern has a grade of 3.

[0188] Finally, the highest possible Gleason score is 10 (5+5), when the primary and secondary patterns both have the most disordered Gleason grades of 5.

[0189] Another way of staging prostate cancer is by using the TNM System. It describes the extent of the primary tumor (T stage), the absence or presence of spread to nearby lymph nodes (N stage) and the absence or presence of distant spread, or metastasis (M stage). Each category of the TNM classification is divided into subcategories representative of its particular state. For example, primary tumors (T stage) may be classified into:

[0190] T1: The tumor cannot be felt during a digital rectal exam, or seen by imaging studies, but cancer cells are found in a biopsy specimen;

[0191] T2: The tumor can be felt during a DRE and the cancer is confined within the prostate gland;

[0192] T3: The tumor has extended through the prostatic capsule (a layer of fibrous tissue surrounding the prostate gland) and/or to the seminal vesicles (two small sacs next to the prostate that store semen), but no other organs are affected;

[0193] T4: The tumor has spread or attached to tissues next to the prostate (other than the seminal vesicles).

[0194] Lymph node involvement is divided into the following 4 categories:

[0195] N0: Cancer has not spread to any lymph nodes;

[0196] N1: Cancer has spread to a single regional lymph node (inside the pelvis) and is not larger than 2 centimeters;

[0197] N2: Cancer has spread to one or more regional lymph nodes and is larger than 2 centimeters, but not larger than 5 centimeters; and

[0198] N3: Cancer has spread to a lymph node and is larger than 5 centimeters (2 inches).

[0199] Metastasis is generally divided into the following two categories:

[0200] M0: The cancer has not metastasized (spread) beyond the regional lymph nodes; and

[0201] M1: The cancer has metastasized to distant lymph nodes (outside of the pelvis), bones, or other distant organs such as lungs, liver, or brain.

[0202] In addition, the Tstage is further divided into subcategories T1a-c T2a-c, T3a-c and T4a-b. The characteristics of each of these subcategories are well known in the art and can be found in a number of textbooks.

[0203] The terms "test compound" and "candidate compound" refer to any chemical entity, pharmaceutical, drug, and the like that is a candidate for use to treat or prevent a disease, illness, sickness, or disorder of bodily function (e.g., cancer). Test compounds comprise both known and potential therapeutic compounds. A test compound can be determined to be therapeutic by screening using the screening methods of the present invention. In some embodiments of the present invention, test compounds include antisense compounds.

[0204] The term "therapeutic effect" refers to a local or systemic effect in animals, particularly mammals, and more particularly humans caused by a pharmacologically active substance. The term thus means any substance intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease, or in the enhancement of desirable physical or mental development and conditions in an animal or human A therapeutic effect can be understood as a decrease in tumor growth, decrease in tumor growth rate, stabilization or decrease in tumor burden, stabilization or reduction in tumor size, stabilization or decrease in tumor malignancy, increase in tumor apoptosis, and/or a decrease in tumor angiogenesis.

[0205] As used herein, "therapeutically effective amount" means the amount of a compound that, when administered to a patient for treating a disease, is sufficient to effect such treatment for the disease, e.g., the amount of such a substance that produces some desired local or systemic effect at a reasonable benefit/risk ratio applicable to any treatment, e.g., is sufficient to ameliorate at least one sign or symptom of the disease, e.g., to prevent progression of the disease or condition, e.g., prevent tumor growth, decrease tumor size, induce tumor cell apoptosis, reduce tumor angiogenesis, prevent metastasis. When administered for preventing a disease, the amount is sufficient to avoid or delay onset of the disease. The "therapeutically effective amount" will vary depending on the compound, its therapeutic index, solubility, the disease and its severity and the age, weight, etc., of the patient to be treated, and the like. For example, certain compounds discovered by the methods of the present invention may be administered in a sufficient amount to produce a reasonable benefit/risk ratio applicable to such treatment. Administration of a therapeutically effective amount of a compound may require the administration of more than one dose of the compound.

[0206] A "transcribed polynucleotide" or "nucleotide transcript" is a polynucleotide (e.g. an mRNA, hnRNA, a cDNA, or an analog of such RNA or cDNA) which is complementary to or having a high percentage of identity (e.g., at least 80% identity) with all or a portion of a mature mRNA made by transcription of a marker of the invention and normal post-transcriptional processing (e.g. splicing), if any, of the RNA transcript, and reverse transcription of the RNA transcript.

[0207] As used herein, "treatment," particularly "active treatment," refers to performing an intervention to treat prostate cancer in a subject, e.g., reduce at least one of the growth rate, reduction of tumor burden, reduce or maintain the tumor size, or the malignancy (e.g., likelihood of metastasis) of the tumor; or to increase apoptosis in the tumor by one or more of administration of a therapeutic agent, e.g., chemotherapy or hormone therapy; administration of radiation therapy (e.g., pellet implantation, brachytherapy), or surgical resection of the tumor, or any combination thereof appropriate for treatment of the subject based on grade and stage of the tumor and other routine considerations. Active treatment is distinguished from "watchful waiting" (i.e., not active treatment) in which the subject and tumor are monitored, but no interventions are performed to affect the tumor. Watchful waiting can include administration of agents that alter effects caused by the tumor (e.g., incontinence, erectile dysfunction) that are not administered to alter the growth or pathology of the tumor itself.

[0208] The recitation of a listing of chemical group(s) in any definition of a variable herein includes definitions of that variable as any single group or combination of listed groups. The recitation of an embodiment for a variable or aspect herein includes that embodiment as any single embodiment or in combination with any other embodiments or portions thereof.

[0209] Any compositions or methods provided herein can be combined with one or more of any of the other compositions and methods provided herein.

[0210] Ranges provided herein are understood to be shorthand for all of the values within the range. For example, a range of 1 to 50 is understood to include any number, combination of numbers, or sub-range from the group consisting 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50.

[0211] Reference will now be made in detail to exemplary embodiments of the invention. While the invention will be described in conjunction with the exemplary embodiments, it will be understood that it is not intended to limit the invention to those embodiments. To the contrary, it is intended to cover alternatives, modifications, and equivalents as may be included within the spirit and scope of the invention as defined by the appended claims.

[0212] Exemplary compositions and methods of the present invention are described in more detail in the following sections: (C) Biomarkers of the invention; (D) Prostate tissue samples; (E) Detection and/or measurement of the biomarkers of the invention; (F) Isolated biomarkers; (G) Applications of biomarkers of the invention; (H) Therapeutics; (I) Drug screening; and (J) Kits/panels.

C. Biomarkers of the Invention

[0213] The present invention is based, at least in part, on the discovery that filamin A is differentially regulated in prostate cancer cells. In particular, the invention is based on the surprising discovery that filamin A levels are significantly elevated in the serum of patients with prostate cancer. Accordingly, the invention provides methods for diagnosing and/or monitoring (e.g., monitoring of disease progression or treatment) and/or prognosing an oncological disease state, e.g., prostate cancer, in a mammal. The invention also provides methods for treating or for adjusting treatment regimens based on diagnostic information relating to the levels of filamin A in the serum of a subject with an oncological disease state, e.g., prostate cancer. The invention further provides panels and kits for practicing the methods of the invention.

[0214] The present invention provides new biomarkers and combinations of biomarkers for use in diagnosing and/or prognosing an oncological disorder, and in particular, biomarkers for use in diagnosing and/or prognosing prostate cancer. The biomarkers of the invention are meant to encompass any measurable characteristic that reflects in a quantitative or qualitative manner the physiological state of an organism, e.g, whether the organism has prostate cancer. The physiological state of an organism is inclusive of any disease or non-disease state, e.g., a subject having prostate cancer or a subject who is otherwise healthy. Said another way, the biomarkers of the invention include characteristics that can be objectively measured and evaluated as indicators of normal processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention, including, in particular, prostate cancer. Biomarkers can be clinical parameters (e.g., age, performance status), laboratory measures (e.g., molecular biomarkers, such as prostate specific antigen), imaging-based measures, or genetic or other molecular determinants, as well as combinations thereof. Examples of biomarkers include, for example, polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites that are diagnostic and/or indicative and/or predictive of an oncological disease, e.g., prostate cancer. Examples of biomarkers also include polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites which are diagnostic and/or indicative and/or predictive of any stage or clinical phase of an oncological disease, such as, prostate cancer. Clinical stage or phase can be represented by any means known in the art, for example, based on the Gleason Score system, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer.

[0215] In one aspect, the present invention relates to using, measuring, detecting, and the like of filamin A alone, or together with one or more additional biomarkers of prostate cancer, which can include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. Other markers that may be used in combination with filamin A include any measurable characteristic described herein that reflects in a quantitative or qualitative manner the physiological state of an organism, e.g, whether the organism has prostate cancer. The physiological state of an organism is inclusive of any disease or non-disease state, e.g., a subject having prostate cancer or a subject who is otherwise healthy. The biomarkers of the invention that may be used in combination with filamin A include characteristics that can be objectively measured and evaluated as indicators of normal processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention, including, in particular, prostate cancer. Such combination biomarkers can be clinical parameters (e.g., age, performance status), laboratory measures (e.g., molecular biomarkers, such as prostate specific antigen), imaging-based measures, or genetic or other molecular determinants Examples of biomarkers for use in combination with filamin A include, for example, polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites that are diagnostic and/or indicative and/or predictive of prostate cancer, or any particular stage or phase of prostate cancer, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer or TNM classifications. In other embodiments, the present invention also involves the analysis and consideration of any clinical and/or patient-related health data, for example, data obtained from an Electronic Medical Record (e.g., collection of electronic health information about individual patients or populations relating to various types of data, such as, demographics, medical history, medication and allergies, immunization status, laboratory test results, radiology images, vital signs, personal statistics like age and weight, and billing information).

[0216] In certain embodiments, filamin A may be used in combination with at least one other biomarker, or more preferably, with at least two other biomarkers, or still more preferably, with at least three other biomarkers, or even more preferably with at least four other biomarkers. Still further, filamin A in certain embodiments, may be used in combination with at least five other markers, or at least six other biomarkers, or at least seven other biomarkers, or at least eight other biomarkers, or at least nine other biomarkers, or at least ten other biomarkers, or at least eleven other biomarkers, or at least twelve other biomarkers, or at least thirteen other biomarkers, or at least fourteen other biomarkers, or at least fifteen other biomarkers, or at least sixteen other biomarkers, or at least seventeen other biomarkers, or at least eighteen other biomarkers, or at least nineteen other biomarkers, or at least twenty other biomarkers. Further, filamin A may be used in combination with a multitude of other biomarkers, including, for example, with between about 20-50 other biomarkers, or between 50-100, or between 100-500, or between 500-1000, or between 1000-10,000 or biomarkers or more.

[0217] In certain embodiments, the present invention involves the detection and/or analysis filamin A I combination with at least one of the following set of biomarkers: prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. The known function of these proteins is provided as follows, without wishing to be bound by theory:

[0218] Filamin A (FLN-A). Filamin A (also known as FLN-A, FLN1, ABP-280, OPD1, OPD2, Endothelial Actin-Binding Protein, CVD1, FMD, MNS, NHBP, XLVD, XMVD, Actin Binding Protein 280, Alpha-Filamin, Filamin-1, Filamin-A--each of which may appear herein and are considered equivalent terms as used herein) is a 280-kD protein that is thought to crosslink actin filaments into orthogonal networks in cortical cytoplasm. The large molecular-weight protein also participates in the anchoring of membrane proteins to the actin cytoskeleton. Remodeling of the cytoskeleton is central to the modulation of cell shape and migration cells. Filamin A, encoded by the FLNA gene, is a widely expressed protein that regulates reorganization of the actin cytoskeleton by interacting with integrins, transmembrane receptor complexes, and second messengers. At least two different isoforms are know, isoform 1 and isoform 2, all of which are contemplated by the invention and encompassed by the term "filamin A." It will be appreciated that isoform 1 is the predominant transcript encoding filamin A. Isoform 2 includes an alternate in-frame exon and encodes a slightly longer protein isoform. Interaction with FLNA may allow neuroblast migration from the ventricular zone into the cortical plate. FLNA tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking. Further reference to filamin A can be found in the scientific literature, for example, in Gorlin J B et la., (October 1993). "Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28". Genomics 17 (2): 496-8, and Robertson S P et al. (March 2003). "Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans". Nat Genet 33 (4): 487-91, each of which are incorporated herein by reference. The nucleotide and amino acid sequences of filamin A can be found as GenBank Accession No. NM_001456.3 (filamin A--isoform 1--mRNA transcript sequence--SEQ ID NO: 46) and the corresponding polypeptide sequence of NP_001447.2 (filamin A--isoform 1--polypeptide sequence--SEQ ID NO: 47) and as GenBank Accession No. NM_001110556.1 (filamin A--isoform 2--mRNA transcript sequence--SEQ ID NO: 48) and the corresponding polypeptide sequence of NP_001104026.1 (filamin A--isoform 2--polypeptide sequence--SEQ ID NO: 49). These GenBank numbers are incorporated herein by reference in the versions available on the earliest effective filing date of this application.

[0219] The present invention is based, at least in part, on the discovery that filamin A is differentially regulated in prostate cancer cells. In particular, the invention is based on the surprising discovery that filamin A levels are significantly elevated in the serum of patients with prostate cancer. Accordingly, the invention provides methods for diagnosing and/or monitoring (e.g., monitoring of disease progression or treatment) and/or prognosing an oncological disease state, e.g., prostate cancer, in a mammal. The invention also provides methods for treating or for adjusting treatment regimens based on diagnostic information relating to the levels of filamin A in the serum of a subject with an oncological disease state, e.g., prostate cancer. The invention further provides panels and kits for practicing the methods of the invention.

[0220] It is understood that the invention includes the use of any combination of one or more of the filamin A sequences provided in the sequence listing or any fragments thereof as long as the fragment can allow for the specific identification of filamin A. Methods of the invention and reagents can be used to detect single isoforms of filamin A, e.g., isoform 1 and isoform 2, combinations of filamin A isoforms, or all of the filamin A isoforms simultaneously. Unless specified, filamin A can be considered to refer to one or more isoforms of filamin A, including total filamin A. Moreover, it is understood that there are naturally occurring variants of filamin A, which may or may not be associated with a specific disease state, the use of which are also included in the instant application.

[0221] It is understood that the invention includes the use of any fragments of filamin A polypeptide as long as the fragment allows for the specific identification of filamin A by a detection method of the invention. For example, an ELISA antibody must be able to bind to the filamin A fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of filamin A which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of filamin A which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding filamin A, including for example, filamin A-encoding DNA, filamin A mRNA, and fragments and/or variants thereof. Reference to "filamin A" may refer to filamin A polypeptide or to the filamin A gene, unless otherwise indicated.

[0222] Keratin 4.

[0223] Keratin 4, also known as as K4; CK4; CK-4; CYK4, is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in differentiated layers of the mucosal and esophageal epithelia with family member KRT13. Mutations in these genes have been associated with White Sponge Nevus, characterized by oral, esophageal, and anal leukoplakia. The type II cytokeratins are clustered in a region of chromosome 12q12-q13.

[0224] As used herein, keratin 4 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 4 is 3851 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 4, GenBank Accession No. NM_002272 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 1 and 2. (The GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0225] It is understood that the invention includes the use of any fragments of keratin 4 polypeptide as long as the fragment allow for the specific identification of keratin 4 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 4 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 4 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 4 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 4, including for example, keratin 4-encoding DNA, keratin 4 mRNA, and fragments and/or variants thereof. Reference to "keratin 4" may refer to keratin 4 polypeptide or to the keratin 4 gene, unless otherwise indicated.

[0226] Keratin 7.

[0227] Keratin 7, also known as as CK7, K2C7, K7, SCL, CK-7; cytokeratin 7; cytokeratin-7; keratin, 55K type II cytoskeletal; keratin, simple epithelial type I, K7; keratin, type II cytoskeletal 7; keratin-7; sarcolectin; type II mesothelial keratin K7; and type-II keratin Kb7, is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains co-expressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the simple epithelia lining the cavities of the internal organs and in the gland ducts and blood vessels. The genes encoding the type II cytokeratins are clustered in a region of chromosome 12q12-q13. Alternative splicing may result in several transcript variants; however, not all variants have been fully described.

[0228] As used herein, keratin 7 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 7 is 3855 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 7, GenBank Accession No. NM_005556 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 3 and 4. (The GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0229] It is understood that the invention includes the use of any fragments of keratin 7 polypeptide as long as the fragment allow for the specific identification of keratin 7 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 7 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 7 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 7 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 7, including for example, keratin 7-encoding DNA, keratin 7 mRNA, and fragments and/or variants thereof. Reference to "keratin 7" may refer to keratin 7 polypeptide or to the keratin 7 gene, unless otherwise indicated.

[0230] Keratin 8.

[0231] Keratin 8, also known as K8; KO; CK8; CK-8; CYK8; K2C8; CARD2 is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene.

[0232] As used herein, keratin 8 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 8 is 3856 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 8, variant 1, GenBank Accession No. NM_001256282 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 5 and 6; and Homo sapiens keratin 8, variant 3, GenBank Acession No. NM_001256293 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 7 and 8. (The GenBank numbers are incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0233] It is understood that the invention includes the use of any fragments of keratin 8 polypeptide as long as the fragment allow for the specific identification of keratin 8 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 8 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 8 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 8 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 8, including for example, keratin 8-encoding DNA, keratin 8 mRNA, and fragments and/or variants thereof. Reference to "keratin 8" may refer to keratin 8 polypeptide or to the keratin 8 gene, unless otherwise indicated.

[0234] Keratin 15.

[0235] Keratin 15, also known as as K15; CK15; K1CO, is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region on chromosome 17q21.2.

[0236] As used herein, keratin 15 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 15 is 3866 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 15, GenBank Accession No. NM_002275 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 9 and 10. (The GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0237] It is understood that the invention includes the use of any fragments of keratin 15 polypeptide as long as the fragment allow for the specific identification of keratin 15 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 15 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 15 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 15 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 15, including for example, keratin 15-encoding DNA, keratin 15 mRNA, and fragments and/or variants thereof. Reference to "keratin 15" may refer to keratin 15 polypeptide or to the keratin 15 gene, unless otherwise indicated.

[0238] Keratin 18.

[0239] Keratin 18, also known as as K18; CYK18, encodes the type I intermediate filament chain keratin 18. Keratin 18, together with its filament partner keratin 8, are perhaps the most commonly found members of the intermediate filament gene family. They are expressed in single layer epithelial tissues of the body. Mutations in this gene have been linked to cryptogenic cirrhosis. Two transcript variants encoding the same protein have been found for this gene.

[0240] As used herein, keratin 18 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 18 is 3875 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 18, variant 1, GenBank Accession No. NM_000224 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 11 and 12, and Homo sapiens keratin 18, variant 2, GenBank Accession No. 199187 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 13 and 14. (The GenBank numbers are incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0241] It is understood that the invention includes the use of any fragments of keratin 18 polypeptide as long as the fragment allow for the specific identification of keratin 18 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 18 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 18 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 18 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 18, including for example, keratin 18-encoding DNA, keratin 18 mRNA, and fragments and/or variants thereof. Reference to "keratin 18" may refer to keratin 18 polypeptide or to the keratin 18 gene, unless otherwise indicated.

[0242] Keratin 19.

[0243] Keratin 19, also known as K19; CK19; K1CS, is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. Unlike its related family members, this smallest known acidic cytokeratin is not paired with a basic cytokeratin in epithelial cells. It is specifically expressed in the periderm, the transiently superficial layer that envelopes the developing epidermis. The type I cytokeratins are clustered in a region of chromosome 17q12-q21.

[0244] As used herein, keratin 19 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human keratin 19 is 3880 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens keratin 19, GenBank Accession No. NM_002276 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 15 and 16. (The GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0245] It is understood that the invention includes the use of any fragments of keratin 19 polypeptide as long as the fragment allow for the specific identification of keratin 19 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the keratin 19 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of keratin 19 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of keratin 19 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding keratin 19, including for example, keratin 19-encoding DNA, keratin 19 mRNA, and fragments and/or variants thereof. Reference to "keratin 19" may refer to keratin 19 polypeptide or to the keratin 8 gene, unless otherwise indicated.

[0246] Tubulin-Beta 3.

[0247] Tubulin-beta 3, also known as CDCBM; TUBB4; beta-4; CFEOM3A, is a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in this gene are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 6.

[0248] As used herein, Tubulin-beta 3 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI Gene ID for human Tubulin-beta 3 is 10381 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens Tubulin-beta 3, variant 2, GenBank Accession No. NM_001197181 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 17 and 18. Homo sapiens Tubulin-beta 3, variant 1, GenBank Accession No. NM_006086 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 19 and 20. (The GenBank numbers are incorporated herein by reference in the versions available on the filing date of the application to which this application claims priority.)

[0249] It is understood that the invention includes the use of any fragments of Tubulin-beta 3 polypeptide as long as the fragment allow for the specific identification of Tubulin-beta 3 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the Tubulin-beta 3 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of Tubulin-beta 3 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of Tubulin-beta 3 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding Tubulin-beta 3, including for example, Tubulin-beta 3-encoding DNA, Tubulin-beta 3 mRNA, and fragments and/or variants thereof. Reference to "Tubulin-beta 3" may refer to Tubulin-beta 3 polypeptide or to the Tubulin-beta 3 gene, unless otherwise indicated.

[0250] Filamin B.

[0251] Filamin B is also known as filamin-3, beta-filamin, ABP-280 homolog, filamin homolog 1, thyroid autoantigen, actin binding protein 278, actin-binding-like protein, Larsen syndrome 1 (autosomal dominant), AOI; FH1; SCT; TAP; LRS1; TABP; FLN-B; FLN1L; ABP-278; and ABP-280. The gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3; boomerang dysplasia; autosomal dominant Larsen syndrome; and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.

[0252] As used herein, filamin B refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI gene ID for filamin B is 2317 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority).

[0253] Homo sapiens filamin B, beta (FLNB), RefSeqGene on chromosome 3, locus NG_012801 is shown in SEQ ID NO: 21. Homo sapiens filamin B, beta (FLNB), transcript variant 1, GenBank Accession No. NM_001164317.1 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 22 and 23. Homo sapiens filamin B, beta (FLNB), transcript variant 3, GenBank Accession No. NM_001164318.1 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 24 and 25. Homo sapiens filamin B, beta (FLNB), transcript variant 4, GenBank Accession No. NM_001164319.1 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 26 and 27. Homo sapiens filamin B, beta (FLNB), transcript variant 2, GenBank Accession No. NM_001457.3 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 28 and 29. (Each GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0254] It is understood that the invention includes the use of any combination of one or more of the filamin B sequences provided in the sequence listing or any fragments thereof as long as the fragment can allow for the specific identification of filamin B. Methods of the invention and reagents can be used to detect single isoforms of filamin B, combinations of filamin B isoforms, or all of the filamin B isoforms simultaneously. Unless specified, filamin B can be considered to refer to one or more isoforms of filamin B, including total filamin B. Moreover, it is understood that there are naturally occurring variants of filamin B, which may or may not be associated with a specific disease state, the use of which are also included in the instant application.

[0255] In addition, it is understood that the invention includes the use of any fragments of filamin B polypeptide as long as the fragment allow for the specific identification of filamin B by a detection method of the invention. For example, an ELISA antibody must be able to bind to the filamin B fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of filamin B which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of filamin B which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding filamin B, including for example, filamin B-encoding DNA, filamin B mRNA, and fragments and/or variants thereof. Reference to "filamin B" may refer to filamin B polypeptide or to the filamin B gene, unless otherwise indicated.

[0256] Lymphocyte Antigen 9.

[0257] Lymphocyte antigen 9 (LY9) is also known as RP11-312J18.1, CD229, SLAMF3, hly9, mLY9, T-lymphocyte surface antigen Ly-9; and cell surface molecule Ly-9. LY9 belongs to the SLAM family of immunomodulatory receptors (see SLAMF1; MIM 603492) and interacts with the adaptor molecule SAP (SH2D1A; MIM 300490) (Graham et al., 2006).

[0258] As used herein, LY9 refers to both the gene and the protein unless clearly indicated otherwise by context. The NCBI gene ID for LY9 is 4063 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority). Homo sapiens lymphocyte antigen 9 (LY9), transcript variant 2, GenBank Accession No. NM_001033667 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 30 and 31. Homo sapiens lymphocyte antigen 9 (LY9), transcript variant 3, GenBank Accession No. NM_001261456 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 32 and 33. Homo sapiens lymphocyte antigen 9 (LY9), transcript variant 4, GenBank Accession No. NM_001261457 amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 34 and 35. Homo sapiens lymphocyte antigen 9 (LY9), transcript variant 1, GenBank Accession No. NM_002348 is shown amino acid and nucleotide sequences, respectively, are provided in SEQ ID NOs: 36 and 37. (Each GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority.)

[0259] It is understood that the invention includes the use of any combination of one or more of the LY9 sequences provided in the sequence listing or any fragments thereof as long as the fragment can allow for the specific identification of LY9. Methods of the invention and reagents can be used to detect single isoforms of LY9, combinations of LY9 isoforms, or all of the LY9 isoforms simultaneously. Unless specified, LY9 can be considered to refer to one or more isoforms of LY9, including total LY9. Moreover, it is understood that there are naturally occurring variants of LY9, which may or may not be associated with a specific disease state, the use of which are also included in the instant application.

[0260] In addition, it is understood that the invention includes the use of any fragments of LY9 polypeptide as long as the fragment allow for the specific identification of LY9 by a detection method of the invention. For example, an ELISA antibody must be able to bind to the LY9 fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of LY9 which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of LY9 which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding LY9, including for example, LY9-encoding DNA, LY9 mRNA, and fragments and/or variants thereof. Reference to "LY9" may refer to LY9 polypeptide or to the LY9 gene, unless otherwise indicated.

[0261] Prostate Specific Antigen.

[0262] Prostate-specific antigen (PSA) is also known as kallikrein-3, seminin, P-30 antigen, semenogelase, gamma-seminoprotein, APS, hK3, and KLK2A1. Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its protein product is a protease present in seminal plasma. It is thought to function normally in the liquefaction of seminal coagulum, presumably by hydrolysis of the high molecular mass seminal vesicle protein. Serum level of this protein, called PSA in the clinical setting, is useful in the diagnosis and monitoring of prostatic carcinoma. Alternate splicing of this gene generates several transcript variants encoding different isoforms.

[0263] As used herein, PSA refers to both the gene and the protein, in both processed and unprocessed forms, unless clearly indicated otherwise by context. The NCBI gene ID for PSA is 354 and detailed information can be found at the NCBI website (incorporated herein by reference in the version available on the filing date of the application to which this application claims priority).

[0264] Homo sapiens PSA is located on chromosome 19 at 19q13.41Sequence: NC_000019.9 (51358171 . . . 51364020). Four splice variants of human PSA are known. Prostate-specific antigen isoform 3 preproprotein, NM_001030047.1, is provided as SEQ ID NOs: 38 and 39. Prostate-specific antigen isoform 4 preproprotein, NM_001030048.1, is provided as SEQ ID NOs: 40 and 41. Prostate-specific antigen isoform 6 preproprotein, NM_001030050.1, is provided as SEQ ID NOs: 42 and 43. Prostate-specific antigen isoform 1 preproprotein, NM_001648.2, is provided in SEQ ID NOs: 44 and 45. (Each GenBank number is incorporated herein by reference in the version available on the filing date of the application to which this application claims priority).

[0265] It is understood that the invention includes the use of any combination of one or more of the PSA sequences provided in the sequence listing or any fragments thereof as long as the fragment can allow for the specific identification of PSA. Methods of the invention and reagents can be used to detect single isoforms of PSA, combinations of PSA isoforms, or all of the PSA isoforms simultaneously. Unless specified, PSA can be considered to refer to one or more isoforms of PSA, including total PSA. Moreover, it is understood that there are naturally occurring variants of PSA, which may or may not be associated with a specific disease state, the use of which are also included in the instant application.

[0266] In addition, it is understood that the invention includes the use of any fragments of PSA polypeptide as long as the fragment allow for the specific identification of PSA by a detection method of the invention. For example, an ELISA antibody must be able to bind to the PSA fragment so that detection is possible. Moreover, it is understood that there are naturally occurring variants of PSA which may or may not be associated with a specific disease state, the use of which are also included in this application. Accordingly, the present inventions also contemplates fragments and variants of PSA which may be associated with a disease state, e.g., prostate cancer, and/or a particular stage or phase of a disease state, e.g., grades 1-5 of prostate cancer. It is also understood that the invention encompasses the use of nucleic acid molecules encoding PSA, including for example, PSA-encoding DNA, PSA mRNA, and fragments and/or variants thereof. Reference to "PSA" may refer to PSA polypeptide or to the PSA gene, unless otherwise indicated.

[0267] Age.

[0268] The age of a subject can be used as a continuous predictive variable for the presence of prostate cancer. For example, increased age is associated with increased risk of prostate cancer. Conversely, decreased age is associated with decreased risk of prostate cancer. Similarly, age can be used as a continuous predictive variable for the stage, or category, of the prostate cancer. For example, age can be used as a continuous predictive variable for the Gleason score of the prostate cancer.

[0269] The biomarkers of the invention, including in particular filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9), may be detected as a polypeptide or a detectable fragment thereof. Alternatively, the biomarkers of the invention, including in particular filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9), may be detected as nucleic acid molecules, such as DNA, RNA, mRNA, microRNA, and the like. In addition, combinations of biomarkers, including filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9), may be detected as any combination of polypeptides and nucleic acid molecules. In certain embodiments, all of the biomarkers are in the form of polypeptides. In certain other embodiments, all of the biomarkers are in the form of polynucleotides. In certain other embodiments, at least filamin A is in the form of a polypeptide, whereas any other markers tested can be a polypeptide or nucleic acid molecule. In still other embodiments, at least filamin A is in the form of a nucleic acid molecule, whereas any other markers tested can be a polypeptide or nucleic acid molecule.

[0270] In other embodiments, the biomarkers of the invention, including in particular filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), lymphocyte antigen 9 (LY9), prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), and non-coding RNAs (ncRNAs), including PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P, may be detected as a polypeptide or a detectable fragment thereof. Alternatively, the biomarkers of the invention, including in particular filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), lymphocyte antigen 9 (LY9), prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), and non-coding RNAs (ncRNAs), including PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P, may be detected as nucleic acid molecules, such as DNA, RNA, mRNA, microRNA, and the like. In addition, combinations of biomarkers, including filamin A alone or in combination with any one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), lymphocyte antigen 9 (LY9), prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), and non-coding RNAs (ncRNAs), including PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P, may be detected as any combination of polypeptides and nucleic acid molecules. In certain embodiments, all of the biomarkers are in the form of polypeptides. In certain other embodiments, all of the biomarkers are in the form of polynucleotides. In certain other embodiments, at least filamin A is in the form of a polypeptide, whereas any other markers tested can be a polypeptide or nucleic acid molecule. In still other embodiments, at least filamin A is in the form of a nucleic acid molecule, whereas any other markers tested can be a polypeptide or nucleic acid molecule.

[0271] The specific marker identified herein as prostate-specific membrane antigen (PSM) is further described in Sokoll et al., 1997, Prostate-specific antigen--Its discovery and biochemical characteristics, Urol. Clin. North Am., 24:253-259, which is incorporated herein by reference.

[0272] The specific marker identified herein as prostate stem cell antigen (PSCA) is further described in Fair et al., 1997, Prostate-specific membrane antigen, Prostate, 32:140-148, which is incorporated herein by reference.

[0273] The specific marker identified herein as TMPRSS2 is further described in Lin et al., 1999, Prostate-localized and androgen-regulated expression of the membrane-bound serine protease TMPRSS2, Cancer Res., 59:4180-4184, which is incorporated herein by reference.

[0274] The specific marker identified herein as PDEF is further described in Oettgen et al., PDEF, a novel prostate epithelium-specific ETS transcription factor interacts with the androgen receptor and activates prostate-specific antigen gene expression, J. Biol. Chem., 275: 1216-1225, which is incorporated herein by reference.

[0275] The specific marker identified herein as prostate-specific gene-1 (HPG-1) is further described in Herness, A novel human prostate-specific gene-1 (HPG-1): molecular cloning, sequencing, and its potential involvement in prostate carcinogenesis, 2003, Cancer Res. 63:329-336, which is incorporated herein by reference.

[0276] The non-coding RNA's (ncRNA's) identified as PCA3 is further described in Bussemakers et al., 1999, DD3: a new prostate-specific gene, highly overexpressed in prostate cancer, Cancer Res. 59:5975-5979, which is incorporated herein by reference.

[0277] The non-coding RNA identified as PCGEM1 is further described in Srikantan et al., 2000. PCGEM1, a prostate-specific gene, is overexpressed in prostate cancer. Proc. Natl. Acad. Sci. USA 97:12216-12221, which is incorporated herein by reference.

[0278] The gene cluster P704P, P712P, and P775P is further described in Stolk et al., 2004. P704P, P712P, and P775P: A genomic cluster of prostate-specific genes. Prostate 60:214-226), which is incorporated herein by reference.

[0279] The present invention also contemplates the use of particular combinations of biomarkers.

[0280] In one embodiment, the invention contemplates marker sets with at least two (2) members, which may include, but are not limited to the following sets: filamin A together with PSA; filamin A together with PSA; filamin A together with LY9; filamin A together with keratin 4; filamin A together with kertain 7; filamin A together with keratin 8; filamin A together with keratin 15; filamin A together with keratin 18; filamin A together with keratin 19; filamin A together with tubulin-beta 3; filamin A together with prostate-specific membrane antigen (PSM); filamin A together with prostate stem cell antigen (PSCA); filamin A together with TMPRSS2; filamin A together with PDEF; filamin A together with prostate-specific gene-1 (HPG-1); filamin A together with PCA3; filamin A together with PCGEM1; and filamin A together with gene cluster P704P, P712P, and P775P; and filamin A together with patient age. Any marker set can additionally be used in combination with PSA.

[0281] In another embodiment, the invention contemplates marker sets with at least three (3) members, wherein one member is filamin A and the additional two members are selected from the following sets of two markers: filamin B, LY9; filamin B, keratin 4; filamin B, keratin 7; filamin B, keratin 8; filamin B, keratin 15; filamin B, keratin 18; filamin B, keratin 19; filamin B, tubulin-beta 3; filamin B, PSM; filamin B, PSCA; filamin B, TMPRSS2; filamin B, PDEF; filamin B, HPG-1; filamin B, PCA3; filamin B, PCGEM1; filamin B, P704P/P712P/P775P; LY9, keratin 4; LY9, keratin 7; LY9, keratin 8; LY9, keratin 15; LY9, keratin 18; LY9, keratin 19; LY9, tubulin-beta 3; LY9, PSM; LY9, PSCA; LY9, TMPRSS2; LY9, PDEF; LY9, HPG-1; LY9, PCA3; LY9, PCGEM1; LY9, P704P/P712P/P775P; keratin 4, keratin 7; keratin 4, keratin 8; keratin 4, keratin 15; keratin 4, keratin 18; keratin 4, keratin 19; keratin 4, tubulin-beta 3; keratin 4, PSM; keratin 4, PSCA; keratin 4, TMPRSS2; keratin 4, PDEF; keratin 4, HPG-1; keratin 4, PCA3; keratin 4, PCGEM1; keratin 4, P704P/P712P/P775P; keratin 7, keratin 8; keratin 7, keratin 15; keratin 7, keratin 18; keratin 7, keratin 19; keratin 7, tubulin-beta 3; keratin 7, PSM; keratin 7, PSCA; keratin 7, TMPRSS2; keratin 7, PDEF; keratin 7, HPG-1; keratin 7, PCA3; keratin 7, PCGEM1; keratin 7, P704P/P712P/P775P; keratin 8, keratin 15; keratin 8, keratin 18; keratin 8, keratin 19; keratin 8, tubulin-beta 3; keratin 8, PSM; keratin 8, PSCA; keratin 8, TMPRSS2; keratin 8, PDEF; keratin 8, HPG-1; keratin 8, PCA3; keratin 8, PCGEM1; keratin 8, P704P/P712P/P775P; keratin 15, keratin 18; keratin 15, keratin 19; keratin 15, tubulin-beta 3; keratin 15, PSM; keratin 15, PSCA; keratin 15, TMPRSS2; keratin 15, PDEF; keratin 15, HPG-1; keratin 15, PCA3; keratin 15, PCGEM1; keratin 15, P704P/P712P/P775P; keratin 18, tubulin-beta 3; keratin 18, keratin 19; and keratin 19, tubulin-beta 3; keratin 18, PSM; keratin 18, PSCA; keratin 18, TMPRSS2; keratin 18, PDEF; keratin 18, HPG-1; keratin 18, PCA3; keratin 18, PCGEM1; keratin 18, P704P/P712P/P775P. Any marker set can be used in combination with patient age. Any marker set can additionally be used in combination with PSA.

[0282] In another embodiment, the invention contemplates marker sets with at least four (4) members, wherein one member is filamin A and the additional three members may include, but are not limited to the following sets: filamin B, LY9, keratin 4; filamin B, LY9, keratin 7; filamin B, LY9, keratin 8; filamin B, LY9, keratin 15; filamin B, LY9, keratin 18; filamin B, LY9, keratin 19; filamin B, LY9, tubulin-beta 3; filamin B, keratin 4, keratin 7; filamin B, keratin 4, keratin 8; filamin B, keratin 4, keratin 15; filamin B, keratin 4, keratin 18; filamin B, keratin 4, keratin 19; filamin B, keratin 4, tubulin-beta 3; filamin B, keratin 7, keratin 8; filamin B, keratin 7, keratin 15; filamin B, keratin 7, keratin 18; filamin B, keratin 7, keratin 19; filamin B, keratin 7, tubulin-beta 3; filamin B, keratin 8, keratin 15; filamin B, keratin 8, keratin 18; filamin B, keratin 8, keratin 19; filamin B, keratin 8, tubulin-beta 3; filamin B, keratin 15, keratin 18; filamin B, keratin 15, keratin 19; filamin B, keratin 15, tubulin-beta 3; filamin B, keratin 18, keratin 19; filamin B, keratin 18, tubulin-beta 3; filamin B, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7; LY9, keratin 4, keratin 8; LY9, keratin 4, keratin 15; LY9, keratin 4, keratin 18; LY9, keratin 4, keratin 19; LY9, keratin 4, tubulin-beta 3; LY9, keratin 7, keratin 8; LY9, keratin 7, keratin 15; LY9, keratin 7, keratin 18; LY9, keratin 7, keratin 19; LY9, keratin 7, tubulin-beta 3; LY9, keratin 8, keratin 15; LY9, keratin 8, keratin 18; LY9, keratin 8, keratin 19; LY9, keratin 8, tubulin-beta 3; LY9, keratin 15, keratin 18; LY9, keratin 15, keratin 19; LY9, keratin 15, tubulin-beta 3; LY9, keratin 18, keratin 19; LY9, keratin 18, tubulin-beta 3; LY9, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 8; keratin 4, keratin 7, keratin 15; keratin 4, keratin 7, keratin 18; keratin 4, keratin 7, keratin 19; keratin 4, keratin 7, tubulin-beta 3; keratin 4, keratin 8, keratin 15; keratin 4, keratin 8, keratin 18; keratin 4, keratin 8, keratin 19; keratin 4, keratin 8, tubulin-beta 3; keratin 4, keratin 15, keratin 18; keratin 4, keratin 15, keratin 19; keratin 4, keratin 15, tubulin-beta 3; keratin 4, keratin 18, keratin 19; keratin 4, keratin 19, tubulin-beta 3; keratin 7, keratin 8, keratin 15; keratin 7, keratin 8, keratin 18; keratin 7, keratin 8, keratin 19; keratin 7, keratin 8, tubulin-beta 3; keratin 7, keratin 8, tubulin-beta 3; keratin 7, keratin 15, keratin 18; keratin 7, keratin 15, keratin 19; keratin 7, keratin 15, tubulin-beta 3; keratin 7, keratin 18, keratin 19; keratin 7, keratin 18, tubulin-beta 3; keratin 15, keratin 18, keratin 19; keratin 15, keratin 18, tubulin-beta 3; and keratin 18, keratin 19, tubulin-beta 3. Any marker set can be used in combination with patient age. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P.

[0283] In another embodiment, the invention contemplates marker sets with at least five (5) members, wherein one member is filamin A and the additional four members may include, but are not limited to the following sets: filamin B, LY9, keratin 4, keratin 7; filamin B, LY9, keratin 4, keratin 8; filamin B, LY9, keratin 4, keratin 15; filamin B, LY9, keratin 4, keratin 18; filamin B, LY9, keratin 4, keratin 19; filamin B, LY9, keratin 4, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8; filamin B, keratin 4, keratin 7, keratin 15; filamin B, keratin 4, keratin 7, keratin 18; filamin B, keratin 4, keratin 7, tubulin-beta 3; filamin B, keratin 4, keratin 7, tubulin-beta 3; filamin B, keratin 7, keratin 8, keratin 15; filamin B, keratin 7, keratin 8, keratin 18; filamin B, keratin 7, keratin 8, keratin 19; filamin B, keratin 7, keratin 8, tubulin-beta 3; filamin B, keratin 8, keratin 15, keratin 18; filamin B, keratin 8, keratin 15, keratin 19; filamin B, keratin 8, keratin 15, tubulin-beta 3; filamin B, keratin 15, keratin 18, keratin 19; filamin B, keratin 15, keratin 18, tubulin-beta 3; filamin B, keratin 18, keratin 19, and tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8; LY9, keratin 4, keratin 7, keratin 15; LY9, keratin 4, keratin 7, keratin 18; LY9, keratin 4, keratin 7, keratin 19; LY9, keratin 4, keratin 7, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 15; LY9, keratin 7, keratin 8, keratin 18; LY9, keratin 7, keratin 8, keratin 19; LY9, keratin 7, keratin 8, tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18; LY9, keratin 8, keratin 15, keratin 19; LY9, keratin 8, keratin 15, tubulin-beta 3; LY9, keratin 15, keratin 18, keratin 19; LY9, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 18, keratin 19, and tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 15; keratin 4, keratin 7, keratin 8, keratin 18; keratin 4, keratin 7, keratin 8, keratin 19; keratin 4, keratin 7, keratin 8, tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18; keratin 4, keratin 8, keratin 15, keratin 19; keratin 4, keratin 8, keratin 15, tubulin-beta 3; keratin 4, keratin 15, keratin 18, keratin 19; keratin 4, keratin 15, keratin 18, tubulin-beta 3; keratin 4, keratin 18, keratin 19, tubulin-beta 3; keratin 8, keratin 15, keratin 18, keratin 19; keratin 8, keratin 15, keratin 18, tubulin-beta 3; and keratin 15, keratin 18, keratin 19, tubulin-beta 3. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any marker set can be used in combination with patient age.

[0284] In another embodiment, the invention contemplates marker sets with at least six (6) members, wherein one member is filamin A and the additional five members may include, but are not limited to the following sets: keratin 8, keratin 15, keratin 18, keratin 19 tubulin-beta 3; keratin 7, keratin 15, keratin 18, keratin 19 tubulin-beta 3; keratin 7, keratin 8, keratin 18, keratin 19 tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 19 tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 18 tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; keratin 4, keratin 15, keratin 18, keratin 19 tubulin-beta 3; keratin 4, keratin 8, keratin 18, keratin 19 tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 19 tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18 tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 8, keratin 18, keratin 19 tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 19 tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, and tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, keratin 19; filamin B, keratin 15, keratin 18, keratin 19 tubulin-beta 3; filamin B, keratin 8, keratin 18, keratin 19 tubulin-beta 3; filamin B, keratin 8, keratin 15, keratin 19 tubulin-beta 3; filamin B, keratin 8, keratin 15, keratin 18, and tubulin-beta 3; filamin B, keratin 8, keratin 15, keratin 18, keratin 19; filamen B, LY9, keratin 18, keratin 19 tubulin-beta 3; filamen B, LY9, keratin 15, keratin 19 tubulin-beta 3; filamen B, LY9, keratin 15, keratin 18, tubulin-beta 3; filamen B, LY9, keratin 15, keratin 18, keratin 19; filamen B, keratin 4, keratin 18, keratin 19 tubulin-beta 3; filamen B, keratin 4, keratin 15, keratin 19 tubulin-beta 3; filamen B, keratin 4, keratin 15, keratin 18, tubulin-beta 3; filamen B, keratin 4, keratin 15, keratin 18, keratin 19; filamen B keratin 7, keratin 18, keratin 19 tubulin-beta 3; filamen B keratin 7, keratin 15, keratin 19, tubulin-beta 3; filamen B keratin 7, keratin 15, keratin 18, tubulin-beta 3; filamen B keratin 7, keratin 15, keratin 18, keratin 19; filamen B, keratin 8, keratin 18, keratin 19 tubulin-beta 3; filamen B, keratin 8, keratin 15, keratin 19 tubulin-beta 3; filamen B, keratin 8, keratin 15, keratin 18 tubulin-beta 3; filamen B, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 4, keratin 18, keratin 19 and tubulin-beta 3; LY9, keratin 4, keratin 15, keratin 19 tubulin-beta 3; LY9, keratin 4, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 15, keratin 18, keratin 19; LY9, keratin 7, keratin 18, keratin 19 tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 19 tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 18, and tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 18, keratin 19; LY9, keratin 8, keratin 18, keratin 19 tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 19 tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, and tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, keratin 19; keratin 4, keratin 7, keratin 18, keratin 19 tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 19 tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 18, and tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 18, keratin 19; keratin 4, keratin 8, keratin 18, keratin 19 tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 19 tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, and tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, keratin 19; keratin 7, keratin 8, keratin 18, keratin 19 tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 19 tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 18, and tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; filamen B, LY9, keratin 4, keratin 19, tubulin-beta 3; filamen B, LY9, keratin 4, keratin 18, ubulin-beta 3; filamen B, LY9, keratin 4, keratin 18, keratin 19; filamen B, LY9, keratin 7, keratin 19, tubulin-beta 3; filamen B, LY9, keratin 7, keratin 18, tubulin-beta 3; filamen B, LY9, keratin 7, keratin 18, keratin 19; filamen B, LY9, keratin 8, keratin 19, tubulin-beta 3; filamen B, LY9, keratin 8, keratin 18, tubulin-beta 3; filamen B, LY9, keratin 8, keratin 18, keratin 19; filamen B, LY9, keratin 15, keratin 19, tubulin-beta 3; filamen B, LY9, keratin 15, keratin 18, tubulin-beta 3; filamen B, LY9, keratin 15, keratin 18, keratin 19; filamen B, keratin 4, keratin 7, keratin 19, tubulin-beta 3; filamen B, keratin 4, keratin 7, keratin 18, tubulin-beta 3; filamen B, keratin 4, keratin 7, keratin 18, keratin 19; filamen B, keratin 4, keratin 8, keratin 19, tubulin-beta 3; filamen B, keratin 4, keratin 8, keratin 18, tubulin-beta 3; filamen B, keratin 4, keratin 8, keratin 18, keratin 19; filamen B, keratin 4, keratin 15, keratin 19, tubulin-beta 3; filamen B, keratin 4, keratin 15, keratin 18, tubulin-beta 3; filamen B, keratin 4, keratin 15, keratin 18, keratin 19; filamen B, keratin 7, keratin 8, keratin 19, tubulin-beta 3; filamen B, keratin 7, keratin 8, keratin 18, tubulin-beta 3; filamen B, keratin 7, keratin 8, keratin 18, keratin 19; filamen B, keratin 8, keratin 15, keratin 19, tubulin-beta 3; filamen B, keratin 8, keratin 15, keratin 18, tubulin-beta 3; filamen B, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 4, keratin 7, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 18, keratin 19; LY9, keratin 4, keratin 8, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 18, keratin 19; LY9, keratin 4, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 15, keratin 18, keratin 19; LY9, keratin 7, keratin 8, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 18, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 18, keratin 19; LY9, keratin 7, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 18, keratin 19; LY9, keratin 8, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 8, keratin 15, keratin 18, keratin 19; keratin 4, keratin 7, keratin 8, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 18, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 18, keratin 19; keratin 4, keratin 7, keratin 15, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 18, tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 18, keratin 19; keratin 4, keratin 8, keratin 15, keratin 19, tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, keratin 19; keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; and keratin 7, keratin 8, keratin 15, keratin 18, keratin 19. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any marker set can be used in combination with patient age.

[0285] In another embodiment, the invention contemplates marker sets with at least seven (7) members, wherein one member is filamin A and the additional six members may include, but are not limited to the following sets: keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3; keratin 4, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3; keratin 4, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 4, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 15, keratin 18, keratin 19; LY9, keratin 4, keratin 7, keratin 18, keratin 19, and tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 15, keratin 19, and tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 15, keratin 18, keratin 19; LY9, keratin 4, keratin 7, keratin 8, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 18, keratin 19; LY9, keratin 4, keratin 7, keratin 8, keratin 15, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 19; and LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any maker set can be used in combination with patient age.

[0286] In another embodiment, the invention contemplates marker sets with at least eight (8) members, wherein one member is filamin A and the additional seven members may include, but are not limited to the following sets: keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; filamin B, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; filamin B, LY9, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19; filamin B, LY9, keratin 4, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 8, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 8, keratin 15, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 8, keratin 15, keratin 18, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 8, keratin 15, keratin 18, keratin 19; filamin B, LY9, keratin 4, keratin 7, keratin 18, keratin 19, and tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 15, keratin 19, and tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 15, keratin 18, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 15, keratin 18, keratin 19; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 18, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 18, keratin 19; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 19; and filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any marker set can be used in combination with patient age.

[0287] In another embodiment, the invention contemplates marker sets with at least nine (9) members, wherein one member is filamin A and the additional eight members may include, but are not limited to the following sets: LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 15, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 18, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 19, tubulin-beta 3; filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, tubulin-beta 3; and filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19. Any marker set can be used in combination with PSA. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any marker set can be used in combination with patient age.

[0288] In another embodiment, the invention contemplates marker sets with at least ten (10) members, wherein one member is filamin A and the additional nine members may include, but are not limited to the following sets: filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3. In addition, any of the above sets may be modified to replace one or more markers in the marker set with one or more of the following additional markers: prostate-specific membrane antigen (PSM), prostate stem cell antigen (PSCA), TMPRSS2, PDEF, prostate-specific gene-1 (HPG-1), PCA3, PCGEM1, and the gene cluster P704P, P712P, and P775P. Any marker set can be used in combination with patient age.

[0289] Any marker set can be used in combination with PSA.

[0290] The invention provides for the use of various combinations and sub-combinations of markers. It is understood that any single marker or combination of the markers provided herein can be used in the invention unless clearly indicated otherwise. Further, any single marker or combination of the markers of the invention can be used in conjunction with patient age. Alternatively, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Alternatively, any single marker or combination of the markers of the invention can be used in conjunction with patient age and PSA.

[0291] Throughout the application, one or more of filamin B, LY9 and keratin 19 is understood as any of: filamin B; LY9; keratin 19; filamin B and LY9; filamin B and keratin 19; LY9 and keratin 19; or filamin B, LY9, and keratin 19. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Further, any single marker or combination of the markers of the invention can be used in conjunction with patient age. Preferably, each marker set includes, in addition if not already indicated, filamin A.

[0292] Throughout the application, combination of the filamin B and LY9 with PSA is understood as any of filamin B; LY9; filamin B and PSA; filamin B and LY9; LY9 and PSA; filamin B, LY9, and PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0293] Throughout the application, one or more prostate cancer markers selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 is understood as any of keratin 4; keratin 7; keratin 8; keratin 15; keratin 18; tubulin beta-3; keratin 4 and keratin 7; keratin 4 and keratin 8; keratin 4 and keratin 15; keratin 4 and keratin 18; keratin 4 and tubulin beta-3; keratin 7 and keratin 8; keratin 7 and keratin 15; keratin 7 and keratin 18; keratin and tubulin beta-3; keratin 8 and keratin 15; keratin 8 and keratin 18; keratin 8 and tubulin beta-3; keratin 15 and keratin 18; keratin 15 and tubulin beta-3; keratin 18 and tubulin beta-3; keratin 4, keratin 7 and keratin 8; keratin 4, keratin 7 and keratin 15; keratin 4, keratin 7 and keratin 18; keratin 4, keratin 7 and tubulin beta-3; keratin 4, keratin 8 and keratin 15; keratin 4, keratin 8 and keratin 18; keratin 4, keratin 8 and tubulin beta-e; keratin 4, keratin 15 and keratin 18; keratin 4, keratin 15 and tubulin beta-e; keratin 4, keratin 18 and tubulin beta-3; kertin 4, keratin 7, keratin 8 and keratin 15; keratin 4, keratin 7, keratin 8 and keratin 18; keratin 4, keratin 7, keratin 8 and tubulin beta-3; keratin 4, keratin 8, keratin 15 and keratin 18; keratin 4, keratin 8, keratin 15 and tubulin beta-3; keratin 4, keratin 15, keratin 18 and tubulin beta-3; keratin 4, keratin 7, keratin 8, keratin 15 and keratin 18; keratin 4, keratin 7, keratin 8, keratin 15, and tubulin beta-3; keratin 4, keratin 7, keratin 8, keratin 18, and tubulin beta-3; keratin 4, keratin 7, keratin 15, keratin 18, and tubulin beta-3; keratin 4, keratin 8, keratin 15, keratin 18, and tubulin beta-3; or keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0294] Throughout the application, one or more prostate cancer markers selected from the group consisting of keratin 7, 15, and 19 is understood as any of keratin 7; keratin 15; keratin 19; keratin 7 and 15; keratin 7 and 19; keratin 15 and 19; and keratin 7, 15, and 19. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0295] Throughout the application, one or more prostate cancer markers selected from the group consisting of keratin 7, 8, and 15 is understood as any of keratin 7; keratin 8; keratin 15; keratin 7 and 8; keratin 7 and 15; keratin 8 and 15; and keratin 7, 8, and 15. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0296] Throughout the application, one or more prostate cancer markers selected from the group consisting of keratin 7 and 15 is understood as any of keratin 7; keratin 15; or keratin 7 and 15. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0297] Throughout the application, one or more prostate cancer markers selected from the group consisting filamin B, LY9, or keratin 19 is understood as any of filamin B; LY9; keratin 19; filamin B and LY9; filamin B and keratin 19; LY9, and keratin 19; and filamin B, LY9, and keratin 19. Further, any single marker or combination of the markers of the invention can be used in conjunction with PSA. Preferably, each marker set includes, in addition if not already indicated, filamin A. Preferably, each marker set includes, in addition if not already indicated, patient age.

[0298] In another aspect, the present invention provides for the identification of a "diagnostic signature" or "disease profile" based on the levels of the biomarkers of the invention in a biological sample, including in a diseased tissue (e.g., prostate tumor) or directly from the serum or blood, that correlates with the presence and/or risk and/or prognosis of prostate cancer. The "levels of the biomarkers" can refer to the expression level of the biomarker genes, e.g., by measuring the expression levels of the biomarker mRNAs. The "levels of the biomarkers" can also refer to level of biomarker polypeptides in a biological sample, e.g., prostate tissue or serum. The collection or totality of expression levels of biomarker polypeptides and/or nucleic acid molecules provide a diagnostic signature that correlates with the presence and/or diagnosis and/or progression of prostate cancer. The biomarkers for obtaining a diagnostic signature or disease profile of the invention are meant to encompass any measurable characteristic that reflects in a quantitative or qualitative manner the physiological state of an organism, e.g, whether the organism has prostate cancer. The physiological state of an organism is inclusive of any disease or non-disease state, e.g., a subject having prostate cancer or a subject who is otherwise healthy. Said another way, the biomarkers used for identifying a diagnostic signature or disease profile of the invention include characteristics that can be objectively measured and evaluated as indicators of normal processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention, including, in particular, prostate cancer. Biomarkers can be clinical parameters (e.g., age, performance status), laboratory measures (e.g., molecular biomarkers, such as prostate specific antigen), imaging-based measures, or genetic or other molecular determinants Examples of biomarkers include, for example, polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites that are diagnostic and/or indicative and/or predictive of an oncological disease, e.g., prostate cancer. Examples of biomarkers also include polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites which are diagnostic and/or indicative and/or predictive of any stage or clinical phase of an oncological disease, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer.

[0299] In a particular embodiment, a prostate cancer disease profile or diagnostic signature is determined on the basis of the combination of filamin A together with one or more additional biomarkers of prostate cancer, which can include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, as well as additional markers PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. Other markers that may be used in combination with filamin A include any measurable characteristic that reflects in a quantitative or qualitative manner the physiological state of an organism, e.g, whether the organism has prostate cancer. Such characteristics may include patient age. The physiological state of an organism is inclusive of any disease or non-disease state, e.g., a subject having prostate cancer or a subject who is otherwise healthy. Said another way, the biomarkers of the invention that may be used in combination with filamin A include characteristics that can be objectively measured and evaluated as indicators of normal processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention, including, in particular, prostate cancer. Such combination biomarkers can be clinical parameters (e.g., age, performance status), laboratory measures (e.g., molecular biomarkers, such as prostate specific antigen), imaging-based measures, or genetic or other molecular determinants Example of biomarkers for use in combination with filamin A include, for example, polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites that are diagnostic and/or indicative and/or predictive of prostate cancer, or any particular stage or phase of prostate cancer, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer. In certain embodiments, biomarkers for use in combination with filamin A include polypeptides, peptides, polypeptide fragments, proteins, antibodies, hormones, polynucleotides, RNA or RNA fragments, microRNA (miRNAs), lipids, polysaccharides, and other bodily metabolites which are diagnostic and/or indicative and/or predictive of prostate cancer, or any stage or clinical phase thereof, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer or TNM classifications. In other embodiments, the present invention also involves the analysis and consideration of any clinical and/or patient-related health data, for example, data obtained from an Electronic Medical Record (e.g., collection of electronic health information about individual patients or populations relating to various types of data, such as, demographics, medical history, medication and allergies, immunization status, laboratory test results, radiology images, vital signs, personal statistics like age and weight, and billing information).

[0300] In certain embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of one or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the one or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the one or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 1 additionally detected biomarker is above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the one or more additional biomarkers.

[0301] In certain other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of two or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the two or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the two or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 2 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the two or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0302] In certain other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of three or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the three or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the three or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 3 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the three or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0303] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of four or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the four or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the four or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 4 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the four or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0304] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of five or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the five or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the five or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 5 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the five or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0305] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of six or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the six or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the six or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 6 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the six or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0306] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of seven or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the seven or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the seven or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 7 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the seven or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0307] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of eight or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the eight or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the eight or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 8 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the eight or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0308] In other embodiments, the diagnostic signature is obtained by (1) detecting the level of filamin A in a biological sample, (2) detecting the level(s) of nine or more additional biomarkers that may include, but are not limited to prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, and (3) comparing the levels of filamin A and the nine or more additional biomarkers to the levels of the same biomarkers from a control sample, (4) determining if the filamin A and the nine or more additional biomarkers detected in the biological sample are above a certain threshold level. If filamin A and at least 9 additionally detected biomarkers are above the threshold level, then the diagnostic signature is indicative of prostate cancer in the biological sample. In certain embodiments, the diagnostic signature can be determined based on an algorithm or computer program that predicts whether the biological sample is cancerous based on the levels of filamin A and the nine or more additional biomarkers. In other embodiments, the diagnostic signature also takes into account the patient's age.

[0309] In accordance with various embodiments, algorithms may be employed to predict whether or not a biological sample is likely to be diseased, e.g., have prostate cancer. The skilled artisan will appreciate that an algorithm can be any computation, formula, statistical survey, nomogram, look-up table, decision tree method, or computer program which processes a set of input variables (e.g., number of markers (n) which have been detected at a level exceeding some threshold level, or number of markers (n) which have been detected at a level below some threshold level) through a number of well-defined successive steps to eventually produce a score or "output," e.g., a diagnosis of prostate cancer. Any suitable algorithm--whether computer-based or manual-based (e.g., look-up table)--is contemplated herein.

[0310] In certain embodiments, an algorithm of the invention used to predict whether a biological sample has prostate cancer producing a score on the basis of the detecte level of filamin A in the sample and the level(s) at least one, or two, or three, or four, or five, or six, or seven, or eight, or nine or more additional prostate cancer markers (e.g., selected from the group consisting of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1), wherein if the score is above a certain threshold score, then the biological sample has prostate cancer. In certain embodiments, the algorithm also produces a score using the patient's age as a continuous predictor variable. For example, increased age is associated with higher risk of prostate cancer.

[0311] In certain embodiments, an algorithm of the invention used to predict whether a biological sample has prostate cancer producing a score on the basis of the detecte level of filamin A in the sample and the level(s) at least one, or two, or three, or four, or five, or six, or seven, or eight, or nine or more additional prostate cancer markers (e.g., selected from the group consisting of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1), wherein if the score is below a certain threshold score, then the biological sample has prostate cancer. In certain embodiments, the algorithm also produces a score using the patient's age as a continuous predictor variable.

[0312] In certain embodiments, an algorithm of the invention used to predict whether a biological sample has prostate cancer producing a score on the basis of the detecte level of filamin A in the sample and the level(s) at least one, or two, or three, or four, or five, or six, or seven, or eight, or nine or more additional prostate cancer markers (e.g., selected from the group consisting of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1), wherein if the score is above a certain threshold score, then the biological sample does not have prostate cancer. In certain embodiments, the algorithm also produces a score using the patient's age as a continuous predictor variable.

[0313] In certain embodiments, an algorithm of the invention used to predict whether a biological sample has prostate cancer producing a score on the basis of the detecte level of filamin A in the sample and the level(s) at least one, or two, or three, or four, or five, or six, or seven, or eight, or nine or more additional prostate cancer markers (e.g., selected from the group consisting of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1), wherein if the score is below a certain threshold score, then the biological sample does not have prostate cancer. In certain embodiments, the algorithm also produces a score using the patient's age as a continuous predictor variable.

[0314] Moreover, a prostate cancer disease profile or signature may be obtained by detecting filamin A in combination with at least one other biomarker, or more preferably, with at least two other biomarkers, or still more preferably, with at least three other biomarkers, or even more preferably with at least four other biomarkers. Still further, filamin A in certain embodiments, may be used in combination with at least five other markers, or at least six other biomarkers, or at least seven other biomarkers, or at least eight other biomarkers, or at least nine other biomarkers, or at least ten other biomarkers, or at least eleven other biomarkers, or at least twelve other biomarkers, or at least thirteen other biomarkers, or at least fourteen other biomarkers, or at least fifteen other biomarkers, or at least sixteen other biomarkers, or at least seventeen other biomarkers, or at least eighteen other biomarkers, or at least nineteen other biomarkers, or at least twenty other biomarkers. Further still, filamin A may be used in combination with a multitude of other biomarkers, including, for example, with between about 20-50 other biomarkers, or between 50-100, or between 100-500, or between 500-1000, or between 1000-10,000 or biomarkers or more. In certain embodiments, the patient's age is also used as a continuous predictor variable. For example, increased age is associated with increased risk of prostate cancer diagnosis.

[0315] In certain embodiments, the biomarkers of the invention can include variant sequences. More particularly, the binding agents/reagents used for detecting the biomarkers of the invention can bind and/or identify variants of the biomarkers of the invention. As used herein, the term "variant" comprehends nucleotide or amino acid sequences different from the specifically identified sequences, wherein one or more nucleotides or amino acid residues is deleted, substituted, or added. Variants may be naturally occurring allelic variants, or non-naturally occurring variants. Variant sequences (polynucleotide or polypeptide) preferably exhibit at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identity to a sequence disclosed herein. The percentage identity is determined by aligning the two sequences to be compared as described below, determining the number of identical residues in the aligned portion, dividing that number by the total number of residues in the inventive (queried) sequence, and multiplying the result by 100.

[0316] In addition to exhibiting the recited level of sequence identity, variants of the disclosed polypeptide biomarkers are preferably themselves expressed in subjects with prostate cancer at levels that are higher or lower than the levels of expression in normal, healthy individuals.

[0317] Variant sequences generally differ from the specifically identified sequence only by conservative substitutions, deletions or modifications. As used herein, a "conservative substitution" is one in which an amino acid is substituted for another amino acid that has similar properties, such that one skilled in the art of peptide chemistry would expect the secondary structure and hydropathic nature of the polypeptide to be substantially unchanged. In general, the following groups of amino acids represent conservative changes: (1) ala, pro, gly, glu, asp, gln, asn, ser, thr; (2) cys, ser, tyr, thr; (3) val, ile, leu, met, ala, phe; (4) lys, arg, his; and (5) phe, tyr, trp, his. Variants may also, or alternatively, contain other modifications, including the deletion or addition of amino acids that have minimal influence on the antigenic properties, secondary structure and hydropathic nature of the polypeptide. For example, a polypeptide may be conjugated to a signal (or leader) sequence at the N-terminal end of the protein which co-translationally or post-translationally directs transfer of the protein. The polypeptide may also be conjugated to a linker or other sequence for ease of synthesis, purification or identification of the polypeptide (e.g., poly-His), or to enhance binding of the polypeptide to a solid support. For example, a polypeptide may be conjugated to an immunoglobulin Fc region.

[0318] Polypeptide and polynucleotide sequences may be aligned, and percentages of identical amino acids or nucleotides in a specified region may be determined against another polypeptide or polynucleotide sequence, using computer algorithms that are publicly available. The percentage identity of a polynucleotide or polypeptide sequence is determined by aligning polynucleotide and polypeptide sequences using appropriate algorithms, such as BLASTN or BLASTP, respectively, set to default parameters; identifying the number of identical nucleic or amino acids over the aligned portions; dividing the number of identical nucleic or amino acids by the total number of nucleic or amino acids of the polynucleotide or polypeptide of the present invention; and then multiplying by 100 to determine the percentage identity.

[0319] Two exemplary algorithms for aligning and identifying the identity of polynucleotide sequences are the BLASTN and FASTA algorithms. The alignment and identity of polypeptide sequences may be examined using the BLASTP algorithm. BLASTX and FASTX algorithms compare nucleotide query sequences translated in all reading frames against polypeptide sequences. The FASTA and FASTX algorithms are described in Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444-2448, 1988; and in Pearson, Methods in Enzymol. 183:63-98, 1990. The FASTA software package is available from the University of Virginia, Charlottesville, Va. 22906-9025. The FASTA algorithm, set to the default parameters described in the documentation and distributed with the algorithm, may be used in the determination of polynucleotide variants. The readme files for FASTA and FASTX Version 2.0x that are distributed with the algorithms describe the use of the algorithms and describe the default parameters.

[0320] The BLASTN software is available on the NCBI anonymous FTP server and is available from the National Center for Biotechnology Information (NCBI), National Library of Medicine, Building 38A, Room 8N805, Bethesda, Md. 20894. The BLASTN algorithm Version 2.0.6 [Sep. 10, 1998] and Version 2.0.11 [Jan. 20, 2000] set to the default parameters described in the documentation and distributed with the algorithm, is preferred for use in the determination of variants according to the present invention. The use of the BLAST family of algorithms, including BLASTN, is described at NCBI's website and in the publication of Altschul, et al., "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs," Nucleic Acids Res. 25:3389-3402, 1997.

[0321] In an alternative embodiment, variant polypeptides are encoded by polynucleotide sequences that hybridize to a disclosed polynucleotide under stringent conditions. Stringent hybridization conditions for determining complementarity include salt conditions of less than about 1 M, more usually less than about 500 mM, and preferably less than about 200 mM. Hybridization temperatures can be as low as 5.degree. C., but are generally greater than about 22.degree. C., more preferably greater than about 30.degree. C., and most preferably greater than about 37.degree. C. Longer DNA fragments may require higher hybridization temperatures for specific hybridization. Since the stringency of hybridization may be affected by other factors such as probe composition, presence of organic solvents and extent of base mismatching, the combination of parameters is more important than the absolute measure of any one alone. An example of "stringent conditions" is prewashing in a solution of 6.times.SSC, 0.2% SDS; hybridizing at 65.degree. C., 6.times.SSC, 0.2% SDS overnight; followed by two washes of 30 minutes each in 1.times.SSC, 0.1% SDS at 65.degree. C. and two washes of 30 minutes each in 0.2.times.SSC, 0.1% SDS at 65.degree. C.

D. Tissue Samples

[0322] The present invention may be practiced with any suitable biological sample that potentially contains, expresses, includes, a detectable disease biomarker, e.g., a polypeptide biomarker, a nucleic acid biomarkers, a mRNA biomarker, a microRNA biomarker. For example, the biological sample may be obtained from sources that include whole blood and serum to diseased and/or healthy tissue, for example, biopsy of prostate tumor. The methods of the invention may especially be applied to the study of any prostate tissue sample, i.e., a sample of prostate tissue or fluid, as well as cells (or their progeny) isolated from such tissue or fluid. In another embodiment, the present invention may be practiced with any suitable Prostate tissue samples which are freshly isolated or which have been frozen or stored after having been collected from a subject, or archival tissue samples, for example, with known diagnosis, treatment and/or outcome history. Prostate tissue may be collected by any non-invasive means, such as, for example, fine needle aspiration and needle biopsy, or alternatively, by an invasive method, including, for example, surgical biopsy.

[0323] The inventive methods may be performed at the single cell level (e.g., isolation and testing of cancerous cells from the prostate tissue sample). However, preferably, the inventive methods are performed using a sample comprising many cells, where the assay is "averaging" expression over the entire collection of cells and tissue present in the sample. Preferably, there is enough of the prostate tissue sample to accurately and reliably determine the expression levels of the set of genes of interest. In certain embodiments, multiple samples may be taken from the same prostate tissue in order to obtain a representative sampling of the tissue. In addition, sufficient biological material can be obtained in order to perform duplicate, triplicate or further rounds of testing.

[0324] Any commercial device or system for isolating and/or obtaining prostate tissue and/or blood or other biological products, and/or for processing said materials prior to conducting a detection reaction is contemplated.

[0325] In certain embodiments, the present invention relates to detecting biomarker nucleic acid molecules (e.g., mRNA encoding filamin A, antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, kertin 18, keratin 19, and tubulin-beta 3). In such embodiments, RNA can be extracted from a biological sample, e.g., a prostate tissue sample, before analysis. Methods of RNA extraction are well known in the art (see, for example, J. Sambrook et al., "Molecular Cloning: A Laboratory Manual", 1989, 2.sup.nd Ed., Cold Spring Harbour Laboratory Press: New York). Most methods of RNA isolation from bodily fluids or tissues are based on the disruption of the tissue in the presence of protein denaturants to quickly and effectively inactivate RNases. Generally, RNA isolation reagents comprise, among other components, guanidinium thiocyanate and/or beta-mercaptoethanol, which are known to act as RNase inhibitors. Isolated total RNA is then further purified from the protein contaminants and concentrated by selective ethanol precipitations, phenol/chloroform extractions followed by isopropanol precipitation (see, for example, P. Chomczynski and N. Sacchi, Anal. Biochem., 1987, 162: 156-159) or cesium chloride, lithium chloride or cesium trifluoroacetate gradient centrifugations.

[0326] Numerous different and versatile kits can be used to extract RNA (i.e., total RNA or mRNA) from bodily fluids or tissues (e.g., prostate tissue samples) and are commercially available from, for example, Ambion, Inc. (Austin, Tex.), Amersham Biosciences (Piscataway, N.J.), BD Biosciences Clontech (Palo Alto, Calif.), BioRad Laboratories (Hercules, Calif.), GIBCO BRL (Gaithersburg, Md.), and Giagen, Inc. (Valencia, Calif.). User Guides that describe in great detail the protocol to be followed are usually included in all these kits. Sensitivity, processing time and cost may be different from one kit to another. One of ordinary skill in the art can easily select the kit(s) most appropriate for a particular situation.

[0327] In certain embodiments, after extraction, mRNA is amplified, and transcribed into cDNA, which can then serve as template for multiple rounds of transcription by the appropriate RNA polymerase. Amplification methods are well known in the art (see, for example, A. R. Kimmel and S. L. Berger, Methods Enzymol. 1987, 152: 307-316; J. Sambrook et al., "Molecular Cloning: A Laboratory Manual", 1989, 2.sup.nd Ed., Cold Spring Harbour Laboratory Press: New York; "Short Protocols in Molecular Biology", F. M. Ausubel (Ed.), 2002, 5.sup.th Ed., John Wiley & Sons; U.S. Pat. Nos. 4,683,195; 4,683,202 and 4,800,159). Reverse transcription reactions may be carried out using non-specific primers, such as an anchored oligo-dT primer, or random sequence primers, or using a target-specific primer complementary to the RNA for each genetic probe being monitored, or using thermostable DNA polymerases (such as avian myeloblastosis virus reverse transcriptase or Moloney murine leukemia virus reverse transcriptase).

[0328] In certain embodiments, the RNA isolated from the prostate tissue sample (for example, after amplification and/or conversion to cDNA or cRNA) is labeled with a detectable agent before being analyzed. The role of a detectable agent is to facilitate detection of RNA or to allow visualization of hybridized nucleic acid fragments (e.g., nucleic acid fragments hybridized to genetic probes in an array-based assay). Preferably, the detectable agent is selected such that it generates a signal which can be measured and whose intensity is related to the amount of labeled nucleic acids present in the sample being analyzed. In array-based analysis methods, the detectable agent is also preferably selected such that it generates a localized signal, thereby allowing spatial resolution of the signal from each spot on the array.

[0329] Methods for labeling nucleic acid molecules are well-known in the art. For a review of labeling protocols, label detection techniques and recent developments in the field, see, for example, L. J. Kricka, Ann. Clin. Biochem. 2002, 39: 114-129; R. P. van Gijlswijk et al., Expert Rev. Mol. Diagn. 2001, 1: 81-91; and S. Joos et al., J. Biotechnol. 1994, 35: 135-153. Standard nucleic acid labeling methods include: incorporation of radioactive agents, direct attachment of fluorescent dyes (see, for example, L. M. Smith et al., Nucl. Acids Res. 1985, 13: 2399-2412) or of enzymes (see, for example, B. A. Connoly and P. Rider, Nucl. Acids. Res. 1985, 13: 4485-4502); chemical modifications of nucleic acid fragments making them detectable immunochemically or by other affinity reactions (see, for example, T. R. Broker et al., Nucl. Acids Res. 1978, 5: 363-384; E. A. Bayer et al., Methods of Biochem. Analysis, 1980, 26: 1-45; R. Langer et al., Proc. Natl. Acad. Sci. USA, 1981, 78: 6633-6637; R. W. Richardson et al., Nucl. Acids Res. 1983, 11: 6167-6184; D. J. Brigati et al., Virol. 1983, 126: 32-50; P. Tchen et al., Proc. Natl Acad. Sci. USA, 1984, 81: 3466-3470; J. E. Landegent et al., Exp. Cell Res. 1984, 15: 61-72; and A. H. Hopman et al., Exp. Cell Res. 1987, 169: 357-368); and enzyme-mediated labeling methods, such as random priming, nick translation, PCR and tailing with terminal transferase (for a review on enzymatic labeling, see, for example, J. Temsamani and S. Agrawal, Mol. Biotechnol. 1996, 5: 223-232).

[0330] Any of a wide variety of detectable agents can be used in the practice of the present invention. Suitable detectable agents include, but are not limited to: various ligands, radionuclides, fluorescent dyes, chemiluminescent agents, microparticles (such as, for example, quantum dots, nanocrystals, phosphors and the like), enzymes (such as, for example, those used in an ELISA, i.e., horseradish peroxidase, beta-galactosidase, luciferase, alkaline phosphatase), colorimetric labels, magnetic labels, and biotin, dioxigenin or other haptens and proteins for which antisera or monoclonal antibodies are available.

[0331] However, in some embodiments, the expression levels are determined by detecting the expression of a gene product (e.g., protein) thereby eliminating the need to obtain a genetic sample (e.g., RNA) from the prostate tissue sample.

[0332] In still other embodiments, the present invention relates to preparing a prediction model for prostate and/or the likelihood of relapse of prostate cancer by preparing a model for prostate cancer based on measuring the biomarkers of the invention in known control samples. More particularly, the present invention relates in some embodiments to preparing a predictive model by evaluating the biomarkers of the invention, e.g., filamin A in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1.

[0333] The skilled person will appreciate that patient tissue samples containing prostate cells or prostate cancer cells may be used in the methods of the present invention including, but not limited to those aimed at predicting relapse probability. In these embodiments, the level of expression of the signature gene can be assessed by assessing the amount, e.g. absolute amount or concentration, of a signature gene product, e.g., protein and RNA transcript encoded by the signature gene and fragments of the protein and RNA transcript) in a sample, e.g., stool and/or blood obtained from a patient. The sample can, of course, be subjected to a variety of well-known post-collection preparative and storage techniques (e.g. fixation, storage, freezing, lysis, homogenization, DNA or RNA extraction, ultrafiltration, concentration, evaporation, centrifugation, etc.) prior to assessing the amount of the signature gene product in the sample.

[0334] The invention further relates to the preparation of a model for prostate cancer or prostate cancer relapse by evaluating the biomarkers of the invention in known samples of prostate cancer. More particularly, the present invention relates to a prostate cancer model for diagnosing and/or monitoring and/or prognosing prostate cancer or prostate cancer relapse using the biomarkers of the invention, which can include filamin A and at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1.

[0335] In the methods of the invention aimed at preparing a model for prostate cancer and/or prostate cancer relapse prediction, it is understood that the particular clinical outcome associated with each sample contributing to the model preferably should be known. Consequently, the model can be established using archived tissue samples. In the methods of the invention aimed at preparing a model for prostate cancer and/or prostate cancer relapse prediction, total RNA can be generally extracted from the source material of interest, generally an archived tissue such as a formalin-fixed, paraffin-embedded tissue, and subsequently purified. Methods for obtaining robust and reproducible gene expression patterns from archived tissues, including formalin-fixed, paraffin-embedded (FFPE) tissues are taught in U.S. Publ. No. 2004/0259105, which is incorporated herein by reference in its entirety. Commercial kits and protocols for RNA extraction from FFPE tissues are available including, for example, ROCHE High Pure RNA Paraffin Kit (Roche) MasterPure.TM. Complete DNA and RNA Purification Kit (EPICENTRE.RTM.Madison, Wis.); Paraffin Block RNA Isolation Kit (Ambion, Inc.) and RNeasy.TM. Mini kit (Qiagen, Chatsworth, Calif.).

[0336] The use of FFPE tissues as a source of RNA for RT-PCR has been described previously (Stanta et al., Biotechniques 11:304-308 (1991); Stanta et al., Methods Mol. Biol. 86:23-26 (1998); Jackson et al., Lancet 1:1391 (1989); Jackson et al., J. Clin. Pathol. 43:499-504 (1999); Finke et al., Biotechniques 14:448-453 (1993); Goldsworthy et al., Mol. Carcinog. 25:86-91 (1999); Stanta and Bonin, Biotechniques 24:271-276 (1998); Godfrey et al., J. Mol. Diagnostics 2:84 (2000); Specht et al., J. Mol. Med. 78:B27 (2000); Specht et al., Am. J. Pathol. 158:419-429 (2001)). For quick analysis of the RNA quality, RT-PCR can be performed utilizing a pair of primers targeting a short fragment in a highly expressed gene, for example, actin, ubiquitin, gapdh or other well-described commonly used housekeeping gene. If the cDNA synthesized from the RNA sample can be amplified using this pair of primers, then the sample is suitable for the a quantitative measurements of RNA target sequences by any method preferred, for example, the DASL assay, which requires only a short cDNA fragment for the annealing of query oligonucleotides.

[0337] There are numerous tissue banks and collections including exhaustive samples from all stages of a wide variety of disease states, most notably cancer and in particular, prostate cancer. The ability to perform genotyping and/or gene expression analysis, including both qualitative and quantitative analysis on these samples enables the application of this methodology to the methods of the invention. In particular, the ability to establish a correlation of gene expression and a known predictor of disease extent and/or outcome by probing the genetic state of tissue samples for which clinical outcome is already known, allows for the establishment of a correlation between a particular molecular signature and the known predictor, such as a Gleason score, to derive a score that allows for a more sensitive prognosis than that based on the known predictor alone. The skilled person will appreciate that by building databases of molecular signatures from tissue samples of known outcomes, many such correlations can be established, thus allowing both diagnosis and prognosis of any condition. Thus, such approaches may be used to correlate the expression levels of the biomarkers of the invention, e.g., filamin A and at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3 and PSA, to a particular stage of prostate cancer.

[0338] Tissue samples useful for preparing a model for prostate cancer prediction include, for example, paraffin and polymer embedded samples, ethanol embedded samples and/or formalin and formaldehyde embedded tissues, although any suitable sample may be used. In general, nucleic acids isolated from archived samples can be highly degraded and the quality of nucleic preparation can depend on several factors, including the sample shelf life, fixation technique and isolation method. However, using the methodologies taught in U.S. Publ. No. 2004/0259105, which have the significant advantage that short or degraded targets can be used for analysis as long as the sequence is long enough to hybridize with the oligonucleotide probes, highly reproducible results can be obtained that closely mimic results found in fresh samples.

[0339] Archived tissue samples, which can be used for all methods of the invention, typically have been obtained from a source and preserved. Preferred methods of preservation include, but are not limited to paraffin embedding, ethanol fixation and formalin, including formaldehyde and other derivatives, fixation as are known in the art. A tissue sample may be temporally "old", e.g. months or years old, or recently fixed. For example, post-surgical procedures generally include a fixation step on excised tissue for histological analysis. In a preferred embodiment, the tissue sample is a diseased tissue sample, particularly a prostate cancer tissue, including primary and secondary tumor tissues as well as lymph node tissue and metastatic tissue.

[0340] Thus, an archived sample can be heterogeneous and encompass more than one cell or tissue type, for example, tumor and non-tumor tissue. Preferred tissue samples include solid tumor samples including, but not limited to, tumors of the prostate. It is understood that in applications of the present invention to conditions other than prostate cancer, the tumor source can be brain, bone, heart, breast, ovaries, prostate, uterus, spleen, pancreas, liver, kidneys, bladder, stomach and muscle. Similarly, depending on the condition, suitable tissue samples include, but are not limited to, bodily fluids (including, but not limited to, blood, urine, serum, lymph, saliva, anal and vaginal secretions, perspiration and semen, of virtually any organism, with mammalian samples being preferred and human samples being particularly preferred). In embodiments directed to methods of establishing a model for prostate cancer relapse prediction, the tissue sample is one for which patient history and outcome is known. Generally, the invention methods can be practiced with the signature gene sequence contained in an archived sample or can be practiced with signature gene sequences that have been physically separated from the sample prior to performing a method of the invention.

E. Detection and/or Measurement of Biomarkers

[0341] The present invention contemplates any suitable means, techniques, and/or procedures for detecting and/or measuring the biomarkers of the invention. The skilled artisan will appreciate that the methodologies employed to measure the biomarkers of the invention will depend at least on the type of biomarker being detected or measured (e.g., mRNA biomarker or polypeptide biomarker) and the source of the biological sample (e.g., whole blood versus prostate biopsy tissue). Certain biological sample may also require certain specialized treatments prior to measuring the biomarkers of the invention, e.g., the preparation of mRNA from a biopsy tissue in the case where mRNA biomarkers are being measured.

[0342] 1. Detection of Nucleic Acid Biomarkers

[0343] In certain embodiments, the invention involves the detection of nucleic acid biomarkers, e.g., mRNA biomarkers of filamin A alone or filamin A in combination with at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1.

[0344] In various embodiments, the diagnostic/prognostic methods of the present invention generally involve the determination of expression levels of a set of genes in a prostate tissue sample. Determination of gene expression levels in the practice of the inventive methods may be performed by any suitable method. For example, determination of gene expression levels may be performed by detecting the expression of mRNA expressed from the genes of interest and/or by detecting the expression of a polypeptide encoded by the genes.

[0345] For detecting nucleic acids encoding biomarkers of the invention, any suitable method can be used, including, but not limited to, Southern blot analysis, Northern blot analysis, polymerase chain reaction (PCR) (see, for example, U.S. Pat. Nos. 4,683,195; 4,683,202, and 6,040,166; "PCR Protocols: A Guide to Methods and Applications", Innis et al. (Eds), 1990, Academic Press: New York), reverse transcriptase PCR (RT-PCT), anchored PCR, competitive PCR (see, for example, U.S. Pat. No. 5,747,251), rapid amplification of cDNA ends (RACE) (see, for example, "Gene Cloning and Analysis: Current Innovations, 1997, pp. 99-115); ligase chain reaction (LCR) (see, for example, EP 01 320 308), one-sided PCR (Ohara et al., Proc. Natl. Acad. Sci., 1989, 86: 5673-5677), in situ hybridization, Taqman-based assays (Holland et al., Proc. Natl. Acad. Sci., 1991, 88: 7276-7280), differential display (see, for example, Liang et al., Nucl. Acid. Res., 1993, 21: 3269-3275) and other RNA fingerprinting techniques, nucleic acid sequence based amplification (NASBA) and other transcription based amplification systems (see, for example, U.S. Pat. Nos. 5,409,818 and 5,554,527), Qbeta Replicase, Strand Displacement Amplification (SDA), Repair Chain Reaction (RCR), nuclease protection assays, subtraction-based methods, Rapid-Scan.RTM., etc.

[0346] In other embodiments, gene expression levels of biomarkers of interest may be determined by amplifying complementary DNA (cDNA) or complementary RNA (cRNA) produced from mRNA and analyzing it using a microarray. A number of different array configurations and methods of their production are known to those skilled in the art (see, for example, U.S. Pat. Nos. 5,445,934; 5,532,128; 5,556,752; 5,242,974; 5,384,261; 5,405,783; 5,412,087; 5,424,186; 5,429,807; 5,436,327; 5,472,672; 5,527,681; 5,529,756; 5,545,531; 5,554,501; 5,561,071; 5,571,639; 5,593,839; 5,599,695; 5,624,711; 5,658,734; and 5,700,637). Microarray technology allows for the measurement of the steady-state mRNA level of a large number of genes simultaneously. Microarrays currently in wide use include cDNA arrays and oligonucleotide arrays. Analyses using microarrays are generally based on measurements of the intensity of the signal received from a labeled probe used to detect a cDNA sequence from the sample that hybridizes to a nucleic acid probe immobilized at a known location on the microarray (see, for example, U.S. Pat. Nos. 6,004,755; 6,218,114; 6,218,122; and 6,271,002). Array-based gene expression methods are known in the art and have been described in numerous scientific publications as well as in patents (see, for example, M. Schena et al., Science, 1995, 270: 467-470; M. Schena et al., Proc. Natl. Acad. Sci. USA 1996, 93: 10614-10619; J. J. Chen et al., Genomics, 1998, 51: 313-324; U.S. Pat. Nos. 5,143,854; 5,445,934; 5,807,522; 5,837,832; 6,040,138; 6,045,996; 6,284,460; and 6,607,885).

[0347] In one particular embodiment, the invention comprises a method for identification of prostate cancer cells in a biological sample by amplifying and detecting nucleic acids corresponding to the novel prostate cancer biomarkers, and or panels of biomarkers that include filamin A alone or filamin A in combination with one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. The biological sample may be any tissue or fluid in which prostate cancer cells might be present. Various embodiments include radical prostatectomy specimens, pathological specimens, bone marrow aspirate, bone marrow biopsy, lymph node aspirate, lymph node biopsy, spleen tissue, fine needle aspirate, skin biopsy or organ tissue biopsy. Other embodiments include samples where the body fluid is peripheral blood, serum, plasma, lymph fluid, ascites, serous fluid, pleural effusion, sputum, cerebrospinal fluid, lacrimal fluid, stool, prostatic fluid or urine.

[0348] Nucleic acid used as a template for amplification can be isolated from cells contained in the biological sample, according to standard methodologies. (Sambrook et al., 1989) The nucleic acid may be genomic DNA or fractionated or whole cell RNA. Where RNA is used, it may be desired to convert the RNA to a complementary cDNA. In one embodiment, the RNA is whole cell RNA and is used directly as the template for amplification.

[0349] Pairs of primers that selectively hybridize to nucleic acids corresponding to any of the prostate cancer biomarker nucleotide sequences identified herein are contacted with the isolated nucleic acid under conditions that permit selective hybridization. Once hybridized, the nucleic acid:primer complex is contacted with one or more enzymes that facilitate template-dependent nucleic acid synthesis. Multiple rounds of amplification, also referred to as "cycles," are conducted until a sufficient amount of amplification product is produced. Next, the amplification product is detected. In certain applications, the detection may be performed by visual means. Alternatively, the detection may involve indirect identification of the product via chemiluminescence, radioactive scintigraphy of incorporated radiolabel or fluorescent label or even via a system using electrical or thermal impulse signals (Affymax technology; Bellus, 1994). Following detection, one may compare the results seen in a given patient with a statistically significant reference group of normal patients and prostate, cancer patients. In this way, it is possible to correlate the amount of nucleic acid detected with various clinical states.

[0350] The term primer, as defined herein, is meant to encompass any nucleic acid that is capable of priming the synthesis of a nascent nucleic acid in a template-dependent process. Typically, primers are oligonucleotides from ten to twenty base pairs in length, but longer sequences may be employed. Primers may be provided in double-stranded or single-stranded form, although the single-stranded form is preferred.

[0351] A number of template dependent processes are available to amplify the nucleic acid sequences present in a given template sample. One of the best known amplification methods is the polymerase chain reaction (referred to as PCR) which is described in detail in U.S. Pat. Nos. 4,683,195, 4,683,202 and 4,800,159, and in Innis et al., 1990, each of which is incorporated herein by reference in its entirety.

[0352] In PCR, two primer sequences are prepared which are complementary to regions on opposite complementary strands of the target nucleic acid sequence. An excess of deoxynucleoside triphosphates are added to a reaction mixture along with a DNA polymerase, e.g., Taq polymerase. If the target nucleic acid sequence is present in a sample, the primers will bind to the target nucleic acid and the polymerase will cause the primers to be extended along the target nucleic acid sequence by adding on nucleotides. By raising and lowering the temperature of the reaction mixture, the extended primers will dissociate from the target nucleic acid to form reaction products, excess primers will bind to the target nucleic acid and to the reaction products and the process is repeated.

[0353] A reverse transcriptase PCR amplification procedure may be performed in order to quantify the amount of mRNA amplified. Methods of reverse transcribing RNA into cDNA are well known and described in Sambrook et al., 1989. Alternative methods for reverse transcription utilize thermostable DNA polymerases. These methods are described in WO 90/07641 filed Dec. 21, 1990. Polymerase chain reaction methodologies are well known in the art.

[0354] Another method for amplification is the ligase chain reaction ("LCR"), disclosed in European Application No. 320 308, incorporated herein by reference in its entirely. In LCR, two complementary probe pairs are prepared, and in the presence of the target sequence, each pair will bind to opposite complementary strands of the target such that they abut. In the presence of a ligase, the two probe pairs will link to form a single unit. By temperature cycling, as in PCR, bound ligated units dissociate from the target and then serve as "target sequences" for ligation of excess probe pairs. U.S. Pat. No. 4,883,750 describes a method similar to LCR for binding probe pairs to a target sequence.

[0355] Qbeta Replicase, described in PCT Application No. PCT/US87/00880, also may be used as still another amplification method in the present invention. In this method, a replicative sequence of RNA which has a region complementary to that of a target is added to a sample in the presence of an RNA polymerase. The polymerase will copy the replicative sequence which may then be detected.

[0356] An isothermal amplification method, in which restriction endonucleases and ligases are used to achieve the amplification of target molecules that contain nucleotide 5'-[.alpha.-thio]triphosphates in one strand of a restriction site also may be useful in the amplification of nucleic acids in the present invention. Walker et al. (1992), incorporated herein by reference in its entirety.

[0357] Strand Displacement Amplification (SDA) is another method of carrying out isothermal amplification of nucleic acids which involves multiple rounds of strand displacement and synthesis, i.e., nick translation. A similar method, called Repair Chain Reaction (RCR), involves annealing several probes throughout a region targeted for amplification, followed by a repair reaction in which only two of the four bases are present. The other two bases may be added as biotinylated derivatives for easy detection. A similar approach is used in SDA. Target specific sequences also may be detected using a cyclic probe reaction (CPR). In CPR, a probe having 3' and 5' sequences of non-specific DNA and a middle sequence of specific RNA is hybridized to DNA which is present in a sample. Upon hybridization, the reaction is treated with RNase H, and the products of the probe identified as distinctive products which are released after digestion. The original template is annealed to another cycling probe and the reaction is repeated.

[0358] Still other amplification methods described in GB Application No. 2 202 328, and in PCT Application No. PCT/US89/01025, each of which is incorporated herein by reference in its entirety, may be used in accordance with the present invention. In the former application, "modified" primers are used in a PCR like, template and enzyme dependent synthesis. The primers may be modified by labeling with a capture moiety (e.g., biotin) and/or a detector moiety (e.g., enzyme). In the latter application, an excess of labeled probes are added to a sample. In the presence of the target sequence, the probe binds and is cleaved catalytically. After cleavage, the target sequence is released intact to be bound by excess probe. Cleavage of the labeled probe signals the presence of the target sequence.

[0359] Other contemplated nucleic acid amplification procedures include transcription-based amplification systems (TAS), including nucleic acid sequence based amplification (NASBA) and 3SR. Kwoh et al. (1989); Gingeras et al., PCT Application WO 88/10315, incorporated herein by reference in their entirety. In NASBA, the nucleic acids may be prepared for amplification by standard phenol/chloroform extraction, heat denaturation of a clinical sample, treatment with lysis buffer and minispin columns for isolation of DNA and RNA or guanidinium chloride extraction of RNA. These amplification techniques involve annealing a primer which has target specific sequences. Following polymerization, DNA/RNA hybrids are digested with RNase H while double stranded DNA molecules are heat denatured again. In either case the single stranded DNA is made fully double stranded by addition of second target specific primer, followed by polymerization. The double-stranded DNA molecules are then multiply transcribed by a polymerase such as T7 or SP6. In an isothermal cyclic reaction, the RNA's are reverse transcribed into double stranded DNA, and transcribed once against with a polymerase such as T7 or SP6. The resulting products, whether truncated or complete, indicate target specific sequences.

[0360] Davey et al., European Application No. 329 822 (incorporated herein by reference in its entirely) disclose a nucleic acid amplification process involving cyclically synthesizing single-stranded RNA ("ssRNA"), ssDNA, and double-stranded DNA (dsDNA), which may be used in accordance with the present invention. The ssRNA is a first template for a first primer oligonucleotide, which is elongated by reverse transcriptase (RNA-dependent DNA polymerase). The RNA is then removed from the resulting DNA:RNA duplex by the action of ribonuclease H(RNase H, an RNase specific for RNA in duplex with either DNA or RNA). The resultant ssDNA is a second template for a second primer, which also includes the sequences of an RNA polymerase promoter (exemplified by T7 RNA polymerase) 5' to its homology to the template. This primer is then extended by DNA polymerase (exemplified by the large "Klenow" fragment of E. coli DNA polymerase 1), resulting in a double-stranded DNA ("dsDNA") molecule, having a sequence identical to that of the original RNA between the primers and having additionally, at one end, a promoter sequence. This promoter sequence may be used by the appropriate RNA polymerase to make many RNA copies of the DNA. These copies may then re-enter the cycle leading to very swift amplification. With proper choice of enzymes, this amplification may be done isothermally without addition of enzymes at each cycle. Because of the cyclical nature of this process, the starting sequence may be chosen to be in the form of either DNA or RNA.

[0361] Miller et al., PCT Application WO 89/06700 (incorporated herein by reference in its entirety) disclose a nucleic acid sequence amplification scheme based on the hybridization of a promoter/primer sequence to a target single-stranded DNA ("ssDNA") followed by transcription of many RNA copies of the sequence. This scheme is not cyclic, i.e., new templates are not produced from the resultant RNA transcripts. Other amplification methods include "race" and "one-sided PCR.TM.." Frohman (1990) and Ohara et al. (1989), each herein incorporated by reference in their entirety.

[0362] Methods based on ligation of two (or more) oligonucleotides in the presence of nucleic acid having the sequence of the resulting "di-oligonucleotide", thereby amplifying the di-oligonucleotide, also may be used in the amplification step of the present invention. Wu et al. (1989), incorporated herein by reference in its entirety.

[0363] Oligonucleotide probes or primers of the present invention may be of any suitable length, depending on the particular assay format and the particular needs and targeted sequences employed. In a preferred embodiment, the oligonucleotide probes or primers are at least 10 nucleotides in length (preferably, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32 . . . ) and they may be adapted to be especially suited for a chosen nucleic acid amplification system and/or hybridization system used. Longer probes and primers are also within the scope of the present invention as well known in the art. Primers having more than 30, more than 40, more than 50 nucleotides and probes having more than 100, more than 200, more than 300, more than 500 more than 800 and more than 1000 nucleotides in length are also covered by the present invention. Of course, longer primers have the disadvantage of being more expensive and thus, primers having between 12 and 30 nucleotides in length are usually designed and used in the art. As well known in the art, probes ranging from 10 to more than 2000 nucleotides in length can be used in the methods of the present invention. As for the % of identity described above, non-specifically described sizes of probes and primers (e.g., 16, 17, 31, 24, 39, 350, 450, 550, 900, 1240 nucleotides, . . . ) are also within the scope of the present invention. In one embodiment, the oligonucleotide probes or primers of the present invention specifically hybridize with a filamin A RNA (or its complementary sequence) or a filamin A mRNA. More preferably, the filamin A primers and probes will be chosen to detect a filamin A RNA which is associated with prostate cancer.

[0364] In other embodiments, the detection means can utilize a hybridization technique, e.g., where a specific primer or probe is selected to anneal to a target biomarker of interest, e.g., filamin A, and thereafter detection of selective hybridization is made. As commonly known in the art, the oligonucleotide probes and primers can be designed by taking into consideration the melting point of hybridization thereof with its targeted sequence (see below and in Sambrook et al., 1989, Molecular Cloning--A Laboratory Manual, 2nd Edition, CSH Laboratories; Ausubel et al., 1994, in Current Protocols in Molecular Biology, John Wiley & Sons Inc., N.Y.).

[0365] To enable hybridization to occur under the assay conditions of the present invention, oligonucleotide primers and probes should comprise an oligonucleotide sequence that has at least 70% (at least 71%, 72%, 73%, 74%), preferably at least 75% (75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%) and more preferably at least 90% (90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 100%) identity to a portion of a filamin A or polynucleotide of another biomarker of the invention. Probes and primers of the present invention are those that hybridize under stringent hybridization conditions and those that hybridize to biomarker homologs of the invention under at least moderately stringent conditions. In certain embodiments probes and primers of the present invention have complete sequence identity to the biomarkers of the invention (filamin A, gene sequences (e.g., cDNA or mRNA). It should be understood that other probes and primers could be easily designed and used in the present invention based on the biomarkers of the invention disclosed herein by using methods of computer alignment and sequence analysis known in the art (cf. Molecular Cloning: A Laboratory Manual, Third Edition, edited by Cold Spring Harbor Laboratory, 2000).

[0366] 2. Detection of Polypeptide Biomarkers

[0367] The present invention contemplates any suitable method for detecting polypeptide biomarkers of the invention. In certain embodiments, the detection method is an immunodetection method involving an antibody that specifically binds to one or more of the biomarkers of the invention invention, e.g., filamin A alone or filamin A in combination with at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. The steps of various useful immunodetection methods have been described in the scientific literature, such as, e.g., Nakamura et al. (1987), which is incorporated herein by reference.

[0368] In general, the immunobinding methods include obtaining a sample suspected of containing a biomarker protein, peptide or antibody, and contacting the sample with an antibody or protein or peptide in accordance with the present invention, as the case may be, under conditions effective to allow the formation of immunocomplexes.

[0369] The immunobinding methods include methods for detecting or quantifying the amount of a reactive component in a sample, which methods require the detection or quantitation of any immune complexes formed during the binding process. Here, one would obtain a sample suspected of containing a prostate specific protein, peptide or a corresponding antibody, and contact the sample with an antibody or encoded protein or peptide, as the case may be, and then detect or quantify the amount of immune complexes formed under the specific conditions.

[0370] In terms of biomarker detection, the biological sample analyzed may be any sample that is suspected of containing a prostate cancer-specific biomarker, such as, filamin A and at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3 and PSA. The biological sample may be, for example, a prostate or lymph node tissue section or specimen, a homogenized tissue extract, an isolated cell, a cell membrane preparation, separated or purified forms of any of the above protein-containing compositions, or even any biological fluid that comes into contact with prostate tissues, including blood or lymphatic fluid.

[0371] Contacting the chosen biological sample with the protein (e.g., filamin A or antigen thereof to bind with a anti-filamin A antibody in the blood), peptide (e.g., filamin A fragment that binds with a anti-filamin A antibody in the blood), or antibody (e.g., as a detection reagent that binds filamin A in a biological sample) under conditions effective and for a period of time sufficient to allow the formation of immune complexes (primary immune complexes). Generally, complex formation is a matter of simply adding the composition to the biological sample and incubating the mixture for a period of time long enough for the antibodies to form immune complexes with, i.e., to bind to, any antigens present. After this time, the sample-antibody composition, such as a tissue section, ELISA plate, dot blot or Western blot, will generally be washed to remove any non-specifically bound antibody species, allowing only those antibodies specifically bound within the primary immune complexes to be detected.

[0372] In general, the detection of immunocomplex formation is well known in the art and may be achieved through the application of numerous approaches. These methods are generally based upon the detection of a label or marker, such as any radioactive, fluorescent, biological or enzymatic tags or labels of standard use in the art. U.S. patents concerning the use of such labels include U.S. Pat. Nos. 3,817,837; 3,850,752; 3,939,350; 3,996,345; 4,277,437; 4,275,149 and 4,366,241, each incorporated herein by reference. Of course, one may find additional advantages through the use of a secondary binding ligand such as a second antibody or a biotin/avidin ligand binding arrangement, as is known in the art.

[0373] The encoded protein (e.g., filamin A), peptide (e.g., filamin A peptide) or corresponding antibody (anti-filamin A antibody as detection reagent) employed in the detection may itself be linked to a detectable label, wherein one would then simply detect this label, thereby allowing the amount of the primary immune complexes in the composition to be determined.

[0374] Alternatively, the first added component that becomes bound within the primary immune complexes may be detected by means of a second binding ligand that has binding affinity for the encoded protein, peptide or corresponding antibody. In these cases, the second binding ligand may be linked to a detectable label. The second binding ligand is itself often an antibody, which may thus be termed a "secondary" antibody. The primary immune complexes are contacted with the labeled, secondary binding ligand, or antibody, under conditions effective and for a period of time sufficient to allow the formation of secondary immune complexes. The secondary immune complexes are then generally washed to remove any non-specifically bound labeled secondary antibodies or ligands, and the remaining label in the secondary immune complexes is then detected.

[0375] Further methods include the detection of primary immune complexes by a two step approach. A second binding ligand, such as an antibody, that has binding affinity for the encoded protein, peptide or corresponding antibody is used to form secondary immune complexes, as described above. After washing, the secondary immune complexes are contacted with a third binding ligand or antibody that has binding affinity for the second antibody, again under conditions effective and for a period of time sufficient to allow the formation of immune complexes (tertiary immune complexes). The third ligand or antibody is linked to a detectable label, allowing detection of the tertiary immune complexes thus formed. This system may provide for signal amplification if this is desired.

[0376] The immunodetection methods of the present invention have evident utility in the diagnosis of conditions such as prostate cancer. Here, a biological or clinical sample suspected of containing either the encoded protein or peptide or corresponding antibody is used. However, these embodiments also have applications to non-clinical samples, such as in the tittering of antigen or antibody samples, in the selection of hybridomas, and the like.

[0377] The present invention, in particular, contemplates the use of ELISAs as a type of immunodetection assay. It is contemplated that the biomarker proteins or peptides of the invention will find utility as immunogens in ELISA assays in diagnosis and prognostic monitoring of prostate cancer. Immunoassays, in their most simple and direct sense, are binding assays. Certain preferred immunoassays are the various types of enzyme linked immunosorbent assays (ELISAs) and radioimmunoassays (RIA) known in the art. Immunohistochemical detection using tissue sections is also particularly useful. However, it will be readily appreciated that detection is not limited to such techniques, and Western blotting, dot blotting, FACS analyses, and the like also may be used.

[0378] In one exemplary ELISA, antibodies binding to the biomarkers of the invention are immobilized onto a selected surface exhibiting protein affinity, such as a well in a polystyrene microtiter plate. Then, a test composition suspected of containing the prostate cancer marker antigen, such as a clinical sample, is added to the wells. After binding and washing to remove non-specifically bound immunecomplexes, the bound antigen may be detected. Detection is generally achieved by the addition of a second antibody specific for the target protein, that is linked to a detectable label. This type of ELISA is a simple "sandwich ELISA." Detection also may be achieved by the addition of a second antibody, followed by the addition of a third antibody that has binding affinity for the second antibody, with the third antibody being linked to a detectable label.

[0379] In another exemplary ELISA, the samples suspected of containing the prostate cancer marker antigen are immobilized onto the well surface and then contacted with the anti-biomarker antibodies of the invention. After binding and washing to remove non-specifically bound immunecomplexes, the bound antigen is detected. Where the initial antibodies are linked to a detectable label, the immunecomplexes may be detected directly. Again, the immunecomplexes may be detected using a second antibody that has binding affinity for the first antibody, with the second antibody being linked to a detectable label.

[0380] Irrespective of the format employed, ELISAs have certain features in common, such as coating, incubating or binding, washing to remove non-specifically bound species, and detecting the bound immunecomplexes. These are described as follows.

[0381] In coating a plate with either antigen or antibody, one will generally incubate the wells of the plate with a solution of the antigen or antibody, either overnight or for a specified period of hours. The wells of the plate will then be washed to remove incompletely adsorbed material. Any remaining available surfaces of the wells are then "coated" with a nonspecific protein that is antigenically neutral with regard to the test antisera. These include bovine serum albumin (BSA), casein and solutions of milk powder. The coating allows for blocking of nonspecific adsorption sites on the immobilizing surface and thus reduces the background caused by nonspecific binding of antisera onto the surface.

[0382] In ELISAs, it is probably more customary to use a secondary or tertiary detection means rather than a direct procedure. Thus, after binding of a protein or antibody to the well, coating with a non-reactive material to reduce background, and washing to remove unbound material, the immobilizing surface is contacted with the control human prostate, cancer and/or clinical or biological sample to be tested under conditions effective to allow immunecomplex (antigen/antibody) formation. Detection of the immunecomplex then requires a labeled secondary binding ligand or antibody, or a secondary binding ligand or antibody in conjunction with a labeled tertiary antibody or third binding ligand.

[0383] The phrase "under conditions effective to allow immunecomplex (antigen/antibody) formation" means that the conditions preferably include diluting the antigens and antibodies with solutions such as BSA, bovine gamma globulin (BGG) and phosphate buffered saline (PBS)/Tween. These added agents also tend to assist in the reduction of nonspecific background.

[0384] The "suitable" conditions also mean that the incubation is at a temperature and for a period of time sufficient to allow effective binding. Incubation steps are typically from about 1 to 2 to 4 h, at temperatures preferably on the order of 25 to 27.degree. C., or may be overnight at about 4.degree. C. or so.

[0385] Following all incubation steps in an ELISA, the contacted surface is washed so as to remove non-complexed material. A preferred washing procedure includes washing with a solution such as PBS/Tween, or borate buffer. Following the formation of specific immunecomplexes between the test sample and the originally bound material, and subsequent washing, the occurrence of even minute amounts of immunecomplexes may be determined.

[0386] To provide a detecting means, the second or third antibody will have an associated label to allow detection. Preferably, this will be an enzyme that will generate color development upon incubating with an appropriate chromogenic substrate. Thus, for example, one will desire to contact and incubate the first or second immunecomplex with a urease, glucose oxidase, alkaline phosphatase or hydrogen peroxidase-conjugated antibody for a period of time and under conditions that favor the development of further immunecomplex formation (e.g., incubation for 2 h at room temperature in a PBS-containing solution such as PBS-Tween).

[0387] After incubation with the labeled antibody, and subsequent to washing to remove unbound material, the amount of label is quantified, e.g., by incubation with a chromogenic substrate such as urea and bromocresol purple. Quantitation is then achieved by measuring the degree of color generation, e.g., using a visible spectra spectrophotometer.

[0388] The protein biomarkers of the invention (e.g., filamin A alone or in combination with any one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) can also be measured, quantitated, detected, and otherwise analyzed using protein mass spectrometry methods and instrumentation. Protein mass spectrometry refers to the application of mass spectrometry to the study of proteins. Although not intending to be limiting, two approaches are typically used for characterizing proteins using mass spectrometry. In the first, intact proteins are ionized and then introduced to a mass analyzer. This approach is referred to as "top-down" strategy of protein analysis. The two primary methods for ionization of whole proteins are electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI). In the second approach, proteins are enzymatically digested into smaller peptides using a protease such as trypsin. Subsequently these peptides are introduced into the mass spectrometer and identified by peptide mass fingerprinting or tandem mass spectrometry. Hence, this latter approach (also called "bottom-up" proteomics) uses identification at the peptide level to infer the existence of proteins.

[0389] Whole protein mass analysis of the biomarkers of the invention can be conducted using time-of-flight (TOF) MS, or Fourier transform ion cyclotron resonance (FT-ICR). These two types of instruments are useful because of their wide mass range, and in the case of FT-ICR, its high mass accuracy. The most widely used instruments for peptide mass analysis are the MALDI time-of-flight instruments as they permit the acquisition of peptide mass fingerprints (PMFs) at high pace (1 PMF can be analyzed in approx. 10 sec). Multiple stage quadrupole-time-of-flight and the quadrupole ion trap also find use in this application.

[0390] The biomarkers of the invention can also be measured in complex mixtures of proteins and molecules that co-exist in a biological medium or sample, however, fractionation of the sample may be required and is contemplated herein. It will be appreciated that ionization of complex mixtures of proteins can result in situation where the more abundant proteins have a tendency to "drown" or suppress signals from less abundant proteins in the same sample. In addition, the mass spectrum from a complex mixture can be difficult to interpret because of the overwhelming number of mixture components. Fractionation can be used to first separate any complex mixture of proteins prior to mass spectrometry analysis. Two methods are widely used to fractionate proteins, or their peptide products from an enzymatic digestion. The first method fractionates whole proteins and is called two-dimensional gel electrophoresis. The second method, high performance liquid chromatography (LC or HPLC) is used to fractionate peptides after enzymatic digestion. In some situations, it may be desirable to combine both of these techniques. Any other suitable methods known in the art for fractionating protein mixtures are also contemplated herein.

[0391] Gel spots identified on a 2D Gel are usually attributable to one protein. If the identity of the protein is desired, usually the method of in-gel digestion is applied, where the protein spot of interest is excised, and digested proteolytically. The peptide masses resulting from the digestion can be determined by mass spectrometry using peptide mass fingerprinting. If this information does not allow unequivocal identification of the protein, its peptides can be subject to tandem mass spectrometry for de novo sequencing.

[0392] Characterization of protein mixtures using HPLC/MS may also be referred to in the art as "shotgun proteomics" and MuDPIT (Multi-Dimensional Protein Identification Technology). A peptide mixture that results from digestion of a protein mixture is fractionated by one or two steps of liquid chromatography (LC). The eluent from the chromatography stage can be either directly introduced to the mass spectrometer through electrospray ionization, or laid down on a series of small spots for later mass analysis using MALDI.

[0393] The biomarkers of the present invention (e.g., filamin A alone or in combination with any one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) can be identified using MS using a variety of techniques, all of which are contemplated herein. Peptide mass fingerprinting uses the masses of proteolytic peptides as input to a search of a database of predicted masses that would arise from digestion of a list of known proteins. If a protein sequence in the reference list gives rise to a significant number of predicted masses that match the experimental values, there is some evidence that this protein was present in the original sample. It will be further appreciated that the development of methods and instrumentation for automated, data-dependent electrospray ionization (ESI) tandem mass spectrometry (MS/MS) in conjunction with microcapillary liquid chromatography (LC) and database searching has significantly increased the sensitivity and speed of the identification of gel-separated proteins. Microcapillary LC-MS/MS has been used successfully for the large-scale identification of individual proteins directly from mixtures without gel electrophoretic separation (Link et al., 1999; Opitek et al., 1997).

