ABHD5 AND PARTIAL HDAC4 FRAGMENTS AND VARIANTS AS A THERAPEUTIC APPROACH FOR THE TREATMENT OF CARDIOVASCULAR DISEASES

Abstract

The present invention relates to Abhydrolase containing domain 5 (ABHD5) and N-terminal fragments of HDAC4 (HDAC4-NT) and variants of the aforementioned peptides for the treatment and prevention of heart failure. The present invention further provides vectors for the cardiomyocyte-specific expression of said peptides and a test system comprising ABHD5 for the identification of novel compounds which are useful for the treatment of heart failure.

Description

[0001] The present invention relates to Abhydrolase containing domain 5 (ABHD5) and N-terminal fragments of HDAC4 (HDAC4-NT) and variants of the aforementioned peptides for the treatment and prevention of heart failure. The present invention further provides vectors for the cardiomyocyte-specific expression of said peptides and a test system comprising ABHD5 for the identification of novel compounds which are useful for the treatment of heart failure.

TECHNICAL BACKGROUND

[0002] Sustained catecholaminergic stress is known to promote heart failure (Cohn et al., 1984 "Plasma Norepinephrine as a Guide to Prognosis in Patients with Chronic Congestive Heart Failure" New England Journal of Medicine, 311: 819-823). In contrast to this, short-term catecholaminergic stimulation (e.g. by physical exercise) promotes cardiac health (Keteyian et al, 2010 "Clinical Role of Exercise Training in the Management of Patients with Chronic Heart Failure" Journal of Cardiopulmonary Rehabilitation and Prevention, 30:67-76). Thus, there appear to be different signaling pathways downstream of the .beta.-adrenergic receptor mediating cardioprotective and pathophysiological effects of .beta.-adrenergic receptor stimulation. One consequence of sustained catecholaminergic stress is myocardial remodeling which causes or exacerbates heart failure. Thus, therapeutic means for influencing said signaling pathways are desirable.

[0003] Full-length histone deacetylase 4 (HDAC4) is proteolytically processed by a previously unknown enzyme yielding an N-terminal fragment (HDAC4-NT) comprising 201 amino acids. In vitro, HDAC4-NT selectively represses myocyte enhancer factor 2 (MEF2) (Backs et al., 2011, "Selective repression of MEF2 Activity by PKA-dependent Proteolysis of HDAC4", Journal of Cell Biology, 195: 403-415).

[0004] Abhydrolase containing domain 5 (ABHD5, also known as "comparative gene identification-58" (CGI-58)) is a protein which has been previously known to be involved in lipid metabolism (Grannemann et al., 2009 "Perilipin controls Lipolysis by regulating the Interactions of AB-hydrolase Containing 5 (Abhd5) and Adipose Triglyceride Lipase (Atgl)", The Journal of Biological Chemistry 284: 34538-34544). Mutations of ABHD5 cause the Chanarin-Dorfman syndrome, a rare genetic disease characterized by excessive accumulation of triacylglycerol in multiple tissues (Lass et al., 2006 "Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome" Cell Metabolism 3: 309-319). It has not been implicated in the regulation of cardiac remodeling.

[0005] Thus, the problem underlying the present invention can be viewed as the provision of novel means and methods for the treatment and prevention of heart failure.

SUMMARY OF THE INVENTION

[0006] In a first aspect, the present invention relates to abhydrolase containing domain 5 (ABHD5) or a variant thereof for use as a medicament.

[0007] In another aspect, the present invention relates to ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0008] In yet another aspect, the present invention relates to a nucleic acid encoding ABHD5 or a variant thereof for use as a medicament.

[0009] In yet another aspect, the present invention relates to a nucleic acid encoding ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0010] In yet another aspect, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof.

[0011] In yet another aspect, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof for use as a medicament.

[0012] In yet another aspect, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0013] In yet another embodiment, the present invention relates to an elongated and/or multimerized variant of the N-terminal fragment of histone deacetylase 4 (HDAC4-NT).