[0394] Several recent methods allow for the quantitation of proteins by mass spectrometry. For example, stable (e.g., non-radioactive) heavier isotopes of carbon (.sup.13C) or nitrogen (.sup.15N) can be incorporated into one sample while the other one can be labeled with corresponding light isotopes (e.g. .sup.12C and .sup.14N). The two samples are mixed before the analysis. Peptides derived from the different samples can be distinguished due to their mass difference. The ratio of their peak intensities corresponds to the relative abundance ratio of the peptides (and proteins). The most popular methods for isotope labeling are SILAC (stable isotope labeling by amino acids in cell culture), trypsin-catalyzed .sup.18O labeling, ICAT (isotope coded affinity tagging), iTRAQ (isobaric tags for relative and absolute quantitation). "Semi-quantitative" mass spectrometry can be performed without labeling of samples. Typically, this is done with MALDI analysis (in linear mode). The peak intensity, or the peak area, from individual molecules (typically proteins) is here correlated to the amount of protein in the sample. However, the individual signal depends on the primary structure of the protein, on the complexity of the sample, and on the settings of the instrument. Other types of "label-free" quantitative mass spectrometry, uses the spectral counts (or peptide counts) of digested proteins as a means for determining relative protein amounts.

[0395] In one embodiment, any one or more of the biomarkers of the invention (e.g., filamin A alone or in combination with any one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) can be identified and quantified from a complex biological sample using mass spectroscopy in accordance with the following exemplary method, which is not intended to limit the invention or the use of other mass spectrometry-based methods.

[0396] In the first step of this embodiment, (A) a biological sample, e.g., a biological sample suspected of having prostate cancer, which comprises a complex mixture of protein (including at least one biomarker of interest) is fragmented and labeled with a stable isotope X. (B) Next, a known amount of an internal standard is added to the biological sample, wherein the internal standard is prepared by fragmenting a standard protein that is identical to the at least one target biomarker of interest, and labeled with a stable isotope Y. (C) This sample obtained is then introduced in an LC-MS/MS device, and multiple reaction monitoring (MRM) analysis is performed using MRM transitions selected for the internal standard to obtain an MRM chromatogram. (D) The MRM chromatogram is then viewed to identify a target peptide biomarker derived from the biological sample that shows the same retention time as a peptide derived from the internal standard (an internal standard peptide), and quantifying the target protein biomarker in the test sample by comparing the peak area of the internal standard peptide with the peak area of the target peptide biomarker.

[0397] Any suitable biological sample may be used as a starting point for LC-MS/MS/MRM analysis, including biological samples derived blood, urine, saliva, hair, cells, cell tissues, biopsy materials, and treated products thereof; and protein-containing samples prepared by gene recombination techniques.

[0398] Each of the above steps (A) to (D) is described further below.

[0399] Step (A) (Fragmentation and Labeling). In step (A), the target protein biomarker is fragmented to a collection of peptides, which is subsequently labeled with a stable isotope X. To fragment the target protein, for example, methods of digesting the target protein with a proteolytic enzyme (protease) such as trypsin, and chemical cleavage methods, such as a method using cyanogen bromide, can be used. Digestion by protease is preferable. It is known that a given mole quantity of protein produces the same mole quantity for each tryptic peptide cleavage product if the proteolytic digest is allowed to proceed to completion. Thus, determining the mole quantity of tryptic peptide to a given protein allows determination of the mole quantity of the original protein in the sample. Absolute quantification of the target protein can be accomplished by determining the absolute amount of the target protein-derived peptides contained in the protease digestion (collection of peptides). Accordingly, in order to allow the proteolytic digest to proceed to completion, reduction and alkylation treatments are preferably performed before protease digestion with trypsin to reduce and alkylate the disulfide bonds contained in the target protein.

[0400] Subsequently, the obtained digest (collection of peptides, comprising peptides of the target biomarker in the biological sample) is subjected to labeling with a stable isotope X. Examples of stable isotopes X include .sup.1H and .sup.2H for hydrogen atoms, .sup.12C and .sup.13C for carbon atoms, and .sup.14N and .sup.15N for nitrogen atoms. Any isotope can be suitably selected therefrom. Labeling by a stable isotope X can be performed by reacting the digest (collection of peptides) with a reagent containing the stable isotope.

[0401] Preferable examples of such reagents that are commercially available include mTRAQ (registered trademark) (produced by Applied Biosystems), which is an amine-specific stable isotope reagent kit. mTRAQ is composed of 2 or 3 types of reagents (mTRAQ-light and mTRAQ-heavy; or mTRAQ-DO, mTRAQ-D4, and mTRAQ-D8) that have a constant mass difference therebetween as a result of isotope-labeling, and that are bound to the N-terminus of a peptide or the primary amine of a lysine residue.

[0402] Step (B) (Addition of the Internal Standard). In step (B), a known amount of an internal standard is added to the sample obtained in step (A). The internal standard used herein is a digest (collection of peptides) obtained by fragmenting a protein (standard protein) consisting of the same amino acid sequence as the target protein (target biomarker) to be measured, and labeling the obtained digest (collection of peptides) with a stable isotope Y. The fragmentation treatment can be performed in the same manner as above for the target protein. Labeling with a stable isotope Y can also be performed in the same manner as above for the target protein. However, the stable isotope Y used herein must be an isotope that has a mass different from that of the stable isotope X used for labeling the target protein digest. For example, in the case of using the aforementioned mTRAQ (registered trademark) (produced by Applied Biosystems), when mTRAQ-light is used to label a target protein digest, mTRAQ-heavy should be used to label a standard protein digest.

[0403] Step (C) (LC-MS/MS and MRM Analysis). In step (C), the sample obtained in step (B) is first placed in an LC-MS/MS device, and then multiple reaction monitoring (MRM) analysis is performed using MRM transitions selected for the internal standard. By LC (liquid chromatography) using the LC-MS/MS device, the sample (collection of peptides labeled with a stable isotope) obtained in step (B) is separated first by one-dimensional or multi-dimensional high-performance liquid chromatography. Specific examples of such liquid chromatography include cation exchange chromatography, in which separation is conducted by utilizing electric charge difference between peptides; and reversed-phase chromatography, in which separation is conducted by utilizing hydrophobicity difference between peptides. Both of these methods may be used in combination.

[0404] Subsequently, each of the separated peptides is subjected to tandem mass spectrometry by using a tandem mass spectrometer (MS/MS spectrometer) comprising two mass spectrometers connected in series. The use of such a mass spectrometer enables the detection of several fmol levels of a target protein. Furthermore, MS/MS analysis enables the analysis of internal sequence information on peptides, thus enabling identification without false positives. Other types of MS analyzers may also be used, including magnetic sector mass spectrometers (Sector MS), quadrupole mass spectrometers (QMS), time-of-flight mass spectrometers (TOFMS), and Fourier transform ion cyclotron resonance mass spectrometers (FT-ICRMS), and combinations of these analyzers.

[0405] Subsequently, the obtained data are put through a search engine to perform a spectral assignment and to list the peptides experimentally detected for each protein. The detected peptides are preferably grouped for each protein, and preferably at least three fragments having an m/z value larger than that of the precursor ion and at least three fragments with an m/z value of, preferably, 500 or more are selected from each MS/MS spectrum in descending order of signal strength on the spectrum. From these, two or more fragments are selected in descending order of strength, and the average of the strength is defined as the expected sensitivity of the MRR transitions. When a plurality of peptides is detected from one protein, at least two peptides with the highest sensitivity are selected as standard peptides using the expected sensitivity as an index.

[0406] Step (D) (Quantification of the Target Protein in the Test Sample). Step (D) comprises identifying, in the MRM chromatogram detected in step (C), a peptide derived from the target protein (a target biomarker of interest) that shows the same retention time as a peptide derived from the internal standard (an internal standard peptide), and quantifying the target protein in the test sample by comparing the peak area of the internal standard peptide with the peak area of the target peptide. The target protein can be quantified by utilizing a calibration curve of the standard protein prepared beforehand.

[0407] The calibration curve can be prepared by the following method. First, a recombinant protein consisting of an amino acid sequence that is identical to that of the target biomarker protein is digested with a protease such as trypsin, as described above. Subsequently, precursor-fragment transition selection standards (PFTS) of a known concentration are individually labeled with two different types of stable isotopes (i.e., one is labeled with a stable isomer used to label an internal standard peptide (labeled with IS), whereas the other is labeled with a stable isomer used to label a target peptide (labeled with T). A plurality of samples are produced by blending a certain amount of the IS-labeled PTFS with various concentrations of the T-labeled PTFS. These samples are placed in the aforementioned LC-MS/MS device to perform MRM analysis. The area ratio of the T-labeled PTFS to the IS-labeled PTFS (T-labeled PTFS/IS-labeled PTFS) on the obtained MRM chromatogram is plotted against the amount of the T-labeled PTFS to prepare a calibration curve. The absolute amount of the target protein contained in the test sample can be calculated by reference to the calibration curve.

[0408] 3. Antibodies and Labels (e.g., Fluorescent Moieties, Dyes)

[0409] In some embodiments, the invention provides methods and compositions that include labels for the highly sensitive detection and quantitation of the biomolecules of the invention, e.g., filamin A alone or in combination with at least one other prostate cancer related marker selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSA, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. One skilled in the art will recognize that many strategies can be used for labeling target molecules to enable their detection or discrimination in a mixture of particles (e.g., labeled anti-filamin A antibody or labeled secondary antibody, or labeled oligonucleotide probe that specifically hybridizes to filamin A mRNA). The labels may be attached by any known means, including methods that utilize non-specific or specific interactions of label and target. Labels may provide a detectable signal or affect the mobility of the particle in an electric field. In addition, labeling can be accomplished directly or through binding partners.

[0410] In some embodiments, the label comprises a binding partner that binds to the biomarker of interest, where the binding partner is attached to a fluorescent moiety. The compositions and methods of the invention may utilize highly fluorescent moieties, e.g., a moiety capable of emitting at least about 200 photons when simulated by a laser emitting light at the excitation wavelength of the moiety, wherein the laser is focused on a spot not less than about 5 microns in diameter that contains the moiety, and wherein the total energy directed at the spot by the laser is no more than about 3 microJoules. Moieties suitable for the compositions and methods of the invention are described in more detail below.

[0411] In some embodiments, the invention provides a label for detecting a biological molecule comprising a binding partner for the biological molecule that is attached to a fluorescent moiety, wherein the fluorescent moiety is capable of emitting at least about 200 photons when simulated by a laser emitting light at the excitation wavelength of the moiety, wherein the laser is focused on a spot not less than about 5 microns in diameter that contains the moiety, and wherein the total energy directed at the spot by the laser is no more than about 3 microJoules. In some embodiments, the moiety comprises a plurality of fluorescent entities, e.g., about 2 to 4, 2 to 5, 2 to 6, 2 to 7, 2 to 8, 2 to 9, 2 to 10, or about 3 to 5, 3 to 6, 3 to 7, 3 to 8, 3 to 9, or 3 to 10 fluorescent entities. In some embodiments, the moiety comprises about 2 to 4 fluorescent entities. In some embodiments, the biological molecule is a protein or a small molecule. In some embodiments, the biological molecule is a protein. The fluorescent entities can be fluorescent dye molecules. In some embodiments, the fluorescent dye molecules comprise at least one substituted indolium ring system in which the substituent on the 3-carbon of the indolium ring contains a chemically reactive group or a conjugated substance. In some embodiments, the dye molecules are Alexa Fluor molecules selected from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 647, Alexa Fluor 680 or Alexa Fluor 700. In some embodiments, the dye molecules are Alexa Fluor molecules selected from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 680 or Alexa Fluor 700. In some embodiments, the dye molecules are Alexa Fluor 647 dye molecules. In some embodiments, the dye molecules comprise a first type and a second type of dye molecules, e.g., two different Alexa Fluor molecules, e.g., where the first type and second type of dye molecules have different emission spectra. The ratio of the number of first type to second type of dye molecule can be, e.g., 4 to 1, 3 to 1, 2 to 1, 1 to 1, 1 to 2, 1 to 3 or 1 to 4. The binding partner can be, e.g., an antibody.

[0412] In some embodiments, the invention provides a label for the detection of a biological marker of the invention, wherein the label comprises a binding partner for the marker and a fluorescent moiety, wherein the fluorescent moiety is capable of emitting at least about 200 photons when simulated by a laser emitting light at the excitation wavelength of the moiety, wherein the laser is focused on a spot not less than about 5 microns in diameter that contains the moiety, and wherein the total energy directed at the spot by the laser is no more than about 3 microJoules. In some embodiments, the fluorescent moiety comprises a fluorescent molecule. In some embodiments, the fluorescent moiety comprises a plurality of fluorescent molecules, e.g., about 2 to 10, 2 to 8, 2 to 6, 2 to 4, 3 to 10, 3 to 8, or 3 to 6 fluorescent molecules. In some embodiments, the label comprises about 2 to 4 fluorescent molecules. In some embodiments, the fluorescent dye molecules comprise at least one substituted indolium ring system in which the substituent on the 3-carbon of the indolium ring contains a chemically reactive group or a conjugated substance. In some embodiments, the fluorescent molecules are selected from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 647, Alexa Fluor 680 or Alexa Fluor 700. In some embodiments, the fluorescent molecules are selected from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 680 or Alexa Fluor 700. In some embodiments, the fluorescent molecules are Alexa Fluor 647 molecules. In some embodiments, the binding partner comprises an antibody. In some embodiments, the antibody is a monoclonal antibody. In other embodiments, the antibody is a polyclonal antibody.

[0413] In various embodiments, the binding partner for detecting a biomarker of interest, e.g., filamin A or filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3 and PSA, is an antibody or antigen-binding fragment thereof. The term "antibody," as used herein, is a broad term and is used in its ordinary sense, including, without limitation, to refer to naturally occurring antibodies as well as non-naturally occurring antibodies, including, for example, single chain antibodies, chimeric, bifunctional and humanized antibodies, as well as antigen-binding fragments thereof. An "antigen-binding fragment" of an antibody refers to the part of the antibody that participates in antigen binding. The antigen binding site is formed by amino acid residues of the N-terminal variable ("V") regions of the heavy ("H") and light ("L") chains. It will be appreciated that the choice of epitope or region of the molecule to which the antibody is raised will determine its specificity, e.g., for various forms of the molecule, if present, or for total (e.g., all, or substantially all of the molecule).

[0414] Methods for producing antibodies are well-established. One skilled in the art will recognize that many procedures are available for the production of antibodies, for example, as described in Antibodies, A Laboratory Manual, Ed Harlow and David Lane, Cold Spring Harbor Laboratory (1988), Cold Spring Harbor, N.Y. One skilled in the art will also appreciate that binding fragments or Fab fragments which mimic antibodies can also be prepared from genetic information by various procedures (Antibody Engineering: A Practical Approach (Borrebaeck, C., ed.), 1995, Oxford University Press, Oxford; J. Immunol. 149, 3914-3920 (1992)). Monoclonal and polyclonal antibodies to molecules, e.g., proteins, and markers also commercially available (R and D Systems, Minneapolis, Minn.; HyTest, HyTest Ltd., Turku Finland; Abcam Inc., Cambridge, Mass., USA, Life Diagnostics, Inc., West Chester, Pa., USA; Fitzgerald Industries International, Inc., Concord, Mass. 01742-3049 USA; BiosPacific, Emeryville, Calif.).

[0415] In some embodiments, the antibody is a polyclonal antibody. In other embodiments, the antibody is a monoclonal antibody.

[0416] Antibodies may be prepared by any of a variety of techniques known to those of ordinary skill in the art (see, for example, Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988). In general, antibodies can be produced by cell culture techniques, including the generation of monoclonal antibodies as described herein, or via transfection of antibody genes into suitable bacterial or mammalian cell hosts, in order to allow for the production of recombinant antibodies.

[0417] Monoclonal antibodies may be prepared using hybridoma methods, such as the technique of Kohler and Milstein (Eur. J. Immunol. 6:511-519, 1976), and improvements thereto. These methods involve the preparation of immortal cell lines capable of producing antibodies having the desired specificity. Monoclonal antibodies may also be made by recombinant DNA methods, such as those described in U.S. Pat. No. 4,816,567. DNA encoding antibodies employed in the disclosed methods may be isolated and sequenced using conventional procedures. Recombinant antibodies, antibody fragments, and/or fusions thereof, can be expressed in vitro or in prokaryotic cells (e.g. bacteria) or eukaryotic cells (e.g. yeast, insect or mammalian cells) and further purified as necessary using well known methods.

[0418] More particularly, monoclonal antibodies (MAbs) may be readily prepared through use of well-known techniques, such as those exemplified in U.S. Pat. No. 4,196,265, incorporated herein by reference. Typically, this technique involves immunizing a suitable animal with a selected immunogen composition, e.g., a purified or partially purified expressed protein, polypeptide or peptide. The immunizing composition is administered in a manner effective to stimulate antibody producing cells. The methods for generating monoclonal antibodies (MAbs) generally begin along the same lines as those for preparing polyclonal antibodies. Rodents such as mice and rats are preferred animals, however, the use of rabbit, sheep or frog cells is also possible. The use of rats may provide certain advantages (Goding, 1986, pp. 60-61), but mice are preferred, with the BALB/c mouse being most preferred as this is most routinely used and generally gives a higher percentage of stable fusions.

[0419] The animals are injected with antigen as described above. The antigen may be coupled to carrier molecules such as keyhole limpet hemocyanin if necessary. The antigen would typically be mixed with adjuvant, such as Freund's complete or incomplete adjuvant. Booster injections with the same antigen would occur at approximately two-week intervals. Following immunization, somatic cells with the potential for producing antibodies, specifically B lymphocytes (B cells), are selected for use in the MAb generating protocol. These cells may be obtained from biopsied spleens, tonsils or lymph nodes, or from a peripheral blood sample. Spleen cells and peripheral blood cells are preferred, the former because they are a rich source of antibody-producing cells that are in the dividing plasmablast stage, and the latter because peripheral blood is easily accessible. Often, a panel of animals will have been immunized and the spleen of the animal with the highest antibody titer will be removed and the spleen lymphocytes obtained by homogenizing the spleen with a syringe.

[0420] The antibody-producing B lymphocytes from the immunized animal are then fused with cells of an immortal myeloma cell, generally one of the same species as the animal that was immunized. Myeloma cell lines suited for use in hybridoma-producing fusion procedures preferably are non-antibody-producing, have high fusion efficiency, and enzyme deficiencies that render then incapable of growing in certain selective media which support the growth of only the desired fused cells (hybridomas).

[0421] The selected hybridomas would then be serially diluted and cloned into individual antibody-producing cell lines, which clones may then be propagated indefinitely to provide MAbs. The cell lines may be exploited for MAb production in two basic ways. A sample of the hybridoma may be injected (often into the peritoneal cavity) into a histocompatible animal of the type that was used to provide the somatic and myeloma cells for the original fusion. The injected animal develops tumors secreting the specific monoclonal antibody produced by the fused cell hybrid. The body fluids of the animal, such as serum or ascites fluid, may then be tapped to provide MAbs in high concentration. The individual cell lines also may be cultured in vitro, where the MAbs are naturally secreted into the culture medium from which they may be readily obtained in high concentrations. MAbs produced by either means may be further purified, if desired, using filtration, centrifugation and various chromatographic methods such as HPLC or affinity chromatography.

[0422] Large amounts of the monoclonal antibodies of the present invention also may be obtained by multiplying hybridoma cells in vivo. Cell clones are injected into mammals which are histocompatible with the parent cells, e.g., syngeneic mice, to cause growth of antibody-producing tumors. Optionally, the animals are primed with a hydrocarbon, especially oils such as pristane (tetramethylpentadecane) prior to injection.

[0423] In accordance with the present invention, fragments of the monoclonal antibody of the invention may be obtained from the monoclonal antibody produced as described above, by methods which include digestion with enzymes such as pepsin or papain and/or cleavage of disulfide bonds by chemical reduction. Alternatively, monoclonal antibody fragments encompassed by the present invention may be synthesized using an automated peptide synthesizer.

[0424] Antibodies may also be derived from a recombinant antibody library that is based on amino acid sequences that have been designed in silico and encoded by polynucleotides that are synthetically generated. Methods for designing and obtaining in silico-created sequences are known in the art (Knappik et al., J. Mol. Biol. 296:254:57-86, 2000; Krebs et al., J. Immunol. Methods 254:67-84, 2001; U.S. Pat. No. 6,300,064).

[0425] Digestion of antibodies to produce antigen-binding fragments thereof can be performed using techniques well known in the art. For example, the proteolytic enzyme papain preferentially cleaves IgG molecules to yield several fragments, two of which (the "F(ab)" fragments) each comprise a covalent heterodimer that includes an intact antigen-binding site. The enzyme pepsin is able to cleave IgG molecules to provide several fragments, including the "F(ab').sub.2" fragment, which comprises both antigen-binding sites. "Fv" fragments can be produced by preferential proteolytic cleavage of an IgM, IgG or IgA immunoglobulin molecule, but are more commonly derived using recombinant techniques known in the art. The Fv fragment includes a non-covalent V.sub.H::V.sub.L heterodimer including an antigen-binding site which retains much of the antigen recognition and binding capabilities of the native antibody molecule (Inbar et al., Proc. Natl. Acad. Sci. USA 69:2659-2662 (1972); Hochman et al., Biochem. 15:2706-2710 (1976); and Ehrlich et al., Biochem. 19:4091-4096 (1980)).

[0426] Antibody fragments that specifically bind to the polypeptide biomarkers disclosed herein can also be isolated from a library of scFvs using known techniques, such as those described in U.S. Pat. No. 5,885,793.

[0427] A wide variety of expression systems are available in the art for the production of antibody fragments, including Fab fragments, scFv, VL and VHs. For example, expression systems of both prokaryotic and eukaryotic origin may be used for the large-scale production of antibody fragments. Particularly advantageous are expression systems that permit the secretion of large amounts of antibody fragments into the culture medium. Eukaryotic expression systems for large-scale production of antibody fragments and antibody fusion proteins have been described that are based on mammalian cells, insect cells, plants, transgenic animals, and lower eukaryotes. For example, the cost-effective, large-scale production of antibody fragments can be achieved in yeast fermentation systems. Large-scale fermentation of these organisms is well known in the art and is currently used for bulk production of several recombinant proteins.

[0428] Antibodies that bind to the polypeptide biomarkers employed in the present methods are well known to those of skill in the art and in some cases are available commercially or can be obtained without undue experimentation.

[0429] In still other embodiments, particularly where oligonucleotides are used as binding partners to detect and hybridize to mRNA biomarkers or other nucleic acid based biomarkers, the binding partners (e.g., oligonucleotides) can comprise a label, e.g., a fluorescent moiety or dye. In addition, any binding partner of the invention, e.g., an antibody, can also be labeled with a fluorescent moiety. The fluorescence of the moiety will be sufficient to allow detection in a single molecule detector, such as the single molecule detectors described herein. A "fluorescent moiety," as that term is used herein, includes one or more fluorescent entities whose total fluorescence is such that the moiety may be detected in the single molecule detectors described herein. Thus, a fluorescent moiety may comprise a single entity (e.g., a Quantum Dot or fluorescent molecule) or a plurality of entities (e.g., a plurality of fluorescent molecules). It will be appreciated that when "moiety," as that term is used herein, refers to a group of fluorescent entities, e.g., a plurality of fluorescent dye molecules, each individual entity may be attached to the binding partner separately or the entities may be attached together, as long as the entities as a group provide sufficient fluorescence to be detected.

[0430] Typically, the fluorescence of the moiety involves a combination of quantum efficiency and lack of photobleaching sufficient that the moiety is detectable above background levels in a single molecule detector, with the consistency necessary for the desired limit of detection, accuracy, and precision of the assay. For example, in some embodiments, the fluorescence of the fluorescent moiety is such that it allows detection and/or quantitation of a molecule, e.g., a marker, at a limit of detection of less than about 10, 5, 4, 3, 2, 1, 0.1, 0.01, 0.001, 0.00001, or 0.000001 pg/ml and with a coefficient of variation of less than about 20, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, 3, 2, 1% or less, e.g., about 10% or less, in the instruments described herein. In some embodiments, the fluorescence of the fluorescent moiety is such that it allows detection and/or quantitation of a molecule, e.g., a marker, at a limit of detection of less than about 5, 1, 0.5, 0.1, 0.05, 0.01, 0.005, 0.001 pg/ml and with a coefficient of variation of less than about 10%, in the instruments described herein. "Limit of detection," or LoD, as those terms are used herein, includes the lowest concentration at which one can identify a sample as containing a molecule of the substance of interest, e.g., the first non-zero value. It can be defined by the variability of zeros and the slope of the standard curve. For example, the limit of detection of an assay may be determined by running a standard curve, determining the standard curve zero value, and adding 2 standard deviations to that value. A concentration of the substance of interest that produces a signal equal to this value is the "lower limit of detection" concentration.

[0431] Furthermore, the moiety has properties that are consistent with its use in the assay of choice. In some embodiments, the assay is an immunoassay, where the fluorescent moiety is attached to an antibody; the moiety must have properties such that it does not aggregate with other antibodies or proteins, or experiences no more aggregation than is consistent with the required accuracy and precision of the assay. In some embodiments, fluorescent moieties that are preferred are fluorescent moieties, e.g., dye molecules that have a combination of 1) high absorption coefficient; 2) high quantum yield; 3) high photostability (low photobleaching); and 4) compatibility with labeling the molecule of interest (e.g., protein) so that it may be analyzed using the analyzers and systems of the invention (e.g., does not cause precipitation of the protein of interest, or precipitation of a protein to which the moiety has been attached).

[0432] Any suitable fluorescent moiety may be used. Examples include, but are not limited to, Alexa Fluor dyes (Molecular Probes, Eugene, Oreg.). The Alexa Fluor dyes are disclosed in U.S. Pat. Nos. 6,977,305; 6,974,874; 6,130,101; and 6,974,305 which are herein incorporated by reference in their entirety. Some embodiments of the invention utilize a dye chosen from the group consisting of Alexa Fluor 647, Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 555, Alexa Fluor 610, Alexa Fluor 680, Alexa Fluor 700, and Alexa Fluor 750. Some embodiments of the invention utilize a dye chosen from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 647, Alexa Fluor 700 and Alexa Fluor 750. Some embodiments of the invention utilize a dye chosen from the group consisting of Alexa Fluor 488, Alexa Fluor 532, Alexa Fluor 555, Alexa Fluor 610, Alexa Fluor 680, Alexa Fluor 700, and Alexa Fluor 750. Some embodiments of the invention utilize the Alexa Fluor 647 molecule, which has an absorption maximum between about 650 and 660 nm and an emission maximum between about 660 and 670 nm. The Alexa Fluor 647 dye is used alone or in combination with other Alexa Fluor dyes.

[0433] In some embodiments, the fluorescent label moiety that is used to detect a biomarker in a sample using the analyzer systems of the invention is a quantum dot. Quantum dots (QDs), also known as semiconductor nanocrystals or artificial atoms, are semiconductor crystals that contain anywhere between 100 to 1,000 electrons and range from 2-10 nm. Some QDs can be between 10-20 nm in diameter. QDs have high quantum yields, which makes them particularly useful for optical applications. QDs are fluorophores that fluoresce by forming excitons, which are similar to the excited state of traditional fluorophores, but have much longer lifetimes of up to 200 nanoseconds. This property provides QDs with low photobleaching. The energy level of QDs can be controlled by changing the size and shape of the QD, and the depth of the QDs' potential. One optical feature of small excitonic QDs is coloration, which is determined by the size of the dot. The larger the dot, the redder, or more towards the red end of the spectrum the fluorescence. The smaller the dot, the bluer or more towards the blue end it is. The bandgap energy that determines the energy and hence the color of the fluoresced light is inversely proportional to the square of the size of the QD. Larger QDs have more energy levels which are more closely spaced, thus allowing the QD to absorb photons containing less energy, i.e., those closer to the red end of the spectrum. Because the emission frequency of a dot is dependent on the bandgap, it is possible to control the output wavelength of a dot with extreme precision. In some embodiments the protein that is detected with the single molecule analyzer system is labeled with a QD. In some embodiments, the single molecule analyzer is used to detect a protein labeled with one QD and using a filter to allow for the detection of different proteins at different wavelengths.

F. Isolated Biomarkers

[0434] 1. Isolated Polypeptide Biomarkers

[0435] One aspect of the invention pertains to isolated marker proteins and biologically active portions thereof, as well as polypeptide fragments suitable for use as immunogens to raise antibodies directed against a marker protein or a fragment thereof. In one embodiment, the native marker protein can be isolated from cells or tissue sources by an appropriate purification scheme using standard protein purification techniques. In another embodiment, a protein or peptide comprising the whole or a segment of the marker protein is produced by recombinant DNA techniques. Alternative to recombinant expression, such protein or peptide can be synthesized chemically using standard peptide synthesis techniques.

[0436] An "isolated" or "purified" protein or biologically active portion thereof is substantially free of cellular material or other contaminating proteins from the cell or tissue source from which the protein is derived, or substantially free of chemical precursors or other chemicals when chemically synthesized. The language "substantially free of cellular material" includes preparations of protein in which the protein is separated from cellular components of the cells from which it is isolated or recombinantly produced. Thus, protein that is substantially free of cellular material includes preparations of protein having less than about 30%, 20%, 10%, or 5% (by dry weight) of heterologous protein (also referred to herein as a "contaminating protein"). When the protein or biologically active portion thereof is recombinantly produced, it is also preferably substantially free of culture medium, i.e., culture medium represents less than about 20%, 10%, or 5% of the volume of the protein preparation. When the protein is produced by chemical synthesis, it is preferably substantially free of chemical precursors or other chemicals, i.e., it is separated from chemical precursors or other chemicals which are involved in the synthesis of the protein. Accordingly such preparations of the protein have less than about 30%, 20%, 10%, 5% (by dry weight) of chemical precursors or compounds other than the polypeptide of interest.

[0437] Biologically active portions of a marker protein include polypeptides comprising amino acid sequences sufficiently identical to or derived from the amino acid sequence of the marker protein, which include fewer amino acids than the full length protein, and exhibit at least one activity of the corresponding full-length protein. Typically, biologically active portions comprise a domain or motif with at least one activity of the corresponding full-length protein. A biologically active portion of a marker protein of the invention can be a polypeptide which is, for example, 10, 25, 50, 100 or more amino acids in length. Moreover, other biologically active portions, in which other regions of the marker protein are deleted, can be prepared by recombinant techniques and evaluated for one or more of the functional activities of the native form of the marker protein.

[0438] Preferred marker proteins are encoded by nucleotide sequences provided in the sequence listing. Other useful proteins are substantially identical (e.g., at least about 40%, preferably 50%, 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%) to one of these sequences and retain the functional activity of the corresponding naturally-occurring marker protein yet differ in amino acid sequence due to natural allelic variation or mutagenesis.

[0439] To determine the percent identity of two amino acid sequences or of two nucleic acids, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in the sequence of a first amino acid or nucleic acid sequence for optimal alignment with a second amino or nucleic acid sequence). The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position. Preferably, the percent identity between the two sequences is calculated using a global alignment. Alternatively, the percent identity between the two sequences is calculated using a local alignment. The percent identity between the two sequences is a function of the number of identical positions shared by the sequences (i.e., % identity=# of identical positions/total # of positions (e.g., overlapping positions).times.100). In one embodiment the two sequences are the same length. In another embodiment, the two sequences are not the same length.

[0440] The determination of percent identity between two sequences can be accomplished using a mathematical algorithm. A preferred, non-limiting example of a mathematical algorithm utilized for the comparison of two sequences is the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87:2264-2268, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-5877. Such an algorithm is incorporated into the BLASTN and BLASTX programs of Altschul, et al. (1990) J. Mol. Biol. 215:403-410. BLAST nucleotide searches can be performed with the BLASTN program, score=100, wordlength=12 to obtain nucleotide sequences homologous to a nucleic acid molecules of the invention. BLAST protein searches can be performed with the BLASTP program, score=50, wordlength=3 to obtain amino acid sequences homologous to a protein molecules of the invention. To obtain gapped alignments for comparison purposes, a newer version of the BLAST algorithm called Gapped BLAST can be utilized as described in Altschul et al. (1997) Nucleic Acids Res. 25:3389-3402, which is able to perform gapped local alignments for the programs BLASTN, BLASTP and BLASTX. Alternatively, PSI-Blast can be used to perform an iterated search which detects distant relationships between molecules. When utilizing BLAST, Gapped BLAST, and PSI-Blast programs, the default parameters of the respective programs (e.g., BLASTX and BLASTN) can be used. See the NCBI website. Another preferred, non-limiting example of a mathematical algorithm utilized for the comparison of sequences is the algorithm of Myers and Miller, (1988) CABIOS 4:11-17. Such an algorithm is incorporated into the ALIGN program (version 2.0) which is part of the GCG sequence alignment software package. When utilizing the ALIGN program for comparing amino acid sequences, a PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4 can be used. Yet another useful algorithm for identifying regions of local sequence similarity and alignment is the FASTA algorithm as described in Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85:2444-2448. When using the FASTA algorithm for comparing nucleotide or amino acid sequences, a PAM120 weight residue table can, for example, be used with a k-tuple value of 2.

[0441] The percent identity between two sequences can be determined using techniques similar to those described above, with or without allowing gaps. In calculating percent identity, only exact matches are counted.

[0442] Another aspect of the invention pertains to antibodies directed against a protein of the invention. In preferred embodiments, the antibodies specifically bind a marker protein or a fragment thereof. The terms "antibody" and "antibodies" as used interchangeably herein refer to immunoglobulin molecules as well as fragments and derivatives thereof that comprise an immunologically active portion of an immunoglobulin molecule, (i.e., such a portion contains an antigen binding site which specifically binds an antigen, such as a marker protein, e.g., an epitope of a marker protein). An antibody which specifically binds to a protein of the invention is an antibody which binds the protein, but does not substantially bind other molecules in a sample, e.g., a biological sample, which naturally contains the protein. Examples of an immunologically active portion of an immunoglobulin molecule include, but are not limited to, single-chain antibodies (scAb), F(ab) and F(ab').sub.2 fragments.

[0443] An isolated protein of the invention or a fragment thereof can be used as an immunogen to generate antibodies. The full-length protein can be used or, alternatively, the invention provides antigenic peptide fragments for use as immunogens. The antigenic peptide of a protein of the invention comprises at least 8 (preferably 10, 15, 20, or 30 or more) amino acid residues of the amino acid sequence of one of the proteins of the invention, and encompasses at least one epitope of the protein such that an antibody raised against the peptide forms a specific immune complex with the protein. Preferred epitopes encompassed by the antigenic peptide are regions that are located on the surface of the protein, e.g., hydrophilic regions. Hydrophobicity sequence analysis, hydrophilicity sequence analysis, or similar analyses can be used to identify hydrophilic regions. In preferred embodiments, an isolated marker protein or fragment thereof is used as an immunogen.

[0444] The invention provides polyclonal and monoclonal antibodies. The term "monoclonal antibody" or "monoclonal antibody composition", as used herein, refers to a population of antibody molecules that contain only one species of an antigen binding site capable of immunoreacting with a particular epitope. Preferred polyclonal and monoclonal antibody compositions are ones that have been selected for antibodies directed against a protein of the invention. Particularly preferred polyclonal and monoclonal antibody preparations are ones that contain only antibodies directed against a marker protein or fragment thereof. Methods of making polyclonal, monoclonal, and recombinant antibody and antibody fragments are well known in the art.

[0445] 2. Isolated Nucleic Acid Biomarkers

[0446] One aspect of the invention pertains to isolated nucleic acid molecules, including nucleic acids which encode a marker protein or a portion thereof. Isolated nucleic acids of the invention also include nucleic acid molecules sufficient for use as hybridization probes to identify marker nucleic acid molecules, and fragments of marker nucleic acid molecules, e.g., those suitable for use as PCR primers for the amplification of a specific product or mutation of marker nucleic acid molecules. As used herein, the term "nucleic acid molecule" is intended to include DNA molecules (e.g., cDNA or genomic DNA) and RNA molecules (e.g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA.

[0447] An "isolated" nucleic acid molecule is one which is separated from other nucleic acid molecules which are present in the natural source of the nucleic acid molecule. In one embodiment, an "isolated" nucleic acid molecule (preferably a protein-encoding sequences) is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5' and 3' ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. For example, in various embodiments, the isolated nucleic acid molecule can contain less than about 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb or 0.1 kb of nucleotide sequences which naturally flank the nucleic acid molecule in genomic DNA of the cell from which the nucleic acid is derived. In another embodiment, an "isolated" nucleic acid molecule, such as a cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or substantially free of chemical precursors or other chemicals when chemically synthesized. A nucleic acid molecule that is substantially free of cellular material includes preparations having less than about 30%, 20%, 10%, or 5% of heterologous nucleic acid (also referred to herein as a "contaminating nucleic acid").

[0448] A nucleic acid molecule of the present invention can be isolated using standard molecular biology techniques and the sequence information in the database records described herein. Using all or a portion of such nucleic acid sequences, nucleic acid molecules of the invention can be isolated using standard hybridization and cloning techniques (e.g., as described in Sambrook et al., ed., Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).

[0449] A nucleic acid molecule of the invention can be amplified using cDNA, mRNA, or genomic DNA as a template and appropriate oligonucleotide primers according to standard PCR amplification techniques. The nucleic acid so amplified can be cloned into an appropriate vector and characterized by DNA sequence analysis. Furthermore, nucleotides corresponding to all or a portion of a nucleic acid molecule of the invention can be prepared by standard synthetic techniques, e.g., using an automated DNA synthesizer.

[0450] In another preferred embodiment, an isolated nucleic acid molecule of the invention comprises a nucleic acid molecule which has a nucleotide sequence complementary to the nucleotide sequence of a marker nucleic acid or to the nucleotide sequence of a nucleic acid encoding a marker protein. A nucleic acid molecule which is complementary to a given nucleotide sequence is one which is sufficiently complementary to the given nucleotide sequence that it can hybridize to the given nucleotide sequence thereby forming a stable duplex.

[0451] Moreover, a nucleic acid molecule of the invention can comprise only a portion of a nucleic acid sequence, wherein the full length nucleic acid sequence comprises a marker nucleic acid or which encodes a marker protein. Such nucleic acids can be used, for example, as a probe or primer. The probe/primer typically is used as one or more substantially purified oligonucleotides. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 15, more preferably at least about 25, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, or 400 or more consecutive nucleotides of a nucleic acid of the invention.

[0452] Probes based on the sequence of a nucleic acid molecule of the invention can be used to detect transcripts or genomic sequences corresponding to one or more markers of the invention. In certain embodiments, the probes hybridize to nucleic acid sequences that traverse splice junctions. The probe comprises a label group attached thereto, e.g., a radioisotope, a fluorescent compound, an enzyme, or an enzyme co-factor. Such probes can be used as part of a diagnostic test kit or panel for identifying cells or tissues which express or mis-express the protein, such as by measuring levels of a nucleic acid molecule encoding the protein in a sample of cells from a subject, e.g., detecting mRNA levels or determining whether a gene encoding the protein or its translational control sequences have been mutated or deleted.

[0453] The invention further encompasses nucleic acid molecules that differ, due to degeneracy of the genetic code, from the nucleotide sequence of nucleic acids encoding a marker protein (e.g., protein having the sequence provided in the sequence listing), and thus encode the same protein.

[0454] It will be appreciated by those skilled in the art that DNA sequence polymorphisms that lead to changes in the amino acid sequence can exist within a population (e.g., the human population). Such genetic polymorphisms can exist among individuals within a population due to natural allelic variation and changes known to occur in cancer. An allele is one of a group of genes which occur alternatively at a given genetic locus. In addition, it will be appreciated that DNA polymorphisms that affect RNA expression levels can also exist that may affect the overall expression level of that gene (e.g., by affecting regulation or degradation).

[0455] As used herein, the phrase "allelic variant" refers to a nucleotide sequence which occurs at a given locus or to a polypeptide encoded by the nucleotide sequence.

[0456] As used herein, the terms "gene" and "recombinant gene" refer to nucleic acid molecules comprising an open reading frame encoding a polypeptide corresponding to a marker of the invention. Such natural allelic variations can typically result in 1-5% variance in the nucleotide sequence of a given gene. Alternative alleles can be identified by sequencing the gene of interest in a number of different individuals. This can be readily carried out by using hybridization probes to identify the same genetic locus in a variety of individuals. Any and all such nucleotide variations and resulting amino acid polymorphisms or variations that are the result of natural allelic variation and that do not alter the functional activity are intended to be within the scope of the invention.

[0457] In another embodiment, an isolated nucleic acid molecule of the invention is at least 15, 20, 25, 30, 40, 60, 80, 100, 150, 200, 250, 300, 350, 400, 450, 550, 650, 700, 800, 900, 1000, 1200, 1400, 1600, 1800, 2000, 2200, 2400, 2600, 2800, 3000, 3500, 4000, 4500, or more nucleotides in length and hybridizes under stringent conditions to a marker nucleic acid or to a nucleic acid encoding a marker protein. As used herein, the term "hybridizes under stringent conditions" is intended to describe conditions for hybridization and washing under which nucleotide sequences at least 60% (65%, 70%, preferably 75%) identical to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found in sections 6.3.1-6.3.6 of Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989). A preferred, non-limiting example of stringent hybridization conditions are hybridization in 6.times. sodium chloride/sodium citrate (SSC) at about 45.degree. C., followed by one or more washes in 0.2.times.SSC, 0.1% SDS at 50-65.degree. C.

G. Biomarker Applications

[0458] The invention provides methods for diagnosing an abnormal prostate state, e.g., BPH or an oncological disease state, e.g., prostate cancer, in a subject. The invention further provides methods for prognosing or monitoring progression or monitoring response of an abnormal prostate state, e.g., BPH or prostate cancer, to a therapeutic treatment during active treatment or watchful waiting.

[0459] In one aspect, the present invention constitutes an application of diagnostic information obtainable by the methods of the invention in connection with analyzing, detecting, and/or measuring the prostate cancer biomarkers of the present invention, including filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, which goes well beyond the discovered correlation between prostate cancer and the biomarkers of the invention.

[0460] For example, when executing the methods of the invention for detecting and/or measuring a polypeptide biomarkers of the present invention, as described herein, one contacts a biological sample with a detection reagent, e.g, a monoclonal antibody, which selectively binds to the biomarker of interest, forming a protein-protein complex, which is then further detected either directly (if the antibody comprises a label) or indirectly (if a secondary detection reagent is used, e.g., a secondary antibody, which in turn is labeled). Thus, the method of the invention transforms the polypeptide markers of the invention to a protein-protein complex that comprises either a detectable primary antibody or a primary and further secondary antibody. Forming such protein-protein complexes is required in order to identify the presence of the biomarker of interest and necessarily changes the physical characteristics and properties of the biomarker of interest as a result of conducting the methods of the invention.

[0461] The same principal applies when conducting the methods of the invention for detecting nucleic acid biomarkers of the invention. In particular, when amplification methods are used to detect a biomarker of the invention (e.g., filamin A mRNA), the amplification process, in fact, results in the formation of a new population of amplicons--i.e., molecules that are newly synthesized and which were not present in the original biological sample, thereby physically transforming the biological sample. Similarly, when hybridization probes are used to detect a target biomarker, a physical new species of molecules is in effect created by the hybridization of the probes (optionally comprising a label) to the target biomarker mRNA (or other nucleic acid), which is then detected. Such polynucleotide products are effectively newly created or formed as a consequence of carrying out the method of the invention.

[0462] The invention provides, in one embodiment, methods for diagnosing an oncological disorder, e.g., prostate cancer. The methods of the present invention can be practiced in conjunction with any other method used by the skilled practitioner to prognose the occurrence or recurrence of an oncologic disorder and/or the survival of a subject being treated for an oncologic disorder. The diagnostic and prognostic methods provided herein can be used to determine if additional and/or more invasive tests or monitoring should be performed on a subject. It is understood that a disease as complex as an oncological disorder is rarely diagnosed using a single test. Therefore, it is understood that the diagnostic, prognostic, and monitoring methods provided herein are typically used in conjunction with other methods known in the art. For example, the methods of the invention may be performed in conjunction with a morphological or cytological analysis of the sample obtained from the subject, imaging analysis, and/or physical exam. Cytological methods would include immunohistochemical or immunofluorescence detection (and quantitation if appropriate) of any other molecular marker either by itself, in conjunction with other markers. Other methods would include detection of other markers by in situ PCR, or by extracting tissue and quantitating other markers by real time PCR. PCR is defined as polymerase chain reaction.

[0463] Methods for assessing tumor progression during watchful waiting or the efficacy of a treatment regimen, e.g., chemotherapy, radiation therapy, surgery, hormone therapy, or any other therapeutic approach useful for treating an oncologic disorder in a subject are also provided. In these methods the amount of marker in a pair of samples (a first sample obtained from the subject at an earlier time point or prior to the treatment regimen and a second sample obtained from the subject at a later time point, e.g., at a later time point when the subject has undergone at least a portion of the treatment regimen) is assessed. It is understood that the methods of the invention include obtaining and analyzing more than two samples (e.g., 3, 4, 5, 6, 7, 8, 9, or more samples) at regular or irregular intervals for assessment of marker levels. Pairwise comparisons can be made between consecutive or non-consecutive subject samples. Trends of marker levels and rates of change of marker levels can be analyzed for any two or more consecutive or non-consecutive subject samples.

[0464] The invention also provides a method for determining whether an oncologic disorder, e.g., prostate cancer, is aggressive. The method comprises determining the amount of a marker present in a sample and comparing the amount to a control amount of the marker present in one or more control samples, as defined in Definitions, thereby determining whether an oncologic disorder is aggressive. Marker levels can be compared to marker levels in samples obtained at different times from the same subject or marker levels from normal or abnormal prostate state subjects. A rapid increase in the level of marker may be indicative of a more aggressive cancer than a slow increase or no increase or change in the marker level.

[0465] The methods of the invention may also be used to select a compound that is capable of modulating, i.e., decreasing, the aggressiveness of an oncologic disorder, e.g., prostate cancer. In this method, a cancer cell is contacted with a test compound, and the ability of the test compound to modulate the expression and/or activity of a marker in the invention in the cancer cell is determined, thereby selecting a compound that is capable of modulating aggressiveness of an oncologic disorder.

[0466] Using the methods described herein, a variety of molecules, may be screened in order to identify molecules which modulate, e.g., increase or decrease the expression and/or activity of a marker of the invention, e.g., filamin A alone or filamin A in combination with one or more of PSA, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9), PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. Compounds so identified can be provided to a subject in order to inhibit the aggressiveness of an oncologic disorder in the subject, to prevent the recurrence of an oncologic disorder in the subject, or to treat an oncologic disorder in the subject.

[0467] The present invention pertains to the field of predictive medicine in which diagnostic assays, prognostic assays, pharmacogenomics, and monitoring clinical trials are used for prognostic (predictive) purposes to thereby treat an individual prophylactically. Accordingly, one aspect of the present invention relates to diagnostic assays for determining the level of expression of one or more marker proteins or nucleic acids, in order to determine whether an individual is at risk of developing a disease or disorder, such as, without limitation, an oncological disorder, e.g., prostate cancer. Such assays can be used for prognostic or predictive purposes to thereby prophylactically treat an individual prior to the onset of the disorder.

[0468] Yet another aspect of the invention pertains to monitoring the influence of agents (e.g., drugs or other therapeutic compounds) on the expression or activity of a biomarker of the invention in clinical trials. These and other applications are described in further detail in the following sections.

[0469] 1. Diagnostic Assays

[0470] An exemplary method for detecting the presence or absence or change of expression level of a marker protein or nucleic acid in a biological sample involves obtaining a biological sample (e.g. an oncological disorder-associated body fluid) from a test subject and contacting the biological sample with a compound or an agent capable of detecting the polypeptide or nucleic acid (e.g., mRNA, genomic DNA, or cDNA). The detection methods of the invention can thus be used to detect mRNA, protein, cDNA, or genomic DNA, for example, in a biological sample in vitro as well as in vivo.

[0471] Methods provided herein for detecting the presence, absence, change of expression level of a marker protein or nucleic acid in a biological sample include obtaining a biological sample from a subject that may or may not contain the marker protein or nucleic acid to be detected, contacting the sample with a marker-specific binding agent (i.e., one or more marker-specific binding agents) that is capable of forming a complex with the marker protein or nucleic acid to be detected, and contacting the sample with a detection reagent for detection of the marker--marker-specific binding agent complex, if formed. It is understood that the methods provided herein for detecting an expression level of a marker in a biological sample includes the steps to perform the assay. In certain embodiments of the detection methods, the level of the marker protein or nucleic acid in the sample is none or below the threshold for detection.

[0472] The methods include formation of either a transient or stable complex between the marker and the marker-specific binding agent. The methods require that the complex, if formed, be formed for sufficient time to allow a detection reagent to bind the complex and produce a detectable signal (e.g., fluorescent signal, a signal from a product of an enzymatic reaction, e.g., a peroxidase reaction, a phosphatase reaction, a beta-galactosidase reaction, or a polymerase reaction).

[0473] In certain embodiments, all markers are detected using the same method. In certain embodiments, all markers are detected using the same biological sample (e.g., same body fluid or tissue). In certain embodiments, different markers are detected using various methods. In certain embodiments, markers are detected in different biological samples.

[0474] 2. Protein Detection

[0475] In certain embodiments of the invention, the marker to be detected is a protein. Proteins are detected using a number of assays in which a complex between the marker protein to be detected and the marker specific binding agent would not occur naturally, for example, because one of the components is not a naturally occurring compound or the marker for detection and the marker specific binding agent are not from the same organism (e.g., human marker proteins detected using marker-specific binding antibodies from mouse, rat, or goat). In a preferred embodiment of the invention, the marker protein for detection is a human marker protein. In certain detection assays, the human markers for detection are bound by marker-specific, non-human antibodies, thus, the complex would not be formed in nature. The complex of the marker protein can be detected directly, e.g., by use of a labeled marker-specific antibody that binds directly to the marker, or by binding a further component to the marker--marker-specific antibody complex. In certain embodiments, the further component is a second marker-specific antibody capable of binding the marker at the same time as the first marker-specific antibody. In certain embodiments, the further component is a secondary antibody that binds to a marker-specific antibody, wherein the secondary antibody preferably linked to a detectable label (e.g., fluorescent label, enzymatic label, biotin). When the secondary antibody is linked to an enzymatic detectable label (e.g., a peroxidase, a phosphatase, a beta-galactosidase), the secondary antibody is detected by contacting the enzymatic detectable label with an appropriate substrate to produce a colorimetric, fluorescent, or other detectable, preferably quantitatively detectable, product. Antibodies for use in the methods of the invention can be polyclonal, however, in a preferred embodiment monoclonal antibodies are used. An intact antibody, or a fragment or derivative thereof (e.g., Fab or F(ab').sub.2) can be used in the methods of the invention. Such strategies of marker protein detection are used, for example, in ELISA, RIA, western blot, and immunofluorescence assay methods.

[0476] In certain detection assays, the marker present in the biological sample for detection is an enzyme and the detection reagent is an enzyme substrate. For example, the enzyme can be a protease and the substrate can be any protein that includes an appropriate protease cleavage site. Alternatively, the enzyme can be a kinase and the substrate can be any substrate for the kinase. In preferred embodiments, the substrate which forms a complex with the marker enzyme to be detected is not the substrate for the enzyme in a human subject.

[0477] In certain embodiments, the marker--marker-specific binding agent complex is attached to a solid support for detection of the marker. The complex can be formed on the substrate or formed prior to capture on the substrate. For example, in an ELISA, RIA, immunoprecipitation assay, western blot, immunofluorescence assay, in gel enzymatic assay the marker for detection is attached to a solid support, either directly or indirectly. In an ELISA, RIA, or immunofluorescence assay, the marker is typically attached indirectly to a solid support through an antibody or binding protein. In a western blot or immunofluorescence assay, the marker is typically attached directly to the solid support. For in-gel enzyme assays, the marker is resolved in a gel, typically an acrylamide gel, in which a substrate for the enzyme is integrated.

[0478] 3. Nucleic Acid Detection

[0479] In certain embodiments of the invention, the marker is a nucleic acid. Nucleic acids are detected using a number of assays in which a complex between the marker nucleic acid to be detected and a marker-specific probe would not occur naturally, for example, because one of the components is not a naturally occurring compound. In certain embodiments, the analyte comprises a nucleic acid and the probe comprises one or more synthetic single stranded nucleic acid molecules, e.g., a DNA molecule, a DNA-RNA hybrid, a PNA, or a modified nucleic acid molecule containing one or more artificial bases, sugars, or backbone moieties. In certain embodiments, the synthetic nucleic acid is a single stranded is a DNA molecule that includes a fluorescent label. In certain embodiments, the synthetic nucleic acid is a single stranded oligonucleotide molecule of about 12 to about 50 nucleotides in length. In certain embodiments, the nucleic acid to be detected is an mRNA and the complex formed is an mRNA hybridized to a single stranded DNA molecule that is complementary to the mRNA. In certain embodiments, an RNA is detected by generation of a DNA molecule (i.e., a cDNA molecule) first from the RNA template using the single stranded DNA that hybridizes to the RNA as a primer, e.g., a general poly-T primer to transcribe poly-A RNA. The cDNA can then be used as a template for an amplification reaction, e.g., PCR, primer extension assay, using a marker-specific probe. In certain embodiments, a labeled single stranded DNA can be hybridized to the RNA present in the sample for detection of the RNA by fluorescence in situ hybridization (FISH) or for detection of the RNA by northern blot.

[0480] For example, in vitro techniques for detection of mRNA include northern hybridizations, in situ hybridizations, and rtPCR. In vitro techniques for detection of genomic DNA include Southern hybridizations. Techniques for detection of mRNA include PCR, northern hybridizations and in situ hybridizations. Methods include both qualitative and quantitative methods.

[0481] A general principle of such diagnostic, prognostic, and monitoring assays involves preparing a sample or reaction mixture that may contain a marker, and a probe, under appropriate conditions and for a time sufficient to allow the marker and probe to interact and bind, thus forming a complex that can be removed and/or detected in the reaction mixture. These assays can be conducted in a variety of ways known in the art, e.g., ELISA assay, PCR, FISH.

[0482] 4. Detection of Expression Levels

[0483] Marker levels can be detected based on the absolute expression level or a normalized or relative expression level. Detection of absolute marker levels may be preferable when monitoring the treatment of a subject or in determining if there is a change in the prostate cancer status of a subject. For example, the expression level of one or more markers can be monitored in a subject undergoing treatment for prostate cancer, e.g., at regular intervals, such a monthly intervals. A modulation in the level of one or more markers can be monitored over time to observe trends in changes in marker levels. Expression levels of the biomarkers of the invention, e.g., filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the subject may be higher than the expression level of those markers in a normal sample, but may be lower than the prior expression level, thus indicating a benefit of the treatment regimen for the subject. Similarly, rates of change of marker levels can be important in a subject who is not subject to active treatment for prostate cancer (e.g., watchful waiting). Changes, or not, in marker levels may be more relevant to treatment decisions for the subject than marker levels present in the population. Rapid changes in marker levels in a subject who otherwise appears to have a normal prostate may be indicative of an abnormal prostate state, even if the markers are within normal ranges for the population.

[0484] As an alternative to making determinations based on the absolute expression level of the marker, determinations may be based on the normalized expression level of the marker. Expression levels are normalized by correcting the absolute expression level of a marker by comparing its expression to the expression of a gene that is not a marker, e.g., a housekeeping gene that is constitutively expressed. Suitable genes for normalization include housekeeping genes such as the actin gene, or epithelial cell-specific genes. This normalization allows the comparison of the expression level in one sample, e.g., a patient sample, to another sample, e.g., a non-cancer sample, or between samples from different sources.

[0485] Alternatively, the expression level can be provided as a relative expression level as compared to an appropriate control, e.g., population control, adjacent normal tissue control, earlier time point control, etc. Preferably, the samples used in the baseline determination will be from non-cancer cells. The choice of the cell source is dependent on the use of the relative expression level. Using expression found in normal tissues as a mean expression score aids in validating whether the marker assayed is cancer specific (versus normal cells). In addition, as more data is accumulated, the mean expression value can be revised, providing improved relative expression values based on accumulated data. Expression data from cancer cells provides a means for grading the severity of the cancer state.

[0486] 5. Diagnostic, Prognostic, and Treatment Methods

[0487] The invention provides methods for detecting an abnormal prostate state in a subject by

[0488] (1) contacting a biological sample from a subject with a panel of one or more detection reagents wherein each detection reagent is specific for one prostate-cancer related protein; wherein the prostate-cancer related proteins are selected from the prostate-cancer related protein set as follows: filamin A alone or filamin A in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1;

[0489] (2) measuring the amount of each prostate-cancer related marker detected in the biological sample by each detection reagent; and

[0490] (3) comparing the level of expression of the one or more prostate-cancer related protein in the biological sample obtained from the subject with a level of expression of the one or more prostate-cancer related protein in a control sample, thereby detecting an abnormal prostate state.

[0491] In certain embodiments, detecting an abnormal prostate state comprises diagnosing prostate cancer status in a subject. In certain embodiments, an abnormal prostate state comprises identifying a predisposition to developing prostate cancer.

[0492] The invention provides methods for monitoring the treatment of prostate cancer in a subject by

[0493] (1) contacting a first biological sample obtained from the subject prior to administering at least a portion of a treatment regimen to the subject with a panel of one or more detection reagents wherein each detection reagent is specific for one prostate-cancer related protein; wherein the prostate-cancer related proteins are selected from the prostate protein set as follows: filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1;

[0494] (2) contacting a second biological sample obtained from the subject after administering at least a portion of a treatment regimen to the subject with a panel of one or more detection reagents wherein each detection reagent is specific for one prostate-cancer related protein; wherein the prostate-cancer related proteins are selected from the prostate protein set as follows: filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1;

[0495] (3) measuring the amount of prostate-cancer related marker detected in each the first biological sample and the second biological sample by each detection reagent; and

[0496] (4) comparing the level of expression of the one or more prostate-cancer related markers in the first sample with the expression level of the one or more prostate-cancer related markers in the second sample, thereby monitoring the treatment of prostate cancer in the subject.

[0497] The invention provides method of selecting for administration of active treatment or against administration of active treatment of prostate cancer in a subject by

[0498] (1) contacting a first biological sample obtained from the subject prior to administering a treatment regimen to the subject with a panel of one or more detection reagents wherein each detection reagent is specific for one prostate-cancer related protein; wherein the prostate-cancer related proteins are selected from the prostate protein set as follows: filamin A alone or in combination with prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1;

[0499] (2) contacting a second biological sample obtained from the subject prior to administering a treatment regimen to the subject with a panel of one or more detection reagents wherein each detection reagent is specific for one prostate-cancer related protein; wherein the prostate-cancer related proteins are selected from the prostate protein set as follows: filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1;

[0500] (3) measuring the amount of prostate-cancer related marker detected in each the first biological sample and the second biological sample by each detection reagent; and

[0501] (4) comparing the level of expression of the one or more prostate-cancer related markers in the first sample with the expression level of the one or more prostate-cancer related markers in the second sample, wherein selecting for administration of active treatment or against administration of active treatment of prostate cancer is based on the presence or absence of changes in the level of expression of one or more markers between the first sample and the second sample.

[0502] In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is two or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is three or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is four or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is five or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is six or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is seven or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is eight or more markers. In certain embodiments of the diagnostic and monitoring methods provided herein, one or more prostate-cancer related markers is nine or more markers.

[0503] In certain embodiments of the diagnostic methods provided herein, an increase in the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the biological sample as compared to the level of expression of the one or more prostate-cancer related markers in a normal control sample is an indication that the subject is afflicted with prostate cancer. In certain embodiments of the diagnostic methods provided herein, no increase in the detected expression level of filamin A or one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the biological sample as compared to the expression level in a normal control sample is an indication that the subject is not afflicted with prostate cancer or not predisposed to developing prostate cancer. In one embodiment, the age of the patient is also determined and used as a predictor variable. For example, increased patient age is an indication that the subject is afflicted with prostate cancer or is predisposed to developing prostate cancer.

[0504] In certain embodiments of the diagnostic methods provided herein, an increase in the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the biological sample as compared to the level of expression of the one or more prostate-cancer related markers in a normal control sample is an indication that the subject is predisposed to developing prostate cancer. In one embodiment, the age of the patient is also determined and used as a predictor variable. For example, increased patient age is an indication that the subject is afflicted with prostate cancer or is predisposed to developing prostate cancer.

[0505] In certain embodiments of the monitoring methods provided herein, no increase in the detected level of expression of any of the one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample as compared to the level of expression of the one or more prostate-cancer related markers in the first sample is an indication that the therapy is efficacious for treating prostate cancer in the subject. In certain embodiments the monitoring methods provided herein, further comprise comparing the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the first sample or the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample with the expression of the one or more prostate-cancer related markers in a control sample.

[0506] In certain embodiments of the monitoring methods provided herein, an increase in the level of expression of the one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample as compared to the level of expression of the one or more prostate-cancer related markers in the first sample is an indication for selection of active treatment of prostate cancer in the subject. In certain embodiments of the monitoring methods provided herein, no increase in the detected level of expression of any of the one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample as compared to the level of expression of the one or more prostate-cancer related markers in the first sample is an indication against selection of active treatment of prostate cancer in the subject. In certain embodiments of the monitoring methods provided herein, wherein an increased expression level of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample as compared to the expression level in the first sample is an indication that the therapy is not efficacious in the treatment of prostate cancer.

[0507] In certain embodiments of the diagnostic and monitoring methods provided herein, the one or more prostate-cancer related markers is selected from the group of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1. In certain embodiments of the diagnostic and monitoring methods provided herein, the one or more prostate-cancer related markers comprise at least keratin 7, keratin 8, and keratin 15. In certain embodiments of the diagnostic and monitoring methods provided herein, the one or more prostate-cancer related markers is selected from the group of keratin 7, keratin 15, and keratin 19. In certain embodiments of the diagnostic and monitoring methods provided herein, the one or more prostate-cancer related markers comprise at least keratin 7 or keratin 15. In certain embodiments of the diagnostic and monitoring methods provided herein, the one or more prostate-cancer related markers comprise at least keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the biological sample is compared to the level of the one or more prostate-cancer related markers in a normal control sample is indicative of a modulation in prostate cancer status.

[0508] In certain embodiments of the monitoring methods provided herein, modulation of the level of expression of the one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 in the second sample as compared to the level of expression of the corresponding marker(s) in the first sample is indicative of a change in prostate cancer status in response to treatment of the prostate cancer in the subject. In certain embodiments of the monitoring methods provided herein, the methods further comprise comparing the level of expression of one or more prostate-cancer related markers selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the first sample; or the level of expression of one or more prostate-cancer related markers selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the second sample to the level of expression of one or more prostate-cancer related markers in a normal control sample.

[0509] In any of the aforementioned embodiments, the methods may also include a step of determining whether a subject having prostate cancer or who is being treated for prostate cancer is responsive to a particular treatment. Such a step can include, for example, measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 prior to administering an anti-prostate cancer treatment, and measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 after administering the anti-prostate cancer treatment, and comparing the expression level before and after treatment. Determining that the prostate cancer is responsive to the treatment if the expression level of the one or more markers is lower than before treatment as compared to after treatment. The method may further include the step of adjusting the treatment to a higher dose in order to increase the responsiveness to the treatment, or adjusting the treatment to a lower dose in order to decrease the responsiveness to the treatment.

[0510] In any of the aforementioned embodiments, the methods may also include a step of determining whether a subject having prostate cancer or who is being treated for prostate cancer is responsive to a particular treatment. Such a step can include, for example, measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 prior to administering an anti-prostate cancer treatment, and measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 after administering the anti-prostate cancer treatment, and comparing the expression level before and after treatment. Determining that the prostate cancer is responsive to the treatment if the expression level of the one or more markers is higher than before treatment as compared to after treatment. The method may further include the step of adjusting the treatment to a higher dose in order to increase the responsiveness to the treatment, or adjusting the treatment to a lower dose in order to decrease the responsiveness to the treatment.

[0511] In any of the aforementioned embodiments, the methods may also include a step of determining whether a subject having prostate cancer or who is being treated for prostate cancer is not responsive to a particular treatment. Such a step can include, for example, measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 prior to administering an anti-prostate cancer treatment, and measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 after administering the anti-prostate cancer treatment, and comparing the expression level before and after treatment. Determining that the prostate cancer is not responsive to the treatment if the expression level of the one or more markers is lower than before treatment as compared to after treatment. The method may further include the step of adjusting the treatment to a higher dose in order to increase the responsiveness to the treatment.

[0512] In any of the aforementioned embodiments, the methods may also include a step of determining whether a subject having prostate cancer or who is being treated for prostate cancer is not responsive to a particular treatment. Such a step can include, for example, measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 prior to administering an anti-prostate cancer treatment, and measuring the level of expression of one or more prostate-cancer related markers selected from the group consisting of filamin A alone or in combination with one or more of prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1 after administering the anti-prostate cancer treatment, and comparing the expression level before and after treatment. Determining that the prostate cancer is not responsive to the treatment if the expression level of the one or more markers is higher than before treatment as compared to after treatment. The method may further include the step of adjusting the treatment to a higher dose in order to increase the responsiveness to the treatment.

[0513] In certain embodiments the diagnostic methods provided herein further comprise detecting the level of expression of prostate specific antigen (PSA) in the biological sample and preferably further comprise comparing the level of expression of PSA in the biological sample to a PSA expression level in a normal control sample. In certain embodiments, the combination of PSA level with one or more of the prostate-cancer maker levels increases the predictive value of the method.

[0514] In certain embodiments the monitoring methods provided herein further comprise detecting the level of expression of prostate specific antigen (PSA) in the first sample and the second sample, and preferably further comprising comparing the level of expression of PSA in the first sample with the level of expression of PSA in the second sample. In certain monitoring methods, the change in PSA level in combination with the change in prostate-cancer maker level increases the predictive value of the method.

[0515] In certain embodiments the diagnostic and monitoring methods provided herein further comprise comparing the detected level of the one or more prostate markers in the biological samples with one or more control samples wherein the control sample is one or more of a sample from the same subject at an earlier time point than the biological sample, a sample from a subject with benign prostatic hyperplasia (BPH), a sample from a subject with non-metastatic prostate cancer, a sample from a subject with metastatic prostate cancer, a sample from a subject with androgen sensitive prostate cancer, a sample from a subject with androgen insensitive prostate cancer, a sample from a subject with aggressive prostate cancer, and sample obtained from a subject with non-aggressive prostate cancer. Comparison of the marker levels in the biological samples with control samples from subjects with various normal and abnormal prostate states facilitates the differentiation between various prostate states including normal prostate and prostate cancer, benign prostate hyperplasia and prostate cancer, benign prostate hyperplasia and normal prostate, androgen dependent and androgen independent prostate cancer, aggressive prostate cancer and non-aggressive prostate cancer, aggressive prostate cancer and non-aggressive prostate cancer, or between any two or more prostate states including normal prostate, prostate cancer, benign prostate hyperplasia, androgen dependent prostate cancer, androgen independent prostate cancer, aggressive prostate cancer, non-aggressive prostate cancer, metastatic prostate cancer, and non-metastatic prostate cancer.

[0516] In certain embodiments the diagnostic and monitoring methods provided herein further comprising detecting the size of the prostate tumor in the subject. In certain embodiments the monitoring methods provided herein further comprise detecting a change in the size or relative aggressiveness of the tumor. In certain embodiments, the size of the prostate tumor in the subject is detected prior to administering the at least a portion of a treatment regimen to the subject. In certain embodiments, the size of the prostate tumor in the subject is detected after administering the at least a portion of a treatment regimen to the subject. Certain monitoring methods, further comprise comparing the size of the prostate tumor in the subject prior to administering the at least a portion of a treatment regimen to the subject to the size of the prostate tumor in the subject after administering the at least a portion of a treatment regimen to the subject. Certain other embodiments of the diagnostic and monitoring methods further comprise determining the particular stage or grade of prostate cancer, e.g., Gleason grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer or TNM classifications. In other embodiments, the present invention also involves the analysis and consideration of any clinical and/or patient-related health data, for example, data obtained from an Electronic Medical Record (e.g., collection of electronic health information about individual patients or populations relating to various types of data, such as, demographics, medical history, medication and allergies, immunization status, laboratory test results, radiology images, vital signs, personal statistics like age and weight, and billing information).

[0517] In certain embodiments the diagnostic and monitoring methods provided herein further comprising obtaining a subject sample.

[0518] In certain embodiments the diagnostic and monitoring methods provided herein further comprising selecting a treatment regimen for the subject based on the level of expression of one or more of the prostate-cancer related markers selected from the group consisting of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1.

[0519] In certain embodiments the diagnostic and monitoring methods provided herein further comprise selecting a subject for having or being suspected of having prostate cancer.

[0520] In certain embodiments the diagnostic and monitoring methods provided herein further comprising treating the subject with a regimen including one or more treatments selected from the group consisting of surgery, radiation, hormone therapy, antibody therapy, therapy with growth factors, cytokines, and chemotherapy.

[0521] In certain embodiments the diagnostic and monitoring methods provided herein further comprise selecting the one or more specific treatment regimens for the subject based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer having the biomarker signature detected in the subject/sample is selected for the subject. In certain embodiments, the treatment method is started, change, revised, or maintained based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject is responding to the treatment regimen, or when it is determined that the subject is not responding to the treatment regimen, or when it is determined that the subject is insufficiently responding to the treatment regimen. In certain embodiments, the treatment method is changed based on the results from the diagnostic or prognostic methods.

[0522] In certain other embodiments the diagnostic and monitoring methods provided herein further comprise introducing one or more specific treatment regimens for the subject based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer is selected for the subject. In certain embodiments, the treatment method is started, change, revised, or maintained based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject is responding to the treatment regimen, or when it is determined that the subject is not responding to the treatment regimen, or when it is determined that the subject is insufficiently responding to the treatment regimen. In certain embodiments, the treatment method is changed based on the results from the diagnostic or prognostic methods.

[0523] In yet other embodiments the diagnostic and monitoring methods provided herein further comprise the step of administering a therapeutically effective amount of an anti-prostate cancer therapy based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer is selected for the subject. In certain embodiments, the treatment method is administered based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject expresses one or more biomarkers of the invention (e.g., filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) above some threshold level that is indicative of prostate cancer.

[0524] In yet other embodiments the diagnostic and monitoring methods provided herein further comprise the step of administering a therapeutically effective amount of an anti-prostate cancer therapy based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer is selected for the subject. In certain embodiments, the treatment method is administered based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject expresses one or more biomarkers of the invention (e.g., filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) below some threshold level that is indicative of prostate cancer.

[0525] In yet other embodiments the diagnostic and monitoring methods provided herein further comprise the step of increasing, decreasing, or changing the dose of an anti-prostate cancer therapy based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer is selected for the subject. In certain embodiments, the treatment method is administered based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject expresses one or more biomarkers of the invention (e.g., filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) above some threshold level that is indicative of prostate cancer.

[0526] In yet other embodiments the diagnostic and monitoring methods provided herein further comprise the step of increasing, decreasing, or changing the dose of an anti-prostate cancer therapy based on the results of the diagnostic and monitoring methods provided herein. In one embodiment, a treatment regimen known to be effective against prostate cancer is selected for the subject. In certain embodiments, the treatment method is administered based on the results from the diagnostic or prognostic methods of the invention, e.g., when it is determined that the subject expresses one or more biomarkers of the invention (e.g., filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1) below some threshold level that is indicative of prostate cancer.

[0527] In certain embodiments, a change in the treatment regimen comprises changing a hormone based therapy treatment. In certain embodiments, treatments for prostate cancer include one or more of surgery, radiation, hormone therapy, antibody therapy, therapy with growth factors, cytokines, or chemotherapy based on the results of a method of any one of claims 1-64 for an interval prior to performing a subsequent diagnostic, prognostic, or monitoring method provided herein.

[0528] In certain embodiments of the diagnostic and monitoring methods provided herein, the method further comprises isolating a component of the biological sample.

[0529] In certain embodiments of the diagnostic and monitoring methods provided herein, the method further comprises labeling a component of the biological sample.

[0530] In certain embodiments of the diagnostic and monitoring methods provided herein, the method further comprises amplifying a component of a biological sample.

[0531] In certain embodiments of the diagnostic and monitoring methods provided herein, the method comprises forming a complex with a probe and a component of a biological sample. In certain embodiments, forming a complex with a probe comprises forming a complex with at least one non-naturally occurring reagent. In certain embodiments of the diagnostic and monitoring methods provided herein, the method comprises processing the biological sample. In certain embodiments of the diagnostic and monitoring methods provided herein, the method of detecting a level of at least two markers comprises a panel of markers. In certain embodiments of the diagnostic and monitoring methods provided herein, the method of detecting a level comprises attaching the marker to be detected to a solid surface.

[0532] The invention provides methods of selecting for administration of active treatment or against administration of active treatment of prostate cancer in a subject comprising:

[0533] (1) detecting a level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta in a first sample obtained from the subject having prostate cancer at a first time wherein the subject has not been actively treated for prostate cancer;

[0534] (2) detecting a level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 in a second sample obtained from the subject at a second time, e.g., wherein the subject has not been actively treated;

[0535] (3) comparing the level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 in the first sample with the level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 in the second sample;

[0536] wherein selecting for administration of active treatment or against administration of active treatment of prostate cancer is based on the presence or absence of changes in the level of expression of one or more markers between the first sample and the second sample.

[0537] In certain embodiments, the method further comprising obtaining a third sample obtained from the subject at a third time (e.g., wherein the subject has not been actively treated), detecting a level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 in the third sample, and comparing the level of one or more markers selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 in the third sample with the level of the one or more markers in the first sample and/or the one or more markers in the second sample.

[0538] In certain embodiments, an increased level of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the second sample as compared to the level of the markers in the first sample is an indication that the therapy is not efficacious in the treatment of prostate cancer.

[0539] In certain embodiments, an increased level of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the second sample as compared to the level of the markers in the first sample is an indication for selecting active treatment for prostate cancer.

[0540] In certain embodiments, the method further comprises comparing the level of one or more markers selected from the group consisting of ilamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the first sample or the level of one or more markers selected from the group consisting of ilamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the second sample with the level of one or more of ilamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in a control sample. In certain embodiments, the method comprises detecting the level of filamin A in combination with one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the first sample; detecting the level of filamin A in combination with one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the second sample; and comparing the level of filamin A in combination with one or more of one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the second sample with the one or more of the level of filamin A in combination with keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in the first sample. In certain embodiments, the method comprises detection of a subset of keratins such as keratin 7, keratin 8, and keratin 15; keratin 7, 15, and 19 in combination with filamin A; and keratin 7 or keratin 15. In certain embodiments, the method further comprises comparing the level of one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in combination with filamin A in the first sample; or the level of expression of one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in combination with filamin A in the second sample to the level of one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, and tubulin beta-3 in combination with filamin A in a control sample.

[0541] In certain embodiments, no change in the level of expression of one or more markers selected from the group consisting of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, between the first sample and the second sample is an indication for selecting against active treatment for prostate cancer.

[0542] In certain embodiments, the methods further comprise detecting the level of prostate specific antigen (PSA) in the first sample and the second sample, and then preferably further comprising comparing the level of PSA in the first sample with the level of PSA in the second sample.

[0543] In certain embodiments, a decrease in the level of one or more of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the second sample as compared to the level of one or more of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the first sample in combination with a decrease in the level of PSA in the second sample as compared to the level of PSA in the first sample has greater predictive value that the therapy is efficacious in treating prostate cancer in the subject than analysis of a single marker alone.

[0544] In certain embodiments, a decrease in the level of one or more of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the second sample as compared to the level of one or more of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1, in the first sample in combination with a decrease in the level of expression of PSA in the second sample as compared to the level of PSA in the first sample has greater predictive value for selecting against active treatment for prostate cancer than analysis of a single marker alone.

[0545] 6. Monitoring Clinical Trials

[0546] Monitoring the influence of agents (e.g., drug compounds) on the level of expression of a marker of the invention can be applied not only in basic drug screening or monitoring the treatment of a single subject, but also in clinical trials. For example, the effectiveness of an agent to affect marker expression can be monitored in clinical trials of subjects receiving treatment for an oncological disorder. In a preferred embodiment, the present invention provides a method for monitoring the effectiveness of treatment of a subject with an agent (e.g., an agonist, antagonist, peptidomimetic, protein, peptide, nucleic acid, small molecule, or other drug candidate) comprising the steps of (i) obtaining a pre-administration sample from a subject prior to administration of the agent; (ii) detecting the level of expression of one or more selected markers of the invention (e.g., filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, optionally in combination with PSA) in the pre-administration sample; (iii) obtaining one or more post-administration samples from the subject; (iv) detecting the level of expression of the marker(s) in the post-administration samples; (v) comparing the level of expression of the marker(s) in the pre-administration sample with the level of expression of the marker(s) in the post-administration sample or samples; and (vi) altering the administration of the agent to the subject accordingly. For example, increased expression of the marker gene(s) during the course of treatment may indicate ineffective dosage and the desirability of increasing the dosage. Conversely, decreased expression of the marker gene(s) may indicate efficacious treatment and no need to change dosage.

H. Treatment/Therapeutics

[0547] The present invention provides methods for use of one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9) markers selected from the group consisting of filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9) to treat disease states in a subject, e.g., a mammal, e.g., a human.

[0548] The present invention also provides methods for treatment of a subject with prostate cancer with a therapeutic, e.g., a nucleic acid based therapeutic, that modulates (e.g., reduces, or increases, and preferably reduces) the expression or activity of one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9) markers selected from the group consisting of filamin A alone or filamin A in combination with one or more of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, PSM, PSCA, TMPRSS2, PDEF, HPG-1, PCA3, and PCGEM1.

[0549] The invention also provides methods for selection and/or administration of known treatment agents, especially hormone based therapies vs. non-hormone based therapies, and aggressive or active treatment vs. "watchful waiting", depending on the detection of a change in the level of one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, or 9) markers selected from the group consisting of filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B (FLNB), and lymphocyte antigen 9 (LY9), as compared to a control. The selection of treatment regimens can further include the detection of PSA to assist in selection of the therapeutic methods. Selection of treatment methods can also include other diagnostic considerations and patient characteristics including results from imaging studies, tumor size or growth rates, risk of poor outcomes, disruption of daily activities, and age, Gleason scores (e.g., grade 1, grade 2, grade 3, grade 4, or grade 5 prostate cancer), TNM classifications, clinical and/or patient-related health data (e.g., data obtained from an Electronic Medical Record (e.g., collection of electronic health information about individual patients or populations relating to various types of data, such as, demographics, medical history, medication and allergies, immunization status, laboratory test results, radiology images, vital signs, personal statistics like age and weight, and billing information).

[0550] As used herein, the term "aggressive oncological disorder", such as aggressive prostate cancer, refers to an oncological disorder involving a fast-growing tumor. An aggressive oncological disorder typically does not respond, responds poorly, or loses response to therapeutic treatment. For example, an prostate cancer may be considered to become an aggressive prostate cancer upon loss of response to hormone therapy, necessitating treatment with chemotherapy, surgery, and/or radiation. As used herein, an aggressive prostate cancer, for example, is one that will likely or has metastasized. As used herein, an aggressive prostate cancer is one that will result in significant changes in quality of life as the tumor grows. Active treatment is therapeutically indicated for an aggressive oncological disorder, e.g., aggressive prostate cancer.

[0551] As used herein, the term "non-aggressive oncological disorder" such as a non-aggressive prostate cancer, refers to an oncological disorder involving a slow-growing tumor. A non-aggressive oncological disorder typically responds favorably or moderately to therapeutic treatment or grows so slowly that immediate treatment is not warranted. A non-aggressive prostate tumor is one that a person skilled in the art, e.g., an oncologist, may decide to not actively treat with routine interventions for the treatment of cancer, e.g., chemotherapy, radiation, surgery, as the active treatment may do more harm than the disease, particularly in an older subject. A non-aggressive prostate tumor is one that a person skilled in the art may decide to monitor with "watchful waiting" rather than subjecting the person to any active therapeutic interventions to alter the presence or growth of the tumor (e.g., radiation, surgery, chemotherapy, hormone therapy).

[0552] 1. Nucleic Acid Therapeutics

[0553] Nucleic acid therapeutics are well known in the art. Nucleic acid therapeutics include both single stranded and double stranded (i.e., nucleic acid therapeutics having a complementary region of at least 15 nucleotides in length that may be one or two nucleic acid strands) nucleic acids that are complementary to a target sequence in a cell. Nucleic acid therapeutics can be delivered to a cell in culture, e.g., by adding the nucleic acid to culture media either alone or with an agent to promote uptake of the nucleic acid into the cell. Nucleic acid therapeutics can be delivered to a cell in a subject, i.e., in vivo, by any route of administration. The specific formulation will depend on the route of administration.

[0554] As used herein, and unless otherwise indicated, the term "complementary," when used to describe a first nucleotide sequence in relation to a second nucleotide sequence, refers to the ability of an oligonucleotide or polynucleotide comprising the first nucleotide sequence to hybridize and form a duplex structure under certain conditions with an oligonucleotide or polynucleotide comprising the second nucleotide sequence, as will be understood by the skilled person. Such conditions can, for example, be stringent conditions, where stringent conditions may include: 400 mM NaCl, 40 mM PIPES pH 6.4, 1 mM EDTA, 50.degree. C. or 70.degree. C. for 12-16 hours followed by washing. Other conditions, such as physiologically relevant conditions as may be encountered inside an organism, can apply. The skilled person will be able to determine the set of conditions most appropriate for a test of complementarity of two sequences in accordance with the ultimate application of the hybridized nucleotides.

[0555] Sequences can be "fully complementary" with respect to each when there is base-pairing of the nucleotides of the first nucleotide sequence with the nucleotides of the second nucleotide sequence over the entire length of the first and second nucleotide sequences. However, where a first sequence is referred to as "substantially complementary" with respect to a second sequence herein, the two sequences can be fully complementary, or they may form one or more, but generally not more than 4, 3 or 2 mismatched base pairs upon hybridization, while retaining the ability to hybridize under the conditions most relevant to their ultimate application. However, where two oligonucleotides are designed to form, upon hybridization, one or more single stranded overhangs as is common in double stranded nucleic acid therapeutics, such overhangs shall not be regarded as mismatches with regard to the determination of complementarity. For example, a dsRNA comprising one oligonucleotide 21 nucleotides in length and another oligonucleotide 23 nucleotides in length, wherein the longer oligonucleotide comprises a sequence of 21 nucleotides that is fully complementary to the shorter oligonucleotide, may yet be referred to as "fully complementary" for the purposes described herein.

[0556] "Complementary" sequences, as used herein, may also include, or be formed entirely from, non-Watson-Crick base pairs and/or base pairs formed from non-natural and modified nucleotides, in as far as the above requirements with respect to their ability to hybridize are fulfilled. Such non-Watson-Crick base pairs includes, but not limited to, G:U Wobble or Hoogstein base pairing.

[0557] The terms "complementary," "fully complementary", and "substantially complementary" herein may be used with respect to the base matching between the sense strand and the antisense strand of a dsRNA, or between an antisense nucleic acid or the antisense strand of dsRNA and a target sequence, as will be understood from the context of their use.

[0558] As used herein, a polynucleotide that is "substantially complementary to at least part of" a messenger RNA (mRNA) refers to a polynucleotide that is substantially complementary to a contiguous portion of the mRNA of interest (e.g., an mRNA encoding filamin B, LY9, a keratin, tubulin-beta 3, or PSA) including a 5' UTR, an open reading frame (ORF), or a 3' UTR. For example, a polynucleotide is complementary to at least a part of filamin B, LY9, a keratin, tubulin-beta 3, or PSA mRNA if the sequence is substantially complementary to a non-interrupted portion of an mRNA encoding filamin B, LY9, a keratin, tubulin-beta 3, or PSA.

[0559] Nucleic acid therapeutics typically include chemical modifications to improve their stability and to modulate their pharmacokinetic and pharmacodynamic properties. For example, the modifications on the nucleotides can include, but are not limited to, LNA, HNA, CeNA, 2'-hydroxyl, and combinations thereof.

[0560] Nucleic acid therapeutics may further comprise at least one phosphorothioate or methylphosphonate internucleotide linkage. The phosphorothioate or methylphosphonate internucleotide linkage modification may occur on any nucleotide of the sense strand or antisense strand or both (in nucleic acid therapeutics including a sense strand) in any position of the strand. For instance, the internucleotide linkage modification may occur on every nucleotide on the sense strand or antisense strand; each internucleotide linkage modification may occur in an alternating pattern on the sense strand or antisense strand; or the sense strand or antisense strand may contain both internucleotide linkage modifications in an alternating pattern. The alternating pattern of the internucleotide linkage modification on the sense strand may be the same or different from the antisense strand, and the alternating pattern of the internucleotide linkage modification on the sense strand may have a shift relative to the alternating pattern of the internucleotide linkage modification on the antisense strand.

[0561] A. Single Stranded Therapeutics

[0562] Antisense nucleic acid therapeutic agent single stranded nucleic acid therapeutics, typically about 16 to 30 nucleotides in length and are complementary to a target nucleic acid sequence in the target cell, either in culture or in an organism.

[0563] Patents directed to antisense nucleic acids, chemical modifications, and therapeutic uses are provided, for example, in U.S. Pat. No. 5,898,031 related to chemically modified RNA-containing therapeutic compounds, and U.S. Pat. No. 6,107,094 related methods of using these compounds as therapeutic agent. U.S. Pat. No. 7,432,250 related to methods of treating patients by administering single-stranded chemically modified RNA-like compounds; and U.S. Pat. No. 7,432,249 related to pharmaceutical compositions containing single-stranded chemically modified RNA-like compounds. U.S. Pat. No. 7,629,321 is related to methods of cleaving target mRNA using a single-stranded oligonucleotide having a plurality RNA nucleosides and at least one chemical modification. Each of the patents listed in the paragraph are incorporated herein by reference.

[0564] B. Double Stranded Therapeutics

[0565] In many embodiments, the duplex region is 15-30 nucleotide pairs in length. In some embodiments, the duplex region is 17-23 nucleotide pairs in length, 17-25 nucleotide pairs in length, 23-27 nucleotide pairs in length, 19-21 nucleotide pairs in length, or 21-23 nucleotide pairs in length.

[0566] In certain embodiments, each strand has 15-30 nucleotides.

[0567] The RNAi agents that are used in the methods of the invention include agents with chemical modifications as disclosed, for example, in Publications WO 2009/073809 and WO/2012/037254, the entire contents of each of which are incorporated herein by reference.

[0568] Nucleic acid therapeutic agents for use in the methods of the invention also include double stranded nucleic acid therapeutics. An "RNAi agent," "double stranded RNAi agent," double-stranded RNA (dsRNA) molecule, also referred to as "dsRNA agent," "dsRNA", "siRNA", "iRNA agent," as used interchangeably herein, refers to a complex of ribonucleic acid molecules, having a duplex structure comprising two anti-parallel and substantially complementary, as defined below, nucleic acid strands. As used herein, an RNAi agent can also include dsiRNA (see, e.g., US Patent publication 20070104688, incorporated herein by reference). In general, the majority of nucleotides of each strand are ribonucleotides, but as described herein, each or both strands can also include one or more non-ribonucleotides, e.g., a deoxyribonucleotide and/or a modified nucleotide. In addition, as used in this specification, an "RNAi agent" may include ribonucleotides with chemical modifications; an RNAi agent may include substantial modifications at multiple nucleotides. Such modifications may include all types of modifications disclosed herein or known in the art. Any such modifications, as used in a siRNA type molecule, are encompassed by "RNAi agent" for the purposes of this specification and claims. The RNAi agents that are used in the methods of the invention include agents with chemical modifications as disclosed, for example, in U.S. Provisional Application No. 61/561,710, filed on Nov. 18, 2011, International Application No. PCT/US2011/051597, filed on Sep. 15, 2010, and PCT Publication WO 2009/073809, the entire contents of each of which are incorporated herein by reference. The two strands forming the duplex structure may be different portions of one larger RNA molecule, or they may be separate RNA molecules. Where the two strands are part of one larger molecule, and therefore are connected by an uninterrupted chain of nucleotides between the 3'-end of one strand and the 5'-end of the respective other strand forming the duplex structure, the connecting RNA chain is referred to as a "hairpin loop." Where the two strands are connected covalently by means other than an uninterrupted chain of nucleotides between the 3'-end of one strand and the 5'-end of the respective other strand forming the duplex structure, the connecting structure is referred to as a "linker." The RNA strands may have the same or a different number of nucleotides. The maximum number of base pairs is the number of nucleotides in the shortest strand of the dsRNA minus any overhangs that are present in the duplex. In addition to the duplex structure, an RNAi agent may comprise one or more nucleotide overhangs. The term "siRNA" is also used herein to refer to an RNAi agent as described above.

[0569] In another aspect, the agent is a single-stranded antisense RNA molecule. An antisense RNA molecule is complementary to a sequence within the target mRNA. Antisense RNA can inhibit translation in a stoichiometric manner by base pairing to the mRNA and physically obstructing the translation machinery, see Dias, N. et al., (2002) Mol Cancer Ther 1:347-355. The antisense RNA molecule may have about 15-30 nucleotides that are complementary to the target mRNA. For example, the antisense RNA molecule may have a sequence of at least 15, 16, 17, 18, 19, 20 or more contiguous nucleotides complementary to the filamin B or LY9 sequences provided herein.

[0570] The term "antisense strand" refers to the strand of a double stranded RNAi agent which includes a region that is substantially complementary to a target sequence (e.g., a human TTR mRNA). As used herein, the term "region complementary to part of an mRNA encoding transthyretin" refers to a region on the antisense strand that is substantially complementary to part of a TTR mRNA sequence. Where the region of complementarity is not fully complementary to the target sequence, the mismatches are most tolerated in the terminal regions and, if present, are generally in a terminal region or regions, e.g., within 6, 5, 4, 3, or 2 nucleotides of the 5' and/or 3' terminus.

[0571] The term "sense strand," as used herein, refers to the strand of a dsRNA that includes a region that is substantially complementary to a region of the antisense strand.

[0572] The invention also includes molecular beacon nucleic acids having at least one region which is complementary to a nucleic acid of the invention, such that the molecular beacon is useful for quantitating the presence of the nucleic acid of the invention in a sample. A "molecular beacon" nucleic acid is a nucleic acid comprising a pair of complementary regions and having a fluorophore and a fluorescent quencher associated therewith. The fluorophore and quencher are associated with different portions of the nucleic acid in such an orientation that when the complementary regions are annealed with one another, fluorescence of the fluorophore is quenched by the quencher. When the complementary regions of the nucleic acid are not annealed with one another, fluorescence of the fluorophore is quenched to a lesser degree. Molecular beacon nucleic acids are described, for example, in U.S. Pat. No. 5,876,930.

I. Drug Screening

[0573] As noted above, sets of biomarkers whose expression levels correlate with one or more selected prostate disease characteristics (e.g., prostate cancer progression) are attractive targets for identification of new therapeutic agents via screens to detect compounds or entities that inhibit or enhance expression of these biomarker genes and/or their products. Accordingly, the present invention provides methods for the identification of compounds potentially useful for modulating prostate cancer progression. In particular, the present invention provides methods for the identification of compounds potentially useful for modulating prostate cancer progression wherein the compounds modulate (e.g., increase or decrease, preferably decrease or inhibit) the expression of filamin A, and/or filamin A in combination with other biomarkers, including prostate specific antigen (PSA), filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, kertin 18, keratin 19, and tubulin-beta 3.

[0574] Such assays typically comprise a reaction between a marker of the invention and one or more assay components. The other components may be either the test compound itself, or a combination of test compounds and a natural binding partner of a marker of the invention. Compounds identified via assays such as those described herein may be useful, for example, for modulating, e.g., inhibiting, ameliorating, treating, or preventing the disease. Compounds identified for modulating the expression level of one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, or LY9; optionally in combination with PSA, are preferably further tested for activity useful in the treatment of cancer, preferably prostate cancer, e.g., inhibiting tumor cell growth, inhibiting tumor angiogenesis, inducing tumor cell apoptosis, etc.

[0575] The test compounds used in the screening assays of the present invention may be obtained from any available source, including systematic libraries of natural and/or synthetic compounds. Test compounds may also be obtained by any of the numerous approaches in combinatorial library methods known in the art, including: biological libraries; peptoid libraries (libraries of molecules having the functionalities of peptides, but with a novel, non-peptide backbone which are resistant to enzymatic degradation but which nevertheless remain bioactive; see, e.g., Zuckermann et al., 1994, J. Med. Chem. 37:2678-85); spatially addressable parallel solid phase or solution phase libraries; synthetic library methods requiring deconvolution; the `one-bead one-compound` library method; and synthetic library methods using affinity chromatography selection. The biological library and peptoid library approaches are limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds (Lam, 1997, Anticancer Drug Des. 12:145).

[0576] Examples of methods for the synthesis of molecular libraries can be found in the art, for example in: DeWitt et al. (1993) Proc. Natl. Acad. Sci. U.S.A. 90:6909; Erb et al. (1994) Proc. Natl. Acad. Sci. USA 91:11422; Zuckermann et al. (1994). J. Med. Chem. 37:2678; Cho et al. (1993) Science 261:1303; Carrell et al. (1994) Angew. Chem. Int. Ed. Engl. 33:2059; Carell et al. (1994) Angew. Chem. Int. Ed. Engl. 33:2061; and in Gallop et al. (1994) J. Med. Chem. 37:1233.

[0577] Libraries of compounds may be presented in solution (e.g., Houghten, 1992, Biotechniques 13:412-421), or on beads (Lam, 1991, Nature 354:82-84), chips (Fodor, 1993, Nature 364:555-556), bacteria and/or spores, (Ladner, U.S. Pat. No. 5,223,409), plasmids (Cull et al, 1992, Proc Natl Acad Sci USA 89:1865-1869) or on phage (Scott and Smith, 1990, Science 249:386-390; Devlin, 1990, Science 249:404-406; Cwirla et al, 1990, Proc. Natl. Acad. Sci. 87:6378-6382; Felici, 1991, J. Mol. Biol. 222:301-310; Ladner, supra.).

[0578] The screening methods of the invention comprise contacting a cell, e.g., a diseased cell, especially a prostate cancer cell, with a test compound and determining the ability of the test compound to modulate the expression and/or activity of filamin B, LY9, or keratin 19, optionally in combination with PSA, in the cell. The expression and/or activity of filamin B, LY9, or keratin 19; optionally in combination with PSA, can be determined using any methods known in the art, such as those described herein.

[0579] In another embodiment, the invention provides assays for screening candidate or test compounds which are substrates of a marker of the invention or biologically active portions thereof. In yet another embodiment, the invention provides assays for screening candidate or test compounds which bind to a marker of the invention or biologically active portions thereof. Determining the ability of the test compound to directly bind to a marker can be accomplished, for example, by any method known in the art.

[0580] This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent capable of modulating the expression and/or activity of a marker of the invention identified as described herein can be used in an animal model to determine the efficacy, toxicity, or side effects of treatment (e.g., of prostate cancer) with such an agent. Alternatively, an agent identified as described herein can be used in an animal model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatment as described above.

[0581] In certain embodiments, the screening methods are performed using cells contained in a plurality of wells of a multi-well assay plate. Such assay plates are commercially available, for example, from Stratagene Corp. (La Jolla, Calif.) and Corning Inc. (Acton, Mass.) and include, for example, 48-well, 96-well, 384-well and 1536-well plates.

[0582] Reproducibility of the results may be tested by performing the analysis more than once with the same concentration of the same candidate compound (for example, by incubating cells in more than one well of an assay plate). Additionally, since candidate compounds may be effective at varying concentrations depending on the nature of the compound and the nature of its mechanism(s) of action, varying concentrations of the candidate compound may be tested. Generally, candidate compound concentrations from 1 fM to about 10 mM are used for screening. Preferred screening concentrations are generally between about 10 pM and about 100 .mu.M.

[0583] The screening methods of the invention will provide "hits" or "leads," i.e., compounds that possess a desired but not optimized biological activity. Lead optimization performed on these compounds to fulfill all physicochemical, pharmacokinetic, and toxicologic factors required for clinical usefulness may provide improved drug candidates. The present invention also encompasses these improved drug candidates and their use as therapeutics for modulating prostate cancer progression.

J. Kits/Panels

[0584] The invention also provides compositions and kits for diagnosing, prognosing, or monitoring a disease or disorder, recurrence of a disorder, or survival of a subject being treated for a disorder (e.g., an abnormal prostate state, BPH, an oncologic disorder, e.g., prostate cancer). These kits include one or more of the following: a detectable antibody that specifically binds to a marker of the invention, a detectable antibody that specifically binds to a marker of the invention, reagents for obtaining and/or preparing subject tissue samples for staining, and instructions for use.

[0585] The invention also encompasses kits for detecting the presence of a marker protein or nucleic acid in a biological sample. Such kits can be used to determine if a subject is suffering from or is at increased risk of developing an abnormal prostate state. For example, the kit can comprise a labeled compound or agent capable of detecting a marker protein or nucleic acid in a biological sample and means for determining the amount of the protein or mRNA in the sample (e.g., an antibody which binds the protein or a fragment thereof, or an oligonucleotide probe which binds to DNA or mRNA encoding the protein). Kits can also include instructions for use of the kit for practicing any of the methods provided herein or interpreting the results obtained using the kit based on the teachings provided herein. The kits can also include reagents for detection of a control protein in the sample not related to the abnormal prostate state, e.g., actin for tissue samples, albumin in blood or blood derived samples for normalization of the amount of the marker present in the sample. The kit can also include the purified marker for detection for use as a control or for quantitation of the assay performed with the kit.

[0586] Kits include a panel of reagents for use in a method to diagnose prostate cancer in a subject (or to identify a subject predisposed to developing prostate cancer, etc.), the panel comprising at least two detection reagents, wherein each detection reagent is specific for one prostate cancer-specific protein, wherein said prostate cancer-specific proteins are selected from the prostate cancer-specific protein sets provided herein.

[0587] For antibody-based kits, the kit can comprise, for example: (1) a first antibody (e.g., attached to a solid support) which binds to a first marker protein; and, optionally, (2) a second, different antibody which binds to either the first marker protein or the first antibody and is conjugated to a detectable label. In certain embodiments, the kit includes (1) a second antibody (e.g., attached to a solid support) which binds to a second marker protein; and, optionally, (2) a second, different antibody which binds to either the second marker protein or the second antibody and is conjugated to a detectable label. The first and second marker proteins are different. In an embodiment, the first and second markers are markers of the invention, e.g., filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, LY9, and PSA. In certain embodiments, neither the first marker nor the second marker is PSA. In certain embodiments, the kit comprises a third antibody which binds to a third marker protein which is different from the first and second marker proteins, and a second different antibody that binds to either the third marker protein or the antibody that binds the third marker protein wherein the third marker protein is different from the first and second marker proteins.

[0588] For oligonucleotide-based kits, the kit can comprise, for example: (1) an oligonucleotide, e.g., a detectably labeled oligonucleotide, which hybridizes to a nucleic acid sequence encoding a marker protein or (2) a pair of primers useful for amplifying a marker nucleic acid molecule. In certain embodiments, the kit can further include, for example: (1) an oligonucleotide, e.g., a second detectably labeled oligonucleotide, which hybridizes to a nucleic acid sequence encoding a second marker protein or (2) a pair of primers useful for amplifying the second marker nucleic acid molecule. The first and second markers are different. In an embodiment, the first and second markers are markers of the invention, e.g., filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, LY9, and PSA. In certain embodiments, neither the first marker nor the second marker is PSA. In certain embodiments, the kit can further include, for example: (1) an oligonucleotide, e.g., a third detectably labeled oligonucleotide, which hybridizes to a nucleic acid sequence encoding a third marker protein or (2) a pair of primers useful for amplifying the third marker nucleic acid molecule wherein the third marker is different from the first and second markers. In certain embodiments, the kit includes a third primer specific for each nucleic acid marker to allow for detection using quantitative PCR methods.

[0589] For chromatography methods, the kit can include markers, including labeled markers, to permit detection and identification of one or more markers of the invention, e.g., filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, LY9, and optionally PSA, by chromatography. In certain embodiments, kits for chromatography methods include compounds for derivatization of one or more markers of the invention. In certain embodiments, kits for chromatography methods include columns for resolving the markers of the method.

[0590] Reagents specific for detection of a marker of the invention, e.g., filamin A, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, filamin B, LY9, and PSA, allow for detection and quantitation of the marker in a complex mixture, e.g., serum, tissue sample. In certain embodiments, the reagents are species specific. In certain embodiments, the reagents are not species specific. In certain embodiments, the reagents are isoform specific. In certain embodiments, the reagents are not isoform specific. In certain embodiments, the reagents detect total keratin 8, keratin 18, filamin B, PSA, or LY9.

[0591] In certain embodiments, the kits for the diagnosis, monitoring, or characterization of prostate cancer comprise at least one reagent specific for the detection of the level of expression of at least one marker selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, filamin B, and LY9. In certain embodiments, the kits further comprise instructions for the diagnosis, monitoring, or characterization of prostate cancer based on the level of expression of the at least one marker selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, filamin B, and LY9. In certain embodiments, the kits further comprise instructions to detect the level of PSA in a sample in which the at least one marker selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, filamin B, and LY9 is detected. In certain embodiments, the kits further comprise at least one reagent for the specific detection of PSA.

[0592] The invention provides kits comprising at least one reagent specific for the detection of a level of expression of at least one marker selected from the group consisting of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, filamin B, and LY9 and at least one reagent specific for the detection of a level of expression of PSA.

[0593] In certain embodiments, the kits can also comprise, e.g., a buffering agents, a preservative, a protein stabilizing agent, reaction buffers. The kit can further comprise components necessary for detecting the detectable label (e.g., an enzyme or a substrate). The kit can also contain a control sample or a series of control samples which can be assayed and compared to the test sample. The controls can be control serum samples or control samples of purified proteins or nucleic acids, as appropriate, with known levels of target markers. Each component of the kit can be enclosed within an individual container and all of the various containers can be within a single package, along with instructions for interpreting the results of the assays performed using the kit.

[0594] The kits of the invention may optionally comprise additional components useful for performing the methods of the invention.

[0595] The invention further provides panels of reagents for detection of one or more prostate-related marker in a subject sample and at least one control reagent. In certain embodiments, the control reagent is to detect the marker for detection in the biological sample wherein the panel is provided with a control sample containing the marker for use as a positive control and optionally to quantitate the amount of marker present in the biological sample. In certain embodiments, the panel includes a detection reagent for a maker not related to an abnormal prostate state that is known to be present or absent in the biological sample to provide a positive or negative control, respectively. The panel can be provided with reagents for detection of a control protein in the sample not related to the abnormal prostate state, e.g., actin for tissue samples, albumin in blood or blood derived samples for normalization of the amount of the marker present in the sample. The panel can be provided with a purified marker for detection for use as a control or for quantitation of the assay performed with the panel.

[0596] In a preferred embodiment, the panel includes reagents for detection of two or more markers of the invention (e.g., 2, 3, 4, 5, 6, 7, 8, 9), preferably in conjunction with a control reagent. In the panel, each marker is detected by a reagent specific for that marker. In certain embodiments, the panel further includes a reagent for the detection of PSA. In certain embodiments, the panel includes replicate wells, spots, or portions to allow for analysis of various dilutions (e.g., serial dilutions) of biological samples and control samples. In a preferred embodiment, the panel allows for quantitative detection of one or more markers of the invention.

[0597] In certain embodiments, the panel is a protein chip for detection of one or more markers. In certain embodiments, the panel is an ELISA plate for detection of one or more markers. In certain embodiments, the panel is a plate for quantitative PCR for detection of one or more markers.

[0598] In certain embodiments, the panel of detection reagents is provided on a single device including a detection reagent for one or more markers of the invention and at least one control sample. In certain embodiments, the panel of detection reagents is provided on a single device including a detection reagent for two or more markers of the invention and at least one control sample. In certain embodiments, multiple panels for the detection of different markers of the invention are provided with at least one uniform control sample to facilitate comparison of results between panels.

[0599] This invention is further illustrated by the following examples which should not be construed as limiting. The contents of all references and published patents and patent applications cited throughout the application are hereby incorporated by reference.

EXAMPLES

[0600] This invention is further illustrated by the following examples which should not be construed as limiting. The contents of all references, GenBank Accession and Gene numbers, and published patents and patent applications cited throughout the application are hereby incorporated by reference. Those skilled in the art will recognize that the invention may be practiced with variations on the disclosed structures, materials, compositions and methods, and such variations are regarded as within the ambit of the invention.

Example 1: Identification of Keratins and Tubulin as Prostate Cancer Markers

[0601] Extracellular Keratins are known to influence the cell proliferation and metastasis of epithelial derived prostate cancers. Androgen refractory prostate cancers exhibit differential expression keratin 8 (K8) when compared to normal tissue. Modulation and degradation of keratins is in turn mediated by mitochondrial generation of Reactive Oxygen Species (ROS). Despite these advances a systematic approach to understanding of keratins and other EC proteins in prostate cancer metastasis and proliferation is lacking.

[0602] An interrogative systems biology based discovery platform (i.e., Interrogative Platform Technology or a.k.a. Interrogative Biology.TM.) disclosed in WO2012119129 (incorporated herein by reference), and shown schematically in FIG. 1, provides new mechanistic insights into understanding mitochondrial role in behavior of prostate cancer cells. The discovery platform involves discovery across a hierarchy of systems including in vitro human cell based models and human serum samples from prostate cancer patients and downstream data integration and mathematical modeling employing an Artificial Intelligence (AI) based informatic module. For cellular models, androgen sensitive LnCAP cell line and metastatic, androgen refractory PC3 cell line were treated with ubidecarenone (coenzyme Q10) in order to engage the mitochondrial machinery. Proteomic signatures were captured using a 2D LC-MS orbitrap technology. Total protein signatures were input to an AI based informatics module to generate causal protein networks (FIG. 2). Wet lab assays that specifically measure mitochondrial ROS, ATP and caspase 3 activation confirmed changes in intracellular levels of these markers.

[0603] As shown in FIG. 3, several novel protein causal interactions that govern induction of mitochondrial machinery by ubidecarenone in PC3 cells were observed. Causal protein maps revealed association of keratins 8 and 15 in PC3 models and not LnCAP. The keratin 8/15 association was lost upon treatment with ubidecarenone, and a direct association of keratins 7 and 15 was established (FIG. 3).

[0604] These results suggest that a change in the interaction among keratins 7, 8, and 15 is particularly useful in demonstrating a response to treatment or a change in prostate cancer status in a subject. Further, keratins 8 and 15 were differentially associated in the androgen refractory, metastatic PC3 cell line and the androgen sensitive LnCAP cell line. This indicates that keratins 8 and 15 could be useful do differentiate between prostate cancer states, e.g., between androgen sensitive and metastatic, androgen refractory prostate cancer.

[0605] An increase in the expression of keratin 19 in relation to prostate cancer was confirmed using a panel of serum samples from subjects suffering from prostate cancer as compared to an appropriate matched control population. (See FIG. 2C and FIG. 3D).

[0606] Thus novel mechanistic insight into prostate cancer proliferation and mitochondrial role in modulating metastasis was gained with a novel chemical systems biology approach.

[0607] The results provided herein demonstrate that modulation of keratin and potential causal association in androgen refractory prostate cancer was inferred by the Platform technology. This provides a potential mechanisms of keratin regulation in response to modulation of mitochondrial function was deciphered by the Platform technology. Thus, novel drivers of cancer pathophysiology were validated in patient serum samples.

Example 2: Identification of Filamin B as a Prostate Cancer Marker

[0608] An interrogative systems biology based discovery platform (i.e., Interrogative Platform Technology or a.k.a. Interrogative Biology.TM.) was used to obtain mechanistic insights into understanding the mitochondrial role in behavior of prostate cancer cells. The Platform technology, which is described in detail in WO2012119129, involves discovery across a hierarchy of systems including in vitro human cell based models and human serum samples from prostate cancer patients and downstream data integration and mathematical modeling employing an Artificial Intelligence (AI) based informatics module.

[0609] The results provided in this Example demonstrate the modulation of filamin B and LY9, and the potential causal association in androgen refractory prostate cancer that was inferred using the Platform technology. The Example provides potential mechanisms of filamin B and LY9 regulation in response to modulation of mitochondrial function that was deciphered by the Platform technology, and provides validation of the markers in patient serum samples.

[0610] Using the Platform methods, human prostate cancer cells PC3 (androgen insensitive, metastatic) and LnCap (androgen sensitive) were modeled in cancer microenvironments including hypoxia, reduced environments, and hyperglycemia and in presence of coenzyme Q10. Normal cells (human dermal fibroblasts (HDFa) and SV40 transformed human liver cells (THLE2)) were modeled under similar conditions mentioned above in Example 2. Proteomics of cellular proteins and proteins secreted in the supernatant were carried out by LCMS. Data were input into the Bayesian Network Inference (BNI) algorithms REFS.TM..

[0611] Causal associations between proteins were derived by the BNI. Differential network analysis was employed to tease out the hubs of activity in prostate cancer when compared to normal cells in normal microenviroments. Filamin B was identified as differential hub of activity in PC3 and not in LnCap and normal cells. That is, Filamin B was found to differ between androgen sensitive LnCAP cell line and metastatic, androgen refractory PC3 cell line. This indicates that Filamin B could be useful to differentiate between prostate cancer states, e.g., between androgen sensitive and metastatic, androgen refractory prostate cancer. The interaction matrix placing filamin B at the center of an interaction hub is shown in FIG. 4. The interaction of LY9 with filamin B is shown in FIG. 5.

Example 3: Validation of Filamin B as a Prostate Cancer Marker in Human Samples

[0612] Having identified filamin B as a prostate cancer marker using the platform technology, human serum samples from normal subjects and subjects with prostate cancer were used to confirm filamin B as a prostate cancer marker.

[0613] Specifically, human serum samples were procured from a commercial vendor that sources human serum. Twenty samples were from normal donors and 20 samples were from patients diagnosed with prostate cancer. Prostate cancer samples were from patients with different prognosis and aggressiveness of cancers reported. Clinical characteristics of the subjects are provided in the table.

TABLE-US-00001 Prostate Cancer Control Group Median Age 61 (47-86) 58 (45-72) Ethnicity Caucasian 75% 85% African American 15% 10% Hispanic 10% 5% Tumor Stage Stage I 20% Stage II 35% Stage III 5% Stage IV 40%

[0614] Commercially available ELISA tests for filamin B and PSA were procured from commercial source. The assays were performed using the manufacturer's instructions. The results from the assay are shown in FIG. 6. The results show the differential levels of FlnB and PSA in patients with a diagnosis for prostate cancer as compared to control subjects without prostate cancer.

[0615] As shown, both filamin B and PSA levels were elevated in serum samples from patients diagnosed with prostate cancer. The correlation between PSA and FlnB expression in serum samples is 0.20075, indicating a relatively low correlation between the variables. This demonstrates that filamin B and PSA are useful for the detection of prostate cancer in different subjects. These results demonstrate that filamin B is useful for the diagnosis of prostate cancer, and that filamin B is useful for improving the detection of prostate cancer by PSA.

Example 4: Validation of LY9 as a Prostate Cancer Marker in Human Samples

[0616] The same human serum samples used in Example 3 were further tested to detect the presence of LY9. A commercially available ELISA test for LY9 was procured from commercial source. The assay was performed using the manufactures' instructions. The results from the assay are shown in FIG. 7. The results show the differential levels of LY9 in patients with a diagnosis for prostate cancer as compared to control subjects without prostate cancer. As shown, samples from subjects with prostate cancer were found to have higher levels of LY9 as compared to normal subjects. Results from assays of expression levels of both filamin B and LY9 in human serum with results expressed as ng/ml of protein are shown in FIG. 8.