[0014] In yet another embodiment, the present invention relates to HDAC4-NT or a variant thereof for use as a medicament.

[0015] In yet another embodiment, the present invention relates to HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0016] In yet another aspect, the present invention relates to a nucleic acid encoding an elongated and/or multimerized variant of HDAC-NT.

[0017] In yet another aspect, the present invention relates to a nucleic acid encoding HDAC4-NT or a variant thereof for use as a medicament.

[0018] In yet another aspect, the present invention relates to a nucleic acid encoding HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0019] In yet another aspect, the present invention relates to a vector comprising nucleic acid encoding HDAC4-NT or a variant thereof.

[0020] In yet another aspect, the present invention relates to a nucleic acid encoding HDAC4-NT or a variant thereof for use as a medicament.

[0021] In yet another aspect, the present invention relates to a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0022] In yet another aspect, the present invention relates to a method for identifying a compound which modulates the activity and/or localization of ABHD5 or a variant thereof comprising the steps of

[0023] a) contacting a test system comprising ABHD5 or a variant thereof with a candidate compound;

[0024] b) determining whether the candidate compound modulates the activity and/or localization of ABHD5 or the variant thereof;

[0025] c) identifying the compound as a compound which modulating the activity and/or localization of ABHD5 based on the comparison of the activity of ABHD5 or the variant thereof in the test system comprising the candidate compound and the activity of ABHD or the variant thereof determined in a control in step b).

[0026] In yet another aspect, the present invention relates to the use of ABHD5 for identifying a compound which suppresses myocardial remodeling.

DETAILED DESCRIPTION OF THE INVENTION

[0027] Before the present invention is described in detail below, it is to be understood that this invention is not limited to the particular methodology, protocols and reagents described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art.

[0028] In the following, the elements of the present invention will be described. These elements are listed with specific embodiments, however, it should be understood that they may be combined in any manner and in any number to create additional embodiments. The variously described examples and preferred embodiments should not be construed to limit the present invention to only the explicitly described embodiments. This description should be understood to support and encompass embodiments which combine the explicitly described embodiments with any number of the disclosed and/or preferred elements. Furthermore, any permutations and combinations of all described elements in this application should be considered disclosed by the description of the present application unless the context indicates otherwise.

[0029] Preferably, the terms used herein are defined as described in "A multilingual glossary of biotechnological terms: (IUPAC Recommendations)", H. G. W. Leuenberger, B. Nagel, and H. Kolbl, Eds., Helvetica Chimica Acta, CH-4010 Basel, Switzerland, (1995).

[0030] To practice the present invention, unless otherwise indicated, conventional methods of chemistry, biochemistry, cell biology, and recombinant DNA techniques are employed which are explained in the literature in the field (cf., e.g., Molecular Cloning: A Laboratory Manual, 2.sup.nd Edition, J. Sambrook et al. eds., Cold Spring Harbor Laboratory Press, Cold Spring Harbor 1989). Furthermore, conventional methods of clinical cardiology are employed which are also explained in the literature in the field (cf., e.g., Practical Methods in Cardiovascular Research, S. Dhein et al. eds., Springer Verlag Berlin Heidelberg, 2005).

[0031] Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. As used in this specification and the appended claims, the singular forms "a", "an", and "the" include plural referents, unless the content clearly dictates otherwise.

[0032] Several documents are cited throughout the text of this specification. Each of the documents cited herein (including all patents, patent applications, scientific publications, manufacturer's specifications, instructions, etc.), whether supra or infra, are hereby incorporated by reference in their entirety. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention.

ABHD5 and Variants Thereof

[0033] It has been surprisingly found in the study underlying the present invention that inhibition of expression of ABHD5 prevents the proteolytic cleavage of full-length HDAC4, thus generating HDAC4-NT. Based on sequence analysis, it is likely that ABHD5 is a serine protease which cleaves HDAC4. Based on this finding, the ABHD5 can be used for generating HDAC4-NT in vivo, thus protecting the myocardium from heart failure.

[0034] Therefore, the present invention relates to abhydrolase containing domain 5 (ABHD5) or a variant thereof for use as a medicament.

[0035] In another embodiment, the present invention relates to ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0036] The term "ABHD5" relates to a polypeptide having an amino acid sequence as defined by one of the sequences SEQ ID NO: 1 to 5 or a variant thereof. Preferably, ABDH5 has an amino acid as defined by SEQ ID NO: 1 (human ABDH5) or a variant thereof.

[0037] "Variants" are preferably N-terminally and/or C-terminally truncated variants, amino acid substitution or deletion variants, or prolonged variants of the sequences of SEQ ID NO: 1 to 5. Variants comprise furthermore an amino acid sequence comprising modified amino acid(s), unnatural amino acid(s) or peptidomimetic(s) or further compounds which can mimic a peptide backbone/structure. Preferably, variants are selected from C-terminally truncated variants of SEQ ID NO.: 1 to 5; amino acid substitution or deletion variants; variants comprising modified amino acid(s), unnatural amino acid(s) or peptidomimetic(s) or further compounds which can mimic a peptide backbone/structure.

[0038] Deletion variants are, preferably, characterized by C-terminal deletion of up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids. Independently of the presence or absence of C-terminal deletions further preferred deletion variants are characterized by N-terminal deletion of up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids.

[0039] The term "ABDH5 variants" preferably includes proteins which have at least 60%, 65%, 70%, 80%, 81%, 82%, 83%, 84%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence similarity, preferably sequence identity over the entire length of the protein according to SEQ ID NO: 1 to 5 or proteins based on SEQ ID NO: 1 to 5 carrying above outlined N- and/or C-terminal deletions using the best sequence alignment and/or over the region of the best sequence alignment, wherein the best sequence alignment is obtainable with art known tools, e.g. Align, using standard settings, preferably EMBOSS::needle, Matrix: Blosum62, Gap Open 10.0, Gap Extend 0.5, with the amino acid sequence set forth in SEQ ID NOs: 1, 2, 3, 4, or 5. It is preferred that when a given ABDH5 variant is aligned with a ABDH5 according to SEQ ID NO:1, 2, 3, 4 or 5 that alignment will be over the entire length of the two proteins and, thus, that the alignment score will be determined on this basis.

[0040] In especially preferred deletion variants, the first 29 or, more preferably, the first 31 amino at the N-terminus are deleted. Human ABHD5 comprises tryptophan residues at positions 19, 23 and 27. Rat and mouse ABHD5 comprise tryptophan residues at positions 21, 25 and 29. Said tryptophan residues are responsible for the binding of ABHD5 to lipid droplets. Deletion of these tryptophan residues creates a variant of ABHD5 which has less affinity to lipid droplets. Thus, such deletion variants move more easily to the nucleus and the cytosol where they mediate cleavage of full-length HDAC4 yielding HDAC4-NT.

[0041] Deletions in further preferred deletion variants are designed to remove only the first or only the first and second tryptophan residues. Thus, these deletion variants have a lower affinity to lipid droplets as compared to full-length ABHD5 but higher affinity as compared to deletion variants missing the first 27 or 30 amino acids.

[0042] Preferred substitution variants are generated by substituting up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids against natural amino acids, unnatural amino acids or peptidomimetics. Preferably, the amino acids of the wild type protein or a deletion variant thereof are substituted for natural amino acids. more preferably, said substitutions are conservative substitutions.