Example 5: Analysis of Filamin B Levels Improves the Detection of Prostate Cancer as Compared to PSA Alone

[0617] Having demonstrated that the level of filamin B is increased in the serum of subjects with prostate cancer, the results were analyzed in conjunction with the study of PSA levels in the same samples to determine if the predictive value of filamin B and PSA together was better than either of the markers alone. Receiver operating characteristic (ROC) curve analysis of sensitivity and false positive rate (FPR) of PSA, filamin B, and the combination of PSA and filamin B was generated. The curves and the area under the curve (AUC) values are shown in FIGS. 9A and B. The goal of this analysis was to gauge the predictive power of the test independent of a specific cut-off. When using an ROC analysis, a test that provides perfect discrimination or accuracy between normal and disease states would have AUC=1, whereas a very poor test that provides no better discrimination than random chance would have AUC=0.5

[0618] As demonstrated by the analysis, filamin B alone performs very well and most importantly somewhat orthogonal to PSA. PSA is reported to have a very high false positive rate, e.g., about 75% (as reported in, Gilligan, "The new data on prostate cancer screening: What should we do now?," Cleveland Clin. J. Med. 76: 446-448, 2009, incorporated herein by reference). That is, it has a high sensitivity and low specificity. In the specific study presented, the AUC for FLNB is lower than that for PSA. However, the correlation level of 0.20075 determined in Example 3, indicates a relatively low correlation between the variables. That is, subjects identified as having an elevated filamin B level did not necessarily have a high PSA level, and the reverse was also true, suggesting that the markers in combination can provide a more predictive test than either marker alone.

[0619] This was confirmed in the ROC analysis. As shown, the combination of PSA and filamin B was found to have a higher AUC indicating better discrimination of the test than PSA alone, and to be more predictive than either of the markers alone. The combination of PSA and filamin B is a very good predictor of prostate cancer and provides a drastic increase over the PSA test specificity, which is the primary problem with the test.

Example 6: Analysis of Filamin B, LY9, and PSA Levels Together Improves the Detection of Prostate Cancer as Compared to any Marker Alone

[0620] Having demonstrated that each of filamin B, LY9, and PSA are all elevated in serum samples from subjects with prostate cancer, the ROC curve analysis was performed comparing each of the three markers individually to the combination of all three markers using a linear scoring function, and comparing the combination of filamin B and LY9, and the combination of filamin B and PSA, against the combination of all three markers using a non-linear scoring function to determine which combinations of the markers were more effective than each single marker for the detection of prostate cancer in a subject. As shown, the combination of all three markers was more predictive than any of the markers alone (FIG. 10A). The combination of filamin B with PSA, either with or without LY9, was more predictive than the combination of filamin B with LY9 (FIG. 10B). Additional samples can be analyzed to further refine the results. The AUC results are summarized in the table.

TABLE-US-00002 Marker AUC LY9 0.85 FLNB 0.78 PSA 0.87 LY9 + FLNB + PSA 0.98

Example 7: Stratification of Subjects with Prostate Cancer Using Keratin 4, Keratin 7, Keratin 8, Keratin 15, Keratin 18, Keratin 19, Tubulin-beta 3

[0621] As demonstrated in Examples 3 and 4 respectively, filamin B levels and LY9 levels can be used to distinguish subjects who are or are not suffering from prostate cancer. Further, as demonstrated in Examples 5 and 6, the analysis of both filamin B and PSA, optionally further in combination with LY9, is more sensitive than an analysis based on either marker alone. The markers keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3 are similarly analyzed, as described in Examples 3-6, in human samples.

[0622] A series of subject samples are obtained from an appropriate source, e.g., a commercial source, wherein the samples were obtained from subjects with different stages of prostate cancer, e.g., aggressive prostate cancer, androgen sensitive, androgen insensitive, metastatic; or from subjects not suffering from prostate cancer, e.g., subjects with normal prostate or subjects with BPH. The samples are analyzed for the expression level of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA. The level of the expression of the makers, alone and in various combinations, correlate with the presence or absence of disease, and with the severity of prostate cancer. For example, an increase in the expression level of one or more of keratin 19, filamin B, LY9, and PSA, as compared to a normal sample from a subject not suffering from prostate cancer, is indicative of prostate cancer in the subject. Expression levels of keratins 7, 8, and 15 may also be particularly useful in the stratification of subjects with prostate cancer.

Example 8: Monitoring of Prostate Cancer Treatment Using Keratin 4, Keratin 7, Keratin 8, Keratin 15, Keratin 18, Keratin 19, Tubulin-Beta 3

[0623] At the time of diagnosis with prostate cancer, subjects are invited to participate in a trial. A subject sample, e.g., blood, is obtained. Periodically, throughout the monitoring, watchful waiting, or active treatment of the subject, e.g., chemotherapy, radiation therapy, surgery, hormone therapy, a new subject sample is obtained. At the end of the study, all subject samples are tested for the expression level of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA. The subject samples are matched to the medical records of the subjects to correlate marker levels with prostate cancer status at the time of diagnosis, rate of progression of disease, response of subjects to one or more interventions, and transitions between androgen dependent and independent status. An increase in the expression level of one or more of keratin 19, filamin B, LY9, and PSA, as compared to a normal sample from a subject not suffering from prostate cancer, is indicative of prostate cancer in the subject. Expression levels of keratins 7, 8, and 15 may also be particularly useful in the diagnosis and monitoring of subjects with prostate cancer.

Example 9: Detection and Monitoring of Prostate Cancer Using Keratin 4, Keratin 7, Keratin 8, Keratin 15, Keratin 18, Keratin 19, Tubulin-Beta 3

[0624] Despite its limitations, including a positive predictive value of only 25-40%, PSA remains the only generally accepted biomarker for prostate cancer. Moreover, as prostate cancer is most commonly a slow growing tumor in men of advanced age, treatment of the cancer may do more harm to the subject than the tumor itself would. Therefore, the tests together for the expression level of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA are used for the detection an monitoring of prostate cancer. The level of the expression of the makers, alone and in various combinations are used in detection, including in routine, preventative, screening methods in men having an increased risk of prostate cancer (e.g., increased age, family history, race, etc.) or in monitoring of subjects diagnosed with prostate cancer prior to or during treatment may be useful to better identify subjects in need of further, potentially more invasive, diagnostic tests, e.g., prostate exam or biopsy, digital rectal exam; or more aggressive treatment. Detection of levels of expression of the markers, or various combinations thereof, may also be indicative of a good or poor response to a specific treatment regimen prior to changes in other signs or symptoms, e.g., loss of tumor response to hormone therapy.

[0625] In routine screening methods for prostate cancer, a serum sample from a subject is tested for the level of expression of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA. The levels are compared to one or more appropriate controls, e.g., other normal subjects, subjects with prostate cancer. Detection of an abnormal level of one or more of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 8, keratin 15, and keratin 19; indicates that the subject should be considered for further tests for the presence of prostate cancer. Changes in the level of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 8, keratin 15, and keratin 19, in the subject may be more indicative of a change in prostate cancer status than comparison to a population control.

[0626] In determining a therapeutic regimen for a subject with prostate cancer not yet being actively treated for prostate cancer (i.e., watchful waiting) can be tested at regular intervals to determine if there is a change in the level of expression of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA. An modulation in the level of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 8, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA indicates that the subject should be considered for further tests to monitor the prostate cancer and more active therapeutic interventions should be considered.

[0627] In a subject undergoing treatment for prostate cancer (e.g., hormone therapy, chemotherapy, radiation therapy, surgery) is tested prior to the initiation of the treatment and during and/or after the treatment to determine if the treatment results in a decrease in the level of expression of at least one of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, preferably at least one of keratin 7, keratin 15, and keratin 19; and optionally further at least one of filamin B, LY9, and PSA. A decrease in the level of keratin 19, filamin B, LY9, or PSA is indicative of response to treatment. Expression levels of keratins 7, 8, and 15 may also be particularly useful in the diagnosis and monitoring of subjects with prostate cancer.

Example 10: Stratification of Subjects with Prostate Cancer Using Filamin B, PSA, or LY9

[0628] As demonstrated in Examples 3 and 4 respectively, filamin B levels and LY9 levels can be used to distinguish subjects who are or are not suffering from prostate cancer. Further, as demonstrated in Examples 5 and 6, the analysis of both filamin B and PSA, optionally further in combination with LY9, is more sensitive than an analysis based on either marker alone.

[0629] A series of subject samples are obtained from an appropriate source, e.g., a commercial source, wherein the samples were obtained from subjects with different stages of prostate cancer, e.g., aggressive prostate cancer, androgen sensitive, androgen insensitive, metastatic; or from subjects not suffering from prostate cancer, e.g., subjects with normal prostate or subjects with BPH. The samples are analyzed for the expression level of filamin B and PSA, and optionally the level of LY9, and further with one or more of keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19. The level of filamin B, LY9, and PSA, alone and in various combinations, optionally with other markers, e.g., keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19, correlate with the presence or absence of disease, and with the severity of prostate cancer.

Example 11: Monitoring of Prostate Cancer Treatment Using Filamin B, PSA, or LY9

[0630] At the time of diagnosis with prostate cancer, subjects are invited to participate in a trial. A subject sample, e.g., blood, is obtained. Periodically, throughout the monitoring, watchful waiting, or active treatment of the subject, e.g., chemotherapy, radiation therapy, surgery, hormone therapy, a new subject sample is obtained. At the end of the study, all subject samples are tested for the level of filamin B, PSA, and optionally in further combination with one or more of LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3. The subject samples are matched to the medical records of the subjects to correlate filamin B, PSA, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, or tubulin-beta 3 levels, as appropriate, with prostate cancer status at the time of diagnosis, rate of progression of disease, response of subjects to one or more interventions, and transitions between androgen dependent and independent status.

Example 12: Detection and Monitoring of Prostate Cancer Using Filamin B, PSA, or LY9

[0631] Despite its limitations, including a positive predictive value of only 25-40%, PSA remains the only generally accepted biomarker for prostate cancer. Moreover, as prostate cancer is most commonly a slow growing tumor in men of advanced age, treatment of the cancer may do more harm to the subject than the tumor itself would. As demonstrated herein, there is a low correlation between elevated levels of filamin B and PSA in subjects with prostate cancer. Further, elevated levels of LY9 have been demonstrated to be associated with prostate cancer. Therefore, the tests together, particularly filamin B and PSA, optionally in combination with one or more of LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19, in detection, including in routine, preventative, screening methods in men having an increased risk of prostate cancer (e.g., increased age, family history, race, etc.) or in monitoring of subjects diagnosed with prostate cancer prior to or during treatment may be useful to better identify subjects in need of further, potentially more invasive, diagnostic tests, e.g., prostate exam or biopsy, digital rectal exam; or more aggressive treatment. Detection of levels of expression of filamin B, PSA, LY9 keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19, may also be indicative of a good or poor response to a specific treatment regimen prior to changes in other signs or symptoms, e.g., loss of tumor response to hormone therapy.

[0632] In routine screening methods for prostate cancer, a serum sample from a subject is tested for the level of expression of both filamin B and PSA, and optionally one or more of LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19. The levels are compared to one or more appropriate controls, e.g., other normal subjects, subjects with prostate cancer. Detection of an abnormal level of one or more of filamin B, PSA, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3, especially keratin 19 indicates that the subject should be considered for further tests for the presence of prostate cancer. Changes in the level of filamin B, optionally in combination with one or more of PSA, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, or tubulin-beta 3, especially keratin 19 with PSA in the subject may be more indicative of a change in prostate cancer status than comparison to a population control.

[0633] In determining a therapeutic regimen for a subject with prostate cancer not yet being actively treated for prostate cancer (i.e., watchful waiting) can be tested at regular intervals to determine if there is a change in the level of expression of filamin B, PSA, LY9 keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3. An increase in the level of filamin B, PSA, keratin 19, or LY9 indicates that the subject should be considered for further tests to monitor the prostate cancer and more active therapeutic interventions should be considered.

[0634] In a subject undergoing treatment for prostate cancer (e.g., hormone therapy, chemotherapy, radiation therapy, surgery) is tested prior to the initiation of the treatment and during and/or after the treatment to determine if the treatment results in a change in the level of expression of one or more of filamin B, PSA, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, and tubulin-beta 3. A decrease in the level of filamin B, PSA, keratin 19, or LY9 is indicative of response to treatment.

Example 13: Detection of Filamin a and Keratin 19 by ELISA in Human Serum from Patients with and without Prostate Cancer

[0635] ELISA assays were conducted on commercially available human serum samples to detect the levels of filamin A and keratin 19 in samples from patients with and without prostate cancer.

[0636] The commercial human serum samples used for the filamin A ELISA are shown in FIG. 11, the data/annotation of which is publicly available at the Asterand and Bioreclamation websites. The commercial human serum samples used for the keratin 19 ELISA are shown in FIG. 12, the data/annotation of which is publicly available at the Asterand and Bioreclamation websites.

[0637] For the filamin A test, the ELISA was conducted in accordance with the Human Filamin A (FLNa) ELISA kit, Catalog No. CSB-EL008724HU, which is commercially and publicly available from CEDARLANE (Cusabio), the contents of which are incorporated herein by reference.

[0638] For the keratin 19 test, the ELISA was conducted in accordance with the Human Keratin-19 (KRT19) ELISA Kit, Catalog No. E91239HU, which is commercially and publicly available from CEDARLANE (Cusabio), the contents of which are incorporated herein by reference.

[0639] FIG. 13 shows the filamin A protein levels in serum from patients with and without prostate cancer as determined by ELISA.

[0640] FIG. 14. shows the keratin 19 protein levels in serum from patients with and without prostate cancer as determined by ELISA.

Example 14: Filamin a and Keratin 19 Differentiate Between Patients with Prostate Cancer and Normal Individuals

[0641] The inventors have developed in-vitro models of prostate cancer based on a number of cancer and normal cell lines including the androgen independent PC3 and the androgen dependent LNCaP prostate cancer cell lines. Key regulatory nodes inferred by Berg Interrogative Biology.TM. were selected for a proof-of-concept validation in human serum as biomarkers of prostate cancer.

[0642] The initial two biomarkers FLNB and LY9 showed predictive power to differentiate between normal serum and serum from prostate cancer patients. This report reviews statistical characteristics of additional biomarkers, FLNA, FLNC, KRT18 and KRT19.

Statistical Performance of Candidate Markers: Bioreclamation

Sample Set #1:

[0643] Human serum samples from normal individuals and individuals with prostate cancer were acquired from a commercial source, as per Example 13. The panel of biomarkers was measured by commercially available ELISA kits, as per Example 13.

[0644] FIG. 15 demonstrates the performance of the candidate markers in the set of 20 normal and 20 prostate cancer samples. FLN-A showed predictive power to differentiate between normal and cancer patients, whereas FLN-C did not show any positive trend. The combination panel of FLN-A and FLN-C did not improve on the performance of FLN-A alone.

Statistical Performance of Candidate Markers: Bioreclamation and Asterand Sample Set #2:

[0645] Human serum samples from normal individuals and individuals with prostate cancer were acquired from two commercial sources, as per Example 13. The panel of biomarkers was measured by commercially available ELISA kits, as per Example 13.

[0646] FIG. 16 demonstrates the performance of the candidate markers in the set of 20 normal and 20 prostate cancer samples. KRT19 showed predictive power to differentiate between normal and cancer patients. KRT18 did not show any differentiation between normal and cancer specimens. The combination panel of KRT18 and KRT19 did not improve on the performance of KRT19 alone.

Conclusion:

[0647] Based on the results of this proof-of-concept study, KRT19 and FLNA have the potential to differentiate between patients with prostate cancer and normal individuals. These two biomarkers may be evaluated in a larger clinical validation study by either a commercial or in-house developed ELISA assay. The results above demonstrate that FLNa and KRT19 are statistically significant biomarkers of prostate cancer and therefore may be a significant improvement over the current screening tools.

Example 15: Filamin a, Filamin B, Keratin 19, and Age Differentiate Between Patients with Prostate Cancer and Normal Individuals

[0648] To study whether the Prostate Cancer Panel test is equivalent, better, or weaker than PSA in screening for prostate cancer, we studied the above 4 comparisons with 4 different MVI (Multivariate Index) models to best study the utility of the panel.

[0649] Samples were divided as training/verification set and validation set. The verification set consisting of 332 samples was used to develop the models. The validation set of 171 samples were used to test the model.

[0650] The annotations of the validation samples were blinded. Probability unit linear regression models were estimated using the verification part of the sample set. Regression models were created to classify samples from the patients with diagnosed prostate cancer, with high Gleason Score (>6 and >7), and with benign prostate hyperplasia. Prostate cancer panel predictive algorithms were implemented based on the regression models and the probability cut-offs selected to achieve a certain level of test sensitivity or specificity. Each predictive algorithm was validated on the left-out validation sample set.

[0651] The biomarkers in the panel are:

[0652] 1) Filamin--A

[0653] 2) Filamin--B

[0654] 3) Keratin--19

[0655] 4) Age was used as a continuous predictor variable.

[0656] Using the panel in various combinations along with clinical information, the predictive power in screening for prostate cancer compared to PSA alone was tested. The specific study objectives were:

[0657] 1) Determine the predictive power and the utility of the Biomarker panel to differentiate between samples from patients with and without prostate cancer.

[0658] 2) Determine the predictive power of the Biomarker panel to differentiate between samples from patients with HIGH Gleason Score (8-10), INTERMEDIATE Gleason Score (7), and LOW Gleason Score (6) prostate cancer.

[0659] 3) Determine the predictive power of the Biomarker panel to identify samples from patients with prostate cancer but low PSA (less than 4 ng/ml) concentration.

[0660] 4) Determine the predictive power of the Biomarker panel to differentiate between samples from patients with prostate cancer and benign prostatic hyperplasia.

[0661] The terminology used for categories of cancer is:

[0662] Super High=Gleason Score 8 and above.

[0663] High=Gleason Score 7 and above

[0664] Low=Gleason score 6

[0665] Else=All other samples when a certain specified category is being compared with the rest of the samples.

[0666] Study Design

[0667] A retrospective and clinically annotated sample set from Mt. Sinai Hospital, Toronto, Canada was obtained. The sample matrix is serum and is frozen since its collection and processing.

[0668] This is a clinically annotated sample set with 662 samples from the patients at a Prostate Center. The patients were all comers for prostate gland biopsy. 120 samples from this set were used as a proof of concept set for the proposed Prostate Cancer Panel. The remaining samples were sorted as per the volume available. Anything short of 350 ul was excluded and the samples were then segregated in 2:1 ratio and identified as `Verification` set and `Validation` set.

[0669] All samples, irrespective of the verification or validation set, were analyzed using the prostate Cancer Panel in the CLIA certified laboratory. The laboratory was blinded to the sample's designation of `verification` or `validation` set.

[0670] The samples were randomized and separated as `verification` and `validation` set.

[0671] Participant Recruitment and Sampling

[0672] Serum samples were collected from 662 male patients. All patients were referred to a Prostate Center for a prostatic biopsy. These patients were suspicious for prostate cancer based on either clinical symptoms, digital-rectal examination, or, more frequently, due to a serum PSA elevation (beyond 3 ng/ml). The patients were consented to participate in this study by a personal interview and blood was drawn before any clinical manipulations or prostatic biopsy.

[0673] To establish the final diagnosis, the pathology report was examined by a clinical associate and patients were categorized as prostate cancer with Gleason score assigned (n=311), benign conditions (n=122), atypical small acini proliferation (n=26), prostatic intraepithelial neoplasia (n=69), benign prostatic hyperplasia (n=60), inflammation (n=58), microfocus adenocarcinoma (n=16).

[0674] Sample Collection Protocol

[0675] Venous blood was collected in SST tube, 5 mL from BD

[0676] Tubes were kept vertically at room temperature for 1/2-1 hour, allowing the blood to clot.

[0677] Samples were centrifuged at 2000 RCF for 10 minutes at 4.degree. C.

[0678] The supernatant serum was collected, aliquoted into 0.5 ml sterile screw-capped tubes, and labeled with the appropriate Identification Number.

[0679] Samples were immediately stored at -80.degree. C.

[0680] Data Collection

[0681] There are 332 samples in the training and 171 samples in the validation dataset. Samples were randomized to make two groups.

[0682] No. of total samples=332

[0683] No. of Gleason above 8=19

[0684] No. of samples with Gleason 6=103

[0685] No. of samples with No-Cancer=159

[0686] No. of BPH samples=23

[0687] Study Population

[0688] The samples were transferred on dry ice and were stored at -80.degree. C. in the CLIA certified laboratory.

[0689] The samples are from a retrospective sample set with the following annotation:

[0690] PSA test values

[0691] Diagnosis

[0692] Patient age

[0693] Reason for biopsy

[0694] Total biopsy cores, staging, and grading (Gleason score)

[0695] Number of positive cores

[0696] Tumor location

[0697] Reference Standard and Rationale

[0698] The PSA test is the reference standard against which the outcome of the Panel was compared.

[0699] This retrospective sample set has documented PSA values which were used in data analysis.

[0700] This set also had documented biopsy results with Gleason scores.

[0701] Validated Assays

[0702] All samples were tested using the assays described below:

[0703] FLN--A ELISA: which measures FLN--A in serum and plasma by ELISA in the range of 3.125-200 ng/ml

[0704] FLN--B ELISA which measures concentration of FLN-B in human serum and plasma by ELISA in the range of 0.156-10 pM

[0705] Keratin--19 ELISA which measures soluble cytokeratin 19 fragments in human serum

[0706] FLN--A IP MRM which measures the concentration of FLN A peptides from human serum using Immunoprecipitation and LC-MS/MS in the range of 125 pg/ml-2000 pg/ml for P2, 250 pg/ml--6000 pg/ml for P3 and 1125 pg/ml--36000 pg/ml for P4.

[0707] Definition and Rationale of Units

[0708] PSA is reported in units of ng/ml. The values are taken from the annotations of the sample set.

[0709] Filamin A ELISA:ng/ml

[0710] Filamin A Peptide IP--MRM:pg/ml

[0711] Keratin--19 fragment ELISA:ng/ml

[0712] Filamin--B ELISA; picomole, pM

[0713] Results

[0714] The models generated from the verification set samples generated the following AUC data in Table 1 and the predictive power data in Table 2.

TABLE-US-00003 TABLE 1 AUC summary for all dataset (Peptide in Log scale) Super High Gleason CA vs Others CA vs BPH High Gleason vs. Low High Gleason vs. Others vs. Others Biomarker AUC Biomarker AUC Biomarker AUC Biomarker AUC Biomarker AUC Individual PSA 0.569 PSA 0.564 PSA 0.619 PSA 0.631 PSA 0.67 Age 0.62 Age 0.621 Age 0.622 Age 0.662 Age 0.7 FLNA 0.574 FLNA 0.696 FLNA 0.515 FLNA 0.56 FLNA 0.542 FLNB 0.51 FLNB 0.516 FLNB 05.28 FLNB 0.515 FLNB 0.515 Krt19 0.519 Krt19 0.618 Krt19 0.573 Krt19 0.567 Krt19 0.574 P2-1 0.55 P2-1 0.636 P2-1 0.527 P2-1 0.551 P2-1 0.528 P2-2 0.502 P2-2 0.582 P2-2 0.528 P2-2 0.552 P2-2 0.53 P3-1 0.51 P3-1 0.524 P3-1 0.547 P3-1 0.529 P3-1 0.5 P4-2 0.522 P4-2 0.595 P4-2 0.551 P4-2 0.555 P4-2 0.578 Two Combined Age & 0.63 FLNA & 0.717 Age & 0.659 Age & 0.696 Age & 0.765 (top) FLNB KRT19 PSA PSA PSA Three Combined Age & 0.635 FLNA & 0.735 PSA & 0.685 PSA & 0.717 PSA & 0.804 (top) FLNB KRT19 & Age & Age & Age & & PSA Age FLNB FLNB FLNB Four Combined Age & 0.637 FLNA & 0.746 PSA & 0.693 PSA & 0.723 PSA & 0.81 (top) FLNA & KRT19 & Age & Age & Age & P2-1 & P2-1 & FLNB & FLNP & FLNB & P2-2 Age P3-1 P3-1 P2-2 FLAN & 0.746 PSA & 0.81 KRT19 & Age & Age & FLNB & P4-2 P2-2 Five Combined Age & 0.644 FLNA & 0.764 PSA & 0.694 No improvement PSA & 0.811 (top) FLNA & KRT19 & Age & Age & PSA & Age & FLNA & FLNB & P2-2 & P2-1 & P3-1 & P2-2 & P2-1 P3-1 KRT19 P2-1

TABLE-US-00004 TABLE 2 Summary of Predictive Power analysis of Verification Samples Cut Sensi- Speci- Goal off tivity ficity PPV NPV Differentiate between Cancer and Non Cancer samples Verification Set 0.4455 0.7712 0.3380 0.5566 0.5783 Gleason Score 8 and above Vs. Other samples Verification Set 0.01997 1.0000 0.2482 0.0752 1.0000 Gleason Score 7 and above Vs. Other samples Verification Set 0.1603 0.8136 0.4915 0.2857 0.9134 Prostate Cancer Vs. BPH samples Verification Set 0.8758 0.8035 0.6087 0.9392 0.2917

[0715] The predictive power and the utility of the Biomarker panel to differentiate between samples from patients with and without prostate cancer is shown below:

TABLE-US-00005 Differentiate between Cancer and Goal Non Cancer Cut off Sensitivity Specificity PPV NPV Comments Verification Set 0.4455 0.7712 0.3380 0.5566 0.5783 Validation Set 0.4455 0.8442 0.3580 0.5556 0.7073 p value significant for Odds Ratio

[0716] Verification Set

[0717] This model was trained to match the sensitivity of PSA=4 cutoff and test the specificity of the above-identified biomarker panel compared to the PSA test. FIG. 18 depicts PCA vs. Else: Sensitivity match PSA with a cutoff of 0.4455.

[0718] Validation Set

[0719] A boxplot of the predicted probability and the accuracy analysis are shown in FIGS. 19 and 20, respectively.

[0720] Next, the predictive power of the biomarker panel to differentiate between samples from patients with SUPER HIGH Gleason Score (8-10), HIGH Gleason Score (7 and above), and LOW Gleason Score (6) prostate cancer was determined.

TABLE-US-00006 Goal Cut off Sensitivity Specificity PPV NPV Comments Gleason Score 8 and above Vs. Other samples Verification Set 0.01997 1.0000 0.2482 0.0752 1.0000 Validation Set 0.01997 0.7500 0.2583 0.0509 0.9512 Gleason Score 7 and above Vs. Other samples Verification Set 0.1603 0.8136 0.4915 0.2857 0.9134 Validation Set 0.1603 0.7000 0.5116 0.2500 0.8800 p value significant for Odds Ratio

[0721] Verification Set

[0722] The model was trained to give a Sensitivity> or =0.95. As per this model, the cut off generated was 0.01997. See FIG. 21.

[0723] Validation Set

[0724] A boxplot of the predicted probability and the accuracy analysis are shown in FIG. 22 and FIG. 23, respectively.

[0725] Next, the predictive power of the biomarker panel to differentiate between samples from patients with a HIGH Gleason Score versus Everything Else was determined.

[0726] Verification Set

[0727] The model was trained to have sensitivity of greater than or equal to 0.8. The outcome was a cut off value for the Biomarker panel which was 0.1603. See FIG. 24.

[0728] Validation Set

[0729] A boxplot of the predicted probability and the accuracy analysis are shown in FIG. 25 and FIG. 26, respectively.

[0730] Next, the predictive power of the biomarker panel to identify samples from patients with prostate cancer but low PSA (less than 4 ng/ml) concentration was determined. For this test, verification samples that had cancer were differentiated as low PSA (less than 4 ng/ml) and high PSA (greater than 4 ng/ml). Thus, the PSA AUC was equal to 1. Next, the low PSA and high PSA were predicted using the above-identified biomarker panel. The Table, below, depicts the AUC Summary for High PSA cancer versus Low PSA cancer.

AUC Summary for High PSA Cancer Vs. Low PSA Cancer

TABLE-US-00007

[0731] High PSA CA versus LPSA CA Biomarker AUC Age 0.598 FLNA 0.608 FLNB 0.517 KRT19 0.517 P3-1 0.532 P4-2 0.506 Two Combined (top) FLNA & Age 0.664 Three Combined (top) FLNA & Age & P4-2 0.669 Four Combined (top) No improvement Five Combined (top) No improvment

[0732] Next, the predictive power of the biomarker panel to differentiate between samples from patients with prostate cancer and benign prostatic hyperplasia was determined. See Table, below.

TABLE-US-00008 Prostate Cancer Goal Vs. BPH Cut off Sensitivity Specificity PPV NPV Comments Verification Set 0.8758 0.8035 0.6087 0.9392 0.2917 Validation Set 0.8758 0.6790 0.3636 0.8871 0.1333

[0733] Verification Set

[0734] The biomarker panel was set to get sensitivity greater than or equal to 0.8. The cut off generated by this model was 0.8758. See FIG. 27.

[0735] Validation Set

[0736] A boxplot of the predicted probability and the accuracy analysis are shown in FIG. 28 and FIG. 29, respectively.

[0737] Conclusion

[0738] The verification and validation study indicates utility in four clinical applications of the PCA panel. The developed model significantly improved the ability to discriminate less aggressive forms from more aggressive forms. The AUC for discriminating samples taken from patients with Gleason Scores 8 and higher was 0.8 (versus 0.67 for PSA alone). The negative predictive value was very high for this model, if the patient value was below the model cutoff, the probability of the patient being disease free was 95%.

[0739] The model also performed well in discriminating patients with BPH versus prostate cancer. A patient value greater than the model cut-off was associated with an approximately 90% probability of the patient having prostate cancer instead of BPH. The AUC for this model was 0.75 (versus 0.56 for PSA alone).

[0740] The capabilities to discriminate samples from patients with prostate cancer from those without prostate cancer had predictive values in the 55-70 percentiles. However, AUC's were improved compared to the use of PSA alone.

[0741] Summary of Predictive Power analysis of Verification/Validation Samples

TABLE-US-00009 Goal Cut off Sensitivity Specificity PPV NPV Comments Differentiate between Cancer and Non Cancer Verification Set 0.4455 0.7712 0.3380 0.5566 0.5783 Validation Set 0.4455 0.8442 0.3580 0.5556 0.7073 p value significant for Odds Ratio Gleason Score 8 and above Vs. Other samples Verification Set 0.01997 1.0000 0.2482 0.0752 1.0000 Validation Set 0.01997 0.7500 0.2583 0.0509 0.9512 Gleason Score 7 and above Vs. Other samples Verification Set 0.1603 0.8136 0.4915 0.2857 0.9134 Validation Set 0.1603 0.7000 0.5116 0.2500 0.8800 p value significant for Odds Ratio Prostate Cancer Vs. BPH Verification Set 0.8758 0.8035 0.6087 0.9392 0.2917 Validation Set 0.8758 0.6790 0.3636 0.8871 0.1333

Example 16: Identification and Validation of Novel Prostate Cancer Biomarkers

[0742] Prostate cancer is the most frequent cancer diagnosis among men and the second leading cause of cancer-related death. Despite the widespread use of digital rectal exam (DRE) and blood-based screening of prostate-specific antigen (PSA) for prostate cancer screening, there are significant limitations in their specificity and prognostic value. Biomarkers which distinguish i) PSA-low prostate cancer from benign prostatic hyperplasia (BPH) and (ii) indolent versus aggressive disease course represent unmet clinical needs. Experimentally, a panel of prostate cancer cell lines and non-tumorigenic, human primary cells were exposed to in vitro conditions designed to stimulate poor oxygenation, low pH, diminished nutrient microenvironments, and metabolic perturbations (24-48 h) followed by iTRAQ proteomic analysis of cell lysates. Using an Interrogative Biology platform, proteomic data were then subjected to Bayesian network learning to map molecular interactions, with cytoskeletal and scaffolding proteins Filamin A (FLNA), Filamin B (FLNB), and Keratin 19 (KRT19) identified as candidate prostate cancer biomarkers.

[0743] To validate biomarker expression, mRNA and protein was quantified in a panel of primary human prostate epithelial cells (HPrEC) and androgen-sensitive (LnCAP) or refractory (DU145, PC-3) prostate cancer cells, and each was differentially detected in one or more prostate cancer cell lines compared to HPrEC (FIGS. 30 and 31). Specifically, basal expression of FLNA, FLNB, and KRT19 in prostate cancer cells in vitro was assessed. mRNA and cell lysates were prepared from HPrEC, LnCAP, DU145, and PC-3 cells. Expression of FLNA, FLNB, and KRT19 was assessed by quantitative RT-PCR and normalized to TBP. Cell lysates were resolved by SDS-PAGE and probed with antibodies specific for FLNA, FLNB, and KRT19. Representative images are shown in FIGS. 30 and 31. Densitometric analysis for FLNA, FLNB, and KRT19 are reported below each blot. Values represent means+SEM, N=3. * p<0.05 compared to HPrEC.

[0744] Using proteomic analysis, peptides from FLNA, FLNB and KRT19 were also detected in cell culture media conditioned by prostate cancer cells (24 h), indicating that they can be secreted (FIG. 32). Specifically, conditioned media from LnCAP, DU145, and PC-3 cells exposed to lypoxia (1% oxygen), TNF.alpha. (10 ng/mL), or R1881 (1 nM) for 24 hours was harvested, and proteomic analysis was performed. Values represent means+SEM, N=3. * p<0.05 compared to normoxia control.

[0745] Importantly, unlike PSA expression, global regulation of FLNA, FLNB, and KRT19 expression remained unaltered after treatment with multiple prostate-cancer relevant stimula (e.g., hypoxia, androgens, and inflammatory stimula) (FIGS. 33-35). Specifically, mRNA was prepared from LnCAP, DU145, and PC-3 cells exposed to hypoxia (1% oxygen; A), TNF.alpha. (10 ng/mL; B), or R1881 (1 nM; C) for 24 h. Expression of FLNA, FLNB, and KRT19 was assessed by quantitative RT-PCR, normalized to TBP, and compared to PSA. Values represent means+SEM, N=3. * p<0.05 compared to normoxia/control.

[0746] Assessment of plasma FLNA and FLNB levels as screening markers were assessed in a proof-of-concept sample cohort of 47 plasma samples (FIG. 36). Residual lithium herpain plasma was collected from patient samples after the ordered tests were completed. The inclusion criteria were elevated PSA results (>2.6 ng/mL), age of 45-70 years, and minimum volume of 700 .mu.L. Results demonstrate that FLNA and FLNB were detected in human plasma and have predictive power in identifying prostate cancer patients.

[0747] Finally, in vivo validation was next conducted in sera from men (N-447) with confirmed prostate cancer, benign prostate tumors, or BPH using LDT ELISA assays in a CLIA-certified laboratory. To assess the sensitivity and specificity of FLNA, FLNB, and KRT19 compared to PSA, ROC curve analysis was performed. The individual predictive power of each biomarker alone was comparable to that of PSA. However, the combination of age, levels of FLNA, FLNB, and KRT19 and PSA out-performed PSA alone in identification of patients with prostate cancer stratified compared to benign status, Gleason scores, and incidence of BPH. Together, these data indicate that FLNA, FLNB, and KRT19 can be used in conjunction with PSA and/or age for more sensitive and specific prostate cancer screening, a critical unmet need in the field.

EQUIVALENTS

[0748] Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments and methods described herein. Such equivalents are intended to be encompassed by the scope of the following claims.

[0749] It is understood that the detailed examples and embodiments described herein are given by way of example for illustrative purposes only, and are in no way considered to be limiting to the invention. Various modifications or changes in light thereof will be suggested to persons skilled in the art and are included within the spirit and purview of this application and are considered within the scope of the appended claims. For example, the relative quantities of the ingredients may be varied to optimize the desired effects, additional ingredients may be added, and/or similar ingredients may be substituted for one or more of the ingredients described. Additional advantageous features and functionalities associated with the systems, methods, and processes of the present invention will be apparent from the appended claims. Moreover, those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.

Sequence CWU 1

1

491520PRTHomo Sapiens 1Met Ile Ala Arg Gln Gln Cys Val Arg Gly Gly Pro Arg Gly Phe Ser1 5 10 15Cys Gly Ser Ala Ile Val Gly Gly Gly Lys Arg Gly Ala Phe Ser Ser 20 25 30Val Ser Met Ser Gly Gly Ala Gly Arg Cys Ser Ser Gly Gly Phe Gly 35 40 45Ser Arg Ser Leu Tyr Asn Leu Arg Gly Asn Lys Ser Ile Ser Met Ser 50 55 60Val Ala Gly Ser Arg Gln Gly Ala Cys Phe Gly Gly Ala Gly Gly Phe65 70 75 80Gly Thr Gly Gly Phe Gly Gly Gly Phe Gly Gly Ser Phe Ser Gly Lys 85 90 95Gly Gly Pro Gly Phe Pro Val Cys Pro Ala Gly Gly Ile Gln Glu Val 100 105 110Thr Ile Asn Gln Ser Leu Leu Thr Pro Leu His Val Glu Ile Asp Pro 115 120 125Glu Ile Gln Lys Val Arg Thr Glu Glu Arg Glu Gln Ile Lys Leu Leu 130 135 140Asn Asn Lys Phe Ala Ser Phe Ile Asp Lys Val Gln Phe Leu Glu Gln145 150 155 160Gln Asn Lys Val Leu Glu Thr Lys Trp Asn Leu Leu Gln Gln Gln Thr 165 170 175Thr Thr Thr Ser Ser Lys Asn Leu Glu Pro Leu Phe Glu Thr Tyr Leu 180 185 190Ser Val Leu Arg Lys Gln Leu Asp Thr Leu Gly Asn Asp Lys Gly Arg 195 200 205Leu Gln Ser Glu Leu Lys Thr Met Gln Asp Ser Val Glu Asp Phe Lys 210 215 220Thr Lys Tyr Glu Glu Glu Ile Asn Lys Arg Thr Ala Ala Glu Asn Asp225 230 235 240Phe Val Val Leu Lys Lys Asp Val Asp Ala Ala Tyr Leu Asn Lys Val 245 250 255Glu Leu Glu Ala Lys Val Asp Ser Leu Asn Asp Glu Ile Asn Phe Leu 260 265 270Lys Val Leu Tyr Asp Ala Glu Leu Ser Gln Met Gln Thr His Val Ser 275 280 285Asp Thr Ser Val Val Leu Ser Met Asp Asn Asn Arg Asn Leu Asp Leu 290 295 300Asp Ser Ile Ile Ala Glu Val Arg Ala Gln Tyr Glu Glu Ile Ala Gln305 310 315 320Arg Ser Lys Ala Glu Ala Glu Ala Leu Tyr Gln Thr Lys Val Gln Gln 325 330 335Leu Gln Ile Ser Val Asp Gln His Gly Asp Asn Leu Lys Asn Thr Lys 340 345 350Ser Glu Ile Ala Glu Leu Asn Arg Met Ile Gln Arg Leu Arg Ala Glu 355 360 365Ile Glu Asn Ile Lys Lys Gln Cys Gln Thr Leu Gln Val Ser Val Ala 370 375 380Asp Ala Glu Gln Arg Gly Glu Asn Ala Leu Lys Asp Ala His Ser Lys385 390 395 400Arg Val Glu Leu Glu Ala Ala Leu Gln Gln Ala Lys Glu Glu Leu Ala 405 410 415Arg Met Leu Arg Glu Tyr Gln Glu Leu Met Ser Val Lys Leu Ala Leu 420 425 430Asp Ile Glu Ile Ala Thr Tyr Arg Lys Leu Leu Glu Gly Glu Glu Tyr 435 440 445Arg Met Ser Gly Glu Cys Gln Ser Ala Val Ser Ile Ser Val Val Ser 450 455 460Gly Ser Thr Ser Thr Gly Gly Ile Ser Gly Gly Leu Gly Ser Gly Ser465 470 475 480Gly Phe Gly Leu Ser Ser Gly Phe Gly Ser Gly Ser Gly Ser Gly Phe 485 490 495Gly Phe Gly Gly Ser Val Ser Gly Ser Ser Ser Ser Lys Ile Ile Ser 500 505 510Thr Thr Thr Leu Asn Lys Arg Arg 515 52022147DNAHomo sapiens 2actcaccggc ctgggccctg tcacttctct gatagctccc agctcgctct ctgcagccat 60gattgccaga cagcagtgtg tccgaggcgg gccccggggc ttcagctgtg gctcggccat 120tgtaggcggt ggcaagagag gtgccttcag ctcagtctcc atgtctggag gtgctggccg 180atgctcttct gggggatttg gcagcagaag cctctacaac ctcaggggga acaaaagcat 240ctccatgagt gtggctgggt cacgacaagg tgcctgcttt gggggtgctg gaggctttgg 300cactggtggc tttggtggtg gatttggggg ctccttcagt ggtaagggtg gccctggctt 360ccccgtctgc cccgctgggg gaattcagga ggtcaccatc aaccagagct tgctcacccc 420cctccacgtg gagattgacc ctgagatcca gaaagtccgg acggaagagc gcgaacagat 480caagctcctc aacaacaagt ttgcctcctt catcgacaag gtgcagttct tagagcaaca 540gaataaggtc ctggagacca aatggaacct gctccagcag cagacgacca ccacctccag 600caaaaacctt gagcccctct ttgagaccta cctcagtgtc ctgaggaagc agctagatac 660cttgggcaat gacaaagggc gcctgcagtc tgagctgaag accatgcagg acagcgtgga 720ggacttcaag actaagtatg aagaggagat caacaaacgc acagcagccg agaatgactt 780tgtggtccta aagaaggacg tggatgctgc ctacctgaac aaggtggagt tggaggccaa 840ggtggacagt cttaatgacg agatcaactt cctgaaggtc ctctatgatg cggagctgtc 900ccagatgcag acccatgtca gcgacacgtc cgtggtcctt tccatggaca acaaccgcaa 960cctggacctg gacagcatta ttgccgaggt ccgtgcccag tacgaggaga ttgcccagag 1020gagcaaggct gaggctgaag ccctgtacca gaccaaggtc cagcagctcc agatctcggt 1080tgaccaacat ggtgacaacc tgaagaacac caagagtgaa attgcagagc tcaacaggat 1140gatccagagg ctgcgggcag agatcgagaa catcaagaag cagtgccaga ctcttcaggt 1200atccgtggct gatgcagagc agcgaggtga gaatgccctt aaagatgccc acagcaagcg 1260cgtagagctg gaggctgccc tgcagcaggc caaggaggag ctggcacgaa tgctgcgtga 1320gtaccaggag ctcatgagtg tgaagctggc cttggacatc gagatcgcca cctaccgcaa 1380actgctggag ggcgaggagt acagaatgtc tggagaatgc cagagtgccg tgagcatctc 1440tgtggtcagc ggtagcacca gcactggagg catcagcgga ggattaggaa gtggctccgg 1500gtttggcctg agtagtggct ttggctccgg ctctggaagt ggctttgggt ttggtggcag 1560tgtctctggc agttccagca gcaagatcat ctctaccacc accctgaaca agagacgata 1620gaggagacga ggtccctgca gctcactgtg tccagctggg cccagcactg gtgtctctgt 1680gcttccttca cttcacctcc atcctctgtc tctggggctc atcttactag tatcccctcc 1740actatcccat gggctctctc tgccccagga tgatcttctg tgctgggaca gggactctgc 1800ctcttggagt ttggtagcta cttcttgatt tgggcctggt gacccacctg gaatgggaag 1860gatgtcagct gacctctcac ctcccatgga cagagaagaa aatgaccagg agtgtcatct 1920ccagaattat tggggtcaca tatgtccctt cccagtccaa tgccatctcc cactagatcc 1980tgtattatcc atctacatca gaaccaaact acttctccaa cacccggcag cacttggccc 2040tgcaagctta ggatgagaac cacttagtgt cccattctac tcctctcatt ccctcttatc 2100catctgcagg tgaatcttca ataaaatgct tttgtcattc attctga 21473469PRTHomo sapiens 3Met Ser Ile His Phe Ser Ser Pro Val Phe Thr Ser Arg Ser Ala Ala1 5 10 15Phe Ser Gly Arg Gly Ala Gln Val Arg Leu Ser Ser Ala Arg Pro Gly 20 25 30Gly Leu Gly Ser Ser Ser Leu Tyr Gly Leu Gly Ala Ser Arg Pro Arg 35 40 45Val Ala Val Arg Ser Ala Tyr Gly Gly Pro Val Gly Ala Gly Ile Arg 50 55 60Glu Val Thr Ile Asn Gln Ser Leu Leu Ala Pro Leu Arg Leu Asp Ala65 70 75 80Asp Pro Ser Leu Gln Arg Val Arg Gln Glu Glu Ser Glu Gln Ile Lys 85 90 95Thr Leu Asn Asn Lys Phe Ala Ser Phe Ile Asp Lys Val Arg Phe Leu 100 105 110Glu Gln Gln Asn Lys Leu Leu Glu Thr Lys Trp Thr Leu Leu Gln Glu 115 120 125Gln Lys Ser Ala Lys Ser Ser Arg Leu Pro Asp Ile Phe Glu Ala Gln 130 135 140Ile Ala Gly Leu Arg Gly Gln Leu Glu Ala Leu Gln Val Asp Gly Gly145 150 155 160Arg Leu Glu Ala Glu Leu Arg Ser Met Gln Asp Val Val Glu Asp Phe 165 170 175Lys Asn Lys Tyr Glu Asp Glu Ile Asn His Arg Thr Ala Ala Glu Asn 180 185 190Glu Phe Val Val Leu Lys Lys Asp Val Asp Ala Ala Tyr Met Ser Lys 195 200 205Val Glu Leu Glu Ala Lys Val Asp Ala Leu Asn Asp Glu Ile Asn Phe 210 215 220Leu Arg Thr Leu Asn Glu Thr Glu Leu Thr Glu Leu Gln Ser Gln Ile225 230 235 240Ser Asp Thr Ser Val Val Leu Ser Met Asp Asn Ser Arg Ser Leu Asp 245 250 255Leu Asp Gly Ile Ile Ala Glu Val Lys Ala Gln Tyr Glu Glu Met Ala 260 265 270Lys Cys Ser Arg Ala Glu Ala Glu Ala Trp Tyr Gln Thr Lys Phe Glu 275 280 285Thr Leu Gln Ala Gln Ala Gly Lys His Gly Asp Asp Leu Arg Asn Thr 290 295 300Arg Asn Glu Ile Ser Glu Met Asn Arg Ala Ile Gln Arg Leu Gln Ala305 310 315 320Glu Ile Asp Asn Ile Lys Asn Gln Arg Ala Lys Leu Glu Ala Ala Ile 325 330 335Ala Glu Ala Glu Glu Arg Gly Glu Leu Ala Leu Lys Asp Ala Arg Ala 340 345 350Lys Gln Glu Glu Leu Glu Ala Ala Leu Gln Arg Gly Lys Gln Asp Met 355 360 365Ala Arg Gln Leu Arg Glu Tyr Gln Glu Leu Met Ser Val Lys Leu Ala 370 375 380Leu Asp Ile Glu Ile Ala Thr Tyr Arg Lys Leu Leu Glu Gly Glu Glu385 390 395 400Ser Arg Leu Ala Gly Asp Gly Val Gly Ala Val Asn Ile Ser Val Met 405 410 415Asn Ser Thr Gly Gly Ser Ser Ser Gly Gly Gly Ile Gly Leu Thr Leu 420 425 430Gly Gly Thr Met Gly Ser Asn Ala Leu Ser Phe Ser Ser Ser Ala Gly 435 440 445Pro Gly Leu Leu Lys Ala Tyr Ser Ile Arg Thr Ala Ser Ala Ser Arg 450 455 460Arg Ser Ala Arg Asp46541753DNAHomo sapiens 4cagccccgcc cctacctgtg gaagcccagc cgcccgctcc cgcggataaa aggcgcggag 60tgtccccgag gtcagcgagt gcgcgctcct cctcgcccgc cgctaggtcc atcccggccc 120agccaccatg tccatccact tcagctcccc ggtattcacc tcgcgctcag ccgccttctc 180gggccgcggc gcccaggtgc gcctgagctc cgctcgcccc ggcggccttg gcagcagcag 240cctctacggc ctcggcgcct cacggccgcg cgtggccgtg cgctctgcct atgggggccc 300ggtgggcgcc ggcatccgcg aggtcaccat taaccagagc ctgctggccc cgctgcggct 360ggacgccgac ccctccctcc agcgggtgcg ccaggaggag agcgagcaga tcaagaccct 420caacaacaag tttgcctcct tcatcgacaa ggtgcggttt ctggagcagc agaacaagct 480gctggagacc aagtggacgc tgctgcagga gcagaagtcg gccaagagca gccgcctccc 540agacatcttt gaggcccaga ttgctggcct tcggggtcag cttgaggcac tgcaggtgga 600tgggggccgc ctggaggcgg agctgcggag catgcaggat gtggtggagg acttcaagaa 660taagtacgaa gatgaaatta accaccgcac agctgctgag aatgagtttg tggtgctgaa 720gaaggatgtg gatgctgcct acatgagcaa ggtggagctg gaggccaagg tggatgccct 780gaatgatgag atcaacttcc tcaggaccct caatgagacg gagttgacag agctgcagtc 840ccagatctcc gacacatctg tggtgctgtc catggacaac agtcgctccc tggacctgga 900cggcatcatc gctgaggtca aggcgcagta tgaggagatg gccaaatgca gccgggctga 960ggctgaagcc tggtaccaga ccaagtttga gaccctccag gcccaggctg ggaagcatgg 1020ggacgacctc cggaataccc ggaatgagat ttcagagatg aaccgggcca tccagaggct 1080gcaggctgag atcgacaaca tcaagaacca gcgtgccaag ttggaggccg ccattgccga 1140ggctgaggag cgtggggagc tggcgctcaa ggatgctcgt gccaagcagg aggagctgga 1200agccgccctg cagcggggca agcaggatat ggcacggcag ctgcgtgagt accaggaact 1260catgagcgtg aagctggccc tggacatcga gatcgccacc taccgcaagc tgctggaggg 1320cgaggagagc cggttggctg gagatggagt gggagccgtg aatatctctg tgatgaattc 1380cactggtggc agtagcagtg gcggtggcat tgggctgacc ctcgggggaa ccatgggcag 1440caatgccctg agcttctcca gcagtgcggg tcctgggctc ctgaaggctt attccatccg 1500gaccgcatcc gccagtcgca ggagtgcccg cgactgagcc gcctcccacc actccactcc 1560tccagccacc acccacaatc acaagaagat tcccacccct gcctcccatg cctggtccca 1620agacagtgag acagtctgga aagtgatgtc agaatagctt ccaataaagc agcctcattc 1680tgaggcctga gtgatccacg tgaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 1740aaaaaaaaaa aaa 17535511PRTHomo sapiens 5Met Asn Gly Val Ser Trp Ser Gln Asp Leu Gln Glu Gly Ile Ser Ala1 5 10 15Trp Phe Gly Pro Pro Ala Ser Thr Pro Ala Ser Thr Met Ser Ile Arg 20 25 30Val Thr Gln Lys Ser Tyr Lys Val Ser Thr Ser Gly Pro Arg Ala Phe 35 40 45Ser Ser Arg Ser Tyr Thr Ser Gly Pro Gly Ser Arg Ile Ser Ser Ser 50 55 60Ser Phe Ser Arg Val Gly Ser Ser Asn Phe Arg Gly Gly Leu Gly Gly65 70 75 80Gly Tyr Gly Gly Ala Ser Gly Met Gly Gly Ile Thr Ala Val Thr Val 85 90 95Asn Gln Ser Leu Leu Ser Pro Leu Val Leu Glu Val Asp Pro Asn Ile 100 105 110Gln Ala Val Arg Thr Gln Glu Lys Glu Gln Ile Lys Thr Leu Asn Asn 115 120 125Lys Phe Ala Ser Phe Ile Asp Lys Val Arg Phe Leu Glu Gln Gln Asn 130 135 140Lys Met Leu Glu Thr Lys Trp Ser Leu Leu Gln Gln Gln Lys Thr Ala145 150 155 160Arg Ser Asn Met Asp Asn Met Phe Glu Ser Tyr Ile Asn Asn Leu Arg 165 170 175Arg Gln Leu Glu Thr Leu Gly Gln Glu Lys Leu Lys Leu Glu Ala Glu 180 185 190Leu Gly Asn Met Gln Gly Leu Val Glu Asp Phe Lys Asn Lys Tyr Glu 195 200 205Asp Glu Ile Asn Lys Arg Thr Glu Met Glu Asn Glu Phe Val Leu Ile 210 215 220Lys Lys Asp Val Asp Glu Ala Tyr Met Asn Lys Val Glu Leu Glu Ser225 230 235 240Arg Leu Glu Gly Leu Thr Asp Glu Ile Asn Phe Leu Arg Gln Leu Tyr 245 250 255Glu Glu Glu Ile Arg Glu Leu Gln Ser Gln Ile Ser Asp Thr Ser Val 260 265 270Val Leu Ser Met Asp Asn Ser Arg Ser Leu Asp Met Asp Ser Ile Ile 275 280 285Ala Glu Val Lys Ala Gln Tyr Glu Asp Ile Ala Asn Arg Ser Arg Ala 290 295 300Glu Ala Glu Ser Met Tyr Gln Ile Lys Tyr Glu Glu Leu Gln Ser Leu305 310 315 320Ala Gly Lys His Gly Asp Asp Leu Arg Arg Thr Lys Thr Glu Ile Ser 325 330 335Glu Met Asn Arg Asn Ile Ser Arg Leu Gln Ala Glu Ile Glu Gly Leu 340 345 350Lys Gly Gln Arg Ala Ser Leu Glu Ala Ala Ile Ala Asp Ala Glu Gln 355 360 365Arg Gly Glu Leu Ala Ile Lys Asp Ala Asn Ala Lys Leu Ser Glu Leu 370 375 380Glu Ala Ala Leu Gln Arg Ala Lys Gln Asp Met Ala Arg Gln Leu Arg385 390 395 400Glu Tyr Gln Glu Leu Met Asn Val Lys Leu Ala Leu Asp Ile Glu Ile 405 410 415Ala Thr Tyr Arg Lys Leu Leu Glu Gly Glu Glu Ser Arg Leu Glu Ser 420 425 430Gly Met Gln Asn Met Ser Ile His Thr Lys Thr Thr Ser Gly Tyr Ala 435 440 445Gly Gly Leu Ser Ser Ala Tyr Gly Gly Leu Thr Ser Pro Gly Leu Ser 450 455 460Tyr Ser Leu Gly Ser Ser Phe Gly Ser Gly Ala Gly Ser Ser Ser Phe465 470 475 480Ser Arg Thr Ser Ser Ser Arg Ala Val Val Val Lys Lys Ile Glu Thr 485 490 495Arg Asp Gly Lys Leu Val Ser Glu Ser Ser Asp Val Leu Pro Lys 500 505 51061807DNAHomo sapiens 6attcagcaaa tgtttgcgga atgaatgggg tgagctggag ccaggacctg caggaaggga 60tctccgcctg gttcggcccg cctgcctcca ctcctgcctc taccatgtcc atcagggtga 120cccagaagtc ctacaaggtg tccacctctg gcccccgggc cttcagcagc cgctcctaca 180cgagtgggcc cggttcccgc atcagctcct cgagcttctc ccgagtgggc agcagcaact 240ttcgcggtgg cctgggcggc ggctatggtg gggccagcgg catgggaggc atcaccgcag 300ttacggtcaa ccagagcctg ctgagccccc ttgtcctgga ggtggacccc aacatccagg 360ccgtgcgcac ccaggagaag gagcagatca agaccctcaa caacaagttt gcctccttca 420tagacaaggt acggttcctg gagcagcaga acaagatgct ggagaccaag tggagcctcc 480tgcagcagca gaagacggct cgaagcaaca tggacaacat gttcgagagc tacatcaaca 540accttaggcg gcagctggag actctgggcc aggagaagct gaagctggag gcggagcttg 600gcaacatgca ggggctggtg gaggacttca agaacaagta tgaggatgag atcaataagc 660gtacagagat ggagaacgaa tttgtcctca tcaagaagga tgtggatgaa gcttacatga 720acaaggtaga gctggagtct cgcctggaag ggctgaccga cgagatcaac ttcctcaggc 780agctatatga agaggagatc cgggagctgc agtcccagat ctcggacaca tctgtggtgc 840tgtccatgga caacagccgc tccctggaca tggacagcat cattgctgag gtcaaggcac 900agtacgagga tattgccaac cgcagccggg ctgaggctga gagcatgtac cagatcaagt 960atgaggagct gcagagcctg gctgggaagc acggggatga cctgcggcgc acaaagactg 1020agatctctga gatgaaccgg aacatcagcc ggctccaggc tgagattgag ggcctcaaag 1080gccagagggc ttccctggag gccgccattg cagatgccga gcagcgtgga gagctggcca 1140ttaaggatgc caacgccaag ttgtccgagc tggaggccgc cctgcagcgg gccaagcagg 1200acatggcgcg gcagctgcgt gagtaccagg agctgatgaa cgtcaagctg gccctggaca 1260tcgagatcgc cacctacagg aagctgctgg agggcgagga gagccggctg gagtctggga 1320tgcagaacat gagtattcat acgaagacca ccagcggcta tgcaggtggt ctgagctcgg 1380cctatggggg cctcacaagc cccggcctca gctacagcct gggctccagc tttggctctg 1440gcgcgggctc cagctccttc agccgcacca gctcctccag ggccgtggtt gtgaagaaga 1500tcgagacacg tgatgggaag ctggtgtctg agtcctctga cgtcctgccc aagtgaacag 1560ctgcggcagc ccctcccagc ctacccctcc tgcgctgccc cagagcctgg gaaggaggcc 1620gctatgcagg gtagcactgg gaacaggaga cccacctgag gctcagccct agccctcagc 1680ccacctgggg agtttactac ctggggaccc cccttgccca tgcctccagc tacaaaacaa 1740ttcaattgct tttttttttt ggtccaaaat aaaacctcag ctagctctgc caatgtcaaa 1800aaaaaaa 18077483PRTHomo sapiens 7Met

Ser Ile Arg Val Thr Gln Lys Ser Tyr Lys Val Ser Thr Ser Gly1 5 10 15Pro Arg Ala Phe Ser Ser Arg Ser Tyr Thr Ser Gly Pro Gly Ser Arg 20 25 30Ile Ser Ser Ser Ser Phe Ser Arg Val Gly Ser Ser Asn Phe Arg Gly 35 40 45Gly Leu Gly Gly Gly Tyr Gly Gly Ala Ser Gly Met Gly Gly Ile Thr 50 55 60Ala Val Thr Val Asn Gln Ser Leu Leu Ser Pro Leu Val Leu Glu Val65 70 75 80Asp Pro Asn Ile Gln Ala Val Arg Thr Gln Glu Lys Glu Gln Ile Lys 85 90 95Thr Leu Asn Asn Lys Phe Ala Ser Phe Ile Asp Lys Val Arg Phe Leu 100 105 110Glu Gln Gln Asn Lys Met Leu Glu Thr Lys Trp Ser Leu Leu Gln Gln 115 120 125Gln Lys Thr Ala Arg Ser Asn Met Asp Asn Met Phe Glu Ser Tyr Ile 130 135 140Asn Asn Leu Arg Arg Gln Leu Glu Thr Leu Gly Gln Glu Lys Leu Lys145 150 155 160Leu Glu Ala Glu Leu Gly Asn Met Gln Gly Leu Val Glu Asp Phe Lys 165 170 175Asn Lys Tyr Glu Asp Glu Ile Asn Lys Arg Thr Glu Met Glu Asn Glu 180 185 190Phe Val Leu Ile Lys Lys Asp Val Asp Glu Ala Tyr Met Asn Lys Val 195 200 205Glu Leu Glu Ser Arg Leu Glu Gly Leu Thr Asp Glu Ile Asn Phe Leu 210 215 220Arg Gln Leu Tyr Glu Glu Glu Ile Arg Glu Leu Gln Ser Gln Ile Ser225 230 235 240Asp Thr Ser Val Val Leu Ser Met Asp Asn Ser Arg Ser Leu Asp Met 245 250 255Asp Ser Ile Ile Ala Glu Val Lys Ala Gln Tyr Glu Asp Ile Ala Asn 260 265 270Arg Ser Arg Ala Glu Ala Glu Ser Met Tyr Gln Ile Lys Tyr Glu Glu 275 280 285Leu Gln Ser Leu Ala Gly Lys His Gly Asp Asp Leu Arg Arg Thr Lys 290 295 300Thr Glu Ile Ser Glu Met Asn Arg Asn Ile Ser Arg Leu Gln Ala Glu305 310 315 320Ile Glu Gly Leu Lys Gly Gln Arg Ala Ser Leu Glu Ala Ala Ile Ala 325 330 335Asp Ala Glu Gln Arg Gly Glu Leu Ala Ile Lys Asp Ala Asn Ala Lys 340 345 350Leu Ser Glu Leu Glu Ala Ala Leu Gln Arg Ala Lys Gln Asp Met Ala 355 360 365Arg Gln Leu Arg Glu Tyr Gln Glu Leu Met Asn Val Lys Leu Ala Leu 370 375 380Asp Ile Glu Ile Ala Thr Tyr Arg Lys Leu Leu Glu Gly Glu Glu Ser385 390 395 400Arg Leu Glu Ser Gly Met Gln Asn Met Ser Ile His Thr Lys Thr Thr 405 410 415Ser Gly Tyr Ala Gly Gly Leu Ser Ser Ala Tyr Gly Gly Leu Thr Ser 420 425 430Pro Gly Leu Ser Tyr Ser Leu Gly Ser Ser Phe Gly Ser Gly Ala Gly 435 440 445Ser Ser Ser Phe Ser Arg Thr Ser Ser Ser Arg Ala Val Val Val Lys 450 455 460Lys Ile Glu Thr Arg Asp Gly Lys Leu Val Ser Glu Ser Ser Asp Val465 470 475 480Leu Pro Lys81901DNAHomo sapiens 8acaggccttt ccttacctcc ctccatgctg tccacttcct ctgtaaagct ctcaaccctg 60tccccttccc cctctctcct gggaaagagc cctcccatgc ctagctgctg ctcttaggga 120ccctgtggct aggtgcgcgg atggaaatcc aggatctccg cctggttcgg cccgcctgcc 180tccactcctg cctctaccat gtccatcagg gtgacccaga agtcctacaa ggtgtccacc 240tctggccccc gggccttcag cagccgctcc tacacgagtg ggcccggttc ccgcatcagc 300tcctcgagct tctcccgagt gggcagcagc aactttcgcg gtggcctggg cggcggctat 360ggtggggcca gcggcatggg aggcatcacc gcagttacgg tcaaccagag cctgctgagc 420ccccttgtcc tggaggtgga ccccaacatc caggccgtgc gcacccagga gaaggagcag 480atcaagaccc tcaacaacaa gtttgcctcc ttcatagaca aggtacggtt cctggagcag 540cagaacaaga tgctggagac caagtggagc ctcctgcagc agcagaagac ggctcgaagc 600aacatggaca acatgttcga gagctacatc aacaacctta ggcggcagct ggagactctg 660ggccaggaga agctgaagct ggaggcggag cttggcaaca tgcaggggct ggtggaggac 720ttcaagaaca agtatgagga tgagatcaat aagcgtacag agatggagaa cgaatttgtc 780ctcatcaaga aggatgtgga tgaagcttac atgaacaagg tagagctgga gtctcgcctg 840gaagggctga ccgacgagat caacttcctc aggcagctat atgaagagga gatccgggag 900ctgcagtccc agatctcgga cacatctgtg gtgctgtcca tggacaacag ccgctccctg 960gacatggaca gcatcattgc tgaggtcaag gcacagtacg aggatattgc caaccgcagc 1020cgggctgagg ctgagagcat gtaccagatc aagtatgagg agctgcagag cctggctggg 1080aagcacgggg atgacctgcg gcgcacaaag actgagatct ctgagatgaa ccggaacatc 1140agccggctcc aggctgagat tgagggcctc aaaggccaga gggcttccct ggaggccgcc 1200attgcagatg ccgagcagcg tggagagctg gccattaagg atgccaacgc caagttgtcc 1260gagctggagg ccgccctgca gcgggccaag caggacatgg cgcggcagct gcgtgagtac 1320caggagctga tgaacgtcaa gctggccctg gacatcgaga tcgccaccta caggaagctg 1380ctggagggcg aggagagccg gctggagtct gggatgcaga acatgagtat tcatacgaag 1440accaccagcg gctatgcagg tggtctgagc tcggcctatg ggggcctcac aagccccggc 1500ctcagctaca gcctgggctc cagctttggc tctggcgcgg gctccagctc cttcagccgc 1560accagctcct ccagggccgt ggttgtgaag aagatcgaga cacgtgatgg gaagctggtg 1620tctgagtcct ctgacgtcct gcccaagtga acagctgcgg cagcccctcc cagcctaccc 1680ctcctgcgct gccccagagc ctgggaagga ggccgctatg cagggtagca ctgggaacag 1740gagacccacc tgaggctcag ccctagccct cagcccacct ggggagttta ctacctgggg 1800accccccttg cccatgcctc cagctacaaa acaattcaat tgcttttttt ttttggtcca 1860aaataaaacc tcagctagct ctgccaatgt caaaaaaaaa a 19019456PRTHomo sapiens 9Met Thr Thr Thr Phe Leu Gln Thr Ser Ser Ser Thr Phe Gly Gly Gly1 5 10 15Ser Thr Arg Gly Gly Ser Leu Leu Ala Gly Gly Gly Gly Phe Gly Gly 20 25 30Gly Ser Leu Ser Gly Gly Gly Gly Ser Arg Ser Ile Ser Ala Ser Ser 35 40 45Ala Arg Phe Val Ser Ser Gly Ser Gly Gly Gly Tyr Gly Gly Gly Met 50 55 60Arg Val Cys Gly Phe Gly Gly Gly Ala Gly Ser Val Phe Gly Gly Gly65 70 75 80Phe Gly Gly Gly Val Gly Gly Gly Phe Gly Gly Gly Phe Gly Gly Gly 85 90 95Asp Gly Gly Leu Leu Ser Gly Asn Glu Lys Ile Thr Met Gln Asn Leu 100 105 110Asn Asp Arg Leu Ala Ser Tyr Leu Asp Lys Val Arg Ala Leu Glu Glu 115 120 125Ala Asn Ala Asp Leu Glu Val Lys Ile His Asp Trp Tyr Gln Lys Gln 130 135 140Thr Pro Thr Ser Pro Glu Cys Asp Tyr Ser Gln Tyr Phe Lys Thr Ile145 150 155 160Glu Glu Leu Arg Asp Lys Ile Met Ala Thr Thr Ile Asp Asn Ser Arg 165 170 175Val Ile Leu Glu Ile Asp Asn Ala Arg Leu Ala Ala Asp Asp Phe Arg 180 185 190Leu Lys Tyr Glu Asn Glu Leu Ala Leu Arg Gln Gly Val Glu Ala Asp 195 200 205Ile Asn Gly Leu Arg Arg Val Leu Asp Glu Leu Thr Leu Ala Arg Thr 210 215 220Asp Leu Glu Met Gln Ile Glu Gly Leu Asn Glu Glu Leu Ala Tyr Leu225 230 235 240Lys Lys Asn His Glu Glu Glu Met Lys Glu Phe Ser Ser Gln Leu Ala 245 250 255Gly Gln Val Asn Val Glu Met Asp Ala Ala Pro Gly Val Asp Leu Thr 260 265 270Arg Val Leu Ala Glu Met Arg Glu Gln Tyr Glu Ala Met Ala Glu Lys 275 280 285Asn Arg Arg Asp Val Glu Ala Trp Phe Phe Ser Lys Thr Glu Glu Leu 290 295 300Asn Lys Glu Val Ala Ser Asn Thr Glu Met Ile Gln Thr Ser Lys Thr305 310 315 320Glu Ile Thr Asp Leu Arg Arg Thr Met Gln Glu Leu Glu Ile Glu Leu 325 330 335Gln Ser Gln Leu Ser Met Lys Ala Gly Leu Glu Asn Ser Leu Ala Glu 340 345 350Thr Glu Cys Arg Tyr Ala Thr Gln Leu Gln Gln Ile Gln Gly Leu Ile 355 360 365Gly Gly Leu Glu Ala Gln Leu Ser Glu Leu Arg Cys Glu Met Glu Ala 370 375 380Gln Asn Gln Glu Tyr Lys Met Leu Leu Asp Ile Lys Thr Arg Leu Glu385 390 395 400Gln Glu Ile Ala Thr Tyr Arg Ser Leu Leu Glu Gly Gln Asp Ala Lys 405 410 415Met Ala Gly Ile Gly Ile Arg Glu Ala Ser Ser Gly Gly Gly Gly Ser 420 425 430Ser Ser Asn Phe His Ile Asn Val Glu Glu Ser Val Asp Gly Gln Val 435 440 445Val Ser Ser His Lys Arg Glu Ile 450 455101861DNAHomo sapiens 10cactcaaggt gtgcaggcag ctgtgtttgt caggaaggca gaaggagttg gctttgcttt 60aggggaggag acgaggtccc acaacaccct ctgaagggta tataaggagc cccagcgtgc 120agcctggcct ggtacctcct gccagcatct cttgggtttg ctgagaactc acgggctcca 180gctacctggc catgaccacc acatttctgc aaacttcttc ctccaccttt gggggtggct 240caacccgagg gggttccctc ctggctgggg gaggtggctt tggtgggggg agtctctctg 300ggggaggtgg aagccgaagt atctcagctt cttctgctag gtttgtctct tcagggtcag 360gaggaggata tgggggtggc atgagggtct gtggctttgg tggaggggct ggtagtgttt 420tcggtggagg ctttggaggg ggcgttggtg ggggttttgg tggtggcttt ggtggtggcg 480atggtggtct cctctctggc aatgagaaaa ttaccatgca gaacctcaat gaccgcctgg 540cctcctacct ggacaaggta cgtgccctgg aggaggccaa tgctgacctg gaggtgaaga 600tccatgactg gtaccagaag cagaccccaa ccagcccaga atgcgactac agccaatact 660tcaagaccat tgaagagctc cgggacaaga tcatggccac caccatcgac aactcccggg 720tcatcctgga gatcgacaat gccaggctgg ctgcggacga cttcaggctc aagtatgaga 780atgagctggc cctgcgccag ggcgttgagg ctgacatcaa cggcttgcgc cgagtcctgg 840atgagctgac cctggccagg actgacctgg agatgcagat cgagggcctg aatgaggagc 900tagcctacct gaagaagaac cacgaagagg agatgaagga gttcagcagc cagctggccg 960gccaggtcaa tgtggagatg gacgcagcac cgggtgtgga cctgacccgt gtgctggcag 1020agatgaggga gcagtacgag gccatggcgg agaagaaccg ccgggatgtc gaggcctggt 1080tcttcagcaa gactgaggag ctgaacaaag aggtggcctc caacacagaa atgatccaga 1140ccagcaagac ggagatcaca gacctgagac gcacgatgca ggagctggag atcgagctgc 1200agtcccagct cagcatgaaa gctgggctgg agaactcact ggccgagaca gagtgccgct 1260atgccacgca gctgcagcag atccaggggc tcattggtgg cctggaggcc cagctgagtg 1320agctccgatg cgagatggag gctcagaacc aggagtacaa gatgctgctt gacataaaga 1380cacggctgga gcaggagatc gctacttacc gcagcctgct cgagggccag gatgccaaga 1440tggctggcat tggcatcagg gaagcctctt caggaggtgg tggtagcagc agcaatttcc 1500acatcaatgt agaagagtca gtggatggac aggtggtttc ttcccacaag agagaaatct 1560aagtgtctat tgcaggagaa acgtcccttg ccactcccca ctctcatcag gccaagtgga 1620ggactggcca gagggcctgc acatgcaaac tccagtccct gccttcagag agctgaaaag 1680ggtccctcgg tcttttattt cagggctttg catgcgctct attccccctc tgcctctccc 1740caccttcttt ggagcaagga gatgcagctg tattgtgtaa caagctcatt tgtacagtgt 1800ctgttcatgt aataaagaat tacttttcct tttgcaaata aaaaaaaaaa aaaaaaaaaa 1860a 186111430PRTHomo sapiens 11Met Ser Phe Thr Thr Arg Ser Thr Phe Ser Thr Asn Tyr Arg Ser Leu1 5 10 15Gly Ser Val Gln Ala Pro Ser Tyr Gly Ala Arg Pro Val Ser Ser Ala 20 25 30Ala Ser Val Tyr Ala Gly Ala Gly Gly Ser Gly Ser Arg Ile Ser Val 35 40 45Ser Arg Ser Thr Ser Phe Arg Gly Gly Met Gly Ser Gly Gly Leu Ala 50 55 60Thr Gly Ile Ala Gly Gly Leu Ala Gly Met Gly Gly Ile Gln Asn Glu65 70 75 80Lys Glu Thr Met Gln Ser Leu Asn Asp Arg Leu Ala Ser Tyr Leu Asp 85 90 95Arg Val Arg Ser Leu Glu Thr Glu Asn Arg Arg Leu Glu Ser Lys Ile 100 105 110Arg Glu His Leu Glu Lys Lys Gly Pro Gln Val Arg Asp Trp Ser His 115 120 125Tyr Phe Lys Ile Ile Glu Asp Leu Arg Ala Gln Ile Phe Ala Asn Thr 130 135 140Val Asp Asn Ala Arg Ile Val Leu Gln Ile Asp Asn Ala Arg Leu Ala145 150 155 160Ala Asp Asp Phe Arg Val Lys Tyr Glu Thr Glu Leu Ala Met Arg Gln 165 170 175Ser Val Glu Asn Asp Ile His Gly Leu Arg Lys Val Ile Asp Asp Thr 180 185 190Asn Ile Thr Arg Leu Gln Leu Glu Thr Glu Ile Glu Ala Leu Lys Glu 195 200 205Glu Leu Leu Phe Met Lys Lys Asn His Glu Glu Glu Val Lys Gly Leu 210 215 220Gln Ala Gln Ile Ala Ser Ser Gly Leu Thr Val Glu Val Asp Ala Pro225 230 235 240Lys Ser Gln Asp Leu Ala Lys Ile Met Ala Asp Ile Arg Ala Gln Tyr 245 250 255Asp Glu Leu Ala Arg Lys Asn Arg Glu Glu Leu Asp Lys Tyr Trp Ser 260 265 270Gln Gln Ile Glu Glu Ser Thr Thr Val Val Thr Thr Gln Ser Ala Glu 275 280 285Val Gly Ala Ala Glu Thr Thr Leu Thr Glu Leu Arg Arg Thr Val Gln 290 295 300Ser Leu Glu Ile Asp Leu Asp Ser Met Arg Asn Leu Lys Ala Ser Leu305 310 315 320Glu Asn Ser Leu Arg Glu Val Glu Ala Arg Tyr Ala Leu Gln Met Glu 325 330 335Gln Leu Asn Gly Ile Leu Leu His Leu Glu Ser Glu Leu Ala Gln Thr 340 345 350Arg Ala Glu Gly Gln Arg Gln Ala Gln Glu Tyr Glu Ala Leu Leu Asn 355 360 365Ile Lys Val Lys Leu Glu Ala Glu Ile Ala Thr Tyr Arg Arg Leu Leu 370 375 380Glu Asp Gly Glu Asp Phe Asn Leu Gly Asp Ala Leu Asp Ser Ser Asn385 390 395 400Ser Met Gln Thr Ile Gln Lys Thr Thr Thr Arg Arg Ile Val Asp Gly 405 410 415Lys Val Val Ser Glu Thr Asn Asp Thr Lys Val Leu Arg His 420 425 430121485DNAHomo sapiens 12tccggggcgg gggcggggcc tcactctgcg atataactcg ggtcgcgcgg ctcgcgcagg 60ccgccaccgt cgtccgcaaa gcctgagtcc tgtcctttct ctctccccgg acagcatgag 120cttcaccact cgctccacct tctccaccaa ctaccggtcc ctgggctctg tccaggcgcc 180cagctacggc gcccggccgg tcagcagcgc ggccagcgtc tatgcaggcg ctgggggctc 240tggttcccgg atctccgtgt cccgctccac cagcttcagg ggcggcatgg ggtccggggg 300cctggccacc gggatagccg ggggtctggc aggaatggga ggcatccaga acgagaagga 360gaccatgcaa agcctgaacg accgcctggc ctcttacctg gacagagtga ggagcctgga 420gaccgagaac cggaggctgg agagcaaaat ccgggagcac ttggagaaga agggacccca 480ggtcagagac tggagccatt acttcaagat catcgaggac ctgagggctc agatcttcgc 540aaatactgtg gacaatgccc gcatcgttct gcagattgac aatgcccgtc ttgctgctga 600tgactttaga gtcaagtatg agacagagct ggccatgcgc cagtctgtgg agaacgacat 660ccatgggctc cgcaaggtca ttgatgacac caatatcaca cgactgcagc tggagacaga 720gatcgaggct ctcaaggagg agctgctctt catgaagaag aaccacgaag aggaagtaaa 780aggcctacaa gcccagattg ccagctctgg gttgaccgtg gaggtagatg cccccaaatc 840tcaggacctc gccaagatca tggcagacat ccgggcccaa tatgacgagc tggctcggaa 900gaaccgagag gagctagaca agtactggtc tcagcagatt gaggagagca ccacagtggt 960caccacacag tctgctgagg ttggagctgc tgagacgacg ctcacagagc tgagacgtac 1020agtccagtcc ttggagatcg acctggactc catgagaaat ctgaaggcca gcttggagaa 1080cagcctgagg gaggtggagg cccgctacgc cctacagatg gagcagctca acgggatcct 1140gctgcacctt gagtcagagc tggcacagac ccgggcagag ggacagcgcc aggcccagga 1200gtatgaggcc ctgctgaaca tcaaggtcaa gctggaggct gagatcgcca cctaccgccg 1260cctgctggaa gatggcgagg actttaatct tggtgatgcc ttggacagca gcaactccat 1320gcaaaccatc caaaagacca ccacccgccg gatagtggat ggcaaagtgg tgtctgagac 1380caatgacacc aaagttctga ggcattaagc cagcagaagc agggtaccct ttggggagca 1440ggaggccaat aaaaagttca gagttcaaaa aaaaaaaaaa aaaaa 148513430PRTHomo sapiens 13Met Ser Phe Thr Thr Arg Ser Thr Phe Ser Thr Asn Tyr Arg Ser Leu1 5 10 15Gly Ser Val Gln Ala Pro Ser Tyr Gly Ala Arg Pro Val Ser Ser Ala 20 25 30Ala Ser Val Tyr Ala Gly Ala Gly Gly Ser Gly Ser Arg Ile Ser Val 35 40 45Ser Arg Ser Thr Ser Phe Arg Gly Gly Met Gly Ser Gly Gly Leu Ala 50 55 60Thr Gly Ile Ala Gly Gly Leu Ala Gly Met Gly Gly Ile Gln Asn Glu65 70 75 80Lys Glu Thr Met Gln Ser Leu Asn Asp Arg Leu Ala Ser Tyr Leu Asp 85 90 95Arg Val Arg Ser Leu Glu Thr Glu Asn Arg Arg Leu Glu Ser Lys Ile 100 105 110Arg Glu His Leu Glu Lys Lys Gly Pro Gln Val Arg Asp Trp Ser His 115 120 125Tyr Phe Lys Ile Ile Glu Asp Leu Arg Ala Gln Ile Phe Ala Asn Thr 130 135 140Val Asp Asn Ala Arg Ile Val Leu Gln Ile Asp Asn Ala Arg Leu Ala145 150 155 160Ala Asp Asp Phe Arg Val Lys Tyr Glu Thr Glu Leu Ala Met Arg Gln 165 170 175Ser Val Glu Asn Asp Ile His Gly Leu Arg Lys Val Ile Asp Asp Thr 180 185 190Asn Ile Thr Arg Leu Gln Leu Glu Thr Glu Ile Glu Ala Leu Lys Glu 195 200 205Glu Leu Leu Phe

Met Lys Lys Asn His Glu Glu Glu Val Lys Gly Leu 210 215 220Gln Ala Gln Ile Ala Ser Ser Gly Leu Thr Val Glu Val Asp Ala Pro225 230 235 240Lys Ser Gln Asp Leu Ala Lys Ile Met Ala Asp Ile Arg Ala Gln Tyr 245 250 255Asp Glu Leu Ala Arg Lys Asn Arg Glu Glu Leu Asp Lys Tyr Trp Ser 260 265 270Gln Gln Ile Glu Glu Ser Thr Thr Val Val Thr Thr Gln Ser Ala Glu 275 280 285Val Gly Ala Ala Glu Thr Thr Leu Thr Glu Leu Arg Arg Thr Val Gln 290 295 300Ser Leu Glu Ile Asp Leu Asp Ser Met Arg Asn Leu Lys Ala Ser Leu305 310 315 320Glu Asn Ser Leu Arg Glu Val Glu Ala Arg Tyr Ala Leu Gln Met Glu 325 330 335Gln Leu Asn Gly Ile Leu Leu His Leu Glu Ser Glu Leu Ala Gln Thr 340 345 350Arg Ala Glu Gly Gln Arg Gln Ala Gln Glu Tyr Glu Ala Leu Leu Asn 355 360 365Ile Lys Val Lys Leu Glu Ala Glu Ile Ala Thr Tyr Arg Arg Leu Leu 370 375 380Glu Asp Gly Glu Asp Phe Asn Leu Gly Asp Ala Leu Asp Ser Ser Asn385 390 395 400Ser Met Gln Thr Ile Gln Lys Thr Thr Thr Arg Arg Ile Val Asp Gly 405 410 415Lys Val Val Ser Glu Thr Asn Asp Thr Lys Val Leu Arg His 420 425 430141439DNAHomo sapiens 14gcagcctcga gggccaacaa cacctgctgt ccgtgtccat gcccggttgg ccaccccgtt 60tctgggggca tgagcttcac cactcgctcc accttctcca ccaactaccg gtccctgggc 120tctgtccagg cgcccagcta cggcgcccgg ccggtcagca gcgcggccag cgtctatgca 180ggcgctgggg gctctggttc ccggatctcc gtgtcccgct ccaccagctt caggggcggc 240atggggtccg ggggcctggc caccgggata gccgggggtc tggcaggaat gggaggcatc 300cagaacgaga aggagaccat gcaaagcctg aacgaccgcc tggcctctta cctggacaga 360gtgaggagcc tggagaccga gaaccggagg ctggagagca aaatccggga gcacttggag 420aagaagggac cccaggtcag agactggagc cattacttca agatcatcga ggacctgagg 480gctcagatct tcgcaaatac tgtggacaat gcccgcatcg ttctgcagat tgacaatgcc 540cgtcttgctg ctgatgactt tagagtcaag tatgagacag agctggccat gcgccagtct 600gtggagaacg acatccatgg gctccgcaag gtcattgatg acaccaatat cacacgactg 660cagctggaga cagagatcga ggctctcaag gaggagctgc tcttcatgaa gaagaaccac 720gaagaggaag taaaaggcct acaagcccag attgccagct ctgggttgac cgtggaggta 780gatgccccca aatctcagga cctcgccaag atcatggcag acatccgggc ccaatatgac 840gagctggctc ggaagaaccg agaggagcta gacaagtact ggtctcagca gattgaggag 900agcaccacag tggtcaccac acagtctgct gaggttggag ctgctgagac gacgctcaca 960gagctgagac gtacagtcca gtccttggag atcgacctgg actccatgag aaatctgaag 1020gccagcttgg agaacagcct gagggaggtg gaggcccgct acgccctaca gatggagcag 1080ctcaacggga tcctgctgca ccttgagtca gagctggcac agacccgggc agagggacag 1140cgccaggccc aggagtatga ggccctgctg aacatcaagg tcaagctgga ggctgagatc 1200gccacctacc gccgcctgct ggaagatggc gaggacttta atcttggtga tgccttggac 1260agcagcaact ccatgcaaac catccaaaag accaccaccc gccggatagt ggatggcaaa 1320gtggtgtctg agaccaatga caccaaagtt ctgaggcatt aagccagcag aagcagggta 1380ccctttgggg agcaggaggc caataaaaag ttcagagttc aaaaaaaaaa aaaaaaaaa 143915400PRTHomo sapiens 15Met Thr Ser Tyr Ser Tyr Arg Gln Ser Ser Ala Thr Ser Ser Phe Gly1 5 10 15Gly Leu Gly Gly Gly Ser Val Arg Phe Gly Pro Gly Val Ala Phe Arg 20 25 30Ala Pro Ser Ile His Gly Gly Ser Gly Gly Arg Gly Val Ser Val Ser 35 40 45Ser Ala Arg Phe Val Ser Ser Ser Ser Ser Gly Ala Tyr Gly Gly Gly 50 55 60Tyr Gly Gly Val Leu Thr Ala Ser Asp Gly Leu Leu Ala Gly Asn Glu65 70 75 80Lys Leu Thr Met Gln Asn Leu Asn Asp Arg Leu Ala Ser Tyr Leu Asp 85 90 95Lys Val Arg Ala Leu Glu Ala Ala Asn Gly Glu Leu Glu Val Lys Ile 100 105 110Arg Asp Trp Tyr Gln Lys Gln Gly Pro Gly Pro Ser Arg Asp Tyr Ser 115 120 125His Tyr Tyr Thr Thr Ile Gln Asp Leu Arg Asp Lys Ile Leu Gly Ala 130 135 140Thr Ile Glu Asn Ser Arg Ile Val Leu Gln Ile Asp Asn Ala Arg Leu145 150 155 160Ala Ala Asp Asp Phe Arg Thr Lys Phe Glu Thr Glu Gln Ala Leu Arg 165 170 175Met Ser Val Glu Ala Asp Ile Asn Gly Leu Arg Arg Val Leu Asp Glu 180 185 190Leu Thr Leu Ala Arg Thr Asp Leu Glu Met Gln Ile Glu Gly Leu Lys 195 200 205Glu Glu Leu Ala Tyr Leu Lys Lys Asn His Glu Glu Glu Ile Ser Thr 210 215 220Leu Arg Gly Gln Val Gly Gly Gln Val Ser Val Glu Val Asp Ser Ala225 230 235 240Pro Gly Thr Asp Leu Ala Lys Ile Leu Ser Asp Met Arg Ser Gln Tyr 245 250 255Glu Val Met Ala Glu Gln Asn Arg Lys Asp Ala Glu Ala Trp Phe Thr 260 265 270Ser Arg Thr Glu Glu Leu Asn Arg Glu Val Ala Gly His Thr Glu Gln 275 280 285Leu Gln Met Ser Arg Ser Glu Val Thr Asp Leu Arg Arg Thr Leu Gln 290 295 300Gly Leu Glu Ile Glu Leu Gln Ser Gln Leu Ser Met Lys Ala Ala Leu305 310 315 320Glu Asp Thr Leu Ala Glu Thr Glu Ala Arg Phe Gly Ala Gln Leu Ala 325 330 335His Ile Gln Ala Leu Ile Ser Gly Ile Glu Ala Gln Leu Gly Asp Val 340 345 350Arg Ala Asp Ser Glu Arg Gln Asn Gln Glu Tyr Gln Arg Leu Met Asp 355 360 365Ile Lys Ser Arg Leu Glu Gln Glu Ile Ala Thr Tyr Arg Ser Leu Leu 370 375 380Glu Gly Gln Glu Asp His Tyr Asn Asn Leu Ser Ala Ser Lys Val Leu385 390 395 400161490DNAHomo sapiens 16agatatccgc ccctgacacc attcctccct tcccccctcc accggccgcg ggcataaaag 60gcgccaggtg agggcctcgc cgctcctccc gcgaatcgca gcttctgaga ccagggttgc 120tccgtccgtg ctccgcctcg ccatgacttc ctacagctat cgccagtcgt cggccacgtc 180gtccttcgga ggcctgggcg gcggctccgt gcgttttggg ccgggggtcg cctttcgcgc 240gcccagcatt cacgggggct ccggcggccg cggcgtatcc gtgtcctccg cccgctttgt 300gtcctcgtcc tcctcggggg cctacggcgg cggctacggc ggcgtcctga ccgcgtccga 360cgggctgctg gcgggcaacg agaagctaac catgcagaac ctcaacgacc gcctggcctc 420ctacctggac aaggtgcgcg ccctggaggc ggccaacggc gagctagagg tgaagatccg 480cgactggtac cagaagcagg ggcctgggcc ctcccgcgac tacagccact actacacgac 540catccaggac ctgcgggaca agattcttgg tgccaccatt gagaactcca ggattgtcct 600gcagatcgac aatgcccgtc tggctgcaga tgacttccga accaagtttg agacggaaca 660ggctctgcgc atgagcgtgg aggccgacat caacggcctg cgcagggtgc tggatgagct 720gaccctggcc aggaccgacc tggagatgca gatcgaaggc ctgaaggaag agctggccta 780cctgaagaag aaccatgagg aggaaatcag tacgctgagg ggccaagtgg gaggccaggt 840cagtgtggag gtggattccg ctccgggcac cgatctcgcc aagatcctga gtgacatgcg 900aagccaatat gaggtcatgg ccgagcagaa ccggaaggat gctgaagcct ggttcaccag 960ccggactgaa gaattgaacc gggaggtcgc tggccacacg gagcagctcc agatgagcag 1020gtccgaggtt actgacctgc ggcgcaccct tcagggtctt gagattgagc tgcagtcaca 1080gctgagcatg aaagctgcct tggaagacac actggcagaa acggaggcgc gctttggagc 1140ccagctggcg catatccagg cgctgatcag cggtattgaa gcccagctgg gcgatgtgcg 1200agctgatagt gagcggcaga atcaggagta ccagcggctc atggacatca agtcgcggct 1260ggagcaggag attgccacct accgcagcct gctcgaggga caggaagatc actacaacaa 1320tttgtctgcc tccaaggtcc tctgaggcag caggctctgg ggcttctgct gtcctttgga 1380gggtgtcttc tgggtagagg gatgggaagg aagggaccct tacccccggc tcttctcctg 1440acctgccaat aaaaatttat ggtccaaggg aaaaaaaaaa aaaaaaaaaa 149017378PRTHomo sapiens 17Met Asp Ser Val Arg Ser Gly Ala Phe Gly His Leu Phe Arg Pro Asp1 5 10 15Asn Phe Ile Phe Gly Gln Ser Gly Ala Gly Asn Asn Trp Ala Lys Gly 20 25 30His Tyr Thr Glu Gly Ala Glu Leu Val Asp Ser Val Leu Asp Val Val 35 40 45Arg Lys Glu Cys Glu Asn Cys Asp Cys Leu Gln Gly Phe Gln Leu Thr 50 55 60His Ser Leu Gly Gly Gly Thr Gly Ser Gly Met Gly Thr Leu Leu Ile65 70 75 80Ser Lys Val Arg Glu Glu Tyr Pro Asp Arg Ile Met Asn Thr Phe Ser 85 90 95Val Val Pro Ser Pro Lys Val Ser Asp Thr Val Val Glu Pro Tyr Asn 100 105 110Ala Thr Leu Ser Ile His Gln Leu Val Glu Asn Thr Asp Glu Thr Tyr 115 120 125Cys Ile Asp Asn Glu Ala Leu Tyr Asp Ile Cys Phe Arg Thr Leu Lys 130 135 140Leu Ala Thr Pro Thr Tyr Gly Asp Leu Asn His Leu Val Ser Ala Thr145 150 155 160Met Ser Gly Val Thr Thr Ser Leu Arg Phe Pro Gly Gln Leu Asn Ala 165 170 175Asp Leu Arg Lys Leu Ala Val Asn Met Val Pro Phe Pro Arg Leu His 180 185 190Phe Phe Met Pro Gly Phe Ala Pro Leu Thr Ala Arg Gly Ser Gln Gln 195 200 205Tyr Arg Ala Leu Thr Val Pro Glu Leu Thr Gln Gln Met Phe Asp Ala 210 215 220Lys Asn Met Met Ala Ala Cys Asp Pro Arg His Gly Arg Tyr Leu Thr225 230 235 240Val Ala Thr Val Phe Arg Gly Arg Met Ser Met Lys Glu Val Asp Glu 245 250 255Gln Met Leu Ala Ile Gln Ser Lys Asn Ser Ser Tyr Phe Val Glu Trp 260 265 270Ile Pro Asn Asn Val Lys Val Ala Val Cys Asp Ile Pro Pro Arg Gly 275 280 285Leu Lys Met Ser Ser Thr Phe Ile Gly Asn Ser Thr Ala Ile Gln Glu 290 295 300Leu Phe Lys Arg Ile Ser Glu Gln Phe Thr Ala Met Phe Arg Arg Lys305 310 315 320Ala Phe Leu His Trp Tyr Thr Gly Glu Gly Met Asp Glu Met Glu Phe 325 330 335Thr Glu Ala Glu Ser Asn Met Asn Asp Leu Val Ser Glu Tyr Gln Gln 340 345 350Tyr Gln Asp Ala Thr Ala Glu Glu Glu Gly Glu Met Tyr Glu Asp Asp 355 360 365Glu Glu Glu Ser Glu Ala Gln Gly Pro Lys 370 375181851DNAHomo sapiens 18agacactcac cccggactcc cttgaacagg gacagggagg aaccccaggc agctagaccc 60cagcagcagc cacacgagca cactgtgggg cagggagggg catctcttga gaacaaaaga 120tccatttctc gactttccaa actggagagc ttcttgagag aaaagagaga gacaggtaca 180ggtccacgcc acccacacac agccctgtgc acacagaccg gacacaggcg tccacagttc 240tgggaagtca tcagtgatga gcatggcatc gaccccagcg gcaactacgt gggcgactcg 300gacttgcagc tggagcggat cagcgtctac tacaacgagg cctcttctca caagtacgtg 360cctcgagcca ttctggtgga cctggaaccc ggaaccatgg acagtgtccg ctcaggggcc 420tttggacatc tcttcaggcc tgacaatttc atctttggtc agagtggggc cggcaacaac 480tgggccaagg gtcactacac ggagggggcg gagctggtgg attcggtcct ggatgtggtg 540cggaaggagt gtgaaaactg cgactgcctg cagggcttcc agctgaccca ctcgctgggg 600ggcggcacgg gctccggcat gggcacgttg ctcatcagca aggtgcgtga ggagtatccc 660gaccgcatca tgaacacctt cagcgtcgtg ccctcaccca aggtgtcaga cacggtggtg 720gagccctaca acgccacgct gtccatccac cagctggtgg agaacacgga tgagacctac 780tgcatcgaca acgaggcgct ctacgacatc tgcttccgca ccctcaagct ggccacgccc 840acctacgggg acctcaacca cctggtatcg gccaccatga gcggagtcac cacctccttg 900cgcttcccgg gccagctcaa cgctgacctg cgcaagctgg ccgtcaacat ggtgcccttc 960ccgcgcctgc acttcttcat gcccggcttc gcccccctca cagcccgggg cagccagcag 1020taccgggccc tgaccgtgcc cgagctcacc cagcagatgt tcgatgccaa gaacatgatg 1080gccgcctgcg acccgcgcca cggccgctac ctgacggtgg ccaccgtgtt ccggggccgc 1140atgtccatga aggaggtgga cgagcagatg ctggccatcc agagcaagaa cagcagctac 1200ttcgtggagt ggatccccaa caacgtgaag gtggccgtgt gtgacatccc gccccgcggc 1260ctcaagatgt cctccacctt catcgggaac agcacggcca tccaggagct gttcaagcgc 1320atctccgagc agttcacggc catgttccgg cgcaaggcct tcctgcactg gtacacgggc 1380gagggcatgg acgagatgga gttcaccgag gccgagagca acatgaacga cctggtgtcc 1440gagtaccagc agtaccagga cgccacggcc gaggaagagg gcgagatgta cgaagacgac 1500gaggaggagt cggaggccca gggccccaag tgaagctgct cgcagctgga gtgagaggca 1560ggtggcggcc ggggccgaag ccagcagtgt ctaaaccccc ggagccatct tgctgccgac 1620accctgcttt cccctcgccc tagggctccc ttgccgccct cctgcagtat ttatggcctc 1680gtcctcccca cctaggccac gtgtgagctg ctcctgtctc tgtcttattg cagctccagg 1740cctgacgttt tacggttttg ttttttactg gtttgtgttt atattttcgg ggatacttaa 1800taaatctatt gctgtcagat acccttaaaa aaaaaaaaaa aaaaaaaaaa a 185119450PRTHomo sapiens 19Met Arg Glu Ile Val His Ile Gln Ala Gly Gln Cys Gly Asn Gln Ile1 5 10 15Gly Ala Lys Phe Trp Glu Val Ile Ser Asp Glu His Gly Ile Asp Pro 20 25 30Ser Gly Asn Tyr Val Gly Asp Ser Asp Leu Gln Leu Glu Arg Ile Ser 35 40 45Val Tyr Tyr Asn Glu Ala Ser Ser His Lys Tyr Val Pro Arg Ala Ile 50 55 60Leu Val Asp Leu Glu Pro Gly Thr Met Asp Ser Val Arg Ser Gly Ala65 70 75 80Phe Gly His Leu Phe Arg Pro Asp Asn Phe Ile Phe Gly Gln Ser Gly 85 90 95Ala Gly Asn Asn Trp Ala Lys Gly His Tyr Thr Glu Gly Ala Glu Leu 100 105 110Val Asp Ser Val Leu Asp Val Val Arg Lys Glu Cys Glu Asn Cys Asp 115 120 125Cys Leu Gln Gly Phe Gln Leu Thr His Ser Leu Gly Gly Gly Thr Gly 130 135 140Ser Gly Met Gly Thr Leu Leu Ile Ser Lys Val Arg Glu Glu Tyr Pro145 150 155 160Asp Arg Ile Met Asn Thr Phe Ser Val Val Pro Ser Pro Lys Val Ser 165 170 175Asp Thr Val Val Glu Pro Tyr Asn Ala Thr Leu Ser Ile His Gln Leu 180 185 190Val Glu Asn Thr Asp Glu Thr Tyr Cys Ile Asp Asn Glu Ala Leu Tyr 195 200 205Asp Ile Cys Phe Arg Thr Leu Lys Leu Ala Thr Pro Thr Tyr Gly Asp 210 215 220Leu Asn His Leu Val Ser Ala Thr Met Ser Gly Val Thr Thr Ser Leu225 230 235 240Arg Phe Pro Gly Gln Leu Asn Ala Asp Leu Arg Lys Leu Ala Val Asn 245 250 255Met Val Pro Phe Pro Arg Leu His Phe Phe Met Pro Gly Phe Ala Pro 260 265 270Leu Thr Ala Arg Gly Ser Gln Gln Tyr Arg Ala Leu Thr Val Pro Glu 275 280 285Leu Thr Gln Gln Met Phe Asp Ala Lys Asn Met Met Ala Ala Cys Asp 290 295 300Pro Arg His Gly Arg Tyr Leu Thr Val Ala Thr Val Phe Arg Gly Arg305 310 315 320Met Ser Met Lys Glu Val Asp Glu Gln Met Leu Ala Ile Gln Ser Lys 325 330 335Asn Ser Ser Tyr Phe Val Glu Trp Ile Pro Asn Asn Val Lys Val Ala 340 345 350Val Cys Asp Ile Pro Pro Arg Gly Leu Lys Met Ser Ser Thr Phe Ile 355 360 365Gly Asn Ser Thr Ala Ile Gln Glu Leu Phe Lys Arg Ile Ser Glu Gln 370 375 380Phe Thr Ala Met Phe Arg Arg Lys Ala Phe Leu His Trp Tyr Thr Gly385 390 395 400Glu Gly Met Asp Glu Met Glu Phe Thr Glu Ala Glu Ser Asn Met Asn 405 410 415Asp Leu Val Ser Glu Tyr Gln Gln Tyr Gln Asp Ala Thr Ala Glu Glu 420 425 430Glu Gly Glu Met Tyr Glu Asp Asp Glu Glu Glu Ser Glu Ala Gln Gly 435 440 445Pro Lys 450201794DNAHomo sapiens 20gacatcagcc gatgcgaagg gcggggccgc ggctataaga gcgcgcggcc gcggtccccg 60accctcagca gccagcccgg cccgcccgcg cccgtccgca gccgcccgcc agacgcgccc 120agtatgaggg agatcgtgca catccaggcc ggccagtgcg gcaaccagat cggggccaag 180ttctgggaag tcatcagtga tgagcatggc atcgacccca gcggcaacta cgtgggcgac 240tcggacttgc agctggagcg gatcagcgtc tactacaacg aggcctcttc tcacaagtac 300gtgcctcgag ccattctggt ggacctggaa cccggaacca tggacagtgt ccgctcaggg 360gcctttggac atctcttcag gcctgacaat ttcatctttg gtcagagtgg ggccggcaac 420aactgggcca agggtcacta cacggagggg gcggagctgg tggattcggt cctggatgtg 480gtgcggaagg agtgtgaaaa ctgcgactgc ctgcagggct tccagctgac ccactcgctg 540gggggcggca cgggctccgg catgggcacg ttgctcatca gcaaggtgcg tgaggagtat 600cccgaccgca tcatgaacac cttcagcgtc gtgccctcac ccaaggtgtc agacacggtg 660gtggagccct acaacgccac gctgtccatc caccagctgg tggagaacac ggatgagacc 720tactgcatcg acaacgaggc gctctacgac atctgcttcc gcaccctcaa gctggccacg 780cccacctacg gggacctcaa ccacctggta tcggccacca tgagcggagt caccacctcc 840ttgcgcttcc cgggccagct caacgctgac ctgcgcaagc tggccgtcaa catggtgccc 900ttcccgcgcc tgcacttctt catgcccggc ttcgcccccc tcacagcccg gggcagccag 960cagtaccggg ccctgaccgt gcccgagctc acccagcaga tgttcgatgc caagaacatg 1020atggccgcct gcgacccgcg ccacggccgc tacctgacgg tggccaccgt gttccggggc 1080cgcatgtcca tgaaggaggt ggacgagcag atgctggcca tccagagcaa gaacagcagc 1140tacttcgtgg agtggatccc caacaacgtg aaggtggccg tgtgtgacat cccgccccgc 1200ggcctcaaga tgtcctccac cttcatcggg aacagcacgg ccatccagga gctgttcaag 1260cgcatctccg agcagttcac ggccatgttc cggcgcaagg ccttcctgca