[0043] A "conservative amino acid substitution" is one in which an amino acid residue is substituted by another amino acid residue having a side chain (R group) with similar chemical properties (e.g., charge or hydrophobicity). In general, a conservative amino acid substitution will not substantially change the functional properties of a protein. In cases, where two or more amino acid sequences differ from each other by conservative substitutions, the number of substitutions may be adjusted upwards to correct for the conservative nature of the substitution. Thus, in the case of conservative amino acid substitutions up to 40, up to 50 or even up to 70 amino acids may be substituted. Examples of groups of amino acids that have side chains with similar chemical properties include: 1) aliphatic side chains: glycine, alanine, valine, leucine and isoleucine;

[0044] 2) aliphatic-hydroxyl side chains: serine and threonine;

[0045] 3) amide-containing side chains: asparagine and glutamine;

[0046] 4) aromatic side chains: phenylalanine, tyrosine, and tryptophan;

[0047] 5) basic side chains: lysine, arginine, and histidine;

[0048] 6) acidic side chains: aspartate and glutamate, and

[0049] 7) sulfur-containing side chains: cysteine and methionine.

[0050] Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, glutamate-aspartate, and asparagine-glutamine. Alternatively, a conservative replacement is any change having a positive value in the PAM250 log-likelihood matrix disclosed in Gonnet G. H. et al, 1992 "Exhaustive matching of the entire protein sequence database." Science 1992, 256:1443-1445. A "moderately conservative" replacement is any change having a non-negative value in the PAM250 log-likelihood matrix.

[0051] In especially preferred substitution variants preferably 1, more preferably 2 and most preferably 3 of the tryptophan residues mentioned above (positions 19, 23 and 27 in human ABHD5; positions 22, 26 and 30 in mouse or rat ABHD5) are substituted by a different amino acid. Preferably, said substitution is not a conservative substitution and more preferably, the amino acid which takes the place of tryptophan is alanine.

[0052] In one preferred embodiment, positions 19 and 23 of human ABHAD5 or positions 22 and 26 of rat ABHD5 are substituted, preferably with alanine.

[0053] In another preferred embodiment, positions 23 and 27 of human ABHAD5 or positions 26 and 30 of rat ABHD5 are substituted, preferably with alanine.

[0054] A "variant" as defined above is, preferably, a functional variant. A functional variant is a variant of the wild type ADHD5 as described above which retains its capability to mediate cleavage of full-length HDAC4 in vitro and, preferably, in vivo. Preferably, the ADHD5 variant has at least 50% of the capability of ADHD5 according to SEQ ID NO: 1 to 5, preferably of SEQ I NO: 1 to mediate cleavage of full-length HDAC4 in vitro and, preferably, in vivo, more preferably at least 60%, 70%, 80%, 90%, 95% or 100% of this activity.

[0055] An assay for testing whether a variant of ABDH5 is still functional can be based on a cell line which does not express ABDH5 due to a knock out. As described in the examples, inhibition of ABHD5 expression inhibits cleavage of HDAC4. If the cells are then transfected with an expression vector encoding the variant of ABHD5 to be tested, a functional variant restores the cell's capability of generating HDAC4-NT from full-length HDAC4, while a non-functional variant does not. Alternatively, the variant of ABDH5 may be administered to the cells as a peptide.

[0056] An even more preferred assay can be conducted in vitro: Since ABDH5 is a putative protease, functional variants of ABDH5 are able to cleave full-length HDAC4 if the required ions and cofactors are present.

Heart Failure

[0057] The term "heart failure" as used in the present application refers to any conditions characterized by the inability of the heart to pump a sufficient amount of blood to meet the body's oxygen demand.

[0058] Heart failure may affect the right ventricle, the left ventricle or both ventricles. The present invention relates to the treatment or prevention of all of the aforementioned types of heart failure and all degrees of heart failure as set forth below.

[0059] The typical symptom experienced by a patient suffering from left-ventricular heart failure is shortness of breath (dyspnea). In mild forms of heart failure, the patient is not limited in ordinary physical activity but experiences dyspnea during periods of increased physical exercise. In more severe cases of heart failure, dyspnea is experienced during ordinary or even light physical activity. In the most severe cases, the patient even experiences dyspnea at rest. The typical symptom of right ventricular heart failure is the congestion of systemic capillaries leading to the accumulation of fluids in various parts of the body. Fluid accumulates in the feet and legs (in people standing up) or in the sacral area (in people lying down). In severe cases fluid accumulates in the abdominal cavity and/or the liver.