ctggtacacg 1320ggcgagggca tggacgagat ggagttcacc gaggccgaga gcaacatgaa cgacctggtg 1380tccgagtacc agcagtacca ggacgccacg gccgaggaag agggcgagat gtacgaagac 1440gacgaggagg agtcggaggc ccagggcccc aagtgaagct gctcgcagct ggagtgagag 1500gcaggtggcg gccggggccg aagccagcag tgtctaaacc cccggagcca tcttgctgcc 1560gacaccctgc tttcccctcg ccctagggct cccttgccgc cctcctgcag tatttatggc 1620ctcgtcctcc ccacctaggc cacgtgtgag ctgctcctgt ctctgtctta ttgcagctcc 1680aggcctgacg ttttacggtt ttgtttttta ctggtttgtg tttatatttt cggggatact 1740taataaatct attgctgtca gataccctta aaaaaaaaaa aaaaaaaaaa aaaa 179421170856DNAHomo sapiens 21gagttagacc caggttcaag tccagctttg tccagtcatt accagctgac caatagcaaa 60tcttatcact taatcactaa tgaggggaac aagcattcaa atatagtcat gtgtacataa 120tgacatttct gtcaacaaca gacagcacaa cacattactg ttgtgtttgt ggtgatgctg 180gtgtaatcat aaccttctgt gctgcagtcc agtaaaaata tagcacaggc cgggggcggt 240ggctcacact tgtggagggc cacctccaca agttgcagtg agctgagatc gcaccactgc 300actccagcct gggcaacaag agtgaaactc catctcaaaa aaataaaaca aacaaacaaa 360caaacaaaca aacacttttt attgcctggg tgtggtggct cacgcctgta atcccagcac 420tttgggaggc tgaggcagga ggattgcttg agcccaggaa ttttagacca gcctgggcaa 480catggcgaaa ccctgtctct acaaaaaata caaaaattag ctgggcatgg tggtgcgccc 540ctatagtccc agctactcag gaggctgaag tgggaagata acctgagccc agggaggtcg 600ataataaaat tttaaaaatt tttagtagag atgggatttc accgtgttgg accaggctga 660tctcgaactc ctggcctcag gtgatctgtg cacctcgacc tcccaaagtg ctgggattac 720aagcgtgagc cactgtgccc agccaacata cttgtttatt atcaaatatt atatactgta 780cataattgta tgttttatat atgtatgtat gtgtgtgtgt gtatatatat atatatatat 840atatatattt tttttttttt tttagacaga gtcttgctct gtcacccagg ctggagtgca 900acggcaccat cttagctcac tgcaacctct gcctcctggg ttcaaaccat tctcccgcct 960cagcctccca agtagctgag attacaggca ctcgccatca tgccccacta attttttttg 1020tatttttgta gagatggggt tccaccgtgt tggccaggct ggtctcgaac tcctgacctc 1080aggtgatccg cctacctcag cctcccaaag tgctgggatt agaggcgtaa cccaccgtgc 1140ctggccaata aaaagtttta aatacagaaa aaagcttaca gaataaggat ttaaagaaag 1200aaagaatttt tgtacagctt ataatgtgtt tgtgttttaa gctgttatta caaaagccaa 1260aaagtcaaag aattaaaaaa tatataaaat taaaaaatta cagtaagcta aggttaattt 1320cttttttatt tttctttttt cttttttttt tttttttgag acggagtctc actctattgg 1380caggttggag tgcagtggcg cgatctcggc tcactgtaac ctccacctcc cggattcaag 1440caactctcct gcctcagcct tccgagtagc tgggactaca ggtgcgtgcc accccaccca 1500gctagttttt gtattttcag tagagacagg gtttcaccac gttggccagg atggtcttga 1560tctcttgacc tcgtgatcca cccgcctcag cctcctaaag tgctgggatt acaggggtga 1620gccaccgtgc ccggcctcta aggttaattt cttattgcag aagaaaaaga ttaaaaaaat 1680aaacttagta tagcctcagt gtacagtgtt tataaagtct acagtagtgc acagtaatgt 1740cctaggcctt cacagtcacg taccactcac tcactgactc acccagagca aattccagtg 1800ctgcaagctc cattcatggc aagtgcccat acaggtagac tatttttatc tttttattta 1860tttatttagt tagttaattt ttgagatgga gtctctctct gtcttccagg ctggagcgca 1920gtggtgcgat cttggctcac tgtaacctct gcctcctggg ttcaagcaat tctcctaccc 1980aagcctcccg agtagctggg attacaggcg cctgccacca tgcctggcta atttttgtat 2040ttttagtaga gaccgagttt tgccatgttg gtcaggctgg tctcgaactc ctgatctcaa 2100gtgatccacc cgccttggcc tcccaaagag ctgggattac aggtgtgagc caccacgccc 2160cgcccaattt tatcttttat atcgtatttt tattataccc ttttaatgtt tagattcaca 2220aatacttatt gtaacaattg cctacagtat caatatagta acttgctgta caggtttgta 2280gcccaggggc aacaggtgat cccctctaac ctggatgtgt ggtcgcctgt accatctagg 2340tctgtgtgaa cacactctct ggtgttccta tcatgacaaa atcctctagc attcctgttg 2400ttaagcaaca catgagtgta gttactgagt ccctattgtg agccagggcc gggtaatata 2460ttctctcccc caggctgttg tgaccatttc cagtgagtca gttcatctgt ctgaacaaag 2520cactctggca ttgattgtat gcaaataacc tgttacagaa tggttctacc cataaactgg 2580ctggcctctt ttgagcaacc ctcaaagttg caagcccttg ccctctgtcc tggtcaacct 2640ctcttcctca gaagcttgcc tgctctgaac tcctctccca aaccgggtta ggagcccctt 2700ctctggtatc agggcaccct gtgcctctct tacagacttg cattatggtt ctaactgtgc 2760tgtgtggcct gggcaagccg ctcaaccact cggttatttc ttcttttttt ttttttgaga 2820cagagtttca ctgttattgc ccaggctgga gtgcaatctt ggctcaccac aacctctgcc 2880tcctgggttc aagcgattct cctgcctcag cctcccaagt agctgggatt acaggcatgc 2940gccaccacgc ccagctaatt ttttgtattt ttagtagagc tagggttttt tcatgttggt 3000caggctggtc tcgaactcct gacctcaggt gatctgccca ccttggcctc ccaaggtgct 3060gggattacag gtgtgagcca ctgcacccga cttgaaagaa attgctttgc actgtgcttg 3120gcacagagga acagcaggtg ttcattcaat gcttgctgtt gtaattattc aggcttttat 3180caacagaggg ctggcctgag actctgccat atctcagaac ctagcacaga acctggatga 3240gtacagagta agtgctcaat gtatgctgtg gtaggcagag taatagcccc caaagacgtt 3300cacatcctaa ctctcaggac ctgtgaacat tcccttaaat ggcaaagggg aattaaggtt 3360gcaaacagga ttagggttct taatcggctg attttaaaat agggagatca tgttggacta 3420accagctggc ccaatgtcat cttaagagtc cttaaaaggg ccaggtgtgg ggaggttgaa 3480gctgcaggga gccgagattg agtcatagca ctccagtttg ggagacggag tgagacaaaa 3540aaaaggctgg gcaaggtggc tcatgcctgt aatcccatca ctttgggagg cagaggctgg 3600tggatcgctt gaggtcagga gttcaagacc agcctggcca acatggtgaa agcccgtctc 3660tattaaaaat acaaaaatta gcggagcgtg gtggcgggtg cctgtaatcc cagccactca 3720ggaggttgag gcaagagaat tgcttgaacc caggaggagg aggttgcagt gagccgagat 3780tgcaccactg gactctagcc tgggcaacgg agtaagactc catcgcagga aaaaaaaaaa 3840aaaggaagat gtgcctatgg agagaggact gtctgaggtc tgagagactc cacctgacat 3900tgcaggcttg cttttctgtt tttttttttt tttttttttt ttttgagacg gagttttgct 3960ctgtcgccca ggctggagtg caatggcacc atctcagctc actgtaacct ctgcctccca 4020ggttcaagcg attctcctat ctcagccttc ccagtagctg ggattacagg tacgcgccac 4080cacacctggc taatttttgt attttaagta gagatggggt tttaccatgt tggccaggct 4140ggtctcgaac tcctgacctc aggtgatcca cccaccttgg cctcccaaag tgctgggatt 4200acaggtgtga gccattgtgc ccagcccatt gcaggctttc acagagaaaa ggggcaggag 4260tcaggcgcgc aggcagcttc tggaagttag aaaacacaag gaaacagatt cttccctaca 4320gcctccagaa gggaatgcat cctgccaaca ctttgttttt agctcagcaa gacctgtgtg 4380ggccatcgaa cctacagaac tgaaggataa tacatttgtg ggtgtgtgtt ttcaaagaca 4440ctaagttttg gtaacttgtt acagcagtaa ctggaaacta agacatgcaa caagccttat 4500tgttcatttt taccaccact actgggctgt tggttatggt ggaattacac ttttctcttc 4560cattaggctg tgtgaactcc ttgaggttgt gcaatacgtt tgtctgattt actactggtt 4620agcaggctct gagaagaatg gctggtacac aggcggagct caataaaagc ccttactgaa 4680ttttattcaa tctatatgtg gatgaagacc tccgccccgc gcgcccctcc cgcaagtccc 4740actgaggccc gacccattct gtccggctcc cagcccccgc gggtcccccc accccggggc 4800tgaccgggtg attcaggcag ccctacatcc tgctggggtg gtgggcttcg agcgcgggtc 4860ccaggacgca gtggggcgca gtgcctgcgg caggcggcag gaggcgagcg tggcccagga 4920actcccgcgg gagggtcggg acggggcggg gcttgggggc ggggcggctc agcgcgcagg 4980cgcggggcca ggcgcctcgc gcggccaggg gcgggcggcc gcagagcagc accggccgtg 5040gctccggtag cagcaagttc gaaccccgct cccgctccgc ttcggttctc gctccttcgg 5100cccttgggcc tccaaacacc agtccccggc agctcgttgc gcattgcgct ctccccgcca 5160ccaggatgcc ggtaaccgag aaggatctag ctgaggacgc gccttggaag aagatccagc 5220agaacacgtt cacacgctgg tgcaacgagc acctcaagtg cgtgaacaaa cgcatcggca 5280acctgcagac cgacctgagc gacgggctgc ggctcatcgc gctgctcgag gtgctcagcc 5340agaagcgcat gtaccgcaag taccatcagc ggcccacctt tcgccagatg cagctcgaga 5400atgtgtccgt ggcgctcgag ttcctggacc gtgagagcat caagctcgtg tccatcggtg 5460agttctctgg ccgggcccag gcgcccactg tggtgccgac ccgcccccgc gcgtgcaccc 5520ctgcggaggg cgaggatttc ccgcagcgcg cccccacctc ggagataagg gggagtcgtc 5580cccaggggtg ggttataggg ggcctagacc ccctccccgg tgtcttcccc tgggatggga 5640cctgttgtga tcgctccccg ccatccgccc cagcagtgca cctttggctg gctaagggtt 5700gagggtttgg gctggggtca caggaggaga ggtggagttg ttgcatttct ctacacctgg 5760ggcgccccta tgggagctag gggactagaa accctcgttc gctgtccccg ggggcgggcc 5820ctagggtcag atgctccgcg gagtgctctc cctgctgcgc ccaggttggt gctctcagag 5880gcagctgaat gggcgttggc tcggaggccg ggccgtgaga cctgaggagg aaccgttctc 5940tgcgcctggg gcctccctgc ccaggtggag acagagacct ggtaccttcc cctgccgtcg 6000ctggaatggg tgtgggcccc gaggttgcaa gggtaggcgc gggtgtgtgt cctcgctctc 6060tctgctccca gctcagctct ggccgcgcgc cgcaggttga acccactcct tgctgccgaa 6120gttataattt agagatggtg gtggtaacag taattgctgt cttgtaggga gcccaactag 6180cgtccactgt gtaccgtcag ccttctaagt tatctccgtc cctacgcatc ctgccatctg 6240gggtgaggct agacccattt tacagataag ggggtccgga gggttaattg acctgtccaa 6300ggtcagcaag tagggcccag ctgagaactg aaggaagtgg gcaacagtta gaaggaggct 6360ttgttttcct ctcctctccc aaacctacac cagggtcttc ctgaaaggag ggagggaatt 6420ggtgtctctt gctggactgg gccttctggt ctggggagga agaataagga tgaagtctcc 6480cttgtggtct gagatagttg gaggcttccc agagggccac aaggctactg atagtgtggg 6540ctgtgatggt aggggctgtg atgtgtgtgt gcatgtgggc gtttgtgcag agaacgtgtg 6600tacacacata gcatgtgtgt atagcatgtg catatgcaaa gagtttgcat gtacacggaa 6660tgtatgcaga gaatgtgtat ccacctacac gtgtgtatgg gtgtgtgtat gtgtgtgtgt 6720gtatgtgggt gggtgggtgt gggttggggc agaggagggt tctgggtctg gatctcttcc 6780taaggagaac cagggactgg ccctggcctg tgatttgggt ctcttcctga ggaaaccagg 6840tcactatagt gaccctagtg acaggaagaa agggagatgg gtgtggctgc caggactttc 6900tccagtggaa aagggattcc ctctaggctg agcctcccct gggccttagg gcctcaccct 6960tcccttcccc cacacctgtc ctggcaggta aggctgcttc ctgcttcctg ggcccagatg 7020gcagccgcac cacccagctg atctccagca gccctccccc tccccaaggg tggcttccct 7080gcagaagaat ctgcatggca cgctgttgtc ttctttctgg ggtccatctc ctgtactggg 7140gagggagaac ctcagaatct cctggaattc tttaccattc agaaaccagc ctcccctctg 7200aagaatccca aggcccagct gggctcaatt tggatctgtt ctttgtttta aaaatgtgta 7260tttatttaat taactgaata aagaaactta aagtaaacca gaagtatcca aatacgacat 7320gaaatctcta aaacaacaac aaaaccaaac caaaccgcag cactagcaaa tcacagactg 7380cctgatctac ccactgttta cagaggcagc agctacttcc agcactgtct ctcatcagtg 7440cccggggctg tgggtctcat tctagatttt gtctacattt ttttacatgg ttctcctgat 7500tccctgctcc ccctccccac caccgccccg cctggagatg gagccttgct ctgtctccag 7560gctggagtac aatggtgcca tctctgctca ctgcaacctc cacctcccgg gttcaagcga 7620ttcttctgcc tcagcctcct gagtagctag aattacaggc acatgccacc acgcccggct 7680aatttttgta ttcttagtag agatggggtt tcaccatgtt ggccaggctg gtctcgaact 7740cttgacctca tgatatgccc gcctcggcct cccaagtgcg ggggttacag ccctgagcca 7800ccgcgcccag cccggtcctc cttttatttt cgaatccact caggccctag ctactcccat 7860tgtcccgacg ttccagggtt agttagcttc ccttcctctg tgctgggcct gtgggctgtt 7920ggcagcttct tcctgttcct accacaactt gcattctatt tttttccttt ttaatgattt 7980cttggatcat attccccaga gtgacattcc tgggttaaag ggtgtgacca catttatgac 8040ttgtatcatt ggctgcctaa ttgctctccc gagagatctt gcaacaaaca ggttttccag 8100cctctggaga ccacagagag ccctggcaag tgccaggact gctgtgggga taaagcagga 8160ggcttcttcc ctaagctctt gaggctgttg tgggtaatgg tccttcatcc ttcaaggcaa 8220agttacctcc agcttggact aaggttcata tattcactgc ttaggttgtg ttacattgtg 8280ctgacaatga cactagcttc aatttggggg cacctactgg gtgttaagtg tgttctgttg 8340atcaccccat tgaattttca tgctaatcat tgattgacag caactactgc cctatctcta 8400atgatctgct tctgcaagtc acttagagag ttcagggctt aacactgtcc tgggcatgtg 8460ttgcttagaa aatggcgcct gttaattaaa taaggtgctg tctaataatt atctcaaaag 8520taatgccagg gctggatgcc gtggctcacg cctgtaatcc cagcacttta ggaggccaag 8580gtgggtggat cacctgaggt caggagttcg agaccagcct ggacaacatg gtgaaaccct 8640agctctacta aaaatacaaa aattagctgg gcatggtggt gcacacctgt agtcccagct 8700actcgggagg ctgaggcagg agaattgctt gaacccggga ggtggaggtt gcagtgagcc 8760gaggtctttg tgtaactgca ctccagcctg ggagagcgag actctgactc aaaaaaaaaa 8820aaaaaaaaaa aagtcatgcc cgaatggttt gcacaccgaa gggacgttca aaattagggg 8880agaacagcct ggttgtttgt ttctgtttgg ttgatcatac tcttgccatg gttagtatta 8940ttatctttat ttaaagatgg gaaacaggag tgaagccact tgtggaggtg acccagctag 9000ctagtaaatg gtgtctgaaa cccaggtctg cccagctgtt gaattggagc cttaactgac 9060ttgccttcca gtttcagaga tgagtaaaat acagcttttc tctccacatc agagggtccc 9120tgcaacacta ggtttgcaag tcttaggtgt tagggtggtg gctggatacc cacactctga 9180acctctgacc ttggacaaaa tagggatgtc agggccttcc atgattggca ggatgaatcc 9240tctgggctgt gatgaaggtc tcacaagttg agagtcagcc gggaattaag tgggatcagt 9300ttgcctcttg tgttttcctc attgtgtttt ggttggttgg ttgagatttc ctactaccca 9360atggatgatg ttttattcca tcgtcaggga aggtatcatt gaatgaatac agggttttgt 9420atgctttgga taagaccaga cagttgtgga gtcattagaa ttgtgtacat gcctccagct 9480ctgagatagg tggtgtttca acagctgcca gaggactctg gcttttctgc ctagaattca 9540ctgaaagaca accctggcta ttgattcaca tttgtggttc attgtaaggt aggcccctag 9600gcgccatcca aaagttgaaa atttccttac gtttcttgtt atgtgatggg cagttcatag 9660tgaggactca gtgtctttaa ttccagctgt ttgccaggag ttggcagttt tatttacttg 9720tttttccaaa aacctttctg acatggggca gtccagccag ctgggaggaa aaggggtctc 9780tcagcccaag aatgatgatc aaggcctaga agtttgggtg gtgtgttttg ttttgggcct 9840ttagagaaag gaattgtttc cttttcagag gatgtggtct aaccctaaag tttacttgac 9900tgacttaaac caggccagcg ccagagcagg cagggtgcgt gttcccaaga cttcgggtca 9960ctaggcagct tccagggtgg tgggtcactg gtccagtcag ctccttttcc ttcctctccc 10020ttttgtgcta ctactaccaa aataatttcc aaataacctt aagttctgct ctttcttgca 10080tgtctagcag atgccagcat gtcttttggg tagtacagag agtgcttaaa aagtagcaaa 10140gttggccgga cgtggtggct catgcctgta atcccagcac cctgggaggc caaggtgggt 10200ggatcacctg aggtctggag tttgagacca gcctgaccaa catggagaaa ccccatctct 10260actaaaaata caaaattaga tggccgtggt ggtgcatgcc tgtaatccca gctacgtggg 10320aggctgaggc aggacaatag cttgaatcca agggcagagg ctgtgttgag ctgagatcat 10380gccattgcac tccagcttgg gcaacaggag caaaactcca tctcaaaaaa aagtagcaaa 10440gtagcatgct ttgtcagaat tattaataac aagttgtggg ccatgtacaa ggtggcacat 10500tagcattcaa tgtcacttgt gtagtagtta agagcaagga ttcttggttc aaatcccact 10560tgccactaag tagctattag aaacttctgt gccttggttt ccttatcact aaaatgggga 10620taataactac cttcttaaaa ggctgttata aagattaaac aagttaataa tttttaaagt 10680gcttggcaca gtttatggta catagtaagt gctctgtgaa tgcctgttaa ttaaataagg 10740cactgtttaa taatctcaaa agtcatgccg gaaaggtttg cacactgaaa gggcatttga 10800aatcagcgcg ctctggggag aacagcttgg ttggctaagg ttgatcctac ttgctaaaat 10860acggctatgg actgcctaga gggtgtcacc tccttgaaag gggctgcccc ctgctatgtt 10920atggctgcct ccagggccca ttcacaccag ctttgtttcc aagctggaca gggagctcca 10980ggcgtctggt cattccagcc tcccacccct ttcaggaatc tctgggccaa atcacttcca 11040gatggtggtt gggcctctgt ggagttctcc cagcaacggc ggagccagca tgccagtcgg 11100cagccgcctt cgttcttgga gagtctgagc taaaggaggg ctttgatttg gagccaaatt 11160gtgtctcttg ggtcctggtt ttgtgctgtg aggcaggtac catggagtgg gctgctggct 11220tagttgagga tggctgccct gctccttagg ggagcagata cccagggcct ggagccttta 11280ggccctgcct ccagtagctc catggtcagg gtgccagtca ccttgcgttt tctttttctt 11340tttttttgag atggagtctt gctctgtcgc ccaggttgga gtgcagtggc gtgatctcgg 11400ctcactgcaa cctctgtctc ccggggtcaa gcaattctcc tgcctcagcc tcctgagtag 11460ctgggattac aggcgtgcgc cactatgtct ggctaatttt tgtattttta gtagagatgg 11520ggtttcacct tgttggtcag gctggtctcg aactcccaac ctcgtgatcc acctgcctcg 11580gcctcccaaa gtgctgggat tacaggcgtg agccaccgga cccagccaac tttgctacat 11640cagtttccag gtagcatatc ctaggcaaaa ctggatgtag cctagtgatt cagggcctcg 11700gtctgaagct agactgtctg gattctaatc cgcactctgc ctgataccag ctgtgcaact 11760ctagtccact gctttaacct ttctgtgcct gcttccctgt ctataaaatg caagagcaaa 11820atagttgcta tcttagagtt gctgggagca ttatatttga tgaggttaag ttatagcaca 11880gtgttgtcat tatcactatg aatattgtgc ttttggaccc aagtccagga ctttgtcttg 11940tcttctgtct attctctggc cagtccagat atttttggaa tcctattgct gtcatctggt 12000gtgttagctg ttccctttct ccaagttcag aacgtctgat gaagatgtct cccaagatcc 12060tttcttcctt tcctcattca acaaatatat gaaagcccat ctctgaacca ggccctgtgc 12120tgggtgctag gacaacagga atgagaggat catgtccttt gcttgcctca gatactgctc 12180agaggagaag agacaagcaa gcagggagag ccatgcagag gagagctgct caaaccttca 12240ggcccatgct catcacctgg ggactttgtt aaaaatgcag gtctgattga gtaggtgctg 12300gggtgtaggc tgggattctg cgtttccagt cagcttcaga tcctgctgtc tgtgcaccgt 12360gctgtaagta gcaaggatct aggtgccaag ccctctgaaa aggaggagca cctgccccta 12420ggctgggtat gggtaatcta gaaggttccc tggaggaagg gacctttcag ctaagaccta 12480aagcgtgact agaattaggc aggcaaacag acatttacac aggagcagac gagtgtgtca 12540gtttagaggt cttgatgctc aggtcagagg ggcagtggag gggtgggcag ggctggttta 12600ccaagggctt tctgaaactg gaggctgcct atggggtatg ctccttgagt ttgtttgttt 12660gttttttttt ttgagttgga gtttcaatct tgtttcctag gctggagtgc agtacagtgg 12720catgatctcg gctcactgca gcctccatct cccgggttca agagattctc ctgcctgagc 12780ctcccaagta gctggaatta taggcatgtg cacacctggc taattttgta tttttagtag 12840atatggtgtt tcaccatgtt ggtcaggctg gcctcgaact cctgacctca ggtgatccac 12900ccacctagcc tcccaaagtg ctgggattac aggcgtgagc cacggcatcc agccccttgt 12960ttagtgtagg gtagtaaacc cagccaaaag gggtcgttta tctcaggggt ctcacctgtt 13020gctccagtca ttcctattag cagaaagttt tgtatgtgcc ccttcctcat atatatatat 13080atttatatat gtatttatat atatttataa gttataaaca tactctactg tcaatttgta 13140tattaaatat tagtaaatct tagtttcttt ttagatgaca aatccaaata taaaatctgt 13200ttttttcctg gctctaacgg attatcttat gtccccttgg ggtggacata cctcttttgg 13260aggctcccgt gaaggtttgt gtttctacat ttagtttttt tcttttttcc atattcttgt 13320tattctgctt ttaattttca tctttgagta ttctaaatta aggagctgga tctgtaattg 13380taacaccttc ccccaacaat aagtttaact aatgaaaata ttcaatggaa tgagccattt 13440taatctaaat ggggctattt cctgctttta taatgattac agttgctttt catgacattc 13500tactagaagc catcttacat tactgttgta aatctagtta ttcattaaac gggcacagta 13560atccctaaat tggctcaggt tattgtataa taaacaacaa tactttcttc ttcaggagct 13620tgagaagtga tcttgtattt ttaaggtgcc taactaactt ttcatgggaa actgagtcca 13680tgtactggga agaaagcttt ttggggaaaa tgattagaaa accaaatggg tctctttatg 13740actgaagtga tgaaccagca ggtgagagta ggtatagatg gtacagagga cggaattact 13800gggtatttta atcaggccca cttagtatca caatttatta ttctattcta tttttattat 13860tattttttga gatggagttt cgctcttgtc atccaggctg gagtgcagtg gcgctatctc 13920agctcactgc aacctccgcc tcccgggttc aagagattct cctgcctcag cctcccaagt 13980agctgggatt acaggcatgc gccatcacac ctggataatt tttttgcatt tttagtagag 14040atgaggtttc tccatgttgg tcaggctggt ctcgaactcc cgatctcagg tgatccgccc 14100gctttggcct ctcaaagtgc tgggattgca ggtgtgagcc atcgcgcctg gccagtgtca 14160ggatttattc tgtgggaggg gaggaggaca aagaaaaata ctgagctatg tttgaagctc 14220ctgccctcta agagccttag agcagctgac ttaaatgtgt tcctttgata aactgtagat 14280ggttgttgta actcttctgc aaactgttta tttttaaaaa caatttgatg agattttact 14340tatgcccatt gtttgagtac agcatttacc aaagaacaat tttggccaga tcccatgcag 14400tagaatgccc ttggccaaaa ttttcttgta ctataagcaa agaagcagtt tggtttttca 14460cttaggcaag actgcctatc agactgagtt attgtgacag agccgctgac tctctccctt 14520tccccattat caaaatctgg

cttttctaag cagcgcatgt aaaaagcttg gcaaggagga 14580cccttgtcct cctacatatt attctttggc tcttcttggt accaagaata catacaaata 14640atgctggctg tgtactgaat gttgaggtgt gcactgttga ggatattcat cctctaatat 14700aacatctagt atttctcaca ccttccgtct gctgagcatt ggtctatctt acttatacta 14760cttctaatcc tcgtgaactc tgcaaaacta gtggctttac atctatgaga aaagaaaaga 14820acttttatcg gaagaaggtg agtcctttta aagtatcagg cctggaaaga cattaaatga 14880gacagcgaac acatcctgct accctctttg agctatgtat tcattgactt tttttttttt 14940tttttttttt ttttgaggca gagttttgct ttgtcaccag gctggagtgt agtggtgcaa 15000tcttggctca ctgcaacctc tgcctccggg gttcaagtga ttctcatgcc acagcctcct 15060gagtagctgg gattacaggc gcctgccacc ttgcctggct agttttggta tttttatttt 15120tatttattta ttttaagaca gggtctcact ctgtcaccca ggctggagta cagtggcgcg 15180atcttggctc actgcaacct ctgcctcccg ggttccagcg attctcctgc ctcaacctct 15240ccagtagctg ggattacagg cgccttggca ccacagccag ttaatttttt gtatttttag 15300tagaaacggg gtttcagcat gttggccagg ctggtctcga actcccaacc tcaggtaatc 15360cgcctgcttt ggcctcccaa agtgctggga ttacgagtgt gagccattgt gccccgccta 15420tgtattcatt tcttaaaatt ggttgctggc taggtgtggt ggtacatgcc tgtcctataa 15480tcacagcact ttggaaggcc ggtgctggag gatctattga ggccaggagt ttaagaccag 15540cctgggtgag atcacatctc tacaaaaaaa aaaaaaaaaa aaaaaattat ctggatgcag 15600tggcacaagc ctacatagtt gtagctgctt gggaggctga gttgggagga tagcttgagc 15660ccaggagttt gagtctgcag tgagctatga ttgcgtcact gcactctagc ctgggcgaca 15720gagtgagacc cgtttctaaa acaaagaaat tgctattgtc acaattagtt ataaattaat 15780ctaataatgc tgcacgcagt accataatcc acaccctata gcttaacgat ggatggccaa 15840ccactaatca atgctatttc tgtacgccaa tgagaattcc tgacaaaaaa ctttgtatca 15900gccccactcc ctgtctgtcc cctcttttgc ttttaaaaac ctgcttgtaa caaaggccaa 15960acagagctca tatccaaggt tacttgggcc tgagtctttc aggcagctgt cttcactttg 16020gctcaagtaa actctttaat agtttaaatt ttaagcctct gcctctttct tttaggttga 16080catctgtttc cattttacag atgagaaaac tgaggctcag ctctgcctca ctttacaggt 16140caggcttaat ccctaatccc tgcctgcatc atgctgtaaa ggacttttgt gtcaaaactg 16200agtttcacac tctgtaaagt aaaatagata tattgtagtg agagggtgta gaagagactg 16260ttttctgctt ctgtggattt tttttcttcc tgttttgctt tgctccaaac tttactcatt 16320tgcgcttgat tcatgtgaaa ctgaaatttc cttctacaga acaaaacttt ttgggggcta 16380cttaccatat cttttcccac accgtggagc tctgactggg accttttcca gtttttggag 16440acattgctcc agttctttcc ctgcctttgg tttccagggg gcagtaatgt caccgcaggt 16500gtggacagta gggaccagct aaaggttgct ttggaggagg tgggcagggc ttttgtttgt 16560gaggtctaga aaccagaggt gaggaaggag gtgtccctgg aactccccct ggctgcaggg 16620ctcacagcac acaccatgac accacagggg tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg 16680tgtgtgtgtg tgtgtgttga ggggagtgtt gttgagagcc aactatgcca ggagatcctt 16740ggtgacagcg gacataggca cagctatgct ctgtcaggaa tgagttcacc cacacccttt 16800tcttctgcta ccttgtttaa ctggtgggag ggtgtgctgg gttgtgtttg ctggtgagcc 16860cagcaactgc acccttcttt ccaggcctag cacccagcct ttatcagtct catggccctg 16920gcacaagtgg gcagcctgct tccaatccaa gcaggcagct ttccgctcat ctgcaggtag 16980cctcgtgctg tggcagcaca aagttgtgtg agccagagct gaacttgtga tccccacggg 17040catctcctga ggcgcacctc tcctgagaga gaaagctggt ccgtccagcc cattcagggc 17100tcagcctccc cagccgtcgc agggctggct tgctgaaagg tctgggtgtt aacacagcac 17160tcctgttctc tctctctgaa ggccctttat gctggcatga attccttttc tcatagagat 17220ctgaaagctc ttttgactaa atgggtcacc tttctgagta ttttcataag gctgtcagcc 17280tttaccatgc cagacaagtt ttctggaatt tcctttccag aaaaaaaaaa aaaaaaggct 17340actaaagagg ttggagttat ttggaacaca gggtggaatt ctggcattcg aactataggg 17400aaacgggtgg ggatttgtgg caggcactat gtaaatttgc cgcaagccca taaattcaga 17460ctttaagatg aaagatggca agcagcagtc agctttcctt caacaggcag gaacggtgct 17520accttccgcc tgtgctgagt gtgactgagg gagaggcagg cctcctaggg aggccggggc 17580aggaaaggtt tcttggtggc taaaatagga tttctcagtt tcccccgtgt cccaagaaaa 17640taagttctta tcatgcttgt accacacttc ttgtgcgtat caccctggtt tccctgcacc 17700tccttgaagt ggtttatcag attccaggga cacaagaatg gtttggcatc tacagcctat 17760tgtgggagca ggggcccggc ctggtgcttc ttgcccagga acaaactgat tgttcccttg 17820gtgtggggta aagcaggcca gagtatggga ccaggccctg cctcccaggg gacctgaggt 17880gcaaggtctt tgagctgaga ccctaaaagg cctttgtgag tctgtagtgc tatcagttga 17940gcagagttca gggttctgtt tacaagattc cctctcagca gaggcaggga ggggtacctg 18000ctggaagacc aggaatgtgc tgctgctggg atgggggccc tcggtggagc ttctagccat 18060ctggaggcag aacccagaat gtgttctgag tgaggcgcct tggcagagtt ggcttgaaag 18120cacctaggca gtggcttgtc acattcctta tctccaccaa aggaggcaag ctagcacctg 18180ggggatggct ctcccatcag ggagtccttt acaggatgtg atccaggtgt cacattacac 18240ttcctgcagg tgtgcacctc ttacctaatt gtctctccta tccctttttc tcagcactat 18300tgtctgacat ccatggggag tcacacccaa agttgggcat gaggtcctct cctgggcacc 18360caacaccttg tttttttgtt tttgtttttt ttggagatag agtcttgctc tgtcacccag 18420gctagagtgc agtggtgcca tcacagctcg ctgcagcctc gacctccttg gctcaagcga 18480tcctcccacc tcagcctccc acgtagtcag aattacaggc acacacacca acactgctgg 18540ctaattttgt attttttgta gattcggttt gctatgttgc ccaggctggt cttgaactcc 18600tgggctcaag cgatctgcct gcctcagcct cccaaagtgt ggggattaca ggcatgagcc 18660acctcacttg gccacactgc cctcttactg agccgtattg gtgttctaaa tggccttctt 18720actctcccac gggtcatcag tgctccaggg gcaggcgctg tgtctcttgt ttacctctgt 18780ggctctgacc ttggcactta ataggaattt aataaataac ttgttaaata aacagtctct 18840agtataatag cttgagtatt aagactggta cattgactta tttgcaattc agaaaatgca 18900aaacagtggt tctttgctgc ctttagtgaa gtgggaatta tatgtagtag acaactgggt 18960ctggggtccc agtggaacac ttcgtttttg gactgtgatg ctgaacttaa agaactcagc 19020agttcatgtt cattctctgg acatctgtga tttgcttcaa caactgttag agaacaaggc 19080cttttccagg tgaagctcag aaaatgaatt taataggaaa ttactgaaag tcacaatcat 19140agtaacagtt tcattagtta cagtgaatat agagagagcc catacaaagt accaggcatt 19200gtgataaacg cttcttacta atagctatac aaaacatcat tgcaattctg agaagtagtt 19260attgttgtaa ttcccgttat gcagatgaga aaactgaggc acacccagat tggccagtga 19320gtgtgtggtt attactcaga ttcttgtctg agattttaat cttcatattt tactgctttc 19380ccaaggaaag ccatcagctc agcaagtctt tgaaatttgc ttcttttttt ttttttgaga 19440cagagtcttg ctgtgtctcc caggctggag tacagtggcg caatcttggc tcactgcaac 19500ctccgcctcc tgggttcaag cgattctctt gcctcagcct cccgagtagc tgggaatata 19560gttgcatgcc accacacctg gctattttgt atttttagta gagacggggt ttcaccatgt 19620tggccagcct ggtcctgaac tcctgatctc gagatccacc tgcctcggcc tcctaaagtg 19680ctgggatcag gcttgagcca ccgaactcgg cctttttttt tttttttttt gaaatgatgt 19740ctccttttgt tgcccaaact gcagtcttgg ctcactgcaa cttctgcctc ctgggttcaa 19800gtgattctcc tgcctcagcc tcccgagtag ctgggactac aggcacgtgc caccatgccc 19860agctaatttt tgtattttta tagagacagg ctaagcttgt cttgaactcc tgacctcaag 19920tgatccacct acctggccct cccaaagtgc tgggattaca ggagtgagcc cctgtgccca 19980gcctgaaatt caattctaat aaatttttat tggagcatta aaaagttaca tctgtagttg 20040ttactctttg caaaaaattg caagaacaca gaaaaatata aagaaaaaaa tcacctgtga 20100agaattttaa tgaatctttt tctactttta ggggattttg cttacagctg ccttttaatc 20160agaataggga agaaagagat tcctttctca ggaaaaaagt gactgtggac tggaaatgct 20220ttgtgaaata attttggtca tactgatggt tataacaaga ttcgtcttca attgagttat 20280tgctgagctt tgtccaacat taaaatgaaa ggtctcattt gagtctcatt gtggtttgca 20340agtctccctt ggtctagaaa tatgtttggt caaccacggc atggaggtgt tccagccact 20400ttctgtctct taaaagtttt taggacctac ttttattggg actgccaggg tctcttaata 20460atagttatta tacttggtaa ctattgtgac cttgtctcat aggcagccca gcatagaaac 20520tcatttagct tttagttgct cagctccatt agctgtttaa acatgtttca gatgtgagcc 20580tgacaatgta cttgggcagc ttggttcacc cttgactgcc tgggaacttt gagaagtctg 20640aaaattatat gtagccctaa ggtcttcatg gtattgtttt tttggaggca ccatttccca 20700atagccctga ggacaccagg cccatgaagc catcctgtct cagccaggag gcagaggaga 20760tggaatggaa accacttctg gatacagatc cagccacttc cggagtgctt cagagcatgg 20820gtcagataga ccttgctgct ttctagctgg cagacttggg gaaggttgtt tgacctctct 20880gagtttgtgt cccagactat agcagtaccc ccttactggc gttatcgaag ataaaatgat 20940ataatcctga taaatcactt gacccagtcc ttggaggtgg tggtgggggc tggggtaagt 21000gccccatgaa tggtggtcat catgctcccc accaacctcc tttctctctt ctcctttccc 21060gtctttcaca cccctaattc ctggacctgg gggtggtctc tccagactag atgaagaagc 21120aatctaatta tctaggaagg tgaaaggtgg ttgggaatac tcccagaaat aggccaaaga 21180taccgcctcc tacctaacag actcttttta gaagaagagg caacctgggt ttttggataa 21240ctgttgagta ggaaccatca tgagtggcat ttctgcattt ctggtcttct ggccaagcct 21300cctttttttt tttttttttt ttttttttta accttgagac agtcttgctt tgttgccagg 21360ctggattgca atggtgcagt cttggctcac tgcaacctcc atctcccagg ttcaagcgat 21420tctcctgcct cagcctcctg agtagctggt actacaggtg ccgccactat gcccagctaa 21480tttttgtatt tttagtaggg acggggtttc atcatattgg ccaggatggt ctcaatctct 21540tgacctcata ctctgcccgc ctcggcctcc caaagtgcca gaattacaag cgtgagccac 21600tgagcccagc cttccttttt tttttttttt tttaagtagc tccattgccc tccctcaccc 21660tttcttttgt ctcctgtaat gtccttccct tccatttctt ttttttcttt tttcttttct 21720tctttctttc tttctttttt ttttttttga gataggatct cattctgtgg caaaggctgg 21780agtgtagtgg cacattcacg gctcattgca gcctcgacct ccaggactca ggtgatcctc 21840acatctcagc ctcccgagta gctgggacca caggcacaca ccaccacacc cggctaattt 21900ttgcattttt tgtagaggta gtgttttgcc atgtttccca ggctggtctt gagctcctgg 21960gctcaagtga tactccctcc tcagcctccc aaattgctga gattacaggc ataagcctct 22020gcacctggcc ttccctctca tttttttttc tttcctggtt ttgcctgtcc cagaccaccc 22080tcttggaaag atgctctccc agcagcggca gtaaggtcct ggtcttgtgt ttgctcctgg 22140gcctgagtct tggctttgct gctttgtagc tagctggctg acaccaggga gctgcttccc 22200tccaggagcc tgtcgtccat atgctgaatg tgatccttaa atgctctgtc ttacaggggc 22260cagacattgt ggctcatgca cttcaggggg ctgaggcgtg cagatcactt gaggccagga 22320gtttgagacc agcctggcca acatggcgaa accctgtctc tactaaaaat acaaaaatta 22380gccggaggtg gtagtgtgtg cctttaattc cagctacttg gaaggctgag gcaggaaaat 22440cgctagaacc tgggaggcgg aggttgcagt gagccgagat catgccactg cactccagcc 22500tgatcaacag agcgagattg tctcaaacaa acaaacaaaa aatgttctgc cttacagagt 22560tcttaggtat aaaagagaag gtgcctctaa agctcttggc accgtgcctg gcttatagta 22620agtgcttggt aaacgtcagc tgctgctgtt gtggtgttag tatcagcatt gttgctgtga 22680gaccctgcac ttcccactta gccttggaaa aataagtctt cacgttaatg ccatgggcta 22740ccgcttctct tttcagggct tcttggagga gggtggagat ggagagacag gtgggggact 22800gccagggtta catcctccat gaggctgagg ctgtgctgac tgccttgtgt gctttcaacc 22860tggagtaaag ggtggctgtg ccagctgctc ccatccccca ggagtctgac tcgtccctgc 22920cttggccctg ggcagcactt tccctcctag ctctttggca tctggggtca tggtggggct 22980gcctgccatc tgtcaaaatt tttgctgccc tgggtgtggt ggtaaacccc cgcactatcc 23040aacttggtgt catggagctg gcgacaatat ttttacagtg gttagtgctt ggaaactgga 23100cttctgggtt atgccctgta caaacagcat caaagtcgct gggctagggt gacagaggag 23160gctgccaaca gggaattctg tggctcctgg gacaggaatg gatatgggag gttgggggcc 23220agtattttcg gttctcttga ggagttggcg agtattagtc tttgccctga tggatagaag 23280gaatctgtct gtgtcttgca tgaaccgtgt acttccccca gttactcctt ggacaccagc 23340tgcctgctgt tcataattgg gccagatttc taatactgca gcgctaccaa atgtcagttt 23400taggccatct ctggtgtagc cagggaacgc ccaacacctt tcccaaaggt agaatttgtg 23460tgggttttac ttcactgagt gactaatgca gatctttatg ttttaatgat gggaagaaat 23520tcgtcagcct gggtactttt tccatgtgat ggggcaaaaa tttaaaacac ttgcacaacg 23580gcttttgttt ctccagctac taaaggtgac tgtcatttag gcattatcag tatgatcagc 23640tgatgttaac ccactcccct tctggagacc cgtttctgtt tctgggaaag gtgtaggaca 23700tgctggattt ggcaagattg caggtcccag gcagatgtcc ggacttagac tctggctctt 23760tttttttttt ccagacaggg tctccctctg tcacccagtc tggagtgcag tggcgcgatc 23820tcggctcacc acaacctccg cctcccaggt tcaagggatt ctcctgcctc agccccctga 23880gtagctggga ttacaggcgt gcaccactat gcccagctaa ttcttttttt ttttttgaga 23940tagaggctca ctgtcaccca ggttggagtg cggtggcccg gtccgcctgc ctcagcctcc 24000caaagtgtta ggattacagg tgtgagccac cgtgcctggc ctcagctaac ttttgtattt 24060ttagtatcaa cgaggtttca ccatgttggc caggctggct ttgaattcct ggcctcaatt 24120gatctgccca cctcggcctc ccaaagtgct gggattacag gcatgagcca ccgcgcctgg 24180cccagaccct ggctcttact cctaggtcta cctctaccat cactggggcc ctcgcctgaa 24240ccttttgccc catctataaa atgggagaac tagactaggt ctgtgtcccc caagcttcaa 24300tcatttgtaa aggaaccacc tttactattt tgccatatcc cacggctgtc tctatttcat 24360ttttcactta atattatttt cccctgcagt tgactcactt gtaaaacaaa tgtatttgaa 24420aaggagactt tgtgtcacta taataacgga aaaacagcgt cactaggtaa atggaaggta 24480accataaata aaccccaaac agttattaaa ttccagccag cactgttgcc tgttcacaac 24540atgaggcata ctctcttttg gttaaaaagg gaaattagca agagatggag aggtgttgaa 24600ggtaacctag cactacattg agccttttcc ttgacctgct caggaggatt gagaaagaac 24660taggagaact gggaagagaa taacgtcttt ttgtgatgca aagtgcctga gtgtgaccaa 24720gagctcagag tagtaatgta tagatgcttt gtttggatac ttatgcagcc attaccatgt 24780gccaggggtg tagaggggct aggagtatag aggggattgg gacttgttca ctgacttctg 24840gttgcttgtg gtctagtagt ggggaggtgg tcatagaata ttgaatacaa acgaagatcg 24900aacaggctgc aggggtttaa taggaaaatc acaggactaa attctgtcat gtgtacatgg 24960ggtctacaaa taagagttgt ttagaatttt ttttaattta aatttcccat gaaatataaa 25020tctatttcat tccagaatga ttctagagaa gctctaaata cattaaagtt gtgttggctg 25080ggtgcagtgg ctcatgcctg taatcccagc actttgggag gctgaggctg gagaatcact 25140tgtggccagg agtttgagac cagcctgggc aacatgggag accttatctc taccaaaaaa 25200aatttttttt tcttttcttt tttttttttt tgagacaaag tttcgctctt gttgcccagg 25260ctagagtgca atggcatgat ctcagctcac tgcaacctcc gcctccctgg ttcaagcaat 25320tctcctgcct cagcctccca agtagctggg attacaggca tgtaccacca cacccagcta 25380attttgtatt ttttttagtg gaggtgggat ttcaccatgt cgatcaggct ggtcttgaac 25440tcctgacctc aggtgatcca cccatctcag tctcacaaag tgttgggatt acaggcgata 25500gccactgcac ctggccaaaa acattttaat aaattagctg ggtatggtgg tatgtgcctg 25560taatcctagc tacttgggag gctggggcag gaggatccct tgagcccagg aattccaagc 25620tgcagtgaac tataatcagg tcactgcact gaagccggag tgacagagtg agaccttgtc 25680tcttaaaata aatttgtgtc attgtttgtt gtttttatgg tgttatgaca atgatccatc 25740ttaacccttt atgtagtggt aactaacttt ctcttttcct aaaagctgat ttgagtttta 25800ggttctcttg gagtctgtga caattgtaaa tagataagat ataacaaaat ggcctgaaat 25860actcttgcaa cactcatatt tcccccctca gattagcatg ttctatactc tctgcaaagc 25920aagatataca ccagaattag gcctctaaaa agcctcatac tgctaatctc tgggaatgaa 25980tggtgttctt tgggataatg ggatatgaag ctcagtctga tttttctgtt ctgctggtag 26040cttagggccc cctttcttct gttgggtttt ttgggagaag ggaagttgtg attaagaatg 26100agaattcttt tttttttttt ttgtctcaag agtcttgctc tgtcgcccag gctggagtgc 26160aatggctcga tctcggctca ctgcagtctt cacctcctgg tgtcaagcga ttctcctgcc 26220ttagcctcca agtagctggg aatacaggca cctgccacca tgcctggcta attttttgta 26280tttttagtaa agatggggtt tcaccatgtt ggccaggctg gtctcgaact actgacccca 26340tgatcccaac ccccccgacc tccccggcct cccaaagtgc tgggattata ggggggagcc 26400actgcgtcca gccaagaatg agaatttggg agtcaggcac ctctgggatt gaatctggaa 26460ttgactgagt gtacatgctt tctctgaggc ctccgtcctc actgctctca tctataaact 26520gggaataatc atagtttcta tctgaaacag tgggtgtgaa gatttaacga gctaaattgt 26580aaagtgcctg agacatggga agaagtcagg atgtgctaat gggtaatctt acacttcccc 26640aatggaaagg gccaggttta tattactcta ggctggtagt aagcgaggca aaggagatat 26700caggtttcag ctttgttaga acatgctaat ggcaccagga cactcagaag agatacagag 26760tttgagacaa atggcaccat gagccctgag acattgtgta tggggtgaat cggatagcaa 26820gaatagactt caaggaggga agtagggcag ttagaatcct ttcagctgca aggaactgaa 26880aactggctca catagaagga aaatgattgg ctcatgtcag caagcctaga tgcagagcaa 26940gttatgggtt tcagggatcc agcatctaaa tgatgtcatc aagaacccaa gttttttggg 27000tctctgctct gttggtttct ttcatcctaa agctggttct cctgtggttt accatagtag 27060agttcctgtg agaactccac tctgaccaat caggccttcc cagagccagg gatggatgga 27120gtcgcttctt ttgaggccca tgggtcctat ctggagggga tggatccaga ctcctatcag 27180gaatctagga ggggccgggc acggtggctc atgcctgtaa tcccagcact tcataatgcc 27240aaggtggaca gatcacttga ggccaggagt tccagatcag cctggccagt atggtgaaac 27300cccatctcta ctaaaaatac aaaaattagc taggcgtggt agcaggcgcc tgttgtccca 27360gctactcggg tggctgaggt gggaggatca cttgagcctg ggcacagagg ttgcggtgag 27420gttgtggtga gctgtggttg cgctgctgcc ctccagcctg ggcaacagag tgagaccctg 27480tctcaaaaac aacaacaaca aaatcttatg taccccataa atatatacac ctactgtgta 27540tccacaaaag ttaaaaatta gaaaaggcaa attgcagaga tttccatatg ctatgatacc 27600gtttatatga agttttacat atgtcataaa aatacagata acctttaggg gaatgatcat 27660taccaaactt ttggataacg gtttctgggg atgggcagag agggctatac agtcatgaag 27720aggtgtatag gggctttcaa ctctttgtag tgttttattt cttcagtccc atggtggtta 27780tatgattctt cactcccctt tttttgtgtg gaatattttt cttataaaaa gtgtgtcttt 27840tatttattta tttatctttt tcacatggag tctcactctg tcgcccaggc tggagtgcag 27900tgttgcgatc tcggctcact gcaagctccg cctcccgggt tcgcgccatt ctcctgcctc 27960agcctcccga gtagctggga ctacaggcgc ccgccaccac gcctggctaa ttttttgtat 28020ttttagcaga gacggggttt cactgtgtta gccaggatgg tctcaatctg ctgaccttgt 28080gatctgcctg cctcggcctc ccaaagtgct aggggattac agacgtgagc caccgtgccc 28140tgcctttttt tttttttttt ttttttttta aaggcagagt cttgccctgt tggccaggct 28200gcagtgcagt ggcctgataa tggctcactg cagcttccac ctcccaggct caagcaatcc 28260tcccacctca gcctcctgag tagctgggac tacaggtatg tgccaccaag cctggctaat 28320ttttccattt ttaaaggttt tgccatgttg cccaggctgg tctcgaaccc ctgggttcaa 28380gccatcctcc caccttggcc tcccaaattg ctgggactat agacgtgaac cactgcaccc 28440ccatccaaaa gtgtcatttt aatgctgaca tactgcatta ctaagcttga ccaggggaag 28500agaaaaaaaa ataccttgtg tttattattt tgtttgtttg tttgtttgag acagggtctt 28560gctctttctc ccaggctaga gtgcagtggc atgaacatgg ctcactgcag cctccacttc 28620ccagggtcaa gccatcctcc cacttcagcc tcccaagtag ctgggattac aggtgtgtgc 28680caccacacct gactaatttt tctttttttc tttttttgta tttttggtag agacagggtt 28740gcccaggctg gtcttgaact cctgagctca agcaatcctc tcttcagcct cccaaagtgc 28800tgggattaca agtatgagcc actgtgcccg gcctgtttgt ttgttttaaa gacaagtttg 28860ggcccagttt ataagaaaag aaaacagacc atccttaggg tgtcaggatg atattttgac 28920aaaggcattc atgcttagca ggatttctct ccccctaccc ccaccccaag tgttgaaacg 28980gctgagctaa ttaccttaga atgtaaggct tcctctgttg cttgtgaacg tggcagactt 29040gggattctca gagacagagg gcttcagaag cttgcctctg ggagcgtcca gtcaatagct 29100ttttgtctga gcagaaggag atattgctca aggtaccatc tcaagggact gctgaatcag 29160ttgcattgtc tctaaaagta ggtaaaagtc tagagtaggg ctggttcaac agtggaatga 29220gtgttaagag agagttgcat tctaagaaca cctttacact gtggccaaat tcaagcaggt 29280ccattttgtg gtttggtggt ccccatctag tgggatgtgg tctggtatcc caggcacctg 29340catatatgag ctcagatggg tttaattttt gaaaaactgc tttattggct gggtgtggta 29400gctcatgcct gtaatcccaa cattttggga ggccaaggca ggaggatctc ttgagcctgg 29460gaattcagga ccagcctggg caacattgag agatccccat ctctactccc ttccccgcca 29520aaaaaaagct aggtgtagtg acatgcacct gtggtcccag ctactcagga ggctgaggtg 29580ggaggattgc ttgagcccgg

gaagtcaaga ctgcagtgag ctgagattgc atgactgcac 29640tccagcctgg gcaaaagagt gagacattgt ctcaatctcc ccacccctgc caagaaaacc 29700caaaaaatat tgaggtataa ttgttataca atgaagaaca cattttgatt agcttataca 29760cacactcctg tgtacacatg tacactcaca catcaggaaa ccatcaccat aatcaagaca 29820gcgaacctcc ctatccagcc ccagaagttt ccttgtgcct ctttgtaatt cttgcctttt 29880atctctccat gtcttccaca cccatgctca agcattcact gatctgcttt ctgtcattat 29940cagtcagttt tcatctttta gccttttata taaatggaat catatagtat gctgttttgt 30000ttttttttga gacaagagtc tcactctgtt acccaggctg gagtgcagtg gtgcgacctc 30060ggctcactac aacctccatc tccccagatt taagtgattc tcctgcccta gcttcccgag 30120tagcagggat tacaggcaca tgctatcatg cctagctaat ttttgtattt ttagtaaaga 30180tggggattca ccatgttggc caggctggtc ccgaactcct gacctcaggt gatcacccgc 30240cttggcctcc caaagtgcta ggatcacagg catgagccac tacgccctgc cagtatgtac 30300tctttttgtc tggcttcttc tagcatagtt attctgaaat tcatccttgt tgcatgtgtc 30360aatagtccta ttccttttta ttgctgagta gtagtccatt gtatggatat actacatttt 30420gtttatacat ccttctgttg ataacatttg ggtggtttct tatttattta tttatttttg 30480agacggagtc tcactctgtt gaacaggctg gagtgcagtg gtgtgatctt ggctcactgc 30540aacctccacc tcccgggttc aagcaattct cctgcctcag ccttctgagt agctgggatt 30600acaggcattt gccaccacac ctggctaatt tttgtatttt tagtagagac ggggtttcac 30660catgttggtc atgctggtct cgaactcctg accttaggcg atccgctcac ctctgcctcc 30720caaagtgcag ggattatagg tgtgagccac cacgcctggc cgggtggttt ctaaataaag 30780ctatcatgaa catcttttac tactctttgt atggatgtat atttctattt ttctgagtgg 30840aatgttagga tcatacatca taggtgtacg tttaactgtt caagaaactg ccaaactgtt 30900tcccaaagtg gttgtattgt tttacatttc cacgagcagt gtttgagagc tccagttctt 30960gcacatccta gccacaaaaa ggttctgttt tttaaagaca attttttttt ttttttgaga 31020gtttcgccct agtcgcccag gctggagtgc agtggtaagc gaatccctgc tacaggccag 31080agactgttct cagttggttt ttacaccaag tatcgcactt cattctaaca ctccaccatt 31140ttacaaatga ggaaaccgag gcactgagag gtttagtaac ttgtggcaca gccaggaagc 31200agtagagaaa gactttgaat ataaatgtat ccattaggat gtatatggtt ccaagtcatg 31260ggaaacctac ctaatcctgg tttatccaaa aagggagctc attggctctc gtaactgaaa 31320agtcaagggg taggcaggca gttggacctg gaagtctcca gggcatcaga gagccttggc 31380tctgcttctc tgattctgtt gtctctccac agacgggtgg gtgtagcagt cccaggcccg 31440cagccacacc ccacacctcc cagaggaaga aggcgggccc tgatcccagc agtcccagga 31500aagccctgag gttcactgtg attggaccag cctatgtcac ctgctcacat ctcagcccac 31560cactggcaag ggtgtttgac tcttgggaat gactcttggg actggcttgt cctagatcac 31620atgttctacc tgaaattggg gacattgcag aggattggtg gagtggacct caaggaggtg 31680tttcacgtgg cttcctgtgt cactaggttg ccatttattc tttagaaagc ccctttgttt 31740gatgaaaccc tggtgtcaca ggctgtgtga cttagggtaa tccccttgtc cacatctgtg 31800aagtgagatt acctcttcac ctcacaggca gatcaaacag gaaaacaaaa acaaaaccaa 31860acccaaaata cacgtaaatt gcagagtgct tgaggtttct tttaagctgt ctatgtaatt 31920aaaagctgtt acttagactt ggatatgaaa taaaatctga cttcaaattt aagtggtgta 31980atttccatgc ctcttaaaat atcaggtaac ttcatttgtg agcctcagtc tgtagacttg 32040agggatttcc atctgaagag ggggcagaat ggtggtttag ggaacgcaac atgtacccca 32100cccccaactt ttttaagagg aagagttgaa agaaataatg aatgtgtgag aaataagggg 32160tttgattgcc ttccagggtc catgttgaag gagaggaaaa tgtagctcaa ccacagtgac 32220tctccccaat taaaaactaa aaaaagatcc gtggttatag ggcttggact tcggacaagc 32280cagcagcctc agtcattgtg agtgtgattc cagattggaa ggttctgcta ggaggaaagt 32340ggaagttttg agaattccta gttggacaga atgcctcttg atcacggcct tagctaaagg 32400agaccactct ttgctggatg gatcagtcag ctacgtgtga agtttggctc agtacaacat 32460tctcggcctg gggcggcagc atgggaaaga tttttattgg aattaacttt ctacagagat 32520gtactttcaa atgagaccat ccttctctca ctggtgagct cacccgggct cttattccac 32580aaagcttaat tgttttggac ccatacattt aaactcctta attaattgac tcaagactta 32640ggacagattt gcttttcttt ataatgactc catggctgta aatgctgctg attcagatga 32700aagaggaccc tagagcacag aatgagaagg acgtggactc aggatacctg tttctttatt 32760ctgactgtgc tcttcgtcag ctctggggct ttggacccca gttttgtaac cacctaacga 32820gttcaccttg cctgctgcct agacggagct gatttatcaa gacagaggaa ttgcaatgga 32880gaaagagtaa gtcacccaga gccagctgtg tgggaggcta gaattttatt gttactgaaa 32940tcagtctccc gagcatttgg gatcagagtt tttaaagata attcggcagg taggggctca 33000ggaagtgggg agtgctgatt ggtcaagttg gagatggagt cacagggggt cgaagtgacg 33060ttttcttgct gtcttctgtt cctgggtggg atggcagaac tggttgagcc agattaccgc 33120tctgggaggt gtcagctgat ccatggagtg cagggtctgc aaactatctc aagcactgat 33180gttaagtttt acagtagtga tgttatctcc agaagcaatt tgtggaggtt cagactcttg 33240cagtttctga cccctaaacc ttaatttcta atcttgtagc taatttgtta gtcctacaaa 33300ggcagactgc tcccaaggca agaagagggt ctttttggga aagggctatt agcagttttt 33360tttcagagtg aaaccataaa ctaaattcat tcccaaggtt agtttggcct atgcccagga 33420atgaacaagg acagcctaaa ggttagaagc aagatggagt cggttaggtc tgacctcttt 33480cactgtctat aatttttgca aaggcagttt cagtttctca cctgtaaacg ttgaagactg 33540agccagaatc agggtcatca aatagcaccc cggctatact ttcttctctt catgacaaac 33600attgctggtc agttgatatg atgttctttc ccactgggcc cagacttgac attagagtct 33660tttttttttt tttttttttt tttttgagac agtctcgctc tatcaccctg gctggagtgc 33720agtggcacca tctcagctca ctgcaacctc cgtctccaga gttcaagcaa ttctcctgcc 33780tcagcctctc aggtagctgg gattacagga gtgcaccacc acacccagca gatttttgta 33840tttttagtag agacggggtt tcgccatgtt ggccaggctt gtctggaact cctgacctca 33900ggccatccgc tcgctttggc ctcccaaagt gctaggatta taggcgtaag ccaccacgcc 33960tggccgacat cagagtcatt ttagcctgca atgcaagttg tcctcagtgg gctgctagca 34020ttggcttcaa ccttcatatc agccagctaa agccccttgt aatgaatggg gaggttcctt 34080cacccttgcc tcccgctgcc tcctcttgac cactcatttt ttttcttgta gttcaggaac 34140caattcagat gatttccctc gtgaagtcct ctcgaaagcc cccaggtaga attattcatt 34200ttttcccttg cattcccaca gcactgtgca cacaaattag aatccttgta aaatggccat 34260gattctgttt atgaccctgg ccctccacca gaccagcctc tctgccctct ggctttttta 34320gatcactggc atggtttctg cctactccag gtgccagtat tattttgtga atgttttttt 34380tcttcatatc tactcatctt tatactactt tactcgtaaa aggaaactag agaacatgat 34440cttaaatgaa aaccacgatc acttgccaga aagaacaggt aactaggctt tgaaaaaata 34500agttagagga gatagcataa gaaaaaatta aaaaataaat aaaatcaatg aaaacaacgt 34560gttactaaat tcttgaaaag ttttttgaag actttgagcc tgaggcctgt tcttattgtt 34620tgtttgtttg tttgtttgtt tgtttttatg acagagtttc gctcttgttg cccaggctag 34680agtgcaatgg catgatctcg gctcattgca gcatttgcct cctgtgttca agcgattctc 34740ctgcctcagc ctcccgagta gctgggatta caggtgcccg ccaccatgcc cagctaattt 34800ttgtatttta gtagagatgg gtttttgcca tgttggccag gctggtctcg aactcctgac 34860ctcaggtgat ccacctgcct tggcctccca aagtgtgggg attacaggcg tgagccacca 34920tgctcggcct gttcttattg ttaaaaagag agatttgtgt gaaagctgct gacgtctttt 34980tggcaccaag tcaagactga gttagttctt gtcagaatct gattgtttgt gaattgatgg 35040cttttttttt tttcctgagt tgggggtctc gctctgttgc ccaggctgga gtacgaccac 35100tataacctca aattgctggg ctcaagcaat ccttccgcct cagctgccca agtagctggg 35160actactaggc atgctccacc atgcccagtt aattaatttt tttttttttt tgagagacag 35220ggtctcacta tgttccccag gctggtctca aattcctggc ctcaagtgat ctcctgcctc 35280agcctcccaa agctctggga ttacaggagc gagccactgt gcctggccgg attttaaagt 35340tctgcccatg cacctcctta gctctggcag ttactacttg caggcatctc ctttgtctgc 35400cctgcccctt gttaggaaag gctgtgctga ctgtcagctg gcacccagtg catagaagag 35460atagttctct gtagatgatg ttgaacaatg tggtactata atcccaacct gttgtatctt 35520tgtttactct caaaagcaac aattgggctg ggcatggtgg ctcatgcctg taatcgcagc 35580actttgggag gctaaggtgg gagggttgct tgaagttagt tccttttttt tttttttttt 35640aaaaaaaaga caagatctcg ctctgtcacc ccggctggaa tgcagtggca tgatcatagc 35700tcactgcagc cttgaccacg tgggctcaag gaatgaacca ttgtgccagg agttcaacac 35760cagcctggat aacatagcga gaccctgtct ctacaggaaa aaaaaaaaaa aagaagaatt 35820gcataagtat catcagaact gttgaatgga aaatcagact ttgtgggttt ggtttgttaa 35880ttacttctcg ttggattaga atttgatagg taaaaaaaaa aaaaaaggtg tagaaaagtg 35940attccagtct tgagcaaatt tttaatggaa aacggtgtct tggttctctg ttcactacaa 36000cttgtatcta agggaaagcc tagtgatgca gacatttcat ttcgtgatgg gaaaactgat 36060gcccagaggt tcacagctga ccaggggcta gtctgactgg ggggatctag gtcaccaccc 36120cccttgcctt gttttcccag ctagtgcatt tcctactaga cttgactcta ctgtaattca 36180agttgctgag tagcaaacaa gaactacaat gactagaagg aacagaacta gcttttttgt 36240gctctgaaag tggaaactta ttgagggttc ttttcctccc agagaatgca gaagtgccct 36300gatttgcttt tggaaggaca ccattcactt tattgcctct tttcattgtt gcccagaata 36360tcaccatgat ttattcatgg gtggtgggga gggtagcact agtgtatgct cccagcaaag 36420aggaacatct cacgttgtga agagatgcgc aaaactaagc cagggcaggg tgtggtggct 36480catgcctgta atcccagcac tttgggaagc tgaggtgggc agatcacctg aggtcaagag 36540ttgaagacca ccctggccaa catggtgaaa ctctgtctgt actaaaaata caaaaattag 36600ctgggtctga ttgcaggtgc ctctaattgc agctacttgg gaggctgagg caggagaatt 36660tcttgaacct gggaggcaga ggttgcagtg agctgagact gtgccgttgt actctagcct 36720gggcaacaag agccatctca aaaaaagaag caagccagat ctttggggtg ctgtgacggc 36780aaatccccca gcgctggcct ctcaggttct cttgcgggat tagtgtttgt tgaataataa 36840gcaatacacc ctgacccagc gagccaaagc aaacaggaca gtaactgaaa ctgcagggga 36900gtgtgagtaa acagttacct tctaccctca tggagctggc ctctggccag caacatgata 36960gctgtttgca tcttactctt atggagccat tggccctctc attaaggtgg gggcagcttc 37020tggtccatgc ctgcaagtcc tcatgggagt gggtacctga cagggtgtaa agggtaggtc 37080tgaggacatg gtttcttttt tttattgttg ttgagatgga atcctgctct tgtcacacag 37140tctggagtgc agtggcctga tctcggctca ctgcaacctc cgtctcactg gttcaagcga 37200ttctcctgcc taagcctcct gagtagctgg gactataggc gcatcctgcc atgcctggct 37260aagttttgta tttttagtag agacggggtt tcaccacgtt ggccaggctg gtctcgaact 37320cctgacctca ggtgatccac ccacctcagc ctcccaaagt gctgggatta caggcgtgag 37380ccaccgtccc cagccaacat ggtttcttta aaatatactc cccgctccat cccattcatg 37440tgtgggagtt gagctgcatc tgggtttttc ttttctcttt ttctgtaaat ctttattgta 37500ttttttttgg atcatagaat ggatacatgt ttcttaaagt ttgatcatta tagaaactta 37560attagactat tatttgagtg ctaaccatag tgagtgagtg cttactgtgt gctaggtggc 37620tttttatgcc tcatgtcact tacatgaggt ctgaggaacg gtgttaatcc cgttttgcag 37680ctgaggaaac tgaggctaca tttacggtca cctagctggc aagcaagtgg ctgagcctgg 37740agcagcagca gatctgggga actccacaaa ccagatttct gtgtggtatc cctgtggaca 37800caaggattta acttgattct ttttgctttc agtatcactt tatgatatta caatgagctt 37860gcagtattta ttttcagaag aaaagccaga ttattcccat ttatgagaga agcagccagg 37920tgggcaggga tttccagcgc tgaaccagcc agtgtgtgca ttgtctcttc ccgctgagcg 37980gccctggtgt gctgggttag tctgtgagcc acaggaaatg ttgtcagggc ctctgggctt 38040ttggatgtca gcaggccttc agtggtgagg aggttgtggc tggactcaga ggactccttg 38100cttttgctga acgaccctcc ccaccaacca ccaccaccac caccagtggg actagcccat 38160gagctgtaag ccaacctttt ccttcctaac ttaattttcc aaagaatagt aacttaccca 38220ccaccactgc agtcactggg ccgggaagac aagcactctt gccttgaatc catgccttga 38280gccagtagcc ttgacccagg gtaaagcagt tatgtgcttg ggtcacctgg gtcatgtttt 38340tgaaattgcc tcaagcctac cttacaaatc cttcctggaa ccctgcttgg cttttctttg 38400tgggcttccc ttaggaggga agcttcccga gcagcttgtc ttgactgtag ccagctgggt 38460ggtcccagcc acagaattta actgtcaaac agcaccagaa gggttcctca tccagctgtc 38520ttgccccaag tgccctcttt gctttctttt tagagagttc tgagactcat tagagagttt 38580agagatttta gcattcttga agttctttct gtggtcagtt tggtgaacca cttcatttct 38640aaagtttctc agttgacccc attcttcccc agctttgcat tctccatgaa gccacctgtg 38700tttggtgtgt atgggttttc tgcaacctag gttgaacaag tcctctagaa tcctgaacaa 38760ttggtgattc atgctggcct ggtttttcta attggcctgg aaatgtggct gtagtggaca 38820caagtggact tggcctcctc tttgatgcgg gtaaacttta gatttgcatt agctctgttt 38880gattagagga tcttactggt ttttgttgtt atttatttac cttttaggag ctttagtctc 38940tgtaggtttt tttttttttt tttttaaagt ccgggtctta ctctgtcacc caggctaggg 39000tgcagtggca tgatcacagc tcactgcagc ccccaccttc ctgggctcag gtgatcctgc 39060caccttagtt tcctgagtag ctgggactac aggcatgtgc caccatgccc agcaaattta 39120tttctacttt ttgaaaacag ggtctcactt tgtcacccag gccagaatgc agtagcacga 39180tcatggctca ctgcagtctc aacctcccag gcttaaggga ttctcccacc tcagcctccc 39240aagtagctgg gaggctactt ggcatgcatc acaaggccca gctaatttgt gttttttctt 39300gtagaggcgg ggttttgcca tgttgcccag gctggtctcg aactcctggg gtcaagttat 39360actctctcct ttgcctccag ccatgagccg ttcgttgcgc ctgggctagt cattatagat 39420ttatcccttc tttcatctca tgctacaaaa gcagttcttg tatttttacc cgacttgtga 39480ttttctactg ggaatgtttg tttgtgatgg ttagcagggt gctgagaggg aattaatccc 39540aggaggccca atattgggcc atgtcgtgct gttgagcaca gtcatttgac acctataact 39600tctcatcaat tcttctgata gactgaggag gaattgggaa atttcctaga gttttgtctg 39660cattattggg ttgttttgag aacataaacc ttaaactcta gctatgtaaa ctggataagt 39720cattttggta atttggcatt cctttttttt tttttttttt tttttgagac agagtttcac 39780tctgttgccc gggggaatga tctctgctca ctgcaacctc tgcctcccag gttcaagcaa 39840ttcttctgcc tcagcctccc aagtagttgg gactacaggc acactccacc gtgtccggct 39900aatttttgta tttttaatag agacaggatt tcatcatgtt gaccaggctg gtaatttggc 39960attcttttga gtacaagtga gagaaactca cttgagctgg cttaagtgaa aaaattcttt 40020gtcaggagag ttttgtgaat ttctgtttag tggcaagttg tagaaaccac ttgaaactgc 40080ttaaaggcaa aagagggagc cacttgtccc agtaactgag acatcccaga gccgactgcc 40140cccaagcatt acttggtccc aagtttcaaa cgggtcttca gggtttgatc tctctcctca 40200tctccagtct gcttcattca ttttggctct atgtggtggc agaagggctt ctggcatctc 40260tggaccttta tgcctcccag gtccaaaccc agccagaaag gagagtgaga gtgctgagtg 40320caaaactctc ctatagctcc tatacaagtc caggatttgc tattagactc cttgaattat 40380gtgcccagct ctgagccaat ggctgtgctt aggaggctcc tgtctcatgc acccacccca 40440gtactgggca tcagaaacaa ccagtgatcc ctataatgaa ccacgggttc acagacttaa 40500gtgtaatcct gcagcagggc ctcaggaaga cttgaaaccc aaaatcagaa agccatggtt 40560tcttgtcttc ctggtgtctg ttttgtccct tccctctgta gaggagtcct gctatcactg 40620caggcaacgg ggctgccctg cagctcctgc tgtttacatt tcactcggtg tagccatagg 40680cagagacctc agggagaacc tgattcggct tggattgagt caggttccac cccagtccag 40740tcagttgtgg actgagaggt gatgaggctg ggccctttaa gacaaatctg ggtgggtgga 40800gtctgtgctt aatgaagttg tgatgttagc tgatggccca gaagggactg gtaggtgcct 40860ctcattgtct ggttgggaag cattctctta agtccaagat gatgataaat agtattaggc 40920caggtgccgt gtcatgcctc tatacccagc actttgagag gccaaggtgg gaggatcgct 40980tgagcccaga agttcaaagc cagagtgggc aacataaaga gaccctgtct ctacaaaaaa 41040caaacaaaca aacaaaccaa aaaaacccca caacaattag ccaggcatga tggcgcacac 41100cagtagtccc agctactcag gaggctgagg tgggaggatt gcttgagcct ggcgggtcga 41160ggttgcagca agctgtgatc acacctctgc gctccagcct gggtgacaga gtgagaccct 41220gtctcaaaaa gtaaaaaatt caaataaata aacaaataat atcaagggcc tctctcccaa 41280gctaggaaga tatcagctga agctctagcc cagctacgtg gatggctgct tcctgcctgg 41340aagcgatgcc cagatcagca ccttgggacc cccctgaact tgcctctgct ccagtgtggg 41400cccttccttc ctgcagagga gacagcactg tctgagaggc atgaatgaga atttcctcct 41460tctaggccca agtcagcatg actcgaggat ggctttgact ggaaaaactg aatcaaagag 41520tgtgctacag ccaaggattt ccccaaacac taatcagtgc tgattacttc cagggtattg 41580cctttggctc tgtggagttt tgtccactgt ggctgcaatg tctggcttct gctgcccaga 41640agatgagaaa tgagtttgta gggatgagcc tgggtgaagg gatgtgcccc ctcaccatcc 41700tgacctctat taggtgtaaa agaccctgat tgccaaattc ataggtcatg ggttggctct 41760gcctccagca ttaacacttg ggggtggagt tggggaatca tagtattact tgcataaatg 41820gaatcctaaa agtttgttgg gacagtttca taaaaatcct caccatgatc agtttgaaaa 41880tgacgttccc ttcacatgtt tgtcttctga actgagttgc aatgctgagt atgagtttga 41940gagtcccaag accatctaaa gcaagcctgt ccaacccaca gactgcaggc tgtaggcagc 42000ccaggacagc tctgaatgcg ccccaacaca aattcgtaaa ctttcttaaa acattatgag 42060atcctttcgc atttgttttt taaagctcat cagctatcat tagtgttagt gtatcttatg 42120tggccaagac aattcttctt cttccagtgt ggcccaggga agccaagaga ttggacaccc 42180ccgatttaaa ggaagtaact caattttgtg aacctgaaac ttgatcttgg atgaaccaaa 42240tgaaatttta tgattctctt aagctcacga aagttcaata actgtgctgt gtaaaataga 42300ggtaaaagac ttgagttgga ccaggaatgg ttgctcatgc ctgtaatccc agcactctgg 42360gaggctgagg cgggtgcatc acttgaagtc aggagttcaa gaccagcccg gccaacatgg 42420tgaaaccctg tttctactaa aaatataaaa attagccggg cgtggtagtg tacgcctgta 42480gtcttagctt cttgggaggc tgaggcagga taatcccttg aacccaggag gtggaggttg 42540cagtgagcaa gatcatacca ctgcactaca gcctgggcta cagagcgaga ctccgtctcc 42600aaaaaaaaaa aaaaaaaaaa aaaaagactt gagttggttc taatagaata ccttggagaa 42660cctcaagatg ccttctggtc cagccaggtt tacagattgg aagatattct gttaatcaga 42720atctcagaga gggacaggcc ctgatcaagg taacacagtg agttgtggta gctgggctgg 42780gctagaacct gggcctcctt ggttccaggt cacagggacc aagggatttg gcttgtctta 42840gtcctacttg taactacaat actgccttct gctaggaaga ataagagctt gcaggctaga 42900ggaatttata ggaattttct ttctttaaaa aaatcccccc aaaaccagct ttactgagat 42960ataactcaca caccataaaa ttcacccttt taaagtatgc aatttttagt atattcacag 43020aattatgcaa ctatcatcac tataatttta gaattgtttt tttttttttg gagacggagt 43080cttactcttg cccaggctgg agtgcagtgg tgcagtcttg gctcactgca acctccatct 43140cccaggttca agcgattctc cttcctcagc cttccgagta gctgggatta taggtgcatg 43200ccaccacacc caactaattt ttgtattttt agtagacatg gggtttcacc attttggtca 43260ggctggtctc aaactccgcc tgccttggcc tcccaaagtg ttgggattac aggtgtgagc 43320cactgtgcct ggccaatttt agaatatttt tattgcctca gaagaacccc tgtatccatt 43380agcagtcact ctccctttcc cttccccaac caggcccaat aaaccactaa tctactctgt 43440ctctatggat ctgtccattc agaacatttc atatggtaaa atcatacacg tgttctggtg 43500ttactgactt ctttcactta gcagaatgtt ttcaaggttc agccatgtta tgtctgtact 43560ttattctttt ttacggccaa gtgttggaat gtgtaggatt tgaattttca aataaagctt 43620taaagttttc agatttattt ttactttgcc tggtgtgttt tttcctggaa agccaacttc 43680tacatttgga gattaaaaga caaactttct caaactccct gtacctaagt ggttgctgct 43740tttcttaaat gttttgacac caaagagaaa aattggtttc tggaagaaag tgtgttttct 43800tttattgcca agaaaattag tgcatgttaa ttaatataga tgctcaggac ccagagttgt 43860aatgaacttt tttcttatat ttattttcta gatgtttgac ttattttaac agttttcatt 43920ttagcaataa tgtttccttc ccactcccaa atttattgga aaccctcaat caaccctatt 43980tatttattta ttttagagat gggatctcac tatgttgtcc aggctggtct ggaaaccctc 44040actcttatag atagtatgaa agaagattat agccaactct tatataacct tccccagagc 44100ctccaattgt taatgttttg ccatatttgc ttgctctatc acttgctcta aagatgcata 44160tcacacactt tttttttttt taatttattt ttgagacaga gtctggctct gtcgcccagg 44220ctgtagtgca gtggcatgat cttggcttac tgcatcctct gcctcctggg ttcaagcgat 44280tctcctgcct tagtctcctg agtagctggg attacaggca cgggccacca tgcccagcta 44340atttttgtat ttttagtaga gatggggttg gccaagctgg tcgtgaacta ttgacctcaa 44400gtgatcctcc tgcctcagcc tcccaaagtg ctaggattac aggagtgagc caccatgcct 44460ggccacatgc gtgtttttta ttgaatcatt tgaaagtact cagctcgtat catgaccctt 44520cacccccaca tactccaaca agcatctcta agaaaaagga cattctccta accacagtgt 44580ctctgcattc ccaggacatt cttctaacca cagcgtcact gcatacccaa gaggttagca 44640ccgatacagt aataacatct

tgtgtaaaac ttcccaaaat gctcccaagt gtcctttatg 44700acagtttaaa aaaaaatggc attttttggg atccaggaac caattaacga ttactcaatt 44760gaatttggtt tcaaagtcac atacctcaac ttttccttta atcaagaaca gcccccctgc 44820cttttacaca tttttttgtc tttcgtgacc gtgtcatttt tgaagaaatc aggcccgttg 44880tcttgtagaa ctggtgtttc tcaagtgtgc ttgggagggt cttggtaaaa tgcacattct 44940gattctggag aacagggtgg agcctgggaa tctgcatttc cagccagcat cccggtgatg 45000ccagtgcagc tggtcttcgg ctgtagaatg ttccacattc taggtctgtc tgtttccttg 45060tgattaaatt caagttgaat atttttggct agggcacttc ctgaggtcat aggtacttcc 45120cactgcctca cagcacaggc tcacaatctc agtttgtcct gttacttcgt ggtgctaagt 45180gtggtcacct gcttcaagtg gtgtccgcct gctctctgtt gaaacaatac ctttctccta 45240gtataatgat taggtaacct gtgattgtaa ttggtaagta atctttgaga ctacatgaat 45300atcctgttcc ccagcagttt tcactcattg gtgaactgtt ttgggaaaaa taatagcatc 45360ttacagttat aataccctgc tggtaacaca tggctcttac ataatcagca gttaattgtt 45420tgtatgtgtg ttaattttta tttttaaaat gtaactagtg actggtaact ctcatttgta 45480ttttaaacat tggcttttac agcttctcag tacatttcac tctgtgtatg tttttggtag 45540agcatttgtt gtcctgtata atggtttagg aaatcctata ggccaaatga agggctggag 45600actcacctgt gttcccacca ctgtgtttca ctgtgtattg ccagagaaaa tacagttaaa 45660tttgaatttc agatagacaa tgaataactt tttagtataa gtatgttcca agtgtggcag 45720acagctctca caagttacaa gtcgttgcgt aggacatacc tatgctaaac gatttgatgt 45780ttatctaaat taatatgtaa ctgatatctt gtatttttat ttgtacgatc ttccaagccc 45840acgtcccacc gccttctcgg ggatggccac catttgtgtt tgctgcctgg tggtgtttgc 45900agctgcgaga agggccttgg aggaggagca aagtgtagtg gtatctccgt gctgtggcct 45960tgggcactgg ggtgggggtt agatgagtaa ttagctgaat atgacctcac ccatgaagaa 46020tgtgcccttg ctaggtatta gcagaggttt aggctccagg gagccattgt cagaagcttg 46080tcagtgatgt catcagctgg aagggccagc tttcaggcct caggaaaaag cttgaaagtc 46140agggctccag ttttggtaat aaatgggaat ggagtttcac aggtagggtg tggaggaatt 46200tattgtgaca ggaagcctga tggagcctct tgcctgtgtg cagcccccag ccaggtttct 46260gagttctgat gaactaccag aaacttccac cacggcctgt gattacactg ttggcccaat 46320gccctggaaa aattggcttg ctctcgggga acactccagg agctgcaaag ggggtgtcag 46380gactgttgtg cagctcccct taaattgggg aggaggggtg gctgatgtgg aaactgttca 46440ttagactgct cagggtagtg tgagaaaacg tgtaatctgt gggcatctac ccctagctgc 46500ccctctgatc tcacccacta ctgtgggagg accccgtgga tgggggcaga ggagggtctt 46560ctggatttag acactcacaa aacttccttt taccttgttc attggaagaa atagaaaatg 46620cctttttttt tttttttttc tttttttttg agacagagtc tcgctctgtt gacaggctgg 46680agtgcagtgg catgatcttg gctcaccgca acctctgcct cccgggttct aacaattctc 46740ctgcctcagc ctctggagta gctgggacta cagccacgtg ccaccacacc cagctaattt 46800ttgtattttt agtacagacg gggtttcacc atgttggcca ggacggtctt gagctcttga 46860cctcgttatc cacccgcctc ggcctcccaa agtgctggga ttacaggcgt gagccaccat 46920gcctggtctc tttttcattt ttaaagggta atttgctgtg caggagtggg ctctcagacc 46980agaagtgggg acctgaatga aatcaaggac tgagtatggt aactacagcc atttaatttt 47040atttgaagtc tcccgtaaaa tgttctggaa aaaacagggg ttccagggct gggtgggcag 47100tttcaatcat ggactggatt ttgtggttca gatttctctg ggcctgttgg aggttcccct 47160taagcaatta cccaaggcag ttctgcccag ctgaagtact gattacctgc acactatacc 47220agtgaggact catgggtgag cagatgggag gcactgagct tgattctgaa accctggcct 47280ccatcccacc tgacattcaa tgtcagatta gaatttggaa gaccctaagt ctccagattg 47340gtgcactggg tagctcctga aatggggtgg ctgagacagg tcctctgtgc ccccttccac 47400agcttcctct ggggcccttc tgctcactgg catgtgcttc tgggcaaata ggcctctccc 47460agcatttgtt ttggctctgt gaaatggggt aatatttgtt cctattgcgg gtgaagcgct 47520gctgttggga tgctcaggta actcactccg tgggtagctg atattgcctg ggcaagtggc 47580attttagagg aaatctgtgc catcaaaaga gttggacctg atcacacttt tgcttttgaa 47640tatgctttgt cccagcctgg ccattcgtca cttgggaccc cctgagtctc tctgacccca 47700ctgtaaaatg gatatgccat ggagttgtcc caggaatcaa gggcaggtcc tctccagtga 47760gtgatgggct tgcctctcac ttctctaaca cccttctgct tccttgtgta agatttcact 47820attagtggct attctctttt acagaagaaa aagggagacg catgcctctt ccagttcact 47880gttcaccatt gcagcatatt tattccaagg gactggccga atcatccctt tctttgttag 47940aatgtggttt tgttgccttg agacaagtgg cccgcatgtc tgcactgaag gaggctttgc 48000gcaatagcct tgggcacctc cggttctgca agcatgtaca gtacttgctc tcctttccct 48060ttctttgtat actttttctg gtctgctacg tgtccatctg catgtggata aagggtcgtc 48120gtcttgagta gtgattttgc tgtgatgtga ttcctgtgag gtctagttgc acacagtgat 48180tccgaaggta gacccagctg gaaagctttt aaattgctga tactccagcc ccactcccca 48240agagatgctg attttgtttt gttttgggga gggcagtttt tttgggtttt ttttttaagc 48300tttttgatgt gtagccaggg ttgagactga agtgattttt gtgagtaacg gagaagtgtt 48360aaggcttgag aagttggaag agccatgctt gagataggac caaggtcata tccccggcat 48420tagcacagag caaccctgac ctgttggaga gttgggctgg atggatgcgg tcaggggaga 48480gactcgcttt attttattta tttagagata cagtttcact cttgtcaccc aggctggagt 48540gtaatggcac gatctcggct cactgcaacc tctgcctcct gggttcaagt gattctcgtg 48600cctcagcctc ctgagtggct gggactccag gcacgcgccg ccacaccctg ctagtttttg 48660tgtttttact agagacaggg tttcaccatt gttggccagg ctggtcttga actcctgacc 48720tcaggtgatc cgcccacctc ggcctaccaa agtgctggga ttatgggtgt gagccactgt 48780gcccagcctc gactcgcttt attatatcca cacttggaat acaattcgga ttgattgtag 48840tggggcattt tataattagg aaaaattaat caggaaaaat cactccatgt agattagtac 48900caccatatga ggggacaaga atttcttcag attaggaact tcttccaaca ggactgacag 48960ggtccaaaac tactcttgga tccagcttta agatggaccc agcccactgt tgagtcccct 49020ctgaggtctt ctctctgtgg atggatttga ttgttaacaa tggctgagtc atgtggcacc 49080cagcccggtg agtaagacag ctgagtaaga ggggaaacag ggcctttggt cagaaaaacc 49140agactgactt cagtcttatc tgtttagaga agccccagaa gctgcaaaaa ttgcagcttc 49200cagactttag tgtgccgtgg tcatgacatc ggtgtggatg gcaggttgtc atctgagcag 49260tcagggtggc agcacacagc ttgcgggctg gctgatggcc gaggtgtgtg aactgacctg 49320ccccaagtga cttcagtgct gggcacagca taggagcagt actaatgata tggacagtat 49380gctcagagga cgttagggag cacagctttg tgtaaagggc atgccctgcc ctgtccggat 49440ttaaagcagc tatagcactg aaaccccatg gtcaccctcg catttctaca cttctgcctg 49500tgccaagtct agtttgtgtg cctcctccat tttgtgtgta catgggggta tttttttctg 49560ctaggcaact gctatttatg cctctcagta ctgtacttag tgtgtaccat tcctgcaagg 49620tatagacatt gtcagcccat tttacagatg aggaaaatgg agtttttgag agggtgagat 49680cattcagtgg cagaatggaa tgttaaccca ggtagtctaa cctctctgct gtagatctga 49740tgtccatttg aactttagac ttcccatctg tgtctacagt ctagccctta aaaaatgtga 49800taaacaggtt tttaggtaag tctgttaatt tcagaaagac attattatta ttttttagaa 49860agttagagct tatgttaggg ctcagtctat cctcctgcct cagctgcctg aatagctggg 49920actgcaggca catgccacca tgcctggtta atttctgtgg tatacatcat tgattactga 49980gaagtcacag tccgttgtta aataactgag ctattcatag ccaaatcatt tttaaaaaca 50040caaatataag caaaaacaaa acatttattt atttatttat tgagacggag tctcgctgtc 50100acccgggctg gagtgcagtg gcgctatctc agctcactgc aacctctgcc tcctgggttc 50160aagtgattct tctgcttcag cctccccagt agctgggact acagacaccc actaccatgc 50220ccggctaatt ttttttttat ttttagtaga gacagggttt cactgtgtta gtcaggatgg 50280tctttatctc ctgaccttgt gatctgcccg cctcggcctc ccaaagtgct gggattacag 50340acgtgagcca ctgtacctgg cccaaacatg tggttttttt aaatgaaagt gtgttcattt 50400tacaaacagt gcattcttac taattttaca ggccctgtgc tagggacatg gcctcgtctt 50460ccgctatctt agagtgaaga agtaaagaca gagaaagtgt tcacaagttg ctgcacaagt 50520ctcattgcag tgcctcccag aggcgcgaag agcaacacct ttcacctggg ctgtcctaga 50580aggcccgtgg cagggtgggg ttggtgaaca ctggggctta agggggtgaa ttcagaagac 50640aaaggacctt ctgggcaaag aagggcccag tagtgggaag tgcaggagtg tgagagtgcc 50700tggaattgcc cactcactgg ctctggagct tggtgctgag tgcttgggaa gtgttgggag 50760gatcagttat attgctggct gggttctaaa gaacctccaa agtttacata aaagttacct 50820ttgatttgac tgttctaccc tccagtcacg tggctaaatt aattaaatca aatttaaaat 50880taagctcagc cataccaagt atatccagtg ttcaataggt acatgtggct tgtggctgat 50940gcactggaca gtgtacatat aaaacatttc catcgttgca gaaacttcta ttgaacagca 51000gttgtattag tccgttctca acactgctgt gaagaaatac ctgagactgg gtaatttata 51060aaggaaagag gtttaattga ttcccagttc cacagggctg gggaagtctc gggaaactta 51120caatcatggc agaaggggaa gcaaacatgt ccttcttcac atggaggccg cagcaaggag 51180aagtgcagag agaagagggg gaaaagcccc ttataaaacc atcagatctt gtgagaacag 51240cagcatgggg gtaaccattc ccctgattca attacctccc accaggtccc tccaatgacc 51300tgtggggatt atgggaacta caatttaaga tgagatttgg gtggggacat agccaagcca 51360catcagtgtt gttacacacc acagtggtgc tgtggtgtgt aggtgggaaa actatggcat 51420gggggccata tctggtcctc tgcctatttt tataaagttt tattggaaca taggccacac 51480tcatttattt atgtactgtc tatggatgct ttcacactgc aacaatagat ccaaatagtt 51540gcaaagagac tgtgtggccc acaaaaccta aatatttact atccaggcca ggcatggtgg 51600ctcatgcctg taattccagc actttgggag gttgaggtgg gcagatccct tgaggtcagg 51660agttcaagac catcctagcc aacatggtga aatcctgtct ctaccaaaaa tacaaaaatt 51720agctaggctt ggtggtgctt gcctgtaatc ccagctactt gggtgtcgag acacgagaat 51780tgcttgaacc cagaaggcag aggttgcagt gagctgggat catgccactg tactccagcc 51840tgggtgacag agtgagattc tgtctctcaa aaaaaaaaaa cttactcttt ggccctttat 51900ggaaagtttg ctgacctctt ctgtagatgg tagggtacgg tagaaggtgt tcaagccagg 51960agtaacatga atgattgtat ttatggccta agaggataac tcgtggtggt gggcgggcca 52020tatttgtgga gagacccatt ttcagtgact tccaagagtc tgcgtgagag atgactgagg 52080tcttgccctg gcaggaatgg ttccattaat ctgtgtctca tttgacaaat gaggaactac 52140aaatgggaac agtttaagat gagatttggg tggggacaca gccaaaccac atcagtggtg 52200ctaatagaca gtggtgctgt ggtgtgtagt agggaaaact atggcctgtg ggccaaattt 52260tgaagtcctt ttactttttg gttctaaaaa ttattaattg tagccagagt tgttaactta 52320atatgtcttg gaccccttgg gctctctgaa gactgtactc tttctttcca cttaataata 52380tacatggaat tgcaaaggaa accaatgata ttgaaataga tatcagaaat aaaattttta 52440gatatagcaa taaatgcaca tctgtattaa aatgtgtaat aacaagatct aacagtgagt 52500ctaagaacta ctataattat catgtagcaa tggcataaag gatagtttgt gctatctaaa 52560acagtcaatg acaggagaaa atctgatttc tttggtgata aaacgacagg tgctgctaat 52620acacctgtgt tttatggtct tcgtttgtaa tgaaaagaaa tgccattaat aaattttatt 52680tatttattta tttatttatt tatttatttt tttttttttt gaggtggagt ctcactctgt 52740cgcccaggct gaagtgcagt ggcatgatct cggctcacta ctacctcctc ctcctgggtt 52800caagggattc ttctgcctca ggctcctgag tagctgggat tacaggcgcc caccaccatg 52860ccaagctaat ttttgtattt ttaatagagg tgggggtttc accatgttga ccaggctagt 52920ctcgaactcc tgaccttgtg atctgcctac ctcgggctcc caaagtcctg ggattacagg 52980tgtgagccac cgcacccggc cagatgctgg gatgtttttt aagaccttag accctaagcc 53040tatcatatca aatacaatga aacacaccca cttttcacac tttaaaaaaa gtgtgttggt 53100gtttattgct gtaaaatagt ttgaaacttt ttaaaaaaag ttttggtctt gctcatactt 53160gtgttttaaa aaagtatttg gctatgacta actcagttat gtatttattt atttattttt 53220gagacggagt ctcgctttgt tgcccaggct ggagtgcagt ggcatgacct cggctcactg 53280cagtcgccgc ctcctgggtt caagcctcag cctctcgagt agctagaatt acaggcgtgc 53340tccaccatac ccagctaatt tttgtatttt tagtagagat ggggttttac catattggtc 53400aggatagtct tgatctcctg acctcctgat ctgcctgcct cggcctccca aagtgctggg 53460attacaggcg tgagccacca cgccctgtga ctaactcagt tatttaacaa ttgactgtaa 53520tttctcagca atcagtgtat acttggaaat tcttgggatg tgagaaaact aacctataac 53580tcattttctt ttttctttga ggtgaggtct ctctttgtta cccaggctgg cgtgcagtgg 53640catgaacagg gctcactgca gccttgacct cctgggctca atcctcccac ctcagtctcc 53700tgagtagctg ggactactgg cacgtgccac catgcctggt taatttttgt attttctgta 53760gaaatggggt ctcactgtgt tgcccaggct gatcctgaac tcctgagctc aagcaatcca 53820cccactttgg cctcccaaca taccgggatt acaggcatga atgagccacc atgcctggcc 53880tgcaacttct ataaatagca aagttagtaa ttagtgaaga tgatggtttg caagcactga 53940attatacttc tattaatttc atttcctttc aattttctaa tgttttgtgc ccaatctgtc 54000ctgtctgcct ctacctagct ttagaagtgt tttgttggtt cctgagatgg agctgtgcct 54060gaagggtatg aggttaccct ctgggttcag cggggagatt tgggaagagt tttgatttgt 54120aggccagtaa aggggcctga cattagatga tggctgctgg gctagggaac aacttagagg 54180cagctaacag gattcaggga gagtggattt ggtgggagag agtagtctag gatgaatcca 54240attgggtttt tatgagtagt ttggtagttg gttgactggg tgggtggtcc cttggtaatt 54300atttgttgat tagtggttgt tgggttaggt tggttacact tacattatag tcgatggaat 54360ctcagatttg gatctaatac cacatgtaag tcgagtggat ttttttttga gacagagttt 54420tgctcttgtt gctcaggctg gagtgcagtg gaacagtctc agctcaccac aacctccgcc 54480tcccaggttc aagcgattct cctacctcag cctcccgagt agctgggatt acaggcatgc 54540gccaccacgc cgggctaatt ttgtattttt aagagttggg ggtttcacca tattggtcag 54600gctggtctcg aactcccgac ctcaggtgat ccgcctgcct tggcctccta aagtgctggc 54660attacagggg tgagccactg tgcctggcca gttgagtgga tttttttagc actcaagctt 54720cgtggctcat tgctattatt gtgcatgtga gcgttttatc tttcagtagc attagggatg 54780ctacttggat gtgttttagt tattacagaa atagttttta ctaactttta ctaagttatc 54840tttcctctcc tgtgtaggaa gtttagagtg aagcggcagt tggctggagg ttctgaaggt 54900ttcccccttt cacataattt gatgttccag ttgcccacat caggacgact ccctctcttt 54960ctactgatgt aagcagtggg ccaaattatg gggctccatc cctgcatctt cctacttgtc 55020taaatcttcg tcacagacaa catattgctc taaaggaaac ctagaaagga ggagaagctg 55080gttttcgccc aaattcctca aaatcatcgc ctgttgttta agaattacag tttgcactgg 55140aacaataaga tgttccttaa tgtggttttt aagtgagttg gttgtcgcct gaatttcata 55200aacactggct aaggattgtg caaaagggtg tgcttccctt tagcatcctt aattagggac 55260agcgttttga aaactgcttt ttattgtcct ttatctgcaa aacttcttga atccaaatag 55320cgagattctc atttcttaat cactgccaca gaaagttgta gattagagaa agctccaatt 55380ccttatttcc tgtcttcctt tctttctgtg tgtttattgc ctgtgtctca tcctcactcc 55440tgccagtttt atagaatgta acctcccagc ctctgggaat gtttgggaga cttgttcata 55500gaggatctga agagcagttt aaagtggact tacccaaact atcttctgga gaacattagt 55560ctctttggag ataaaatttt taaacatccg ctagtccaat agtgttggca aattccctgt 55620gacactgtag ccctctcttt gagattgtca atgtacgttg gcatgttaaa ggctctgaga 55680agtcctgcag cagttaaaaa attgtttagt ctagtgtgcc cccagttgtt tggccactga 55740aacccccttt tctggaaaaa ccagctaaca tctggtagtc ttttctaaga ggtggtactg 55800aagatgatac tcatgttaca catttaaaaa ttctaacatg tgtttttcat gtgtttataa 55860aatgcaacta atgtatcaaa cctgtgattt ccaggacata attacttaag ctaaggaaaa 55920aagaaaacat gagtgaagga aaaactttag taaataggcc aggtggtaag aggagagagc 55980cttgtctgtg agtgtggtct agggggatgc tggacctagc ttttcagagc taggttcagg 56040cagagctgct ctgagatgta gacactgcag ctggggttct tgttgagccg ggaagcagct 56100tctgactaag gtgcagactg tttagatgag ctggtcataa agagccctga ctgtggactg 56160cgtctccagc cacggcagca gctggtggat ggggtgatgc cttggatatt tatcgtgtgt 56220ttcttgcctg gcctgccctt ggacagtgcg cctcaggaat gttagaatgt gttccccctt 56280tagcagcaaa gccgatctgc tgtgtacttg ttctgtttat cttactgcca cgaccgttta 56340tcacgggcca gagttcaggg gcacactgat aaatctcttt taggaggatg atgtaaccct 56400cagcattttc cccctacttg gttctgagtt tttaaagctt ttgtaacacc atcatgtcct 56460tgtttgggca tcttcctgtg tactcccgtt tgggtctcca gggtgaaata gccaacagtg 56520gattctggag tcatggcctg ggttcaaatt cctgctctgc tgcttatcaa ctctgacttt 56580gggtttaatt gacctattca ttatttttct taatctggaa aatggagcca acagcagttc 56640ctcataaagc agctgtaagg attcaggggg gtaactgcac agggccaagc cctcaggttt 56700cacctctcac tgggaggtcg gacctctgca taatggacaa gctctcctag ggtgcaagtg 56760aacgggggcg caagggagtt aggaaggtgg gtgttttttg tttttgtttt ttggtggctt 56820gaaaaacatg cccaaggctg ggtgtggtgg ctcatgcctg taattccagc actttggaag 56880gcagaggcgg gagcattgtt tgagcccggg agtttgagat cagcctgggc aacatggtga 56940gaccctgtct ctcttttttt tttttttttt ttgagatgga gtctcgctct gttgcccaga 57000ctggagtgca gtggcgcaat ctcagctcac tgcaaccttc acccccaggt tcaagtgatt 57060ctcctgcctc agcctcccaa gtagctggga ttacaggcgt gtgccattgt gcccagctaa 57120tttttgtgct tttagtagag atggggtttt gtcatgttgg ccaggctggt ctcgaactcc 57180tgatcacagg tgacccatcc accttggcct cccaaagtgc taggattata ggcgtgagct 57240actgtgcctg gctgacccaa aaaattagct gggcgtggtg gcacacaccc ctgtagtccc 57300agctacttgt gaggctgggg caggaggatt gcttgaggcc agcctgggca acagagcaag 57360accttgtctc aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa gaaagaaaga aaagaaaaga 57420aaagaaaaga aaaacatgcc caaaggcaac caaatgactc catcttttgc aatgtaatct 57480tcaacatcga ctcctctggc aagctgtttg gaaatggcaa agtccatctc ctgaggctgg 57540gagattgctt gtccaggacg ggtgtgtctg gtgaggaatg gaaggcattt ggatggccac 57600tgagaaagct gagccaagga gcatcagaaa gacaatcagg caaacccaca gagtctccag 57660gtattccttt gctgataggt aacattgcac tagcgattta aacaaacagg tgaaaggcca 57720ttgccctacc accccacctc acctctattc cttgctgctc tttccagaag caactgcatg 57780gtctgggaac agttttttgt cttgtcaaga gacagtctgt acatagatga attcaattat 57840attacttctg tagtaccctg tactcaaatt tgaacctgtc atacacattg cttttatcat 57900ttcataatac ctgttgattt tcccacgtta gtacctatag atcctgacaa gcaattttgt 57960taagatgaag agttcttcat atgtattgta ctatgtttct ttttttgatg atgtatgtca 58020agatttatta taaaagtaac agatgggtag ggcatggtgg ctcattcctg tgatcccagc 58080actttgggag accgagatgg gaggattgct tgagcccggg agtttaagac aagcctggga 58140aacctggcga aatcctgtct ctacaaaaat tacgaaaatt agccaggcat ggtggtgact 58200gtcccagcta cttgggaccc aaatgtccca gatactcagg aagctgagtc gggagcctga 58260tcctcagagg tcgaggttgc agtgagccgt gattgcacca ctgcactcca gcctaggtga 58320cagagtgaga ccctgtctcc ccctggcctc caaaaaaaaa aaaaaaagta acatatgtag 58380tttaaatttt aaaaattaaa tttttggggg ggctgggtgt ggtggctcat gcctgtaatc 58440ccagcacttt gggaggccaa ggtgggcaga tcacctgaga tcaggagttc aagaccagcc 58500tggccaacat ggtgaaaccc tgtctctaga aaaacacaaa aattagctgg gcatgatggg 58560gggcgcctgt aatcccagct acttgggagg ctgaggtggg agaatcgctt gaacctggga 58620ggcggaggtt gcagtaagcc gaaatcatgc cactgcactc cagcctgggt gacagagcga 58680gactccatta aaaaataaaa ataaaaaatc aagcaatgca gaataaataa caacaataaa 58740atgaaagccc atcttccacc atcagcttct tagttttctt cctagaagga gccagtgagg 58800acagtttggt gtttatgctt ccagatcttt ctgttcagat gcagtcatga cttctgaaaa 58860acaggattgt acaattcata cttttctaca aattatcccc ttcccttaat acatcataga 58920agcctattca tattggaaca aacaaacatt tcttattctt ttcacagcac cctgttttcc 58980tcttgcttga atgtaaagtt tatttaacca cttactgtca gggaggcatt tgttttcagt 59040tctccctccc tccccccacc agttgtcttg taatgaactg ctttaatggc taaagatcac 59100tttaatatca aaacctcccc cacctcccat tagaaaaaga aatcatgtta gggaacttca 59160aattgaattt acggaccttg tgtttaattt tctatcagca gtggccccag cctggcccct 59220gcagactgcc ccggaatctg tgggaggagt tggggtggcc tgcagactag agcacactgc 59280cagttcattc agcagctcac cgagcaagaa acatcttgat tctatcagcc ttaatgctgt 59340gtcccattag ggacccagct cttgtggtca ttagcagatg gaatgctcat ctgtgctaga 59400aggcggaatt ctagggcatt cggctctgag cagtcttgaa ccagaattga atggcttgaa 59460tccttttcac aatgccaacg gggaggcacc cttagctccc aaacttgtgt gtgttataat 59520actatggtag taataacagt ggttgtagta gcccccgtga atttgatggg acagtcgtca 59580ggcagtgctg cttgcttgct ttactccatc gtatcaccgc agcctgatga ggcgagggag 59640ttacgactct cattttgcag gtgaggacac tgagcacagg gaatcgaccc actcatggtc 59700acacagcttg ccaagtcgct

gtgcttggga ggtgaaccag gcttctctga cgccccagca 59760ggacgtctga acttctagct gccccatcac taactgactt aatgcccctg actcctgggt 59820gacttggcca ccagttactt cagccagcga cctgcccttt ctttgagtgg gttccaccca 59880tccctgcacc atgcctttta ctttggatgt tggtggcatg gaattccacc cgtaagaagg 59940aggtcggtcc ctgggctgag agagtttgca gagagctctg ttgggattgg gtgggacgtg 60000tgtttggagg cctcctcaca taattgtggg ctgaaaggtc cagatttggg gatataaagt 60060tgagccgtca gctgagctaa agacagggca cagggaggag ccatccagaa agtgtcagtg 60120taggtaaagc aggcagagtt ccccctatct gtcctctgag ggcctccttt cttgtggttt 60180cctccctttt ctgtggtgat ggtcagagcc agcggttata aattatttgg aattttcctc 60240agcttggttc ctactcaaga ctttaaatta ggagttttgt tcccttttat gacttcacaa 60300tctttgggca ggctgccatc tctacagcag gctaatatga gttgtaactt gaggtgagtt 60360acaggggaaa aatggaagct gatttctccc cttttaaacc aaggaagcca ccttgatctg 60420actttgtaac aaagctcaac ttttgtaagt ttgcaattaa aggataaata cctatcctat 60480ttattattat tattaacttt ttattataaa aggggaaaaa actcccagga aacatagcct 60540aatatgaggg acaaaaagcc aaaaggtttt ttttttcttc ctttaaaagg tcctcaatgt 60600cttgccctgt ggagacacca gttttcatta taataacgcc attatctctt tgtagagtca 60660tttcaagcca atttaacttt ctcatttaaa agtataattg gtattcagca cagagctggg 60720agctcagtag gcagttagaa aatatgtgta tattttttga gacgaagttt cactcttgtc 60780acctaggctg gagtgcagtg gtgcgatctt ggcttactgc aacctccacc tcccgggttc 60840aagcaattct cctgcctcag cctcccaaat agctggaact acaggcactc accaccacgc 60900ccaactaatt ttcgtatttt tagtagagat ggggtttcac catggctggt ctcaaactcc 60960tgagtttcgc caggctggtt tcaaactcct gatttcaggt gatctacctg ccttggcctc 61020ctaaagtgct ggcattatag gcatgagcca cagcacctgg ctggcagtta ggaaatattt 61080attgaatatg agaaaagaaa aatagagcaa attgaatctt caagtagtat gtgagtaact 61140ctaattcctg ttttctggaa aacacacagg ctgataggtt tgggtaaata agagcagagc 61200tgcatcttct ctcaagttcc ctgattccct caaggagtta cctgagaata gctctgtgcc 61260aagcagtgcg gcatgcatag gggacctctt gaatggaggg acagtccatt atcattagaa 61320tccccagttc cagccaggtg cagtggctca tgcctgtaat cccagcactt tgagaggcca 61380atgtgggcag attgcttgag ttcaggagtt caagactagc ctgggcaaca tggcaaaacc 61440ttgtctcccc ccgccacaca cacaccacac agacacacag acacacacac actggctagg 61500cgtggtggca ggtgtctgta gtcccagcta cttagaaagc tgaggtagga ggattgcttg 61560agacttggag gtcgatactg cagtgagctg tgatcgtgcc actgcactcc agcttgggtg 61620acagagcaag accccggacc ctgtctcaaa aaaaaaattc cccagttctc agggtgtggt 61680agaggccgag tcagtcatgg ctgagacaag gggactgtgc tctgtgtgct tctgtgccct 61740gtgtttatat ggttcatacg ctgcctgtcc accatgtttt tcccgagagc ctcggcagcg 61800caggcatcat gggaatgact gagtcaggtg gaaattcaga ggccctgccc tggtgggcag 61860agaagcctgg cttacctccc aagcacagca tgtgtgtgga tcacttctgt gcactgtctc 61920ctcatctcca aaatgggagt cataactgaa ctcacctcat caagttgtta tgagatgatg 61980tagattcagc gaagtagcaa gagtaggagt ttgggctttg ataacagaga gaagtgagtt 62040tccatctaga ttctccccct gtgtcacttt tggcagttgg cttcacctct gtgggcctct 62100gttatgtcat ctgtaaaatg ggattaaccc taaaagccac cctcacaggg tcattgtgag 62160gattgcacaa ggtgatgcaa gtggcacagg gtctggccca ggagaggggg ctggaagaga 62220gcgagctgcc attgtatttt ggttgctgtg gatctaagga gaagagatgt ttaggagtct 62280ttccctggca tggttcctcc tgccttcacc catcactctt ttcctcgagg gattccctgt 62340ggggtgcaca gccccagggt gggccagact gagctcacag gagcatgggc tgtgtttcag 62400gtgaggtggc ctcaccacat gacaaactga gctggagtca aagggtcacg aggacctcca 62460ttcacagcca gcatttatta tttcagctgg aaatgtttgc cgagcagttg tagctggaag 62520ctgtgagcga gacacagact gccatcaggc tgaggcctcc agagctcatg ctgggcttta 62580acctgagcct cttgggggct gggctctgag ctcctccact tctgctcatg cccaggcgtc 62640cttgggggcc ttgaactgtc agttgtccag gagaactgtg tggcagcaac agaatgagtt 62700tgtatagcaa cctgttgctt tgaggtttaa aacttagttt agaacgcaat tgctttgacc 62760attttggagt gtctatactt tttttcttct tctttaagtt ttcttttttc tttttttctt 62820tttttttttt ttgagacaga gttttgctct tgttgcccag tggcaacaag agtgcaatgg 62880cgaaatctcg gctcaccaca acctctacct cctgggttca agctattctc ctgcctcggc 62940cttctgagta gctgggatta caggcgcccg ccaccatgcc tgaccaattt ttgtattttt 63000agtagagacg ggtttcaccg tgttcaccag gctggtctcg aactcctgac ctcaggtgat 63060tcatctgcct tggcctccca aaatgctggg attacaggca taagccatca agccctgctt 63120ttttgtttcc cttcttcgac ctttctaaca agaggttgga atcctcgttt tgacttttaa 63180aggatttccc agtgctagaa agtggtaaga tagttactgt atcctaggcc ctttagcaga 63240cctgtctcat tgatcattta tttagtccag tgtggctttg ttgttggata ttaagtaatt 63300ctcaaaattt taccttttca aaagtggcat tgaaaataaa ggcattgggt gatgaaaatg 63360gaacttttaa atacagtgat tcctgttaac cagaaatagg gtgtttggga taatttatga 63420agcagtacac catcatagat actatgagct gaaagttcac caaactctct atcccaaaat 63480aacaataagg tatttatgaa gtgattcgtt ccaactattt gaggcaaaaa ttgtccagca 63540agtgagagag aacagaagga atagttggca aaatagggaa tttgaagtct gaggttatgc 63600ataaggaatg tgttatgggc ctatagtaga aatctcaaat cagggattag ggaatgttta 63660ctcagttctg ttgcagagaa atcctggcca cgactccccc atgccatgcc cagggcaggc 63720attgctaatc ttcactgcct ccattctcca tgccctgttc acggaagaca tttctaatgc 63780attttagcag tctttttttt ttttgctgaa tccagatgtg gcctcagaat ccttctcaac 63840acagtgtact agcaccactt ggtgctcctg atctactgta tcatctcttg aaaaactact 63900aacatgaaaa gacctgccaa gtcaacttta tattaactga acccttgaca cagtgatgga 63960taaaaattaa ttcaaacagc ttctttgtga tctttgagta gttcatgagc aagaaagaga 64020attggaaatc cagccaactt cggccccctt gtctacttgt attttactgt ggtttatgtt 64080ttctcttacc aattgagata ggcccatgag acttctggtc ttccaaagcc cagaacatcc 64140ccacattata gtttaaccac tgtaacaaag aggttttttt tgtttgtttt tttgtttttt 64200ttttgttttt tttttgggac agaatctcgc tctgtcgccc aggctggagt gcagtggcat 64260gatcttggct cactgcaagc tccgcctccc aggttcacgc cattctcctg cctcagcctc 64320ctgagtagct ggggttacag gcgcccacca tcacgcccgg ctaatttttt gcatttttta 64380atagagacgg ggtgtctgga tctctgacct cgtgatccgc ccacctccgc ctcccaaagt 64440gctgggatta caggcgtgag ccaccacgcc tggccagagg ttttcttaaa aacaataaca 64500acaaaaacag ttgtggaaag catgtagagt gtgggttttt tcggtcttca ggttggcagg 64560gcatctgata ctgggaccca ggttccttcc ctcaccttgc tgtgcctctc ctagtgcagg 64620ccaaagccag gtgactgcgc tgtctgggct cctggctggc aatcggggaa agagtgcatg 64680gagcaggcat gcccactgtt caggtcctga agccgtggct catttcatat catttgttgc 64740ttatttgaaa gacaggcaca gcactgactt ccaggggagg ctgactgacc atctaggtgg 64800aagttgcatg cctgggaggg agaaggggac aaaggccaca gataggcatc agttatcagg 64860gccttaagtc tgccttgttg gcatgcagcc ttttattgga tcaaggccct ggagaaaagc 64920cctgagcagg aggagataag ccagcttggt ccccttcatc ctacccaggg gcctctgggg 64980tacctgagcc aaagtgcaca gttcattggc tgtgtggatg gaagggatat gggacttgaa 65040aatgggacac tggtcctggg cagctgaccg acatggtcct ccttaacctg ctgtctgggg 65100agatgggttg catctggcta ggttttgact gaggaactga ggagagctgt cagctgtccc 65160cgctttggtt cagaatgccc ttttgtttgg acagctgaag cctacaattc agccatggtt 65220tgtttgggct cagaaaacag gcaaggatgg agagaaactg caaagctgac ctgggctgtc 65280agtgggcacc aggtcctgct ggcctggggt ctggatgcag gagatctgag ctcttcaatg 65340tggggtggtc ttgcagcagc tcttcacagg ctgctgctgc tgctgctgta ggctcaccca 65400agcagccaag acggacagga tctattctag ttttgtgcag agttggatat agaagaggca 65460ttagagggag aggggatggg gaaggagttc caggccaggt gagcatgggg cacagtaaac 65520tgggatgtta aggaggggcc agtttgtgac cagcctgggc aacatggcgg aaccctgtct 65580ctataaaaaa ttaaattagc caggtgggtg gcatgtgcct gtagtcctag ctacccagga 65640ggctgaggtg gaaggatcgc ttgagcccag gaggcggatg ttgcagtgag cagagattgt 65700accattgtat tctagcctgg atgaccgaga ccctgtcttt aaaaaaaaaa aaaaaggagg 65760ggccagaccc ctgacccata tgtgctgctc ttttctttca gggaggtctg ataaaatatc 65820agtagttcaa ttcttttttt tttttttttt ttttttctga gatggagtct tgctctgttg 65880cccaggctgg agtgcaatgg agtgatttcg gctcactgag acctccgtct cccaggttca 65940agtgattctt gtgcctcagc ctcccaagta gctgggatta caaggtgccc accgccatgc 66000ctggctgatt tttgtatttt tagtagcgac agggtttcac catattgtcc aggctggtct 66060cgaactcgtg acctcaggag gtcctcctgc ctcagcctcc caaagtgctg ggattatagg 66120cgtgagccac catgcccggc ccatagttca gttctttagg tggttcttgg tgctgcatat 66180gagatctctg caagaaggac acgtctgagc cgggtggttt agaagaccag catggcccaa 66240gaccctcaga gcaacaccaa gaaccaccta aaattctttc tcagacgtgt ccttcttgca 66300gagatctcac gtgccccagg ttcgctgcag cgttaggggt cagcctccct ttggagcagg 66360agagcagggg ccttggaggt ggcagtcatg gccctcctaa ttaattgctt ggctcagaga 66420agtgacaaat tgaacatttc aaccacctgt taattcacaa ggtacttctt ttcatttctt 66480gctgcttgca caaaacactt ggagtatggc ttgtggatgt ctggccctag ggaagagtgt 66540ttggcacata gcaggtactt aagtattagg aaaatgagga tggaggggag ggagggaaca 66600ttattaagcg gccaactgtg agacaggcat tgtgcttgac tctttctttc tttttttttt 66660tttttttgag acagagtctc tttctgtcac ccaggctgga gtgcagtggt gtgatctcgg 66720atcactgcaa ccgcgcctcc tgggttcaag tgattttcgt gcctcagcct cccaagtagc 66780tgggattaca ggcgcctgcc attatgccct gctaatttta tttttagtgg agacagggtt 66840tcaccatgtt ggccaggctg gtctcgaact cctgacctca gtgatctgcc tgcctcggcc 66900tcccaaagtg ccaggattac aggcgtgagc cactgtgccc ggccgacact tggcattctc 66960taacctacct actccttata acagccctgg gaagtagttg accatggcca tttctatttg 67020gtagatgagg aaaaataagg ttcagagatg gattgttcaa accgatgtat ctagtcaagc 67080tactggttcc cgagcctgtg tttgcaaccc ctctaccatg tagcctctcc gggtggtaga 67140gatgaggggg cagagtgcac agtgcatggc atcctgttcc ccagatggcc aagtcttagt 67200gcgagtgtgt gtggccttgg taacttgtgt caagcacaca ccccatctct ctctctctct 67260cttttttttt ttttttttga aacggagtct cactcggtca cccaggctgg agtgcagtgg 67320tgctatcttg gctcactgca acctctgcct cctgggttca ggcgattctc ttgcctcagc 67380ctcccgagta gctgggacta caggcacatg ccaccacgcc cagcaaattt ttagaagaga 67440ctgggtttca ccatgttggc caggatggtc ttgaactcct gacctcgtga tctgccctcc 67500ttggcctccc aaagtgctag gattacaggc tctcttgctc tctctctctc ttgttttttt 67560ttttttgaga cagagtctta ctttgttgcc cagcttggag tgcagtggcg tgatcatggt 67620tcactgcagc ctcgatctcc tggctcaagc aatcctcctg cctcagcctc tcaagtacta 67680gttggtacta atgggcatgc accactacac ctgactaatt ttttttatta tttgtaggga 67740cagggtgtcc ctatgttgcc caggctctgg tcttgaactc ctgggctcga gctatcctcc 67800tgtctcagct tcccatagtg ctgggattac agagatgaac cgcctggcct acacacccct 67860atctctcctc gattcttttt tttttttttt tttttttgag acagagtctc cctctgtctc 67920ccaggctgga gtgcagtggg gtgatcttgg ctcactgtag cctatggctc ccaggttcaa 67980gcgattcttg tgcttcagcc acccaagtag ctgggattac aggcacacac caccatgccc 68040agctaatttt tgtattttga gtagagacag ggtttcaccg tgttagccag gctggcctcg 68100aactcctgac cccaagtgat cctcctgcct cggcctccca aagtgttgag attataggtg 68160tgagccacca tgcctggcct ctccttgatt cttacagtca ctttgttggc tgtttctgac 68220tcagcagcta cctgcattgt ggccaaagga tgacctattc cttctcagga gggcaaaaat 68280gtggaatagt gtctgtccat gcctctcctc atgggctacc acctctgcca ccgtggttaa 68340tcagtaacaa ccaggagaga agctgctgga actgacctct gggaactccc tggatggttt 68400ggtgcaggaa tgtagtaggc atacacgtgg ttgcgtggat ctgggccctc ctgatgtgag 68460tagagaggta aaaggccacc atctccttga cctctgggga actcatccac aaagaagatg 68520tttccaagat gcttctgaag attgcctaaa aatagccggt ttccaccccc gtgaatgcat 68580ccattctaga atgctccttc accaggacca gagaactgat ttacagaagt gacatgaaaa 68640cattccatcc cagaatttgc agtagctcaa attaagtttc tagctattaa aaagaaaaga 68700aaacaaaact aaacaaaaca cacccaccct gctcacttag aagcaacact gagtaatttt 68760aagtagttcg agaaaatgta tgtggtttga gggtcagggt tgtccagagc caagaccagt 68820tatgtgggaa ttgttattgg ctggatttgg ggaggagaaa cccatggccc aattccaacc 68880cactgaaatc taagcagatt ctaggtggtt aggcggacct ggtaggcgtt ggtttatttt 68940attcccgaaa aaggccctgg agcaagtctt cacatggaat cctgctgaaa ggcttccggc 69000tcatctggcc ttttcctcct cttaaggttc tgctccatgt tttaccctcg gcgtaaacat 69060tgcagagcac gttcagatct gaaaagtgtc tcatctacgt gatggtcaga cgttgttgac 69120cctgtgatgc tgtgtaacat ttcattttcg aggcttgggg agtctcctat ttcatgtgga 69180tgggaacctg gaggtctttg ggcaagtcgc catcttttta ttgttccaag agtttggtga 69240agcgtttgaa ccttcacctg tcaaaatcag ttttggaatg agaactgctc tctctctagt 69300ccttataata gcagaaggaa ggtatcattt atcccaatga gaccataaag ggggctttcc 69360cgtgtggaca cccaccttga attcaattgg aaacagaaat tctgggcatt gtattttttg 69420taaatttggc tcagacttca actggatcat atttccccca aaatcttttc gaaaaagact 69480tgtgtctcat tcctttagac tagcatgtgt aagctgggta aaaatagagc aagccgattt 69540catgttaatg atttcatgtt aggtttgtga atcaaatctg caagtctgct tttgaaaagc 69600atttaacata taacttggga aagtttgagt tttgcagact aatgcctgtg gccggatgag 69660acttcatagc tccatccaat ccctcctggt gcaagagatc aatgccttga gggtgcctgg 69720ccaccaccat taccctgaca gtatacccac tatttattta tttatttatt tatttattta 69780cttatttatt gtttaccctt ttgaagattg ctcttctccc tttaacttaa aggaattggc 69840atggaaactt gtttgatctg gaatttctga taatcagtag gtagtaactc cgtaatcaat 69900agcacttcaa aacaacaacc aaataacagg ataactaatc caaaaaattc agtcatggtc 69960aaggacttcc agctcaggaa atgtctggtc ccgtggggtg gattccttgg ataaccaagt 70020tccgtgcagg gcctggagtt ttatgcagac cattgctcct tgattgacca caggacctca 70080aaaggagggc tggcttcatg accacatgac ccgtgtgctc agaagggccc tgtacttggt 70140ttattgctct gctgttgctg tcttgaagtt cttaattttt tttttttttt tggcactggg 70200gagttgcagt ttcaaacaac acttattcat tgtctcacag tttctgtggg ccaggagtcc 70260agccatggct taagaccagg tcctctgctc cgggtctcac gagactacaa ggaaggtgcc 70320atctagggtg tgttttcatc tgaatgccta actaaggaaa aatccacttc attcaggttc 70380attcaggttt ttaaaagaat ccatttctgt gtgattgtcc cactgacagg tcccagcttt 70440ttactagctg ttgcttggag gctaacctca ggttttacag gctacgctca tatctctgcc 70500atgaggcctt ctgcataggc aattcataac acaggtgcct gtttcctcac agccagcaag 70560agaatctgtc tcctgtctgc taaagtggag tttcatgcat cgtaatatgg tcatgggagt 70620aatagcccgt cacctctgcc atttttctgt tggttagaat aaaggcacag gttttcccca 70680cactcaggaa gaacccatga tataaaggct ttcagtaaag gagacgacaa acagaatatg 70740gaatgatcag aattactctt atgacccaga ccaagaacat cagcattacc tacgaattta 70800ttggaaattc aaattctcct gtttcacccc aggcctgtta aatcagaaac tttaaaagcg 70860agcccagcat tctgtggttt aacagatcct tcaggtgatt ctgacacctg ctgaattttg 70920agaaccactg gtctagaggc aggcaggtct tgctccccta ggagttaagt ttgatgtatc 70980ttctggtaat actgagaaat gagctgggaa atggttccaa aatcagatta tcctccccag 71040gattaacaag actcatactt gcaaaagaga gtgaagaaga gaaactaaaa aaagcaagag 71100gctgtgtgtg aagctagatt caaacagtta aagacagcaa cacatggcaa aggatgggaa 71160tttgaggaag tgggtagtga aagcaattct tgagctaaat tacaagaaaa cacggtgaat 71220ttgtatctgt ttcctatatt tagggggctg gcttaaacgt tagtgataca tttggggagt 71280agaaaatgga tgttggtgtg aagttcttaa gttttggaca aggaaccctg tattttcatt 71340tttctctgag ccccatgaat tatgtagaca gtcctgcttc gaagttatta tttatacaat 71400tcattataga gaaagtcctt gggaacctta actttgagtg aggattgctt gagttagttt 71460ttcttaccag ccactccatg atactctttg ttttttccag gttagatgat cgagttttat 71520tatgactgaa tctgcacctg caaaattaat tctgattaat taatttaata attaaattct 71580gatgatttct ctctgatggt ttgggtgtgg gctcttaaag agggtctttt tttgcaagag 71640gatataacaa taatcaggtt aattaaaaaa ataaggctct caccctttca tttttgagtg 71700gcatgccatg caccccttat cagcatgtga gtatgctttt catgtggtcg tggttgggtt 71760tcattaagtg taatttggca tgtgttcaac cagcattcag gtggctcttg gtgggtggct 71820ggggagacac caagatgcag atagctcagt cactcctcaa caagcggctt agttctggaa 71880tgaggtggga ggccaaggaa ctcacacata aatgctggtg ggagtgaagt gccaccagct 71940gtagaatctg gtgtcagaat gatgagccag gagttatccc acaggaggat gggtgaaggt 72000cttcccatca aagggataga gaacatgtga agaggtccag gggctcaggg caagatgtag 72060tccaggaaca aggagtcttt gagcctgcag tatggtgggt ggaagtggca agagtggaaa 72120gcggattgga tggggtttat gtaggttctg aggtgctgtg tatgtttaag gagctgattg 72180tgtgcagcgg gaaccctggt gaatttggaa gcacagaggc acctgacgag aaagatggtt 72240ctggggttat gtgaacagtg attcggcttc aaggctatca aagacaaaaa tgtttattgg 72300gagggtatag aaaagggttt gccaaaagag ttaggtaggg atagaattga cacattgtgg 72360aaactatacc cagagtttaa gaggtggagt ccaggatagt gcccatgttt gtagcttggg 72420gtcctggtag aatgggagct ggctatggag tatctttgtt ggagagtggg tatagggaaa 72480cggagagaga gagaaagttg cagggggtgc gggagatgga tagctgcaga gaaggcaagg 72540gcagggaaag tggaaacaaa tggcagtgag actcctggaa ggtgctggcc aggggcatgg 72600catggcatgt tctgttaagc aaggaaagga ctagaaaggg gccatgattt tggctgggca 72660cttatcctcc tcacaacagg acgcatttgt gtcatggctt actcttaaga atgactgacg 72720tgtcagaata gcaaatatga aaatgattga taacacctag cattggtgag atttgcaggg 72780ataactagct ggcctcttaa atctatagat aggaatgtaa acagaaacaa actttttata 72840gggaaaagat atctaggaca taatgattaa tgaaaagaaa aaaattccta cctatcgaaa 72900aacgtgaatt caggcagcaa acacacatgc atgtatacac atacacacgt gcacacacgc 72960atacacacac aatctggtag gctgtatact accagtttag caggttgtta cctctgggat 73020gcagtcactc ctttttgttg tgtatatttg tgaaatgatt tctttcaatt tttgagacag 73080ggtctcactc tgttgcccag gctggagtgc agtggcgtga cgtcagctct ctgcaacttt 73140cacttcccgg gctcaagcga tcctccaacc tcagtctcct gagtagctgg gactacagga 73200gtgagccacc atgctcggct aatttttttt ttttttttgg gtagagaggg agttttgcca 73260tgttgcccag gctggtcttg aactcctaag ctcaaagcaa tcctcctgcc tcggcctccc 73320aaaagtgctg gggttacagg agtgtgccac tgcacctggc cattattatg gaaaatttta 73380ggcgtataca aaagtagaga cagtggtgtc ttacatgctc atgaacccat gatccagtga 73440catccgttaa tggcattttg gaatcatatt tcatctgttt ttgtcctcaa atgttttgaa 73500gcaaatttca gcattacatc atttcactct taaatatctc agtatggttc tctaatagtt 73560gaagactcca tttacattta tataaggagc ataatttaca cttgtgtaac ccaaaggaat 73620gaccaagcct gtgcttctct ccccagatag caaagccatt gtggatggga acctgaagct 73680catcttgggt ctggtgtgga cgctgatcct ccactactcc atctccatgc ccgtgtggga 73740ggatgaaggg gatgatgatg ccaagaagca gacgccaaag cagaggctgc tggggtggat 73800tcagaacaag atcccctact tgcccatcac caactttaac cagaactggc aagacggcaa 73860agccctggga gccctggtag acagctgtgc tccaggtaag tggccagggc tgcctaaacc 73920atctgtccag gatgggggtg tgtgggtccc aaacattctg gttttcaacg ggaatgctat 73980ctttgctttg attagcgtat ttctccaggt cttagcccat tataagccca ttataaggaa 74040actaaaactg gctctgtgta cccttccaag ggcagatttt ctaggtatat ccatagacat 74100gtttgagcat caagttgagt cttttatcca aattccaatg aaggagttgg tgcttagaag 74160caagacttgg gtttaggttc cagactccaa aatcctgtgt cttcccacat tggtgctcag 74220tttctcattg gatttggaga aacatttggt cctattaggt ggcttggcat gaaaatctga 74280aaacttccat ggagtggaaa gtacccattt ttattaacca ctggtttgac tatatatggc 74340attctccacc cttttctttc tgtgttgctg tgaaatagca tttggtcagg atccagttgg 74400agccttttcc acccttgatg ggctgctcat ttcttagtgg ttgagtgtat atgaaggttg 74460taattattcc cactggaggg tttagattga tgggtagagt ttgctggtac acactcagta 74520gaaagaccag agtcagagtt tacacacacc ccctaaagtt gattttaata aaaaaaaaag 74580gtattaatca tattttccat ttactgtgta ttctgtattt actgggcaca ttagtattta 74640gttagttagt ggttcttgac atactcaaag cagaactagt gtcagttggg taggggaggg 74700ctgaaggcct cattcttact tgagagccta taagttggtg tcatccagga aaaattcaaa 74760gtgcagcatt aattgatttc

ctaatatcct cttctttact tccatttaag gacacatttt 74820aggatacctc tttccaattt aaacctggga gtttttactc tagtccttta cctcatgtgc 74880ttacaaaggc ttttaagata attctaggtt tgtgcctttg agcaagtgga tttttgaatc 74940acacaggatg ctattctaga ctttttagat atatccagga atagagtaaa aaataaaatc 75000cctcctgcat aaaggcacca ggctttttcc aagctttgtt tattttttaa caccacttct 75060tcaaggaatg gataatcccc atcttcatgc aagaacatag cacccggagg agaagtctca 75120gtaatggagg atagtttaca ccctggcaca ctcatacctg tgatactttt tgcctattaa 75180atatatgatt tgctcagatt ttaggaaaaa atcattctct gaactaaaag aaaaaatggg 75240gttagtttag gcacatggtt tcctttaatc tctttggtca gctaatgcta aaagaatctt 75300ttgtgttctg ttaacaggtc tgtgcccaga ctgggaatcc tgggacccgc agaagcctgt 75360ggataatgca cgagaagcca tgcagcaggc agatgactgg ctgggtgtcc cacaggtatg 75420cacaagtgtg ccaggtcctg tgaggctgcc cccacccact agcttgttct gtggatgcct 75480tcccgggtca ggcagcccga ccttcttggc attgagactt cagagagcat tgcctgtgat 75540gctctctcat cttcctcagt ttacccataa taatagtagg ttctcattga ctcaggtgct 75600tatagatctt agtgtgttgg tttaatgtag atcatccaga aattttcatg tcactcttct 75660ttgtcacaca ctggcaaatt ttctagtatt tcttctctaa atattttgaa gactaccttt 75720aaaccccaga ctacaaatat ggaccctaac tattaggttg agccataaga aattgatagt 75780atttgaccat ttttcaatct acattttaaa aggtaatttt aatccaatag cttaagaaaa 75840gtcacaggac ttaaaatttt tttttttttt tgagatggag tctcgctttg tcgcccaggc 75900tggagtgcag tggtgtgatc tccactcact gcaacctctg cctcccgggt tcaagcaatt 75960ctcctgcctc agcctcctga gtagctggga ttataggtgc gcaccaccac acctggctaa 76020tttttgtatt tttagtagag acagggtttt accatgttgg tcaggctagt ctcgaactcc 76080tgacctcgtg atctgcccgc ctcagcctcc caaagtgctg ggattacagg cgtgagccac 76140tgtgcctggc cgacttaaaa cttttaaaaa catgtaagcc aggataatcc accattaatg 76200gaaactgtgg aagaatctct atcacccata atcctatcac aggaatataa caagagaact 76260cagaaatcaa ataagtcttg gataccatct acagtagtca cattgcttag ttgaagtctg 76320atcttcctag ctgggaggaa aaccagtgtt ttctttccag aaactccctc taacagttag 76380gcaccatgag tcccgtgtcc aaaggctagc cagggaagat tgcaggtagc cagtgccatg 76440ggactgatgg cgtcactata ggctgcattg aggtctgagt tcagtgtatt ttgtaacagg 76500gtcccttgga aggtagaaca acatgcctgt ttctttggtt tggttttgga gtcatgtctc 76560tcctacatgg ctcattggtt tcttggctcg tccaccctca ggaagtggtg tggtgtgttt 76620ttcatctccg cttaaaccta aaccgtctcc tttttacgtt cacgtgatgt tggcatgggt 76680gaagttgttg aaggagctgc tgggaagaaa tgccaaatcg acacacatcc tactttttat 76740ggaatgtatt gaaggcgact gttcaaaccc aagtagctct tttgttcctg caggctaatg 76800gtcagaatgt tttctggtgc tttttatcac atggggaggg aagttggaca catctgttgt 76860tcattgcaca tggttaacct ggtccatgag acagagcctc tgttcatctg aggaagtgtg 76920atttacctcc ttagcaccat tactggaggc agggaggact ctgcaagctg tttagggctg 76980ggtcagatga tggtactgaa actgaggtgg tggcaccttc agggaagtca cctgtccagg 77040atgggtctag tcttgctcct aagctgaata tcaagagaag ttcacccatt ccctattttt 77100tttttttttt tttgagatgg agtcttgctc tgtcacatag gctggagtgc agtggcacga 77160tctcagctca ctgcaacctc cgcctcctag gtacaagcga ttctcctgtc tcagcctccc 77220gagtagctgg gactgcaggt gtatgccacc atgcctggct aattttgtat ttttagtaga 77280aatggggttt caccatgttg gccaggcttg tcttgaactc ctgacctcgt gatccaccca 77340cctcggcctc ccaaagtgct gggattacag gtgtgagcta ctgcgtctgg cctttttttt 77400ttttttaaag agacagcgtc ttactcctct gttacccagg ctggagtgca gtggcatgat 77460ctcggttcac tgaaacctcc acctgctggg ttcaagccat cctcctgcct cagcctccct 77520agtagctggg attacaggtg tctgccacca cactgggcta atttttgtat ttttagtaga 77580gactgggttt taccatgttg gccaggcttg tctcgaactc ctgacctcaa gtgatttctc 77640ttgtcttggc ctcctaaagt gatgggatta cagtcatgag ctaccacgcc tggcttccct 77700atttttttaa tggctcctaa tatattgaga tcacatatct aatatttaca tgttatttct 77760tttttattta ccttttttaa ttagtagagt taatacagat acagaccatg agtatacaag 77820caaaggaaaa agctggttaa cctgtgcact tttttgtaac atgctctaat cccatgtgtg 77880cttgtttctt cattttcctg ccttgctata gcttatcctt ttatcatttt tgaaattttg 77940accagaggag taaatggact tttggggaat ggggaggaca atgaactttt ggaagttaca 78000tgcagaattt tttggagagg ggcccctagc tttcaaaggg gtctgcaatt tctcaaaaat 78060ggttaaaaac actgatattg gtgtgttggt ttaaagtaat ttcacttaat tgagaagctg 78120actcagtttc ttaatatttg tagtgcttgg tttaagaggc atttgcaaac acttcaatag 78180ttgcaaagtg atgtgttctg ggtgttcatc caccatgtca ttatcctagg tcatcactcc 78240tgaagaaatc attcacccgg atgtggacga gcactcagtt atgacttacc tgtcccagtt 78300ccccaaagcc aagctcaagc cgggggctcc tctcaaaccc aaactcaacc cgaagaaagc 78360cagggcctat ggcagaggtg agtgctggtc ctctggtgtt gtattggaga catgtcctct 78420ggtgttggag atgatttcat ggcttcaaga gtgatgttct tagaatcaaa aatagatagg 78480tgtaatcctc aaagagaccc caagcctcct ttgtaacaca ttttatgact gttttattct 78540gccttgtttt tctaaggctt taagaaatgt ttctgcttag atggaaaggg caagtttgct 78600gcttggtgat tttagtgcag tagcccattg ctcccatttt tcagaagagg aatcgcgggg 78660tagggagtcg ggggagtttg gtcttgcccc agatcaccac agtcagtgat gggggtgggc 78720catctggctg ctgattcatt tctccttctg ttacactaag cctgcctcag atttccagcc 78780ggagtgggag ctattgttaa cccctggcag atacttcctt gctaagacat cctgtttatg 78840actgcgaggc agctgcggaa caccgttttg ctcagaacat tatagtgggt agaagccatt 78900tcaaggcatt tggtgttgtg attggcacct gacttcaagc acactagctt tgtgaagaga 78960acagttacat ggctgcaaag tgtggtttct ggtgaagatc aacatggcca gatacaactt 79020aatgcctttt ctatggggga ggggaaggag tgcattttat ttctcatttt tcataattaa 79080gaaaatatcg gccgggtgtg atggttcatg cctataatct cagcactttg agaggccgag 79140gcgggcagat cacctgaggt caggagttgg agaccagcct ggccaacatg gtgaaaccct 79200gtctctacaa aaaatacaaa aattagccag gcatggtggc gggtgcctgt aatcccagct 79260attcaggagg ctgaggcagg agaatcgctt gaacccagga ggcagaggtt gcatcgagcc 79320gagatcttgc cactgcactc cagcctgggt gacagagtgc gtgagcctcc gtctcaaaaa 79380aaaaaaacga gaaagaaaat gttatcccag tgggataata gttatacaca cagtattctg 79440tatatcttct cccagaattg acagttgtta ccattctagc ttaatagttt tctcttgccc 79500tttgtgtgtg tttgcatatg tgttcatgtg tatgattgct gaattatttg aaaataagtt 79560gcaagcatgg tgacagttct gtcctcagta catcactaag cttctcctaa gaataggata 79620tcctctagca taaccacagt attcattgcc acatgtaaga aaattaacaa tagtttcata 79680taatctaata ttcagtttgt tgtagaattt ctctattgtc ctaagattat cttttatagt 79740tgttgctgtt ttacaaacta agatctgatt aaggttcact tactacattt gtttgttatt 79800tctctttaga ctcttttcat gctaaataat ttccccaaac tttttttttt ttttttttaa 79860atgacactga ctttctgaat agttaagggc atgtgtcttg taggatgttc cttccctaca 79920aatgttccct ttgaataaag tattttcctg cttggtatca gcttagtctt tttttttttt 79980tttttttttg agagtcttgc tctgtcgccc aggctggagt gcagtggcac gatctcagct 80040cactgcaacc tctgcctcct gggttcaagc gatcctcctg cctcagcctc ccgagtagct 80100gggattacag gcatccacca ccatgcctgg ctaatttttg tatttttagt agagatgggg 80160tttcaccatg ttggccaggc tggtctccaa ctcctggcct caggtgatct gcccggctcg 80220gcctcccaat ccgcttattc ttaagacgac acatggctag ggcagtgatg ctgaccacgt 80280gctgttctca cctcagtggt cgagtcttct catctgactt tttgggcatg atttagaccg 80340gcagatagtt ctggaacaaa ccccttacca tttgaggttc cgtttgcagt gggttgtgag 80400gtgtgtgaga catcacttgt gttatgtagg gactagggac ttcaaagccc tcctcccatt 80460cacagtcact tgaaggctgg catgtcctca ctttctttaa aagtgctttc tttggccggg 80520cttggtggct cacacctgta atcctagcac tttggaggct gaggcaggca gatcacaagg 80580tcagaagatt gagaccatcc tggctaacaa ggtgaaaccc catctctact aaaaatacaa 80640aaattagctt ggcgtggtgg tacaagcctg tagtcccagc tactcgggag gctgaggcag 80700gagaattgct tgaacctggg aggcggaggt tgcagtgagc cgagatcgcg ccactgcact 80760ccagcctggg tgacagaacg agactctgtc tcaaaaaaaa aaaaaaaaaa gtgctttctt 80820taaggcatac cacaggtggt ggctggaatg aggaatctct gactttaaag gttatgcttc 80880cttaatgaca aaacagttgc aaacaaccaa ttaaatcctt tgtcaaccag attggtcaaa 80940tggactgaat ctaatcaagg catagtgtat gtttgtaata accttatcac tggccatccg 81000gcttccctgt tgttaatgtg agacggtttc ctttcacggt gctattttct agaaaatgat 81060cacttgttat ggttcaggaa tgtggctggt cattgccatt tccttcatct gcctcttagc 81120aagtgtggtg cacttgtaga ggaaacacac ccttttaaaa aaaaattttt ttttatatgt 81180gtgctttttg cattttttta attgtgggaa aatatccata acataaaatt cactatttta 81240accattttta agtgtggcat taagtgtatt cacgttgttg tgcaaccgcc actgctatcc 81300atctccagaa ctttttcaac ttcccaaact gaaactccat actcattaaa caatagcgcc 81360ccattctccc ctctcctctg ctcctggtaa cctttattct actccctgtc tctatgaatt 81420tgcttattct agggacctcc tagaagtgaa atcatatgct gtctgttagg tacctcctag 81480aagtggaatc atacgctgtc tgttaggtac ctcctagaag tagaatcata tgctgtcttt 81540ttttctctgg cttacttcat ttgtcatatg ttttcagggt tcaccatgtt gtagcatgtg 81600ttagaatttc attccttttt aaggctgaat aatattcctt tgtacgtgta tatcacattt 81660tgcttataca ttcgtctgct gatagacatt tgggttgtta cattcttttg gctattgtga 81720ataatgctgc tatgaaaaca tgggtgtaca agtgctgttt gagaccctgc tttcaattct 81780tttagggata tacccagaag tggaattggt ggatcatatg gtaattctat atgcagctta 81840tttttcagga ggaagtggcc tcactctgct ttttaaagta ggagacaaaa tggtcatatt 81900aggtgacagg gtcacaaggc cacatgggtg gggctgtgag atatgtccct gtcatgtggt 81960tagatgaaag ccggggtcag ttttggtctt ctctgtgtga ccacattgct tcatttctgc 82020cacctgagcc caggaagaga gaccgtttca tcttctagtt tctaaaagat ttgaaagtgt 82080tgttttattt tttatttcct gattgtttaa tagatgccag ttgccagcca gttagcattt 82140gttgatccat tcactgagtc ccaccttgct tagttctagt gggttgaaag gagagagggc 82200tggggtgagg tggacctcca gccacaaaca gatctttgtg gtgggcttcc ttgcagggtt 82260agctatgtga aaagcattcg tccatgagct aatcagaaat ctttgtaaaa atctagttct 82320ctatgaagca tttactgtag agcaatcctt aagcaccctt ctatctgagt aatcagaggg 82380gtaccagttg tctcctttca tggtaagcaa agctccgcag aagtttacag agttggggtg 82440tggttcaact ttctaaccag ccatggttag ccacgggtga ccaacccaag cccagacctt 82500tgacaagctg cagagtacgt tgtttcttag gctgctggag tcacacgaag tggaactttt 82560agtattttag gtgcatgttt atttacttac ttatttttgt tgttgtcgtt ttcagataga 82620gtctcactct ctctctctgt gtgtggagtg tcgtgatgcc atcacggcta actgcagcct 82680tgaccttctg ggctcaagtg attctccctc ctcagcttcc ctagtagttc ggaccacagg 82740tgtgcaccac catgtccagc tttttttttt tttaatattt tagtttgaga ccagcctggc 82800catgttgccc aggctggtct caaaatcctg agctcaagca atccccctgc cttggccccc 82860tcaaagtgct gggattacag gcatgagcca ccatgcttgg ctattaggtg tatgtttaaa 82920tccatttgct tatatcagtt acataacctg agtgttatgt aaatcttaag caaaagaaaa 82980atatatgaaa taaaaattga aactcacttc ccaactgcca atctcattcc tgccttcaaa 83040gtttcaggta tttatttcta gccttttttc tatgctgagt taaactgtgt atcttctttg 83100ctttgcattt cttactgagc agtgtgggaa ggctaccttt taaaatttat ttgtagttct 83160ttataatttt tacctttctt tttaggcaga aagattatct tattatataa cagtctacgg 83220ccattttttc ttaaactaaa ttattgggaa atgaatagaa atccagagta tagtaacaaa 83280tgacctagtg tctttaacag attggtagct aggaaaagga agtggtggag agacagccgg 83340agattaaatg agacttaaga gacttagcaa ccatttgtaa tatgtgacct tatttggatc 83400ctattcaaac taatggttaa aaaaattcat gatagctggg catggtggct cacgcctgta 83460atcccagtac tttgggaggc tgaggtgggt ggatcacgag gtcaggagat cgagaccatc 83520ctggccaacg tggtgaaacc ccctttacca aaaatacaaa aattagctgg gcatggcggc 83580atgtgcctgt agtcccagct acttgggagg ctgaggcagg aaaatcgctt gaacctggga 83640ggtggaggtt gcagtgaacc gagatggcgc cactgcactc caggctggcg acagagctag 83700actctgtctc aaacaaacaa acaaacaaat aaaaattcat gataaagcag cagctcaagg 83760tgctgtaaga aattcatgat atttataaga taattgaaaa tttgaacact gaatatttga 83820cattaaggaa ttattttttt ttatatggta tcgatattgt gggtactttg caagtatctt 83880ttaaggatac atagtgattg tggataaaaa atctgaggtc taggatttgt gtcaaaataa 83940tacaggaagg ggaggtggcg ggagtgaagg tgaaacaaga ccagctgtga gttgatagtt 84000gttgaagctg ggtacaggag gtccactgtg cagtgctctc tacatctgtg tttgtaattc 84060tttttttttt ttgagacgga gtctcactct gtcgcccagg ctggagtgca gtggcatgat 84120ctcggcccac tgcaacctct gctgcccggg ttcaagcgtt ctcctgcctc agcctgccaa 84180gtagctggga ttacaggcgc ccaccaccac acccggctaa ttttgtagtt ttagtagaga 84240tggggtttca ccatcttggc caggctggtc ttgaactcct gacctcgtga tccacctgcc 84300tcggcctccc gaagtgttgg gattacaggt gtgagccact gcgcccagcc ttttttttga 84360gacagagttt cgctcttgtt gcccaggctg gagtgcaatg gcacgatctc ggctcactgc 84420aacctctgcc tcctggattc aagtaattct cctgcctcag cctcccaagt agctgggatt 84480acaggcatgc accaccacac cccgccaatt ttgtattttt agtagagaca aggttacacc 84540atgttggtca ggctggtctt gaactgctga ccttgggtga tctgcccacc ttggcctcga 84600aagtgctgag attacaggtg tgaaccacgg cgcccagcct tttttttttt tttttttttt 84660tgctgaagtt tcacttctgt ttcacaggtt ggagtgcaat ggtatgatct tggctcgctg 84720caacccccgc ctctgcctcc tgggttcaag ggattctcct gcctcagcct cccgagtagc 84780tgagattata ggcatctacc atcacacctg gctaattttt gtatttttag tagagacgga 84840gtttcaccat gttggccagg ctggtctcga actcctgacc tcaggtaatc cacctgcctt 84900ggcctcccaa attgctggaa ttacaggtgt gagccactgt gtccagccta gtttggaatt 84960cttcataata aaaagctttt taaaaaggta atatttggac ttctgctcct gggaagatgg 85020aataggactt ttcctaattc tttcttctaa ctacaactaa aacccctggg ctatacataa 85080ggaaaacaca gggagcctct gaaaaaggat gaggcagacc aaccagggat cttgggactc 85140gaggaatgac acagtactga gttccttggg tttactttgc tttatatatc ccagacttgg 85200agccaaagaa agaagctgac aacctgaaaa tgccagtggg cacaaacaca gaaagtgcca 85260acaaaagctc ccctgtccag ccagaagacc aggaaagggc agcccagtga ggcagaaaac 85320ttaaagagtc actgctctac tccaggtcca caccatagaa aaaactatgc agccccacac 85380ttacacccgc agaggtgaat ggggagccta ggctttgaca acagtctagc aataaggaag 85440ccactctccg gggccatgga ggagcagtaa tgaggcactc ctacttcctc cagccagaac 85500tcccaccttc acgcaccagt aatgagcccc ccaatcttga gcatcagtcg aggttgaatg 85560gagagcctag acttcttccc ccactgttag taacaaggtg tgtacccttc cctcccctgc 85620cacagtggta tcataaaatg ccagctacaa cagaacattt acagaagacc cagagtctca 85680ttacatgata ccccaaatat ccagtttcaa aaaaaaaaag aaatcacttg tcataccaag 85740aaccaggaag atctcaaact gaatgaaaaa gacagttgat gccaacactg aggtgataga 85800gatgttagaa tcctatgaca aaaattttaa agcagccatt aaaaaaggct tcagtagcca 85860ggcgtggtgg ctcactttgg gaggcttgta atcccaggac tttgggaggc cgaggcgggc 85920agatcacctg aggtcaggaa ttcgatacca gcctgaccaa ccttatgaaa cccagtctct 85980actaaaaata caaaaaatta gccaggtgag gtggtgggca cctgtaatcc cagctactcg 86040ggaggctgag gcaggagaat cgcttgaaac tgggaggtgg aggttgcagt gagctgaggt 86100catgccgttg ccctccagcc tgggcaagaa gagtgagact ccatctcaaa aaaaaaaaaa 86160aaggcttcgg taggcagtta agaacaatca tgaaaaaaat gaaaaaatta aaaatctcaa 86220caaagaaata caatgtccca gcaaaataat aataaaaatt taggagataa aaagaaccaa 86280atggacattt tagaattgga aattgcagta actgaaataa aaacttattg gataagcgca 86340atagcagggt ggaaggacag agaaaagaat ccttcaactg gacaacaatt ggttgttttg 86400ttctgaggtg gagttttgct cttgtcaccc aggctagagt acagtggagt gatcttggct 86460tactgcaacc tctgcctcct gggttcaagc tattctcctg cctcagcctc cctagtagct 86520gggcttacag gtgcccacca ccacttctgg ctaatttttt tatttttagt agagacgtag 86580tttcaccctg ttggcctggc tggtcttgaa ctcctgacct taggtgatcc acctcggtaa 86640tccaccttag gtgatccaaa gtgctgggat tacaggtgtg agccactgga cccggcctct 86700gtaagctttt ttctgtgttt aaaacttttc atttttgtac ttttaaaact tttttttttt 86760tttaaacaca cacattagtc tagacttaca cagggtcagg atcatcatta tcactatctt 86820ccacctccaa atcctgtccc actgtcccac tggtaggtcg tcaagagcag taatgtgtgg 86880aaccgccgtc tcctataata acaatgcctt cttctagaat atttcctgaa ggacttgctt 86940gaggctgctt tacagttaac ttaattttta aatagaagat gcccactcta aaatataatg 87000ataaaaagta tagcatatta aatacataaa ccagtagcat tgtcatttat catcaagtat 87060tatgtattga acataattgt ctgtgctata tatgtttcta tggccggtag cccagtgggt 87120ttgtttatac cagcatcatc acaaatacat gagtaatgcg atgcgttact gtgacgtcag 87180taggcaacag gaattttttg gctctattta taatcttacg ggaccatcat tgtatgtgtg 87240gactattttt gactgaaact tcattattta gcaaatgact atattagcaa ataaaattga 87300gctgtatata atgaagaagt atgcattata accaagtggg gtttattgca gggatgcaag 87360gcctcgttca ctattagaaa atcagtcaac agcctggctc ggtggctcac gcctgtaatc 87420ccagcacttt gggaggccga ggtgggcgat gggcggatca tgaggtcagg agatcaagac 87480catcctggct aacacggtga aaccctgtct ctactaaaaa tacaaaaaat tagctgggcg 87540tggtggtggg tgcctgtagt cccagctact cgggaggctg aggcaggaga atggcatgaa 87600cccgggaggc agagcttgca gtgagccaag attgtgccac cgcactgtag cctgggcgac 87660agagcgagac tccgtctcaa aaaaaaaaaa aaaaagtcaa atagtaaaga taccacctct 87720cctcaaattg tcattcaggt ttgatgcaat tgctgtcaaa atcccagcaa gagtttttgc 87780agatagcaag attattattt taaaacctat atgaaaaggc aaaggaatta aagtagcaaa 87840aacaattttg agaaagaagt acaacatgga ggaatcagcc ttcctgattt caagacttgc 87900tgtatagcta cagaagtcca gattttgtag tattggtcaa aggatagaca ttatagatca 87960gtgaaacaga attgcagccc cacacaaata tgcacaactg attattgaca aaggtgcaaa 88020gataagtcat tgggggaaaa aaccttttcg gcacatggtg gcagagaaat tgaacatccc 88080taggcaaaac aaaacaaaag caaaccccaa accaaaaaac aaaaaaccca tataactata 88140aaactttgag aaaaaaacat agaagagaat ctttgagatc tagagctagg caaatagttc 88200tcagatttga caccaaaaac atgatccatt aaaaaaaaat aagttggatt tcatcaaaat 88260taaaaacttt ttaatgtttt aagaaggatg gtctgtctca aagactcaac atggtacatg 88320gtggttggcc tttatgtgct gttgagggtt ttcctgcatt gaagggtgca ctcctgggtc 88380acctactgtc ctgcaagaca agctgtctta gccctcacac tataaaagcc acccggacac 88440cgtctcaaac agaactcaaa atgttgctga gactgggatc tgggggctgg attttacttt 88500tacaaacaat ttaaaacttt ttacagttaa gaggatgaat atacaggcta aagactggga 88560gaaaaaattt gcaaaccata tgtccaacag aacactagta tctagaacat gtagaaagaa 88620ctctcaagtc ttagtcgtta aaaaacagac aaacatttaa ccaaacaacc caataagaaa 88680atgggcaaaa gacataaaca gtttctgctg aagagaacgt ccatatgaca aaaaaacaca 88740tcgaaatttg ttcagtatca ttaaccatga gaaaaatgcg aattaatcct agtacacact 88800atcagaacgg ctaaaataaa aaatattaat actgataaca ctaaatgcag aacggatgga 88860gagaaactga atctggatca ctcactcata cattgctggt gggaatgtaa aatggtgtag 88920ctactttgga acactgtttg gtagtttctt aataaagaaa taggctgggc acagtgactc 88980ccttctgtaa tcccagcact ttgggaggct gaggctggag gatcacttga gcccaggagt 89040ttgagaccag cctgggcaac atagggagat tgcatctcta caaataattt ttaaaaatta 89100tacaggtgtg gtggtatgca cctgtggtcc cagctactca ggagattgag gcaggaggat 89160tgcctgagcc tgggaggtcg aggttgcagt gagccgtaat tgtgccactg tgctccagcc 89220tgggctacag agtgagactt ggtctcaaaa caaaaacaaa aacaaaacct caaaaaacag 89280tacatgcaac taccatatgg cccaacaatt gcactccttg gcatttatcc cagaggaatg 89340aaaacttact gtatatgaga gccactgttt ttccttctat agtctcacag ctaaagaaaa 89400aaaacttttc tcatcttctc tactactcct ctcagtattt cgcttccggt caccaaaatc 89460tatggatttc tgtcccccat actgacaagt tctccaattt tatgtggaca acaagtaggt 89520gtcctataat caattccctt caattctgac actatctacc tgaagttagt gcagacgcca 89580ttaagggctc ggtccctcaa aactgcccct gacttcagag gccagtcaga agtggtgggt 89640cctcaggtaa cccacagctt ctgtccaggt ttgctacaaa tcagaaggtc ccattacccc 89700ttcctcatgt tatgttattt gctagagtgg ctcacagaac tcagggaaac acttaccttt 89760agcagttgtg tagtgaagga tatgatagag gatacagatg atgccccaga tgaagaggtg 89820cacggggcaa agtttagagg

cgttttgaac acaggagcgt ctgtccccat gaagttgggg 89880tgggccatcc tcttggcaca tggatgtgtt caccaaccca gaagctctct aaactccata 89940cttcagggat gtggaggcta agtcacgtag gcgtgattga cattaactga gactacagtt 90000cctctccctt ccctgtagga tggggagtgg ggccgaaagt tctaagcttc tgatcatgac 90060ttggtctttc tgttgattag ccacatcttg aaagctatcc gggagcccac taagagttgc 90120ctgattagaa cagaagatgc tcttgtcacc aaggacattc caaggggttt aggaactctg 90180gaaccagggg cagagaccta tatatataat ttcttactat tttatactta tgttcacaca 90240cacacacaca cacacacaca cccctatgca cagatgttta cagcagcttt attggtaaga 90300gacaactaga aacaacccag atgttcttca gtgggcgaat ggttaaactg tggtacatct 90360ataccatgga atattagcta ctcagcaata aaaaggaaaa aaaccattga cagaagcaac 90420aacctgggtg aacctgtaga caattatatg tagtgaaaaa ggccactcct aaaaggttac 90480atagttatga ttccattgat gtgacgttac cgaaataata aaattacagt gtggagaacg 90540ggttagtggt tatcagggct aaggagagtg tgggtgtggt tatgcaaggg cagcaggagg 90600gctccctgtg ctaaagggaa tgttctctat tttgattgta tcaacgtcaa taccctggtt 90660gtgagattga gtcatagctt tttaccgtgt taccactggg gaaactattt tgagatggag 90720tcatgctctg ccgcctagga tgcgatctgg gctcactgca acctccacct ccctggttca 90780agcaattctc ctgcctcagc ctcccaagta gctgggatta caggcatgtg ccaccacgtt 90840gtatttttag tagagacagg gtttcaccat gttggccagg ctggtcttga acgcctgact 90900tcaggtgatc cacctgcctc agcctcccaa agtgctggga ttacaggcat gagccaccgc 90960tcccagcaag ggcattgttt cttacaccta caggtaaaat ctgtctcgat gaatttgctc 91020gatcatctta aaataaaaag gttaattaaa aaaatgattg aatataattt ttaaaaatgt 91080caggcaatac aataaatgct gtttaatgag aaataagctt cgctcctccc tgctgtgttg 91140cttccatcaa ggcaagctct gctactactt attaaccaca ttatttccac aattttatat 91200agactcctga ctgaggttct ctgaatatca aaattggata ttacttcaat aacatgggca 91260aaattaaggc tttcgacctg cctgattttc cttgtcaagg cagtttgtcc ccatttccca 91320catgggatct gcagggctgg gtcccatctc tcagttccct gaaagagatg cagtgggcga 91380tggctcatga cacaccctcg cctggcttct aacatgtctg tgtaaacctg tggcaggaat 91440cgagcccact ggaaacatgg tgaagcagcc agccaagttc actgtggaca ccatcagcgc 91500cgggcaagga gacgtgatgg tgtttgttga ggacccagaa gggaacaaag aggaggtatg 91560ttggaggatg ctgcctctcc tttccagcac ctcatggagc ttttggggct tgtaatgcgg 91620ccagggactg tgcctccatt ttcatttcag ctcacaacca aaagtgtttt ttaccaaaag 91680gatactgagg cttatagctg ttaaagtaac ctgcccaaga ggtgagcctt gaaatcaaat 91740ttaaattgat tgccagggac acagtgttta atgaaataaa ggatactttg gatttagcaa 91800aggtgccttg tcagttgagg tttatgtatg tatttattta tttatttatt tatttattga 91860gacagagttt cactcctgtt gcccgggttg gagtgcagtg gcacaatctt ggctcacggc 91920aacattcacc tactgggttc aggcgattct cctgcctcag cccggctaat ttttgtaacc 91980caagtaactg ggattacagg gacctgccac cacgcctggc taatttttgt atttttagta 92040gagacagggt ttcaccacat tggccaggct ggtcttgaac tcctgacctc aggtgatcca 92100cctgcctctg cctcccaaac tgctgggatt acaggtgtga gccaccgtgc ccagcctcag 92160ttgaggtttt atatactgat ggccagaata ataagagtct tgccctgctc tcttcccaca 92220ttggccattc tttggttcct ccctcagagc ctttgcacat gctgttcttt ctgtcactta 92280ttttcgtagg accatatttt attcttggca tttagcataa tttgcaattc taagtttaca 92340gatggatggt ccatttcccc caccggggca gggattgtat ctgacttgct catgttttat 92400ttttagtacc taacactggg ccctgcattt cataagcttt caatgaacta ttgagtggat 92460aaaggtttaa gtttcttgct tcatattctc tcttacctag agagtgccag cctgacactg 92520gacactggag agtcctgact ctgttatgcc tctgtgctgc atggttttgt ttctgtgact 92580tcaagcagtt tctctctagg ggcgttgtgc aagagggaca ggagctcgcc agcaccttca 92640gtgtttccga cctggcagct cctgcagaac ccctgctgac acagcatgct ccttactcac 92700acccggcacc ttttctaact gttgcccacc ttccctccta ggcacaagtg acccctgaca 92760gtgacaagaa caagacatac tctgtggagt atctgcccaa ggtcaccggg ctacacaaag 92820taagatgaag cagcatggct gtggcttggg ctgctctggg gctaggagaa gaaagatagc 92880ccaggaagaa gagtgttttt cttaagtgaa tttctgattt tcctttctga ttatagaagg 92940atctatgctc atgatagaaa attggaatca ctaggattcc ctctactagc taggatgagt 93000tgtttgcaat gtcgtaagat ttttccaact ccatctaggt aactaatggt tgcagctgtg 93060tgtctggagt gtagatgctg tggtgactac actatagatg ggttctttgt ccttgattct 93120ttttttggag acagggtctt gctctgtcac ccaagctgga gtgcagtggt gtggtctcag 93180ctcactgcaa cccccgcctc ctgggctcaa gcgatcctct cacctcagcc tcccaagtag 93240gtgggattat aggcacccac aaccactccc agctaatttt tgcattttta gtagagacca 93300ggtttcacca ggtcacctag actgttcttg aactcctgac ctcaaactat cctcctgcct 93360cagcctccca aagtgctggg attatagaca tgagccacca caccctgctg gctctttgtc 93420cttaatgctt tcttaagaac tctccttgga ggtgctctgg aggagctgtc agcattgaag 93480gctgaggatg gagtagttca gctgaatata gtagagggaa atggccctct cagcacctgg 93540agaaatgata gggattgagg cctcaggctc tttgtcttgg cagcctttcg agttctgttt 93600gagatgacat ccaggtgacc tatagggcaa gggctgagag agcctgtctt gcaggagagt 93660ggggtgaccc aggagtacac ttttcattgg aagaaagccc tcaacagcac ataaaggcca 93720atcccatcat gtacctgccc agactttgga atacagactg tactcaccac cttgggcttt 93780agtgaattca cctggaatga tggccttagc gttctcttag actcttagac tatgatgcat 93840ttggagtaaa tgctcttgaa gggagcattt ataatgtaat taattaattc cagtcaagta 93900taggttcaca tgaaacccaa cccaattacc ccccaaaaat ttcagagatg agaacagtga 93960ctcaagtttt agatggaaat cattctactt tgtcccaaat ccatgtatct aagaatgatt 94020ttcgtccctt gaaaaaacag tttggctgtg gatttgaaat cctggaactg catattttat 94080tctgagggat agtggcccat tcagcccccg aaaggactca atgtccagag attgaaatgt 94140gtttgtttcc tattaaagag actaagtgta tataaggtca gcatttttat tttgctaaag 94200gtgtgatgtc ccagacccag ctgtatggct gaaggggcca ggtgggagtc ccattcaggc 94260tgttaaactt ggttccaggg ctccttattc tagacacctt gtgtgtgcca tcatgggagg 94320gtaggagagg tgatcatcaa tgtatgtggc ttgatgtcag tcttgctggg cacagagaag 94380tgattatgta tttctcacct atctgtcacc tataggtcac agtcctcttt gcaggacagc 94440acatctccaa gagcccattt gaagtgagtg ttgacaaggc ccagggagat gccagtaaag 94500tcactgcaaa aggtccaggg ttggaagctg tagggaacat cgccaataag cccacctact 94560ttgacatcta tacggcaggt aacgtgcctc tcctccatgg atctgacctt tgcgctttct 94620tccagaggct gaaatataat cctcggggac ttgaaggcct gaccttttgt cttttaaatc 94680aaataaataa tcacaaagac aattttttca aatgtgttat attagatttt tcaaaaccag 94740cttttcttct ctaaaatact caggcttcac ttgaataaga catacttctt gaattgttgg 94800cttcttttcc atgtagtaaa tagaaaatgc agaagaagga aacattcaac cataaaccct 94860tcaaccccta gaaaatagtt gttaacatct tggtgtggac ctctctgagg gcctgtctcc 94920tgtttacttg ttttgttgtt gttgttgggg gaacagagaa tcactctatt gcccagactg 94980gagtgcagtg gcgtgatctt ggctcaacgc aacctccgcc tcctgggttc aagcgattct 95040catacatcag cctctcaagt agctgggatt acaggcgtgc gccaccatgc ttggctaatt 95100tttgtatttt ttttagtaga gacggatttc accatgttgg ccaggctggt ctcgaaatcc 95160tgacctcaag tgatctaccc acctcggcct ctcgaagtgc tgggattaca agcatgagcc 95220accacactgg tcctgtttgc attttgcact cagcagcagt gagctttcag agagggtgac 95280ttgggctcat ggaatgcttg ctttcttgta ggagctggtg tgggtgacat tggtgtggag 95340gtggaagatc cccaggggaa gaacaccgtg gagttgctcg tggaagacaa aggaaaccag 95400gtgtatcgat gtgtgtacaa acccatgcag cctggccctc acgtggtcaa gatcttcttt 95460gctggggaca ctattcctaa gagtcccttc gttgtgcagg ttggggaagg tgagtgctgg 95520gctgctggcc acatgtgctt ctcataggga agctgactgc acagctgggc agggaggcca 95580ggaaaacagt cagggcccaa cattgacctt atgcctatcc cttttctgcc agggctactt 95640cagcagtaag tggcttactt tgtcctcaat atattaatat taatatcttc tatgagccac 95700gcagagacct aaatgctttg cttatattaa ctcatttact tctctccaaa acacatgtac 95760aggagagtaa ttatcctcat ggagggaggt gggactgagg cagtgggagg actcggtagc 95820ataactgaag ttagcagcag caacatgggc cctgcagcct ccattgcttg gcctttactg 95880gcccaggcac ttaccatgac tgcatctaat cattgcacca gcctgtgtgt tgcaggtgct 95940attattatcc ctagcttgca ggtggagatg ctgaggctta gatagcgtta ggtatcagta 96000ctacaaggca tcagcagggc tagaaccaca gactctgttg gccttaccct taactactct 96060gctaaactcc ctctggcgct gggggtacgc atttttctca aatgttagac tctctccctc 96120tgactttgtt gccccttttt ttctgttttg ttttgttttg ttttgttttc caactgtact 96180accttttcta acccacactt gcctttccct gttctgtcct ctgaatctgc gtctgcagac 96240gtggcttcct cttccgaatc ctacctctgg gccagcctgg accctgaagc tgttggcttc 96300ctagttgaga ccactgggcc agaggcctct tgcttggtaa gggctggttg ggtgggactt 96360ccttgccagt tctttgtgct gcttgtgaat gttagctggg cccgtgttct gtgtgatttt 96420aggaaactct gtgcaggtgt tattattaca gcctgtccag ccggaaccca aacccactgt 96480ctaattgcct ttaaacacat ctagggcttt tttagatggt gaaggagctg gtggtgccct 96540tcagactcta gccccattta atgtttatat gaactcagca attactcttt tgatgttgag 96600actgttgcac atgttcataa tttccatgag tgtgtgtgtg tttcttaaga cacattaaag 96660ccctccgagg aagtcctgtc attgtattgt gactgacttc tggtatgacc aacttttctc 96720cccttgacaa agaaaaaaca ggcaaaaaaa attctaacat attcctaagc aaagctcttt 96780tttacataag agagcatttt gaatagcttt cctaattcta ctattgtttt ccaacctttc 96840ctcactcgtg gacttccttt ttcttttctg gcctgtacat cctatactat ttagcattta 96900atgaataacc tttttctttt aatttactaa catcctctct cccacctaaa tgattttaca 96960tatgtaaaaa aaaaatatat atatatttgc aggggcgcgg tgggaaggat acagggtctc 97020actctgtctt ttgggctgga gtgcagtggt accatcatgg ctcacttgta gcctcgacct 97080cccaggctca aatgatcctc ccacttcagc ctcttgagta gctaagactg tagatgtgcg 97140ccaccatgcc tggttacatt ttttaccctt tttttttctt tttctttttc tttttttttt 97200tgttttgttt tgttttgaga cagagtctca ctctctcacc catgctggag tgtggtggtg 97260tgatcttggc tcactgcagc ttctgcttcc ctggttcaag tgattcttgc ctcagccacc 97320tgagtagctg ggactacagg tgcacaccac cacgcctggc taagtttttt tgtactttta 97380gcagacacag ggtttcacta tgttggccag gctggtctcg aactcctgat gtcaagtgat 97440ccacctgcct cggcctccca aaatgctggg tttacaggca taagccacca tgcctgacct 97500aatttttctt ttttttgtag aggtggggtc tcactctgtt gtccagactg gtcttaaacc 97560cctggactca agcaatctcc ccgcctcagc ctcccaaagt gctgggttta cagatgtaaa 97620ttattttatg ttaaaagaaa ctttatatca ctttcacaat ggaaaaccaa agtcacttgc 97680cataaagtgc caccgtaagc ttatgttcat ccataaacca tctaaaatca tctctaactc 97740caagggtatg tgtatgactc tttgggaagc agttgtttgc caaatagcca gctaaggcca 97800ttgcaggaag gaggaaccag aggaggaatt accttccgtc tgtggagtag agtcccgtct 97860tctggagtct gtgaccttcc tgtatagaga tttgtcaaat tttcagtgtt agatttggaa 97920aggaaaagcc acttaataac atgacatttt ccccactagt ctcccgtttc tatttactga 97980aaaggttgtc cgtgctgggc agaagattta ttctagggca taaaggtatc ttttatcaac 98040ctctagatac catggaacag tagttctgtg gacatttcaa gtaaggcata ttggaagcta 98100tcttcgccct taacttttag acttacaact ctaggttttc aagctagacc cggaaatgaa 98160atcagcaatg gtgtttactg ctaattattg cctttatagc cacccacatt ctgaaggcct 98220tgtaacagac agcacgaaaa gattggtctg cctcagccaa ggtggggctg aactggtctc 98280tttccaagct gtgttggttg tttttgcctg gttgttcagg cggaagacaa caacatttag 98340acacttaaaa atggctgacc caggttttgg aacccagaca ggcattttca agtactgcat 98400tttccaagaa gacttgaaaa agtccagtct atccaattac tgagcccttg agtatggcag 98460tgaggtttga ataatgtcca gcactcggcc ttaactccct ttcacaaatg aaaggttaaa 98520tgctggaagc aggagcacag catggatttg ctgtgctctc ctgttttctt tgccaaagtc 98580acttttctcc agtccttctg tggtgtcact ggacaaagtt atattgtgtc tgtatttgct 98640agcctggtgt gctccctgag tgggacccct ggtcttgggc aactactgca tactatttgt 98700gcaaagcaaa tattttcttg gcgggtggct ccaggttacc ttggctttca cgactctgac 98760taaagaatga aagattgaat tgatgtcaaa actgtgcttg cagcctgcaa tccaaatgcc 98820tgccgggcca gtggccgagg cctacaaccc aaaggcgtcc gtatccggga gaccacagat 98880ttcaaggttg acaccaaagc tgcaggaagt ggggagctcg gtgtaaccat gaagggtcct 98940agtaagtgtt cctttgtttc tctatctcag gtgtggtttt ggctaacttt gcagccatgg 99000catatggatt tcatcccacg gccagttgtc ctcaataatc ccagaaggct atgtcaagga 99060tttgaggcta tctgggctcc ttggggaaga cggcagtgat tgattagtaa tgtctgccct 99120ggatgcggcc agtgggtggc ttgacagctt tacattacat caagacttct gggagtagaa 99180aaagcagtga tgtaaaggag ttggggaaat gctgctgttg gaacaagtgg ctcatttttt 99240attttagaca tctgggctca gagaggaagg ctcttgccta aggtcataca gcgtttgtaa 99300tcatctgagc tggaattcaa gcacagtctc caaagccagt gattttccca ctacaggtta 99360cattttatag agtatgaaat tatgtcaagt acttaattac tatgatcagt gcttatagaa 99420ggagaataaa attccctaag attaagtttt ctttgtagat aaatgccatt tgtggaggta 99480caggttaaac cctgcaaccc attctctctc cctcttttgg ggaaggagac agcagatgtg 99540gggatgggtg tcttcacttt tttcgttgga acagagaagc atttcagcac ttctagtctc 99600gggtgtagca gcctttggtg gttttactcc catgcctgtg gaatcttgag cttcctgtac 99660caggattgct cttaccttct gtgttcccaa caggctgggg caggagcatt ctgagctcca 99720gaaagttaat atttgacttc acagcaccag gctttgggtc aggctgtgcc ctgagggtag 99780ccgaggttct agactgccca gacctggagt caagctgctt ggggactgtc ttccctccca 99840gattattcca acaggagcca aggagggtgt gtgtgtgtgt gtgtgtgtgt gtgtgcacgc 99900gcgtgcatgc ctctgcgtat gtgtgcgtac gtgtgtgttt tctcctgacc ttgaatactt 99960gcttgactca acggctttcc tggccaaacc tcagggctca acacaaaaca agttcctgcc 100020tgatggctgg gtttggagtt tgcagcgtca catctaaaac ctgtcctctt gcagatagcg 100080tctgaggact ttcttgcttt tgttgtccag ctttagatgg aaaagtatac gctggaacac 100140tgaacctaaa actcatacca aatacttcta aaggtttact tcttccccag tttttgtggg 100200ggactaggaa gggtagctat gattattggg aaatactgaa atgtgactgg atttatcttt 100260atgcaggccc agggagttca ggacctcagg gcccctcgta gccaagcaag atttctaaag 100320ccaattagct gggaaatcct ccatttcctc ataccttgaa gcagagatgg ctgtgttttt 100380agctttgaaa taatctccca ggctttgagg ggagaggtcc catactctgg ggcagcccac 100440ttggttttta tgtatggttt atgttttgtt cagtgtggct gcctctctgt tcttgtcctt 100500ttgattctca ttttgggcct aggattgtgt tggaaagatt atctccttcc ttcccacaga 100560gggtctggag gagctggtga agcagaaaga ctttctggat ggggtctacg cattcgagta 100620ttaccccagc accccgggga gatacagcat tgccatcaca tgggggggac accacattcc 100680aaagaggtga ggctcctgct gcagaggggt cttctctgga gggtgctcgg cccagggcgg 100740actcatgggt agttgcttcc cgggctgcag gagggaaaga gatctgcttt gttgaaaact 100800tttttttttt ttttttcgga gcagcacaga catttggcct gttctcaaaa gcagcagaaa 100860gttgctgtgg ttttagctga cttgctttaa atcaaatgct ggtggttagg ggctggtggg 100920aggcagggga ggcagaagga gcagttagag caaatgggct gtgtgtctag atgcccgcat 100980ataaactgag attctctttt tcaatgaact cctttgttca tgaatgccac ggggcagaat 101040ctgctgtggt ttacattaag accgtctacg tgagtgctgt caggggccaa gggacgcagt 101100ctacagcttt gccttgtggg cattgcactt gcccctctgc gttctgtgtt ttccagctcc 101160cctggaggtg caactttaaa ctccgaataa attcagttag ccttgagaaa tatttgggca 101220ttattgggtt ccgaatacct accacgcttt tttttttaag cctcccatgc caaggttaca 101280gcacattcat tcatgtatga gataaagccc attcaaccaa gttttctggt tatagcataa 101340gcaggatata gtgtgtggac tctctcactt tccagggtca tagtctgggg aggcctgcac 101400acaaaggtaa agggccagga ggctggtgca aagcagcgtg gcttgagtgc caacccagtg 101460gccacctgag ctcccagaag cagtcacatt acattatatt gttgacataa cagtagctat 101520gggtgagagg cctgcaggag gaagggcttg gctgcagttt gggatgccag atgaaaggat 101580caggcaagtg gaaagaatgt gcaaaggaac tgcagcttat ggctatagtg acaccttact 101640ttactcttct ttgatgcttc ttctattcct ttccctgtag cccctttgaa gttcaagttg 101700gccctgaagc gggtatgcag aaagtccgtg cttggggccc tgggctccat ggtgggattg 101760tcgggcggtc agcggacttc gtggtagaat ccattggctc tgaagtgggg tctctgggta 101820agtggacaca gctgaccagc atcttctgga ggactgagga ttacagggct tccgggctgt 101880gtcaggctgg atgttggggc cttgcctagc ctcaatacct ttagcttcct ggcctcctgg 101940ccaccctaag ccatctctgc gtgctgctgt acatttgcag ttgcctctga taccagcatt 102000gattcattca ggagaccttg agggcagaaa ccttatgtgg gtattgtgcc taaaacaatg 102060cttggaacgt agtaaacact tagcaaatag tgttgactga cctttatagt ttagatgaat 102120gaatgaatga attttgctga aatttggatt tggaagataa atatttcctt tggagcacag 102180ctgaagtata ttttaaatac atgtctaatg tatatatgat cattttatat caggagtcag 102240ccagcttttt ctataaaagg ccagatggca aatattttcc acctgtgggc cttatggtct 102300ctgtcacagt tatttgactc tgccgttgta gcctgaaagc agctatagga atacgtaaac 102360aaacgtgtgt ggccatgttc cagtaaaact ttatttgcaa aagtaagcaa tgggccagat 102420gtggccttca gactgtcgtt tagcaacccg ttttaggtaa tagcaataag caaaagagaa 102480aaataagaaa tcacatttaa ttttcccttc tagagagatg atatgaatcg tcttgtatat 102540tcttagtcta gagataatat taagtctttt agtgtatcct tctagacttt tttctctata 102600tatgcatgca aatattgatt tggtacagaa aatatcttag acaagtcttt atatctttat 102660gcgtaaatat agggtatgcc ttcattttcc atagcttcca tggaattcca ttgtatggct 102720ctatccattg tcaggctctt cagttatttc cagggttttg ctataaaaac agtgctgact 102780gtgtatcctt ggtaattgcc ttcagataaa aacccagaag tggatttggt ggtgctaaga 102840gtgggtgttg gttcaaggct tttgccacat gttgccacat ctccaacaga agggtttgct 102900ggttggactt cccctgttgg atgatgataa aatacatata atgtatttaa tactatatat 102960atatatatat atatatatcc tcctggcctc aagtgatcca cctgcctcgg ccctcccaaa 103020gtgctgggat gacaggtgtg agccaccaca cccagcccag gcctacattt gaaaaaaaaa 103080aaatatatat atattttcca ccccttccat ctctactgaa gacttaatga gcttggtttt 103140ggaagaaagg gatacaaaca gatttcaatc ttctggccaa cacttggctt ttagggaggc 103200agcgggaatg agctgtcgta acatagaata ggtgctttcc accatataac cagggagacc 103260cttccacctc caccccctag ggtttgccat tgaaggcccc tctcaggcaa agattgagta 103320caacgaccag aatgatggat cgtgtgatgt caaatactgg cccaaggagc ctggcgaata 103380tgctgttcac atcatgtgtg acgacgaaga catcaaggac agcccgtaca tggccttcat 103440ccacccagcc acgggaggct acaaccctga tctggtgaat cagctgctgt gcttctgtct 103500tcttgtccct ggcccctggt tcctcacccc catgcccgaa gttgccttaa gcagcatgtt 103560gagagatggc agagaggaat catttggatt ttaggaagga aacaggcctg catttgtttg 103620tttgtttgtt tgtttgtttg tttgttttga gacagactct tgctctgtcg cccaggctgg 103680ggtacggtgg catgatcaca gctcactgga acctctgcct cctgggttca agtgattctc 103740gtgccttagc ctcccaagta gctggaacta caggcatgtg ccaccacagc tggctaatct 103800ttgtattgtt tagtagagat ggggtttcac catgttggcc aggctggtct cgaactcctg 103860gcctcaagtg atccacccgc ctcggccctc ccaaagtgct gggattacag gtgtgagcct 103920ccacacccag cccaggccta catttgaatc ctggtagtag cacttagcac ttttatagtg 103980ttgggcaagt aacttaccta tctgactctt ggtgtcttcc tctataagac aggaatgata 104040gtagtctctg cttctagaga gcttctagga tgattcagga ggtggcatgc ataaagaccg 104100cctttggctt atgcctggcc catgcaggga gctccataag ctgttatttt cttgcaactc 104160cggggatcat atgtcagtct tacagccatt ttctatagtt attatttcaa ggtgctccat 104220agataaagga tttttttttc ctagttccgt gtctcttaag ttggagcaat gtttccaaga 104280gtgtcctctc aaacccttag caggctgata agcatcaagt ctgagccagc ctggctgaca 104340gggagttggc cccagaggcc acgtgtgcta ctgttggccc acacgggcag ctgtccatag 104400gctgatgtca gtctgggctg gtagctaccc cgttttggcc aaatgatatt cctttgccct 104460ctagggcaaa tgttgtccgt ggtaaagatt ctgagtcccc tcaaagtggg aacgttgaaa 104520ctgggcatga ctagaggtct ctgccccagt tgttagaagt tctttaggtc aactcagaat 104580aaggcaggga gcatgggtta gtttgggcat ggttttagaa caggggtttc caatattttg 104640ccttccctgg gccacactgg aaggagaaga attgtcttgg gccacacata aaatactaat 104700gatagccgat gaacaaaaac aaaaacaaaa aaaaaattgc aaaaaatttt ataacatttt 104760aagaaagttt acaaatttgt gttgggctgc attcaaagcc atcctgggcc gcatgcgggc 104820ttcaggccgt gggttggatt tgtttagaga gttttctccc ttatgaggga gagacatttg 104880tttttaagtt acaacctact

ttagcacttt acttcccata accaacctct tatgtggata 104940ctgtaaaacc agacacaggt cattttgttc ttcccccacc ccctggttac ctgtctttgt 105000ataagggttt agttggggca ttacacagaa agagacttac tatctgcctt tgcttcaggt 105060tcgagcatac gggccaggtt tggagaaatc tggatgcatt gtcaacaacc tggccgagtt 105120cactgtggat cctaaggatg ctggaaaagc tcccttaaag atatttgctc aggtaaattt 105180cagggggcca cctgtgcagg taattgtcag gtaacaagat ctgaccacgt aatggcaagt 105240tgctgagtcc atctgatctt cagtttcctc atctgcaccg tggaaatgat aagaagatta 105300tcttataggg ttatgtgagg gttcagtgag actaccatgt agagtactgg gctttaaaaa 105360aatcagcttt ctgatttata ttctgtggaa atgaggcttg tttgtttcag gttattctat 105420aatgtctttt ggtgtggctg aagctgctga ggccatgggg ggagatttgt aaacaaggat 105480ttaaaaagta tgtttattta atctaattga atttggccaa aggacttaaa tgcaggaatt 105540gagtggccaa agctttgttt ttgggtcact tgctcttaat aactaaaaat aaataaatgc 105600atgtcatatt ttgtcactgg ttgtcaccgt gttgtgaaaa tatggcacat tgtagttggt 105660ccatgaagtt ttgttgtata agcaagtggt gacttggctg tcttgggagg ccacagtgac 105720cctgtctgat agagacagtg tgagggccac ctctggtcct agctctggct tttttgcagg 105780atggggaagg ccaacgcatt gacatccaga tgaagaaccg gatggacggc acatatgcat 105840gctcatacac cccggtgaag gccatcaagc acaccattgc tgtggtctgg ggaggcgtga 105900acatcccgca cagcccctac agggtaggtt gtgaggcaga atcctggctg ttttatggaa 105960atgcctggtc atacaccagg tctgggatcc atgcctgaca gccaaggcag acatatggaa 106020ggaacccatc cctggtgggc cttgaatgat ggaggggccc gaagggcaga gtgctccagc 106080ctgctcagaa gaactatttc taacaatgtt ttttaatagt attttactgg gtccaagtgg 106140aggagaactt gatgaccttc tccatgtctt ctctaggtca acatcgggca aggtagccat 106200cctcagaagg tcaaagtgtt tgggccaggt gtggagagaa gtggtctgaa ggcaaatgaa 106260cctacacact tcacggtgga ctgtactgag gctggggaag gtgagaaagg gctttgttca 106320acccagtgat cattgctccg tggggaaggc agttcttttc ataacgtttc aatgcctttt 106380gaactaggaa gtagtccatc tgaataggta atcatctact gagcctctga gtcattcctt 106440agtgatatct ttgctaatcc atcatccctt tccccaaatc cttactcttt ctcaggtttc 106500ttactagaaa cttcccaatt gctttttgag ggtgttaacc tgagctggaa gagattgcac 106560aggacatgct gtttcttgta agctggtgct aataagctgg tctgttccag gtgatgtcag 106620tgttggcatt aagtgtgatg cccgggtgtt aagtgaagat gaggaagacg tggattttga 106680cattattcac aatgccaatg atacgttcac agtcaaatat gtgcctcctg ctgctgggcg 106740atacactatc aaagttctct ttgcatctca ggtacgtggt ggggcctggg aggagatggg 106800tggagtaggc ctggattctc tttggccact tgtgtgcatg tctcatctac tttttggtgt 106860tttgttagta ttattatttt tgagatggag tctcactctt tcacccaagc tagagtgcag 106920tggtgtgatc ttggctcact gcaacctctg cctcccaggt tcaagtgatc ctcccacctc 106980agcctcccaa gtagctgggg actacaggct cataccacca cccagctaat ttttttttaa 107040tttgttttta tttttttatt ttttttttga gatggagttt tgctcttgtt gcccaagctg 107100gagtgcaatg gcatgatctt ggctcactgc aacctctgcc tcccgggttc aagtgattct 107160cctgcctcag cctcccaagt agctgggatt acaggccacc acgcctggct aatttttttg 107220tatttttata gaaatggggt ttcaccatgt tagccaggct ggtctcaaac ttctgacctc 107280agatgatacg cctgccttgg cctcccaaag tgctgggatt ctaggtgtga gccaccgtgc 107340ctggccactc agctaattgt tttgcatttt tagtagagac ggttgcccag actgctctcg 107400agctcctgac ctcaggccca cctggcctcc caaagtgttg ggattatagg catgagccac 107460cacatttggc ctcctttttg gtgttttact gacagggaag ttgtcttgag aacactgctc 107520aatcgttttc tctctggctc cttacaacca agaaggaaaa aaaatttacc cagagctaaa 107580ttattaccac tttctaacaa aagtgaggca gtgtgttcag tggttaaaag caggggtctg 107640gagagagact agtttgtaat aaattttcat caatattttg gttgaaatgc agttagcttc 107700tagatatgtt ctactttgat gcctttgaag caatgactgt ggtctccacc cttaaatttt 107760tatagagaga ggtgatttga agtttcaggt atgcaatagt gaagataggg tgagcaggat 107820cctgaaagag agaattttga aatcctaggg attaaaatta accttacata aaaatggaaa 107880tcttagtaga atgttctgtg cctaaaggta gtggtcttga catccattta acctcttctg 107940cctttattcc aatagtctgc aacattcttt ttgaagaatt ataatcattc tgtctctgat 108000cacttcttgc atttccccag accttagctc tcagctgtcc ctggaggaca tttccttccc 108060ccagccccat gtattattgt cgtttttggt tttattcttg ttggcatttt tcatcctgag 108120tactcaacat tcagtattaa aggctcaaag tcctcgggtt tgtttgtgac atcagggatc 108180caggcattag agagtgacct gttatagaag gccctttccc aatgctgggc ccttttggct 108240tatcttaccc ttctgtttac ctgtggtaat agaagtctgc tcaccactcg ctaagtcaga 108300gtgatgctaa ggttcaccct ttgttgaagg ctccctgagc tctggctgtt gcttcagggg 108360ctttcctact aagactgtgt ctctgctaca ggaaatcccc gccagccctt tcagagtcaa 108420agttgaccct tcccacgatg ccagcaaagt gaaggcagaa ggcccagggc tcagcaaagc 108480aggtaagatg gcacgtctag gttgtcctgg gcccctctgc cagccggtgg cactgggcgt 108540gtttcatcca cggccttgag gaacttcatc tccaccaaca ccaacaccaa gctggcaggt 108600tttctgtgca gctctgatgc agcagtggct ggccaggccc gttgctggct gtcataatag 108660acctggtgct gttgaacctg tctgacgggt tctcaaagtg aaactactcc agctggtctg 108720tctcctcact tcacagtata tctttccagg tgtggaaaat gggaaaccga cccacttcac 108780tgtctacacc aagggggctg ggaaagcccc gctcaacgtg cagttcaaca gccctcttcc 108840tggcgatgca gtgaaggatt tggatatcat cgataattat gactactctc acacggttaa 108900atatacaccc acccaacagg tagggtcctt ctcccctctg ctcccctggc ccccagccag 108960gcccctttct atgcagtcgg tgctgggtca ctgtggacac caaggggtgt gagaggtgct 109020ctgccaaagt gctccctgat gggaggcagc tcctggcact ttgaacccct ctgggagcac 109080ctataggaag cccaatgggt tctatcaggt gaactgcaga attccccaaa agcaagcagg 109140aagctggtcc catatctcca cctttggttt gcattttatc agagaaatgc tcagttcttg 109200atattcaggc cctaatatct atctttctgt tacacatgtg cacacatgtg cacacacaca 109260cacatacaca cacacacgtg cattccctcg cggcctcacc agctgccttt tagtcttttc 109320attaattacc cacagaaaaa gagctgctac acctttgtgt ttccttcctg gtccttttag 109380cttagtttac cctttttatg aggtgttgga atgaggtctt ttctcaaaga gccagttcag 109440cctttcgtcc ctaaggccca gcacactatt tagggcagca aattattccc ctttacaaaa 109500tgcaggattt cacatgtgat cttaccatct aggctggctt actctgatta tttcaggcca 109560taagggcctt aaaactgcct ctctgtacaa gttaatgttt atttgtttaa aaacattaaa 109620aaaaatttgt atcgtggtaa aatacacata acacaaaatt taccgtctta accattttta 109680agtgtatagt tcattagtgt taagtgcatt cattatgtcg tgcacccatc accaccatcc 109740atctccataa ttctttacat cttgtaaaac tgaagccctg tatccattat atttgtttaa 109800aattttgttt cgcttcatgt tcacacctct ggggtctgga gagcagacat cctggcagaa 109860aagtctggat tttaatactt aagcctagtg ttcgaagtgg ttgttccaag cctctgagat 109920tcctttattc ttaagggaaa tgatcctgct gtgtttgaaa tgccatttgt aggagaagaa 109980gggcaacgct ttctgcagaa gcactgctca gaagccttgc tcccgtctgg gtcctctcag 110040cgaggagcag tcaagagtca agtggggaag aaagaggatt atagtgagga aggggtcatg 110100gtgtaactgt cccctgagtt tgggggctgc actcccttgg agatggaatc cttactgtga 110160gaacatccct gcagtgggag ggattccctg ggcgaaggga ttctgtgtgt cgtgttataa 110220atgtggcccc ttacatccag gcttgctgct gtttgtgctt tcttccccaa atttttattt 110280ttatttattt attttttaga caaaagtctt gctctgttgc ccaagctgga gtgcagtggc 110340atgatctcag ctcactgcaa cctctgcctc ccaggttcaa gcgattctcc tgcctcagcc 110400tcccgagcag gtgggattac aggcacatgc caccacacct ggctaatttt tgtatttttg 110460gtagagacgg ggtttcgcca tgttggccag gctggtctcc aactcctggg ctgaggcaat 110520cctttcacct cagcctccaa acctgcggat attacaggca tgagccactg cgcctgacct 110580cagtatttgt ctttttgtga ctgatttatt tttcttccta tatgtcctcc atgttgtagc 110640acgtgtcaga acttcattcc ttttcgaggc tgcattccac tgtatgtata tatgttttgc 110700ttctctcttc gtctgttttt tgtttgtttt ttcttgagac tcgctctgtt cctcaagctg 110760gagtggcact gtctcggctc actgcaacct ctgtctcctg ggttcaagtg attgtcctgc 110820ctcagcctac cgagtagctg gaagtacagg cacgtgccac catgcccagc taatttttgt 110880atttttagta tagatgtttc accatgttgg ccaaggtttc accatggggt ttcaccatgt 110940tggccaggcc ggtcttgaat tcctgatctc aggtgatctg cccacctcag cctccgaaag 111000tgctgggatt ataggcatga gccaccgcgc ccggccatct tcatttgttg aagaacattt 111060gggttgcttc cgtcttttgt ctgttgtgaa taatgctggg tgtacaaata tctctttgag 111120tctctgcatt taattcttgt gattataaac ccgaaatgga attgctggat catatggaaa 111180tctcttttta attttttgag aaactactat actgtattcc acagtggctg cactacttta 111240cagtcctgcc aacagcatgc aagggtcctg gtttctccac atccttgcta acatttgttt 111300tttttctgtt tttttttttt gttgttgttg ttgttgttga tagtgaccat cctgttgagt 111360gtaagatggt gtcttattgt ggttttgatt tgcattttcc taatgattag tgatgctgat 111420catcttttca tgtgcttatt ggtcctttgc atattttctt tggagaatta tctacttgcc 111480catttttata tcaaccttct taattttatg ttgagtttta ggaattctcc atgtattctg 111540gatattagtt ccttatcaga taaatgattt gcaaatatat tctctcactc cttggtttgc 111600cttttcacgc cgttaacagt tctcgtgtgc aggttataaa cgcggcttct tatctccaga 111660cttgctcttc ctgtgcttta aaataaaaaa tccaaaacaa aacattcatt attagtaatg 111720ataaaactaa cacttttata gatagagcat tcttttctca tcaggccact caatagtaag 111780taggtaatta ttttcctgct gatggttctg agggttggtg ggagccttac tactgggtgc 111840accacgctga atcttctttg ttgccaaatt ctccatattc tttaggagaa agcaccagaa 111900agccatagct gtctgcgtac aatgactggg atcacaaggc catgacgtct tctaaaaaca 111960ttttgtgact tctgctttat tctatgtcta tatgcctttt agtgttttgg ctgagccgtt 112020agaaagtaag ttgcagatat caggacaggg tcagggtttg acctgcatcc ttggaaagga 112080ctgcagaacc cagtacccca gacgtcccct gctgctggtt gaggcagaag tggagattag 112140gagcctaggt ccggttttgt cccctttgaa gtaatgctgg agtgggaggc tccttacttc 112200agagtcaccc caaggtcaca ttcatccagt tctctgatag cagcaggttt gagaactgct 112260gccatgctga gtactcactt agggctttgt gtccggatgc tcccaggatg cattcaagga 112320gccgggtggg ccttggtggc ggtcgttgcc accaagtggc aacatccaag ctgcttgaag 112380ccacccacaa ccccacaacc aagagaagag aagaccaaag tcctcaggta aatcacaagt 112440gtgaatgact tgcagggtgg cactggggtc cttcttgttg tttgttgctt ggagctgggt 112500ttattgtttc attatttggg caacttgcaa ttctgcctat ttttctatgg caaagaacac 112560attaaatctc tccttagatt gaatttcctt cccaccccca cccccagcac agagcctggc 112620cctataagtg ctctgtgtgg attaatggct gtgagtgagc gaataaatga catggcgcct 112680ggattcacaa gcggagatgg cctaagaacg ttgtaatctg gtagaggagt gatgccaaca 112740cctcctcatt ctcctttgaa ctctgttttc tgaagagcag ctaaaagctc aagactgggc 112800taaggaagtg tgcccttgga tgtggttaag agacctgggt cagcccagaa agccaccccc 112860tgacacgggg gagggagcat actttgaggg ctgacaccca caggcacacc ttctcatggt 112920agttttaggg tataacaggc tggaaatccc cagaaaggtg gctgcttggg catgggtgtg 112980tcctggcctg gtgtgggcgc ttccccctca gaacacaggc tgtgccacgt ggggagccga 113040ggtcctgcct gagtaaccca ggtccctgat tgctggtttt gctccctgac acctgcaggc 113100ctgccactcc acctcgcaaa gtccctgagt gacagcttgc aggtgcttgc ctgcctgggg 113160tggatgagtg atgtggatgg ctgtaggatc ctgtgagtcc cttgaggatg caaaagtaga 113220gcgcgttttg ccttagagga atggacttgt tggcttgggg cttgaggacc ctcccagagg 113280tcaaagactc ggttttatag aagggaagtg atttccctga ggactttggt cttctcttct 113340cttggttgtg ggtggcttca agcagcttaa atttctcacc gcacgttccc ctgcgcagag 113400cagtttgaga agctggtggc aatgtctcca ttacgtgctg tgctgggagc cactaggatt 113460ggggaccact ccatgtagta ctctggcacc tttagaaatc cctgtgagct cacagaccct 113520cacagagtaa cagcttctac cttgaaatgt tcttaacgtg gtggtcctgg ctgctcctgg 113580agggccctaa aagggatggt gctgagggtg gctctctcag tcccatcctc ttctgagctg 113640tctggtcagt gtcttgtgta tgtatatttt gaagaataag attcaggttt cagaagcatg 113700tagaggagag tgaaactgtc ttgcagcctg cgaagtcgtg gcgaaatgca ctggccatca 113760ctacccagac atccctcact tcatagccct gttggggaat aaacacagtc cattccttag 113820ttggggcctc aggggacact ttaaaatgct gtaggcattg taggtgtaaa tctccgagat 113880tttttccctc ccccttctta ggttatttaa ggtacagttc attttctatc tgagtttttg 113940ttttgttttt gactggtaac aagagcatac tttcttttat gggatgggtg ggcttaactg 114000gaagagggtt tttccctctc ttttttagca cttcagagaa gaggccagaa aactttatgc 114060gggtgaggga ggaggtatcc ccaagacctc tggttagcct gaggtctgct tagtgagccc 114120ctgaattgtt aggggctgtg gggaaacgga agctcgggaa gagttggcac gttgggaatg 114180ccacgttggc tgaagtagcg agtcagtcct gccttaaaca gtacaaaaag gagacctttc 114240ctgccccttg gctggctccc agctctgttg aatttgacct gtacacattt taccaggaaa 114300tgttgttcac atgaggcagg gggccaattg gttttgtgtg cagtgcttaa aaatgctgga 114360aaattaatcc tctcttcatt gatgcaacca gttttttttt ttttttcttg gcctttaccc 114420ccttccttat tacaaaagga atgtgacaaa atatacatag gccaaatgct acaccctttt 114480aacacttgat cagcaacagc tttcagcagg gcctgcattc cagcaaggct gctggattct 114540tggggggaac tcgtctctcc ctcacacttt cctgttacat tatgcctggc cgattgtggt 114600gaaggggatc ttgatctact gagacagcca tgagatttct tggagcctcg atttggaggg 114660agggaacttg gccaaccatg gagagaagaa gccggctgtg tgccagcctg gaaccggcga 114720gaggagagaa atggcgcaca catggctatc gcgtgccacc cggccacccg tgagggtgcc 114780tgccaatcct gcaagcacca tctgccttca cacttgcaat tttattttct ttcacatgga 114840aatggaagtt cagatattgt gcgatggtct tagcacaggt ctaggtgaac tcttgcaaat 114900ccctgttgca gcctgggggc ctcaaactga ttcctaggac agaaatggtt ctgtttggtg 114960agtggcccca ggcccagctg cactggctgg cactgggtat gatgatgggg aggtggtgtg 115020gcagagcagc taggacacag atttgggggc catgggtatg aggcccagct cgcaccctta 115080ccaaggtgtg tgacttgggg cacgttcctt taccagtctg agccacagtt tcctctcctg 115140aaaaaatgag atgacagtag gaactacccc ttaggactgt tttgatcttg aattgaggaa 115200atgcataaaa gcacatagca tggtgcttgg tgtgtagaaa atgctcatta agttgcttct 115260gttattatta gctgctctta tttgatctaa tttttctgtt attcttgcct tgtggtcaaa 115320agctagaaga aatagatcta agatactttc tacattgatt ggaatcaagt ctcccctgtc 115380cgtgagaaga atgagggatc ttgaggggat tttaaatgcc aagttagctt tttggtaccc 115440aaaggtaaac tgagttttct ctcttgttcc agggcaacat gcaggttctg gtgacttacg 115500gtggcgatcc catccctaaa agccctttca ctgtgggtgt tgctgcaccg ctggatctga 115560gcaagataaa actcaatggg ctggaaaaca gtaagtgcct gaatggagag cagatgggtt 115620gttgatgacc ccccaacgtg gctgctggtt agattttctt caaaaggtga aatttgcaga 115680gaagcaaatt ctatgttaag agactttgca gttgcacaga ctttggttcg aattaaggcc 115740gtggtgtgaa gtaactgtga ctgtgtctgc cccttagcca caccgagact cagctttctc 115800atttgtacag tggggggtgg tcggcgggga gaggttgaga acacccatgg gaatattttg 115860aaaattatat gagctaatgg ttcagaggct ggcacgtagt cagccccctg gcattgcagt 115920aggaagtttt cattaaaaag agaatttggg ctatgttgct ttctgatgag tttctaactg 115980tgccagctat ccttggcaac tgaatccgca ctaaggttgc gagtcaagca taaatgccaa 116040atccctggca ctcagaagtc actaccacca cacctctgcc ccatcccaat gttcctttag 116100cttgttaggg attttactag tataagctca tttcgcttat tttcaatttt ctgattattt 116160tttagtaggg aaaatttcaa acagaaaagg aaagagaata gtataacatg aacactgatg 116220tacttatcac tcagcttcag atgtgcaaca catgctcata aaatgatttt tttatacaag 116280taaaaatata tccatttttc atctaaaaaa cattacagtt aagggataat tccactttaa 116340ccctcacctc tccttctccc tagggttaac caaagttttc aattcagttt ctgttcttcc 116400agatcttctc tctgcatcta tacatataga tgtgcctgtg gaacacattt ggctgtattt 116460attttgcatt aaagttgccc tgctgtataa acctacttct tcggcctgcc ttccaacagt 116520gcatctcggg aatcattcac tcctacatct tttccgtctg tgtttactgc tgagtggctc 116580cagactggat gtacctcagg gctcacattc acctggtttc aggcttactg aggcagggct 116640gagtgcatac ccccaggacg gggcctcctg tattcacctg tgagggtttc tccagagtac 116700cactagcagt gccattagtg agcatcttcc ttcactcgtg acccaagtgc acaagttgca 116760agcaaggcca gctcccagtt gcagagatcc aaagtgagag ctcactgttg gcttttgtgg 116820ctggagcagc cagctctgag tgtgtaaacg tccactgccc aaccctgtca tgtgtcccct 116880tgtcactcct ttccccaaga cactgagagc tttgactcca gaacaggaaa agcagggtgc 116940caattaggaa agcctctttt ccggtgggaa gtagcgatcc gggacctcct tgcctgtggt 117000tcggcagtgt ccatcttgcc aggccctatg ttccttcaga gtcaaggttc tctgggttgt 117060ggcaggggcc ctgtgttccc agtgcttttg ttttgggtaa agtcctttcc ctgttcttgt 117120ctaatctaac acttgggctt cctgcagccc tgctttgcag agaccttttg gaaaccatca 117180cggtacagtc agttctcagc acttgcttca atcggctcgc atttggcagc tctgtgactt 117240ctgctttctt gagggggagg ggtgcctata agatggagtt ggctgccaag aattagtaaa 117300taaaacattg acttatgagg gtgtttggat atcaagttaa caccaaaagt aagtaaataa 117360gagacgacag tgtcagatta caactttctg gtcagcaaag attgtggggt caggtaaatt 117420tcactttgag tcccagcttg gcaggctgct gcatatgtca ccctggacaa gttacttaac 117480ctctctgagc atcagtttcc ccatctgtga aagccattgg ttaataataa ataccccata 117540ggattgtggt gaaaattaag acaataacct atttgtgctt ggcatataaa atgcattcag 117600taaatgatag ccgttattgc tgtcatcact aattgattat tgtgccgaca cttgttgtta 117660ctgaggctga gatgctgatg atacttactc agctttgctg cttgtcctct gcagcagctg 117720ttgcttacag tggaggctga gataagtccc cgtgtccaaa gaaccattgc ttctgtgctc 117780tggattgttc ctgctgctga aaagggtcag ctcttcacct cagcttgtgt ttcttttcca 117840ggggtggaag ttgggaagga tcaggagttc accgttgata ccaggggggc aggaggccag 117900gggaagctgg acgtgacaat cctcagcccc tctcggaagg tcgtgccatg cctagtgaca 117960cctgtgacag gccgggagaa cagcacggcc aagttcatcc ctcgggagga ggggctgtat 118020gctgtagacg tgacctacga tggacaccct gtgcccggga gcccctacac agtggaggcc 118080tcgctgccac cagatcccag caaggtcagc ctttgctttt gtcccagaac ttgtctcatt 118140gctgtcaaac atgacaccat agtccttctc tggttcttcc tggcaaagac cttctgaaaa 118200tcgttttgtg atgaaagtta gcacaattca ctgtgaaagg tcccctgggt aggtgggtca 118260caaccctgct cctcctcttg ctctctgact acaagacttt ggtgaggggc tccctgtccc 118320agagtcttct ttcttcgctt gttagcataa tcacagtcct cactacaaag ccagcctgta 118380aggggtaggt gagttagcaa acgtggaggc ctctgcccag cacccagctc acagacggag 118440ctcaccctcc agaagctaga atcatgtaat ataaaaatac attattctgg ccaggcgcgg 118500tggctcatgc ctgtaatccc agcactttgg gaggccgagg cgggcggatc atgaggtcag 118560gagatcaaga ccatcctggc taccacggtg aaaccccgtc tccactaaaa atacaaaaaa 118620ttagctgggc atggtggcgg gcacctgtag tcccagctac tcgggaggct gaggcaggag 118680aatggtgtga acctgggagg cggagcttgc agtgagctga gatcacacca ctgcactcca 118740gcctgggcga cagagcaaga ctccgtctca aaaaaaaaaa aaaaaaaacc acaaaaaaaa 118800acattattct tggctgggcg cagcggctca cgcctgtaat cactgcactt tgggaggcca 118860aggtggatgg ataacttgag gtcaggagtt tgagaccaac ctggccaaca tggtgaaacc 118920ccatctctac taaaaataca aagattagct gggtgtggtg acgcatgcct gtaatcccag 118980ctactcggga ggctgaggtg ggataatcgc ttgaacctgg gaggcagagg ttgcagtgag 119040ctgagattgt gccactgcac tccagcctgg gcaacagagt gagattccgt cccctccaaa 119100aaaaaaaaaa aaagttcatc gtcatttctt catagtaacc ctgactcaag gggttttgga 119160agatttccag tggtctcaat ggtgtgaatc ctatgaaggt gtcttatttg ttgaattaga 119220ggtgaaagcc tccttcctca ctctttttta gaaacagttt agttttatta ttatgcagaa 119280tttgttgagc aaattgcaac agcccaagcc acagctagct ccacaagagc ccttccatga 119340gccctcaacc tgggatctcg tgtatctttg ttggaatgga cattaggttt ccaagtccag 119400gcctgtgatt tagaagggtc aggttgggta ggagagagga gagtcttgga ggggctgctc 119460catgggggtc acacctctct cctgtgggtt ttcgctggtg attgagttct gaggcatttg 119520ctgcattgac tgttgtagct ttaactcgtg tgcacgtgtg acacataaag ccccaagaga 119580agggctgcct ggctcagatg cacttccatg ctgattatat gcatgggtgt tgaaagcagt 119640gctggctgag cagcgatccc agtgcagttt gactttattc tttgctcaaa taggtgaagg 119700cccacggtcc cggcctcgaa ggtggtctcg tgggcaagcc tgccgagttc accatcgata 119760ccaaaggagc tggtactgga ggtctgggct taacggtgga aggtccgtgc gaggccaaaa 119820tcgagtgctc cgacaatggt gatgggacct gctccgtctc ttaccttccc acaaaacccg 119880gggagtactt cgtcaacatc ctctttgaag aagtccacat acctgggtct cccttcaaag 119940ctgacattga aatgcccttt

gacccctcta aagtcgtggc atcggggcca ggtctcgagc 120000acgggaaggt gggtgaagct ggcctcctta gcgtcgactg ctcggaagcg ggaccggggg 120060ccctgggcct ggaagctgtc tcggactcgg gaacaaaagc cgaagtcagt attcagaaca 120120acaaagatgg cacctacgcg gtgacctacg tgcccctgac ggccggcatg tacacgttga 120180ccatgaagta tggtggcgaa ctcgtgccac acttccccgc ccgggtcaag gtggagcccg 120240ccgtggacac cagcaggatc aaagtctttg gaccaggaat agaagggaaa ggtgggtttc 120300atttaaaaaa aaaaaaaaaa aaaaaaagac aagctgggac ttaagggcta cctgaaactt 120360ggagctgcaa actcagccac ctgcaggagc caggtgacat ataaggcggt gctcacctgt 120420tccctctgcc tcggggagta gttggggggc cctggtgaag gttaagcaca ttgcatttct 120480ggggaccgtg ctactcaacc cctgttttct gtttctccat ggggaacagg acctagcatt 120540gtcagcagaa tctctagttt tttggcaaag gcagaaatct tgatttttct ctggaaactc 120600aacatacaac atgttggcat ttaattggaa aaaagtttaa aatgtagtgt tgtctaacac 120660ctgcatgcca cacagcaggt tagtcttcaa cctttaacct gtcctcgagc ccggtgtgag 120720cagtcgtgtt gtcacttagc cgtggctact ctagaaaggc cttctttggg atggaggggg 120780ttaatattct tgatttgaga gttagaaaaa ccagttttcc agttactgaa attggacttc 120840atgtgtcctg aagtgccaag aaccttggtt ctggggtttg cttttgggtc tggggtactg 120900gtggcagtgt tagctatgtg cttgctctgc agatgtgttc cgggaagcta ccaccgactt 120960tacagttgac tctcggccgc tgacccaggt tgggggtgac cacatcaagg cccacattgc 121020caacccctca ggggcctcca ccgagtgctt tgtcacagac aatgcggatg ggacctacca 121080ggtggaatac acaccctttg agaaaggtga gccgccctgt cctcggactg gaccctcgtt 121140cagagctgcc cttggtcatt gcctcctggt ggctggtact gatgcctgcc ccatgtgcta 121200ggcctgtctc agcagggcca cgtgcagagt gacagagtgg aagtcagcgt ccgctgcagt 121260cacctgccca ctcagtgcct ggcttgctgg ccttgtgtaa taggtgggct gggtttagcc 121320tcagtctcac ctcagcaagt tatggggtaa tgtcatgatg ttgctcattt gtgccatttt 121380tctttgcgta tgaatttctt tcttcttgag tattaggaat tataaaaaat ttcaataaat 121440agaaaaccat aaagaaaaaa aagtgccatg tatatctcca ctacctggag atcggaagcc 121500tgcgatattc tgatatagat attttcagtc ttcttgtgga tgcctgtttc ttctgtttca 121560cgggtttcgc tttttctttt ggttaatggc tggatggtgt tttcccgaat gagagtagtc 121620tgtttaggat gactgacttg aatatttgct tggttggggt ggagtggctt atgtgactgc 121680agatagacgg tttgtattat ttaaaagtca gatcatacct acattactgt gggattgttt 121740tgttttgttt tgaaacagga tgtcactctg ttgcccaggc tggagtgcag tggtgtgatc 121800acggctcact gcaggctcaa cctcctgggc tcaaatgatc ctcctgcctc agccccctga 121860gtagctggaa ctgcaggtgt gcaccaccac actcagctaa tttttgtatt ttttgtagag 121920atggggtctc gccatgttgc ccaggctggt cttgaactcc tggactcaag tgatctaccc 121980acctcggcct cccaaagtgc tgggattata ggtgtaagcc actgccccca gccacattac 122040tgtgttttta accccctttt ccaaataaca tagtatagca tgcagacttc gatgctagat 122100gaaactctga agtagagaat catttttcac aaatagggga tttgtatgca aatatgcgtt 122160tctgtttgtt gttttgagca ggtctccatg tagtggaggt gacatatgat gacgtgccta 122220tcccaaacag tcccttcaag gtggctgtca ctgaaggctg ccagccatct agggtgcaag 122280cccaaggacc tggattgaaa gaggccttta ccaacaagcc caatgtcttc accgtggtta 122340ccaggtaggc aaggccctac atttggtgtc ttgagtctca cttttgtggc tagattctac 122400ctatgtgtca tggtttccta acttttgata agatgaattt ttatttttat aacatgtatt 122460tccttctgta gagacttatg ttacatagaa agaccaagca tacctaaaaa acataccaaa 122520gcacttgata atggtcatga aactatttag caaaccagga gtcaatcaag ctctataact 122580tgataatgta aaaatttgta gccaaccttg taagtatttt tattaaagtt ggttgcaagg 122640catatgcctg cgttgtactt gcagtcctag ccagtgcaat tagataagaa aaataggctg 122700ggtgtggcgg ctcacacctg taatctcagc acttcaggtg gccgagacgg gacaattgct 122760tgaggccagg agtttgagac cagcctggcc aacatggcaa aaccccatcc ctacaagaaa 122820tataaaaatt agctgggctt ggtagtacac gcctgtaatc ccagctacta cttgggaggc 122880tgaggcatgt gaattgcttg aacccaagag acataggttg cagtgagccg agaccgcgcc 122940actgcactcc agcctgggca atggagtgag actctgtctc aggaaaaaga aaaataaatg 123000aagcataagc attgaaaatg aggggtcaga gtgtctttac ttacattata ctaatgtgaa 123060attccctatg tgagaggtgt agtaattgag ttggggtggc tacgtggaat agtttataaa 123120gggaatttgc atgaattttg gcaataagca gaccagcata aataaatggt gcacatttca 123180ctttcttttc cactctttcc agaggcgcag gaattggtgg gcttggcata actgttgagg 123240gaccatcaga gtcgaagata aattgcagag acaacaagga tggcagctgc agtgctgagt 123300acattccttt cgcaccgggg gattacgatg ttaatatcac atatggagga gcccacatcc 123360ccggtgagct attcctcaga gaggacccca gagaataatt gattttgcag gaaaatgggt 123420ttgattttgg ttatctctct gagtggggaa aacaatctga tatttgtaat agctgcaaaa 123480ggagagtttt tcttagggct acatctccaa gattatctca actcccagta gaaccggtaa 123540catggcaaaa agcatcggct tagaattttg actggaaaca gttgtgcgtg tgttggagga 123600cctagttctt gattcagggg aaagctggtt ctttacaaag ttgaaaatca cagtggctca 123660cacctgtaat ccccaaactt tgggaggcca aggcatgcag attgcttcag gtcaggagtt 123720tgagaccagc ccaggcaaca tggggaatcc ccatctttac aagaaataca aaacttagct 123780gagtgtgatg gtgcgtgcct gtaatcctag ctatgtgggg tgggggctgt gatgggacga 123840tgtctgagat gggagcctgg gaggttgagt gagctgagat tgcgccactg cgctccagct 123900tgggtgacag aggaagaccc tgtctcaaaa aaaaaaaaaa agaaaaagaa agaaaatttc 123960taccttattt tgtgcttggc tccttattca tgtgtcttgg tttctttttt ttcactgaca 124020atactagtag ctgatcaaga tatgcagatt caaattcttt cttttgtatt tagtgatgtc 124080atgtgtaatc actgtgaaac acggtttctc aactccggca ctatgacact ttgggctaga 124140tgattctttg tggtgtgggg ctgtcctgtt cattgtagac ttttgtcagc atccctgccc 124200tgtacctgct agatgcccat agcagacttc tccttcccca ttcttatttg tggcaaccaa 124260aaatgtctcc atatcttgcc agatgtctta agggacaaaa tcacttcagc ctgaaccact 124320gctgtaaaga ttcaaacaat aaataaatat atgacttaag tagtgaaaga ccctcctcca 124380tttgttttgg ggggaggact ctccataggt tctagttatc tactcaaatg attgtcaccc 124440ccacacattt tatttattta tttcaatagc tttggggtac aagtcgtttg tggttacatg 124500gatgaattct atagtggtga attctgagac cacctccccc gcccccattt ctaaaagggc 124560aggcaagtgt gtggtgtgga cagaagaccg agggctgggg ctgttctggg ccacttatgc 124620cttgtcttag gtgtggtgtg aagagggcaa agccccaccc caggacccca ggagcagaaa 124680gagcctcagc ggggtcttgt tcttctttct ctgggtcacg ctgagagggg aagggcaggt 124740tgaggggccc actgctgggt tctgggttaa ctctcaggca gctggagtgt ccactgacca 124800cacgctttcc tgattccatt cctgcttccc ccttaccaca tggaaatgtg cacacacact 124860cacactcact ctctctcaca ctgatcagaa agtattgaca ttcaactcag actgattcta 124920ctcagatact catttaagcc tcaagtcatt taaaacaaca tgtttctcct caaacttgtg 124980cttgcggctc attcaatata gatttaaaaa attcctataa tcactagtct aggggacttc 125040agctgtgggc aagacaaagt tcctgccctc agggagctta ctgtctaggg cttttacaac 125100taaaacttgt gatgactgct atgaagaatg agaatggggc tcggtgacag aattcagagc 125160tacgggcttg ttttggagtt ttgtaacact tgcgttagga gagagttggg cacaggaaac 125220gggtagaagg ctgctcccag gaggggtgat gtggctccga cctggcaggc aacagtggag 125280atgaacatct cctgtggcaa tgaaactttt tgactatggg gaaaggctgg tgagtgccac 125340cagcttccga atccccctta cagaaagggg tcagagtttg tcccctgtgg ccgacctgtg 125400agcttaaagc aaatggtcgt ctttgagcat aacaacagaa agacactcat ttgtggtttt 125460cccatcaggt gtggatggtg cctttttatg tttcaggctc tctgttgcct cccagagagc 125520caaatgccgg cttttccaga accccagaac tttcccaggc agagatattt agtgaagtgt 125580tggttggttt tctaagcatc aggcttctta gctaaggcaa cctatggggg tactgccggg 125640aaacagtcgg ctacctgcca ccttctaatt tgctttcatg gtaattctgg gtgcttaaat 125700attagcctag tttttcctgg cctggttaaa aacccggagt ggagttattt ttaacaacgt 125760gtcctgtctt acccgtaatg gcatgttgat ttcctgtggt aggccagctg tggttggttg 125820gtggcggctc cctagaccac tggattgact ggggttcaga gtgcatgagg aagaagatct 125880ggcatgaggg aatggtgaca tgtgtctggg catggaacag gggagtggcg gataatgctt 125940ggggtctgcc atcttggaca gtttatctta cccgggtttg ttggtttttg gctactctca 126000tgctgagctc agacaacttc tagtggaggc tctgacttaa agattggcct cagaggtagt 126060cccttgccat cagctgttga cattgaaatc ctcaactgtc actctctaaa gtaaagcccc 126120cttttgttcc tctcacccca gtgtggaggc ctgtgcttgt ttgccagggc cagccattta 126180tttcacgtag ctaaagacct ggatgccgtt gaaacccagc tgttgttaga aagccaggga 126240ctcaattctt tgtgtgtctt ggctgtctac catctctaat tctacaaagt ataaattctc 126300tgggatgcaa agcagagatc cctcagcttt cacggcagtc attaactttg ccagatacca 126360tggggagcac caggactccc atgcgaggca gaggtgcacg tagccccttg gtgatgggcg 126420tggtagcctg aggcatgctg ccgttcgctg gatggggagg tccccctcca cagtggagtc 126480catgagtgtc cttggcctag cccttgtttc tctgtttagc acttctctag caaatcacta 126540tctcctctcc tcgactcctc tgtgcttcat ctttaaaact gacaccctca aggagtcaga 126600ggccctcagg gtcccccggg gggtcagcca tgtagcagga gctcagctta cactcaggaa 126660gacggcaagg cttcaccagg tggccgagtg accgagaagg ctgagtgtgg tcagaaggtg 126720ccagctgcat tggagggaga ggagtctggg ggacacacag gagccatgtg tgggggacag 126780ggctggatgt gggctgcagg gcctgcccat ctctctccgt tctgttgttc caccacttgg 126840cttcctcctt cagttgctcc agcagcctgt ctcctccctc gcctctaggc tcctgcatgt 126900gctgaggcct ctctacttga agcacctctc tgtctgctcc ctcttgtgcc gcaactgaga 126960tgttactgga aagctttctc tggtctcccg cagaccaggt taattgcctc ctgagtgctc 127020caccttccac accccaaata tgttatgtag gatgttagag tgacttgctt gcctcatcct 127080tctcctgcag ttgtgggttc ctggggggtg ttaaccgctc aggatccagc acgtggcaca 127140acatctgcac gtagtaggtg ttctgtgaga atggttgaca acaatgagta ggcacatgag 127200cagtgcacac agtgaggcag ggggagctga ccgaggcctg catggccgag gtcccggggg 127260agcagcagtg ctattctggg tgtgcacaag gtggtctcca attcccagct tgtgctcaga 127320atcccacaac ctctcttcca ggcagcccct tcagggttcc tgtgaaggat gttgtggacc 127380ccagcaaggt caagattgcc ggccccgggc tgggctcagg cgtccgagcc cgtgtcctgc 127440agtccttcac ggtggacagc agcaaggctg gcctggctcc gctggaagtg agggttctgg 127500gcccacgagg taagtgtgca ccctgccttc ctgcagacat tcatctgccc caggcagggg 127560cagctgtaac ccagagcaga tgctttgctt ttgagtttgc tcatgagctt aaaattaaat 127620taaaaaaaat tattgtttca tttctagtta aacagtagaa attcctgctt acaagtaagc 127680aggcttgtta tttctccagt gatctgtccc cccatttaat aatatggcta tcaatttctt 127740agaggaagca gcagtatttg ggctgtcata tgtaatatgg tggcgactgt ttcattatgt 127800gtttcagcat ttgtgagggg gtgggttgct ctggatgtgg cagatggtgg ggtttggagg 127860tgataactca ttgagatatc ttggtgtcca tgtggtacat accagaacct ctgggaatgc 127920caggcacatg atgcacgtga tacgtggctt tgtcattgtc ttagttcccc agagagagag 127980tgtgtcttgg ggaatgggct ttgttggcaa tttggcctgc cttgttggca gcttggaact 128040tgggtttggt aaggctagcg ggccatatag ggacaaagcc ctgaagtgca ttggaacttg 128100ccttttttga taagtgacca tgtttcctcc tccagcactt aaaatgtgcc tttctcccac 128160atagaggaca gtgtgcctaa tttcttacgt aatctggatt ttcctcgcca atgatatgtt 128220cttggattca cagaagtggc aaatggggtt ttccctcttt gaagaggaac cttctccttc 128280atggggttca gcaggaggtt ttatcttttg aagctcaggg cagaaatggt ttgggggaaa 128340ttaggtcatg ggtctgggat cagattctgt gaagttactg agcttcagga cctgcatgtg 128400tttgtgtgca tgtatgtgtc cctgtgtatg tgtgaatgag agagggagaa aaagaagaaa 128460gagaagcttt acttggatat ctgcctctat tatgaaggac tctcaagtaa cagccttttg 128520attttagctg acgacacgga ttcccagtca tggcgcagcc ccttgaaagc cctttcagag 128580ttctttaaag gtgacccgaa gggtgacttt aataagacag gtttgcattt tcccatggct 128640gctgaattat gtaacccaaa tgcttcttgc tggcctcact tctaaaattg cttacacctg 128700cctcatctgc tttgcttaat gagcatgcca tcctttgatt aacctaccct ggagttgacc 128760catccttgac tgtcacgttg gaagctggga tctggactct gcaacccaac gcgtgccttg 128820attatgtttt agcataatct ctaacatctc cacaggcttc accttgaggg tccccttgcc 128880ccatgagatt ggcaccctca cctgccctgc acctatgccc cagcatgctg gtaccacagt 128940gttctttgct caaaggtggc cacaagtctt gactagccag cccattggtt aatttttgct 129000cttcacaatt ctggactctt tggcagtgtc tcagctgtag agtaaaattg ccacatccta 129060agcgtgccta accagcttga aaggttatat tgtgtcttca acacacatca tccacataca 129120ccctccagca gcaagcacag gcagtctcct taattatact ctagggcaga ctgagtgtat 129180tttagccaac aaaaagctaa aggtgtctct cggggtcatt tctgcaacca tgaattgggg 129240atcctgtgat ttttttcagg cctgtgatta tggttgctgg cctttttgtt actcatcagt 129300ggaaaccaat agctcttggg gatggatgtg gtcctatttc agactcagcc aagggtggag 129360taaaggtgag gccaggcagc tccttaaacc tctcatctct gtcctcaggc ttggtggagc 129420cagtgaacgt ggtggacaat ggagatggca cacacacagt aacctacacc ccatctcagg 129480agggacctta catggtctca gttaaatatg ctgatgaaga gattcctcgc aggtaagctc 129540catccatctg cccatccatt cctccatcag tctatctgtc cacccatcca ttcctccatc 129600agtccatcca cccatccgtt cctccatcat tccatccatc cactcatcca ttcctccatc 129660agtccatcca tccacccatc cattcctcca tcagtccatc catccatcca ttctttcatc 129720attccatcca tccacccatc cattcctcca tcagtccgtc tacccattca tagaggcagc 129780aagtattaca tagaacctgc aacttgtcac cacacactag ccttgatatt tgtggctccc 129840gctctctcac tcccccagtt cctttcagac atctttagtt taaaggtgag ctgaaattaa 129900gaagttggaa atcctaacca cgtgtggtgg gattcgcctg taatcccagc tacttgggag 129960actgagatga gaggatcact tgagcccaag agtttgaggc cagcctgggc aacatagacc 130020ctcccctgac atctctggaa aaaaaaaaaa aaaaaaaaaa aaaaaagcaa tagtagtaga 130080caatcattga tgaaataaat aatttattag tttattagag gcttcctttt ggtgttttgg 130140tgaacctgca agtagttttc tgattgggac aggacaaagg tctttacttc agggtttgct 130200tgataaaagc atttccaaaa ggttttacat agaaaccttg ttccttgttg atattaatac 130260aaaaaaaaat gttacataag ctcttcacct cttggaacaa tctctaaggg ttttcttttc 130320tttttttaaa aaatcatgcc ccttaagatg aaaaactttc acccatatcc cctaacacat 130380attttatata gagataagca tattagctct atgtagaaat atgtaattta taaattacat 130440ttgtatattg ctttactaat ataccatgta ccatatgaag catactatag aataattata 130500gatacagaat atagaataag atgagatata aatattaaaa ctgaagttcc agtattctct 130560ttccatttgg tgaccatgat cttagcataa caaaagtggg gtaaatgtgt ttaaccctgt 130620gtttcccaaa ctaatttgtg aactcttcct ccccaaacta cttgtatccc ttggaacaga 130680ggtccccaac ccttggagcg tggactggtg tgggtgcacg gcatgttagg aattgggccg 130740cacggtggtg ggtgagccat cattactgcc tgagccctgc ctcctgtcag atcagcagct 130800gcattagatt ctcataggag tgcgaaccct attgtgaact gcacatgaga aggatctaga 130860ttgcacactc cttgtgagaa tctaactagt gcctgatgat ctgaggtgga acagttttat 130920cctgaaagca ttcccccacc aggccccctg gtcttctacg aaaccagtcc ctagtgccaa 130980aaaggttggg gaccgctgcc ttggaacaca ctcaggacaa aaccagtctg tcatatgatg 131040gttactacct catagttgta aatttctgct agacttaggc accttgacta actcactgtc 131100ttatctgctg tagaaatccc cttttccatc ccactcttat gtgtaagaaa agtcagatgc 131160agctgggttg acatgtatct ttattgacta gggtgtgtgt gtgtgtgtct atcaagtccc 131220ttcaaggtca aggtccttcc cacatatgat gccagcaaag tgactgccag tggccccggc 131280cttagttcct atggtgtgcc tgccagtcta cctgtggact ttgcaattga tgcccgagat 131340gccggggaag gcctgcttgc tgttcaaata acggtaactt ggagttattt tctgagccaa 131400accttaatcc taagacttaa tttctgggcc agatttaaga acaagggttt caataaccga 131460tttctgactc aatgcaagtt gtttgttaga ttttcccacc aaagagtcag taaatgtgca 131520gaagcagaag cagctcacct gagagatttg agggtgtagc tccaagaacc actttttggt 131580gaattttcat gtttttttac tacatctatt cctatgtttt tatttttatt ttttttaaag 131640atggggtttc accatgttgc ccaatctggt cttgaactct cttgggttca agcagtctgc 131700ctgcctcaac ctcccaaagt gctgggattg cagacatgag acactgtgcc cgtcccctat 131760gtttttattt ttaaatgttt taaattactc tttggttcat ttaagactaa gttatgctgc 131820atatcacagt aaaccttaaa ataagagtgg ctgaaataaa tgagattatt ctctcttgtt 131880aaggaacccc aggctaagcc acctgggtgc cctgcagctc accaaggaag tcagctccat 131940ctctctgctc ctctacctag catgtggctt ctgtccttaa ggtctcctcc tggaccataa 132000ggctgccagt gctctggcca tcacatccac atggcaggcc agaaggagga agaaagaagg 132060gaaaaagggg tcctcccagc tcagtgggct ctcttaagca gccctgccaa aagtccatca 132120tagacttcca ttcccttctg atttgttggg ggttggtcac aattcacatt acctagtggc 132180aaggatgcta ggaagtggat tcccatcttc tgggagcggt gcacctagct aagagttatg 132240gtcctgttaa taaagagaaa agggagactg gatgtggtgg tgtgtgagca gaagcctctg 132300cctcctcccc tccctacatt tcagaggatt tcgagctaaa acactcttgg ttcacctgac 132360aacaaaatta ctaaaaattg gccatgtctg tcatggtgtt aaagggatct gtgaccctct 132420actctcccta ccaaaaaaca aaacaaaact agattgtatt aagccatcaa ttctgtctgt 132480ttccactaga ggcactaatt ggaaaatatg tcagggtttt ccatgaatgt tttctacatc 132540ttgacaacat cctaaatagc atttctctat gatccacagg accaagaagg aaaacccaaa 132600agagccattg tccatgacaa taaagatggc acgtatgctg tcacctacat ccccgacaag 132660actgggcgct atatgattgg agtcacctac gggggtgacg acatcccact ttctccttat 132720cgcatccgag ccacacagac gggtgatgcc agcaagtgcc tggccacggg tgagtacagg 132780gcatctcaag gtcaggggca caggctttgc aatcagaaag ccgggccgta gcccttctct 132840gtgacttaca agctacatga tctgggcacg ttgctcaacc tcactgaact tcagtttgac 132900atagattgaa gctctttgtt tttatttgga gaacatttag atccaagaag ctcttctaag 132960gaacagagac tgttttacag ggttactgca aagattagat gaggtcaggc atgaaaaatg 133020cttagcacag tgctaggtac atgataacta ttattatatg cttttgaaat gttgagaacc 133080caactctgat ggcggctccc atgaaaagca gcacatttct gccttttatg agtagatagt 133140tactcaggat tcattcaaga gcatttcagg tcagcattag agaaacacat ttaaggatct 133200aggttttttt catcatgcat atgtaaacct ctcaggaatt ctccatgaat atttgagcat 133260cacagtttct ttggtttctt tctttttttt tcccctcctt tttccttcag tttctaagac 133320acaactattg actgtcacag gccattcttt tttttttttt tttttttttt gagatggagt 133380cttgctctgt tgcccaggct ggagtgcagt gacgcaatct cagctcactg cagcctcagc 133440ctcctgagta gctgggacca caggtgccca cgaccatgcc cggctaagtt ttgtattttt 133500agtggattca gggtttcacc ataattggcc aggctggtct cgaactcctg gcctcaagtg 133560atctgccctc ctcagcctcc caaagtgctg ggattacagg tgtgagcacc acgcctggcc 133620ggcctttcag tttttaagaa cagcccttgg gcagctcagt gctgctgctc aagcagattt 133680taaaacacga atccccatct ctaaaatgag acagatttac ttctttttaa ataagaagac 133740taaacacagg accacccttg atgtgttctg tttctctctt agcccatctt tttttgaatg 133800gagaaaatct gggctttcac ggcaaggttg tgaattgctc agcgtggccc tttttggctc 133860acccatggca aaaaatggaa aaattttgga atgcaggcca atccaccacc tcctaggtct 133920atgcagctgc cagcgacaac cagatcatct ttactaattg atggcatgtt aacgttggat 133980ggggacttcc cccttgcctt gcaggcccta tttcctcccc cagcttgggc agaagcctga 134040gctgaatact tgccttttgg ccacacctct gggtctgtca ttcagggtct tccacagatt 134100gactccagtc ttctcttcca ctcctccctg aacaaactgt tcttgccacc ctccctatta 134160ctcctacgca cttggctcat atctaccaat gtgcttttag ttcatgcttt tctgcatttc 134220ctgatatgtg gatcctgtgt aaaggggcgc cagaaatcaa gagagagact ggtcactggg 134280gagaggttgc aagtctccct tagctaacag cacccatcct tcagggttca gccatgtttc 134340ctttctttag gaagcccttt gtcagtgcgg caaccctggg atataaattc ttagaacctt 134400tgcctagata tgctgccaga cacttctctg aggaacagtt tgttattttt tctgtaactt 134460agttcctctt cagcatttcc actgcagttg gaaatgtcgt tcttggtgcc tggccctgtt 134520aacatcttga gagcagggac tgtgtcttgc ccacctttat gtgtacctgg cacttaagaa 134580aatgcccaat atgtttgcta ttgaaagtca accttcattg ccataccttt aaatgctggc 134640aaacccaggc taacctttag tcaacactca gagcttacag atgctcctta tttagtaagt 134700aattgatgac gtaacccttt gagcaacacc tgatcagggg atctttggga tatccctctg 134760aatggcagca gttggaggcc taacatttac aggcacagac aacatggatg ggtatgattt 134820gttcttgggc ctccaggatg tgtgtccata cttccattct cttcccctga actcttctcc 134880aggtcctgga atcgcctcca ctgtgaaaac tggcgaagaa gtaggctttg tggttgatgc 134940caagactgcc gggaagggta aagtgacctg cacggttctg accccagatg gcactgaggc 135000cgaggccgat gtcattgaga