[0060] Heart failure may be divided into inherited and acquired forms of the disease. Inherited forms of the disease include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, isolated ventricular non-compaction and mitochondrial myopathy. Acquired heart failure is typically caused by coronary artery disease, arterial hypertension, loss of viable myocardium due to myocardial infarction, cigarette smoking, obesity, diabetes, metabolic syndrome, kidney disease, environmental stress, depressive or mood disorders, lipid storage disease, cancer, chronic inflammation, postpartal cardiomyopathy, stress induced cardiomyopathy, transient cardiac dysfunction or valvular heart disease. It is particularly preferred that acquired cardiomyopathies are treated, in particular postpartal cardiomyopathy, stress induced cardiomyopathy, transient cardiac dysfunction.

[0061] The means and methods of the present invention are suited for the treatment of all the aforementioned types of heart failure.

[0062] Heart failure is caused or accompanied by myocardial remodeling. In myocardial remodeling, terminally differentiated cardiomyocytes increase in size in order to increase the contractility of the myocardium. However, this leads to increasing stiffness of the heart and concomitantly to difficulties in filling the ventricles during diastole. Moreover, the ventricles enlarge contributing to a more spherical form of the heart. This spherical shape of the heart decreases the stroke volume. Since myocardial remodeling tends to decrease myocardial output rather than increasing it, the process of myocardial remodeling causes and exacerbates heart failure.

[0063] As a consequence of myocardial remodeling, the risk of cardiac dysrhythmia increases. The term "cardiac dysrhythmia" refers to all types abnormal electric activity of the myocardium. Preferably, cardiac dysrhythmia is tachycardia (pathologically increased heart beat) or bradycardia (pathologically decreased heart beat). Cardiac dysrhythmia may originate from the atria or the ventricles. Particularly relevant types of dysrhythmia are atrial fibrillation and ventricular tachycardia.

[0064] Therefore, the means and methods of the present invention which suppress or reverse the process of myocardial remodeling during heart failure are well suited for the treatment or prevention of myocardial remodeling, thus increasing cardiac output and decreasing the risk of complications of cardiac remodeling, particularly cardiac dysrhythmia as defined above.

[0065] The success of the treatment according to the present invention may be verified by echocardiography or magnetic resonance imaging. Moreover, decreasing levels of natriuretic peptides, particularly nT-proBNP after onset of treatment indicate that the treatment is successful.

Patient

[0066] The patient receiving the pharmaceutical compounds and pharmaceutical compositions disclosed in the present application is preferably a primate, rodent, pig, sheep, cow or goat. The rodent is, preferably, a rat and more preferably a mouse. The primate is, preferably, a human, chimpanzee or macaque. Most preferably, the patient is a human.

[0067] Preferably, the patient suffers from heart failure.

Treatment

[0068] As used herein, "treat", "treating" or "treatment" of a heart failure means refers to at least one of the following: (a) reducing the severity of heart failure, (b) limiting or preventing the symptoms typical for heart failure, (c) reversing myocardial remodeling, (d) preventing further progress of myocardial remodeling, and (e) decreasing the likelihood of the negative consequences of myocardial remodeling described above. Preferably, a patient to be treated already suffers from heart failure and/or myocardial remodeling.

[0069] As used herein, "prevent", "preventing" or "prevention" refer to the inhibition of the onset of heart failure and/or myocardial remodeling in a patient not yet suffering from the aforementioned disorders. Thus, a patient receiving preventive treatment is healthy with respect to the disorder to be prevented by said treatment. In a preferred embodiment of the present invention, the patient suffers from heart failure but does not yet show signs and symptoms of myocardial remodeling.

[0070] It is understood by the person skilled in the art that "treatment" or prevention" may not be successful in every patient receiving the pharmaceutical compounds or composition of the present invention. However, the terms "treatment" and "prevention" require that a significant proportion of patient benefits from said treatment.