atgaagatgg aacctatgac atcttctaca cagctgccaa 135060gccgggcaca tatgtgatct atgtgcgctt cggtggtgtt gatattccta acagcccctt 135120cactgtcatg gtaaggaaaa ttccttctcc cgagcatgct gttattggtg gaaactgtaa 135180cagctgccgt ttgttgaacc ctgactagga tatcctcttc accttttttt tcctttggaa 135240aaaaatttgt taagcagtca tgaccttgta gagtcccaga gtaatctcta gaaactcaga 135300gaccctttgg ctgtaagggt ttttagggaa tcttactggc caccaaggtg tctatcataa 135360taagggactt gggcaatatc ctggcctaag cccaggcatt ttgaaagata actcctcaga 135420aaaacacacc tttatgaaaa tgtttctaca taaaacatga caggttttta accggccagc 135480tcttccttct tccatcttca tggccattct ccatggctgg aggagagagc ttcctgatgc 135540tgttttgttt ggagacttga ctctgaaatc ccaggactca aagtacctcc acttgtgttt 135600tggaaagatt cacactttat gtatgagggg gaaatacctc gtcttttgca gctaggaaca 135660tctggaataa aaggaggaaa ccattatgca aacacctggg ttagtgaatg accaaggtct 135720ttcattttca gttgtgagtt acttatagat cttcctctgt ttatttattt ttattattac 135780ataatagatc ttcttctgaa tattcttcaa ccaggaaaag ggttagaaac cttggggaca 135840ttacctcatt gaaccctcaa aaccaagcat cgttggcttt tttacaaatg aagcatgctt 135900ggtctagaca gacaccaaat accatgctgt catcctcact ggtgtccttt gatactgtgg 135960tcagcagccg cacttgacca caaggtttat aggcccttaa tgacctggcc ttgtgcacag 136020ccgacaaagc accttctaat tatttcattt tgtgcagcaa tggagaggtg catgaagact 136080ccattccaaa ctccaaagct cagggacttt cttccgaaca gtctatactc tgttgtagta 136140ttattccctt ccatcgacgt ctgtttatct gtaaacagca tgccagagat ctggaggctc 136200ttttatgtct caagtatgta aatgtaaaca cttgtcaact tttgacattg ttcatttaag 136260agtgtttttc tcctgtagga agaaagaaat acagctggga agttgatgtc cttattcaca 136320gagaagggta ccagttgtag ttttcagaat ctgtttttag cccatagtgg gttttatctg 136380gttggttaga attaggtgga aggagggaag agcagccaag cactgagcag tggtcatggg 136440cctgctggtg caatgatttg ggggtaagag aagaccatat tgggaaggtc tacgtgagaa 136500agtcagagta aaaaaattga ggaccctttt tgcagaagtg gaggcttcca aactcagtaa 136560taagtgtctt ctagcccctg aatacacaca aagcaagaat actttgtgtt tacccactgc 136620cccctgacca ctgctgaagg cagaaaggga cgatcaccta cagtacctgg tttgggtctt 136680tattctctca ttccagggag agaaccttaa ctagatggac tgactgactg ttcattggct 136740ttggttgggt agattccctg cttccctcta taagtttgac gccaaaaaag gacaccgacc 136800agcactgcag tcatagcaaa tgtctcaagg agacccacag ggtggtttct tcaaatacac 136860tactcacaca cagcacatgg agtcatggac aaacagctta actgcccatt gcctttgaga 136920agtcctggac caaaggccat agctcagcca ttgaaagatc ttccttctga ctgatatgtc 136980cctgcatagc tccaacctgt gcaggcagag gatagggctg ttccaaatgt cgctcacaga 137040gctgcctttg cctttctgca gatcccaaga tacacacaaa gcagttaaca tgggtaaata 137100ggccttcctc tgtaggagag ggcttctgat tcttattctt tcttatggcg gaagagggtg 137160ttgagagggg ttcccttgct gttggttctg ttgaatcagg agcattaaat cttttttgtt 137220tttttttgag acagaatctc actctgtcac ccaggctgga gtacagtggt gcaatctcag 137280ctctctgcaa cctccacctc ctgggtttaa gcgattctcc tgcctcagcc tcccgagtag 137340ctgggattat aggcacctgc caccacgcct ggctattttt tgtatattta gtagagatgg 137400ggtttcacca tgttggccag gctggtaact cctgacctcc agtgatccac ctgccttggc 137460ctcccaaagt gctgggatta ccggcatgag ccactgcgcc cagccatgag cattaaagct 137520aagatttgtt gaaaatgaat ttataaaaaa ctttagaaac attaactgct gagcatggtg 137580gctcatgcct gaaatctcag cagtttggga ggccaaggtg agagggttgc tggatcccag 137640gagtttaaga ccagcctggg caatacagtg agaccccatc tctaccaaaa aaaaaaaata 137700ataattagcc tggtgtggtg gtgcacgcct ctagtcccaa ctgctcagga ggctgaggtg 137760ggaggatcac ctgggcccag aaggttgagg ctgtagtaag ctgagattgc gccactgcac 137820tccagcctgg atgacagagc aaaactctgc ctcaaaaaaa attaaataat taaccacagt 137880agacatttat caagtaaaaa aagaactttt tcctgattct gtgctgcaga gatgccttgt 137940gttagttttt acctacttac acttcacaca cctcactttc atgcctgggg tcacaccgta 138000catactgctt tcgcaccttg cttccttccc tcaatgtgtc ataggtaccc ttacatattg 138060attcattgga cctgactgcc atgttccact ggacagactc accagaattt atttgaccaa 138120atcccttcca gatggacatt gggttgcttt agttttgcac gaccacagac agcaccagtc 138180aaggtcctta cacacatcaa ttaactatgg agtctcccgc cagcttaggt ctgcgtgcta 138240caagtggggt tgtgggctca cagggcatgc gcatctgaca gttgaagaga ggacaccaac 138300tgccttccaa aagggcagta agaaagtgtc cttcgctaga gtgagtggct cactgcagtt 138360caagatggag cagtggggga agcagctctg tggtggtagt ctactgagtg tatccttcca 138420gtatggttcc caactaatct ccatttgcca ctgaccaggc cacagatggg gaagtcacag 138480ccgtggagga ggcaccggta aatgcatgtc cccctggatt caggccctgg gtacaatttt 138540ggttttttcc tttttgtgtt tctgtgttta ctcagccttc atttcagaaa atctgccatc 138600tgcttctggg attgcttaag ccctgtgggt gtcctggtca ttggtgtgcc cctcactgat 138660cagcccatca cgatgatccc tgctttttct gtaataagat cacctttgcg tcaccatccg 138720tgctccacga atcgccagcc gtcgtgtctg tgatcacgct cggtgcagtt tgtctctgtg 138780tttaaagaga aagacagaca gctgtctgca gccctcctgc tgcctctcaa agccgccact 138840tgcacattca gtttctgttc agggggaaag ccacccactg ctactctctg ccacttaaaa 138900tgcaccttct tttccaggcc acaagcaact aaacctttcc agatggagcc tcttgggact 138960catagacatt gctgtctctc acttttccac tttcccgtgg gtgctgctgg gaattttaca 139020aacagactcc cgagtgattg ctaacagttg gtcagcatga cctctccagt ccctcaggtt 139080ctaccctggg tctggagcca cttagacaaa gcccatacca caatgggcag ccgcattccc 139140aaatcccggc ctcactggct tgtagaattc ccagcagctc taacccctgt agcttcacca 139200gctcccgctg ttgtctgctt tacccagtga ccactgcctt ctgtttttag gtgaccgaag 139260aggcctatgt cccagtgagt gacatgaacg gcctgggatt taagcctttt gacctggtca 139320ttccgtttgc tgtcaggaaa ggagaaatca ctggtaagca cttgccataa aggccgtctc 139380attctcactt gctctcacga gcttcccaga atggtgctgg ggaggtgtgt ccactgtccc 139440ccagacccag gctccttaac ccagggtcac gagttcttgg tctccggtgt tgggccgtgg 139500gctcctgaaa ctacagaata tgccacgtgt gtgtttctct gaagaagtgg ctcactgaca 139560acttgcatta ctttcttgag cagtcccatg attctctcta ggttaaaaac tgctgtgttt 139620agatacctca tgactgtcgg gttcttgttt gccccttttt cctgccttct cttatttgac 139680ttttccagat gtgactttga cactgagtct gtcatacagg agttcctttc tcccctcagc 139740ctcttttcaa tggcccactt ctctttggtt tgatgctcta tgtatccagc tggtttcatg 139800gtgttctcaa gtcctttctg agcttgattt tgccagttgt agaaaactct ttaagagttg 139860tctgctatat tttgtggaag ccaaatggaa ctggaaaaaa aaaaaagaaa agagcaaatg 139920gtctctccca ttgtgggact tgaatgtttt aggcagcaac gaatgttctt gggtctggaa 139980acctttattt tgaatacatc tgtgccttgg gctctgcttc tctggggaag gttgctggtg 140040ggcttcattg ccccgtctct ctgtgctcca taggagaggt ccacatgcct tctgggaaga 140100cagccacacc tgagattgtg gacaacaagg acggcacggt cactgttaga tatgccccca 140160ctgaggtcgg gctccatgag atgcacatca aatacatggg cagccacatc cctggtaagc 140220tgagtcagca ggcccagcag ggctccacca ttcaggggca tccgggcagc ctgcagacac 140280tcctcagccg ctttgcaggg agcagctctc ggcagcaggc tggagaatgc agcgttggta 140340cccctgtgaa accaaacagt ctgggaccct agcaggtcca gctgatttct ggaagggatg 140400atgtagctca gtgtcttggg tcacagtgca ggcctttggg tctgtggttg tttatctttg 140460tcactacgct gagtgtggcc agaggtcaag ctgggagaaa aatgggaggc atggtgaggg 140520actttccagc ctggcctgca gagccctgtg tgggctggag gcttggggcc aggtcagagg 140580tggaagaaga ggaccagcag ccctggaaga agaggaccag cagccctcta caagggaagc 140640cagcccaggt ttcatgggtc accaaccagc acagtgtcac cagttcattc tttctttttg 140700tagttgtatt tgttttttaa tttagtattt tgaataggta acacattctc atggttcaaa 140760aataaaaatg atacgaagaa agttttcctt cctacccctc tccttgaact agactatcat 140820aaattttttt atgttcgatt tcagagtttc agggttttat tttttatttt tttgtggaga 140880tagggtctca ctgtgttgca cagattggtc tcaaactcct gtcctcaagc agacctcccg 140940cctttgtctc ctaaagtgtt gggataacag gcatgagccg ccacgcctgg ccaatttcag 141000agtattttta agactctcca tgcaaacgga aatacagata tataagagag tgtcttccca 141060gccttccctc atgtggacga accattacat atttgaccat ttccctattg gagggcattt 141120tggttcttcc tgccctcgct gtccccagtg ttgctgcgca aatcgacttt tcccctagtc 141180acctcacact cacaaagatg tatctgtgag atttagttac cagaggaggc aatgctaggg 141240ccccagtgca ggcatctatg attttgacag atcttgccaa attgcccttc agaggggctg 141300ttgcagttca cacgccctct ggccatggag aagagcacct tcttttccac aaaatttgcc 141360agtagaatat ggtatcaaat ttttggagct ttgccagtct gatggttgga aagaaacaga 141420atctcagcgt tgctttattt gtatttctct tgtgaatgag accacacaac tttccctatg 141480tctatttgta tttctttttc tgtgaactga acatttggat ccacggcctg tttttctatt 141540tggttattgg cctttgtcat atagtttcta agagcaatgt aaacattgga gagattagcc 141600ctttgtggta ggagttgcaa atgtttctct gagattggca tttactttag ttgtctgtat 141660gtaatattgg tttaaagcaa aaatgtatta tctgcttcta tttaaatatt ctaaagcggc 141720agatggagag agaggaaaaa atgtctttct cacatctgcc atccacttcc actgctggtg 141780tgagttgtgt atcttttcag atgtttctct ctgtatctac aaacatacat ataattttat 141840tctattttgt ttttaaagga atagcataat ggtattcata gtttatagca acttgctttt 141900tttcttttta atgcatcata ttatggataa tttctcaagt cagtaaacat gggtcttcct 141960cactcttttt aatggcccat gagtagatca gcatttattt aaccggtccc ctgttgtgaa 142020cacttaggtc ttttcctgat gtgcacccga acactgcaga aatgaaagtg cttacatagg 142080gctaggagtc ggggtgggca gagaagacca ctgtggggtt gattccttac aggttgaatg 142140gcatgggcaa atggccttcc aaaagccctt tccacttacc ttccctctgg ccatgggtcc 142200tttcaccacc cagtgcaaaa gtttcttcct tatttgtcag gttgggctgg taccttacct 142260tagccccctt cctcatctgg agcagcttcc aggattgttt ttcttatgtt gtgattgaag 142320gaataatact gcgtagaccc tctctgatgt cctaggatgg cgggggatgg gaggtgcatg 142380tgcatctcct tctgtctctt catgcctctg cttaggaggc gccagacctg tagagaggtg 142440gacgtcaaga tgccagttgt ccagggtctt cgttcacccc ttaatgagca ccaattttgt 142500ttgtgtcctt cgtaaaccca gagagcccac tccagttcta cgtgaactac cccaacagtg 142560gaagtgtttc tgcatacggt ccaggcctcg tgtatggagt ggccaacaaa actgccacct 142620tcaccatcgt cacagaggat gcaggagaag gtactgtgtg gtttacgtgt ttatacgcct 142680ccagctgtcc atttggaggg tgaagtggac acggttccag ggtggctttt aaaagtgaga 142740caatcgaatg gtagtatttg tcttgtcttt tctctcgtgt aaatctgttt cttctttaga 142800gccgcttcgt cttctaccca gacagacatt tttgaagtcc tttgtgttct aactgaaatc 142860agattcatgc tatgaaatac tttatgtgac ttgtctggaa tttaagtgtg ttttggttgg 142920tgatgttttt gttcttgttg cacatgtatc cacaagacca catgacttac tgagtggctc 142980tttttgataa agctgtgtgc ccattcccgt ggtattcatg gataatccca aatctgtggt 143040tctaatggga tttccgtgat ggcagccagt gcctgatggg cagggacaat ccacctctgc 143100cctccaccac ccaccgtctc ctatgtgtaa ttgatgtaca cggctccttc cttttctcat 143160cccatgcatc ctgagagtag agagagctcc agggttactt gcagtgaaga actcagatgt 143220ttggggtttc ttctcagtgg gtgtttttac tgcgtggact gcttcattct gacagatgtc 143280cctttgccca cagctcacgt ggagtgcgtc aatccattgt ccccagcatc agggctgccc 143340tggatgagtt gttaaaagga aactcttaaa acaaggcaac tctctcccta acacccctgc 143400atccctgttc ccacttgtag gtggtctgga cttggctatt gagggcccct caaaagcaga 143460aatcagctgc attgacaata aagatgggac atgcacagtg acctacctgc cgactctgcc 143520aggcgactac agcattctgg tcaagtacaa tgacaagcac atccctggca gccccttcac 143580agccaagatc acaggtaggg ttgtctggct tctggggtct tcctcgtggg aagtatggct 143640gcctctgact gccaccctcc ttatcagacc cctggcagca ggctagacgt ctctttgagt 143700ttaggtttca cagagacttg ttgaggagga gcaggggatg gaatgcaatt ttggattagc 143760taaatccttc tcttgctgat aatccaggaa aatgcgagag ctagtatttg gagcacactt 143820ttattgtgcc agtgtgactc tagggtgcaa agagaaagct ctcagatgga gtgttcgaat 143880catacttact gcaatagtgc atgaagtgca tgagcttaga catgcccttc agcgtcacta 143940ctaggtaaat tttctgctat cccttttaca gatgggaaaa ctgaggcttg gcaaggtagt 144000ggtgtagcca agttcacata taggtaaaca gatccaggtt atcaaattcc aaagcccatg 144060ctcctcacct tgctgtgttc aggttatgct ttcagtgggt tataaggaag atgcacaagg 144120cagatcctgt ttccccaccg tatttagacc tgtctgtgaa gcagccagta gtactgtgtg 144180gaatgtggtc attgtttacc tagaaatgcc cacagccatg ccaggcaggt atgaggtgcc 144240ttcaactaac aaaaattcct atattttatt ttatttttga gacagagtct cactctatca 144300cccaggctgg agttttagtg gcatgatctc ggctcactgt gacctctacc tcctgggttc 144360aagcgattct cctgcctcag cctcctgaat agctgggatt acagcaccca ccaccacacc 144420cagcttattt ttgtattttt aatagagatg aagtttcacc atgttggaca ggctggtctt 144480gaactcctga cctcaagtga ttcgtctgcc tcagcctctc aaagtgttgg gattaggcac 144540ctggcccaaa gattccttta aaatgtggtc catgaggact caagtctcta ggtcctgcca 144600gcttcttgtc tttgctgcaa gcaggcatga atcccatcat tcttcattgg ttgggtctac 144660tcagtgttca aggctcattt ttttttcact taactttgtg taattagttc ttgcgtgttc 144720atccgtgaac agcatatggc atggcagctc tgtgaagcca gggtaaccac atgtaacggg 144780agtccttttt gggggatgtt tcccagatga cagcaggcgg tgctcccagg tgaagttggg 144840ctcagccgct gacttcctgc tcgacatcag tgagactgac ctcagcagcc tgacggccag 144900cattaaggcc ccatctggcc gagacgagcc ctgtctcctg aagaggctgc ccaacaacca 144960cattggtgag ctaggctacc cttcctggct ggagccagga catcttgggt gggagatggg 145020gactcttgca gtcctttctt gggaatgggt agcacaatgg agtgtgatgt gataaacctg 145080ctgggtcaca cgcacgataa atgcccaagc gtatttgtgc attgtgatat cgacactctg 145140gattgttggg tgtcaggaaa gaggacatat ttctatttct gagagtgtgt ctctctcctg 145200cttcctctcc gccatcccct tacaagcccc aatctgtgtt ctggtccagg catctccttc 145260atcccccggg aagtgggcga acatctggtc agcatcaaga aaaatggcaa ccatgtggcc 145320aacagccccg tgtctatcat ggtggtccag tcggagattg gtgacgcccg ccgagccaaa 145380gtctatggcc gcggcctgtc agaaggccgg actttcgaga tgtctgactt catcgtggac 145440acaagggatg caggtctgtg tggtcccagg ggagaggccc agagcttgtg ggaaccgact 145500tattttgctg aggcagcgtc atcttttcat cctaccaact ccttttcctt tctgagcatc 145560cttcaagcta taggtccttc tgcctgcatt gtcttttatg cctcatgacc attggcaaaa 145620atgggattgt ctttgttttt tagatgatga aactgaggct tgcaaggttt agagccccct 145680ctgcactagg atctgaaccc agagccacaa cacctcgcaa acccctgttt tcttatctgc 145740tctcccaccc ttgttctcag cttcccagcg tctctccaag caaagaatgt tgggttgatt 145800ggccaagacc atggtcatct gagcagagct tttgtggaaa tgaagcatct ctttctgttt 145860tctctttgag atggtttgag ttagattgtg tctcttccaa gcttgccaca ccccagtgcc 145920tccagtcatc tgctttcttg aaggatggcc acgctggtga attctagaca aattctaacc 145980cggggagagg gctggagaat ttctggtcct ggttgggaga tactccctgt taaaccttcg 146040gatatgctga cctagctgag gtagccaggg gctatttaaa aattcaaaat ctcagatctg 146100gctgtggata aacccccaag gtggtacgtg cagtacttgg aggcgtgagg gcagaaggtc 146160ctccccagca gtttgtacgg gacacatcat ctatgggata ttagtaaata tccttaagga 146220aaggcttctg tggtcaaaac caggttcagc aggttatttc actatggggc ttctcaggac 146280gcttaaccta ctcatccccc tctgggcttt gcaaacgagg ccgccattgc tttctttctg 146340ctatgtagaa atagattgag gcgtaagggt cggatgtcct ttctccattc atcaggctcc 146400ctcttcctga ggagctgctg tcagaacagc ctggggctgc tgtgttgcag gttatggtgg 146460catatccttg gcggtggaag gccccagcaa agtggacatc cagacggagg acctggaaga 146520tggcacctgc aaagtctcct acttccctac cgtgcctggg gtttatatcg tctccaccaa 146580attcgctgac gagcacgtgc ctggtatgtg cattccattc ccctccaggt gggatgcttg 146640ggttttctgt aaatgctgtg ccttggcctc tggcctgctc acaggagcct tcttgggtct 146700tgcagggagc ccatttaccg tgaagatcag tggggaggga agagtcaaag agagcatcac 146760ccgcaccagt cgggccccgt ccgtggccac tgtcgggagc atttgtgacc tgaacctgaa 146820aatcccaggt gggcgtcggg gactagtagg gtggggaagc cttggctcca gccttcaggg 146880cagtgggtgc ctttgggaac caagtttagg catggcccag aacacagtat ccaagtcggc 146940tgtgctgacc ttttcatttc acttcatttc attatgttct tctatgttta ttttcacaga 147000gtctcatcca agaaaaacaa atgtttacct tgctaccttt ttcctcttcc aaataaaaat 147060agctttattg tgtcacatgg gggaaacgta gatatgcttt tagattttta gattaactat 147120ctgtcaaata gaatcatgtc agtgaaagaa ctggccctgc cgatgccagg gtctggaagt 147180atttaagagg tggcagccca gcggcatcct tctagtattt ctctttcatt cctgaaatta 147240gaacgagggc tgtgctgcag aactcgctgg gccacatcta gccctttggt ggtgaattgt 147300tcttcttggg ccccgattag ccagtcaaca ggtcacacag tctgtctgaa atgtgttcca 147360agttctttct ataaagaatc cttccagagg gaagccactg tgagtgaaaa ttttgaggct 147420cctctgccca gaagttggca tgtcctgtgg aattgcacaa attctacaga gaagggaaat 147480ctaaatcgtc ttcagatgga gcttgtgttg cgagctctgg agagggggtt gtctttctac 147540actgcatctc ccatccttcc taacgagtca cggagctgtc gactccgcct tcttggcttt 147600agttaacagg ttcttcttgt gtagtcacat caacgtcggg tcacatggga atgtggtaaa 147660gcctcattac tgtagagttc agacatgatc acttaaaaag agctttattg ggccgggcgc 147720ggtggcttac tcctataatc ccagcacttt ggggggccga ggcaggcaga tcacctgagg 147780tcaggagttc gagaccagcc tggctaacat ggcaaaaccc tatctcttct aaaaatacaa 147840aaataagcag ggcgtggtgg cgggcacctg taatcccacc tactcaggag gctgaggcac 147900aagaattgcg taaacctggg aggtggaggt tgcagtgagc tgaaattgca ccgctgcact 147960ccagcctggg caacaaagtg agactccttc tcaaaaaaaa aaaaaaaaaa aaaaaagagc 148020tgtactgatc gtttgtagtc ataaacagtt cgtgtgcctc aaggtggggg gaggaagtgt 148080cacctcccag agagagcttg gttcacattt taggtacaga gttggaccct ggctgcccca 148140tcctcatagc cacgtctgct cactttccag tcacattggt gtactcatcc actgtttttg 148200tgggcatctt cccacctcaa aaaatagaca tccacatcat ctctttcatg accctgataa 148260aatgccattt cattcaatgg aactattggt gatagaaaaa gagagattcc atttcatgtc 148320tagatgcatc aaccttcgtt actcatctct gtgcctcagc tcccatcatc agggctgctg 148380tgacatttgc caccctgtgc tcaggctgtg ggctggatgc ccaggagtgg gctgggctgg 148440tgcatttcag atgctgccat gccttggcag accgccctcc acatttctcc atactccccc 148500accagcactg gggctgtctc tccttctcac tttggccaac ctgatggaaa aacatggcat 148560tcagtgttca gtttcatatc ttcgattact agtgatatgt gtactgtgtt ttcttttcat 148620ttgctttaca tttctcattt ggcaaaattt ctgtgctctg cttatttctt gaggaactag 148680caagtatctg cagtgtggac gtttaccctt tctcttaagt ctcttccagc tcttggccat 148740tttgttattc ttttagttac ttagtaccag atgactctgg gtgaggctcg attttccact 148800cattacccaa atgatcctct cggagatccc ctcctcctta atggaggaca gctcactaac 148860ttcagatgtc ctccggaccc aggttttgcg gggcatcttt gtcagtttgg gctgctgtag 148920caaaatcaca tgaactaggt ggcaaccaac agaaatgtat gcctcacagt tgtggaggct 148980ggaagtccaa gatcaggtgc cagcatggcc agattgtggt gagggcctcc ttccaggctg 149040caaaccgaca gcgtcccctt gtatcctcac atgctggaga acggagggag ccagctgtct 149100gggactctta caaggccact gaccccatca cagggtcgct ccactttcat gaccttatct 149160aatcctaatt gcctcctcaa ggcccatgat aatcccatca cattgttggg ggtagggttt 149220caatatttga attttggagg gacacaaaca ttcagttcat tacatgggtg accctctttt 149280caacctccct tcccttttct gtcctcaggg gtcagagtca tgaactgctc tgcccagatc 149340ctgtggggct ggagggtgca gtttcatact ggctctaggt gatggcagtg ctccgtgccc 149400cgcatgcggc cgcctggcct caccacggca gtgcaggcac agtcgttggc atgacgtgag 149460cagctcacgg agagtgatgt ggtcttgcgt cctagcactg gtgacccgag acattgcttt 149520tctgaaagtg tggcccctgg tctttggttt gctcaaagct ttgctcacgc atggtttccc 149580ctctgccatt gggacttaca tatgttcacc tttttctcta actttgtctt gttgcctaaa 149640agaaatgcca aagcttcttg acggtaaagg atgatggctc ttgttttcta cccttaccta 149700tctgtggaaa ggagcccgtc tgtgcatgat ggatgaccac gtcacctttg gcaaaaagtc 149760tcagtgcccc cagcatgggt ggcctgaagg gccctgccca ctccatgctg gccacagaag 149820ggcaggcacc cagcctgaag ggaaggaagc ctgggcacct cacgtccacc gggctgcaca 149880caccttgctc tcggctgctt gccctgcatg tcctgccctg tctcaggccc ttgccctaac 149940cctcttctct cccccaacct ccctccctct ttcagaaatc aacagcagtg atatgtcggc 150000ccacgtcacc agcccctctg gccgtgtgac tgaggcagag attgtgccca tggggaagaa 150060ctcacactgc gtccggtttg

tgccccagga gatgggcgtg cacacggtca gcgtcaagta 150120ccgtgggcag cacgtcaccg gcagcccctt ccagttcacc gtggggccac ttggtgaagg 150180aggcgcccac aaggtgcggg caggaggccc tggcctggag agaggagaag cgggagtccc 150240aggtgagcat tgcgggcagg attttcactt gggaagaata gagttgagcc caggcagtgt 150300gggcacccac atactttttt gccccatttg aaagagaaga cttctgatag gtggcattaa 150360gggcattatt taaaacaagg catcatgact aagtctggca cagtttgtaa ctaagctttg 150420ctcacttacg taaagccaaa caggtttctt actgggagcc tccttggagc ccgtatctta 150480ttagtgtgca cctgagtctc taattgggga gcagagtaat acggtttcca gagcatcttt 150540cagggctgat gttctgtgga acatactaga aagctacaaa actgactgta agcatccttt 150600cctgtggttg ccgctggtgg gaagatctgt agggaaaaaa tggaacattc tcatctttct 150660ctggcttggt taaggtgtat tcatttttta aattttttat ttaatatctt tttctctctt 150720gtttgttaga gatggggtcc cactatcttg ctcagactgg tcttgaactc ctgggctcaa 150780gtgatcctcc tgccttggcc tcctaaagtg ctgggattat aggcatgagc cactgtgcct 150840ggccggttaa gatgtattca gggctgggcg tggtggctca cacctgtaac tctagcactt 150900tgcaaggccg aggcaggcag actgcctgag ctcaggagtt caagaccagc ctgggcaaca 150960cggtgaaacc ccatctttac taaaatataa aagaaattag ctgggcatgg cggcatgagc 151020ctgtagtctc agctactcgg gaggctgaga caggagaatt gcttgaacac aggagatgga 151080gcttgcagtg agctgagatt gcaccactgc actccagcct gggcagcaga gcaagactcc 151140gtctcaaaaa aaaaaaaaaa aagacatgtc ttcagaggac tccagatgtc ctgtgaattt 151200agttatcact agtgatgctt aggaaacttc agcaatggac cttggacctt gcttgggttc 151260tgcttggggt tggagaaaga ggaaagggct agcaacagac gaaacctagc actgcaggtt 151320tgaacaagga tggaagaggg acaggggctc tgtggggctc agtcactaac caggtttctc 151380tttgctctca gctgagttca gcatttggac ccgggaagca ggcgctggag gcctctccat 151440cgctgttgag ggccccagta aggccgagat tacattcgat gaccataaaa atgggtcgtg 151500cggtgtatct tatattgccc aagagcctgg tatgtattca gggttcacaa gaggacattt 151560tccttgtttg aacatgatta ggttgcaagg aacagaaatc catcaagttt gctgaagtca 151620atgaggaatc tatgtgtatg ggcacatggg acagcctcct agaaatccag ttgcaagata 151680catggccaga cctcttaagg gtgggaacgc ttgttctggt tgccttttgc ctttctccat 151740tagcctctct gcttcttgct ttcattcaat tgctccattc tttccaccaa ccagcctctg 151800tctgcccacc catggctacc ctggctggct gccccagaag agtggccttg gcatctgagc 151860tccctctagc aggagctctt aaccttttgt gtgccattga ctcttgccat ctggcgaagc 151920ctatggggac tgttcttggg ataatgtttt aaagcacata aaatgaaata tgtcacatta 151980taaaagaaat cattgatatt atagtacagt taccaaaatc ttacaagaac aaatatgcaa 152040catagaaaca tgcatatctt cgttaataca ttaaatcata agatttggtg acagtatatt 152100aactgtcatc aaagtgacaa agtaataagt gaaaatgata cgtcaaaata actgtaaaat 152160gacataaaaa tatatgattt ttaatggtga tgtaagtcat atgtacttat aatgtgctgt 152220gatttcttgt caacatttct gaagaaagga aatggtaaat ttcagttaga gaatggtgaa 152280aattaaaacg taattttttc cccattgaag tccatggatc tgctgaattc aatacaggcc 152340atttggggac cctgtgagcc ccggttaaga gtccctggcc ttaccccact aaggaaatca 152400tatcggccca gcctcagcca ggcgactccc actcaaccaa tcagctgtgg ccattgagga 152460gggctgggtc tctctgaagg cattttagcc cttggtgaga agcaagagtc cactctgggt 152520ccagagtctc tgaaatgatg ggactttcct gtcctcatag gtaactacga ggtgtccatc 152580aagttcaatg atgagcacat cccggaaagc ccctacctgg tgccggtcat cgcaccctcc 152640gacgacgccc gccgcctcac tgttatgagc cttcaggtga gatgcaagga agcatccatc 152700tccttggccg caggccacca gtgagacccc tggactcctg aggctgcttc aatgtcccct 152760taggtgctga ggcccctttt cacattttga ccacagatgt cacccagtca ctggggagct 152820ttcctgtggc agagtcaact ccccatacac ttagggcgga tgacacttgg ggcgagcaaa 152880aacagagcca cagtcaacaa cacaccttaa tgtttgggga cacgtttgtt tttaaaggtt 152940tatttaagag aaacaaagga agcctgttca taactggtta agggataaca agggctttca 153000aaacaaaacc aacacaaaaa taacagtgca gtgatgtttt agcctgctgt tgttggctgc 153060ctttcttcaa gaaagtcagt tgcaacttac tgtgattcat taataagtgt gcagggaact 153120atattaagag ctttatcagt gttacctcag taaatccttg caatagcctg acaagtaggt 153180tctcttgacc ccattttaat gatggaaaaa cagagataca aggaggtttt gtccactggg 153240aaccagctag tatgaggcag aacaggcaca gtgtggctcc agaacctgta tttttgtttg 153300tttgttgttg ttgttgaggc agagtctcgc tctgtcaccc aggctggagt gcagtggcat 153360gatctcggct cactgaaacc tctgcctccc aggttcaagt gattcttctg cctcagcctc 153420ctgagtagct gagactccag gcacgcgcca tcacacccgg ctaatttttg gatttttcgt 153480agagatgggg ttgcaccatg ttggccaggc tggtctcaaa ctcctgacct gaggtgatcc 153540accccactca acctcccaaa gtgctgggat tacagacgtg agccactgtg cctggccaga 153600acctgtgccc ttaacggcaa cctctctaac ccccacctga tgttgtggca cacggttgca 153660tagtccatcc cattaggata ccaggagatg caacattttt cctcgtccta aacaggtcac 153720ttaattcaag gttgtactag caccttcagc caaactaaga accatcgggg atgcctctgg 153780gtttttgccc aggacactga aaaataatta ggtgtctgaa ctgggagtag caattaagtt 153840gtgaaataac atcgaaatcc caaagtatga tttctgggta agagtttcta aatagccttg 153900agctgccccc agttcttgaa aatattggat tcattaaaat ccaatctgat gtctaagatt 153960ggtgatatca ttggctttag ttccatacac ttggtttaca tttgagattc taatcttact 154020ctgaggggaa ctgggatacc tccagttgtt ccaaacatta gtctttcatt tagagacgta 154080aacagaaccc aaaccagact cagtccacac attgaagcgg cctcatccgg agaataccaa 154140gggtactaac tggttactgt ggtgtagatg tttttcttgt gtttcattta aaggcttctt 154200aacagaagtg tcttttgtgg ccaacttaac taaaacctac ggagggagat aaacccagca 154260cttattgagg gcaggagctg ccctcatgca tctcgaagat ttctttcaaa tctgccgagg 154320catttatctc cctcttgagg atttagcggc aagcggattc aggtaatgta aatgattctg 154380tctaaaagga gctggtttgg aaaaatcccc tccaggaaac ttctgtagag tgctctcgtc 154440atagctgggt cataaatgtt tcagtaagtg cacagcaggc tgtttcttaa gcttttgtaa 154500ccagctgctg ccgcaggaga agtgtgttca tcagcatcgc cccctgttct tcccgggtca 154560tttgatgccg agtgatatgt aaattattga tcagagattt tgcggaggcc cacgcaagca 154620acatctggtg ctggttagca aagagaggca tgtatcgttt tgtcttgctt ttgagacttt 154680ttaggaaatt ggagtaggct ggcacttggg gtgggggtgg gatgggagtg atctggtgat 154740caaagaccct ctaattctgt gttctgtcct ccctcctcag tctatatccc ctagggcagc 154800acagtccaat agtaggttct gcagtgatca aaatgcttca agtctatgct atgcagcatg 154860atagccacta accatatgtg actattgaac atctgaaatg tggccagagg aaccaaggag 154920ctggatgttt agttttattt aagtgcatta agttgaaata tatgtatata tggcctcgtg 154980gctggtgact accaaattag ccagtgcagc tttaggacct tgccatgaag atgtggttct 155040tgggccagtt cttggacctc agcatcacct gagaacttca gtcccagacc cactggaaaa 155100gaatctgtat tttaataaga tccccagatg gtttgcttac acattaagtg tgagccatgc 155160tgcttcagag ttattgcctg aggagtggct gtccgaccaa gtctaaatca aaattactga 155220cttgtaaaat gctgctgttc aggattggct agtcttaaaa tatctcaaat gttgttgctc 155280agctttgttc ttaaccatct gaacttctaa tcccctcctc ccagaagagg agatagtttc 155340caagacaaag tatggggagt gaaactgatc cagggaagag caaaagctat gtctttctat 155400ggcttcttgt ggggatacaa cctctaaatg catattaata tttaataata agctgacgtt 155460ttcgagcctc tctgtgtatg ggctaggccc tgtgataaat gttttgcatg cacagcttca 155520tttgatcttt atagtagccc tcgagataga tcgttattat gcccatttta cagatgagga 155580aactgagact cgaagaggtt tggcacccta gatatatagc taggaaatgg taggaaatcc 155640agatccagct gattcttaac tgctatggag tactgccttc tttgcacacg tagcccttta 155700taatatgttc ctccaggtct gcccttgaga taacaaacag cataacataa aactgtgttc 155760gtgttcgtga gtgcatgact ttgttagctg cagtatcctc ttaaaagagg acactttttt 155820gacctggaac atactgggtt ttctggcctg catgggcatt attttggatg ctgagatgat 155880agtccttttg accaggatgt ctcaagtatc caagcccaga aatcatctct tctaggctga 155940atcaagatgg tttgcataag agaccatgca gatgcacgtc tctgctatct tacattaaaa 156000atgcagaatg gctcacctgc cctttgttgt catatgttat atagaaaaac ctatttgcat 156060gagaactgtc acccacagtt ttgggtaggg tcagtgtgtg ccactgagca ggaacgccga 156120gggccataac ctgtctgatg tattaaattc tcaggaatcg ggattaaaag ttaaccagcc 156180agcatccttt gctataaggt tgaatggcgc aaaaggcaag attgatgcaa aggtgcacag 156240cccctctgga gccgtggagg agtgccacgt gtctgagctg gagccaggtg agcaggaggc 156300ctgctggggg gtcccagcac cagcactttc cagcagaatg ttcctgtaaa tgtgtgtccc 156360aagggagggc tgatcagttt cattactgcc agtgagcctc tgaattccct ttgctgttgc 156420cagatattgt ttataaatta gggtttaaac atgtgccagg gatagggaga ccctttatgc 156480taggagagaa tgctcattct ttctttcttt tttaaacaaa tgctgggctg ggtacagtgc 156540cttaacctga gaggtcaagg ctgcagtgag ctatgatgca gtgagctatg attgtgccac 156600tgaactccag cctgggtgac agagtgagac cctgtctcca gaaaaaaaac aaaaaaacaa 156660aaaaacacat acacacaaca caaaaacaaa tgcttctttg ttttctgtta gtttttcaga 156720ttccttttgc atgacattca tcataatttt tctttcatat tgtaacaaca tcttacagat 156780ttttattcat tgaccttatg gcacgagtaa gcatattttg atctcacttt actctaaagg 156840aaaagtaggt taatgttctg taaatttaaa aaagaaaatc tgggtctcta ggccctaatg 156900tcctaagatt tttcttgctt ggtgccttgg tatatggaat tctctgattt aatcaacttt 156960aaagagacag tgttaccggt gaacataata aatttattaa gtgtcagaaa cttgaaggaa 157020ggtataaggc tcaaagagtt gctcaaagtt tagtgaaggc ctggccaaaa agcagatgat 157080gaccccaaat gatcactagt accacaggag aactgtgaag caaatggtaa agatggtcag 157140agcaggagag agaaatagtt tctgcctcgg tgagttcagg agggcttctc agaggaggtg 157200acatttgatg tgggccttga tgtatgagga ggagacctat gattactgcc ttatagggca 157260tttgttgtgt gcctggctgt atttgtatag tgtagttgga aatctaggct ctgaccaggc 157320atggtggctc acacctgtaa tctcagcact ttgggaggat cagttgagcc caggagtttg 157380ggaccaacct gggtaacata gtgagacccc ttctctacaa aaaaaagtaa aaaaaaaatt 157440agccaggcat ggtggcacac acctgtagtc tacttgtggg ggatgaggtg ggaggattgc 157500ttatgtccag gaggtcgaga ctgctgtgag ctgtgatcat gccattgcac tccagcctgg 157560gtaacacagc aagaccctgt ctcaaaaaga aagaaaaagg aatgtaggct ctgtgtgaac 157620atttagatct atgtttccta gtaggcagaa aggcagtggg gagcctcagg aggaacaagt 157680gtaaaggatg gggtcagatc ctggttttag tctgaaaggc caagtggcaa gctggtgctc 157740ccagagtggt ccatttgagg aagcagtggc actggaaatg gagaggaggg acttgaggcc 157800agagatctat ggtggctata gagagtgaga gagagaatcc attccaaaat gttccacgta 157860gcttagtgat tgggtcggaa gatgacagtg cagttatcag aactagggcc agccaggcag 157920agggtgggtg aggattggtc agggccttaa agggtttaat attttacttt gaggggtttt 157980gaaggatccc caatacccaa atggagatgt ttactagatc actgtgaggt ttggtggcct 158040cagccccaac agtccctcac tgggtaccct ccctcttctc ttaaagccaa tgtgcttcag 158100gggaagctaa ctccacccca gacaggattt gaacccctac agatgtatga gatcattagc 158160atgacacagt tactattgat tgcaaattac agaataccca gctcaagcca actcacacaa 158220taaaggggcc cagtaagttg cataactaga aagttcaaga catccaagac aggtttcagc 158280aatttgattt ggtcattgag ctgcgccctg caaggcgtca aatatttctg ctgttctgct 158340ttgtgggcct ggttctggcc ttcctcttgg tggcaggatg gccttcctct tggtggcagg 158400atggctgcag cagcaccaga tgtcccacct tcacgccaca tcaattaaga gagacaccct 158460ctcaggattc ttagaagtcg agagcctcct ttcccagaag tctccagcac gtctgccttc 158520ccctctcact gacctggaca catgcccact gctgagtcat ttcctgtggc taaagaaatg 158580ccatgtgctc attgactaag gcttagtgaa gaaggatttt tccctgatcc actcagggac 158640cacacctgga catggcggtg gagccagctt cccctacaac acattggctt taagggaggc 158700ggatggggac tgttggagga tgttcagtgc caaaggacgt agggtgcaca gcttcatgga 158760ggtgcacctc tgtggagacg tccagaggca gggagaagag ctttggggaa cacaaattct 158820gagagggatg aagagtacta ggcaccaggg agagaccgag agactacctg gagaggtagg 158880aggagaacag gctctgcacc ctgggcagga gggcttcaag gaggaagcgg cagtcaggtg 158940gtgcacaatg ggtagatgtt ctaggtgccc acttcagtta acagattacc ttgctacatg 159000ctgtgaccca aacgcacagc cacaaacctg ccctgtgggg gcagttccta gctttgagct 159060taattaagga gcattaatgc cagttggaac cgtttttttt ccccttcaag tggccaaata 159120gagaaacata gaagaagtga ggttttcttt tttcccttca tatatattcc tttttatttc 159180ttgttatgcc ttcccaaaac agagacattg aacagtagtt agaatggcca tctcccaatg 159240tttaaaaaca aactgaactc cccaatgggt gaacaaagta aagagtagta acctggagtt 159300cagctgagta agccgctgcg gagccttaag tggtgaggtc ttccaatttc agagtgctgt 159360gtcttcaact tgtatcatca ttttagtgga aaaacataat ttaattttgg tgaaatgaga 159420ttcatctcgt gacaggatta gtaacagcat tcacagaatt tcacactgaa gaagtgaggt 159480tttctaaaga aaggaagtgt tcttctgagg caggggtcag agtcttgtcc tgtgtttata 159540ggatttgcaa tgtggatgcg tttcccttgg ggctgatgag ggatacccag ggggtctgtc 159600tggttctgaa atccaggatg ctgagtgcca ggctccctgt agaactgttg attttaaatg 159660ggccatctca gcttggcctc catcctttat cctcactgaa ctcaggggtg tccatttgct 159720tgatttcacc ctgtgccttt gctcattctc ctagataagt atgctgttcg cttcatccct 159780catgagaatg gtgtccacac catcgatgtc aagttcaatg ggagccacgt ggttggaagc 159840cccttcaaag tgcgcgttgg ggagcctgga caagcgggga accctgccct ggtgtccgcc 159900tatggcacgg gactcgaagg gggcaccaca ggtaacccac tcttctgctt cttgaagcct 159960taactgaacc agctccaggg accaagccag atggaaatcc tcaagcccca tgaaagcttt 160020ttacacgtac tccccgtgga aactggggtc atgcacactt cggaggcgct tgctgtccaa 160080agctgttttg ggagttgcgg tttgacccac gataaatcca gagtgagagc tcgatggccg 160140tgttatcaca cctcattact gttagttgtg attcagattc cttcctctgc caagtttctt 160200gactttcaga acaggatgct gatagtcagg gaacacagca cagtgtcatt aattttgagg 160260gtttctttgc ctgcacagaa ttcatgatgc gtccaagtgg gctcctaccc gtctgttctt 160320tcatggtacc aggctcccag aaatgcactg aagcagcaat aagacctgtc ccagcctatc 160380tcctcctctt tttactctca gatcttaatg gaggaggaga aaagactgaa atgttcaaag 160440aattctgaag ctttttagac ccgttacaat ttacttttat tctttgccac agatgggaca 160500tgtttgatta tgaaagatac aggcagtgaa gaagtaaata aagtgagact cactccatct 160560tctctcctcc tcccccacct gggtctggaa gcaaacggct ctgggaaggg aggaccttca 160620ccctgtctgt catctcattg tctgtcttca ttcttggttg ctgggttggt tagctaattg 160680gttcattaga caagcagaca cagagttttg cttttgtctt acagaaagaa tcttactgta 160740tccactgtgt ggtatagctt gtgtttttgc tttgacatct taaagatctt tccatgtcag 160800aacagatctt cccctccttt tcctggctgt agtgagaatt cctgctgtga atcgcagtta 160860tttgaacagg tggcatcggg tggtgcgcag tgagtgcgtc actgttatgg aggctgccag 160920ggtggagagt cagtccttag tctttgcagg ggaagtgcgc agtgtggact cactggggca 160980tgtttgcatt tggtgttact ttggaccctc ttgggaaagc agtatgtcct ggtttcttga 161040gtctcttgtg tgtgtacccc caccccgcat aaggagagtg ggatggagca gacttgcctc 161100ccaggggtga ggggtgagtg gctgcatggt tgcctggcat ccagccctag gagcaagtga 161160cctgtgtggc caaggggccc tctccgggtg caggagtgac tggtgggctg gcaggctgcc 161220cgggactctg gccaaagcag tggcctcagc aaagccaccc acaggggtgg tgtgagtgct 161280gccagactcc ccaggcaaat ccagcccggc tccacgctga actctgggcc tgcggcttgc 161340cttttgtgaa aggcatggta tcattttacc gtaagtgatg tccattttac agatgtggaa 161400agtgagatgc agaggttgag tcactcccca aacaacactc ccccaaaaag cagtcagctg 161460ggaggaggca gaaccaggaa tcagtctaca tccgtgacct cagagcctat gcgctgaacc 161520cccgagcttg gccccctctc taagtggctg gctcacccag aggcagtgac tgcatcccca 161580gcccactttg gggatgtcct aaaccaggac ccctgtcctc ccagccactc aggagtactt 161640tccaggcagc agtgctggca cttgggccct gacaaggtac tcacctttga gggcccaggt 161700ggggtcctct cggcacttgg agcgcgtggc aggcttcagg ccaggcctca cagcagctgc 161760tggggtctcc cacactggcc aggaagcatc tcaccctcct gctggctcat gccgctgtgc 161820ctgggccctc tcccatttcc ttttggctgt tcgcacacct ttttgggagc ttgggtttca 161880ggctgtgctc tgcaagtgct ggacgctgct gagagaagga gttgctcttg cagggaagct 161940cctagccagg aggggagagg tacagaaccg cctgcttcaa accctgtgta aatattgctc 162000ttgtcacagg gaaggcgcct tgtttttcca gccctcctgc tcccaagcct ttccctaaat 162060atccattctg agattacaca gctgcagtgt gcatggaatg aaaaggtatc tgtgcttggc 162120cgccagagcg cccagtatcc tgaccttctg aacaaagcaa acctccctct gtttttaatg 162180ggtgagtttg ctgtatctct tggctcaagc tttaaatggt ccattctgta gattttggag 162240taggggaatg tggagaattt ggggcgggac cctgctggag gcggcttgag aggctgggag 162300atagaccagg gagctccaga ttctttggag ccgctgagca attttcctaa tgaaatggtc 162360caggaacccc agtgtgctcg gggtatacca gaagggcctc cttccttaac tgccttgaag 162420aacaagcagt gctgcgttta acatgcatta aactcacagg aactgagctg gacatatttg 162480agggggtggg ggaagaccgc cacgcccaga gatgttttgt ggtgtcagat acaggttata 162540gctagaggca gtggtgagag acttctgctt gtggattttt ttccttccat cttctctcag 162600gtaagtgctt tagctccaag ttggacagac tttatgttta aatcccagtt ctgctggtcc 162660ccagctgtgt gactccagat gaattatctg acttcactgt gcctctgctt cctttcctgt 162720aaaacaggat taataacagg acccacctaa taggcttgtt tggagctgta gaggaggtaa 162780cagccaagta gtagctcttg tcccataacc cctgctttct cttttcccac ctcgtcttcc 162840ctgccctttt gggccctcac agtcaagatg aactgatttt tggttggtca aaatattgca 162900ttagggccaa atgggtgcgg tggctcatgc ctgtaatcaa agcactttgg aaggccaagg 162960cagaaagatt gtttgaggcc aagagtttga gaccagcctg ggtgacatag taaaactcca 163020tctctaccaa aaaaaaaaat ttttaaagac gaacttagga atgaaacagc ttgttaaaaa 163080atggtggaac tttcccctgc agccacatca tttcaacttc actttaaaaa tatctttttg 163140gcctggcaca gtggctcaca cctgtaatcc cagcactttg ggaggtggag gtgggaggat 163200cacttgagcc taggagtttg agaccagccc aggcaacaca gcaaaacccc atctctacaa 163260aaaaatttaa aaattagcca ggcgtggtgg tgcatgcctg aagtcccagc tactttggag 163320gctgaggcag gaggatggct tgagcctgga agattgacgc tgtggtgagc tgtgatcatg 163380ccaccgtact ccagcctggg caacagagga agactttatc taaaaaaaaa aatattagta 163440ataaggccgg gtgcgttggc tcatgcctgt aatcctagca ctttgggaga ccaaggtggg 163500cagatcactt gaggtcagga gctcaagacc agcctggcca acatggtgag accccatctc 163560tactaaagaa atacaaaaat tagctgggca tggtggcgag tgcctgtaat cccagctaat 163620caggaagctg aagcaggaga atcgcttgaa cctgggaggc ggaggttgca ataagccaag 163680atcatggtac tgcactccag cctgggcaac agagcgagac tctatctcaa tcaatcaatc 163740aataaaatat ctttccttat catcacctta cagctgcttc ctggatggac acactgtctc 163800cttgttgctc acctcccgct tcttccctac gtagccccag gcctcagagc tgctgcttga 163860ggggcttctt ggctgcacag attagatacc atgatgaggt tgagatagtg ttgggggtgg 163920accttggggc aggagcctca agagcttcca ggaacagctg ggttgtgttt gagagttgca 163980cgatagcagc tcttttgttt ttattgatat ccagaacaat aattctttct ctggactagg 164040agctataatt aaaccaaaat atttcccagc tggggcagtg tctagggctc tggcagaagc 164100atagccctgc atggggatgc tatgccaggc atgccccata gagggcactg tagcaggcat 164160gcgccagacc tgatgactga aggaggctct ccctgggcca gctaagttgt ctcagggctg 164220cagttagggg atctgaggca gctccactgc ccatccaggg gtcaagagat gagcctggca 164280ccagagccat gcagacatgg ttcaaacccg gctctaccac tttctggttg tgtagcgtga 164340ctggccccct ccctgagccg cagagtcatt tgtgaagcag gaatcacgga aaggattcca 164400taccacatgc gtaaatggtg ctgtgcacag gacctggagc cggagtgggg tacgcatgcc 164460ccgtcagcgg gagctgctgt tctgttcctg tgcttgttgc tggaattcac ggcaaagtgg 164520gtgggctggc aggtcacagt ggctgcaccc ggtctgcagc acagtgcctg gggtgagggc 164580tgaggaggaa gggaggagat gcttggcctc cctggcttct ccaagtctac ccggagaaga 164640aaggacagtc agaggggccc acgcctcccc cacacccctg gagggagagc tggactctgg 164700tggctgaagc agcacttcag gctcacagtg tgactcaggc ttcttgccct cagccacaat 164760ggctcatgcc cagaggagag aacagggtgt ccaggctgtt ggtgcttgtg ggcgaaatgt 164820cagccatgct cctcctgcct tggcctagaa aagggagccc ccaccccgca gggcctgagg 164880ttctctctgc cagaagttca gagctagtgc cagtgggttc ccatgccacc agggtgagcc 164940ctctgtaagg ggatctatgt gtgtccctca ccacggcctc agtgctccca ggaaagccct 165000ccaagtcatc aacacagcat tttctattcc tttctcccag gtatccagtc ggaattcttt 165060attaacacca cccgagcagg tccagggaca ttatccgtca ccatcgaagg cccatccaag 165120gttaaaatgg attgccagga

aacacctgaa gggtacaaag tcatgtacac ccccatggct 165180cctggtaact acctgatcag cgtcaaatac ggtgggccca accacatcgt gggcagtccc 165240ttcaaggcca aggtgacagg taacgaacaa ccaccttcgg agttactctc ccttcctggg 165300gagctggttg tgtcagatca atcatagtgg aaactatgga tggttttaga tgtgttaaag 165360ctactttgaa ctttgaatgt cagtaaatag tatgagatgt cagagggcag tgtttgaaac 165420ttacaaaagt ccacagagtg gagccgtgca gaagttgaga aagcatgtta ggatgttagg 165480tggttttcta tctctaacag gaaagaatac atattgaaat cttacgtatt tgtttagatc 165540agggtctgaa aaatcccctg atttctaatt ttcacttgaa aaataatcaa aaagttttcc 165600tatacttata aaaatgtgtc tcctccaaaa cactggaaaa aataccaaac tatgaaaacc 165660acttcacagc caccacccaa ggtaaccacc ataaacactg tagtaaatcc cttccacacg 165720tcatgattca ctgttacata aagaatgtag gttcatcgca ggaaaattag aaaattcaga 165780tagaaaaatc atcctttctc atccacagaa tcattttttg atatttcatt atatgtcatc 165840ccaaactttt acactgctta tacatagact attttatgtc aatagaaaga tgtgaattcc 165900acaggcacat ctttggtggg tagggggtgg ggggattggg agggtccttg gccttgtcag 165960ccaaggccag actcatccat ttgcccagaa agccagatcc tagttgtatg ggggtgggat 166020cctaggggtt tagaagacat tatgggtgtg agatacaggt gtggtggctt ttgtgttggg 166080gtgcgcgggc tctcctgggg ttactgtgta gggtactcgc ctgtcctctg gctgagagac 166140ccctcttgat ctggccattc atgcctgtcc ccctccctcc tgtatcttag gccagcgtct 166200agttagccct ggctcagcca acgagacctc atccatcctg gtggagtcag tgaccaggtc 166260gtctacagag acctgctata gcgccattcc caaggcatcc tcggacgcca gcaaggtgac 166320ctctaagggg gcagggctct caaaggcctt tgtgggccag aagagttcct tcctggtgga 166380ctgcagcaaa gctggtaggt gtctgggcct tttcaagggt ggggtggggc aggggcaggc 166440tgggcaccct gggtacactg gccttccctg ctgaggtctc ctgcagtgcc cacccccatg 166500taggccagcc gtttgcaagt aaccatcgtc atgaccctgt tctcctgcac ttaatatttt 166560taaatgattt ccttctcttt tgccttttga acttgggtat ttatttgggt ttcaagggtc 166620ggttgcctgg gttctggcat ccagtacacc tgggctggaa acctagtacc gccacttcat 166680tcattcattc gtttgttcta aaacttattt agccatgtga ccttggaaag ttattaaatc 166740tctttccaaa agtcagtttc ctcttctcgg aagtaccttc cttaaggtgc ttgtgagagt 166800aaacaagaag attctcatag ccaacactta gaatagccct tactgtgtgc taggttttga 166860cacccataac tcttaaacct cacaactagt tcgtgaggta tgtgctgttc tcattccctg 166920tttacagatg gggaagctga gctagggaga ggtgagattc cagtccaagg tcacccaggt 166980agcaagtggc agggcaggga ttcgaaccca caccgtcagg ctctatgagc ctctgcttgt 167040aattgccacg ctctcccacc tcttaggggc cccagcatta tcgtggaagc accttacctt 167100tggctctcat atttcctctt cttcctgtgc ctgtcctgat gcatccgggt ggagtaacca 167160ccttttgcct cctaggctcc aacatgctgc tgatcggggt ccatgggccc accaccccct 167220gcgaggaggt ctccatgaag catgtaggca accagcaata caacgtcaca tacgtcgtca 167280aggagagggg cgattatgtg ctggctgtga agtgggggga ggaacacatc cctggcagcc 167340cttttcatgt cacagtgcct taaaacagtt ttctcaaatc ctggagagag ttcttgtggt 167400tgcttttgtt gcttgtttgt aattcatttt atacaaagcc ctccagcctg tttgtggggc 167460tgaaacccca tccctaaaat attgctgttg taaaatgcct tcagaaataa gtcctagact 167520ggactcttga gggacatatt ggagaatctt aagaaatgca agcttgttca gggggctgag 167580aagatcctga gtacactagg tgcaaaccag aactcttggt ggaacagacc agccactgca 167640gcagacagac caggaacaca atgagactga catttcaaaa aaacaaaact ggctagcctg 167700agctgctggt tcactcttca gcatttatga aacaaggcta ggggaagatg ggcagagaaa 167760aaggggacac ctagtttggt tgtcatttgg caaaggagat gacttaaaat ccgcttaatc 167820tcttccagtg tccgtgttaa tgtatttggc tattagatca ctagcactgc tttaccgctc 167880ctcatcgcca acacccccat gctctgtggc cttcttacac ttctcagagg gcagagtggc 167940agccgggcac cctacagaaa ctcagagggc agagtggcag ccaggcccac atgtctctca 168000agtacctgtc ccctcgctct ggtgattatt tcttgcagaa tcaccacacg agaccatccc 168060ggcagtcatg gttttgcttt agttttccaa gtccgtttca gtcccttcct tggtctgaag 168120aaattctgca gtggcgagca gtttcccact tgccaaagat cccttttaac caacactagc 168180ccttgttttt aacacacgct ccagcccttc atcagcctgg gcagtcttac caaaatgttt 168240aaagtgatct cagaggggcc catggattaa cgccctcatc ccaaggtccg tcccatgaca 168300taacactcca cacccgcccc agccaacttc atgggtcact ttttctggaa aataatgatc 168360tgtacagaca ggacagaatg aaactcctgc gggtctttgg cctgaaagtt gggaatggtt 168420gggggagaga agggcagcag cttattggtg gtcttttcac cattggcaga aacagtgaga 168480gctgtgtggt gcagaaatcc agaaatgagg tgtagggaat tttgcctgcc ttcctgcaga 168540cctgagctgg ctttggaatg aggttaaagt gtcagggacg ttgcctgagc ccaaatgtgt 168600agtgtggtct gggcaggcag acctttaggt tttgctgctt agtcctgagg aagtggccac 168660tcttgtggca ggtgtagtat ctggggcgag tgttgggggt aaaagcccac cctacagaaa 168720gtggaacagc ccggagcctg atgtgaaagg accacgggtg ttgtaagctg ggacacggaa 168780gccaaactgg aatcaaacgc cgactgtaaa ttgtatctta taacttatta aataaaacat 168840ttgctccgta aagttgcctt ggtgttcttg gatgatgtcg cttctgaata aattgtttaa 168900tcctaggagt tcaacaccct cagcctgggt aacagcaaga cccagcctct acaaaaaatt 168960aaaaaattag ccagcatggt gatgcatgcc tgcagtccca gctactcagg aggcggaggc 169020aggaggattg cttgagcctg agaggccaag gttgcagtga gctgtgtttg caaccctgca 169080ctctagcctg ggcaacagag caagacagtg taacacacac acacacacac acacacacac 169140acacacacac acaggcacat cgttggagcc ccagatcagc tctcccaacc ccttaaggga 169200cacaaaacta gcaacttgtt ttgacaatga acctgggctc cttttgtggg ggtggggtgg 169260ggctggtaaa caagctgtca cctgtcaccc tgctgtgctt attgttgctg ctgcctctgt 169320ttctcttttt tttttttttt taattttcct tttttgagac agagtctcac tctgttgccc 169380aggctggagt gcagtggcag gatctctgct cactgcagcc tccgcctccc aggttcaagt 169440gattcttctg cctcagcttc ccaagtagct gggactacag gcgtgcacca ccatgcctgg 169500ctaatttttg tctttttagt agagatgtgg tttcgccgtg ttggccaggc tggtcttgaa 169560ctcctgacct caagtgatcc gccctgcctt ggtcttccaa agtgctgtat tacaggcgtc 169620aaccactgcg actggcctgt ttctcctttt tctagaagag cttttgattg ctgaatgctt 169680acgaggtacc tagcacccct cctccgcccc cacctcctcc tcctctgtct ccgcctcctc 169740cccaccccac agcagtgata ccgctttaca gatggcacta ccacctcagg tgctgcaatg 169800acatgtttgc agatgcaaag ctcacttggg ggaagaccct aggcccctgc cttcttgacc 169860ccagggtgct agctctaccc cctggtgata ccgctgtgga aacaggagtc cccagatagg 169920ccccggcagg tgccacggtg atgggaaatc acggctgggc ccccagccct ccagatgggg 169980gttgggggtg gagagaaaag cagggaaggg agactggatt cttctgacac ctggctgtca 170040attgggatca attgtttgcc tctgagagga gggaggaaga gagtggagga aaggtcctct 170100cctcccggag ggagcagcct tatctgtggc ctgcaccagg aagcactgct tcctggactc 170160ctatctgaga aggtccgtgg gcttcgggat tctgcagtgg cgggcagttc ccccacttgc 170220caaagagtcc attcaggctc tgcccggtgg ggtctggccg ggccacagta tcatgctagt 170280ttgcccacag aggagcacag ggcgcagcca ttggtctctc cactgtgaag cctggcggct 170340ttctgttggg ggaggcagca tttgtaaatt aacagcatgg gctttggtgt caggcacccc 170400agagcttcaa cgctggctct gccgttcatt agctgtgtgg ccctggggaa gtcgccttgc 170460ctcacctctc tgggtggtcg tgaggatcaa ataagagccc acagggagct gtaaggaaca 170520attccctgcc agagtctcag ccactgctgt ctgtgaccaa cacctgctgg aagtgatgtt 170580cctggcagaa ggccgccccc tggctgcttg ttggcatctg gggctacact tggttgtccc 170640ctgcatggga gcgatggtga tgttaccctg gggtaaattt ccccactaga agccactgcc 170700tcctgttaca tcaaagacat cccagggtgg gatgcacctc tttatcagtc aatggctagg 170760accacagggc aacccttacc tgcacctggg cttggctgct atggaaacca gctgtttgtg 170820caaatacctt gaaaactttg aaacttgacc ccggac 170856222633PRTHomo sapiens 22Met Pro Val Thr Glu Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys1 5 10 15Ile Gln Gln Asn Thr Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys 20 25 30Val Asn Lys Arg Ile Gly Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu 35 40 45Arg Leu Ile Ala Leu Leu Glu Val Leu Ser Gln Lys Arg Met Tyr Arg 50 55 60Lys Tyr His Gln Arg Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val65 70 75 80Ser Val Ala Leu Glu Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser 85 90 95Ile Asp Ser Lys Ala Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly 100 105 110Leu Val Trp Thr Leu Ile Leu His Tyr Ser Ile Ser Met Pro Val Trp 115 120 125Glu Asp Glu Gly Asp Asp Asp Ala Lys Lys Gln Thr Pro Lys Gln Arg 130 135 140Leu Leu Gly Trp Ile Gln Asn Lys Ile Pro Tyr Leu Pro Ile Thr Asn145 150 155 160Phe Asn Gln Asn Trp Gln Asp Gly Lys Ala Leu Gly Ala Leu Val Asp 165 170 175Ser Cys Ala Pro Gly Leu Cys Pro Asp Trp Glu Ser Trp Asp Pro Gln 180 185 190Lys Pro Val Asp Asn Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp 195 200 205Leu Gly Val Pro Gln Val Ile Thr Pro Glu Glu Ile Ile His Pro Asp 210 215 220Val Asp Glu His Ser Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala225 230 235 240Lys Leu Lys Pro Gly Ala Pro Leu Lys Pro Lys Leu Asn Pro Lys Lys 245 250 255Ala Arg Ala Tyr Gly Arg Gly Ile Glu Pro Thr Gly Asn Met Val Lys 260 265 270Gln Pro Ala Lys Phe Thr Val Asp Thr Ile Ser Ala Gly Gln Gly Asp 275 280 285Val Met Val Phe Val Glu Asp Pro Glu Gly Asn Lys Glu Glu Ala Gln 290 295 300Val Thr Pro Asp Ser Asp Lys Asn Lys Thr Tyr Ser Val Glu Tyr Leu305 310 315 320Pro Lys Val Thr Gly Leu His Lys Val Thr Val Leu Phe Ala Gly Gln 325 330 335His Ile Ser Lys Ser Pro Phe Glu Val Ser Val Asp Lys Ala Gln Gly 340 345 350Asp Ala Ser Lys Val Thr Ala Lys Gly Pro Gly Leu Glu Ala Val Gly 355 360 365Asn Ile Ala Asn Lys Pro Thr Tyr Phe Asp Ile Tyr Thr Ala Gly Ala 370 375 380Gly Val Gly Asp Ile Gly Val Glu Val Glu Asp Pro Gln Gly Lys Asn385 390 395 400Thr Val Glu Leu Leu Val Glu Asp Lys Gly Asn Gln Val Tyr Arg Cys 405 410 415Val Tyr Lys Pro Met Gln Pro Gly Pro His Val Val Lys Ile Phe Phe 420 425 430Ala Gly Asp Thr Ile Pro Lys Ser Pro Phe Val Val Gln Val Gly Glu 435 440 445Ala Cys Asn Pro Asn Ala Cys Arg Ala Ser Gly Arg Gly Leu Gln Pro 450 455 460Lys Gly Val Arg Ile Arg Glu Thr Thr Asp Phe Lys Val Asp Thr Lys465 470 475 480Ala Ala Gly Ser Gly Glu Leu Gly Val Thr Met Lys Gly Pro Lys Gly 485 490 495Leu Glu Glu Leu Val Lys Gln Lys Asp Phe Leu Asp Gly Val Tyr Ala 500 505 510Phe Glu Tyr Tyr Pro Ser Thr Pro Gly Arg Tyr Ser Ile Ala Ile Thr 515 520 525Trp Gly Gly His His Ile Pro Lys Ser Pro Phe Glu Val Gln Val Gly 530 535 540Pro Glu Ala Gly Met Gln Lys Val Arg Ala Trp Gly Pro Gly Leu His545 550 555 560Gly Gly Ile Val Gly Arg Ser Ala Asp Phe Val Val Glu Ser Ile Gly 565 570 575Ser Glu Val Gly Ser Leu Gly Phe Ala Ile Glu Gly Pro Ser Gln Ala 580 585 590Lys Ile Glu Tyr Asn Asp Gln Asn Asp Gly Ser Cys Asp Val Lys Tyr 595 600 605Trp Pro Lys Glu Pro Gly Glu Tyr Ala Val His Ile Met Cys Asp Asp 610 615 620Glu Asp Ile Lys Asp Ser Pro Tyr Met Ala Phe Ile His Pro Ala Thr625 630 635 640Gly Gly Tyr Asn Pro Asp Leu Val Arg Ala Tyr Gly Pro Gly Leu Glu 645 650 655Lys Ser Gly Cys Ile Val Asn Asn Leu Ala Glu Phe Thr Val Asp Pro 660 665 670Lys Asp Ala Gly Lys Ala Pro Leu Lys Ile Phe Ala Gln Asp Gly Glu 675 680 685Gly Gln Arg Ile Asp Ile Gln Met Lys Asn Arg Met Asp Gly Thr Tyr 690 695 700Ala Cys Ser Tyr Thr Pro Val Lys Ala Ile Lys His Thr Ile Ala Val705 710 715 720Val Trp Gly Gly Val Asn Ile Pro His Ser Pro Tyr Arg Val Asn Ile 725 730 735Gly Gln Gly Ser His Pro Gln Lys Val Lys Val Phe Gly Pro Gly Val 740 745 750Glu Arg Ser Gly Leu Lys Ala Asn Glu Pro Thr His Phe Thr Val Asp 755 760 765Cys Thr Glu Ala Gly Glu Gly Asp Val Ser Val Gly Ile Lys Cys Asp 770 775 780Ala Arg Val Leu Ser Glu Asp Glu Glu Asp Val Asp Phe Asp Ile Ile785 790 795 800His Asn Ala Asn Asp Thr Phe Thr Val Lys Tyr Val Pro Pro Ala Ala 805 810 815Gly Arg Tyr Thr Ile Lys Val Leu Phe Ala Ser Gln Glu Ile Pro Ala 820 825 830Ser Pro Phe Arg Val Lys Val Asp Pro Ser His Asp Ala Ser Lys Val 835 840 845Lys Ala Glu Gly Pro Gly Leu Ser Lys Ala Gly Val Glu Asn Gly Lys 850 855 860Pro Thr His Phe Thr Val Tyr Thr Lys Gly Ala Gly Lys Ala Pro Leu865 870 875 880Asn Val Gln Phe Asn Ser Pro Leu Pro Gly Asp Ala Val Lys Asp Leu 885 890 895Asp Ile Ile Asp Asn Tyr Asp Tyr Ser His Thr Val Lys Tyr Thr Pro 900 905 910Thr Gln Gln Gly Asn Met Gln Val Leu Val Thr Tyr Gly Gly Asp Pro 915 920 925Ile Pro Lys Ser Pro Phe Thr Val Gly Val Ala Ala Pro Leu Asp Leu 930 935 940Ser Lys Ile Lys Leu Asn Gly Leu Glu Asn Arg Val Glu Val Gly Lys945 950 955 960Asp Gln Glu Phe Thr Val Asp Thr Arg Gly Ala Gly Gly Gln Gly Lys 965 970 975Leu Asp Val Thr Ile Leu Ser Pro Ser Arg Lys Val Val Pro Cys Leu 980 985 990Val Thr Pro Val Thr Gly Arg Glu Asn Ser Thr Ala Lys Phe Ile Pro 995 1000 1005Arg Glu Glu Gly Leu Tyr Ala Val Asp Val Thr Tyr Asp Gly His 1010 1015 1020Pro Val Pro Gly Ser Pro Tyr Thr Val Glu Ala Ser Leu Pro Pro 1025 1030 1035Asp Pro Ser Lys Val Lys Ala His Gly Pro Gly Leu Glu Gly Gly 1040 1045 1050Leu Val Gly Lys Pro Ala Glu Phe Thr Ile Asp Thr Lys Gly Ala 1055 1060 1065Gly Thr Gly Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala 1070 1075 1080Lys Ile Glu Cys Ser Asp Asn Gly Asp Gly Thr Cys Ser Val Ser 1085 1090 1095Tyr Leu Pro Thr Lys Pro Gly Glu Tyr Phe Val Asn Ile Leu Phe 1100 1105 1110Glu Glu Val His Ile Pro Gly Ser Pro Phe Lys Ala Asp Ile Glu 1115 1120 1125Met Pro Phe Asp Pro Ser Lys Val Val Ala Ser Gly Pro Gly Leu 1130 1135 1140Glu His Gly Lys Val Gly Glu Ala Gly Leu Leu Ser Val Asp Cys 1145 1150 1155Ser Glu Ala Gly Pro Gly Ala Leu Gly Leu Glu Ala Val Ser Asp 1160 1165 1170Ser Gly Thr Lys Ala Glu Val Ser Ile Gln Asn Asn Lys Asp Gly 1175 1180 1185Thr Tyr Ala Val Thr Tyr Val Pro Leu Thr Ala Gly Met Tyr Thr 1190 1195 1200Leu Thr Met Lys Tyr Gly Gly Glu Leu Val Pro His Phe Pro Ala 1205 1210 1215Arg Val Lys Val Glu Pro Ala Val Asp Thr Ser Arg Ile Lys Val 1220 1225 1230Phe Gly Pro Gly Ile Glu Gly Lys Asp Val Phe Arg Glu Ala Thr 1235 1240 1245Thr Asp Phe Thr Val Asp Ser Arg Pro Leu Thr Gln Val Gly Gly 1250 1255 1260Asp His Ile Lys Ala His Ile Ala Asn Pro Ser Gly Ala Ser Thr 1265 1270 1275Glu Cys Phe Val Thr Asp Asn Ala Asp Gly Thr Tyr Gln Val Glu 1280 1285 1290Tyr Thr Pro Phe Glu Lys Gly Leu His Val Val Glu Val Thr Tyr 1295 1300 1305Asp Asp Val Pro Ile Pro Asn Ser Pro Phe Lys Val Ala Val Thr 1310 1315 1320Glu Gly Cys Gln Pro Ser Arg Val Gln Ala Gln Gly Pro Gly Leu 1325 1330 1335Lys Glu Ala Phe Thr Asn Lys Pro Asn Val Phe Thr Val Val Thr 1340 1345 1350Arg Gly Ala Gly Ile Gly Gly Leu Gly Ile Thr Val Glu Gly Pro 1355 1360 1365Ser Glu Ser Lys Ile Asn Cys Arg Asp Asn Lys Asp Gly Ser Cys 1370 1375 1380Ser Ala Glu Tyr Ile Pro Phe Ala Pro Gly Asp Tyr Asp Val Asn 1385 1390 1395Ile Thr Tyr Gly Gly Ala His Ile Pro Gly Ser Pro Phe Arg Val 1400 1405 1410Pro Val Lys Asp Val Val Asp Pro Ser Lys Val Lys Ile Ala Gly 1415 1420 1425Pro Gly Leu Gly Ser Gly Val Arg Ala Arg Val Leu Gln Ser Phe 1430 1435 1440Thr Val Asp Ser Ser Lys Ala Gly Leu Ala Pro Leu Glu Val Arg 1445 1450 1455Val Leu Gly Pro Arg Ala Asp Asp Thr Asp Ser Gln Ser Trp Arg 1460 1465 1470Ser Pro Leu Lys Ala Leu Ser Glu Phe Phe Lys Gly Asp Pro Lys 1475 1480 1485Gly Asp Phe Asn Lys Thr Gly Leu Val Glu Pro Val Asn Val Val 1490 1495 1500Asp Asn Gly Asp Gly Thr His Thr Val Thr Tyr Thr Pro Ser Gln 1505 1510 1515Glu Gly Pro Tyr

Met Val Ser Val Lys Tyr Ala Asp Glu Glu Ile 1520 1525 1530Pro Arg Ser Pro Phe Lys Val Lys Val Leu Pro Thr Tyr Asp Ala 1535 1540 1545Ser Lys Val Thr Ala Ser Gly Pro Gly Leu Ser Ser Tyr Gly Val 1550 1555 1560Pro Ala Ser Leu Pro Val Asp Phe Ala Ile Asp Ala Arg Asp Ala 1565 1570 1575Gly Glu Gly Leu Leu Ala Val Gln Ile Thr Asp Gln Glu Gly Lys 1580 1585 1590Pro Lys Arg Ala Ile Val His Asp Asn Lys Asp Gly Thr Tyr Ala 1595 1600 1605Val Thr Tyr Ile Pro Asp Lys Thr Gly Arg Tyr Met Ile Gly Val 1610 1615 1620Thr Tyr Gly Gly Asp Asp Ile Pro Leu Ser Pro Tyr Arg Ile Arg 1625 1630 1635Ala Thr Gln Thr Gly Asp Ala Ser Lys Cys Leu Ala Thr Gly Pro 1640 1645 1650Gly Ile Ala Ser Thr Val Lys Thr Gly Glu Glu Val Gly Phe Val 1655 1660 1665Val Asp Ala Lys Thr Ala Gly Lys Gly Lys Val Thr Cys Thr Val 1670 1675 1680Leu Thr Pro Asp Gly Thr Glu Ala Glu Ala Asp Val Ile Glu Asn 1685 1690 1695Glu Asp Gly Thr Tyr Asp Ile Phe Tyr Thr Ala Ala Lys Pro Gly 1700 1705 1710Thr Tyr Val Ile Tyr Val Arg Phe Gly Gly Val Asp Ile Pro Asn 1715 1720 1725Ser Pro Phe Thr Val Met Ala Thr Asp Gly Glu Val Thr Ala Val 1730 1735 1740Glu Glu Ala Pro Val Asn Ala Cys Pro Pro Gly Phe Arg Pro Trp 1745 1750 1755Val Thr Glu Glu Ala Tyr Val Pro Val Ser Asp Met Asn Gly Leu 1760 1765 1770Gly Phe Lys Pro Phe Asp Leu Val Ile Pro Phe Ala Val Arg Lys 1775 1780 1785Gly Glu Ile Thr Gly Glu Val His Met Pro Ser Gly Lys Thr Ala 1790 1795 1800Thr Pro Glu Ile Val Asp Asn Lys Asp Gly Thr Val Thr Val Arg 1805 1810 1815Tyr Ala Pro Thr Glu Val Gly Leu His Glu Met His Ile Lys Tyr 1820 1825 1830Met Gly Ser His Ile Pro Glu Ser Pro Leu Gln Phe Tyr Val Asn 1835 1840 1845Tyr Pro Asn Ser Gly Ser Val Ser Ala Tyr Gly Pro Gly Leu Val 1850 1855 1860Tyr Gly Val Ala Asn Lys Thr Ala Thr Phe Thr Ile Val Thr Glu 1865 1870 1875Asp Ala Gly Glu Gly Gly Leu Asp Leu Ala Ile Glu Gly Pro Ser 1880 1885 1890Lys Ala Glu Ile Ser Cys Ile Asp Asn Lys Asp Gly Thr Cys Thr 1895 1900 1905Val Thr Tyr Leu Pro Thr Leu Pro Gly Asp Tyr Ser Ile Leu Val 1910 1915 1920Lys Tyr Asn Asp Lys His Ile Pro Gly Ser Pro Phe Thr Ala Lys 1925 1930 1935Ile Thr Asp Asp Ser Arg Arg Cys Ser Gln Val Lys Leu Gly Ser 1940 1945 1950Ala Ala Asp Phe Leu Leu Asp Ile Ser Glu Thr Asp Leu Ser Ser 1955 1960 1965Leu Thr Ala Ser Ile Lys Ala Pro Ser Gly Arg Asp Glu Pro Cys 1970 1975 1980Leu Leu Lys Arg Leu Pro Asn Asn His Ile Gly Ile Ser Phe Ile 1985 1990 1995Pro Arg Glu Val Gly Glu His Leu Val Ser Ile Lys Lys Asn Gly 2000 2005 2010Asn His Val Ala Asn Ser Pro Val Ser Ile Met Val Val Gln Ser 2015 2020 2025Glu Ile Gly Asp Ala Arg Arg Ala Lys Val Tyr Gly Arg Gly Leu 2030 2035 2040Ser Glu Gly Arg Thr Phe Glu Met Ser Asp Phe Ile Val Asp Thr 2045 2050 2055Arg Asp Ala Gly Tyr Gly Gly Ile Ser Leu Ala Val Glu Gly Pro 2060 2065 2070Ser Lys Val Asp Ile Gln Thr Glu Asp Leu Glu Asp Gly Thr Cys 2075 2080 2085Lys Val Ser Tyr Phe Pro Thr Val Pro Gly Val Tyr Ile Val Ser 2090 2095 2100Thr Lys Phe Ala Asp Glu His Val Pro Gly Ser Pro Phe Thr Val 2105 2110 2115Lys Ile Ser Gly Glu Gly Arg Val Lys Glu Ser Ile Thr Arg Thr 2120 2125 2130Ser Arg Ala Pro Ser Val Ala Thr Val Gly Ser Ile Cys Asp Leu 2135 2140 2145Asn Leu Lys Ile Pro Glu Ile Asn Ser Ser Asp Met Ser Ala His 2150 2155 2160Val Thr Ser Pro Ser Gly Arg Val Thr Glu Ala Glu Ile Val Pro 2165 2170 2175Met Gly Lys Asn Ser His Cys Val Arg Phe Val Pro Gln Glu Met 2180 2185 2190Gly Val His Thr Val Ser Val Lys Tyr Arg Gly Gln His Val Thr 2195 2200 2205Gly Ser Pro Phe Gln Phe Thr Val Gly Pro Leu Gly Glu Gly Gly 2210 2215 2220Ala His Lys Val Arg Ala Gly Gly Pro Gly Leu Glu Arg Gly Glu 2225 2230 2235Ala Gly Val Pro Ala Glu Phe Ser Ile Trp Thr Arg Glu Ala Gly 2240 2245 2250Ala Gly Gly Leu Ser Ile Ala Val Glu Gly Pro Ser Lys Ala Glu 2255 2260 2265Ile Thr Phe Asp Asp His Lys Asn Gly Ser Cys Gly Val Ser Tyr 2270 2275 2280Ile Ala Gln Glu Pro Gly Asn Tyr Glu Val Ser Ile Lys Phe Asn 2285 2290 2295Asp Glu His Ile Pro Glu Ser Pro Tyr Leu Val Pro Val Ile Ala 2300 2305 2310Pro Ser Asp Asp Ala Arg Arg Leu Thr Val Met Ser Leu Gln Glu 2315 2320 2325Ser Gly Leu Lys Val Asn Gln Pro Ala Ser Phe Ala Ile Arg Leu 2330 2335 2340Asn Gly Ala Lys Gly Lys Ile Asp Ala Lys Val His Ser Pro Ser 2345 2350 2355Gly Ala Val Glu Glu Cys His Val Ser Glu Leu Glu Pro Asp Lys 2360 2365 2370Tyr Ala Val Arg Phe Ile Pro His Glu Asn Gly Val His Thr Ile 2375 2380 2385Asp Val Lys Phe Asn Gly Ser His Val Val Gly Ser Pro Phe Lys 2390 2395 2400Val Arg Val Gly Glu Pro Gly Gln Ala Gly Asn Pro Ala Leu Val 2405 2410 2415Ser Ala Tyr Gly Thr Gly Leu Glu Gly Gly Thr Thr Gly Ile Gln 2420 2425 2430Ser Glu Phe Phe Ile Asn Thr Thr Arg Ala Gly Pro Gly Thr Leu 2435 2440 2445Ser Val Thr Ile Glu Gly Pro Ser Lys Val Lys Met Asp Cys Gln 2450 2455 2460Glu Thr Pro Glu Gly Tyr Lys Val Met Tyr Thr Pro Met Ala Pro 2465 2470 2475Gly Asn Tyr Leu Ile Ser Val Lys Tyr Gly Gly Pro Asn His Ile 2480 2485 2490Val Gly Ser Pro Phe Lys Ala Lys Val Thr Gly Gln Arg Leu Val 2495 2500 2505Ser Pro Gly Ser Ala Asn Glu Thr Ser Ser Ile Leu Val Glu Ser 2510 2515 2520Val Thr Arg Ser Ser Thr Glu Thr Cys Tyr Ser Ala Ile Pro Lys 2525 2530 2535Ala Ser Ser Asp Ala Ser Lys Val Thr Ser Lys Gly Ala Gly Leu 2540 2545 2550Ser Lys Ala Phe Val Gly Gln Lys Ser Ser Phe Leu Val Asp Cys 2555 2560 2565Ser Lys Ala Gly Ser Asn Met Leu Leu Ile Gly Val His Gly Pro 2570 2575 2580Thr Thr Pro Cys Glu Glu Val Ser Met Lys His Val Gly Asn Gln 2585 2590 2595Gln Tyr Asn Val Thr Tyr Val Val Lys Glu Arg Gly Asp Tyr Val 2600 2605 2610Leu Ala Val Lys Trp Gly Glu Glu His Ile Pro Gly Ser Pro Phe 2615 2620 2625His Val Thr Val Pro 2630239560DNAHomo sapiens 23gcggccaggg gcgggcggcc gcagagcagc accggccgtg gctccggtag cagcaagttc 60gaaccccgct cccgctccgc ttcggttctc gctccttcgg cccttgggcc tccaaacacc 120agtccccggc agctcgttgc gcattgcgct ctccccgcca ccaggatgcc ggtaaccgag 180aaggatctag ctgaggacgc gccttggaag aagatccagc agaacacgtt cacacgctgg 240tgcaacgagc acctcaagtg cgtgaacaaa cgcatcggca acctgcagac cgacctgagc 300gacgggctgc ggctcatcgc gctgctcgag gtgctcagcc agaagcgcat gtaccgcaag 360taccatcagc ggcccacctt tcgccagatg cagctcgaga atgtgtccgt ggcgctcgag 420ttcctggacc gtgagagcat caagctcgtg tccatcgata gcaaagccat tgtggatggg 480aacctgaagc tcatcttggg tctggtgtgg acgctgatcc tccactactc catctccatg 540cccgtgtggg aggatgaagg ggatgatgat gccaagaagc agacgccaaa gcagaggctg 600ctggggtgga ttcagaacaa gatcccctac ttgcccatca ccaactttaa ccagaactgg 660caagacggca aagccctggg agccctggta gacagctgtg ctccaggtct gtgcccagac 720tgggaatcct gggacccgca gaagcctgtg gataatgcac gagaagccat gcagcaggca 780gatgactggc tgggtgtccc acaggtcatc actcctgaag aaatcattca cccggatgtg 840gacgagcact cagttatgac ttacctgtcc cagttcccca aagccaagct caagccgggg 900gctcctctca aacccaaact caacccgaag aaagccaggg cctatggcag aggaatcgag 960cccactggaa acatggtgaa gcagccagcc aagttcactg tggacaccat cagcgccggg 1020caaggagacg tgatggtgtt tgttgaggac ccagaaggga acaaagagga ggcacaagtg 1080acccctgaca gtgacaagaa caagacatac tctgtggagt atctgcccaa ggtcaccggg 1140ctacacaaag tcacagtcct ctttgcagga cagcacatct ccaagagccc atttgaagtg 1200agtgttgaca aggcccaggg agatgccagt aaagtcactg caaaaggtcc agggttggaa 1260gctgtaggga acatcgccaa taagcccacc tactttgaca tctatacggc aggagctggt 1320gtgggtgaca ttggtgtgga ggtggaagat ccccagggga agaacaccgt ggagttgctc 1380gtggaagaca aaggaaacca ggtgtatcga tgtgtgtaca aacccatgca gcctggccct 1440cacgtggtca agatcttctt tgctggggac actattccta agagtccctt cgttgtgcag 1500gttggggaag cctgcaatcc aaatgcctgc cgggccagtg gccgaggcct acaacccaaa 1560ggcgtccgta tccgggagac cacagatttc aaggttgaca ccaaagctgc aggaagtggg 1620gagctcggtg taaccatgaa gggtcctaag ggtctggagg agctggtgaa gcagaaagac 1680tttctggatg gggtctacgc attcgagtat taccccagca ccccggggag atacagcatt 1740gccatcacat gggggggaca ccacattcca aagagcccct ttgaagttca agttggccct 1800gaagcgggta tgcagaaagt ccgtgcttgg ggccctgggc tccatggtgg gattgtcggg 1860cggtcagcgg acttcgtggt agaatccatt ggctctgaag tggggtctct ggggtttgcc 1920attgaaggcc cctctcaggc aaagattgag tacaacgacc agaatgatgg atcgtgtgat 1980gtcaaatact ggcccaagga gcctggcgaa tatgctgttc acatcatgtg tgacgacgaa 2040gacatcaagg acagcccgta catggccttc atccacccag ccacgggagg ctacaaccct 2100gatctggttc gagcatacgg gccaggtttg gagaaatctg gatgcattgt caacaacctg 2160gccgagttca ctgtggatcc taaggatgct ggaaaagctc ccttaaagat atttgctcag 2220gatggggaag gccaacgcat tgacatccag atgaagaacc ggatggacgg cacatatgca 2280tgctcataca ccccggtgaa ggccatcaag cacaccattg ctgtggtctg gggaggcgtg 2340aacatcccgc acagccccta cagggtcaac atcgggcaag gtagccatcc tcagaaggtc 2400aaagtgtttg ggccaggtgt ggagagaagt ggtctgaagg caaatgaacc tacacacttc 2460acggtggact gtactgaggc tggggaaggt gatgtcagtg ttggcattaa gtgtgatgcc 2520cgggtgttaa gtgaagatga ggaagacgtg gattttgaca ttattcacaa tgccaatgat 2580acgttcacag tcaaatatgt gcctcctgct gctgggcgat acactatcaa agttctcttt 2640gcatctcagg aaatccccgc cagccctttc agagtcaaag ttgacccttc ccacgatgcc 2700agcaaagtga aggcagaagg cccagggctc agcaaagcag gtgtggaaaa tgggaaaccg 2760acccacttca ctgtctacac caagggggct gggaaagccc cgctcaacgt gcagttcaac 2820agccctcttc ctggcgatgc agtgaaggat ttggatatca tcgataatta tgactactct 2880cacacggtta aatatacacc cacccaacag ggcaacatgc aggttctggt gacttacggt 2940ggcgatccca tccctaaaag ccctttcact gtgggtgttg ctgcaccgct ggatctgagc 3000aagataaaac tcaatgggct ggaaaacagg gtggaagttg ggaaggatca ggagttcacc 3060gttgatacca ggggggcagg aggccagggg aagctggacg tgacaatcct cagcccctct 3120cggaaggtcg tgccatgcct agtgacacct gtgacaggcc gggagaacag cacggccaag 3180ttcatccctc gggaggaggg gctgtatgct gtagacgtga cctacgatgg acaccctgtg 3240cccgggagcc cctacacagt ggaggcctcg ctgccaccag atcccagcaa ggtgaaggcc 3300cacggtcccg gcctcgaagg tggtctcgtg ggcaagcctg ccgagttcac catcgatacc 3360aaaggagctg gtactggagg tctgggctta acggtggaag gtccgtgcga ggccaaaatc 3420gagtgctccg acaatggtga tgggacctgc tccgtctctt accttcccac aaaacccggg 3480gagtacttcg tcaacatcct ctttgaagaa gtccacatac ctgggtctcc cttcaaagct 3540gacattgaaa tgccctttga cccctctaaa gtcgtggcat cggggccagg tctcgagcac 3600gggaaggtgg gtgaagctgg cctccttagc gtcgactgct cggaagcggg accgggggcc 3660ctgggcctgg aagctgtctc ggactcggga acaaaagccg aagtcagtat tcagaacaac 3720aaagatggca cctacgcggt gacctacgtg cccctgacgg ccggcatgta cacgttgacc 3780atgaagtatg gtggcgaact cgtgccacac ttccccgccc gggtcaaggt ggagcccgcc 3840gtggacacca gcaggatcaa agtctttgga ccaggaatag aagggaaaga tgtgttccgg 3900gaagctacca ccgactttac agttgactct cggccgctga cccaggttgg gggtgaccac 3960atcaaggccc acattgccaa cccctcaggg gcctccaccg agtgctttgt cacagacaat 4020gcggatggga cctaccaggt ggaatacaca ccctttgaga aaggtctcca tgtagtggag 4080gtgacatatg atgacgtgcc tatcccaaac agtcccttca aggtggctgt cactgaaggc 4140tgccagccat ctagggtgca agcccaagga cctggattga aagaggcctt taccaacaag 4200cccaatgtct tcaccgtggt taccagaggc gcaggaattg gtgggcttgg cataactgtt 4260gagggaccat cagagtcgaa gataaattgc agagacaaca aggatggcag ctgcagtgct 4320gagtacattc ctttcgcacc gggggattac gatgttaata tcacatatgg aggagcccac 4380atccccggca gccccttcag ggttcctgtg aaggatgttg tggaccccag caaggtcaag 4440attgccggcc ccgggctggg ctcaggcgtc cgagcccgtg tcctgcagtc cttcacggtg 4500gacagcagca aggctggcct ggctccgctg gaagtgaggg ttctgggccc acgagctgac 4560gacacggatt cccagtcatg gcgcagcccc ttgaaagccc tttcagagtt ctttaaaggt 4620gacccgaagg gtgactttaa taagacaggc ttggtggagc cagtgaacgt ggtggacaat 4680ggagatggca cacacacagt aacctacacc ccatctcagg agggacctta catggtctca 4740gttaaatatg ctgatgaaga gattcctcgc agtcccttca aggtcaaggt ccttcccaca 4800tatgatgcca gcaaagtgac tgccagtggc cccggcctta gttcctatgg tgtgcctgcc 4860agtctacctg tggactttgc aattgatgcc cgagatgccg gggaaggcct gcttgctgtt 4920caaataacgg accaagaagg aaaacccaaa agagccattg tccatgacaa taaagatggc 4980acgtatgctg tcacctacat ccccgacaag actgggcgct atatgattgg agtcacctac 5040gggggtgacg acatcccact ttctccttat cgcatccgag ccacacagac gggtgatgcc 5100agcaagtgcc tggccacggg tcctggaatc gcctccactg tgaaaactgg cgaagaagta 5160ggctttgtgg ttgatgccaa gactgccggg aagggtaaag tgacctgcac ggttctgacc 5220ccagatggca ctgaggccga ggccgatgtc attgagaatg aagatggaac ctatgacatc 5280ttctacacag ctgccaagcc gggcacatat gtgatctatg tgcgcttcgg tggtgttgat 5340attcctaaca gccccttcac tgtcatggcc acagatgggg aagtcacagc cgtggaggag 5400gcaccggtaa atgcatgtcc ccctggattc aggccctggg tgaccgaaga ggcctatgtc 5460ccagtgagtg acatgaacgg cctgggattt aagccttttg acctggtcat tccgtttgct 5520gtcaggaaag gagaaatcac tggagaggtc cacatgcctt ctgggaagac agccacacct 5580gagattgtgg acaacaagga cggcacggtc actgttagat atgcccccac tgaggtcggg 5640ctccatgaga tgcacatcaa atacatgggc agccacatcc ctgagagccc actccagttc 5700tacgtgaact accccaacag tggaagtgtt tctgcatacg gtccaggcct cgtgtatgga 5760gtggccaaca aaactgccac cttcaccatc gtcacagagg atgcaggaga aggtggtctg 5820gacttggcta ttgagggccc ctcaaaagca gaaatcagct gcattgacaa taaagatggg 5880acatgcacag tgacctacct gccgactctg ccaggcgact acagcattct ggtcaagtac 5940aatgacaagc acatccctgg cagccccttc acagccaaga tcacagatga cagcaggcgg 6000tgctcccagg tgaagttggg ctcagccgct gacttcctgc tcgacatcag tgagactgac 6060ctcagcagcc tgacggccag cattaaggcc ccatctggcc gagacgagcc ctgtctcctg 6120aagaggctgc ccaacaacca cattggcatc tccttcatcc cccgggaagt gggcgaacat 6180ctggtcagca tcaagaaaaa tggcaaccat gtggccaaca gccccgtgtc tatcatggtg 6240gtccagtcgg agattggtga cgcccgccga gccaaagtct atggccgcgg cctgtcagaa 6300ggccggactt tcgagatgtc tgacttcatc gtggacacaa gggatgcagg ttatggtggc 6360atatccttgg cggtggaagg ccccagcaaa gtggacatcc agacggagga cctggaagat 6420ggcacctgca aagtctccta cttccctacc gtgcctgggg tttatatcgt ctccaccaaa 6480ttcgctgacg agcacgtgcc tgggagccca tttaccgtga agatcagtgg ggagggaaga 6540gtcaaagaga gcatcacccg caccagtcgg gccccgtccg tggccactgt cgggagcatt 6600tgtgacctga acctgaaaat cccagaaatc aacagcagtg atatgtcggc ccacgtcacc 6660agcccctctg gccgtgtgac tgaggcagag attgtgccca tggggaagaa ctcacactgc 6720gtccggtttg tgccccagga gatgggcgtg cacacggtca gcgtcaagta ccgtgggcag 6780cacgtcaccg gcagcccctt ccagttcacc gtggggccac ttggtgaagg aggcgcccac 6840aaggtgcggg caggaggccc tggcctggag agaggagaag cgggagtccc agctgagttc 6900agcatttgga cccgggaagc aggcgctgga ggcctctcca tcgctgttga gggccccagt 6960aaggccgaga ttacattcga tgaccataaa aatgggtcgt gcggtgtatc ttatattgcc 7020caagagcctg gtaactacga ggtgtccatc aagttcaatg atgagcacat cccggaaagc 7080ccctacctgg tgccggtcat cgcaccctcc gacgacgccc gccgcctcac tgttatgagc 7140cttcaggaat cgggattaaa agttaaccag ccagcatcct ttgctataag gttgaatggc 7200gcaaaaggca agattgatgc aaaggtgcac agcccctctg gagccgtgga ggagtgccac 7260gtgtctgagc tggagccaga taagtatgct gttcgcttca tccctcatga gaatggtgtc 7320cacaccatcg atgtcaagtt caatgggagc cacgtggttg gaagcccctt caaagtgcgc 7380gttggggagc ctggacaagc ggggaaccct gccctggtgt ccgcctatgg cacgggactc 7440gaagggggca ccacaggtat ccagtcggaa ttctttatta acaccacccg agcaggtcca 7500gggacattat ccgtcaccat cgaaggccca tccaaggtta aaatggattg ccaggaaaca 7560cctgaagggt acaaagtcat gtacaccccc atggctcctg gtaactacct gatcagcgtc 7620aaatacggtg ggcccaacca catcgtgggc agtcccttca aggccaaggt gacaggccag 7680cgtctagtta gccctggctc agccaacgag acctcatcca tcctggtgga gtcagtgacc 7740aggtcgtcta cagagacctg ctatagcgcc attcccaagg catcctcgga cgccagcaag 7800gtgacctcta agggggcagg gctctcaaag gcctttgtgg gccagaagag ttccttcctg 7860gtggactgca gcaaagctgg ctccaacatg ctgctgatcg gggtccatgg gcccaccacc 7920ccctgcgagg aggtctccat gaagcatgta ggcaaccagc aatacaacgt cacatacgtc 7980gtcaaggaga ggggcgatta tgtgctggct gtgaagtggg gggaggaaca catccctggc 8040agcccttttc atgtcacagt gccttaaaac agttttctca aatcctggag agagttcttg 8100tggttgcttt tgttgcttgt ttgtaattca ttttatacaa agccctccag cctgtttgtg

8160gggctgaaac cccatcccta aaatattgct gttgtaaaat gccttcagaa ataagtccta 8220gactggactc ttgagggaca tattggagaa tcttaagaaa tgcaagcttg ttcagggggc 8280tgagaagatc ctgagtacac taggtgcaaa ccagaactct tggtggaaca gaccagccac 8340tgcagcagac agaccaggaa cacaatgaga ctgacatttc aaaaaaacaa aactggctag 8400cctgagctgc tggttcactc ttcagcattt atgaaacaag gctaggggaa gatgggcaga 8460gaaaaagggg acacctagtt tggttgtcat ttggcaaagg agatgactta aaatccgctt 8520aatctcttcc agtgtccgtg ttaatgtatt tggctattag atcactagca ctgctttacc 8580gctcctcatc gccaacaccc ccatgctctg tggccttctt acacttctca gagggcagag 8640tggcagccgg gcaccctaca gaaactcaga gggcagagtg gcagccaggc ccacatgtct 8700ctcaagtacc tgtcccctcg ctctggtgat tatttcttgc agaatcacca cacgagacca 8760tcccggcagt catggttttg ctttagtttt ccaagtccgt ttcagtccct tccttggtct 8820gaagaaattc tgcagtggcg agcagtttcc cacttgccaa agatcccttt taaccaacac 8880tagcccttgt ttttaacaca cgctccagcc cttcatcagc ctgggcagtc ttaccaaaat 8940gtttaaagtg atctcagagg ggcccatgga ttaacgccct catcccaagg tccgtcccat 9000gacataacac tccacacccg ccccagccaa cttcatgggt cactttttct ggaaaataat 9060gatctgtaca gacaggacag aatgaaactc ctgcgggtct ttggcctgaa agttgggaat 9120ggttggggga gagaagggca gcagcttatt ggtggtcttt tcaccattgg cagaaacagt 9180gagagctgtg tggtgcagaa atccagaaat gaggtgtagg gaattttgcc tgccttcctg 9240cagacctgag ctggctttgg aatgaggtta aagtgtcagg gacgttgcct gagcccaaat 9300gtgtagtgtg gtctgggcag gcagaccttt aggttttgct gcttagtcct gaggaagtgg 9360ccactcttgt ggcaggtgta gtatctgggg cgagtgttgg gggtaaaagc ccaccctaca 9420gaaagtggaa cagcccggag cctgatgtga aaggaccacg ggtgttgtaa gctgggacac 9480ggaagccaaa ctggaatcaa acgccgactg taaattgtat cttataactt attaaataaa 9540acatttgctc cgtaaagttg 9560242591PRTHomo sapiens 24Met Pro Val Thr Glu Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys1 5 10 15Ile Gln Gln Asn Thr Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys 20 25 30Val Asn Lys Arg Ile Gly Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu 35 40 45Arg Leu Ile Ala Leu Leu Glu Val Leu Ser Gln Lys Arg Met Tyr Arg 50 55 60Lys Tyr His Gln Arg Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val65 70 75 80Ser Val Ala Leu Glu Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser 85 90 95Ile Asp Ser Lys Ala Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly 100 105 110Leu Val Trp Thr Leu Ile Leu His Tyr Ser Ile Ser Met Pro Val Trp 115 120 125Glu Asp Glu Gly Asp Asp Asp Ala Lys Lys Gln Thr Pro Lys Gln Arg 130 135 140Leu Leu Gly Trp Ile Gln Asn Lys Ile Pro Tyr Leu Pro Ile Thr Asn145 150 155 160Phe Asn Gln Asn Trp Gln Asp Gly Lys Ala Leu Gly Ala Leu Val Asp 165 170 175Ser Cys Ala Pro Gly Leu Cys Pro Asp Trp Glu Ser Trp Asp Pro Gln 180 185 190Lys Pro Val Asp Asn Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp 195 200 205Leu Gly Val Pro Gln Val Ile Thr Pro Glu Glu Ile Ile His Pro Asp 210 215 220Val Asp Glu His Ser Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala225 230 235 240Lys Leu Lys Pro Gly Ala Pro Leu Lys Pro Lys Leu Asn Pro Lys Lys 245 250 255Ala Arg Ala Tyr Gly Arg Gly Ile Glu Pro Thr Gly Asn Met Val Lys 260 265 270Gln Pro Ala Lys Phe Thr Val Asp Thr Ile Ser Ala Gly Gln Gly Asp 275 280 285Val Met Val Phe Val Glu Asp Pro Glu Gly Asn Lys Glu Glu Ala Gln 290 295 300Val Thr Pro Asp Ser Asp Lys Asn Lys Thr Tyr Ser Val Glu Tyr Leu305 310 315 320Pro Lys Val Thr Gly Leu His Lys Val Thr Val Leu Phe Ala Gly Gln 325 330 335His Ile Ser Lys Ser Pro Phe Glu Val Ser Val Asp Lys Ala Gln Gly 340 345 350Asp Ala Ser Lys Val Thr Ala Lys Gly Pro Gly Leu Glu Ala Val Gly 355 360 365Asn Ile Ala Asn Lys Pro Thr Tyr Phe Asp Ile Tyr Thr Ala Gly Ala 370 375 380Gly Val Gly Asp Ile Gly Val Glu Val Glu Asp Pro Gln Gly Lys Asn385 390 395 400Thr Val Glu Leu Leu Val Glu Asp Lys Gly Asn Gln Val Tyr Arg Cys 405 410 415Val Tyr Lys Pro Met Gln Pro Gly Pro His Val Val Lys Ile Phe Phe 420 425 430Ala Gly Asp Thr Ile Pro Lys Ser Pro Phe Val Val Gln Val Gly Glu 435 440 445Ala Cys Asn Pro Asn Ala Cys Arg Ala Ser Gly Arg Gly Leu Gln Pro 450 455 460Lys Gly Val Arg Ile Arg Glu Thr Thr Asp Phe Lys Val Asp Thr Lys465 470 475 480Ala Ala Gly Ser Gly Glu Leu Gly Val Thr Met Lys Gly Pro Lys Gly 485 490 495Leu Glu Glu Leu Val Lys Gln Lys Asp Phe Leu Asp Gly Val Tyr Ala 500 505 510Phe Glu Tyr Tyr Pro Ser Thr Pro Gly Arg Tyr Ser Ile Ala Ile Thr 515 520 525Trp Gly Gly His His Ile Pro Lys Ser Pro Phe Glu Val Gln Val Gly 530 535 540Pro Glu Ala Gly Met Gln Lys Val Arg Ala Trp Gly Pro Gly Leu His545 550 555 560Gly Gly Ile Val Gly Arg Ser Ala Asp Phe Val Val Glu Ser Ile Gly 565 570 575Ser Glu Val Gly Ser Leu Gly Phe Ala Ile Glu Gly Pro Ser Gln Ala 580 585 590Lys Ile Glu Tyr Asn Asp Gln Asn Asp Gly Ser Cys Asp Val Lys Tyr 595 600 605Trp Pro Lys Glu Pro Gly Glu Tyr Ala Val His Ile Met Cys Asp Asp 610 615 620Glu Asp Ile Lys Asp Ser Pro Tyr Met Ala Phe Ile His Pro Ala Thr625 630 635 640Gly Gly Tyr Asn Pro Asp Leu Val Arg Ala Tyr Gly Pro Gly Leu Glu 645 650 655Lys Ser Gly Cys Ile Val Asn Asn Leu Ala Glu Phe Thr Val Asp Pro 660 665 670Lys Asp Ala Gly Lys Ala Pro Leu Lys Ile Phe Ala Gln Asp Gly Glu 675 680 685Gly Gln Arg Ile Asp Ile Gln Met Lys Asn Arg Met Asp Gly Thr Tyr 690 695 700Ala Cys Ser Tyr Thr Pro Val Lys Ala Ile Lys His Thr Ile Ala Val705 710 715 720Val Trp Gly Gly Val Asn Ile Pro His Ser Pro Tyr Arg Val Asn Ile 725 730 735Gly Gln Gly Ser His Pro Gln Lys Val Lys Val Phe Gly Pro Gly Val 740 745 750Glu Arg Ser Gly Leu Lys Ala Asn Glu Pro Thr His Phe Thr Val Asp 755 760 765Cys Thr Glu Ala Gly Glu Gly Asp Val Ser Val Gly Ile Lys Cys Asp 770 775 780Ala Arg Val Leu Ser Glu Asp Glu Glu Asp Val Asp Phe Asp Ile Ile785 790 795 800His Asn Ala Asn Asp Thr Phe Thr Val Lys Tyr Val Pro Pro Ala Ala 805 810 815Gly Arg Tyr Thr Ile Lys Val Leu Phe Ala Ser Gln Glu Ile Pro Ala 820 825 830Ser Pro Phe Arg Val Lys Val Asp Pro Ser His Asp Ala Ser Lys Val 835 840 845Lys Ala Glu Gly Pro Gly Leu Ser Lys Ala Gly Val Glu Asn Gly Lys 850 855 860Pro Thr His Phe Thr Val Tyr Thr Lys Gly Ala Gly Lys Ala Pro Leu865 870 875 880Asn Val Gln Phe Asn Ser Pro Leu Pro Gly Asp Ala Val Lys Asp Leu 885 890 895Asp Ile Ile Asp Asn Tyr Asp Tyr Ser His Thr Val Lys Tyr Thr Pro 900 905 910Thr Gln Gln Gly Asn Met Gln Val Leu Val Thr Tyr Gly Gly Asp Pro 915 920 925Ile Pro Lys Ser Pro Phe Thr Val Gly Val Ala Ala Pro Leu Asp Leu 930 935 940Ser Lys Ile Lys Leu Asn Gly Leu Glu Asn Arg Val Glu Val Gly Lys945 950 955 960Asp Gln Glu Phe Thr Val Asp Thr Arg Gly Ala Gly Gly Gln Gly Lys 965 970 975Leu Asp Val Thr Ile Leu Ser Pro Ser Arg Lys Val Val Pro Cys Leu 980 985 990Val Thr Pro Val Thr Gly Arg Glu Asn Ser Thr Ala Lys Phe Ile Pro 995 1000 1005Arg Glu Glu Gly Leu Tyr Ala Val Asp Val Thr Tyr Asp Gly His 1010 1015 1020Pro Val Pro Gly Ser Pro Tyr Thr Val Glu Ala Ser Leu Pro Pro 1025 1030 1035Asp Pro Ser Lys Val Lys Ala His Gly Pro Gly Leu Glu Gly Gly 1040 1045 1050Leu Val Gly Lys Pro Ala Glu Phe Thr Ile Asp Thr Lys Gly Ala 1055 1060 1065Gly Thr Gly Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala 1070 1075 1080Lys Ile Glu Cys Ser Asp Asn Gly Asp Gly Thr Cys Ser Val Ser 1085 1090 1095Tyr Leu Pro Thr Lys Pro Gly Glu Tyr Phe Val Asn Ile Leu Phe 1100 1105 1110Glu Glu Val His Ile Pro Gly Ser Pro Phe Lys Ala Asp Ile Glu 1115 1120 1125Met Pro Phe Asp Pro Ser Lys Val Val Ala Ser Gly Pro Gly Leu 1130 1135 1140Glu His Gly Lys Val Gly Glu Ala Gly Leu Leu Ser Val Asp Cys 1145 1150 1155Ser Glu Ala Gly Pro Gly Ala Leu Gly Leu Glu Ala Val Ser Asp 1160 1165 1170Ser Gly Thr Lys Ala Glu Val Ser Ile Gln Asn Asn Lys Asp Gly 1175 1180 1185Thr Tyr Ala Val Thr Tyr Val Pro Leu Thr Ala Gly Met Tyr Thr 1190 1195 1200Leu Thr Met Lys Tyr Gly Gly Glu Leu Val Pro His Phe Pro Ala 1205 1210 1215Arg Val Lys Val Glu Pro Ala Val Asp Thr Ser Arg Ile Lys Val 1220 1225 1230Phe Gly Pro Gly Ile Glu Gly Lys Asp Val Phe Arg Glu Ala Thr 1235 1240 1245Thr Asp Phe Thr Val Asp Ser Arg Pro Leu Thr Gln Val Gly Gly 1250 1255 1260Asp His Ile Lys Ala His Ile Ala Asn Pro Ser Gly Ala Ser Thr 1265 1270 1275Glu Cys Phe Val Thr Asp Asn Ala Asp Gly Thr Tyr Gln Val Glu 1280 1285 1290Tyr Thr Pro Phe Glu Lys Gly Leu His Val Val Glu Val Thr Tyr 1295 1300 1305Asp Asp Val Pro Ile Pro Asn Ser Pro Phe Lys Val Ala Val Thr 1310 1315 1320Glu Gly Cys Gln Pro Ser Arg Val Gln Ala Gln Gly Pro Gly Leu 1325 1330 1335Lys Glu Ala Phe Thr Asn Lys Pro Asn Val Phe Thr Val Val Thr 1340 1345 1350Arg Gly Ala Gly Ile Gly Gly Leu Gly Ile Thr Val Glu Gly Pro 1355 1360 1365Ser Glu Ser Lys Ile Asn Cys Arg Asp Asn Lys Asp Gly Ser Cys 1370 1375 1380Ser Ala Glu Tyr Ile Pro Phe Ala Pro Gly Asp Tyr Asp Val Asn 1385 1390 1395Ile Thr Tyr Gly Gly Ala His Ile Pro Gly Ser Pro Phe Arg Val 1400 1405 1410Pro Val Lys Asp Val Val Asp Pro Ser Lys Val Lys Ile Ala Gly 1415 1420 1425Pro Gly Leu Gly Ser Gly Val Arg Ala Arg Val Leu Gln Ser Phe 1430 1435 1440Thr Val Asp Ser Ser Lys Ala Gly Leu Ala Pro Leu Glu Val Arg 1445 1450 1455Val Leu Gly Pro Arg Gly Leu Val Glu Pro Val Asn Val Val Asp 1460 1465 1470Asn Gly Asp Gly Thr His Thr Val Thr Tyr Thr Pro Ser Gln Glu 1475 1480 1485Gly Pro Tyr Met Val Ser Val Lys Tyr Ala Asp Glu Glu Ile Pro 1490 1495 1500Arg Ser Pro Phe Lys Val Lys Val Leu Pro Thr Tyr Asp Ala Ser 1505 1510 1515Lys Val Thr Ala Ser Gly Pro Gly Leu Ser Ser Tyr Gly Val Pro 1520 1525 1530Ala Ser Leu Pro Val Asp Phe Ala Ile Asp Ala Arg Asp Ala Gly 1535 1540 1545Glu Gly Leu Leu Ala Val Gln Ile Thr Asp Gln Glu Gly Lys Pro 1550 1555 1560Lys Arg Ala Ile Val His Asp Asn Lys Asp Gly Thr Tyr Ala Val 1565 1570 1575Thr Tyr Ile Pro Asp Lys Thr Gly Arg Tyr Met Ile Gly Val Thr 1580 1585 1590Tyr Gly Gly Asp Asp Ile Pro Leu Ser Pro Tyr Arg Ile Arg Ala 1595 1600 1605Thr Gln Thr Gly Asp Ala Ser Lys Cys Leu Ala Thr Gly Pro Gly 1610 1615 1620Ile Ala Ser Thr Val Lys Thr Gly Glu Glu Val Gly Phe Val Val 1625 1630 1635Asp Ala Lys Thr Ala Gly Lys Gly Lys Val Thr Cys Thr Val Leu 1640 1645 1650Thr Pro Asp Gly Thr Glu Ala Glu Ala Asp Val Ile Glu Asn Glu 1655 1660 1665Asp Gly Thr Tyr Asp Ile Phe Tyr Thr Ala Ala Lys Pro Gly Thr 1670 1675 1680Tyr Val Ile Tyr Val Arg Phe Gly Gly Val Asp Ile Pro Asn Ser 1685 1690 1695Pro Phe Thr Val Met Ala Thr Asp Gly Glu Val Thr Ala Val Glu 1700 1705 1710Glu Ala Pro Val Thr Glu Glu Ala Tyr Val Pro Val Ser Asp Met 1715 1720 1725Asn Gly Leu Gly Phe Lys Pro Phe Asp Leu Val Ile Pro Phe Ala 1730 1735 1740Val Arg Lys Gly Glu Ile Thr Gly Glu Val His Met Pro Ser Gly 1745 1750 1755Lys Thr Ala Thr Pro Glu Ile Val Asp Asn Lys Asp Gly Thr Val 1760 1765 1770Thr Val Arg Tyr Ala Pro Thr Glu Val Gly Leu His Glu Met His 1775 1780 1785Ile Lys Tyr Met Gly Ser His Ile Pro Glu Ser Pro Leu Gln Phe 1790 1795 1800Tyr Val Asn Tyr Pro Asn Ser Gly Ser Val Ser Ala Tyr Gly Pro 1805 1810 1815Gly Leu Val Tyr Gly Val Ala Asn Lys Thr Ala Thr Phe Thr Ile 1820 1825 1830Val Thr Glu Asp Ala Gly Glu Gly Gly Leu Asp Leu Ala Ile Glu 1835 1840 1845Gly Pro Ser Lys Ala Glu Ile Ser Cys Ile Asp Asn Lys Asp Gly 1850 1855 1860Thr Cys Thr Val Thr Tyr Leu Pro Thr Leu Pro Gly Asp Tyr Ser 1865 1870 1875Ile Leu Val Lys Tyr Asn Asp Lys His Ile Pro Gly Ser Pro Phe 1880 1885 1890Thr Ala Lys Ile Thr Asp Asp Ser Arg Arg Cys Ser Gln Val Lys 1895 1900 1905Leu Gly Ser Ala Ala Asp Phe Leu Leu Asp Ile Ser Glu Thr Asp 1910 1915 1920Leu Ser Ser Leu Thr Ala Ser Ile Lys Ala Pro Ser Gly Arg Asp 1925 1930 1935Glu Pro Cys Leu Leu Lys Arg Leu Pro Asn Asn His Ile Gly Ile 1940 1945 1950Ser Phe Ile Pro Arg Glu Val Gly Glu His Leu Val Ser Ile Lys 1955 1960 1965Lys Asn Gly Asn His Val Ala Asn Ser Pro Val Ser Ile Met Val 1970 1975 1980Val Gln Ser Glu Ile Gly Asp Ala Arg Arg Ala Lys Val Tyr Gly 1985 1990 1995Arg Gly Leu Ser Glu Gly Arg Thr Phe Glu Met Ser Asp Phe Ile 2000 2005 2010Val Asp Thr Arg Asp Ala Gly Tyr Gly Gly Ile Ser Leu Ala Val 2015 2020 2025Glu Gly Pro Ser Lys Val Asp Ile Gln Thr Glu Asp Leu Glu Asp 2030 2035 2040Gly Thr Cys Lys Val Ser Tyr Phe Pro Thr Val Pro Gly Val Tyr 2045 2050 2055Ile Val Ser Thr Lys Phe Ala Asp Glu His Val Pro Gly Ser Pro 2060 2065 2070Phe Thr Val Lys Ile Ser Gly Glu Gly Arg Val Lys Glu Ser Ile 2075 2080 2085Thr Arg Thr Ser Arg Ala Pro Ser Val Ala Thr Val Gly Ser Ile 2090 2095 2100Cys Asp Leu Asn Leu Lys Ile Pro Glu Ile Asn Ser Ser Asp Met 2105 2110 2115Ser Ala His Val Thr Ser Pro Ser Gly Arg Val Thr Glu Ala Glu 2120 2125 2130Ile Val Pro Met Gly Lys Asn Ser His Cys Val Arg Phe Val Pro 2135 2140 2145Gln Glu Met Gly Val His Thr Val Ser Val Lys Tyr Arg Gly Gln 2150 2155 2160His Val Thr Gly Ser Pro Phe Gln Phe Thr Val Gly Pro Leu Gly 2165 2170 2175Glu Gly Gly Ala His Lys Val Arg Ala Gly Gly Pro Gly Leu Glu 2180 2185 2190Arg Gly Glu Ala Gly Val Pro Ala Glu Phe Ser Ile Trp Thr Arg 2195 2200 2205Glu Ala Gly Ala Gly Gly Leu Ser Ile Ala Val Glu Gly