[0071] In patients suffering from primary heart failure as defined above, treatment according to the present invention preferably cures heart failure because it removes or alleviates the underlying cause.

[0072] In patients suffering from secondary heart failure as defined above, the treatment according to the present invention preferably decreases the speed of progression of heart failure or even stops progression of heart failure completely.

Nucleic Acid

[0073] In yet another aspect, the present invention relates to a nucleic acid encoding ABHD5 or a variant thereof for use as a medicament.

[0074] In yet another aspect, the present invention relates to a nucleic acid encoding ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0075] The term "nucleic acid" refers to a polymeric macromolecule made from nucleotide monomers. Nucleotide monomers are composed of a nucleobase, a five-carbon sugar (such as but not limited to ribose or 2'-deoxyribose), and one to three phosphate groups. Typically, a polynucleotide is formed through phosphodiester bonds between the individual nucleotide monomers. In the context of the present invention preferred nucleic acid molecules include but are not limited to ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). Moreover, the term "polynucleotide" also includes artificial analogs of DNA or RNA, such as peptide nucleic acid (PNA).

[0076] The nucleic acid of the present invention encodes ABHD5 or a variant thereof. Since the genetic code is degenerated, i.e. each amino acid is encoded by more than one nucleic acid, each peptide or its variant may be encoded by a multiplicity of different nucleic acid sequences.

[0077] Preferably, the nucleic acid encoding ABHD5 is selected from the group consisting of SEQ ID NOs: 6, 7, 8, 9 and 10. More preferably, the nucleic acid encoding ABHD5 has a sequence as defined by SEQ ID NO: 6.

Vector

[0078] For an effective treatment of heart failure, the increase of the amount of functional ABHD5 is advantageous. The administration of ABHD5 may pose practical difficulties. Therefore, the use of expression systems which mediate expression of ABHD5 by the cardiomyocytes of the patient are a solution for the problem underlying the present invention.

[0079] Thus, in yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof.

[0080] In yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof for use as a medicament.

[0081] In yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding ABHD5 or a variant thereof for use in the treatment or prevention of heart failure.

[0082] As used herein, the term "vector" refers to at least one nucleic acid or to a mixture of at least one nucleic acid and at least one protein which is capable of introducing the nucleic acid comprised therein into a cell. At least one nucleic acid comprised by the vector consists of or comprises at least one nucleic acid encoding ABHD5 or a variant thereof. In addition to the nucleic acid consisting of or comprising the nucleic acid encoding ABHD5 or the variant thereof, additional nucleic acids and/or polypeptides may be introduced into the cell. The addition of additional nucleic acids and/or polypeptides is especially preferred if said additional nucleic acids and/or polypeptides are required to introduce the nucleic acid encoding ABHD5 or the variant thereof into the cell.

[0083] In the context of the present invention it is preferred that ABHD5 or the variant thereof is expressed within the cell upon introduction of the vector or vectors. Examples of suitable vectors include but are not limited to plasmids, cosmids, phages, viruses or artificial chromosomes.

[0084] In preferred embodiments, the vector is selected from the group consisting of plasmids, cosmids, phages, viruses, and artificial chromosomes. More preferably, a vector suitable for practicing the present invention is a phage vector, preferably lambda phage and filamentous phage vectors, or a viral vector.

[0085] Preferred viral vectors are based on naturally occurring vectors, which are modified to be replication incompetent also referred to as non-replicating. Non-replicating viruses require the provision of proteins in trans for replication. Typically those proteins are stably or transiently expressed in a viral producer cell line, thereby allowing replication of the virus. The viral vectors are, thus, preferably infectious and non-replicating. The skilled person is aware of how to render various viruses replication incompetent.