Pro Ser 2210 2215 2220Lys Ala Glu Ile Thr Phe Asp Asp His Lys Asn Gly Ser Cys Gly 2225 2230 2235Val Ser Tyr Ile Ala Gln Glu Pro Gly Asn Tyr Glu Val Ser Ile 2240 2245 2250Lys Phe Asn Asp Glu His Ile Pro Glu Ser Pro Tyr Leu Val Pro 2255 2260 2265Val Ile Ala Pro Ser Asp Asp Ala Arg Arg Leu Thr Val Met Ser 2270 2275 2280Leu Gln Glu Ser Gly Leu Lys Val Asn Gln Pro Ala Ser Phe Ala 2285 2290 2295Ile Arg Leu Asn Gly Ala Lys Gly Lys Ile Asp Ala Lys Val His 2300 2305 2310Ser Pro Ser Gly Ala Val Glu Glu Cys His Val Ser Glu Leu Glu 2315 2320 2325Pro Asp Lys Tyr Ala Val Arg Phe Ile Pro His Glu Asn Gly Val 2330 2335 2340His Thr Ile Asp Val Lys Phe Asn Gly Ser His Val Val Gly Ser 2345 2350 2355Pro Phe Lys Val Arg Val Gly Glu Pro Gly Gln Ala Gly Asn Pro 2360 2365 2370Ala Leu Val Ser Ala Tyr Gly Thr Gly Leu Glu Gly Gly Thr Thr 2375 2380 2385Gly Ile Gln Ser Glu Phe Phe Ile Asn Thr Thr Arg Ala Gly Pro 2390 2395 2400Gly Thr Leu Ser Val Thr Ile Glu Gly Pro Ser Lys Val Lys Met 2405 2410 2415Asp Cys Gln Glu Thr Pro Glu Gly Tyr Lys Val Met Tyr Thr Pro 2420 2425 2430Met Ala Pro Gly Asn Tyr Leu Ile Ser Val Lys Tyr Gly Gly Pro 2435 2440 2445Asn His Ile Val Gly Ser Pro Phe Lys Ala Lys Val Thr Gly Gln 2450 2455 2460Arg Leu Val Ser Pro Gly Ser Ala Asn Glu Thr Ser Ser Ile Leu 2465 2470 2475Val Glu Ser Val Thr Arg Ser Ser Thr Glu Thr Cys Tyr Ser Ala 2480 2485 2490Ile Pro Lys Ala Ser Ser Asp Ala Ser Lys Val Thr Ser Lys Gly 2495 2500 2505Ala Gly Leu Ser Lys Ala Phe Val Gly Gln Lys Ser Ser Phe Leu 2510 2515 2520Val Asp Cys Ser Lys Ala Gly Ser Asn Met Leu Leu Ile Gly Val 2525 2530 2535His Gly Pro Thr Thr Pro Cys Glu Glu Val Ser Met Lys His Val 2540 2545 2550Gly Asn Gln Gln Tyr Asn Val Thr Tyr Val Val Lys Glu Arg Gly 2555 2560 2565Asp Tyr Val Leu Ala Val Lys Trp Gly Glu Glu His Ile Pro Gly 2570 2575 2580Ser Pro Phe His Val Thr Val Pro 2585 2590259434DNAHomo sapiens 25gcggccaggg gcgggcggcc gcagagcagc accggccgtg gctccggtag cagcaagttc 60gaaccccgct cccgctccgc ttcggttctc gctccttcgg cccttgggcc tccaaacacc 120agtccccggc agctcgttgc gcattgcgct ctccccgcca ccaggatgcc ggtaaccgag 180aaggatctag ctgaggacgc gccttggaag aagatccagc agaacacgtt cacacgctgg 240tgcaacgagc acctcaagtg cgtgaacaaa cgcatcggca acctgcagac cgacctgagc 300gacgggctgc ggctcatcgc gctgctcgag gtgctcagcc agaagcgcat gtaccgcaag 360taccatcagc ggcccacctt tcgccagatg cagctcgaga atgtgtccgt ggcgctcgag 420ttcctggacc gtgagagcat caagctcgtg tccatcgata gcaaagccat tgtggatggg 480aacctgaagc tcatcttggg tctggtgtgg acgctgatcc tccactactc catctccatg 540cccgtgtggg aggatgaagg ggatgatgat gccaagaagc agacgccaaa gcagaggctg 600ctggggtgga ttcagaacaa gatcccctac ttgcccatca ccaactttaa ccagaactgg 660caagacggca aagccctggg agccctggta gacagctgtg ctccaggtct gtgcccagac 720tgggaatcct gggacccgca gaagcctgtg gataatgcac gagaagccat gcagcaggca 780gatgactggc tgggtgtccc acaggtcatc actcctgaag aaatcattca cccggatgtg 840gacgagcact cagttatgac ttacctgtcc cagttcccca aagccaagct caagccgggg 900gctcctctca aacccaaact caacccgaag aaagccaggg cctatggcag aggaatcgag 960cccactggaa acatggtgaa gcagccagcc aagttcactg tggacaccat cagcgccggg 1020caaggagacg tgatggtgtt tgttgaggac ccagaaggga acaaagagga ggcacaagtg 1080acccctgaca gtgacaagaa caagacatac tctgtggagt atctgcccaa ggtcaccggg 1140ctacacaaag tcacagtcct ctttgcagga cagcacatct ccaagagccc atttgaagtg 1200agtgttgaca aggcccaggg agatgccagt aaagtcactg caaaaggtcc agggttggaa 1260gctgtaggga acatcgccaa taagcccacc tactttgaca tctatacggc aggagctggt 1320gtgggtgaca ttggtgtgga ggtggaagat ccccagggga agaacaccgt ggagttgctc 1380gtggaagaca aaggaaacca ggtgtatcga tgtgtgtaca aacccatgca gcctggccct 1440cacgtggtca agatcttctt tgctggggac actattccta agagtccctt cgttgtgcag 1500gttggggaag cctgcaatcc aaatgcctgc cgggccagtg gccgaggcct acaacccaaa 1560ggcgtccgta tccgggagac cacagatttc aaggttgaca ccaaagctgc aggaagtggg 1620gagctcggtg taaccatgaa gggtcctaag ggtctggagg agctggtgaa gcagaaagac 1680tttctggatg gggtctacgc attcgagtat taccccagca ccccggggag atacagcatt 1740gccatcacat gggggggaca ccacattcca aagagcccct ttgaagttca agttggccct 1800gaagcgggta tgcagaaagt ccgtgcttgg ggccctgggc tccatggtgg gattgtcggg 1860cggtcagcgg acttcgtggt agaatccatt ggctctgaag tggggtctct ggggtttgcc 1920attgaaggcc cctctcaggc aaagattgag tacaacgacc agaatgatgg atcgtgtgat 1980gtcaaatact ggcccaagga gcctggcgaa tatgctgttc acatcatgtg tgacgacgaa 2040gacatcaagg acagcccgta catggccttc atccacccag ccacgggagg ctacaaccct 2100gatctggttc gagcatacgg gccaggtttg gagaaatctg gatgcattgt caacaacctg 2160gccgagttca ctgtggatcc taaggatgct ggaaaagctc ccttaaagat atttgctcag 2220gatggggaag gccaacgcat tgacatccag atgaagaacc ggatggacgg cacatatgca 2280tgctcataca ccccggtgaa ggccatcaag cacaccattg ctgtggtctg gggaggcgtg 2340aacatcccgc acagccccta cagggtcaac atcgggcaag gtagccatcc tcagaaggtc 2400aaagtgtttg ggccaggtgt ggagagaagt ggtctgaagg caaatgaacc tacacacttc 2460acggtggact gtactgaggc tggggaaggt gatgtcagtg ttggcattaa gtgtgatgcc 2520cgggtgttaa gtgaagatga ggaagacgtg gattttgaca ttattcacaa tgccaatgat 2580acgttcacag tcaaatatgt gcctcctgct gctgggcgat acactatcaa agttctcttt 2640gcatctcagg aaatccccgc cagccctttc agagtcaaag ttgacccttc ccacgatgcc 2700agcaaagtga aggcagaagg cccagggctc agcaaagcag gtgtggaaaa tgggaaaccg 2760acccacttca ctgtctacac caagggggct gggaaagccc cgctcaacgt gcagttcaac 2820agccctcttc ctggcgatgc agtgaaggat ttggatatca tcgataatta tgactactct 2880cacacggtta aatatacacc cacccaacag ggcaacatgc aggttctggt gacttacggt 2940ggcgatccca tccctaaaag ccctttcact gtgggtgttg ctgcaccgct ggatctgagc 3000aagataaaac tcaatgggct ggaaaacagg gtggaagttg ggaaggatca ggagttcacc 3060gttgatacca ggggggcagg aggccagggg aagctggacg tgacaatcct cagcccctct 3120cggaaggtcg tgccatgcct agtgacacct gtgacaggcc gggagaacag cacggccaag 3180ttcatccctc gggaggaggg gctgtatgct gtagacgtga cctacgatgg acaccctgtg 3240cccgggagcc cctacacagt ggaggcctcg ctgccaccag atcccagcaa ggtgaaggcc 3300cacggtcccg gcctcgaagg tggtctcgtg ggcaagcctg ccgagttcac catcgatacc 3360aaaggagctg gtactggagg tctgggctta acggtggaag gtccgtgcga ggccaaaatc 3420gagtgctccg acaatggtga tgggacctgc tccgtctctt accttcccac aaaacccggg 3480gagtacttcg tcaacatcct ctttgaagaa gtccacatac ctgggtctcc cttcaaagct 3540gacattgaaa tgccctttga cccctctaaa gtcgtggcat cggggccagg tctcgagcac 3600gggaaggtgg gtgaagctgg cctccttagc gtcgactgct cggaagcggg accgggggcc 3660ctgggcctgg aagctgtctc ggactcggga acaaaagccg aagtcagtat tcagaacaac 3720aaagatggca cctacgcggt gacctacgtg cccctgacgg ccggcatgta cacgttgacc 3780atgaagtatg gtggcgaact cgtgccacac ttccccgccc gggtcaaggt ggagcccgcc 3840gtggacacca gcaggatcaa agtctttgga ccaggaatag aagggaaaga tgtgttccgg 3900gaagctacca ccgactttac agttgactct cggccgctga cccaggttgg gggtgaccac 3960atcaaggccc acattgccaa cccctcaggg gcctccaccg agtgctttgt cacagacaat 4020gcggatggga cctaccaggt ggaatacaca ccctttgaga aaggtctcca tgtagtggag 4080gtgacatatg atgacgtgcc tatcccaaac agtcccttca aggtggctgt cactgaaggc 4140tgccagccat ctagggtgca agcccaagga cctggattga aagaggcctt taccaacaag 4200cccaatgtct tcaccgtggt taccagaggc gcaggaattg gtgggcttgg cataactgtt 4260gagggaccat cagagtcgaa gataaattgc agagacaaca aggatggcag ctgcagtgct 4320gagtacattc ctttcgcacc gggggattac gatgttaata tcacatatgg aggagcccac 4380atccccggca gccccttcag ggttcctgtg aaggatgttg tggaccccag caaggtcaag 4440attgccggcc ccgggctggg ctcaggcgtc cgagcccgtg tcctgcagtc cttcacggtg 4500gacagcagca aggctggcct ggctccgctg gaagtgaggg ttctgggccc acgaggcttg 4560gtggagccag tgaacgtggt ggacaatgga gatggcacac acacagtaac ctacacccca 4620tctcaggagg gaccttacat ggtctcagtt aaatatgctg atgaagagat tcctcgcagt 4680cccttcaagg tcaaggtcct tcccacatat gatgccagca aagtgactgc cagtggcccc 4740ggccttagtt cctatggtgt gcctgccagt ctacctgtgg actttgcaat tgatgcccga 4800gatgccgggg aaggcctgct tgctgttcaa ataacggacc aagaaggaaa acccaaaaga 4860gccattgtcc atgacaataa agatggcacg tatgctgtca cctacatccc cgacaagact 4920gggcgctata tgattggagt cacctacggg ggtgacgaca tcccactttc tccttatcgc 4980atccgagcca cacagacggg tgatgccagc aagtgcctgg ccacgggtcc tggaatcgcc 5040tccactgtga aaactggcga agaagtaggc tttgtggttg atgccaagac tgccgggaag 5100ggtaaagtga cctgcacggt tctgacccca gatggcactg aggccgaggc cgatgtcatt 5160gagaatgaag atggaaccta tgacatcttc tacacagctg ccaagccggg cacatatgtg 5220atctatgtgc gcttcggtgg tgttgatatt cctaacagcc ccttcactgt catggccaca 5280gatggggaag tcacagccgt ggaggaggca ccggtgaccg aagaggccta tgtcccagtg 5340agtgacatga acggcctggg atttaagcct tttgacctgg tcattccgtt tgctgtcagg 5400aaaggagaaa tcactggaga ggtccacatg ccttctggga agacagccac acctgagatt 5460gtggacaaca aggacggcac ggtcactgtt agatatgccc ccactgaggt cgggctccat 5520gagatgcaca tcaaatacat gggcagccac atccctgaga gcccactcca gttctacgtg 5580aactacccca acagtggaag tgtttctgca tacggtccag gcctcgtgta tggagtggcc 5640aacaaaactg ccaccttcac catcgtcaca gaggatgcag gagaaggtgg tctggacttg 5700gctattgagg gcccctcaaa agcagaaatc agctgcattg acaataaaga tgggacatgc 5760acagtgacct acctgccgac tctgccaggc gactacagca ttctggtcaa gtacaatgac 5820aagcacatcc ctggcagccc cttcacagcc aagatcacag atgacagcag gcggtgctcc 5880caggtgaagt tgggctcagc cgctgacttc ctgctcgaca tcagtgagac tgacctcagc 5940agcctgacgg ccagcattaa ggccccatct ggccgagacg agccctgtct cctgaagagg 6000ctgcccaaca accacattgg catctccttc atcccccggg aagtgggcga acatctggtc 6060agcatcaaga aaaatggcaa ccatgtggcc aacagccccg tgtctatcat ggtggtccag 6120tcggagattg gtgacgcccg ccgagccaaa gtctatggcc gcggcctgtc agaaggccgg 6180actttcgaga tgtctgactt catcgtggac acaagggatg caggttatgg tggcatatcc 6240ttggcggtgg aaggccccag caaagtggac atccagacgg aggacctgga agatggcacc 6300tgcaaagtct cctacttccc taccgtgcct ggggtttata tcgtctccac caaattcgct 6360gacgagcacg tgcctgggag cccatttacc gtgaagatca gtggggaggg aagagtcaaa 6420gagagcatca cccgcaccag tcgggccccg tccgtggcca ctgtcgggag catttgtgac 6480ctgaacctga aaatcccaga aatcaacagc agtgatatgt cggcccacgt caccagcccc 6540tctggccgtg tgactgaggc agagattgtg cccatgggga agaactcaca ctgcgtccgg 6600tttgtgcccc aggagatggg cgtgcacacg gtcagcgtca agtaccgtgg gcagcacgtc 6660accggcagcc ccttccagtt caccgtgggg ccacttggtg aaggaggcgc ccacaaggtg 6720cgggcaggag gccctggcct ggagagagga gaagcgggag tcccagctga gttcagcatt 6780tggacccggg aagcaggcgc tggaggcctc tccatcgctg ttgagggccc cagtaaggcc 6840gagattacat tcgatgacca taaaaatggg tcgtgcggtg tatcttatat tgcccaagag 6900cctggtaact acgaggtgtc catcaagttc aatgatgagc acatcccgga aagcccctac 6960ctggtgccgg tcatcgcacc ctccgacgac gcccgccgcc tcactgttat gagccttcag 7020gaatcgggat taaaagttaa ccagccagca tcctttgcta taaggttgaa tggcgcaaaa 7080ggcaagattg atgcaaaggt gcacagcccc tctggagccg tggaggagtg ccacgtgtct 7140gagctggagc cagataagta tgctgttcgc ttcatccctc atgagaatgg tgtccacacc 7200atcgatgtca agttcaatgg gagccacgtg gttggaagcc ccttcaaagt gcgcgttggg 7260gagcctggac aagcggggaa ccctgccctg gtgtccgcct atggcacggg actcgaaggg 7320ggcaccacag gtatccagtc ggaattcttt attaacacca cccgagcagg tccagggaca 7380ttatccgtca ccatcgaagg cccatccaag gttaaaatgg attgccagga aacacctgaa 7440gggtacaaag tcatgtacac ccccatggct cctggtaact acctgatcag cgtcaaatac 7500ggtgggccca accacatcgt gggcagtccc ttcaaggcca aggtgacagg ccagcgtcta 7560gttagccctg gctcagccaa cgagacctca tccatcctgg tggagtcagt gaccaggtcg 7620tctacagaga cctgctatag cgccattccc aaggcatcct cggacgccag caaggtgacc 7680tctaaggggg cagggctctc aaaggccttt gtgggccaga agagttcctt cctggtggac 7740tgcagcaaag ctggctccaa catgctgctg atcggggtcc atgggcccac caccccctgc 7800gaggaggtct ccatgaagca tgtaggcaac cagcaataca acgtcacata cgtcgtcaag 7860gagaggggcg attatgtgct ggctgtgaag tggggggagg aacacatccc tggcagccct 7920tttcatgtca cagtgcctta aaacagtttt ctcaaatcct ggagagagtt cttgtggttg 7980cttttgttgc ttgtttgtaa ttcattttat acaaagccct ccagcctgtt tgtggggctg 8040aaaccccatc cctaaaatat tgctgttgta aaatgccttc agaaataagt cctagactgg 8100actcttgagg gacatattgg agaatcttaa gaaatgcaag cttgttcagg gggctgagaa 8160gatcctgagt acactaggtg caaaccagaa ctcttggtgg aacagaccag ccactgcagc 8220agacagacca ggaacacaat gagactgaca tttcaaaaaa acaaaactgg ctagcctgag 8280ctgctggttc actcttcagc atttatgaaa caaggctagg ggaagatggg cagagaaaaa 8340ggggacacct agtttggttg tcatttggca aaggagatga cttaaaatcc gcttaatctc 8400ttccagtgtc cgtgttaatg tatttggcta ttagatcact agcactgctt taccgctcct 8460catcgccaac acccccatgc tctgtggcct tcttacactt ctcagagggc agagtggcag 8520ccgggcaccc tacagaaact cagagggcag agtggcagcc aggcccacat gtctctcaag 8580tacctgtccc ctcgctctgg tgattatttc ttgcagaatc accacacgag accatcccgg 8640cagtcatggt tttgctttag ttttccaagt ccgtttcagt cccttccttg gtctgaagaa 8700attctgcagt ggcgagcagt ttcccacttg ccaaagatcc cttttaacca acactagccc 8760ttgtttttaa cacacgctcc agcccttcat cagcctgggc agtcttacca aaatgtttaa 8820agtgatctca gaggggccca tggattaacg ccctcatccc aaggtccgtc ccatgacata 8880acactccaca cccgccccag ccaacttcat gggtcacttt ttctggaaaa taatgatctg 8940tacagacagg acagaatgaa actcctgcgg gtctttggcc tgaaagttgg gaatggttgg 9000gggagagaag ggcagcagct tattggtggt cttttcacca ttggcagaaa cagtgagagc 9060tgtgtggtgc agaaatccag aaatgaggtg tagggaattt tgcctgcctt cctgcagacc 9120tgagctggct ttggaatgag gttaaagtgt cagggacgtt gcctgagccc aaatgtgtag 9180tgtggtctgg gcaggcagac ctttaggttt tgctgcttag tcctgaggaa gtggccactc 9240ttgtggcagg tgtagtatct ggggcgagtg ttgggggtaa aagcccaccc tacagaaagt 9300ggaacagccc ggagcctgat gtgaaaggac cacgggtgtt gtaagctggg acacggaagc 9360caaactggaa tcaaacgccg actgtaaatt gtatcttata acttattaaa taaaacattt 9420gctccgtaaa gttg 9434262578PRTHomo sapiens 26Met Pro Val Thr Glu Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys1 5 10 15Ile Gln Gln Asn Thr Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys 20 25 30Val Asn Lys Arg Ile Gly Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu 35 40 45Arg Leu Ile Ala Leu Leu Glu Val Leu Ser Gln Lys Arg Met Tyr Arg 50 55 60Lys Tyr His Gln Arg Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val65 70 75 80Ser Val Ala Leu Glu Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser 85 90 95Ile Asp Ser Lys Ala Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly 100 105 110Leu Val Trp Thr Leu Ile Leu His Tyr Ser Ile Ser Met Pro Val Trp 115 120 125Glu Asp Glu Gly Asp Asp Asp Ala Lys Lys Gln Thr Pro Lys Gln Arg 130 135 140Leu Leu Gly Trp Ile Gln Asn Lys Ile Pro Tyr Leu Pro Ile Thr Asn145 150 155 160Phe Asn Gln Asn Trp Gln Asp Gly Lys Ala Leu Gly Ala Leu Val Asp 165 170 175Ser Cys Ala Pro Gly Leu Cys Pro Asp Trp Glu Ser Trp Asp Pro Gln 180 185 190Lys Pro Val Asp Asn Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp 195 200 205Leu Gly Val Pro Gln Val Ile Thr Pro Glu Glu Ile Ile His Pro Asp 210 215 220Val Asp Glu His Ser Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala225 230 235 240Lys Leu Lys Pro Gly Ala Pro Leu Lys Pro Lys Leu Asn Pro Lys Lys 245 250 255Ala Arg Ala Tyr Gly Arg Gly Ile Glu Pro Thr Gly Asn Met Val Lys 260 265 270Gln Pro Ala Lys Phe Thr Val Asp Thr Ile Ser Ala Gly Gln Gly Asp 275 280 285Val Met Val Phe Val Glu Asp Pro Glu Gly Asn Lys Glu Glu Ala Gln 290 295 300Val Thr Pro Asp Ser Asp Lys Asn Lys Thr Tyr Ser Val Glu Tyr Leu305 310 315 320Pro Lys Val Thr Gly Leu His Lys Val Thr Val Leu Phe Ala Gly Gln 325 330 335His Ile Ser Lys Ser Pro Phe Glu Val Ser Val Asp Lys Ala Gln Gly 340 345 350Asp Ala Ser Lys Val Thr Ala Lys Gly Pro Gly Leu Glu Ala Val Gly 355 360 365Asn Ile Ala Asn Lys Pro Thr Tyr Phe Asp Ile Tyr Thr Ala Gly Ala 370 375 380Gly Val Gly Asp Ile Gly Val Glu Val Glu Asp Pro Gln Gly Lys Asn385 390 395 400Thr Val Glu Leu Leu Val Glu Asp Lys Gly Asn Gln Val Tyr Arg Cys 405 410 415Val Tyr Lys Pro Met Gln Pro Gly Pro His Val Val Lys Ile Phe Phe 420 425 430Ala Gly Asp Thr Ile Pro Lys Ser Pro Phe Val Val Gln Val Gly Glu 435 440 445Ala Cys Asn Pro Asn Ala Cys Arg Ala Ser Gly Arg Gly Leu Gln Pro 450 455 460Lys Gly Val Arg Ile Arg Glu Thr Thr Asp Phe Lys Val Asp Thr Lys465 470 475 480Ala Ala Gly Ser Gly Glu Leu Gly Val Thr Met Lys Gly Pro Lys Gly 485 490 495Leu Glu Glu Leu Val Lys Gln Lys Asp Phe Leu Asp Gly Val Tyr Ala 500 505 510Phe Glu Tyr Tyr Pro Ser Thr Pro Gly Arg Tyr Ser Ile Ala Ile Thr 515 520 525Trp

Gly Gly His His Ile Pro Lys Ser Pro Phe Glu Val Gln Val Gly 530 535 540Pro Glu Ala Gly Met Gln Lys Val Arg Ala Trp Gly Pro Gly Leu His545 550 555 560Gly Gly Ile Val Gly Arg Ser Ala Asp Phe Val Val Glu Ser Ile Gly 565 570 575Ser Glu Val Gly Ser Leu Gly Phe Ala Ile Glu Gly Pro Ser Gln Ala 580 585 590Lys Ile Glu Tyr Asn Asp Gln Asn Asp Gly Ser Cys Asp Val Lys Tyr 595 600 605Trp Pro Lys Glu Pro Gly Glu Tyr Ala Val His Ile Met Cys Asp Asp 610 615 620Glu Asp Ile Lys Asp Ser Pro Tyr Met Ala Phe Ile His Pro Ala Thr625 630 635 640Gly Gly Tyr Asn Pro Asp Leu Val Arg Ala Tyr Gly Pro Gly Leu Glu 645 650 655Lys Ser Gly Cys Ile Val Asn Asn Leu Ala Glu Phe Thr Val Asp Pro 660 665 670Lys Asp Ala Gly Lys Ala Pro Leu Lys Ile Phe Ala Gln Asp Gly Glu 675 680 685Gly Gln Arg Ile Asp Ile Gln Met Lys Asn Arg Met Asp Gly Thr Tyr 690 695 700Ala Cys Ser Tyr Thr Pro Val Lys Ala Ile Lys His Thr Ile Ala Val705 710 715 720Val Trp Gly Gly Val Asn Ile Pro His Ser Pro Tyr Arg Val Asn Ile 725 730 735Gly Gln Gly Ser His Pro Gln Lys Val Lys Val Phe Gly Pro Gly Val 740 745 750Glu Arg Ser Gly Leu Lys Ala Asn Glu Pro Thr His Phe Thr Val Asp 755 760 765Cys Thr Glu Ala Gly Glu Gly Asp Val Ser Val Gly Ile Lys Cys Asp 770 775 780Ala Arg Val Leu Ser Glu Asp Glu Glu Asp Val Asp Phe Asp Ile Ile785 790 795 800His Asn Ala Asn Asp Thr Phe Thr Val Lys Tyr Val Pro Pro Ala Ala 805 810 815Gly Arg Tyr Thr Ile Lys Val Leu Phe Ala Ser Gln Glu Ile Pro Ala 820 825 830Ser Pro Phe Arg Val Lys Val Asp Pro Ser His Asp Ala Ser Lys Val 835 840 845Lys Ala Glu Gly Pro Gly Leu Ser Lys Ala Gly Val Glu Asn Gly Lys 850 855 860Pro Thr His Phe Thr Val Tyr Thr Lys Gly Ala Gly Lys Ala Pro Leu865 870 875 880Asn Val Gln Phe Asn Ser Pro Leu Pro Gly Asp Ala Val Lys Asp Leu 885 890 895Asp Ile Ile Asp Asn Tyr Asp Tyr Ser His Thr Val Lys Tyr Thr Pro 900 905 910Thr Gln Gln Gly Asn Met Gln Val Leu Val Thr Tyr Gly Gly Asp Pro 915 920 925Ile Pro Lys Ser Pro Phe Thr Val Gly Val Ala Ala Pro Leu Asp Leu 930 935 940Ser Lys Ile Lys Leu Asn Gly Leu Glu Asn Arg Val Glu Val Gly Lys945 950 955 960Asp Gln Glu Phe Thr Val Asp Thr Arg Gly Ala Gly Gly Gln Gly Lys 965 970 975Leu Asp Val Thr Ile Leu Ser Pro Ser Arg Lys Val Val Pro Cys Leu 980 985 990Val Thr Pro Val Thr Gly Arg Glu Asn Ser Thr Ala Lys Phe Ile Pro 995 1000 1005Arg Glu Glu Gly Leu Tyr Ala Val Asp Val Thr Tyr Asp Gly His 1010 1015 1020Pro Val Pro Gly Ser Pro Tyr Thr Val Glu Ala Ser Leu Pro Pro 1025 1030 1035Asp Pro Ser Lys Val Lys Ala His Gly Pro Gly Leu Glu Gly Gly 1040 1045 1050Leu Val Gly Lys Pro Ala Glu Phe Thr Ile Asp Thr Lys Gly Ala 1055 1060 1065Gly Thr Gly Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala 1070 1075 1080Lys Ile Glu Cys Ser Asp Asn Gly Asp Gly Thr Cys Ser Val Ser 1085 1090 1095Tyr Leu Pro Thr Lys Pro Gly Glu Tyr Phe Val Asn Ile Leu Phe 1100 1105 1110Glu Glu Val His Ile Pro Gly Ser Pro Phe Lys Ala Asp Ile Glu 1115 1120 1125Met Pro Phe Asp Pro Ser Lys Val Val Ala Ser Gly Pro Gly Leu 1130 1135 1140Glu His Gly Lys Val Gly Glu Ala Gly Leu Leu Ser Val Asp Cys 1145 1150 1155Ser Glu Ala Gly Pro Gly Ala Leu Gly Leu Glu Ala Val Ser Asp 1160 1165 1170Ser Gly Thr Lys Ala Glu Val Ser Ile Gln Asn Asn Lys Asp Gly 1175 1180 1185Thr Tyr Ala Val Thr Tyr Val Pro Leu Thr Ala Gly Met Tyr Thr 1190 1195 1200Leu Thr Met Lys Tyr Gly Gly Glu Leu Val Pro His Phe Pro Ala 1205 1210 1215Arg Val Lys Val Glu Pro Ala Val Asp Thr Ser Arg Ile Lys Val 1220 1225 1230Phe Gly Pro Gly Ile Glu Gly Lys Asp Val Phe Arg Glu Ala Thr 1235 1240 1245Thr Asp Phe Thr Val Asp Ser Arg Pro Leu Thr Gln Val Gly Gly 1250 1255 1260Asp His Ile Lys Ala His Ile Ala Asn Pro Ser Gly Ala Ser Thr 1265 1270 1275Glu Cys Phe Val Thr Asp Asn Ala Asp Gly Thr Tyr Gln Val Glu 1280 1285 1290Tyr Thr Pro Phe Glu Lys Gly Leu His Val Val Glu Val Thr Tyr 1295 1300 1305Asp Asp Val Pro Ile Pro Asn Ser Pro Phe Lys Val Ala Val Thr 1310 1315 1320Glu Gly Cys Gln Pro Ser Arg Val Gln Ala Gln Gly Pro Gly Leu 1325 1330 1335Lys Glu Ala Phe Thr Asn Lys Pro Asn Val Phe Thr Val Val Thr 1340 1345 1350Arg Gly Ala Gly Ile Gly Gly Leu Gly Ile Thr Val Glu Gly Pro 1355 1360 1365Ser Glu Ser Lys Ile Asn Cys Arg Asp Asn Lys Asp Gly Ser Cys 1370 1375 1380Ser Ala Glu Tyr Ile Pro Phe Ala Pro Gly Asp Tyr Asp Val Asn 1385 1390 1395Ile Thr Tyr Gly Gly Ala His Ile Pro Gly Ser Pro Phe Arg Val 1400 1405 1410Pro Val Lys Asp Val Val Asp Pro Ser Lys Val Lys Ile Ala Gly 1415 1420 1425Pro Gly Leu Gly Ser Gly Val Arg Ala Arg Val Leu Gln Ser Phe 1430 1435 1440Thr Val Asp Ser Ser Lys Ala Gly Leu Ala Pro Leu Glu Val Arg 1445 1450 1455Val Leu Gly Pro Arg Gly Leu Val Glu Pro Val Asn Val Val Asp 1460 1465 1470Asn Gly Asp Gly Thr His Thr Val Thr Tyr Thr Pro Ser Gln Glu 1475 1480 1485Gly Pro Tyr Met Val Ser Val Lys Tyr Ala Asp Glu Glu Ile Pro 1490 1495 1500Arg Ser Pro Phe Lys Val Lys Val Leu Pro Thr Tyr Asp Ala Ser 1505 1510 1515Lys Val Thr Ala Ser Gly Pro Gly Leu Ser Ser Tyr Gly Val Pro 1520 1525 1530Ala Ser Leu Pro Val Asp Phe Ala Ile Asp Ala Arg Asp Ala Gly 1535 1540 1545Glu Gly Leu Leu Ala Val Gln Ile Thr Asp Gln Glu Gly Lys Pro 1550 1555 1560Lys Arg Ala Ile Val His Asp Asn Lys Asp Gly Thr Tyr Ala Val 1565 1570 1575Thr Tyr Ile Pro Asp Lys Thr Gly Arg Tyr Met Ile Gly Val Thr 1580 1585 1590Tyr Gly Gly Asp Asp Ile Pro Leu Ser Pro Tyr Arg Ile Arg Ala 1595 1600 1605Thr Gln Thr Gly Asp Ala Ser Lys Cys Leu Ala Thr Gly Pro Gly 1610 1615 1620Ile Ala Ser Thr Val Lys Thr Gly Glu Glu Val Gly Phe Val Val 1625 1630 1635Asp Ala Lys Thr Ala Gly Lys Gly Lys Val Thr Cys Thr Val Leu 1640 1645 1650Thr Pro Asp Gly Thr Glu Ala Glu Ala Asp Val Ile Glu Asn Glu 1655 1660 1665Asp Gly Thr Tyr Asp Ile Phe Tyr Thr Ala Ala Lys Pro Gly Thr 1670 1675 1680Tyr Val Ile Tyr Val Arg Phe Gly Gly Val Asp Ile Pro Asn Ser 1685 1690 1695Pro Phe Thr Val Met Val Thr Glu Glu Ala Tyr Val Pro Val Ser 1700 1705 1710Asp Met Asn Gly Leu Gly Phe Lys Pro Phe Asp Leu Val Ile Pro 1715 1720 1725Phe Ala Val Arg Lys Gly Glu Ile Thr Gly Glu Val His Met Pro 1730 1735 1740Ser Gly Lys Thr Ala Thr Pro Glu Ile Val Asp Asn Lys Asp Gly 1745 1750 1755Thr Val Thr Val Arg Tyr Ala Pro Thr Glu Val Gly Leu His Glu 1760 1765 1770Met His Ile Lys Tyr Met Gly Ser His Ile Pro Glu Ser Pro Leu 1775 1780 1785Gln Phe Tyr Val Asn Tyr Pro Asn Ser Gly Ser Val Ser Ala Tyr 1790 1795 1800Gly Pro Gly Leu Val Tyr Gly Val Ala Asn Lys Thr Ala Thr Phe 1805 1810 1815Thr Ile Val Thr Glu Asp Ala Gly Glu Gly Gly Leu Asp Leu Ala 1820 1825 1830Ile Glu Gly Pro Ser Lys Ala Glu Ile Ser Cys Ile Asp Asn Lys 1835 1840 1845Asp Gly Thr Cys Thr Val Thr Tyr Leu Pro Thr Leu Pro Gly Asp 1850 1855 1860Tyr Ser Ile Leu Val Lys Tyr Asn Asp Lys His Ile Pro Gly Ser 1865 1870 1875Pro Phe Thr Ala Lys Ile Thr Asp Asp Ser Arg Arg Cys Ser Gln 1880 1885 1890Val Lys Leu Gly Ser Ala Ala Asp Phe Leu Leu Asp Ile Ser Glu 1895 1900 1905Thr Asp Leu Ser Ser Leu Thr Ala Ser Ile Lys Ala Pro Ser Gly 1910 1915 1920Arg Asp Glu Pro Cys Leu Leu Lys Arg Leu Pro Asn Asn His Ile 1925 1930 1935Gly Ile Ser Phe Ile Pro Arg Glu Val Gly Glu His Leu Val Ser 1940 1945 1950Ile Lys Lys Asn Gly Asn His Val Ala Asn Ser Pro Val Ser Ile 1955 1960 1965Met Val Val Gln Ser Glu Ile Gly Asp Ala Arg Arg Ala Lys Val 1970 1975 1980Tyr Gly Arg Gly Leu Ser Glu Gly Arg Thr Phe Glu Met Ser Asp 1985 1990 1995Phe Ile Val Asp Thr Arg Asp Ala Gly Tyr Gly Gly Ile Ser Leu 2000 2005 2010Ala Val Glu Gly Pro Ser Lys Val Asp Ile Gln Thr Glu Asp Leu 2015 2020 2025Glu Asp Gly Thr Cys Lys Val Ser Tyr Phe Pro Thr Val Pro Gly 2030 2035 2040Val Tyr Ile Val Ser Thr Lys Phe Ala Asp Glu His Val Pro Gly 2045 2050 2055Ser Pro Phe Thr Val Lys Ile Ser Gly Glu Gly Arg Val Lys Glu 2060 2065 2070Ser Ile Thr Arg Thr Ser Arg Ala Pro Ser Val Ala Thr Val Gly 2075 2080 2085Ser Ile Cys Asp Leu Asn Leu Lys Ile Pro Glu Ile Asn Ser Ser 2090 2095 2100Asp Met Ser Ala His Val Thr Ser Pro Ser Gly Arg Val Thr Glu 2105 2110 2115Ala Glu Ile Val Pro Met Gly Lys Asn Ser His Cys Val Arg Phe 2120 2125 2130Val Pro Gln Glu Met Gly Val His Thr Val Ser Val Lys Tyr Arg 2135 2140 2145Gly Gln His Val Thr Gly Ser Pro Phe Gln Phe Thr Val Gly Pro 2150 2155 2160Leu Gly Glu Gly Gly Ala His Lys Val Arg Ala Gly Gly Pro Gly 2165 2170 2175Leu Glu Arg Gly Glu Ala Gly Val Pro Ala Glu Phe Ser Ile Trp 2180 2185 2190Thr Arg Glu Ala Gly Ala Gly Gly Leu Ser Ile Ala Val Glu Gly 2195 2200 2205Pro Ser Lys Ala Glu Ile Thr Phe Asp Asp His Lys Asn Gly Ser 2210 2215 2220Cys Gly Val Ser Tyr Ile Ala Gln Glu Pro Gly Asn Tyr Glu Val 2225 2230 2235Ser Ile Lys Phe Asn Asp Glu His Ile Pro Glu Ser Pro Tyr Leu 2240 2245 2250Val Pro Val Ile Ala Pro Ser Asp Asp Ala Arg Arg Leu Thr Val 2255 2260 2265Met Ser Leu Gln Glu Ser Gly Leu Lys Val Asn Gln Pro Ala Ser 2270 2275 2280Phe Ala Ile Arg Leu Asn Gly Ala Lys Gly Lys Ile Asp Ala Lys 2285 2290 2295Val His Ser Pro Ser Gly Ala Val Glu Glu Cys His Val Ser Glu 2300 2305 2310Leu Glu Pro Asp Lys Tyr Ala Val Arg Phe Ile Pro His Glu Asn 2315 2320 2325Gly Val His Thr Ile Asp Val Lys Phe Asn Gly Ser His Val Val 2330 2335 2340Gly Ser Pro Phe Lys Val Arg Val Gly Glu Pro Gly Gln Ala Gly 2345 2350 2355Asn Pro Ala Leu Val Ser Ala Tyr Gly Thr Gly Leu Glu Gly Gly 2360 2365 2370Thr Thr Gly Ile Gln Ser Glu Phe Phe Ile Asn Thr Thr Arg Ala 2375 2380 2385Gly Pro Gly Thr Leu Ser Val Thr Ile Glu Gly Pro Ser Lys Val 2390 2395 2400Lys Met Asp Cys Gln Glu Thr Pro Glu Gly Tyr Lys Val Met Tyr 2405 2410 2415Thr Pro Met Ala Pro Gly Asn Tyr Leu Ile Ser Val Lys Tyr Gly 2420 2425 2430Gly Pro Asn His Ile Val Gly Ser Pro Phe Lys Ala Lys Val Thr 2435 2440 2445Gly Gln Arg Leu Val Ser Pro Gly Ser Ala Asn Glu Thr Ser Ser 2450 2455 2460Ile Leu Val Glu Ser Val Thr Arg Ser Ser Thr Glu Thr Cys Tyr 2465 2470 2475Ser Ala Ile Pro Lys Ala Ser Ser Asp Ala Ser Lys Val Thr Ser 2480 2485 2490Lys Gly Ala Gly Leu Ser Lys Ala Phe Val Gly Gln Lys Ser Ser 2495 2500 2505Phe Leu Val Asp Cys Ser Lys Ala Gly Ser Asn Met Leu Leu Ile 2510 2515 2520Gly Val His Gly Pro Thr Thr Pro Cys Glu Glu Val Ser Met Lys 2525 2530 2535His Val Gly Asn Gln Gln Tyr Asn Val Thr Tyr Val Val Lys Glu 2540 2545 2550Arg Gly Asp Tyr Val Leu Ala Val Lys Trp Gly Glu Glu His Ile 2555 2560 2565Pro Gly Ser Pro Phe His Val Thr Val Pro 2570 2575279395DNAHomo sapiens 27gcggccaggg gcgggcggcc gcagagcagc accggccgtg gctccggtag cagcaagttc 60gaaccccgct cccgctccgc ttcggttctc gctccttcgg cccttgggcc tccaaacacc 120agtccccggc agctcgttgc gcattgcgct ctccccgcca ccaggatgcc ggtaaccgag 180aaggatctag ctgaggacgc gccttggaag aagatccagc agaacacgtt cacacgctgg 240tgcaacgagc acctcaagtg cgtgaacaaa cgcatcggca acctgcagac cgacctgagc 300gacgggctgc ggctcatcgc gctgctcgag gtgctcagcc agaagcgcat gtaccgcaag 360taccatcagc ggcccacctt tcgccagatg cagctcgaga atgtgtccgt ggcgctcgag 420ttcctggacc gtgagagcat caagctcgtg tccatcgata gcaaagccat tgtggatggg 480aacctgaagc tcatcttggg tctggtgtgg acgctgatcc tccactactc catctccatg 540cccgtgtggg aggatgaagg ggatgatgat gccaagaagc agacgccaaa gcagaggctg 600ctggggtgga ttcagaacaa gatcccctac ttgcccatca ccaactttaa ccagaactgg 660caagacggca aagccctggg agccctggta gacagctgtg ctccaggtct gtgcccagac 720tgggaatcct gggacccgca gaagcctgtg gataatgcac gagaagccat gcagcaggca 780gatgactggc tgggtgtccc acaggtcatc actcctgaag aaatcattca cccggatgtg 840gacgagcact cagttatgac ttacctgtcc cagttcccca aagccaagct caagccgggg 900gctcctctca aacccaaact caacccgaag aaagccaggg cctatggcag aggaatcgag 960cccactggaa acatggtgaa gcagccagcc aagttcactg tggacaccat cagcgccggg 1020caaggagacg tgatggtgtt tgttgaggac ccagaaggga acaaagagga ggcacaagtg 1080acccctgaca gtgacaagaa caagacatac tctgtggagt atctgcccaa ggtcaccggg 1140ctacacaaag tcacagtcct ctttgcagga cagcacatct ccaagagccc atttgaagtg 1200agtgttgaca aggcccaggg agatgccagt aaagtcactg caaaaggtcc agggttggaa 1260gctgtaggga acatcgccaa taagcccacc tactttgaca tctatacggc aggagctggt 1320gtgggtgaca ttggtgtgga ggtggaagat ccccagggga agaacaccgt ggagttgctc 1380gtggaagaca aaggaaacca ggtgtatcga tgtgtgtaca aacccatgca gcctggccct 1440cacgtggtca agatcttctt tgctggggac actattccta agagtccctt cgttgtgcag 1500gttggggaag cctgcaatcc aaatgcctgc cgggccagtg gccgaggcct acaacccaaa 1560ggcgtccgta tccgggagac cacagatttc aaggttgaca ccaaagctgc aggaagtggg 1620gagctcggtg taaccatgaa gggtcctaag ggtctggagg agctggtgaa gcagaaagac 1680tttctggatg gggtctacgc attcgagtat taccccagca ccccggggag atacagcatt 1740gccatcacat gggggggaca ccacattcca aagagcccct ttgaagttca agttggccct 1800gaagcgggta tgcagaaagt ccgtgcttgg ggccctgggc tccatggtgg gattgtcggg 1860cggtcagcgg acttcgtggt agaatccatt ggctctgaag tggggtctct ggggtttgcc 1920attgaaggcc cctctcaggc aaagattgag tacaacgacc agaatgatgg atcgtgtgat 1980gtcaaatact ggcccaagga gcctggcgaa tatgctgttc acatcatgtg tgacgacgaa 2040gacatcaagg acagcccgta catggccttc atccacccag ccacgggagg ctacaaccct 2100gatctggttc gagcatacgg gccaggtttg gagaaatctg gatgcattgt caacaacctg 2160gccgagttca ctgtggatcc taaggatgct ggaaaagctc ccttaaagat atttgctcag 2220gatggggaag gccaacgcat tgacatccag atgaagaacc ggatggacgg cacatatgca 2280tgctcataca ccccggtgaa ggccatcaag cacaccattg ctgtggtctg gggaggcgtg 2340aacatcccgc acagccccta cagggtcaac atcgggcaag gtagccatcc tcagaaggtc 2400aaagtgtttg

ggccaggtgt ggagagaagt ggtctgaagg caaatgaacc tacacacttc 2460acggtggact gtactgaggc tggggaaggt gatgtcagtg ttggcattaa gtgtgatgcc 2520cgggtgttaa gtgaagatga ggaagacgtg gattttgaca ttattcacaa tgccaatgat 2580acgttcacag tcaaatatgt gcctcctgct gctgggcgat acactatcaa agttctcttt 2640gcatctcagg aaatccccgc cagccctttc agagtcaaag ttgacccttc ccacgatgcc 2700agcaaagtga aggcagaagg cccagggctc agcaaagcag gtgtggaaaa tgggaaaccg 2760acccacttca ctgtctacac caagggggct gggaaagccc cgctcaacgt gcagttcaac 2820agccctcttc ctggcgatgc agtgaaggat ttggatatca tcgataatta tgactactct 2880cacacggtta aatatacacc cacccaacag ggcaacatgc aggttctggt gacttacggt 2940ggcgatccca tccctaaaag ccctttcact gtgggtgttg ctgcaccgct ggatctgagc 3000aagataaaac tcaatgggct ggaaaacagg gtggaagttg ggaaggatca ggagttcacc 3060gttgatacca ggggggcagg aggccagggg aagctggacg tgacaatcct cagcccctct 3120cggaaggtcg tgccatgcct agtgacacct gtgacaggcc gggagaacag cacggccaag 3180ttcatccctc gggaggaggg gctgtatgct gtagacgtga cctacgatgg acaccctgtg 3240cccgggagcc cctacacagt ggaggcctcg ctgccaccag atcccagcaa ggtgaaggcc 3300cacggtcccg gcctcgaagg tggtctcgtg ggcaagcctg ccgagttcac catcgatacc 3360aaaggagctg gtactggagg tctgggctta acggtggaag gtccgtgcga ggccaaaatc 3420gagtgctccg acaatggtga tgggacctgc tccgtctctt accttcccac aaaacccggg 3480gagtacttcg tcaacatcct ctttgaagaa gtccacatac ctgggtctcc cttcaaagct 3540gacattgaaa tgccctttga cccctctaaa gtcgtggcat cggggccagg tctcgagcac 3600gggaaggtgg gtgaagctgg cctccttagc gtcgactgct cggaagcggg accgggggcc 3660ctgggcctgg aagctgtctc ggactcggga acaaaagccg aagtcagtat tcagaacaac 3720aaagatggca cctacgcggt gacctacgtg cccctgacgg ccggcatgta cacgttgacc 3780atgaagtatg gtggcgaact cgtgccacac ttccccgccc gggtcaaggt ggagcccgcc 3840gtggacacca gcaggatcaa agtctttgga ccaggaatag aagggaaaga tgtgttccgg 3900gaagctacca ccgactttac agttgactct cggccgctga cccaggttgg gggtgaccac 3960atcaaggccc acattgccaa cccctcaggg gcctccaccg agtgctttgt cacagacaat 4020gcggatggga cctaccaggt ggaatacaca ccctttgaga aaggtctcca tgtagtggag 4080gtgacatatg atgacgtgcc tatcccaaac agtcccttca aggtggctgt cactgaaggc 4140tgccagccat ctagggtgca agcccaagga cctggattga aagaggcctt taccaacaag 4200cccaatgtct tcaccgtggt taccagaggc gcaggaattg gtgggcttgg cataactgtt 4260gagggaccat cagagtcgaa gataaattgc agagacaaca aggatggcag ctgcagtgct 4320gagtacattc ctttcgcacc gggggattac gatgttaata tcacatatgg aggagcccac 4380atccccggca gccccttcag ggttcctgtg aaggatgttg tggaccccag caaggtcaag 4440attgccggcc ccgggctggg ctcaggcgtc cgagcccgtg tcctgcagtc cttcacggtg 4500gacagcagca aggctggcct ggctccgctg gaagtgaggg ttctgggccc acgaggcttg 4560gtggagccag tgaacgtggt ggacaatgga gatggcacac acacagtaac ctacacccca 4620tctcaggagg gaccttacat ggtctcagtt aaatatgctg atgaagagat tcctcgcagt 4680cccttcaagg tcaaggtcct tcccacatat gatgccagca aagtgactgc cagtggcccc 4740ggccttagtt cctatggtgt gcctgccagt ctacctgtgg actttgcaat tgatgcccga 4800gatgccgggg aaggcctgct tgctgttcaa ataacggacc aagaaggaaa acccaaaaga 4860gccattgtcc atgacaataa agatggcacg tatgctgtca cctacatccc cgacaagact 4920gggcgctata tgattggagt cacctacggg ggtgacgaca tcccactttc tccttatcgc 4980atccgagcca cacagacggg tgatgccagc aagtgcctgg ccacgggtcc tggaatcgcc 5040tccactgtga aaactggcga agaagtaggc tttgtggttg atgccaagac tgccgggaag 5100ggtaaagtga cctgcacggt tctgacccca gatggcactg aggccgaggc cgatgtcatt 5160gagaatgaag atggaaccta tgacatcttc tacacagctg ccaagccggg cacatatgtg 5220atctatgtgc gcttcggtgg tgttgatatt cctaacagcc ccttcactgt catggtgacc 5280gaagaggcct atgtcccagt gagtgacatg aacggcctgg gatttaagcc ttttgacctg 5340gtcattccgt ttgctgtcag gaaaggagaa atcactggag aggtccacat gccttctggg 5400aagacagcca cacctgagat tgtggacaac aaggacggca cggtcactgt tagatatgcc 5460cccactgagg tcgggctcca tgagatgcac atcaaataca tgggcagcca catccctgag 5520agcccactcc agttctacgt gaactacccc aacagtggaa gtgtttctgc atacggtcca 5580ggcctcgtgt atggagtggc caacaaaact gccaccttca ccatcgtcac agaggatgca 5640ggagaaggtg gtctggactt ggctattgag ggcccctcaa aagcagaaat cagctgcatt 5700gacaataaag atgggacatg cacagtgacc tacctgccga ctctgccagg cgactacagc 5760attctggtca agtacaatga caagcacatc cctggcagcc ccttcacagc caagatcaca 5820gatgacagca ggcggtgctc ccaggtgaag ttgggctcag ccgctgactt cctgctcgac 5880atcagtgaga ctgacctcag cagcctgacg gccagcatta aggccccatc tggccgagac 5940gagccctgtc tcctgaagag gctgcccaac aaccacattg gcatctcctt catcccccgg 6000gaagtgggcg aacatctggt cagcatcaag aaaaatggca accatgtggc caacagcccc 6060gtgtctatca tggtggtcca gtcggagatt ggtgacgccc gccgagccaa agtctatggc 6120cgcggcctgt cagaaggccg gactttcgag atgtctgact tcatcgtgga cacaagggat 6180gcaggttatg gtggcatatc cttggcggtg gaaggcccca gcaaagtgga catccagacg 6240gaggacctgg aagatggcac ctgcaaagtc tcctacttcc ctaccgtgcc tggggtttat 6300atcgtctcca ccaaattcgc tgacgagcac gtgcctggga gcccatttac cgtgaagatc 6360agtggggagg gaagagtcaa agagagcatc acccgcacca gtcgggcccc gtccgtggcc 6420actgtcggga gcatttgtga cctgaacctg aaaatcccag aaatcaacag cagtgatatg 6480tcggcccacg tcaccagccc ctctggccgt gtgactgagg cagagattgt gcccatgggg 6540aagaactcac actgcgtccg gtttgtgccc caggagatgg gcgtgcacac ggtcagcgtc 6600aagtaccgtg ggcagcacgt caccggcagc cccttccagt tcaccgtggg gccacttggt 6660gaaggaggcg cccacaaggt gcgggcagga ggccctggcc tggagagagg agaagcggga 6720gtcccagctg agttcagcat ttggacccgg gaagcaggcg ctggaggcct ctccatcgct 6780gttgagggcc ccagtaaggc cgagattaca ttcgatgacc ataaaaatgg gtcgtgcggt 6840gtatcttata ttgcccaaga gcctggtaac tacgaggtgt ccatcaagtt caatgatgag 6900cacatcccgg aaagccccta cctggtgccg gtcatcgcac cctccgacga cgcccgccgc 6960ctcactgtta tgagccttca ggaatcggga ttaaaagtta accagccagc atcctttgct 7020ataaggttga atggcgcaaa aggcaagatt gatgcaaagg tgcacagccc ctctggagcc 7080gtggaggagt gccacgtgtc tgagctggag ccagataagt atgctgttcg cttcatccct 7140catgagaatg gtgtccacac catcgatgtc aagttcaatg ggagccacgt ggttggaagc 7200cccttcaaag tgcgcgttgg ggagcctgga caagcgggga accctgccct ggtgtccgcc 7260tatggcacgg gactcgaagg gggcaccaca ggtatccagt cggaattctt tattaacacc 7320acccgagcag gtccagggac attatccgtc accatcgaag gcccatccaa ggttaaaatg 7380gattgccagg aaacacctga agggtacaaa gtcatgtaca cccccatggc tcctggtaac 7440tacctgatca gcgtcaaata cggtgggccc aaccacatcg tgggcagtcc cttcaaggcc 7500aaggtgacag gccagcgtct agttagccct ggctcagcca acgagacctc atccatcctg 7560gtggagtcag tgaccaggtc gtctacagag acctgctata gcgccattcc caaggcatcc 7620tcggacgcca gcaaggtgac ctctaagggg gcagggctct caaaggcctt tgtgggccag 7680aagagttcct tcctggtgga ctgcagcaaa gctggctcca acatgctgct gatcggggtc 7740catgggccca ccaccccctg cgaggaggtc tccatgaagc atgtaggcaa ccagcaatac 7800aacgtcacat acgtcgtcaa ggagaggggc gattatgtgc tggctgtgaa gtggggggag 7860gaacacatcc ctggcagccc ttttcatgtc acagtgcctt aaaacagttt tctcaaatcc 7920tggagagagt tcttgtggtt gcttttgttg cttgtttgta attcatttta tacaaagccc 7980tccagcctgt ttgtggggct gaaaccccat ccctaaaata ttgctgttgt aaaatgcctt 8040cagaaataag tcctagactg gactcttgag ggacatattg gagaatctta agaaatgcaa 8100gcttgttcag ggggctgaga agatcctgag tacactaggt gcaaaccaga actcttggtg 8160gaacagacca gccactgcag cagacagacc aggaacacaa tgagactgac atttcaaaaa 8220aacaaaactg gctagcctga gctgctggtt cactcttcag catttatgaa acaaggctag 8280gggaagatgg gcagagaaaa aggggacacc tagtttggtt gtcatttggc aaaggagatg 8340acttaaaatc cgcttaatct cttccagtgt ccgtgttaat gtatttggct attagatcac 8400tagcactgct ttaccgctcc tcatcgccaa cacccccatg ctctgtggcc ttcttacact 8460tctcagaggg cagagtggca gccgggcacc ctacagaaac tcagagggca gagtggcagc 8520caggcccaca tgtctctcaa gtacctgtcc cctcgctctg gtgattattt cttgcagaat 8580caccacacga gaccatcccg gcagtcatgg ttttgcttta gttttccaag tccgtttcag 8640tcccttcctt ggtctgaaga aattctgcag tggcgagcag tttcccactt gccaaagatc 8700ccttttaacc aacactagcc cttgttttta acacacgctc cagcccttca tcagcctggg 8760cagtcttacc aaaatgttta aagtgatctc agaggggccc atggattaac gccctcatcc 8820caaggtccgt cccatgacat aacactccac acccgcccca gccaacttca tgggtcactt 8880tttctggaaa ataatgatct gtacagacag gacagaatga aactcctgcg ggtctttggc 8940ctgaaagttg ggaatggttg ggggagagaa gggcagcagc ttattggtgg tcttttcacc 9000attggcagaa acagtgagag ctgtgtggtg cagaaatcca gaaatgaggt gtagggaatt 9060ttgcctgcct tcctgcagac ctgagctggc tttggaatga ggttaaagtg tcagggacgt 9120tgcctgagcc caaatgtgta gtgtggtctg ggcaggcaga cctttaggtt ttgctgctta 9180gtcctgagga agtggccact cttgtggcag gtgtagtatc tggggcgagt gttgggggta 9240aaagcccacc ctacagaaag tggaacagcc cggagcctga tgtgaaagga ccacgggtgt 9300tgtaagctgg gacacggaag ccaaactgga atcaaacgcc gactgtaaat tgtatcttat 9360aacttattaa ataaaacatt tgctccgtaa agttg 9395282602PRTHomo sapiens 28Met Pro Val Thr Glu Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys1 5 10 15Ile Gln Gln Asn Thr Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys 20 25 30Val Asn Lys Arg Ile Gly Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu 35 40 45Arg Leu Ile Ala Leu Leu Glu Val Leu Ser Gln Lys Arg Met Tyr Arg 50 55 60Lys Tyr His Gln Arg Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val65 70 75 80Ser Val Ala Leu Glu Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser 85 90 95Ile Asp Ser Lys Ala Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly 100 105 110Leu Val Trp Thr Leu Ile Leu His Tyr Ser Ile Ser Met Pro Val Trp 115 120 125Glu Asp Glu Gly Asp Asp Asp Ala Lys Lys Gln Thr Pro Lys Gln Arg 130 135 140Leu Leu Gly Trp Ile Gln Asn Lys Ile Pro Tyr Leu Pro Ile Thr Asn145 150 155 160Phe Asn Gln Asn Trp Gln Asp Gly Lys Ala Leu Gly Ala Leu Val Asp 165 170 175Ser Cys Ala Pro Gly Leu Cys Pro Asp Trp Glu Ser Trp Asp Pro Gln 180 185 190Lys Pro Val Asp Asn Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp 195 200 205Leu Gly Val Pro Gln Val Ile Thr Pro Glu Glu Ile Ile His Pro Asp 210 215 220Val Asp Glu His Ser Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala225 230 235 240Lys Leu Lys Pro Gly Ala Pro Leu Lys Pro Lys Leu Asn Pro Lys Lys 245 250 255Ala Arg Ala Tyr Gly Arg Gly Ile Glu Pro Thr Gly Asn Met Val Lys 260 265 270Gln Pro Ala Lys Phe Thr Val Asp Thr Ile Ser Ala Gly Gln Gly Asp 275 280 285Val Met Val Phe Val Glu Asp Pro Glu Gly Asn Lys Glu Glu Ala Gln 290 295 300Val Thr Pro Asp Ser Asp Lys Asn Lys Thr Tyr Ser Val Glu Tyr Leu305 310 315 320Pro Lys Val Thr Gly Leu His Lys Val Thr Val Leu Phe Ala Gly Gln 325 330 335His Ile Ser Lys Ser Pro Phe Glu Val Ser Val Asp Lys Ala Gln Gly 340 345 350Asp Ala Ser Lys Val Thr Ala Lys Gly Pro Gly Leu Glu Ala Val Gly 355 360 365Asn Ile Ala Asn Lys Pro Thr Tyr Phe Asp Ile Tyr Thr Ala Gly Ala 370 375 380Gly Val Gly Asp Ile Gly Val Glu Val Glu Asp Pro Gln Gly Lys Asn385 390 395 400Thr Val Glu Leu Leu Val Glu Asp Lys Gly Asn Gln Val Tyr Arg Cys 405 410 415Val Tyr Lys Pro Met Gln Pro Gly Pro His Val Val Lys Ile Phe Phe 420 425 430Ala Gly Asp Thr Ile Pro Lys Ser Pro Phe Val Val Gln Val Gly Glu 435 440 445Ala Cys Asn Pro Asn Ala Cys Arg Ala Ser Gly Arg Gly Leu Gln Pro 450 455 460Lys Gly Val Arg Ile Arg Glu Thr Thr Asp Phe Lys Val Asp Thr Lys465 470 475 480Ala Ala Gly Ser Gly Glu Leu Gly Val Thr Met Lys Gly Pro Lys Gly 485 490 495Leu Glu Glu Leu Val Lys Gln Lys Asp Phe Leu Asp Gly Val Tyr Ala 500 505 510Phe Glu Tyr Tyr Pro Ser Thr Pro Gly Arg Tyr Ser Ile Ala Ile Thr 515 520 525Trp Gly Gly His His Ile Pro Lys Ser Pro Phe Glu Val Gln Val Gly 530 535 540Pro Glu Ala Gly Met Gln Lys Val Arg Ala Trp Gly Pro Gly Leu His545 550 555 560Gly Gly Ile Val Gly Arg Ser Ala Asp Phe Val Val Glu Ser Ile Gly 565 570 575Ser Glu Val Gly Ser Leu Gly Phe Ala Ile Glu Gly Pro Ser Gln Ala 580 585 590Lys Ile Glu Tyr Asn Asp Gln Asn Asp Gly Ser Cys Asp Val Lys Tyr 595 600 605Trp Pro Lys Glu Pro Gly Glu Tyr Ala Val His Ile Met Cys Asp Asp 610 615 620Glu Asp Ile Lys Asp Ser Pro Tyr Met Ala Phe Ile His Pro Ala Thr625 630 635 640Gly Gly Tyr Asn Pro Asp Leu Val Arg Ala Tyr Gly Pro Gly Leu Glu 645 650 655Lys Ser Gly Cys Ile Val Asn Asn Leu Ala Glu Phe Thr Val Asp Pro 660 665 670Lys Asp Ala Gly Lys Ala Pro Leu Lys Ile Phe Ala Gln Asp Gly Glu 675 680 685Gly Gln Arg Ile Asp Ile Gln Met Lys Asn Arg Met Asp Gly Thr Tyr 690 695 700Ala Cys Ser Tyr Thr Pro Val Lys Ala Ile Lys His Thr Ile Ala Val705 710 715 720Val Trp Gly Gly Val Asn Ile Pro His Ser Pro Tyr Arg Val Asn Ile 725 730 735Gly Gln Gly Ser His Pro Gln Lys Val Lys Val Phe Gly Pro Gly Val 740 745 750Glu Arg Ser Gly Leu Lys Ala Asn Glu Pro Thr His Phe Thr Val Asp 755 760 765Cys Thr Glu Ala Gly Glu Gly Asp Val Ser Val Gly Ile Lys Cys Asp 770 775 780Ala Arg Val Leu Ser Glu Asp Glu Glu Asp Val Asp Phe Asp Ile Ile785 790 795 800His Asn Ala Asn Asp Thr Phe Thr Val Lys Tyr Val Pro Pro Ala Ala 805 810 815Gly Arg Tyr Thr Ile Lys Val Leu Phe Ala Ser Gln Glu Ile Pro Ala 820 825 830Ser Pro Phe Arg Val Lys Val Asp Pro Ser His Asp Ala Ser Lys Val 835 840 845Lys Ala Glu Gly Pro Gly Leu Ser Lys Ala Gly Val Glu Asn Gly Lys 850 855 860Pro Thr His Phe Thr Val Tyr Thr Lys Gly Ala Gly Lys Ala Pro Leu865 870 875 880Asn Val Gln Phe Asn Ser Pro Leu Pro Gly Asp Ala Val Lys Asp Leu 885 890 895Asp Ile Ile Asp Asn Tyr Asp Tyr Ser His Thr Val Lys Tyr Thr Pro 900 905 910Thr Gln Gln Gly Asn Met Gln Val Leu Val Thr Tyr Gly Gly Asp Pro 915 920 925Ile Pro Lys Ser Pro Phe Thr Val Gly Val Ala Ala Pro Leu Asp Leu 930 935 940Ser Lys Ile Lys Leu Asn Gly Leu Glu Asn Arg Val Glu Val Gly Lys945 950 955 960Asp Gln Glu Phe Thr Val Asp Thr Arg Gly Ala Gly Gly Gln Gly Lys 965 970 975Leu Asp Val Thr Ile Leu Ser Pro Ser Arg Lys Val Val Pro Cys Leu 980 985 990Val Thr Pro Val Thr Gly Arg Glu Asn Ser Thr Ala Lys Phe Ile Pro 995 1000 1005Arg Glu Glu Gly Leu Tyr Ala Val Asp Val Thr Tyr Asp Gly His 1010 1015 1020Pro Val Pro Gly Ser Pro Tyr Thr Val Glu Ala Ser Leu Pro Pro 1025 1030 1035Asp Pro Ser Lys Val Lys Ala His Gly Pro Gly Leu Glu Gly Gly 1040 1045 1050Leu Val Gly Lys Pro Ala Glu Phe Thr Ile Asp Thr Lys Gly Ala 1055 1060 1065Gly Thr Gly Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala 1070 1075 1080Lys Ile Glu Cys Ser Asp Asn Gly Asp Gly Thr Cys Ser Val Ser 1085 1090 1095Tyr Leu Pro Thr Lys Pro Gly Glu Tyr Phe Val Asn Ile Leu Phe 1100 1105 1110Glu Glu Val His Ile Pro Gly Ser Pro Phe Lys Ala Asp Ile Glu 1115 1120 1125Met Pro Phe Asp Pro Ser Lys Val Val Ala Ser Gly Pro Gly Leu 1130 1135 1140Glu His Gly Lys Val Gly Glu Ala Gly Leu Leu Ser Val Asp Cys 1145 1150 1155Ser Glu Ala Gly Pro Gly Ala Leu Gly Leu Glu Ala Val Ser Asp 1160 1165 1170Ser Gly Thr Lys Ala Glu Val Ser Ile Gln Asn Asn Lys Asp Gly 1175 1180 1185Thr Tyr Ala Val Thr Tyr Val Pro Leu Thr Ala Gly Met Tyr Thr 1190 1195 1200Leu Thr Met Lys Tyr Gly Gly Glu Leu Val Pro His Phe Pro Ala 1205 1210 1215Arg Val Lys Val Glu Pro Ala Val Asp Thr Ser Arg Ile Lys Val 1220 1225 1230Phe Gly Pro Gly Ile Glu Gly Lys Asp Val Phe Arg Glu Ala Thr 1235 1240 1245Thr Asp Phe Thr Val Asp Ser Arg Pro Leu Thr Gln Val Gly Gly 1250 1255 1260Asp His Ile Lys Ala His Ile Ala Asn Pro Ser Gly Ala Ser Thr 1265 1270 1275Glu Cys Phe Val Thr Asp Asn Ala Asp Gly Thr Tyr Gln Val Glu 1280 1285 1290Tyr Thr Pro Phe Glu Lys Gly Leu His Val Val Glu Val Thr Tyr 1295 1300 1305Asp Asp Val Pro Ile Pro Asn Ser Pro

Phe Lys Val Ala Val Thr 1310 1315 1320Glu Gly Cys Gln Pro Ser Arg Val Gln Ala Gln Gly Pro Gly Leu 1325 1330 1335Lys Glu Ala Phe Thr Asn Lys Pro Asn Val Phe Thr Val Val Thr 1340 1345 1350Arg Gly Ala Gly Ile Gly Gly Leu Gly Ile Thr Val Glu Gly Pro 1355 1360 1365Ser Glu Ser Lys Ile Asn Cys Arg Asp Asn Lys Asp Gly Ser Cys 1370 1375 1380Ser Ala Glu Tyr Ile Pro Phe Ala Pro Gly Asp Tyr Asp Val Asn 1385 1390 1395Ile Thr Tyr Gly Gly Ala His Ile Pro Gly Ser Pro Phe Arg Val 1400 1405 1410Pro Val Lys Asp Val Val Asp Pro Ser Lys Val Lys Ile Ala Gly 1415 1420 1425Pro Gly Leu Gly Ser Gly Val Arg Ala Arg Val Leu Gln Ser Phe 1430 1435 1440Thr Val Asp Ser Ser Lys Ala Gly Leu Ala Pro Leu Glu Val Arg 1445 1450 1455Val Leu Gly Pro Arg Gly Leu Val Glu Pro Val Asn Val Val Asp 1460 1465 1470Asn Gly Asp Gly Thr His Thr Val Thr Tyr Thr Pro Ser Gln Glu 1475 1480 1485Gly Pro Tyr Met Val Ser Val Lys Tyr Ala Asp Glu Glu Ile Pro 1490 1495 1500Arg Ser Pro Phe Lys Val Lys Val Leu Pro Thr Tyr Asp Ala Ser 1505 1510 1515Lys Val Thr Ala Ser Gly Pro Gly Leu Ser Ser Tyr Gly Val Pro 1520 1525 1530Ala Ser Leu Pro Val Asp Phe Ala Ile Asp Ala Arg Asp Ala Gly 1535 1540 1545Glu Gly Leu Leu Ala Val Gln Ile Thr Asp Gln Glu Gly Lys Pro 1550 1555 1560Lys Arg Ala Ile Val His Asp Asn Lys Asp Gly Thr Tyr Ala Val 1565 1570 1575Thr Tyr Ile Pro Asp Lys Thr Gly Arg Tyr Met Ile Gly Val Thr 1580 1585 1590Tyr Gly Gly Asp Asp Ile Pro Leu Ser Pro Tyr Arg Ile Arg Ala 1595 1600 1605Thr Gln Thr Gly Asp Ala Ser Lys Cys Leu Ala Thr Gly Pro Gly 1610 1615 1620Ile Ala Ser Thr Val Lys Thr Gly Glu Glu Val Gly Phe Val Val 1625 1630 1635Asp Ala Lys Thr Ala Gly Lys Gly Lys Val Thr Cys Thr Val Leu 1640 1645 1650Thr Pro Asp Gly Thr Glu Ala Glu Ala Asp Val Ile Glu Asn Glu 1655 1660 1665Asp Gly Thr Tyr Asp Ile Phe Tyr Thr Ala Ala Lys Pro Gly Thr 1670 1675 1680Tyr Val Ile Tyr Val Arg Phe Gly Gly Val Asp Ile Pro Asn Ser 1685 1690 1695Pro Phe Thr Val Met Ala Thr Asp Gly Glu Val Thr Ala Val Glu 1700 1705 1710Glu Ala Pro Val Asn Ala Cys Pro Pro Gly Phe Arg Pro Trp Val 1715 1720 1725Thr Glu Glu Ala Tyr Val Pro Val Ser Asp Met Asn Gly Leu Gly 1730 1735 1740Phe Lys Pro Phe Asp Leu Val Ile Pro Phe Ala Val Arg Lys Gly 1745 1750 1755Glu Ile Thr Gly Glu Val His Met Pro Ser Gly Lys Thr Ala Thr 1760 1765 1770Pro Glu Ile Val Asp Asn Lys Asp Gly Thr Val Thr Val Arg Tyr 1775 1780 1785Ala Pro Thr Glu Val Gly Leu His Glu Met His Ile Lys Tyr Met 1790 1795 1800Gly Ser His Ile Pro Glu Ser Pro Leu Gln Phe Tyr Val Asn Tyr 1805 1810 1815Pro Asn Ser Gly Ser Val Ser Ala Tyr Gly Pro Gly Leu Val Tyr 1820 1825 1830Gly Val Ala Asn Lys Thr Ala Thr Phe Thr Ile Val Thr Glu Asp 1835 1840 1845Ala Gly Glu Gly Gly Leu Asp Leu Ala Ile Glu Gly Pro Ser Lys 1850 1855 1860Ala Glu Ile Ser Cys Ile Asp Asn Lys Asp Gly Thr Cys Thr Val 1865 1870 1875Thr Tyr Leu Pro Thr Leu Pro Gly Asp Tyr Ser Ile Leu Val Lys 1880 1885 1890Tyr Asn Asp Lys His Ile Pro Gly Ser Pro Phe Thr Ala Lys Ile 1895 1900 1905Thr Asp Asp Ser Arg Arg Cys Ser Gln Val Lys Leu Gly Ser Ala 1910 1915 1920Ala Asp Phe Leu Leu Asp Ile Ser Glu Thr Asp Leu Ser Ser Leu 1925 1930 1935Thr Ala Ser Ile Lys Ala Pro Ser Gly Arg Asp Glu Pro Cys Leu 1940 1945 1950Leu Lys Arg Leu Pro Asn Asn His Ile Gly Ile Ser Phe Ile Pro 1955 1960 1965Arg Glu Val Gly Glu His Leu Val Ser Ile Lys Lys Asn Gly Asn 1970 1975 1980His Val Ala Asn Ser Pro Val Ser Ile Met Val Val Gln Ser Glu 1985 1990 1995Ile Gly Asp Ala Arg Arg Ala Lys Val Tyr Gly Arg Gly Leu Ser 2000 2005 2010Glu Gly Arg Thr Phe Glu Met Ser Asp Phe Ile Val Asp Thr Arg 2015 2020 2025Asp Ala Gly Tyr Gly Gly Ile Ser Leu Ala Val Glu Gly Pro Ser 2030 2035 2040Lys Val Asp Ile Gln Thr Glu Asp Leu Glu Asp Gly Thr Cys Lys 2045 2050 2055Val Ser Tyr Phe Pro Thr Val Pro Gly Val Tyr Ile Val Ser Thr 2060 2065 2070Lys Phe Ala Asp Glu His Val Pro Gly Ser Pro Phe Thr Val Lys 2075 2080 2085Ile Ser Gly Glu Gly Arg Val Lys Glu Ser Ile Thr Arg Thr Ser 2090 2095 2100Arg Ala Pro Ser Val Ala Thr Val Gly Ser Ile Cys Asp Leu Asn 2105 2110 2115Leu Lys Ile Pro Glu Ile Asn Ser Ser Asp Met Ser Ala His Val 2120 2125 2130Thr Ser Pro Ser Gly Arg Val Thr Glu Ala Glu Ile Val Pro Met 2135 2140 2145Gly Lys Asn Ser His Cys Val Arg Phe Val Pro Gln Glu Met Gly 2150 2155 2160Val His Thr Val Ser Val Lys Tyr Arg Gly Gln His Val Thr Gly 2165 2170 2175Ser Pro Phe Gln Phe Thr Val Gly Pro Leu Gly Glu Gly Gly Ala 2180 2185 2190His Lys Val Arg Ala Gly Gly Pro Gly Leu Glu Arg Gly Glu Ala 2195 2200 2205Gly Val Pro Ala Glu Phe Ser Ile Trp Thr Arg Glu Ala Gly Ala 2210 2215 2220Gly Gly Leu Ser Ile Ala Val Glu Gly Pro Ser Lys Ala Glu Ile 2225 2230 2235Thr Phe Asp Asp His Lys Asn Gly Ser Cys Gly Val Ser Tyr Ile 2240 2245 2250Ala Gln Glu Pro Gly Asn Tyr Glu Val Ser Ile Lys Phe Asn Asp 2255 2260 2265Glu His Ile Pro Glu Ser Pro Tyr Leu Val Pro Val Ile Ala Pro 2270 2275 2280Ser Asp Asp Ala Arg Arg Leu Thr Val Met Ser Leu Gln Glu Ser 2285 2290 2295Gly Leu Lys Val Asn Gln Pro Ala Ser Phe Ala Ile Arg Leu Asn 2300 2305 2310Gly Ala Lys Gly Lys Ile Asp Ala Lys Val His Ser Pro Ser Gly 2315 2320 2325Ala Val Glu Glu Cys His Val Ser Glu Leu Glu Pro Asp Lys Tyr 2330 2335 2340Ala Val Arg Phe Ile Pro His Glu Asn Gly Val His Thr Ile Asp 2345 2350 2355Val Lys Phe Asn Gly Ser His Val Val Gly Ser Pro Phe Lys Val 2360 2365 2370Arg Val Gly Glu Pro Gly Gln Ala Gly Asn Pro Ala Leu Val Ser 2375 2380 2385Ala Tyr Gly Thr Gly Leu Glu Gly Gly Thr Thr Gly Ile Gln Ser 2390 2395 2400Glu Phe Phe Ile Asn Thr Thr Arg Ala Gly Pro Gly Thr Leu Ser 2405 2410 2415Val Thr Ile Glu Gly Pro Ser Lys Val Lys Met Asp Cys Gln Glu 2420 2425 2430Thr Pro Glu Gly Tyr Lys Val Met Tyr Thr Pro Met Ala Pro Gly 2435 2440 2445Asn Tyr Leu Ile Ser Val Lys Tyr Gly Gly Pro Asn His Ile Val 2450 2455 2460Gly Ser Pro Phe Lys Ala Lys Val Thr Gly Gln Arg Leu Val Ser 2465 2470 2475Pro Gly Ser Ala Asn Glu Thr Ser Ser Ile Leu Val Glu Ser Val 2480 2485 2490Thr Arg Ser Ser Thr Glu Thr Cys Tyr Ser Ala Ile Pro Lys Ala 2495 2500 2505Ser Ser Asp Ala Ser Lys Val Thr Ser Lys Gly Ala Gly Leu Ser 2510 2515 2520Lys Ala Phe Val Gly Gln Lys Ser Ser Phe Leu Val Asp Cys Ser 2525 2530 2535Lys Ala Gly Ser Asn Met Leu Leu Ile Gly Val His Gly Pro Thr 2540 2545 2550Thr Pro Cys Glu Glu Val Ser Met Lys His Val Gly Asn Gln Gln 2555 2560 2565Tyr Asn Val Thr Tyr Val Val Lys Glu Arg Gly Asp Tyr Val Leu 2570 2575 2580Ala Val Lys Trp Gly Glu Glu His Ile Pro Gly Ser Pro Phe His 2585 2590 2595Val Thr Val Pro 2600299467DNAHomo sapiens 29gcggccaggg gcgggcggcc gcagagcagc accggccgtg gctccggtag cagcaagttc 60gaaccccgct cccgctccgc ttcggttctc gctccttcgg cccttgggcc tccaaacacc 120agtccccggc agctcgttgc gcattgcgct ctccccgcca ccaggatgcc ggtaaccgag 180aaggatctag ctgaggacgc gccttggaag aagatccagc agaacacgtt cacacgctgg 240tgcaacgagc acctcaagtg cgtgaacaaa cgcatcggca acctgcagac cgacctgagc 300gacgggctgc ggctcatcgc gctgctcgag gtgctcagcc agaagcgcat gtaccgcaag 360taccatcagc ggcccacctt tcgccagatg cagctcgaga atgtgtccgt ggcgctcgag 420ttcctggacc gtgagagcat caagctcgtg tccatcgata gcaaagccat tgtggatggg 480aacctgaagc tcatcttggg tctggtgtgg acgctgatcc tccactactc catctccatg 540cccgtgtggg aggatgaagg ggatgatgat gccaagaagc agacgccaaa gcagaggctg 600ctggggtgga ttcagaacaa gatcccctac ttgcccatca ccaactttaa ccagaactgg 660caagacggca aagccctggg agccctggta gacagctgtg ctccaggtct gtgcccagac 720tgggaatcct gggacccgca gaagcctgtg gataatgcac gagaagccat gcagcaggca 780gatgactggc tgggtgtccc acaggtcatc actcctgaag aaatcattca cccggatgtg 840gacgagcact cagttatgac ttacctgtcc cagttcccca aagccaagct caagccgggg 900gctcctctca aacccaaact caacccgaag aaagccaggg cctatggcag aggaatcgag 960cccactggaa acatggtgaa gcagccagcc aagttcactg tggacaccat cagcgccggg 1020caaggagacg tgatggtgtt tgttgaggac ccagaaggga acaaagagga ggcacaagtg 1080acccctgaca gtgacaagaa caagacatac tctgtggagt atctgcccaa ggtcaccggg 1140ctacacaaag tcacagtcct ctttgcagga cagcacatct ccaagagccc atttgaagtg 1200agtgttgaca aggcccaggg agatgccagt aaagtcactg caaaaggtcc agggttggaa 1260gctgtaggga acatcgccaa taagcccacc tactttgaca tctatacggc aggagctggt 1320gtgggtgaca ttggtgtgga ggtggaagat ccccagggga agaacaccgt ggagttgctc 1380gtggaagaca aaggaaacca ggtgtatcga tgtgtgtaca aacccatgca gcctggccct 1440cacgtggtca agatcttctt tgctggggac actattccta agagtccctt cgttgtgcag 1500gttggggaag cctgcaatcc aaatgcctgc cgggccagtg gccgaggcct acaacccaaa 1560ggcgtccgta tccgggagac cacagatttc aaggttgaca ccaaagctgc aggaagtggg 1620gagctcggtg taaccatgaa gggtcctaag ggtctggagg agctggtgaa gcagaaagac 1680tttctggatg gggtctacgc attcgagtat taccccagca ccccggggag atacagcatt 1740gccatcacat gggggggaca ccacattcca aagagcccct ttgaagttca agttggccct 1800gaagcgggta tgcagaaagt ccgtgcttgg ggccctgggc tccatggtgg gattgtcggg 1860cggtcagcgg acttcgtggt agaatccatt ggctctgaag tggggtctct ggggtttgcc 1920attgaaggcc cctctcaggc aaagattgag tacaacgacc agaatgatgg atcgtgtgat 1980gtcaaatact ggcccaagga gcctggcgaa tatgctgttc acatcatgtg tgacgacgaa 2040gacatcaagg acagcccgta catggccttc atccacccag ccacgggagg ctacaaccct 2100gatctggttc gagcatacgg gccaggtttg gagaaatctg gatgcattgt caacaacctg 2160gccgagttca ctgtggatcc taaggatgct ggaaaagctc ccttaaagat atttgctcag 2220gatggggaag gccaacgcat tgacatccag atgaagaacc ggatggacgg cacatatgca 2280tgctcataca ccccggtgaa ggccatcaag cacaccattg ctgtggtctg gggaggcgtg 2340aacatcccgc acagccccta cagggtcaac atcgggcaag gtagccatcc tcagaaggtc 2400aaagtgtttg ggccaggtgt ggagagaagt ggtctgaagg caaatgaacc tacacacttc 2460acggtggact gtactgaggc tggggaaggt gatgtcagtg ttggcattaa gtgtgatgcc 2520cgggtgttaa gtgaagatga ggaagacgtg gattttgaca ttattcacaa tgccaatgat 2580acgttcacag tcaaatatgt gcctcctgct gctgggcgat acactatcaa agttctcttt 2640gcatctcagg aaatccccgc cagccctttc agagtcaaag ttgacccttc ccacgatgcc 2700agcaaagtga aggcagaagg cccagggctc agcaaagcag gtgtggaaaa tgggaaaccg 2760acccacttca ctgtctacac caagggggct gggaaagccc cgctcaacgt gcagttcaac 2820agccctcttc ctggcgatgc agtgaaggat ttggatatca tcgataatta tgactactct 2880cacacggtta aatatacacc cacccaacag ggcaacatgc aggttctggt gacttacggt 2940ggcgatccca tccctaaaag ccctttcact gtgggtgttg ctgcaccgct ggatctgagc 3000aagataaaac tcaatgggct ggaaaacagg gtggaagttg ggaaggatca ggagttcacc 3060gttgatacca ggggggcagg aggccagggg aagctggacg tgacaatcct cagcccctct 3120cggaaggtcg tgccatgcct agtgacacct gtgacaggcc gggagaacag cacggccaag 3180ttcatccctc gggaggaggg gctgtatgct gtagacgtga cctacgatgg acaccctgtg 3240cccgggagcc cctacacagt ggaggcctcg ctgccaccag atcccagcaa ggtgaaggcc 3300cacggtcccg gcctcgaagg tggtctcgtg ggcaagcctg ccgagttcac catcgatacc 3360aaaggagctg gtactggagg tctgggctta acggtggaag gtccgtgcga ggccaaaatc 3420gagtgctccg acaatggtga tgggacctgc tccgtctctt accttcccac aaaacccggg 3480gagtacttcg tcaacatcct ctttgaagaa gtccacatac ctgggtctcc cttcaaagct 3540gacattgaaa tgccctttga cccctctaaa gtcgtggcat cggggccagg tctcgagcac 3600gggaaggtgg gtgaagctgg cctccttagc gtcgactgct cggaagcggg accgggggcc 3660ctgggcctgg aagctgtctc ggactcggga acaaaagccg aagtcagtat tcagaacaac 3720aaagatggca cctacgcggt gacctacgtg cccctgacgg ccggcatgta cacgttgacc 3780atgaagtatg gtggcgaact cgtgccacac ttccccgccc gggtcaaggt ggagcccgcc 3840gtggacacca gcaggatcaa agtctttgga ccaggaatag aagggaaaga tgtgttccgg 3900gaagctacca ccgactttac agttgactct cggccgctga cccaggttgg gggtgaccac 3960atcaaggccc acattgccaa cccctcaggg gcctccaccg agtgctttgt cacagacaat 4020gcggatggga cctaccaggt ggaatacaca ccctttgaga aaggtctcca tgtagtggag 4080gtgacatatg atgacgtgcc tatcccaaac agtcccttca aggtggctgt cactgaaggc 4140tgccagccat ctagggtgca agcccaagga cctggattga aagaggcctt taccaacaag 4200cccaatgtct tcaccgtggt taccagaggc gcaggaattg gtgggcttgg cataactgtt 4260gagggaccat cagagtcgaa gataaattgc agagacaaca aggatggcag ctgcagtgct 4320gagtacattc ctttcgcacc gggggattac gatgttaata tcacatatgg aggagcccac 4380atccccggca gccccttcag ggttcctgtg aaggatgttg tggaccccag caaggtcaag 4440attgccggcc ccgggctggg ctcaggcgtc cgagcccgtg tcctgcagtc cttcacggtg 4500gacagcagca aggctggcct ggctccgctg gaagtgaggg ttctgggccc acgaggcttg 4560gtggagccag tgaacgtggt ggacaatgga gatggcacac acacagtaac ctacacccca 4620tctcaggagg gaccttacat ggtctcagtt aaatatgctg atgaagagat tcctcgcagt 4680cccttcaagg tcaaggtcct tcccacatat gatgccagca aagtgactgc cagtggcccc 4740ggccttagtt cctatggtgt gcctgccagt ctacctgtgg actttgcaat tgatgcccga 4800gatgccgggg aaggcctgct tgctgttcaa ataacggacc aagaaggaaa acccaaaaga 4860gccattgtcc atgacaataa agatggcacg tatgctgtca cctacatccc cgacaagact 4920gggcgctata tgattggagt cacctacggg ggtgacgaca tcccactttc tccttatcgc 4980atccgagcca cacagacggg tgatgccagc aagtgcctgg ccacgggtcc tggaatcgcc 5040tccactgtga aaactggcga agaagtaggc tttgtggttg atgccaagac tgccgggaag 5100ggtaaagtga cctgcacggt tctgacccca gatggcactg aggccgaggc cgatgtcatt 5160gagaatgaag atggaaccta tgacatcttc tacacagctg ccaagccggg cacatatgtg 5220atctatgtgc gcttcggtgg tgttgatatt cctaacagcc ccttcactgt catggccaca 5280gatggggaag tcacagccgt ggaggaggca ccggtaaatg catgtccccc tggattcagg 5340ccctgggtga ccgaagaggc ctatgtccca gtgagtgaca tgaacggcct gggatttaag 5400ccttttgacc tggtcattcc gtttgctgtc aggaaaggag aaatcactgg agaggtccac 5460atgccttctg ggaagacagc cacacctgag attgtggaca acaaggacgg cacggtcact 5520gttagatatg cccccactga ggtcgggctc catgagatgc acatcaaata catgggcagc 5580cacatccctg agagcccact ccagttctac gtgaactacc ccaacagtgg aagtgtttct 5640gcatacggtc caggcctcgt gtatggagtg gccaacaaaa ctgccacctt caccatcgtc 5700acagaggatg caggagaagg tggtctggac ttggctattg agggcccctc aaaagcagaa 5760atcagctgca ttgacaataa agatgggaca tgcacagtga cctacctgcc gactctgcca 5820ggcgactaca gcattctggt caagtacaat gacaagcaca tccctggcag ccccttcaca 5880gccaagatca cagatgacag caggcggtgc tcccaggtga agttgggctc agccgctgac 5940ttcctgctcg acatcagtga gactgacctc agcagcctga cggccagcat taaggcccca 6000tctggccgag acgagccctg tctcctgaag aggctgccca acaaccacat tggcatctcc 6060ttcatccccc gggaagtggg cgaacatctg gtcagcatca agaaaaatgg caaccatgtg 6120gccaacagcc ccgtgtctat catggtggtc cagtcggaga ttggtgacgc ccgccgagcc 6180aaagtctatg gccgcggcct gtcagaaggc cggactttcg agatgtctga cttcatcgtg 6240gacacaaggg atgcaggtta tggtggcata tccttggcgg tggaaggccc cagcaaagtg 6300gacatccaga cggaggacct ggaagatggc acctgcaaag tctcctactt ccctaccgtg 6360cctggggttt atatcgtctc caccaaattc gctgacgagc acgtgcctgg gagcccattt 6420accgtgaaga tcagtgggga gggaagagtc aaagagagca tcacccgcac cagtcgggcc 6480ccgtccgtgg ccactgtcgg gagcatttgt gacctgaacc tgaaaatccc agaaatcaac 6540agcagtgata tgtcggccca cgtcaccagc ccctctggcc gtgtgactga ggcagagatt 6600gtgcccatgg ggaagaactc acactgcgtc cggtttgtgc cccaggagat gggcgtgcac 6660acggtcagcg tcaagtaccg tgggcagcac gtcaccggca gccccttcca gttcaccgtg 6720gggccacttg gtgaaggagg cgcccacaag gtgcgggcag gaggccctgg cctggagaga 6780ggagaagcgg gagtcccagc tgagttcagc atttggaccc gggaagcagg cgctggaggc 6840ctctccatcg ctgttgaggg ccccagtaag gccgagatta cattcgatga ccataaaaat 6900gggtcgtgcg gtgtatctta tattgcccaa gagcctggta actacgaggt gtccatcaag 6960ttcaatgatg agcacatccc ggaaagcccc tacctggtgc cggtcatcgc accctccgac 7020gacgcccgcc gcctcactgt tatgagcctt caggaatcgg gattaaaagt

taaccagcca 7080gcatcctttg ctataaggtt gaatggcgca aaaggcaaga ttgatgcaaa ggtgcacagc 7140ccctctggag ccgtggagga gtgccacgtg tctgagctgg agccagataa gtatgctgtt 7200cgcttcatcc ctcatgagaa tggtgtccac accatcgatg tcaagttcaa tgggagccac 7260gtggttggaa gccccttcaa agtgcgcgtt ggggagcctg gacaagcggg gaaccctgcc 7320ctggtgtccg cctatggcac gggactcgaa gggggcacca caggtatcca gtcggaattc 7380tttattaaca ccacccgagc aggtccaggg acattatccg tcaccatcga aggcccatcc 7440aaggttaaaa tggattgcca ggaaacacct gaagggtaca aagtcatgta cacccccatg 7500gctcctggta actacctgat cagcgtcaaa tacggtgggc ccaaccacat cgtgggcagt 7560cccttcaagg ccaaggtgac aggccagcgt ctagttagcc ctggctcagc caacgagacc 7620tcatccatcc tggtggagtc agtgaccagg tcgtctacag agacctgcta tagcgccatt 7680cccaaggcat cctcggacgc cagcaaggtg acctctaagg gggcagggct ctcaaaggcc 7740tttgtgggcc agaagagttc cttcctggtg gactgcagca aagctggctc caacatgctg 7800ctgatcgggg tccatgggcc caccaccccc tgcgaggagg tctccatgaa gcatgtaggc 7860aaccagcaat acaacgtcac atacgtcgtc aaggagaggg gcgattatgt gctggctgtg 7920aagtgggggg aggaacacat ccctggcagc ccttttcatg tcacagtgcc ttaaaacagt 7980tttctcaaat cctggagaga gttcttgtgg ttgcttttgt tgcttgtttg taattcattt 8040tatacaaagc cctccagcct gtttgtgggg ctgaaacccc atccctaaaa tattgctgtt 8100gtaaaatgcc ttcagaaata agtcctagac tggactcttg agggacatat tggagaatct 8160taagaaatgc aagcttgttc agggggctga gaagatcctg agtacactag gtgcaaacca 8220gaactcttgg tggaacagac cagccactgc agcagacaga ccaggaacac aatgagactg 8280acatttcaaa aaaacaaaac tggctagcct gagctgctgg ttcactcttc agcatttatg 8340aaacaaggct aggggaagat gggcagagaa aaaggggaca cctagtttgg ttgtcatttg 8400gcaaaggaga tgacttaaaa tccgcttaat ctcttccagt gtccgtgtta atgtatttgg 8460ctattagatc actagcactg ctttaccgct cctcatcgcc aacaccccca tgctctgtgg 8520ccttcttaca cttctcagag ggcagagtgg cagccgggca ccctacagaa actcagaggg 8580cagagtggca gccaggccca catgtctctc aagtacctgt cccctcgctc tggtgattat 8640ttcttgcaga atcaccacac gagaccatcc cggcagtcat ggttttgctt tagttttcca 8700agtccgtttc agtcccttcc ttggtctgaa gaaattctgc agtggcgagc agtttcccac 8760ttgccaaaga tcccttttaa ccaacactag cccttgtttt taacacacgc tccagccctt 8820catcagcctg ggcagtctta ccaaaatgtt taaagtgatc tcagaggggc ccatggatta 8880acgccctcat cccaaggtcc gtcccatgac ataacactcc acacccgccc cagccaactt 8940catgggtcac tttttctgga aaataatgat ctgtacagac aggacagaat gaaactcctg 9000cgggtctttg gcctgaaagt tgggaatggt tgggggagag aagggcagca gcttattggt 9060ggtcttttca ccattggcag aaacagtgag agctgtgtgg tgcagaaatc cagaaatgag 9120gtgtagggaa ttttgcctgc cttcctgcag acctgagctg gctttggaat gaggttaaag 9180tgtcagggac gttgcctgag cccaaatgtg tagtgtggtc tgggcaggca gacctttagg 9240ttttgctgct tagtcctgag gaagtggcca ctcttgtggc aggtgtagta tctggggcga 9300gtgttggggg taaaagccca ccctacagaa agtggaacag cccggagcct gatgtgaaag 9360gaccacgggt gttgtaagct gggacacgga agccaaactg gaatcaaacg ccgactgtaa 9420attgtatctt ataacttatt aaataaaaca tttgctccgt aaagttg 946730193PRTHomo sapiens 30Met Val Ala Pro Lys Ser His Thr Asp Asp Trp Ala Pro Gly Pro Phe1 5 10 15Ser Ser Lys Pro Gln Arg Ser Gln Leu Gln Ile Phe Ser Ser Val Leu 20 25 30Gln Thr Ser Leu Leu Phe Leu Leu Met Gly Leu Arg Ala Ser Gly Lys 35 40 45Asp Ser Ala Pro Thr Val Val Ser Gly Ile Leu Gly Gly Ser Val Thr 50 55 60Leu Pro Leu Asn Ile Ser Val Asp Thr Glu Ile Glu Asn Val Ile Trp65 70 75 80Ile Gly Pro Lys Asn Ala Leu Ala Phe Ala Arg Pro Lys Glu Asn Val 85 90 95Thr Ile Met Val Lys Ser Tyr Leu Gly Arg Leu Asp Ile Thr Lys Trp 100 105 110Ser Tyr Ser Leu Cys Ile Ser Asn Leu Thr Leu Asn Asp Ala Gly Ser 115 120 125Tyr Lys Ala Gln Ile Asn Gln Arg Asn Phe Glu Val Thr Thr Glu Glu 130 135 140Glu Phe Thr Leu Phe Val Tyr Ala Pro Phe Ile Glu Lys Leu Ser Val145 150 155 160His Val Ile Glu Gly Asp His Arg Thr Leu Leu Glu Gly Ser Gly Leu 165 170 175Glu Ser Ile Ile Ser Thr Leu Ala Glu Pro Arg Val Ser Val Arg Glu 180 185 190Gly311525DNAHomo sapiens 31acatacacat acacatgcac acacacactc atatacacat gcagaagctg tgacacgtgc 60ggaagctgtg gtaagtgcat cctccttcag tctcagttct gaaaatagat catcatggtg 120gcaccaaaga gtcacacaga tgactgggct cctgggcctt tctccagtaa gccacagagg 180agtcagctgc aaatattctc ttctgttcta cagacctctc tcctcttcct gctcatggga 240ctaagagcct ctggaaagga ctcagcccca acagtggtgt cagggatcct agggggttcc 300gtgactctcc ccctaaacat ctcagtagac acagagattg agaacgtcat ctggattggt 360cccaaaaatg ctcttgcttt cgcacgtccc aaagaaaatg taaccattat ggtcaaaagc 420tacctgggcc gactagacat caccaagtgg agttactccc tgtgcatcag caatctgact 480ctgaatgatg caggatccta caaagcccag ataaaccaaa ggaattttga agtcaccact 540gaggaggaat tcaccctgtt cgtctatgca ccatttattg aaaagttgtc cgtccacgtc 600atcgagggtg accaccgcac actcctggag ggcagcggcc tggagtccat catcagcacc 660ctggctgagc cacgtgtgag cgtgcgggag ggctaggccc tcgcccccac ctgccactgg 720agaccgctcc gccatcccca cctcaccgcc gcgcagcaga gctggaaggg tcctgccgat 780gggaccctgc caggcccagt gccactgccc cccgaggctg ctagacgtgg gcgttaggcg 840tgtcccaccc acccgccgcc tcccatggca cgtcgggaac accggagccg ccaacttgga 900gactcctggt ctgtgaagag ccgctgacgc ccgcaggaac cgggctgggc cttgtgtgcc 960agtggggttt gtgcttggtc tttctccgct tggatttgct tatttattgc attgctggta 1020gagactccca agcctgtcca ccctgcaaag actcctcggg cagcatgcgg gtcccgcaca 1080ctgcacccat ttcctggatg tcccctgcag gcgcgggagg ccatccgggc ctgctggctg 1140cggccccctc tcagccaggc ctggctcagc ccactgcgtg ggaggtcacc ggccactccc 1200cgaggagctg ggatccccgg gatgcaggcc cacagtgcgg ggctgcaccc atgatgcgga 1260gctggcctcc aaccctgcgg gccgcgccag gcaccaactc agtgtttgtc agtgtttgtt 1320tttccaagaa atggttcaaa ttgctgctca gatttttaaa tttactgtag ctgccagtgt 1380acacgtgtgg accccatttt atttttacac caatttggtg aaaatgctgc tttcctcagc 1440ctccccacaa ttaaactgca catggtctct aaaaaaataa aaataaataa ataaataaat 1500aaataaaaag tatcttttct cccca 152532641PRTHomo sapiens 32Met Val Ala Pro Lys Ser His Thr Asp Asp Trp Ala Pro Gly Pro Phe1 5 10 15Ser Ser Lys Pro Gln Arg Ser Gln Leu Gln Ile Phe Ser Ser Val Leu 20 25 30Gln Thr Ser Leu Leu Phe Leu Leu Met Gly Leu Arg Ala Ser Gly Lys 35 40 45Asp Ser Ala Pro Thr Val Val Ser Gly Ile Leu Gly Gly Ser Val Thr 50 55 60Leu Pro Leu Asn Ile Ser Val Asp Thr Glu Ile Glu Asn Val Ile Trp65 70 75 80Ile Gly Pro Lys Asn Ala Leu Ala Phe Ala Arg Pro Lys Glu Asn Val 85 90 95Thr Ile Met Val Lys Ser Tyr Leu Gly Arg Leu Asp Ile Thr Lys Trp 100 105 110Ser Tyr Ser Leu Cys Ile Ser Asn Leu Thr Leu Asn Asp Ala Gly Ser 115 120 125Tyr Lys Ala Gln Ile Asn Gln Arg Asn Phe Glu Val Thr Thr Glu Glu 130 135 140Glu Phe Thr Leu Phe Val Tyr Glu Gln Leu Gln Glu Pro Gln Val Thr145 150 155 160Met Lys Ser Val Lys Val Ser Glu Asn Phe Ser Cys Asn Ile Thr Leu 165 170 175Met Cys Ser Val Lys Gly Ala Glu Lys Ser Val Leu Tyr Ser Trp Thr 180 185 190Pro Arg Glu Pro His Ala Ser Glu Ser Asn Gly Gly Ser Ile Leu Thr 195 200 205Val Ser Arg Thr Pro Cys Asp Pro Asp Leu Pro Tyr Ile Cys Thr Ala 210 215 220Gln Asn Pro Val Ser Gln Arg Ser Ser Leu Pro Val His Val Gly Gln225 230 235 240Phe Cys Thr Asp Pro Gly Ala Ser Arg Gly Gly Thr Thr Gly Glu Thr 245 250 255Val Val Gly Val Leu Gly Glu Pro Val Thr Leu Pro Leu Ala Leu Pro 260 265 270Ala Cys Arg Asp Thr Glu Lys Val Val Trp Leu Phe Asn Thr Ser Ile 275 280 285Ile Ser Lys Glu Arg Glu Glu Ala Ala Thr Ala Asp Pro Leu Ile Lys 290 295 300Ser Arg Asp Pro Tyr Lys Asn Arg Val Trp Val Ser Ser Gln Asp Cys305 310 315 320Ser Leu Lys Ile Ser Gln Leu Lys Ile Glu Asp Ala Gly Pro Tyr His 325 330 335Ala Tyr Val Cys Ser Glu Ala Ser Ser Val Thr Ser Met Thr His Val 340 345 350Thr Leu Leu Ile Tyr Arg Arg Leu Arg Lys Pro Lys Ile Thr Trp Ser 355 360 365Leu Arg His Ser Glu Asp Gly Ile Cys Arg Ile Ser Leu Thr Cys Ser 370 375 380Val Glu Asp Gly Gly Asn Thr Val Met Tyr Thr Trp Thr Pro Leu Gln385 390 395 400Lys Glu Ala Val Val Ser Gln Gly Glu Ser His Leu Asn Val Ser Trp 405 410 415Arg Ser Ser Glu Asn His Pro Asn Leu Thr Cys Thr Ala Ser Asn Pro 420 425 430Val Ser Arg Ser Ser His Gln Phe Leu Ser Glu Asn Ile Cys Ser Gly 435 440 445Pro Glu Arg Asn Thr Lys Leu Trp Ile Gly Leu Phe Leu Met Val Cys 450 455 460Leu Leu Cys Val Gly Ile Phe Ser Trp Cys Ile Trp Lys Arg Lys Gly465 470 475 480Arg Cys Ser Val Pro Ala Phe Cys Ser Ser Gln Ala Glu Ala Pro Ala 485 490 495Asp Thr Pro Gly Tyr Glu Lys Leu Asp Thr Pro Leu Arg Pro Ala Arg 500 505 510Gln Gln Pro Thr Pro Thr Ser Asp Ser Ser Ser Asp Ser Asn Leu Thr 515 520 525Thr Glu Glu Asp Glu Asp Arg Pro Glu Val His Lys Pro Ile Ser Gly 530 535 540Arg Tyr Glu Val Phe Asp Gln Val Thr Gln Glu Gly Ala Gly His Asp545 550 555 560Pro Ala Pro Glu Gly Gln Ala Asp Tyr Asp Pro Val Thr Pro Tyr Val 565 570 575Thr Glu Val Glu Ser Val Val Gly Glu Asn Thr Met Tyr Ala Gln Val 580 585 590Phe Asn Leu Gln Gly Lys Thr Pro Val Ser Gln Lys Glu Glu Ser Ser 595 600 605Ala Thr Ile Tyr Cys Ser Ile Arg Lys Pro Gln Val Val Pro Pro Pro 610 615 620Gln Gln Asn Asp Leu Glu Ile Pro Glu Ser Pro Thr Tyr Glu Asn Phe625 630 635 640Thr332508DNAHomo sapiens 33acatacacat acacatgcac acacacactc atatacacat gcagaagctg tgacacgtgc 60ggaagctgtg gtaagtgcat cctccttcag tctcagttct gaaaatagat catcatggtg 120gcaccaaaga gtcacacaga tgactgggct cctgggcctt tctccagtaa gccacagagg 180agtcagctgc aaatattctc ttctgttcta cagacctctc tcctcttcct gctcatggga 240ctaagagcct ctggaaagga ctcagcccca acagtggtgt cagggatcct agggggttcc 300gtgactctcc ccctaaacat ctcagtagac acagagattg agaacgtcat ctggattggt 360cccaaaaatg ctcttgcttt cgcacgtccc aaagaaaatg taaccattat ggtcaaaagc 420tacctgggcc gactagacat caccaagtgg agttactccc tgtgcatcag caatctgact 480ctgaatgatg caggatccta caaagcccag ataaaccaaa ggaattttga agtcaccact 540gaggaggaat tcaccctgtt cgtctatgag cagctgcagg agccccaagt caccatgaag 600tctgtgaagg tgtctgagaa cttctcctgt aacatcactc taatgtgctc cgtgaagggg 660gcagagaaaa gtgttctgta cagctggacc ccaagggaac cccatgcttc tgagtccaat 720ggaggctcca ttcttaccgt ctcccgaaca ccatgtgacc cagacctgcc atacatctgc 780acagcccaga accccgtcag ccagagaagc tccctccctg tccatgttgg gcagttctgt 840acagatccag gagcctccag aggaggaaca acgggggaga ctgtggtagg ggtcctggga 900gagccagtca ccctgccact tgcactccca gcctgccggg acacagagaa ggttgtctgg 960ttgtttaaca catccatcat tagcaaagag agggaagaag cagcaacggc agatccactc 1020attaaatcca gggatcctta caagaacagg gtgtgggtct ccagccagga ctgctccctg 1080aagatcagcc agctgaagat agaggacgcc ggcccctacc atgcctacgt gtgctcagag 1140gcctccagcg tcaccagcat gacacatgtc accctgctca tctaccgcag gctgaggaag 1200cccaaaatca cgtggagcct caggcacagt gaggatggca tctgcaggat cagcctgacc 1260tgctccgtgg aggacggggg aaacactgtc atgtacacat ggaccccgct gcagaaggaa 1320gctgttgtgt cccaagggga atcacacctc aatgtctcat ggagaagcag tgaaaatcac 1380cccaacctca catgcacagc cagcaaccct gtcagcagga gttcccacca gtttctttct 1440gagaacatct gttcaggacc tgagagaaac acaaagcttt ggattgggtt gttcctgatg 1500gtttgccttc tgtgcgttgg gatcttcagc tggtgcattt ggaagcgaaa aggacggtgt 1560tcagtcccag ccttctgttc cagccaagct gaggccccag cggatacacc aggatatgag 1620aagctggaca ctcccctcag gcctgccagg caacagccta cacccacctc agacagcagc 1680tctgacagca acctcacaac tgaggaggat gaggacaggc ctgaggtgca caagcccatc 1740agtggaagat atgaggtatt tgaccaggtc actcaggagg gcgctggaca tgacccagcc 1800cctgagggcc aagcagacta tgatcccgtc actccatatg tcacggaagt tgagtctgtg 1860gttggagaga acaccatgta tgcacaagtg ttcaacttac agggaaagac cccagtttct 1920cagaaggaag agagctcagc cacaatctac tgctccatac ggaaacctca ggtggtgcca 1980ccaccacaac agaatgatct tgagattcct gaaagtccta cctatgaaaa tttcacctga 2040aaggaaaagc agctgctgcc tctctcctgg gaccgtgggg ttggaaagtc agctggacct 2100catggggcct ggggctcaca gacagaagca cctcagaatt tccttcagtg cctcagagat 2160gcctggatgt ggcccctccc cctccttctc acccttaagg actcccaaac ccattaatag 2220ttcagacaca ggctccttct tggagcctat gggcttcaga tgtctttgcc ccatttgtca 2280cctcgcacac ttatagcgtt tcctcctcga aattctacca agactggtca aatgttgctg 2340aggggcctgg accagctgtc ctttacacca ccttctcaac actgctgaaa agaacccaag 2400agaattgtca cacatgacac aagatgtaca taatatcatg ctcactgcag tgttatttaa 2460aataaaaggc aggaaataaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 250834565PRTHomo sapiens 34Met Val Ala Pro Lys Ser His Thr Asp Asp Trp Ala Pro Gly Pro Phe1 5 10 15Ser Ser Lys Pro Gln Arg Ser Gln Leu Gln Ile Phe Ser Ser Val Leu 20 25 30Gln Thr Ser Leu Leu Phe Leu Leu Met Gly Leu Arg Ala Ser Gly Lys 35 40 45Asp Ser Ala Pro Thr Val Val Ser Gly Ile Leu Gly Gly Ser Val Thr 50 55 60Leu Pro Leu Asn Ile Ser Val Asp Thr Glu Ile Glu Asn Val Ile Trp65 70 75 80Ile Gly Pro Lys Asn Ala Leu Ala Phe Ala Arg Pro Lys Glu Asn Val 85 90 95Thr Ile Met Val Lys Ser Tyr Leu Gly Arg Leu Asp Ile Thr Lys Trp 100 105 110Ser Tyr Ser Leu Cys Ile Ser Asn Leu Thr Leu Asn Asp Ala Gly Ser 115 120 125Tyr Lys Ala Gln Ile Asn Gln Arg Asn Phe Glu Val Thr Thr Glu Glu 130 135 140Glu Phe Thr Leu Phe Val Tyr Glu Gln Leu Gln Glu Pro Gln Val Thr145 150 155 160Met Lys Ser Val Lys Val Ser Glu Asn Phe Ser Cys Asn Ile Thr Leu 165 170 175Met Cys Ser Val Lys Gly Ala Glu Lys Ser Val Leu Tyr Ser Trp Thr 180 185 190Pro Arg Glu Pro His Ala Ser Glu Ser Asn Gly Gly Ser Ile Leu Thr 195 200 205Val Ser Arg Thr Pro Cys Asp Pro Asp Leu Pro Tyr Ile Cys Thr Ala 210 215 220Gln Asn Pro Val Ser Gln Arg Ser Ser Leu Pro Val His Val Gly Gln225 230 235 240Phe Cys Thr Asp Pro Gly Ala Ser Arg Gly Gly Thr Thr Gly Glu Thr 245 250 255Val Val Gly Val Leu Gly Glu Pro Val Thr Leu Pro Leu Ala Leu Pro 260 265 270Ala Cys Arg Asp Thr Glu Lys Val Val Trp Leu Phe Asn Thr Ser Ile 275 280 285Ile Ser Lys Glu Arg Glu Glu Ala Ala Thr Ala Asp Pro Leu Ile Lys 290 295 300Ser Arg Asp Pro Tyr Lys Asn Arg Val Trp Val Ser Ser Gln Asp Cys305 310 315 320Ser Leu Lys Ile Ser Gln Leu Lys Ile Glu Asp Ala Gly Pro Tyr His 325 330 335Ala Tyr Val Cys Ser Glu Ala Ser Ser Val Thr Ser Met Thr His Val 340 345 350Thr Leu Leu Ile Tyr Arg Pro Glu Arg Asn Thr Lys Leu Trp Ile Gly 355 360 365Leu Phe Leu Met Val Cys Leu Leu Cys Val Gly Ile Phe Ser Trp Cys 370 375 380Ile Trp Lys Arg Lys Gly Arg Cys Ser Val Pro Ala Phe Cys Ser Ser385 390 395 400Gln Ala Glu Ala Pro Ala Asp Thr Pro Glu Pro Thr Ala Gly His Thr 405 410 415Leu Tyr Ser Val Leu Ser Gln Gly Tyr Glu Lys Leu Asp Thr Pro Leu 420 425 430Arg Pro Ala Arg Gln Gln Pro Thr Pro Thr Ser Asp Ser Ser Ser Asp 435 440 445Ser Asn Leu Thr Thr Glu Glu Asp Glu Asp Arg Pro Glu Val His Lys 450 455 460Pro Ile Ser Gly Arg Tyr Glu Val Phe Asp Gln Val Thr Gln Glu Gly465 470 475 480Ala Gly His Asp Pro Ala Pro Glu Gly Gln Ala Asp Tyr Asp Pro Val 485 490 495Thr Pro Tyr Val Thr Glu Val Glu Ser Val Val Gly Glu Asn Thr Met 500 505 510Tyr Ala Gln Val Phe Asn Leu Gln Gly Lys Thr Pro Val Ser Gln Lys 515 520 525Glu Glu Ser Ser Ala Thr Ile Tyr Cys Ser Ile Arg Lys Pro Gln Val 530 535 540Val Pro Pro Pro Gln Gln Asn Asp Leu Glu Ile Pro Glu Ser Pro Thr545 550 555

560Tyr Glu Asn Phe Thr 565352280DNAHomo sapiens 35acatacacat acacatgcac acacacactc atatacacat gcagaagctg tgacacgtgc 60ggaagctgtg gtaagtgcat cctccttcag tctcagttct gaaaatagat catcatggtg 120gcaccaaaga gtcacacaga tgactgggct cctgggcctt tctccagtaa gccacagagg 180agtcagctgc aaatattctc ttctgttcta cagacctctc tcctcttcct gctcatggga 240ctaagagcct ctggaaagga ctcagcccca acagtggtgt cagggatcct agggggttcc 300gtgactctcc ccctaaacat ctcagtagac acagagattg agaacgtcat ctggattggt 360cccaaaaatg ctcttgcttt cgcacgtccc aaagaaaatg taaccattat ggtcaaaagc 420tacctgggcc gactagacat caccaagtgg agttactccc tgtgcatcag caatctgact 480ctgaatgatg caggatccta caaagcccag ataaaccaaa ggaattttga agtcaccact 540gaggaggaat tcaccctgtt cgtctatgag cagctgcagg agccccaagt caccatgaag 600tctgtgaagg tgtctgagaa cttctcctgt aacatcactc taatgtgctc cgtgaagggg 660gcagagaaaa gtgttctgta cagctggacc ccaagggaac cccatgcttc tgagtccaat 720ggaggctcca ttcttaccgt ctcccgaaca ccatgtgacc cagacctgcc atacatctgc 780acagcccaga accccgtcag ccagagaagc tccctccctg tccatgttgg gcagttctgt 840acagatccag gagcctccag aggaggaaca acgggggaga ctgtggtagg ggtcctggga 900gagccagtca ccctgccact tgcactccca gcctgccggg acacagagaa ggttgtctgg 960ttgtttaaca catccatcat tagcaaagag agggaagaag cagcaacggc agatccactc 1020attaaatcca gggatcctta caagaacagg gtgtgggtct ccagccagga ctgctccctg 1080aagatcagcc agctgaagat agaggacgcc ggcccctacc atgcctacgt gtgctcagag 1140gcctccagcg tcaccagcat gacacatgtc accctgctca tctaccgacc tgagagaaac 1200acaaagcttt ggattgggtt gttcctgatg gtttgccttc tgtgcgttgg gatcttcagc 1260tggtgcattt ggaagcgaaa aggacggtgt tcagtcccag ccttctgttc cagccaagct 1320gaggccccag cggatacacc agaacccaca gctggccaca cgctatactc tgtgctctcc 1380caaggatatg agaagctgga cactcccctc aggcctgcca ggcaacagcc tacacccacc 1440tcagacagca gctctgacag caacctcaca actgaggagg atgaggacag gcctgaggtg 1500cacaagccca tcagtggaag atatgaggta tttgaccagg tcactcagga gggcgctgga 1560catgacccag cccctgaggg ccaagcagac tatgatcccg tcactccata tgtcacggaa 1620gttgagtctg tggttggaga gaacaccatg tatgcacaag tgttcaactt acagggaaag 1680accccagttt ctcagaagga agagagctca gccacaatct actgctccat acggaaacct 1740caggtggtgc caccaccaca acagaatgat cttgagattc ctgaaagtcc tacctatgaa 1800aatttcacct gaaaggaaaa gcagctgctg cctctctcct gggaccgtgg ggttggaaag 1860tcagctggac ctcatggggc ctggggctca cagacagaag cacctcagaa tttccttcag 1920tgcctcagag atgcctggat gtggcccctc cccctccttc tcacccttaa ggactcccaa 1980acccattaat agttcagaca caggctcctt cttggagcct atgggcttca gatgtctttg 2040ccccatttgt cacctcgcac acttatagcg tttcctcctc gaaattctac caagactggt 2100caaatgttgc tgaggggcct ggaccagctg tcctttacac caccttctca acactgctga 2160aaagaaccca agagaattgt cacacatgac acaagatgta cataatatca tgctcactgc 2220agtgttattt aaaataaaag gcaggaaata aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 228036655PRTHomo sapiens 36Met Val Ala Pro Lys Ser His Thr Asp Asp Trp Ala Pro Gly Pro Phe1 5 10 15Ser Ser Lys Pro Gln Arg Ser Gln Leu Gln Ile Phe Ser Ser Val Leu 20 25 30Gln Thr Ser Leu Leu Phe Leu Leu Met Gly Leu Arg Ala Ser Gly Lys 35 40 45Asp Ser Ala Pro Thr Val Val Ser Gly Ile Leu Gly Gly Ser Val Thr 50 55 60Leu Pro Leu Asn Ile Ser Val Asp Thr Glu Ile Glu Asn Val Ile Trp65 70 75 80Ile Gly Pro Lys Asn Ala Leu Ala Phe Ala Arg Pro Lys Glu Asn Val 85 90 95Thr Ile Met Val Lys Ser Tyr Leu Gly Arg Leu Asp Ile Thr Lys Trp 100 105 110Ser Tyr Ser Leu Cys Ile Ser Asn Leu Thr Leu Asn Asp Ala Gly Ser 115 120 125Tyr Lys Ala Gln Ile Asn Gln Arg Asn Phe Glu Val Thr Thr Glu Glu 130 135 140Glu Phe Thr Leu Phe Val Tyr Glu Gln Leu Gln Glu Pro Gln Val Thr145 150 155 160Met Lys Ser Val Lys Val Ser Glu Asn Phe Ser Cys Asn Ile Thr Leu 165 170 175Met Cys Ser Val Lys Gly Ala Glu Lys Ser Val Leu Tyr Ser Trp Thr 180 185 190Pro Arg Glu Pro His Ala Ser Glu Ser Asn Gly Gly Ser Ile Leu Thr 195 200 205Val Ser Arg Thr Pro Cys Asp Pro Asp Leu Pro Tyr Ile Cys Thr Ala 210 215 220Gln Asn Pro Val Ser Gln Arg Ser Ser Leu Pro Val His Val Gly Gln225 230 235 240Phe Cys Thr Asp Pro Gly Ala Ser Arg Gly Gly Thr Thr Gly Glu Thr 245 250 255Val Val Gly Val Leu Gly Glu Pro Val Thr Leu Pro Leu Ala Leu Pro 260 265 270Ala Cys Arg Asp Thr Glu Lys Val Val Trp Leu Phe Asn Thr Ser Ile 275 280 285Ile Ser Lys Glu Arg Glu Glu Ala Ala Thr Ala Asp Pro Leu Ile Lys 290 295 300Ser Arg Asp Pro Tyr Lys Asn Arg Val Trp Val Ser Ser Gln Asp Cys305 310 315 320Ser Leu Lys Ile Ser Gln Leu Lys Ile Glu Asp Ala Gly Pro Tyr His 325 330 335Ala Tyr Val Cys Ser Glu Ala Ser Ser Val Thr Ser Met Thr His Val 340 345 350Thr Leu Leu Ile Tyr Arg Arg Leu Arg Lys Pro Lys Ile Thr Trp Ser 355 360 365Leu Arg His Ser Glu Asp Gly Ile Cys Arg Ile Ser Leu Thr Cys Ser 370 375 380Val Glu Asp Gly Gly Asn Thr Val Met Tyr Thr Trp Thr Pro Leu Gln385 390 395 400Lys Glu Ala Val Val Ser Gln Gly Glu Ser His Leu Asn Val Ser Trp 405 410 415Arg Ser Ser Glu Asn His Pro Asn Leu Thr Cys Thr Ala Ser Asn Pro 420 425 430Val Ser Arg Ser Ser His Gln Phe Leu Ser Glu Asn Ile Cys Ser Gly 435 440 445Pro Glu Arg Asn Thr Lys Leu Trp Ile Gly Leu Phe Leu Met Val Cys 450 455 460Leu Leu Cys Val Gly Ile Phe Ser Trp Cys Ile Trp Lys Arg Lys Gly465 470 475 480Arg Cys Ser Val Pro Ala Phe Cys Ser Ser Gln Ala Glu Ala Pro Ala 485 490 495Asp Thr Pro Glu Pro Thr Ala Gly His Thr Leu Tyr Ser Val Leu Ser 500 505 510Gln Gly Tyr Glu Lys Leu Asp Thr Pro Leu Arg Pro Ala Arg Gln Gln 515 520 525Pro Thr Pro Thr Ser Asp Ser Ser Ser Asp Ser Asn Leu Thr Thr Glu 530 535 540Glu Asp Glu Asp Arg Pro Glu Val His Lys Pro Ile Ser Gly Arg Tyr545 550 555 560Glu Val Phe Asp Gln Val Thr Gln Glu Gly Ala Gly His Asp Pro Ala 565 570 575Pro Glu Gly Gln Ala Asp Tyr Asp Pro Val Thr Pro Tyr Val Thr Glu 580 585 590Val Glu Ser Val Val Gly Glu Asn Thr Met Tyr Ala Gln Val Phe Asn 595 600 605Leu Gln Gly Lys Thr Pro Val Ser Gln Lys Glu Glu Ser Ser Ala Thr 610 615 620Ile Tyr Cys Ser Ile Arg Lys Pro Gln Val Val Pro Pro Pro Gln Gln625 630 635 640Asn Asp Leu Glu Ile Pro Glu Ser Pro Thr Tyr Glu Asn Phe Thr 645 650 655372550DNAHomo sapiens 37acatacacat acacatgcac acacacactc atatacacat gcagaagctg tgacacgtgc 60ggaagctgtg gtaagtgcat cctccttcag tctcagttct gaaaatagat catcatggtg 120gcaccaaaga gtcacacaga tgactgggct cctgggcctt tctccagtaa gccacagagg 180agtcagctgc aaatattctc ttctgttcta cagacctctc tcctcttcct gctcatggga 240ctaagagcct ctggaaagga ctcagcccca acagtggtgt cagggatcct agggggttcc 300gtgactctcc ccctaaacat ctcagtagac acagagattg agaacgtcat ctggattggt 360cccaaaaatg ctcttgcttt cgcacgtccc aaagaaaatg taaccattat ggtcaaaagc 420tacctgggcc gactagacat caccaagtgg agttactccc tgtgcatcag caatctgact 480ctgaatgatg caggatccta caaagcccag ataaaccaaa ggaattttga agtcaccact 540gaggaggaat tcaccctgtt cgtctatgag cagctgcagg agccccaagt caccatgaag 600tctgtgaagg tgtctgagaa cttctcctgt aacatcactc taatgtgctc cgtgaagggg 660gcagagaaaa gtgttctgta cagctggacc ccaagggaac cccatgcttc tgagtccaat 720ggaggctcca ttcttaccgt ctcccgaaca ccatgtgacc cagacctgcc atacatctgc 780acagcccaga accccgtcag ccagagaagc tccctccctg tccatgttgg gcagttctgt 840acagatccag gagcctccag aggaggaaca acgggggaga ctgtggtagg ggtcctggga 900gagccagtca ccctgccact tgcactccca gcctgccggg acacagagaa ggttgtctgg 960ttgtttaaca catccatcat tagcaaagag agggaagaag cagcaacggc agatccactc 1020attaaatcca gggatcctta caagaacagg gtgtgggtct ccagccagga ctgctccctg 1080aagatcagcc agctgaagat agaggacgcc ggcccctacc atgcctacgt gtgctcagag 1140gcctccagcg tcaccagcat gacacatgtc accctgctca tctaccgcag gctgaggaag 1200cccaaaatca cgtggagcct caggcacagt gaggatggca tctgcaggat cagcctgacc 1260tgctccgtgg aggacggggg aaacactgtc atgtacacat ggaccccgct gcagaaggaa 1320gctgttgtgt cccaagggga atcacacctc aatgtctcat ggagaagcag tgaaaatcac 1380cccaacctca catgcacagc cagcaaccct gtcagcagga gttcccacca gtttctttct 1440gagaacatct gttcaggacc tgagagaaac acaaagcttt ggattgggtt gttcctgatg 1500gtttgccttc tgtgcgttgg gatcttcagc tggtgcattt ggaagcgaaa aggacggtgt 1560tcagtcccag ccttctgttc cagccaagct gaggccccag cggatacacc agaacccaca 1620gctggccaca cgctatactc tgtgctctcc caaggatatg agaagctgga cactcccctc 1680aggcctgcca ggcaacagcc tacacccacc tcagacagca gctctgacag caacctcaca 1740actgaggagg atgaggacag gcctgaggtg cacaagccca tcagtggaag atatgaggta 1800tttgaccagg tcactcagga gggcgctgga catgacccag cccctgaggg ccaagcagac 1860tatgatcccg tcactccata tgtcacggaa gttgagtctg tggttggaga gaacaccatg 1920tatgcacaag tgttcaactt acagggaaag accccagttt ctcagaagga agagagctca 1980gccacaatct actgctccat acggaaacct caggtggtgc caccaccaca acagaatgat 2040cttgagattc ctgaaagtcc tacctatgaa aatttcacct gaaaggaaaa gcagctgctg 2100cctctctcct gggaccgtgg ggttggaaag tcagctggac ctcatggggc ctggggctca 2160cagacagaag cacctcagaa tttccttcag tgcctcagag atgcctggat gtggcccctc 2220cccctccttc tcacccttaa ggactcccaa acccattaat agttcagaca caggctcctt 2280cttggagcct atgggcttca gatgtctttg ccccatttgt cacctcgcac acttatagcg 2340tttcctcctc gaaattctac caagactggt caaatgttgc tgaggggcct ggaccagctg 2400tcctttacac caccttctca acactgctga aaagaaccca agagaattgt cacacatgac 2460acaagatgta cataatatca tgctcactgc agtgttattt aaaataaaag gcaggaaata 2520aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 255038238PRTHomo sapiens 38Met Trp Val Pro Val Val Phe Leu Thr Leu Ser Val Thr Trp Ile Gly1 5 10 15Ala Ala Pro Leu Ile Leu Ser Arg Ile Val Gly Gly Trp Glu Cys Glu 20 25 30Lys His Ser Gln Pro Trp Gln Val Leu Val Ala Ser Arg Gly Arg Ala 35 40 45Val Cys Gly Gly Val Leu Val His Pro Gln Trp Val Leu Thr Ala Ala 50 55 60His Cys Ile Arg Asn Lys Ser Val Ile Leu Leu Gly Arg His Ser Leu65 70 75 80Phe His Pro Glu Asp Thr Gly Gln Val Phe Gln Val Ser His Ser Phe 85 90 95Pro His Pro Leu Tyr Asp Met Ser Leu Leu Lys Asn Arg Phe Leu Arg 100 105 110Pro Gly Asp Asp Ser Ser His Asp Leu Met Leu Leu Arg Leu Ser Glu 115 120 125Pro Ala Glu Leu Thr Asp Ala Val Lys Val Met Asp Leu Pro Thr Gln 130 135 140Glu Pro Ala Leu Gly Thr Thr Cys Tyr Ala Ser Gly Trp Gly Ser Ile145 150 155 160Glu Pro Glu Glu Phe Leu Thr Pro Lys Lys Leu Gln Cys Val Asp Leu 165 170 175His Val Ile Ser Asn Asp Val Cys Ala Gln Val His Pro Gln Lys Val 180 185 190Thr Lys Phe Met Leu Cys Ala Gly Arg Trp Thr Gly Gly Lys Ser Thr 195 200 205Cys Ser Trp Val Ile Leu Ile Thr Glu Leu Thr Met Pro Ala Leu Pro 210 215 220Met Val Leu His Gly Ser Leu Val Pro Trp Arg Gly Gly Val225 230 235391906DNAHomo sapiens 39agccccaagc ttaccacctg cacccggaga gctgtgtcac catgtgggtc ccggttgtct 60tcctcaccct gtccgtgacg tggattggtg ctgcacccct catcctgtct cggattgtgg 120gaggctggga gtgcgagaag cattcccaac cctggcaggt gcttgtggcc tctcgtggca 180gggcagtctg cggcggtgtt ctggtgcacc cccagtgggt cctcacagct gcccactgca 240tcaggaacaa aagcgtgatc ttgctgggtc ggcacagcct gtttcatcct gaagacacag 300gccaggtatt tcaggtcagc cacagcttcc cacacccgct ctacgatatg agcctcctga 360agaatcgatt cctcaggcca ggtgatgact ccagccacga cctcatgctg ctccgcctgt 420cagagcctgc cgagctcacg gatgctgtga aggtcatgga cctgcccacc caggagccag 480cactggggac cacctgctac gcctcaggct ggggcagcat tgaaccagag gagttcttga 540ccccaaagaa acttcagtgt gtggacctcc atgttatttc caatgacgtg tgtgcgcaag 600ttcaccctca gaaggtgacc aagttcatgc tgtgtgctgg acgctggaca gggggcaaaa 660gcacctgctc gtgggtcatt ctgatcaccg aactgaccat gccagccctg ccgatggtcc 720tccatggctc cctagtgccc tggagaggag gtgtctagtc agagagtagt cctggaaggt 780ggcctctgtg aggagccacg gggacagcat cctgcagatg gtcctggccc ttgtcccacc 840gacctgtcta caaggactgt cctcgtggac cctcccctct gcacaggagc tggaccctga 900agtcccttcc ccaccggcca ggactggagc ccctacccct ctgttggaat ccctgcccac 960cttcttctgg aagtcggctc tggagacatt tctctcttct tccaaagctg ggaactgcta 1020tctgttatct gcctgtccag gtctgaaaga taggattgcc caggcagaaa ctgggactga 1080cctatctcac tctctccctg cttttaccct tagggtgatt ctgggggccc acttgtctgt 1140aatggtgtgc ttcaaggtat cacgtcatgg ggcagtgaac catgtgccct gcccgaaagg 1200ccttccctgt acaccaaggt ggtgcattac cggaagtgga tcaaggacac catcgtggcc 1260aacccctgag cacccctatc aaccccctat tgtagtaaac ttggaacctt ggaaatgacc 1320aggccaagac tcaagcctcc ccagttctac tgacctttgt ccttaggtgt gaggtccagg 1380gttgctagga aaagaaatca gcagacacag gtgtagacca gagtgtttct taaatggtgt 1440aattttgtcc tctctgtgtc ctggggaata ctggccatgc ctggagacat atcactcaat 1500ttctctgagg acacagatag gatggggtgt ctgtgttatt tgtggggtac agagatgaaa 1560gaggggtggg atccacactg agagagtgga gagtgacatg tgctggacac tgtccatgaa 1620gcactgagca gaagctggag gcacaacgca ccagacactc acagcaagga tggagctgaa 1680aacataaccc actctgtcct ggaggcactg ggaagcctag agaaggctgt gagccaagga 1740gggagggtct tcctttggca tgggatgggg atgaagtaag gagagggact ggaccccctg 1800gaagctgatt cactatgggg ggaggtgtat tgaagtcctc cagacaaccc tcagatttga 1860tgatttccta gtagaactca cagaaataaa gagctgttat actgtg 190640218PRTHomo sapiens 40Met Trp Val Pro Val Val Phe Leu Thr Leu Ser Val Thr Trp Ile Gly1 5 10 15Ala Ala Pro Leu Ile Leu Ser Arg Ile Val Gly Gly Trp Glu Cys Glu 20 25 30Lys His Ser Gln Pro Trp Gln Val Leu Val Ala Ser Arg Gly Arg Ala 35 40 45Val Cys Gly Gly Val Leu Val His Pro Gln Trp Val Leu Thr Ala Ala 50 55 60His Cys Ile Arg Lys Pro Gly Asp Asp Ser Ser His Asp Leu Met Leu65 70 75 80Leu Arg Leu Ser Glu Pro Ala Glu Leu Thr Asp Ala Val Lys Val Met 85 90 95Asp Leu Pro Thr Gln Glu Pro Ala Leu Gly Thr Thr Cys Tyr Ala Ser 100 105 110Gly Trp Gly Ser Ile Glu Pro Glu Glu Phe Leu Thr Pro Lys Lys Leu 115 120 125Gln Cys Val Asp Leu His Val Ile Ser Asn Asp Val Cys Ala Gln Val 130 135 140His Pro Gln Lys Val Thr Lys Phe Met Leu Cys Ala Gly Arg Trp Thr145 150 155 160Gly Gly Lys Ser Thr Cys Ser Gly Asp Ser Gly Gly Pro Leu Val Cys 165 170 175Asn Gly Val Leu Gln Gly Ile Thr Ser Trp Gly Ser Glu Pro Cys Ala 180 185 190Leu Pro Glu Arg Pro Ser Leu Tyr Thr Lys Val Val His Tyr Arg Lys 195 200 205Trp Ile Lys Asp Thr Ile Val Ala Asn Pro 210 215411335DNAHomo sapiens 41agccccaagc ttaccacctg cacccggaga gctgtgtcac catgtgggtc ccggttgtct 60tcctcaccct gtccgtgacg tggattggtg ctgcacccct catcctgtct cggattgtgg 120gaggctggga gtgcgagaag cattcccaac cctggcaggt gcttgtggcc tctcgtggca 180gggcagtctg cggcggtgtt ctggtgcacc cccagtgggt cctcacagct gcccactgca 240tcaggaagcc aggtgatgac tccagccacg acctcatgct gctccgcctg tcagagcctg 300ccgagctcac ggatgctgtg aaggtcatgg acctgcccac ccaggagcca gcactgggga 360ccacctgcta cgcctcaggc tggggcagca ttgaaccaga ggagttcttg accccaaaga 420aacttcagtg tgtggacctc catgttattt ccaatgacgt gtgtgcgcaa gttcaccctc 480agaaggtgac caagttcatg ctgtgtgctg gacgctggac agggggcaaa agcacctgct 540cgggtgattc tgggggccca cttgtctgta atggtgtgct tcaaggtatc acgtcatggg 600gcagtgaacc atgtgccctg cccgaaaggc cttccctgta caccaaggtg gtgcattacc 660ggaagtggat caaggacacc atcgtggcca acccctgagc acccctatca accccctatt 720gtagtaaact tggaaccttg gaaatgacca ggccaagact caagcctccc cagttctact 780gacctttgtc cttaggtgtg aggtccaggg ttgctaggaa aagaaatcag cagacacagg 840tgtagaccag agtgtttctt aaatggtgta attttgtcct ctctgtgtcc tggggaatac 900tggccatgcc tggagacata tcactcaatt tctctgagga cacagatagg atggggtgtc 960tgtgttattt gtggggtaca gagatgaaag aggggtggga tccacactga gagagtggag 1020agtgacatgt gctggacact gtccatgaag cactgagcag aagctggagg cacaacgcac 1080cagacactca cagcaaggat ggagctgaaa acataaccca ctctgtcctg gaggcactgg 1140gaagcctaga gaaggctgtg agccaaggag ggagggtctt cctttggcat gggatgggga 1200tgaagtaagg agagggactg gaccccctgg aagctgattc actatggggg gaggtgtatt 1260gaagtcctcc agacaaccct cagatttgat gatttcctag tagaactcac agaaataaag 1320agctgttata ctgtg

13354269PRTHomo sapiens 42Met Trp Val Pro Val Val Phe Leu Thr Leu Ser Val Thr Trp Ile Gly1 5 10 15Ala Ala Pro Leu Ile Leu Ser Arg Ile Val Gly Gly Trp Glu Cys Glu 20 25 30Lys His Ser Gln Pro Trp Gln Val Leu Val Ala Ser Arg Gly Arg Ala 35 40 45Val Cys Gly Gly Val Leu Val His Pro Gln Trp Val Leu Thr Ala Ala 50 55 60His Cys Ile Arg Lys6543555DNAHomo sapiens 43agccccaagc ttaccacctg cacccggaga gctgtgtcac catgtgggtc ccggttgtct 60tcctcaccct gtccgtgacg tggattggtg ctgcacccct catcctgtct cggattgtgg 120gaggctggga gtgcgagaag cattcccaac cctggcaggt gcttgtggcc tctcgtggca 180gggcagtctg cggcggtgtt ctggtgcacc cccagtgggt cctcacagct gcccactgca 240tcaggaagtg agtaggggcc tggggtctgg ggagcaggtg tctgtgtccc agaggaataa 300cagctgggca ttttccccag gataacctct aaggccagcc ttgggactgg gggagagagg 360gaaagttctg gttcaggtca catggggagg cagggttggg gctggaccac cctccccatg 420gctgcctggg tctccatctg tgttcctcta tgtctctttg tgtcgctttc attatgtctc 480ttggtaactg gcttcggttg tgtctctccg tgtgactatt ttgttctctc tctccctctc 540ttctctgtct tcagt 55544261PRTHomo sapiens 44Met Trp Val Pro Val Val Phe Leu Thr Leu Ser Val Thr Trp Ile Gly1 5 10 15Ala Ala Pro Leu Ile Leu Ser Arg Ile Val Gly Gly Trp Glu Cys Glu 20 25 30Lys His Ser Gln Pro Trp Gln Val Leu Val Ala Ser Arg Gly Arg Ala 35 40 45Val Cys Gly Gly Val Leu Val His Pro Gln Trp Val Leu Thr Ala Ala 50 55 60His Cys Ile Arg Asn Lys Ser Val Ile Leu Leu Gly Arg His Ser Leu65 70 75 80Phe His Pro Glu Asp Thr Gly Gln Val Phe Gln Val Ser His Ser Phe 85 90 95Pro His Pro Leu Tyr Asp Met Ser Leu Leu Lys Asn Arg Phe Leu Arg 100 105 110Pro Gly Asp Asp Ser Ser His Asp Leu Met Leu Leu Arg Leu Ser Glu 115 120 125Pro Ala Glu Leu Thr Asp Ala Val Lys Val Met Asp Leu Pro Thr Gln 130 135 140Glu Pro Ala Leu Gly Thr Thr Cys Tyr Ala Ser Gly Trp Gly Ser Ile145 150 155 160Glu Pro Glu Glu Phe Leu Thr Pro Lys Lys Leu Gln Cys Val Asp Leu 165 170 175His Val Ile Ser Asn Asp Val Cys Ala Gln Val His Pro Gln Lys Val 180 185 190Thr Lys Phe Met Leu Cys Ala Gly Arg Trp Thr Gly Gly Lys Ser Thr 195 200 205Cys Ser Gly Asp Ser Gly Gly Pro Leu Val Cys Asn Gly Val Leu Gln 210 215 220Gly Ile Thr Ser Trp Gly Ser Glu Pro Cys Ala Leu Pro Glu Arg Pro225 230 235 240Ser Leu Tyr Thr Lys Val Val His Tyr Arg Lys Trp Ile Lys Asp Thr 245 250 255Ile Val Ala Asn Pro 260451464DNAHomo sapiens 45agccccaagc ttaccacctg cacccggaga gctgtgtcac catgtgggtc ccggttgtct 60tcctcaccct gtccgtgacg tggattggtg ctgcacccct catcctgtct cggattgtgg 120gaggctggga gtgcgagaag cattcccaac cctggcaggt gcttgtggcc tctcgtggca 180gggcagtctg cggcggtgtt ctggtgcacc cccagtgggt cctcacagct gcccactgca 240tcaggaacaa aagcgtgatc ttgctgggtc ggcacagcct gtttcatcct gaagacacag 300gccaggtatt tcaggtcagc cacagcttcc cacacccgct ctacgatatg agcctcctga 360agaatcgatt cctcaggcca ggtgatgact ccagccacga cctcatgctg ctccgcctgt 420cagagcctgc cgagctcacg gatgctgtga aggtcatgga cctgcccacc caggagccag 480cactggggac cacctgctac gcctcaggct ggggcagcat tgaaccagag gagttcttga 540ccccaaagaa acttcagtgt gtggacctcc atgttatttc caatgacgtg tgtgcgcaag 600ttcaccctca gaaggtgacc aagttcatgc tgtgtgctgg acgctggaca gggggcaaaa 660gcacctgctc gggtgattct gggggcccac ttgtctgtaa tggtgtgctt caaggtatca 720cgtcatgggg cagtgaacca tgtgccctgc ccgaaaggcc ttccctgtac accaaggtgg 780tgcattaccg gaagtggatc aaggacacca tcgtggccaa cccctgagca cccctatcaa 840ccccctattg tagtaaactt ggaaccttgg aaatgaccag gccaagactc aagcctcccc 900agttctactg acctttgtcc ttaggtgtga ggtccagggt tgctaggaaa agaaatcagc 960agacacaggt gtagaccaga gtgtttctta aatggtgtaa ttttgtcctc tctgtgtcct 1020ggggaatact ggccatgcct ggagacatat cactcaattt ctctgaggac acagatagga 1080tggggtgtct gtgttatttg tggggtacag agatgaaaga ggggtgggat ccacactgag 1140agagtggaga gtgacatgtg ctggacactg tccatgaagc actgagcaga agctggaggc 1200acaacgcacc agacactcac agcaaggatg gagctgaaaa cataacccac tctgtcctgg 1260aggcactggg aagcctagag aaggctgtga gccaaggagg gagggtcttc ctttggcatg 1320ggatggggat gaagtaagga gagggactgg accccctgga agctgattca ctatgggggg 1380aggtgtattg aagtcctcca gacaaccctc agatttgatg atttcctagt agaactcaca 1440gaaataaaga gctgttatac tgtg 1464468533DNAHomo sapiens 46attcgcgtgg aggcgcgtcg cgcgcagcgg acgccgacag aatccccgag gcgcctggcg 60cgggcgcggg cgcgaaggcg atccgggcgc caccccgcgg tcatcggtca ccggtcgctc 120tcaggaacag cagcgcaacc tctgctccct gcctcgcctc ccgcgcgcct aggtgcctgc 180gactttaatt aaagggccgt cccctcgccg aggctgcagc accgcccccc cggcttctcg 240cgcctcaaaa tgagtagctc ccactctcgg gcgggccaga gcgcagcagg cgcggctccg 300ggcggcggcg tcgacacgcg ggacgccgag atgccggcca ccgagaagga cctggcggag 360gacgcgccgt ggaagaagat ccagcagaac actttcacgc gctggtgcaa cgagcacctg 420aagtgcgtga gcaagcgcat cgccaacctg cagacggacc tgagcgacgg gctgcggctt 480atcgcgctgt tggaggtgct cagccagaag aagatgcacc gcaagcacaa ccagcggccc 540actttccgcc aaatgcagct tgagaacgtg tcggtggcgc tcgagttcct ggaccgcgag 600agcatcaaac tggtgtccat cgacagcaag gccatcgtgg acgggaacct gaagctgatc 660ctgggcctca tctggaccct gatcctgcac tactccatct ccatgcccat gtgggacgag 720gaggaggatg aggaggccaa gaagcagacc cccaagcaga ggctcctggg ctggatccag 780aacaagctgc cgcagctgcc catcaccaac ttcagccggg actggcagag cggccgggcc 840ctgggcgccc tggtggacag ctgtgccccg ggcctgtgtc ctgactggga ctcttgggac 900gccagcaagc ccgttaccaa tgcgcgagag gccatgcagc aggcggatga ctggctgggc 960atcccccagg tgatcacccc cgaggagatt gtggacccca acgtggacga gcactctgtc 1020atgacctacc tgtcccagtt ccccaaggcc aagctgaagc caggggctcc cttgcggccc 1080aaactgaacc cgaagaaagc ccgtgcctac gggccaggca tcgagcccac aggcaacatg 1140gtgaagaagc gggcagagtt cactgtggag accagaagtg ctggccaggg agaggtgctg 1200gtgtacgtgg aggacccggc cggacaccag gaggaggcaa aagtgaccgc caataacgac 1260aagaaccgca ccttctccgt ctggtacgtc cccgaggtga cggggactca taaggttact 1320gtgctctttg ctggccagca catcgccaag agccccttcg aggtgtacgt ggataagtca 1380cagggtgacg ccagcaaagt gacagcccaa ggtcccggcc tggagcccag tggcaacatc 1440gccaacaaga ccacctactt tgagatcttt acggcaggag ctggcacggg cgaggtcgag 1500gttgtgatcc aggaccccat gggacagaag ggcacggtag agcctcagct ggaggcccgg 1560ggcgacagca cataccgctg cagctaccag cccaccatgg agggcgtcca caccgtgcac 1620gtcacgtttg ccggcgtgcc catccctcgc agcccctaca ctgtcactgt tggccaagcc 1680tgtaacccga gtgcctgccg ggcggttggc cggggcctcc agcccaaggg tgtgcgggtg 1740aaggagacag ctgacttcaa ggtgtacaca aagggcgctg gcagtgggga gctgaaggtc 1800accgtgaagg gccccaaggg agaggagcgc gtgaagcaga aggacctggg ggatggcgtg 1860tatggcttcg agtattaccc catggtccct ggaacctata tcgtcaccat cacgtggggt 1920ggtcagaaca tcgggcgcag tcccttcgaa gtgaaggtgg gcaccgagtg tggcaatcag 1980aaggtacggg cctggggccc tgggctggag ggcggcgtcg ttggcaagtc agcagacttt 2040gtggtggagg ctatcgggga cgacgtgggc acgctgggct tctcggtgga agggccatcg 2100caggctaaga tcgaatgtga cgacaagggc gacggctcct gtgatgtgcg ctactggccg 2160caggaggctg gcgagtatgc cgttcacgtg ctgtgcaaca gcgaagacat ccgcctcagc 2220cccttcatgg ctgacatccg tgacgcgccc caggacttcc acccagacag ggtgaaggca 2280cgtgggcctg gattggagaa gacaggtgtg gccgtcaaca agccagcaga gttcacagtg 2340gatgccaagc acggtggcaa ggccccactt cgggtccaag tccaggacaa tgaaggctgc 2400cctgtggagg cgttggtcaa ggacaacggc aatggcactt acagctgctc ctacgtgccc 2460aggaagccgg tgaagcacac agccatggtg tcctggggag gcgtcagcat ccccaacagc 2520cccttcaggg tgaatgtggg agctggcagc caccccaaca aggtcaaagt atacggcccc 2580ggagtagcca agacagggct caaggcccac gagcccacct acttcactgt ggactgcgcc 2640gaggctggcc agggggacgt cagcatcggc atcaagtgtg cccctggagt ggtaggcccc 2700gccgaagctg acatcgactt cgacatcatc cgcaatgaca atgacacctt cacggtcaag 2760tacacgcccc ggggggctgg cagctacacc attatggtcc tctttgctga ccaggccacg 2820cccaccagcc ccatccgagt caaggtggag ccctctcatg acgccagtaa ggtgaaggcc 2880gagggccctg gcctcagtcg cactggtgtc gagcttggca agcccaccca cttcacagta 2940aatgccaaag ctgctggcaa aggcaagctg gacgtccagt tctcaggact caccaagggg 3000gatgcagtgc gagatgtgga catcatcgac caccatgaca acacctacac agtcaagtac 3060acgcctgtcc agcagggtcc agtaggcgtc aatgtcactt atggagggga tcccatccct 3120aagagccctt tctcagtggc agtatctcca agcctggacc tcagcaagat caaggtgtct 3180ggcctgggag agaaggtgga cgttggcaaa gaccaggagt tcacagtcaa atcaaagggt 3240gctggtggtc aaggcaaagt ggcatccaag attgtgggcc cctcgggtgc agcggtgccc 3300tgcaaggtgg agccaggcct gggggctgac aacagtgtgg tgcgcttcct gccccgtgag 3360gaagggccct atgaggtgga ggtgacctat gacggcgtgc ccgtgcctgg cagccccttt 3420cctctggaag ctgtggcccc caccaagcct agcaaggtga aggcgtttgg gccggggctg 3480cagggaggca gtgcgggctc ccccgcccgc ttcaccatcg acaccaaggg cgccggcaca 3540ggtggcctgg gcctgacggt ggagggcccc tgtgaggcgc agctcgagtg cttggacaat 3600ggggatggca catgttccgt gtcctacgtg cccaccgagc ccggggacta caacatcaac 3660atcctcttcg ctgacaccca catccctggc tccccattca aggcccacgt ggttccctgc 3720tttgacgcat ccaaagtcaa gtgctcaggc cccgggctgg agcgggccac cgctggggag 3780gtgggccaat tccaagtgga ctgctcgagc gcgggcagcg cggagctgac cattgagatc 3840tgctcggagg cggggcttcc ggccgaggtg tacatccagg accacggtga tggcacgcac 3900accattacct acattcccct ctgccccggg gcctacaccg tcaccatcaa gtacggcggc 3960cagcccgtgc ccaacttccc cagcaagctg caggtggaac ctgcggtgga cacttccggt 4020gtccagtgct atgggcctgg tattgagggc cagggtgtct tccgtgaggc caccactgag 4080ttcagtgtgg acgcccgggc tctgacacag accggagggc cgcacgtcaa ggcccgtgtg 4140gccaacccct caggcaacct gacggagacc tacgttcagg accgtggcga tggcatgtac 4200aaagtggagt acacgcctta cgaggaggga ctgcactccg tggacgtgac ctatgacggc 4260agtcccgtgc ccagcagccc cttccaggtg cccgtgaccg agggctgcga cccctcccgg 4320gtgcgtgtcc acgggccagg catccaaagt ggcaccacca acaagcccaa caagttcact 4380gtggagacca ggggagctgg cacgggcggc ctgggcctgg ctgtagaggg cccctccgag 4440gccaagatgt cctgcatgga taacaaggac ggcagctgct cggtcgagta catcccttat 4500gaggctggca cctacagcct caacgtcacc tatggtggcc atcaagtgcc aggcagtcct 4560ttcaaggtcc ctgtgcatga tgtgacagat gcgtccaagg tcaagtgctc tgggcccggc 4620ctgagcccag gcatggttcg tgccaacctc cctcagtcct tccaggtgga cacaagcaag 4680gctggtgtgg ccccattgca ggtcaaagtg caagggccca aaggcctggt ggagccagtg 4740gacgtggtag acaacgctga tggcacccag accgtcaatt atgtgcccag ccgagaaggg 4800ccctacagca tctcagtact gtatggagat gaagaggtac cccggagccc cttcaaggtc 4860aaggtgctgc ctactcatga tgccagcaag gtgaaggcca gtggccccgg gctcaacacc 4920actggcgtgc ctgccagcct gcccgtggag ttcaccatcg atgcaaagga cgccggggag 4980ggcctgctgg ctgtccagat cacggatccc gaaggcaagc cgaagaagac acacatccaa 5040gacaaccatg acggcacgta tacagtggcc tacgtgccag acgtgacagg tcgctacacc 5100atcctcatca agtacggtgg tgacgagatc cccttctccc cgtaccgcgt gcgtgccgtg 5160cccaccgggg acgccagcaa gtgcactgtc acaggtgctg gcatcggccc caccattcag 5220attggggagg agacggtgat cactgtggac actaaggcgg caggcaaagg caaagtgacg 5280tgcaccgtgt gcacgcctga tggctcagag gtggatgtgg acgtggtgga gaatgaggac 5340ggcactttcg acatcttcta cacggccccc cagccgggca aatacgtcat ctgtgtgcgc 5400tttggtggcg agcacgtgcc caacagcccc ttccaagtga cggctctggc tggggaccag 5460ccctcggtgc agccccctct acggtctcag cagctggccc cacagtacac ctacgcccag 5520ggcggccagc agacttgggc cccggagagg cccctggtgg gtgtcaatgg gctggatgtg 5580accagcctga ggccctttga ccttgtcatc cccttcacca tcaagaaggg cgagatcaca 5640ggggaggttc ggatgccctc aggcaaggtg gcgcagccca ccatcactga caacaaagac 5700ggcaccgtga ccgtgcggta tgcacccagc gaggctggcc tgcacgagat ggacatccgc 5760tatgacaaca tgcacatccc aggaagcccc ttgcagttct atgtggatta cgtcaactgt 5820ggccatgtca ctgcctatgg gcctggcctc acccatggag tagtgaacaa gcctgccacc 5880ttcaccgtca acaccaagga tgcaggagag gggggcctgt ctctggccat tgagggcccg 5940tccaaagcag aaatcagctg cactgacaac caggatggga catgcagcgt gtcctacctg 6000cctgtgctgc cgggggacta cagcattcta gtcaagtaca atgaacagca cgtcccaggc 6060agccccttca ctgctcgggt cacaggtgac gactccatgc gtatgtccca cctaaaggtc 6120ggctctgctg ccgacatccc catcaacatc tcagagacgg atctcagcct gctgacggcc 6180actgtggtcc cgccctcggg ccgggaggag ccctgtttgc tgaagcggct gcgtaatggc 6240cacgtgggga tttcattcgt gcccaaggag acgggggagc acctggtgca tgtgaagaaa 6300aatggccagc acgtggccag cagccccatc ccggtggtga tcagccagtc ggaaattggg 6360gatgccagtc gtgttcgggt ctctggtcag ggccttcacg aaggccacac ctttgagcct 6420gcagagttta tcattgatac ccgcgatgca ggctatggtg ggctcagcct gtccattgag 6480ggccccagca aggtggacat caacacagag gacctggagg acgggacgtg cagggtcacc 6540tactgcccca cagagccagg caactacatc atcaacatca agtttgccga ccagcacgtg 6600cctggcagcc ccttctctgt gaaggtgaca ggcgagggcc gggtgaaaga gagcatcacc 6660cgcaggcgtc gggctccttc agtggccaac gttggtagtc attgtgacct cagcctgaaa 6720atccctgaaa ttagcatcca ggatatgaca gcccaggtga ccagcccatc gggcaagacc 6780catgaggccg agatcgtgga aggggagaac cacacctact gcatccgctt tgttcccgct 6840gagatgggca cacacacagt cagcgtgaag tacaagggcc agcacgtgcc tgggagcccc 6900ttccagttca ccgtggggcc cctaggggaa gggggagccc acaaggtccg agctgggggc 6960cctggcctgg agagagctga agctggagtg ccagccgaat tcagtatctg gacccgggaa 7020gctggtgctg gaggcctggc cattgctgtc gagggcccca gcaaggctga gatctctttt 7080gaggaccgca aggacggctc ctgtggtgtg gcttatgtgg tccaggagcc aggtgactac 7140gaagtctcag tcaagttcaa cgaggaacac attcccgaca gccccttcgt ggtgcctgtg 7200gcttctccgt ctggcgacgc ccgccgcctc actgtttcta gccttcagga gtcagggcta 7260aaggtcaacc agccagcctc ttttgcagtc agcctgaacg gggccaaggg ggcgatcgat 7320gccaaggtgc acagcccctc aggagccctg gaggagtgct atgtcacaga aattgaccaa 7380gataagtatg ctgtgcgctt catccctcgg gagaatggcg tttacctgat tgacgtcaag 7440ttcaacggca cccacatccc tggaagcccc ttcaagatcc gagttgggga gcctgggcat 7500ggaggggacc caggcttggt gtctgcttac ggagcaggtc tggaaggcgg tgtcacaggg 7560aacccagctg agttcgtcgt gaacacgagc aatgcgggag ctggtgccct gtcggtgacc 7620attgacggcc cctccaaggt gaagatggat tgccaggagt gccctgaggg ctaccgcgtc 7680acctataccc ccatggcacc tggcagctac ctcatctcca tcaagtacgg cggcccctac 7740cacattgggg gcagcccctt caaggccaaa gtcacaggcc cccgtctcgt cagcaaccac 7800agcctccacg agacatcatc agtgtttgta gactctctga ccaaggccac ctgtgccccc 7860cagcatgggg ccccgggtcc tgggcctgct gacgccagca aggtggtggc caagggcctg 7920gggctgagca aggcctacgt aggccagaag agcagcttca cagtagactg cagcaaagca 7980ggcaacaaca tgctgctggt gggggttcat ggcccaagga ccccctgcga ggagatcctg 8040gtgaagcacg tgggcagccg gctctacagc gtgtcctacc tgctcaagga caagggggag 8100tacacactgg tggtcaaatg gggggacgag cacatcccag gcagccccta ccgcgttgtg 8160gtgccctgag tctggggccc gtgccagccg gcagccccca agcctgcccc gctacccaag 8220cagccccgcc ctcttcccct caaccccggc ccaggccgcc ctggccgccc gcctgtcact 8280gcagccgccc ctgccctgtg ccgtgctgcg ctcacctgcc tccccagcca gccgctgacc 8340tctcggcttt cacttgggca gagggagcca tttggtggcg ctgcttgtct tctttggttc 8400tgggaggggt gagggatggg ggtcctgtac acaaccaccc actagttctc ttctccagcc 8460aagaggaata aagttttgct tccattaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 8520aaaaaaaaaa aaa 8533472639PRTHomo sapiens 47Met Ser Ser Ser His Ser Arg Ala Gly Gln Ser Ala Ala Gly Ala Ala1 5 10 15Pro Gly Gly Gly Val Asp Thr Arg Asp Ala Glu Met Pro Ala Thr Glu 20 25 30Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys Ile Gln Gln Asn Thr 35 40 45Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys Val Ser Lys Arg Ile 50 55 60Ala Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu Arg Leu Ile Ala Leu65 70 75 80Leu Glu Val Leu Ser Gln Lys Lys Met His Arg Lys His Asn Gln Arg 85 90 95Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val Ser Val Ala Leu Glu 100 105 110Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser Ile Asp Ser Lys Ala 115 120 125Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly Leu Ile Trp Thr Leu 130 135 140Ile Leu His Tyr Ser Ile Ser Met Pro Met Trp Asp Glu Glu Glu Asp145 150 155 160Glu Glu Ala Lys Lys Gln Thr Pro Lys Gln Arg Leu Leu Gly Trp Ile 165 170 175Gln Asn Lys Leu Pro Gln Leu Pro Ile Thr Asn Phe Ser Arg Asp Trp 180 185 190Gln Ser Gly Arg Ala Leu Gly Ala Leu Val Asp Ser Cys Ala Pro Gly 195 200 205Leu Cys Pro Asp Trp Asp Ser Trp Asp Ala Ser Lys Pro Val Thr Asn 210 215 220Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp Leu Gly Ile Pro Gln225 230 235 240Val Ile Thr Pro Glu Glu Ile Val Asp Pro Asn Val Asp Glu His Ser 245 250 255Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala Lys Leu Lys Pro Gly 260 265 270Ala Pro Leu Arg Pro Lys Leu Asn Pro Lys Lys Ala Arg Ala Tyr Gly 275 280 285Pro Gly Ile Glu Pro Thr Gly Asn Met Val Lys Lys Arg Ala Glu Phe 290 295 300Thr Val Glu Thr Arg Ser Ala Gly Gln Gly Glu Val Leu Val Tyr Val305 310 315 320Glu Asp Pro Ala Gly His Gln Glu Glu Ala Lys Val Thr Ala Asn Asn 325 330 335Asp Lys Asn Arg Thr Phe Ser Val Trp Tyr Val Pro Glu Val Thr Gly 340 345 350Thr His Lys Val Thr Val Leu Phe Ala Gly Gln His Ile Ala Lys Ser 355 360 365Pro Phe Glu Val Tyr Val Asp

Lys Ser Gln Gly Asp Ala Ser Lys Val 370 375 380Thr Ala Gln Gly Pro Gly Leu Glu Pro Ser Gly Asn Ile Ala Asn Lys385 390 395 400Thr Thr Tyr Phe Glu Ile Phe Thr Ala Gly Ala Gly Thr Gly Glu Val 405 410 415Glu Val Val Ile Gln Asp Pro Met Gly Gln Lys Gly Thr Val Glu Pro 420 425 430Gln Leu Glu Ala Arg Gly Asp Ser Thr Tyr Arg Cys Ser Tyr Gln Pro 435 440 445Thr Met Glu Gly Val His Thr Val His Val Thr Phe Ala Gly Val Pro 450 455 460Ile Pro Arg Ser Pro Tyr Thr Val Thr Val Gly Gln Ala Cys Asn Pro465 470 475 480Ser Ala Cys Arg Ala Val Gly Arg Gly Leu Gln Pro Lys Gly Val Arg 485 490 495Val Lys Glu Thr Ala Asp Phe Lys Val Tyr Thr Lys Gly Ala Gly Ser 500 505 510Gly Glu Leu Lys Val Thr Val Lys Gly Pro Lys Gly Glu Glu Arg Val 515 520 525Lys Gln Lys Asp Leu Gly Asp Gly Val Tyr Gly Phe Glu Tyr Tyr Pro 530 535 540Met Val Pro Gly Thr Tyr Ile Val Thr Ile Thr Trp Gly Gly Gln Asn545 550 555 560Ile Gly Arg Ser Pro Phe Glu Val Lys Val Gly Thr Glu Cys Gly Asn 565 570 575Gln Lys Val Arg Ala Trp Gly Pro Gly Leu Glu Gly Gly Val Val Gly 580 585 590Lys Ser Ala Asp Phe Val Val Glu Ala Ile Gly Asp Asp Val Gly Thr 595 600 605Leu Gly Phe Ser Val Glu Gly Pro Ser Gln Ala Lys Ile Glu Cys Asp 610 615 620Asp Lys Gly Asp Gly Ser Cys Asp Val Arg Tyr Trp Pro Gln Glu Ala625 630 635 640Gly Glu Tyr Ala Val His Val Leu Cys Asn Ser Glu Asp Ile Arg Leu 645 650 655Ser Pro Phe Met Ala Asp Ile Arg Asp Ala Pro Gln Asp Phe His Pro 660 665 670Asp Arg Val Lys Ala Arg Gly Pro Gly Leu Glu Lys Thr Gly Val Ala 675 680 685Val Asn Lys Pro Ala Glu Phe Thr Val Asp Ala Lys His Gly Gly Lys 690 695 700Ala Pro Leu Arg Val Gln Val Gln Asp Asn Glu Gly Cys Pro Val Glu705 710 715 720Ala Leu Val Lys Asp Asn Gly Asn Gly Thr Tyr Ser Cys Ser Tyr Val 725 730 735Pro Arg Lys Pro Val Lys His Thr Ala Met Val Ser Trp Gly Gly Val 740 745 750Ser Ile Pro Asn Ser Pro Phe Arg Val Asn Val Gly Ala Gly Ser His 755 760 765Pro Asn Lys Val Lys Val Tyr Gly Pro Gly Val Ala Lys Thr Gly Leu 770 775 780Lys Ala His Glu Pro Thr Tyr Phe Thr Val Asp Cys Ala Glu Ala Gly785 790 795 800Gln Gly Asp Val Ser Ile Gly Ile Lys Cys Ala Pro Gly Val Val Gly 805 810 815Pro Ala Glu Ala Asp Ile Asp Phe Asp Ile Ile Arg Asn Asp Asn Asp 820 825 830Thr Phe Thr Val Lys Tyr Thr Pro Arg Gly Ala Gly Ser Tyr Thr Ile 835 840 845Met Val Leu Phe Ala Asp Gln Ala Thr Pro Thr Ser Pro Ile Arg Val 850 855 860Lys Val Glu Pro Ser His Asp Ala Ser Lys Val Lys Ala Glu Gly Pro865 870 875 880Gly Leu Ser Arg Thr Gly Val Glu Leu Gly Lys Pro Thr His Phe Thr 885 890 895Val Asn Ala Lys Ala Ala Gly Lys Gly Lys Leu Asp Val Gln Phe Ser 900 905 910Gly Leu Thr Lys Gly Asp Ala Val Arg Asp Val Asp Ile Ile Asp His 915 920 925His Asp Asn Thr Tyr Thr Val Lys Tyr Thr Pro Val Gln Gln Gly Pro 930 935 940Val Gly Val Asn Val Thr Tyr Gly Gly Asp Pro Ile Pro Lys Ser Pro945 950 955 960Phe Ser Val Ala Val Ser Pro Ser Leu Asp Leu Ser Lys Ile Lys Val 965 970 975Ser Gly Leu Gly Glu Lys Val Asp Val Gly Lys Asp Gln Glu Phe Thr 980 985 990Val Lys Ser Lys Gly Ala Gly Gly Gln Gly Lys Val Ala Ser Lys Ile 995 1000 1005Val Gly Pro Ser Gly Ala Ala Val Pro Cys Lys Val Glu Pro Gly 1010 1015 1020Leu Gly Ala Asp Asn Ser Val Val Arg Phe Leu Pro Arg Glu Glu 1025 1030 1035Gly Pro Tyr Glu Val Glu Val Thr Tyr Asp Gly Val Pro Val Pro 1040 1045 1050Gly Ser Pro Phe Pro Leu Glu Ala Val Ala Pro Thr Lys Pro Ser 1055 1060 1065Lys Val Lys Ala Phe Gly Pro Gly Leu Gln Gly Gly Ser Ala Gly 1070 1075 1080Ser Pro Ala Arg Phe Thr Ile Asp Thr Lys Gly Ala Gly Thr Gly 1085 1090 1095Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala Gln Leu Glu 1100 1105 1110Cys Leu Asp Asn Gly Asp Gly Thr Cys Ser Val Ser Tyr Val Pro 1115 1120 1125Thr Glu Pro Gly Asp Tyr Asn Ile Asn Ile Leu Phe Ala Asp Thr 1130 1135 1140His Ile Pro Gly Ser Pro Phe Lys Ala His Val Val Pro Cys Phe 1145 1150 1155Asp Ala Ser Lys Val Lys Cys Ser Gly Pro Gly Leu Glu Arg Ala 1160 1165 1170Thr Ala Gly Glu Val Gly Gln Phe Gln Val Asp Cys Ser Ser Ala 1175 1180 1185Gly Ser Ala Glu Leu Thr Ile Glu Ile Cys Ser Glu Ala Gly Leu 1190 1195 1200Pro Ala Glu Val Tyr Ile Gln Asp His Gly Asp Gly Thr His Thr 1205 1210 1215Ile Thr Tyr Ile Pro Leu Cys Pro Gly Ala Tyr Thr Val Thr Ile 1220 1225 1230Lys Tyr Gly Gly Gln Pro Val Pro Asn Phe Pro Ser Lys Leu Gln 1235 1240 1245Val Glu Pro Ala Val Asp Thr Ser Gly Val Gln Cys Tyr Gly Pro 1250 1255 1260Gly Ile Glu Gly Gln Gly Val Phe Arg Glu Ala Thr Thr Glu Phe 1265 1270 1275Ser Val Asp Ala Arg Ala Leu Thr Gln Thr Gly Gly Pro His Val 1280 1285 1290Lys Ala Arg Val Ala Asn Pro Ser Gly Asn Leu Thr Glu Thr Tyr 1295 1300 1305Val Gln Asp Arg Gly Asp Gly Met Tyr Lys Val Glu Tyr Thr Pro 1310 1315 1320Tyr Glu Glu Gly Leu His Ser Val Asp Val Thr Tyr Asp Gly Ser 1325 1330 1335Pro Val Pro Ser Ser Pro Phe Gln Val Pro Val Thr Glu Gly Cys 1340 1345 1350Asp Pro Ser Arg Val Arg Val His Gly Pro Gly Ile Gln Ser Gly 1355 1360 1365Thr Thr Asn Lys Pro Asn Lys Phe Thr Val Glu Thr Arg Gly Ala 1370 1375 1380Gly Thr Gly Gly Leu Gly Leu Ala Val Glu Gly Pro Ser Glu Ala 1385 1390 1395Lys Met Ser Cys Met Asp Asn Lys Asp Gly Ser Cys Ser Val Glu 1400 1405 1410Tyr Ile Pro Tyr Glu Ala Gly Thr Tyr Ser Leu Asn Val Thr Tyr 1415 1420 1425Gly Gly His Gln Val Pro Gly Ser Pro Phe Lys Val Pro Val His 1430 1435 1440Asp Val Thr Asp Ala Ser Lys Val Lys Cys Ser Gly Pro Gly Leu 1445 1450 1455Ser Pro Gly Met Val Arg Ala Asn Leu Pro Gln Ser Phe Gln Val 1460 1465 1470Asp Thr Ser Lys Ala Gly Val Ala Pro Leu Gln Val Lys Val Gln 1475 1480 1485Gly Pro Lys Gly Leu Val Glu Pro Val Asp Val Val Asp Asn Ala 1490 1495 1500Asp Gly Thr Gln Thr Val Asn Tyr Val Pro Ser Arg Glu Gly Pro 1505 1510 1515Tyr Ser Ile Ser Val Leu Tyr Gly Asp Glu Glu Val Pro Arg Ser 1520 1525 1530Pro Phe Lys Val Lys Val Leu Pro Thr His Asp Ala Ser Lys Val 1535 1540 1545Lys Ala Ser Gly Pro Gly Leu Asn Thr Thr Gly Val Pro Ala Ser 1550 1555 1560Leu Pro Val Glu Phe Thr Ile Asp Ala Lys Asp Ala Gly Glu Gly 1565 1570 1575Leu Leu Ala Val Gln Ile Thr Asp Pro Glu Gly Lys Pro Lys Lys 1580 1585 1590Thr His Ile Gln Asp Asn His Asp Gly Thr Tyr Thr Val Ala Tyr 1595 1600 1605Val Pro Asp Val Thr Gly Arg Tyr Thr Ile Leu Ile Lys Tyr Gly 1610 1615 1620Gly Asp Glu Ile Pro Phe Ser Pro Tyr Arg Val Arg Ala Val Pro 1625 1630 1635Thr Gly Asp Ala Ser Lys Cys Thr Val Thr Gly Ala Gly Ile Gly 1640 1645 1650Pro Thr Ile Gln Ile Gly Glu Glu Thr Val Ile Thr Val Asp Thr 1655 1660 1665Lys Ala Ala Gly Lys Gly Lys Val Thr Cys Thr Val Cys Thr Pro 1670 1675 1680Asp Gly Ser Glu Val Asp Val Asp Val Val Glu Asn Glu Asp Gly 1685 1690 1695Thr Phe Asp Ile Phe Tyr Thr Ala Pro Gln Pro Gly Lys Tyr Val 1700 1705 1710Ile Cys Val Arg Phe Gly Gly Glu His Val Pro Asn Ser Pro Phe 1715 1720 1725Gln Val Thr Ala Leu Ala Gly Asp Gln Pro Ser Val Gln Pro Pro 1730 1735 1740Leu Arg Ser Gln Gln Leu Ala Pro Gln Tyr Thr Tyr Ala Gln Gly 1745 1750 1755Gly Gln Gln Thr Trp Ala Pro Glu Arg Pro Leu Val Gly Val Asn 1760 1765 1770Gly Leu Asp Val Thr Ser Leu Arg Pro Phe Asp Leu Val Ile Pro 1775 1780 1785Phe Thr Ile Lys Lys Gly Glu Ile Thr Gly Glu Val Arg Met Pro 1790 1795 1800Ser Gly Lys Val Ala Gln Pro Thr Ile Thr Asp Asn Lys Asp Gly 1805 1810 1815Thr Val Thr Val Arg Tyr Ala Pro Ser Glu Ala Gly Leu His Glu 1820 1825 1830Met Asp Ile Arg Tyr Asp Asn Met His Ile Pro Gly Ser Pro Leu 1835 1840 1845Gln Phe Tyr Val Asp Tyr Val Asn Cys Gly His Val Thr Ala Tyr 1850 1855 1860Gly Pro Gly Leu Thr His Gly Val Val Asn Lys Pro Ala Thr Phe 1865 1870 1875Thr Val Asn Thr Lys Asp Ala Gly Glu Gly Gly Leu Ser Leu Ala 1880 1885 1890Ile Glu Gly Pro Ser Lys Ala Glu Ile Ser Cys Thr Asp Asn Gln 1895 1900 1905Asp Gly Thr Cys Ser Val Ser Tyr Leu Pro Val Leu Pro Gly Asp 1910 1915 1920Tyr Ser Ile Leu Val Lys Tyr Asn Glu Gln His Val Pro Gly Ser 1925 1930 1935Pro Phe Thr Ala Arg Val Thr Gly Asp Asp Ser Met Arg Met Ser 1940 1945 1950His Leu Lys Val Gly Ser Ala Ala Asp Ile Pro Ile Asn Ile Ser 1955 1960 1965Glu Thr Asp Leu Ser Leu Leu Thr Ala Thr Val Val Pro Pro Ser 1970 1975 1980Gly Arg Glu Glu Pro Cys Leu Leu Lys Arg Leu Arg Asn Gly His 1985 1990 1995Val Gly Ile Ser Phe Val Pro Lys Glu Thr Gly Glu His Leu Val 2000 2005 2010His Val Lys Lys Asn Gly Gln His Val Ala Ser Ser Pro Ile Pro 2015 2020 2025Val Val Ile Ser Gln Ser Glu Ile Gly Asp Ala Ser Arg Val Arg 2030 2035 2040Val Ser Gly Gln Gly Leu His Glu Gly His Thr Phe Glu Pro Ala 2045 2050 2055Glu Phe Ile Ile Asp Thr Arg Asp Ala Gly Tyr Gly Gly Leu Ser 2060 2065 2070Leu Ser Ile Glu Gly Pro Ser Lys Val Asp Ile Asn Thr Glu Asp 2075 2080 2085Leu Glu Asp Gly Thr Cys Arg Val Thr Tyr Cys Pro Thr Glu Pro 2090 2095 2100Gly Asn Tyr Ile Ile Asn Ile Lys Phe Ala Asp Gln His Val Pro 2105 2110 2115Gly Ser Pro Phe Ser Val Lys Val Thr Gly Glu Gly Arg Val Lys 2120 2125 2130Glu Ser Ile Thr Arg Arg Arg Arg Ala Pro Ser Val Ala Asn Val 2135 2140 2145Gly Ser His Cys Asp Leu Ser Leu Lys Ile Pro Glu Ile Ser Ile 2150 2155 2160Gln Asp Met Thr Ala Gln Val Thr Ser Pro Ser Gly Lys Thr His 2165 2170 2175Glu Ala Glu Ile Val Glu Gly Glu Asn His Thr Tyr Cys Ile Arg 2180 2185 2190Phe Val Pro Ala Glu Met Gly Thr His Thr Val Ser Val Lys Tyr 2195 2200 2205Lys Gly Gln His Val Pro Gly Ser Pro Phe Gln Phe Thr Val Gly 2210 2215 2220Pro Leu Gly Glu Gly Gly Ala His Lys Val Arg Ala Gly Gly Pro 2225 2230 2235Gly Leu Glu Arg Ala Glu Ala Gly Val Pro Ala Glu Phe Ser Ile 2240 2245 2250Trp Thr Arg Glu Ala Gly Ala Gly Gly Leu Ala Ile Ala Val Glu 2255 2260 2265Gly Pro Ser Lys Ala Glu Ile Ser Phe Glu Asp Arg Lys Asp Gly 2270 2275 2280Ser Cys Gly Val Ala Tyr Val Val Gln Glu Pro Gly Asp Tyr Glu 2285 2290 2295Val Ser Val Lys Phe Asn Glu Glu His Ile Pro Asp Ser Pro Phe 2300 2305 2310Val Val Pro Val Ala Ser Pro Ser Gly Asp Ala Arg Arg Leu Thr 2315 2320 2325Val Ser Ser Leu Gln Glu Ser Gly Leu Lys Val Asn Gln Pro Ala 2330 2335 2340Ser Phe Ala Val Ser Leu Asn Gly Ala Lys Gly Ala Ile Asp Ala 2345 2350 2355Lys Val His Ser Pro Ser Gly Ala Leu Glu Glu Cys Tyr Val Thr 2360 2365 2370Glu Ile Asp Gln Asp Lys Tyr Ala Val Arg Phe Ile Pro Arg Glu 2375 2380 2385Asn Gly Val Tyr Leu Ile Asp Val Lys Phe Asn Gly Thr His Ile 2390 2395 2400Pro Gly Ser Pro Phe Lys Ile Arg Val Gly Glu Pro Gly His Gly 2405 2410 2415Gly Asp Pro Gly Leu Val Ser Ala Tyr Gly Ala Gly Leu Glu Gly 2420 2425 2430Gly Val Thr Gly Asn Pro Ala Glu Phe Val Val Asn Thr Ser Asn 2435 2440 2445Ala Gly Ala Gly Ala Leu Ser Val Thr Ile Asp Gly Pro Ser Lys 2450 2455 2460Val Lys Met Asp Cys Gln Glu Cys Pro Glu Gly Tyr Arg Val Thr 2465 2470 2475Tyr Thr Pro Met Ala Pro Gly Ser Tyr Leu Ile Ser Ile Lys Tyr 2480 2485 2490Gly Gly Pro Tyr His Ile Gly Gly Ser Pro Phe Lys Ala Lys Val 2495 2500 2505Thr Gly Pro Arg Leu Val Ser Asn His Ser Leu His Glu Thr Ser 2510 2515 2520Ser Val Phe Val Asp Ser Leu Thr Lys Ala Thr Cys Ala Pro Gln 2525 2530 2535His Gly Ala Pro Gly Pro Gly Pro Ala Asp Ala Ser Lys Val Val 2540 2545 2550Ala Lys Gly Leu Gly Leu Ser Lys Ala Tyr Val Gly Gln Lys Ser 2555 2560 2565Ser Phe Thr Val Asp Cys Ser Lys Ala Gly Asn Asn Met Leu Leu 2570 2575 2580Val Gly Val His Gly Pro Arg Thr Pro Cys Glu Glu Ile Leu Val 2585 2590 2595Lys His Val Gly Ser Arg Leu Tyr Ser Val Ser Tyr Leu Leu Lys 2600 2605 2610Asp Lys Gly Glu Tyr Thr Leu Val Val Lys Trp Gly Asp Glu His 2615 2620 2625Ile Pro Gly Ser Pro Tyr Arg Val Val Val Pro 2630 2635488557DNAHomo sapiens 48attcgcgtgg aggcgcgtcg cgcgcagcgg acgccgacag aatccccgag gcgcctggcg 60cgggcgcggg cgcgaaggcg atccgggcgc caccccgcgg tcatcggtca ccggtcgctc 120tcaggaacag cagcgcaacc tctgctccct gcctcgcctc ccgcgcgcct aggtgcctgc 180gactttaatt aaagggccgt cccctcgccg aggctgcagc accgcccccc cggcttctcg 240cgcctcaaaa tgagtagctc ccactctcgg gcgggccaga gcgcagcagg cgcggctccg 300ggcggcggcg tcgacacgcg ggacgccgag atgccggcca ccgagaagga cctggcggag 360gacgcgccgt ggaagaagat ccagcagaac actttcacgc gctggtgcaa cgagcacctg 420aagtgcgtga gcaagcgcat cgccaacctg cagacggacc tgagcgacgg gctgcggctt 480atcgcgctgt tggaggtgct cagccagaag aagatgcacc gcaagcacaa ccagcggccc 540actttccgcc aaatgcagct tgagaacgtg tcggtggcgc tcgagttcct ggaccgcgag 600agcatcaaac tggtgtccat cgacagcaag gccatcgtgg acgggaacct gaagctgatc 660ctgggcctca tctggaccct gatcctgcac tactccatct ccatgcccat gtgggacgag 720gaggaggatg aggaggccaa gaagcagacc cccaagcaga ggctcctggg ctggatccag 780aacaagctgc cgcagctgcc catcaccaac ttcagccggg actggcagag cggccgggcc 840ctgggcgccc tggtggacag ctgtgccccg ggcctgtgtc ctgactggga ctcttgggac 900gccagcaagc ccgttaccaa tgcgcgagag gccatgcagc aggcggatga ctggctgggc 960atcccccagg tgatcacccc cgaggagatt gtggacccca acgtggacga gcactctgtc 1020atgacctacc tgtcccagtt ccccaaggcc aagctgaagc caggggctcc cttgcggccc 1080aaactgaacc

cgaagaaagc ccgtgcctac gggccaggca tcgagcccac aggcaacatg 1140gtgaagaagc gggcagagtt cactgtggag accagaagtg ctggccaggg agaggtgctg 1200gtgtacgtgg aggacccggc cggacaccag gaggaggcaa aagtgaccgc caataacgac 1260aagaaccgca ccttctccgt ctggtacgtc cccgaggtga cggggactca taaggttact 1320gtgctctttg ctggccagca catcgccaag agccccttcg aggtgtacgt ggataagtca 1380cagggtgacg ccagcaaagt gacagcccaa ggtcccggcc tggagcccag tggcaacatc 1440gccaacaaga ccacctactt tgagatcttt acggcaggag ctggcacggg cgaggtcgag 1500gttgtgatcc aggaccccat gggacagaag ggcacggtag agcctcagct ggaggcccgg 1560ggcgacagca cataccgctg cagctaccag cccaccatgg agggcgtcca caccgtgcac 1620gtcacgtttg ccggcgtgcc catccctcgc agcccctaca ctgtcactgt tggccaagcc 1680tgtaacccga gtgcctgccg ggcggttggc cggggcctcc agcccaaggg tgtgcgggtg 1740aaggagacag ctgacttcaa ggtgtacaca aagggcgctg gcagtgggga gctgaaggtc 1800accgtgaagg gccccaaggg agaggagcgc gtgaagcaga aggacctggg ggatggcgtg 1860tatggcttcg agtattaccc catggtccct ggaacctata tcgtcaccat cacgtggggt 1920ggtcagaaca tcgggcgcag tcccttcgaa gtgaaggtgg gcaccgagtg tggcaatcag 1980aaggtacggg cctggggccc tgggctggag ggcggcgtcg ttggcaagtc agcagacttt 2040gtggtggagg ctatcgggga cgacgtgggc acgctgggct tctcggtgga agggccatcg 2100caggctaaga tcgaatgtga cgacaagggc gacggctcct gtgatgtgcg ctactggccg 2160caggaggctg gcgagtatgc cgttcacgtg ctgtgcaaca gcgaagacat ccgcctcagc 2220cccttcatgg ctgacatccg tgacgcgccc caggacttcc acccagacag ggtgaaggca 2280cgtgggcctg gattggagaa gacaggtgtg gccgtcaaca agccagcaga gttcacagtg 2340gatgccaagc acggtggcaa ggccccactt cgggtccaag tccaggacaa tgaaggctgc 2400cctgtggagg cgttggtcaa ggacaacggc aatggcactt acagctgctc ctacgtgccc 2460aggaagccgg tgaagcacac agccatggtg tcctggggag gcgtcagcat ccccaacagc 2520cccttcaggg tgaatgtggg agctggcagc caccccaaca aggtcaaagt atacggcccc 2580ggagtagcca agacagggct caaggcccac gagcccacct acttcactgt ggactgcgcc 2640gaggctggcc agggggacgt cagcatcggc atcaagtgtg cccctggagt ggtaggcccc 2700gccgaagctg acatcgactt cgacatcatc cgcaatgaca atgacacctt cacggtcaag 2760tacacgcccc ggggggctgg cagctacacc attatggtcc tctttgctga ccaggccacg 2820cccaccagcc ccatccgagt caaggtggag ccctctcatg acgccagtaa ggtgaaggcc 2880gagggccctg gcctcagtcg cactggtgtc gagcttggca agcccaccca cttcacagta 2940aatgccaaag ctgctggcaa aggcaagctg gacgtccagt tctcaggact caccaagggg 3000gatgcagtgc gagatgtgga catcatcgac caccatgaca acacctacac agtcaagtac 3060acgcctgtcc agcagggtcc agtaggcgtc aatgtcactt atggagggga tcccatccct 3120aagagccctt tctcagtggc agtatctcca agcctggacc tcagcaagat caaggtgtct 3180ggcctgggag agaaggtgga cgttggcaaa gaccaggagt tcacagtcaa atcaaagggt 3240gctggtggtc aaggcaaagt ggcatccaag attgtgggcc cctcgggtgc agcggtgccc 3300tgcaaggtgg agccaggcct gggggctgac aacagtgtgg tgcgcttcct gccccgtgag 3360gaagggccct atgaggtgga ggtgacctat gacggcgtgc ccgtgcctgg cagccccttt 3420cctctggaag ctgtggcccc caccaagcct agcaaggtga aggcgtttgg gccggggctg 3480cagggaggca gtgcgggctc ccccgcccgc ttcaccatcg acaccaaggg cgccggcaca 3540ggtggcctgg gcctgacggt ggagggcccc tgtgaggcgc agctcgagtg cttggacaat 3600ggggatggca catgttccgt gtcctacgtg cccaccgagc ccggggacta caacatcaac 3660atcctcttcg ctgacaccca catccctggc tccccattca aggcccacgt ggttccctgc 3720tttgacgcat ccaaagtcaa gtgctcaggc cccgggctgg agcgggccac cgctggggag 3780gtgggccaat tccaagtgga ctgctcgagc gcgggcagcg cggagctgac cattgagatc 3840tgctcggagg cggggcttcc ggccgaggtg tacatccagg accacggtga tggcacgcac 3900accattacct acattcccct ctgccccggg gcctacaccg tcaccatcaa gtacggcggc 3960cagcccgtgc ccaacttccc cagcaagctg caggtggaac ctgcggtgga cacttccggt 4020gtccagtgct atgggcctgg tattgagggc cagggtgtct tccgtgaggc caccactgag 4080ttcagtgtgg acgcccgggc tctgacacag accggagggc cgcacgtcaa ggcccgtgtg 4140gccaacccct caggcaacct gacggagacc tacgttcagg accgtggcga tggcatgtac 4200aaagtggagt acacgcctta cgaggaggga ctgcactccg tggacgtgac ctatgacggc 4260agtcccgtgc ccagcagccc cttccaggtg cccgtgaccg agggctgcga cccctcccgg 4320gtgcgtgtcc acgggccagg catccaaagt ggcaccacca acaagcccaa caagttcact 4380gtggagacca ggggagctgg cacgggcggc ctgggcctgg ctgtagaggg cccctccgag 4440gccaagatgt cctgcatgga taacaaggac ggcagctgct cggtcgagta catcccttat 4500gaggctggca cctacagcct caacgtcacc tatggtggcc atcaagtgcc aggcagtcct 4560ttcaaggtcc ctgtgcatga tgtgacagat gcgtccaagg tcaagtgctc tgggcccggc 4620ctgagcccag gcatggttcg tgccaacctc cctcagtcct tccaggtgga cacaagcaag 4680gctggtgtgg ccccattgca ggtcaaagtg caagggccca aaggcctggt ggagccagtg 4740gacgtggtag acaacgctga tggcacccag accgtcaatt atgtgcccag ccgagaaggg 4800ccctacagca tctcagtact gtatggagat gaagaggtac cccggagccc cttcaaggtc 4860aaggtgctgc ctactcatga tgccagcaag gtgaaggcca gtggccccgg gctcaacacc 4920actggcgtgc ctgccagcct gcccgtggag ttcaccatcg atgcaaagga cgccggggag 4980ggcctgctgg ctgtccagat cacggatccc gaaggcaagc cgaagaagac acacatccaa 5040gacaaccatg acggcacgta tacagtggcc tacgtgccag acgtgacagg tcgctacacc 5100atcctcatca agtacggtgg tgacgagatc cccttctccc cgtaccgcgt gcgtgccgtg 5160cccaccgggg acgccagcaa gtgcactgtc acagtgtcaa tcggaggtca cgggctaggt 5220gctggcatcg gccccaccat tcagattggg gaggagacgg tgatcactgt ggacactaag 5280gcggcaggca aaggcaaagt gacgtgcacc gtgtgcacgc ctgatggctc agaggtggat 5340gtggacgtgg tggagaatga ggacggcact ttcgacatct tctacacggc cccccagccg 5400ggcaaatacg tcatctgtgt gcgctttggt ggcgagcacg tgcccaacag ccccttccaa 5460gtgacggctc tggctgggga ccagccctcg gtgcagcccc ctctacggtc tcagcagctg 5520gccccacagt acacctacgc ccagggcggc cagcagactt gggccccgga gaggcccctg 5580gtgggtgtca atgggctgga tgtgaccagc ctgaggccct ttgaccttgt catccccttc 5640accatcaaga agggcgagat cacaggggag gttcggatgc cctcaggcaa ggtggcgcag 5700cccaccatca ctgacaacaa agacggcacc gtgaccgtgc ggtatgcacc cagcgaggct 5760ggcctgcacg agatggacat ccgctatgac aacatgcaca tcccaggaag ccccttgcag 5820ttctatgtgg attacgtcaa ctgtggccat gtcactgcct atgggcctgg cctcacccat 5880ggagtagtga acaagcctgc caccttcacc gtcaacacca aggatgcagg agaggggggc 5940ctgtctctgg ccattgaggg cccgtccaaa gcagaaatca gctgcactga caaccaggat 6000gggacatgca gcgtgtccta cctgcctgtg ctgccggggg actacagcat tctagtcaag 6060tacaatgaac agcacgtccc aggcagcccc ttcactgctc gggtcacagg tgacgactcc 6120atgcgtatgt cccacctaaa ggtcggctct gctgccgaca tccccatcaa catctcagag 6180acggatctca gcctgctgac ggccactgtg gtcccgccct cgggccggga ggagccctgt 6240ttgctgaagc ggctgcgtaa tggccacgtg gggatttcat tcgtgcccaa ggagacgggg 6300gagcacctgg tgcatgtgaa gaaaaatggc cagcacgtgg ccagcagccc catcccggtg 6360gtgatcagcc agtcggaaat tggggatgcc agtcgtgttc gggtctctgg tcagggcctt 6420cacgaaggcc acacctttga gcctgcagag tttatcattg atacccgcga tgcaggctat 6480ggtgggctca gcctgtccat tgagggcccc agcaaggtgg acatcaacac agaggacctg 6540gaggacggga cgtgcagggt cacctactgc cccacagagc caggcaacta catcatcaac 6600atcaagtttg ccgaccagca cgtgcctggc agccccttct ctgtgaaggt gacaggcgag 6660ggccgggtga aagagagcat cacccgcagg cgtcgggctc cttcagtggc caacgttggt 6720agtcattgtg acctcagcct gaaaatccct gaaattagca tccaggatat gacagcccag 6780gtgaccagcc catcgggcaa gacccatgag gccgagatcg tggaagggga gaaccacacc 6840tactgcatcc gctttgttcc cgctgagatg ggcacacaca cagtcagcgt gaagtacaag 6900ggccagcacg tgcctgggag ccccttccag ttcaccgtgg ggcccctagg ggaaggggga 6960gcccacaagg tccgagctgg gggccctggc ctggagagag ctgaagctgg agtgccagcc 7020gaattcagta tctggacccg ggaagctggt gctggaggcc tggccattgc tgtcgagggc 7080cccagcaagg ctgagatctc ttttgaggac cgcaaggacg gctcctgtgg tgtggcttat 7140gtggtccagg agccaggtga ctacgaagtc tcagtcaagt tcaacgagga acacattccc 7200gacagcccct tcgtggtgcc tgtggcttct ccgtctggcg acgcccgccg cctcactgtt 7260tctagccttc aggagtcagg gctaaaggtc aaccagccag cctcttttgc agtcagcctg 7320aacggggcca agggggcgat cgatgccaag gtgcacagcc cctcaggagc cctggaggag 7380tgctatgtca cagaaattga ccaagataag tatgctgtgc gcttcatccc tcgggagaat 7440ggcgtttacc tgattgacgt caagttcaac ggcacccaca tccctggaag ccccttcaag 7500atccgagttg gggagcctgg gcatggaggg gacccaggct tggtgtctgc ttacggagca 7560ggtctggaag gcggtgtcac agggaaccca gctgagttcg tcgtgaacac gagcaatgcg 7620ggagctggtg ccctgtcggt gaccattgac ggcccctcca aggtgaagat ggattgccag 7680gagtgccctg agggctaccg cgtcacctat acccccatgg cacctggcag ctacctcatc 7740tccatcaagt acggcggccc ctaccacatt gggggcagcc ccttcaaggc caaagtcaca 7800ggcccccgtc tcgtcagcaa ccacagcctc cacgagacat catcagtgtt tgtagactct 7860ctgaccaagg ccacctgtgc cccccagcat ggggccccgg gtcctgggcc tgctgacgcc 7920agcaaggtgg tggccaaggg cctggggctg agcaaggcct acgtaggcca gaagagcagc 7980ttcacagtag actgcagcaa agcaggcaac aacatgctgc tggtgggggt tcatggccca 8040aggaccccct gcgaggagat cctggtgaag cacgtgggca gccggctcta cagcgtgtcc 8100tacctgctca aggacaaggg ggagtacaca ctggtggtca aatgggggga cgagcacatc 8160ccaggcagcc cctaccgcgt tgtggtgccc tgagtctggg gcccgtgcca gccggcagcc 8220cccaagcctg ccccgctacc caagcagccc cgccctcttc ccctcaaccc cggcccaggc 8280cgccctggcc gcccgcctgt cactgcagcc gcccctgccc tgtgccgtgc tgcgctcacc 8340tgcctcccca gccagccgct gacctctcgg ctttcacttg ggcagaggga gccatttggt 8400ggcgctgctt gtcttctttg gttctgggag gggtgaggga tgggggtcct gtacacaacc 8460acccactagt tctcttctcc agccaagagg aataaagttt tgcttccatt aaaaaaaaaa 8520aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaa 8557492647PRTHomo sapiens 49Met Ser Ser Ser His Ser Arg Ala Gly Gln Ser Ala Ala Gly Ala Ala1 5 10 15Pro Gly Gly Gly Val Asp Thr Arg Asp Ala Glu Met Pro Ala Thr Glu 20 25 30Lys Asp Leu Ala Glu Asp Ala Pro Trp Lys Lys Ile Gln Gln Asn Thr 35 40 45Phe Thr Arg Trp Cys Asn Glu His Leu Lys Cys Val Ser Lys Arg Ile 50 55 60Ala Asn Leu Gln Thr Asp Leu Ser Asp Gly Leu Arg Leu Ile Ala Leu65 70 75 80Leu Glu Val Leu Ser Gln Lys Lys Met His Arg Lys His Asn Gln Arg 85 90 95Pro Thr Phe Arg Gln Met Gln Leu Glu Asn Val Ser Val Ala Leu Glu 100 105 110Phe Leu Asp Arg Glu Ser Ile Lys Leu Val Ser Ile Asp Ser Lys Ala 115 120 125Ile Val Asp Gly Asn Leu Lys Leu Ile Leu Gly Leu Ile Trp Thr Leu 130 135 140Ile Leu His Tyr Ser Ile Ser Met Pro Met Trp Asp Glu Glu Glu Asp145 150 155 160Glu Glu Ala Lys Lys Gln Thr Pro Lys Gln Arg Leu Leu Gly Trp Ile 165 170 175Gln Asn Lys Leu Pro Gln Leu Pro Ile Thr Asn Phe Ser Arg Asp Trp 180 185 190Gln Ser Gly Arg Ala Leu Gly Ala Leu Val Asp Ser Cys Ala Pro Gly 195 200 205Leu Cys Pro Asp Trp Asp Ser Trp Asp Ala Ser Lys Pro Val Thr Asn 210 215 220Ala Arg Glu Ala Met Gln Gln Ala Asp Asp Trp Leu Gly Ile Pro Gln225 230 235 240Val Ile Thr Pro Glu Glu Ile Val Asp Pro Asn Val Asp Glu His Ser 245 250 255Val Met Thr Tyr Leu Ser Gln Phe Pro Lys Ala Lys Leu Lys Pro Gly 260 265 270Ala Pro Leu Arg Pro Lys Leu Asn Pro Lys Lys Ala Arg Ala Tyr Gly 275 280 285Pro Gly Ile Glu Pro Thr Gly Asn Met Val Lys Lys Arg Ala Glu Phe 290 295 300Thr Val Glu Thr Arg Ser Ala Gly Gln Gly Glu Val Leu Val Tyr Val305 310 315 320Glu Asp Pro Ala Gly His Gln Glu Glu Ala Lys Val Thr Ala Asn Asn 325 330 335Asp Lys Asn Arg Thr Phe Ser Val Trp Tyr Val Pro Glu Val Thr Gly 340 345 350Thr His Lys Val Thr Val Leu Phe Ala Gly Gln His Ile Ala Lys Ser 355 360 365Pro Phe Glu Val Tyr Val Asp Lys Ser Gln Gly Asp Ala Ser Lys Val 370 375 380Thr Ala Gln Gly Pro Gly Leu Glu Pro Ser Gly Asn Ile Ala Asn Lys385 390 395 400Thr Thr Tyr Phe Glu Ile Phe Thr Ala Gly Ala Gly Thr Gly Glu Val 405 410 415Glu Val Val Ile Gln Asp Pro Met Gly Gln Lys Gly Thr Val Glu Pro 420 425 430Gln Leu Glu Ala Arg Gly Asp Ser Thr Tyr Arg Cys Ser Tyr Gln Pro 435 440 445Thr Met Glu Gly Val His Thr Val His Val Thr Phe Ala Gly Val Pro 450 455 460Ile Pro Arg Ser Pro Tyr Thr Val Thr Val Gly Gln Ala Cys Asn Pro465 470 475 480Ser Ala Cys Arg Ala Val Gly Arg Gly Leu Gln Pro Lys Gly Val Arg 485 490 495Val Lys Glu Thr Ala Asp Phe Lys Val Tyr Thr Lys Gly Ala Gly Ser 500 505 510Gly Glu Leu Lys Val Thr Val Lys Gly Pro Lys Gly Glu Glu Arg Val 515 520 525Lys Gln Lys Asp Leu Gly Asp Gly Val Tyr Gly Phe Glu Tyr Tyr Pro 530 535 540Met Val Pro Gly Thr Tyr Ile Val Thr Ile Thr Trp Gly Gly Gln Asn545 550 555 560Ile Gly Arg Ser Pro Phe Glu Val Lys Val Gly Thr Glu Cys Gly Asn 565 570 575Gln Lys Val Arg Ala Trp Gly Pro Gly Leu Glu Gly Gly Val Val Gly 580 585 590Lys Ser Ala Asp Phe Val Val Glu Ala Ile Gly Asp Asp Val Gly Thr 595 600 605Leu Gly Phe Ser Val Glu Gly Pro Ser Gln Ala Lys Ile Glu Cys Asp 610 615 620Asp Lys Gly Asp Gly Ser Cys Asp Val Arg Tyr Trp Pro Gln Glu Ala625 630 635 640Gly Glu Tyr Ala Val His Val Leu Cys Asn Ser Glu Asp Ile Arg Leu 645 650 655Ser Pro Phe Met Ala Asp Ile Arg Asp Ala Pro Gln Asp Phe His Pro 660 665 670Asp Arg Val Lys Ala Arg Gly Pro Gly Leu Glu Lys Thr Gly Val Ala 675 680 685Val Asn Lys Pro Ala Glu Phe Thr Val Asp Ala Lys His Gly Gly Lys 690 695 700Ala Pro Leu Arg Val Gln Val Gln Asp Asn Glu Gly Cys Pro Val Glu705 710 715 720Ala Leu Val Lys Asp Asn Gly Asn Gly Thr Tyr Ser Cys Ser Tyr Val 725 730 735Pro Arg Lys Pro Val Lys His Thr Ala Met Val Ser Trp Gly Gly Val 740 745 750Ser Ile Pro Asn Ser Pro Phe Arg Val Asn Val Gly Ala Gly Ser His 755 760 765Pro Asn Lys Val Lys Val Tyr Gly Pro Gly Val Ala Lys Thr Gly Leu 770 775 780Lys Ala His Glu Pro Thr Tyr Phe Thr Val Asp Cys Ala Glu Ala Gly785 790 795 800Gln Gly Asp Val Ser Ile Gly Ile Lys Cys Ala Pro Gly Val Val Gly 805 810 815Pro Ala Glu Ala Asp Ile Asp Phe Asp Ile Ile Arg Asn Asp Asn Asp 820 825 830Thr Phe Thr Val Lys Tyr Thr Pro Arg Gly Ala Gly Ser Tyr Thr Ile 835 840 845Met Val Leu Phe Ala Asp Gln Ala Thr Pro Thr Ser Pro Ile Arg Val 850 855 860Lys Val Glu Pro Ser His Asp Ala Ser Lys Val Lys Ala Glu Gly Pro865 870 875 880Gly Leu Ser Arg Thr Gly Val Glu Leu Gly Lys Pro Thr His Phe Thr 885 890 895Val Asn Ala Lys Ala Ala Gly Lys Gly Lys Leu Asp Val Gln Phe Ser 900 905 910Gly Leu Thr Lys Gly Asp Ala Val Arg Asp Val Asp Ile Ile Asp His 915 920 925His Asp Asn Thr Tyr Thr Val Lys Tyr Thr Pro Val Gln Gln Gly Pro 930 935 940Val Gly Val Asn Val Thr Tyr Gly Gly Asp Pro Ile Pro Lys Ser Pro945 950 955 960Phe Ser Val Ala Val Ser Pro Ser Leu Asp Leu Ser Lys Ile Lys Val 965 970 975Ser Gly Leu Gly Glu Lys Val Asp Val Gly Lys Asp Gln Glu Phe Thr 980 985 990Val Lys Ser Lys Gly Ala Gly Gly Gln Gly Lys Val Ala Ser Lys Ile 995 1000 1005Val Gly Pro Ser Gly Ala Ala Val Pro Cys Lys Val Glu Pro Gly 1010 1015 1020Leu Gly Ala Asp Asn Ser Val Val Arg Phe Leu Pro Arg Glu Glu 1025 1030 1035Gly Pro Tyr Glu Val Glu Val Thr Tyr Asp Gly Val Pro Val Pro 1040 1045 1050Gly Ser Pro Phe Pro Leu Glu Ala Val Ala Pro Thr Lys Pro Ser 1055 1060 1065Lys Val Lys Ala Phe Gly Pro Gly Leu Gln Gly Gly Ser Ala Gly 1070 1075 1080Ser Pro Ala Arg Phe Thr Ile Asp Thr Lys Gly Ala Gly Thr Gly 1085 1090 1095Gly Leu Gly Leu Thr Val Glu Gly Pro Cys Glu Ala Gln Leu Glu 1100 1105 1110Cys Leu Asp Asn Gly Asp Gly Thr Cys Ser Val Ser Tyr Val Pro 1115 1120 1125Thr Glu Pro Gly Asp Tyr Asn Ile Asn Ile Leu Phe Ala Asp Thr 1130 1135 1140His Ile Pro Gly Ser Pro Phe Lys Ala His Val Val Pro Cys Phe 1145 1150 1155Asp Ala Ser Lys Val Lys Cys Ser Gly Pro Gly Leu Glu Arg Ala 1160 1165 1170Thr Ala Gly Glu Val Gly Gln Phe Gln Val Asp Cys Ser Ser Ala 1175 1180 1185Gly Ser Ala Glu Leu Thr Ile Glu Ile Cys Ser Glu Ala Gly Leu 1190 1195 1200Pro Ala Glu Val Tyr Ile Gln Asp His Gly Asp Gly Thr His Thr 1205 1210 1215Ile Thr Tyr Ile Pro Leu Cys Pro Gly Ala Tyr Thr Val Thr Ile 1220 1225 1230Lys Tyr Gly Gly

Gln Pro Val Pro Asn Phe Pro Ser Lys Leu Gln 1235 1240 1245Val Glu Pro Ala Val Asp Thr Ser Gly Val Gln Cys Tyr Gly Pro 1250 1255 1260Gly Ile Glu Gly Gln Gly Val Phe Arg Glu Ala Thr Thr Glu Phe 1265 1270 1275Ser Val Asp Ala Arg Ala Leu Thr Gln Thr Gly Gly Pro His Val 1280 1285 1290Lys Ala Arg Val Ala Asn Pro Ser Gly Asn Leu Thr Glu Thr Tyr 1295 1300 1305Val Gln Asp Arg Gly Asp Gly Met Tyr Lys Val Glu Tyr Thr Pro 1310 1315 1320Tyr Glu Glu Gly Leu His Ser Val Asp Val Thr Tyr Asp Gly Ser 1325 1330 1335Pro Val Pro Ser Ser Pro Phe Gln Val Pro Val Thr Glu Gly Cys 1340 1345 1350Asp Pro Ser Arg Val Arg Val His Gly Pro Gly Ile Gln Ser Gly 1355 1360 1365Thr Thr Asn Lys Pro Asn Lys Phe Thr Val Glu Thr Arg Gly Ala 1370 1375 1380Gly Thr Gly Gly Leu Gly Leu Ala Val Glu Gly Pro Ser Glu Ala 1385 1390 1395Lys Met Ser Cys Met Asp Asn Lys Asp Gly Ser Cys Ser Val Glu 1400 1405 1410Tyr Ile Pro Tyr Glu Ala Gly Thr Tyr Ser Leu Asn Val Thr Tyr 1415 1420 1425Gly Gly His Gln Val Pro Gly Ser Pro Phe Lys Val Pro Val His 1430 1435 1440Asp Val Thr Asp Ala Ser Lys Val Lys Cys Ser Gly Pro Gly Leu 1445 1450 1455Ser Pro Gly Met Val Arg Ala Asn Leu Pro Gln Ser Phe Gln Val 1460 1465 1470Asp Thr Ser Lys Ala Gly Val Ala Pro Leu Gln Val Lys Val Gln 1475 1480 1485Gly Pro Lys Gly Leu Val Glu Pro Val Asp Val Val Asp Asn Ala 1490 1495 1500Asp Gly Thr Gln Thr Val Asn Tyr Val Pro Ser Arg Glu Gly Pro 1505 1510 1515Tyr Ser Ile Ser Val Leu Tyr Gly Asp Glu Glu Val Pro Arg Ser 1520 1525 1530Pro Phe Lys Val Lys Val Leu Pro Thr His Asp Ala Ser Lys Val 1535 1540 1545Lys Ala Ser Gly Pro Gly Leu Asn Thr Thr Gly Val Pro Ala Ser 1550 1555 1560Leu Pro Val Glu Phe Thr Ile Asp Ala Lys Asp Ala Gly Glu Gly 1565 1570 1575Leu Leu Ala Val Gln Ile Thr Asp Pro Glu Gly Lys Pro Lys Lys 1580 1585 1590Thr His Ile Gln Asp Asn His Asp Gly Thr Tyr Thr Val Ala Tyr 1595 1600 1605Val Pro Asp Val Thr Gly Arg Tyr Thr Ile Leu Ile Lys Tyr Gly 1610 1615 1620Gly Asp Glu Ile Pro Phe Ser Pro Tyr Arg Val Arg Ala Val Pro 1625 1630 1635Thr Gly Asp Ala Ser Lys Cys Thr Val Thr Val Ser Ile Gly Gly 1640 1645 1650His Gly Leu Gly Ala Gly Ile Gly Pro Thr Ile Gln Ile Gly Glu 1655 1660 1665Glu Thr Val Ile Thr Val Asp Thr Lys Ala Ala Gly Lys Gly Lys 1670 1675 1680Val Thr Cys Thr Val Cys Thr Pro Asp Gly Ser Glu Val Asp Val 1685 1690 1695Asp Val Val Glu Asn Glu Asp Gly Thr Phe Asp Ile Phe Tyr Thr 1700 1705 1710Ala Pro Gln Pro Gly Lys Tyr Val Ile Cys Val Arg Phe Gly Gly 1715 1720 1725Glu His Val Pro Asn Ser Pro Phe Gln Val Thr Ala Leu Ala Gly 1730 1735 1740Asp Gln Pro Ser Val Gln Pro Pro Leu Arg Ser Gln Gln Leu Ala 1745 1750 1755Pro Gln Tyr Thr Tyr Ala Gln Gly Gly Gln Gln Thr Trp Ala Pro 1760 1765 1770Glu Arg Pro Leu Val Gly Val Asn Gly Leu Asp Val Thr Ser Leu 1775 1780 1785Arg Pro Phe Asp Leu Val Ile Pro Phe Thr Ile Lys Lys Gly Glu 1790 1795 1800Ile Thr Gly Glu Val Arg Met Pro Ser Gly Lys Val Ala Gln Pro 1805 1810 1815Thr Ile Thr Asp Asn Lys Asp Gly Thr Val Thr Val Arg Tyr Ala 1820 1825 1830Pro Ser Glu Ala Gly Leu His Glu Met Asp Ile Arg Tyr Asp Asn 1835 1840 1845Met His Ile Pro Gly Ser Pro Leu Gln Phe Tyr Val Asp Tyr Val 1850 1855 1860Asn Cys Gly His Val Thr Ala Tyr Gly Pro Gly Leu Thr His Gly 1865 1870 1875Val Val Asn Lys Pro Ala Thr Phe Thr Val Asn Thr Lys Asp Ala 1880 1885 1890Gly Glu Gly Gly Leu Ser Leu Ala Ile Glu Gly Pro Ser Lys Ala 1895 1900 1905Glu Ile Ser Cys Thr Asp Asn Gln Asp Gly Thr Cys Ser Val Ser 1910 1915 1920Tyr Leu Pro Val Leu Pro Gly Asp Tyr Ser Ile Leu Val Lys Tyr 1925 1930 1935Asn Glu Gln His Val Pro Gly Ser Pro Phe Thr Ala Arg Val Thr 1940 1945 1950Gly Asp Asp Ser Met Arg Met Ser His Leu Lys Val Gly Ser Ala 1955 1960 1965Ala Asp Ile Pro Ile Asn Ile Ser Glu Thr Asp Leu Ser Leu Leu 1970 1975 1980Thr Ala Thr Val Val Pro Pro Ser Gly Arg Glu Glu Pro Cys Leu 1985 1990 1995Leu Lys Arg Leu Arg Asn Gly His Val Gly Ile Ser Phe Val Pro 2000 2005 2010Lys Glu Thr Gly Glu His Leu Val His Val Lys Lys Asn Gly Gln 2015 2020 2025His Val Ala Ser Ser Pro Ile Pro Val Val Ile Ser Gln Ser Glu 2030 2035 2040Ile Gly Asp Ala Ser Arg Val Arg Val Ser Gly Gln Gly Leu His 2045 2050 2055Glu Gly His Thr Phe Glu Pro Ala Glu Phe Ile Ile Asp Thr Arg 2060 2065 2070Asp Ala Gly Tyr Gly Gly Leu Ser Leu Ser Ile Glu Gly Pro Ser 2075 2080 2085Lys Val Asp Ile Asn Thr Glu Asp Leu Glu Asp Gly Thr Cys Arg 2090 2095 2100Val Thr Tyr Cys Pro Thr Glu Pro Gly Asn Tyr Ile Ile Asn Ile 2105 2110 2115Lys Phe Ala Asp Gln His Val Pro Gly Ser Pro Phe Ser Val Lys 2120 2125 2130Val Thr Gly Glu Gly Arg Val Lys Glu Ser Ile Thr Arg Arg Arg 2135 2140 2145Arg Ala Pro Ser Val Ala Asn Val Gly Ser His Cys Asp Leu Ser 2150 2155 2160Leu Lys Ile Pro Glu Ile Ser Ile Gln Asp Met Thr Ala Gln Val 2165 2170 2175Thr Ser Pro Ser Gly Lys Thr His Glu Ala Glu Ile Val Glu Gly 2180 2185 2190Glu Asn His Thr Tyr Cys Ile Arg Phe Val Pro Ala Glu Met Gly 2195 2200 2205Thr His Thr Val Ser Val Lys Tyr Lys Gly Gln His Val Pro Gly 2210 2215 2220Ser Pro Phe Gln Phe Thr Val Gly Pro Leu Gly Glu Gly Gly Ala 2225 2230 2235His Lys Val Arg Ala Gly Gly Pro Gly Leu Glu Arg Ala Glu Ala 2240 2245 2250Gly Val Pro Ala Glu Phe Ser Ile Trp Thr Arg Glu Ala Gly Ala 2255 2260 2265Gly Gly Leu Ala Ile Ala Val Glu Gly Pro Ser Lys Ala Glu Ile 2270 2275 2280Ser Phe Glu Asp Arg Lys Asp Gly Ser Cys Gly Val Ala Tyr Val 2285 2290 2295Val Gln Glu Pro Gly Asp Tyr Glu Val Ser Val Lys Phe Asn Glu 2300 2305 2310Glu His Ile Pro Asp Ser Pro Phe Val Val Pro Val Ala Ser Pro 2315 2320 2325Ser Gly Asp Ala Arg Arg Leu Thr Val Ser Ser Leu Gln Glu Ser 2330 2335 2340Gly Leu Lys Val Asn Gln Pro Ala Ser Phe Ala Val Ser Leu Asn 2345 2350 2355Gly Ala Lys Gly Ala Ile Asp Ala Lys Val His Ser Pro Ser Gly 2360 2365 2370Ala Leu Glu Glu Cys Tyr Val Thr Glu Ile Asp Gln Asp Lys Tyr 2375 2380 2385Ala Val Arg Phe Ile Pro Arg Glu Asn Gly Val Tyr Leu Ile Asp 2390 2395 2400Val Lys Phe Asn Gly Thr His Ile Pro Gly Ser Pro Phe Lys Ile 2405 2410 2415Arg Val Gly Glu Pro Gly His Gly Gly Asp Pro Gly Leu Val Ser 2420 2425 2430Ala Tyr Gly Ala Gly Leu Glu Gly Gly Val Thr Gly Asn Pro Ala 2435 2440 2445Glu Phe Val Val Asn Thr Ser Asn Ala Gly Ala Gly Ala Leu Ser 2450 2455 2460Val Thr Ile Asp Gly Pro Ser Lys Val Lys Met Asp Cys Gln Glu 2465 2470 2475Cys Pro Glu Gly Tyr Arg Val Thr Tyr Thr Pro Met Ala Pro Gly 2480 2485 2490Ser Tyr Leu Ile Ser Ile Lys Tyr Gly Gly Pro Tyr His Ile Gly 2495 2500 2505Gly Ser Pro Phe Lys Ala Lys Val Thr Gly Pro Arg Leu Val Ser 2510 2515 2520Asn His Ser Leu His Glu Thr Ser Ser Val Phe Val Asp Ser Leu 2525 2530 2535Thr Lys Ala Thr Cys Ala Pro Gln His Gly Ala Pro Gly Pro Gly 2540 2545 2550Pro Ala Asp Ala Ser Lys Val Val Ala Lys Gly Leu Gly Leu Ser 2555 2560 2565Lys Ala Tyr Val Gly Gln Lys Ser Ser Phe Thr Val Asp Cys Ser 2570 2575 2580Lys Ala Gly Asn Asn Met Leu Leu Val Gly Val His Gly Pro Arg 2585 2590 2595Thr Pro Cys Glu Glu Ile Leu Val Lys His Val Gly Ser Arg Leu 2600 2605 2610Tyr Ser Val Ser Tyr Leu Leu Lys Asp Lys Gly Glu Tyr Thr Leu 2615 2620 2625Val Val Lys Trp Gly Asp Glu His Ile Pro Gly Ser Pro Tyr Arg 2630 2635 2640Val Val Val Pro 2645

Claims

1. A method for detecting the level of filamin A in a sample from a subject comprising: (a) selecting a subject who has elevated PSA and is symptomatic of prostate cancer; (b) isolating a serum sample or a plasma sample from the subject, and (c) detecting the protein level of filamin A in the serum sample or plasma sample.

2. The method of claim 1, further comprising detecting the level of one or more additional markers of prostate cancer in the sample.

3. The method of claim 2, wherein the one or more additional markers of prostate cancer is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, and prostate specific antigen (PSA).

4. (canceled)

5. The method of claim 96, wherein the reagent is an anti-filamin A antibody that selectively binds to at least one epitope of filamin A.

6. The method of claim 5, wherein the level of filamin A protein is determined by immunoassay or ELISA.

7. (canceled)

8. (canceled)

9. (canceled)

10. (canceled)

11. (canceled)

12. (canceled)

13. (canceled)

14. (canceled)

15. A method for detecting the level of filamin A in a sample from a subject comprising: (a) obtaining a serum sample or a plasma sample from a subject, wherein the subject has elevated PSA and is symptomatic of prostate cancer, and (b) detecting the protein level of filamin A in the serum sample or plasma sample.

16. The method of claim 97, wherein the reagent is an anti-filamin A antibody that selectively binds to at least one epitope of filamin A.

17. The method of claim 16, wherein the antibody comprises a detectable label.

18. The method of claim 16, wherein the step of detecting the level of the complex further comprises contacting the complex with a detectable secondary antibody and measuring the level of the secondary antibody.

19. The method of claim 15, further comprising detecting the level of one or more additional markers of prostate cancer.

20. The method of claim 19, wherein the one or more additional markers of prostate cancer is selected from the group consisting of filamin B, LY9, keratin 4, keratin 7, keratin 8, keratin 15, keratin 18, keratin 19, tubulin-beta 3, and prostate specific antigen (PSA).

21. (canceled)

22. (canceled)

23. (canceled)

24. The method of claim 16, wherein the level of the complex is detected by immunoassay or ELISA.

25.-67.

68. A kit for detecting filamin A in a biological sample from a subject having, suspected of having, or at risk for having prostate cancer comprising at least one reagent for measuring the level of filamin A in the biological sample from the subject, and a set of instructions for measuring the level of filamin A in the biological sample from the subject.

69-86. (canceled)

87. The method of any one of claims 1-3, 5, 6, 15-20, 24, and 94-97, further comprising determining the age of the subject.

88.-93. (canceled)

94. The method of claim 5, wherein the antibody comprises a detectable label.

95. The method of claim 5, wherein the step of detecting the level of the complex further comprises contacting the complex with a detectable secondary antibody and measuring the level of the secondary antibody.

96. The method of claim 1, wherein detecting the protein level of filamin A in the serum sample or plasma sample is by contacting the sample with a reagent that selectively binds keratin A, allowing a complex to form between the reagent and filamin A, and detecting the level of the complex.

97. The method of claim 15, wherein detecting the protein level of filamin A in the serum sample or plasma sample is by contacting the sample with a reagent that selectively binds keratin A, allowing a complex to form between the reagent and filamin A, and detecting the level of the complex.