[0086] In a preferred embodiment of the present invention the vector is selected from the group consisting of adenovirus vectors, adeno-associated virus (AAV) vectors (e.g., AAV type 6, type 1, type 5, type 9 and type 2), alphavirus vectors (e.g., Venezuelan equine encephalitis virus (VEE), sindbis virus (SIN), semliki forest virus (SFV), and VEE-SIN chimeras), herpes virus vectors (e.g. vectors derived from cytomegaloviruses, like rhesus cytomegalovirus (RhCMV) (14)), arena virus vectors (e.g. lymphocytic choriomeningitis virus (LCMV) vectors (15)), measles virus vectors, pox virus vectors (e.g., vaccinia virus, modified vaccinia virus Ankara (MVA), NYVAC (derived from the Copenhagen strain of vaccinia), and avipox vectors: canarypox (ALVAC) and fowlpox (FPV) vectors), vesicular stomatitis virus vectors, retrovirus, lentivirus, viral like particles, and bacterial spores.

[0087] The most preferred vector is an adenovirus, more preferably adeno associated virus (AAV) type 1, type 6 or type 9. For use in humans, AAV types 1 or 6 are preferred, for use in mice AAV type 9.

[0088] An especially preferred vector given in SEQ ID NO: 18. Also preferred is a vector as defined by SEQ ID NO: 19. Said sequences comprise HDAC4-NT or luciferase instead of a ABHD5. However, the exchange of these inserts for ABHD5 is easily accomplished.

[0089] To direct expression of ABHD5 or the variant thereof, the nucleic acid encoding it is operationally linked to an internal promoter and/or enhancer that is recognized by the transcriptional machinery of the cell. Suitable promoters may be derived from the genome of mamnmalian cells (e. g., MHCII promoter, EF1alpha promoter) or from mammalian viruses (e.g., the cytomegalovirus promoter, the spleen focus-forming virus SFFV promoter). Especially preferred are promoters which enable the expression of the above-mentioned gene in cardiomyocytes.

[0090] One preferred promoter is defined by SEQ ID NO: 22. In an especially preferred embodiment, the promoter is a human toponin promoter, more preferably the human troponin T promoter, as this promoter is especially well suited for cardiomyocyte-specific expression of transgenes. Preferably, the human troponin T promoter has a nucleic acid sequence as defined by SEQ ID NO: 21.

[0091] In another preferred embodiment, the vector encodes a recognition site for micro-RNA 122 between the coding sequence of the HDAC4, ABHD5 or their variants and the terminator sequence so that said recognition site becomes part of the transcript which also encodes HDAC4, ABHD5 or a variant thereof produced from this vector. Since micro-RNA 122 is found in many types of cells but not in cardiomyocytes, said recognition site causes breakdown of the mRNA in those types of cells where micro-RNA 122 is present, thus preventing translation of the transcript. Preferably the recognition site for micro-RNA 122 has a nucleic acid sequence as defined by SEQ ID NO: 20.

[0092] Since the two elements described above are advantageous for the cardiomyocyte-specific expression of many other peptides besides HDAC4-NT and ABHD5, the present invention relates in a further embodiment to the use of a recognition site for micro-RNA 122 for the cardiomyocyte-specific expression of transgenes. Preferably, said recognition site has a nucleic acid sequence as defined by SEQ ID NO: 20.

[0093] In yet another embodiment, the present invention relates to the use of a combination of the human troponin promoter and the recognition site for micro-RNA 122 for the cardiomyocyte-specific expression of transgenes. Preferably, said recognition site has a nucleic acid sequence as defined by SEQ ID NO: 20.

[0094] In yet another embodiment, the present invention relates to a vector encoding a recognition site for micro-RNA 122 between the promoter and the terminator sequence so that said recognition site becomes part of the transcript which also encode HDAC4-NT or a variant thereof produced from this vector. Preferably, said recognition site has a nucleic acid sequence as defined by SEQ ID NO: 20. Preferably, the vector additionally comprises a human troponin promoter. More preferably, the human troponin promoter controls transcription of the nucleic sequence which comprises the aforementioned recognition site for micro-RNA 122.

[0095] In a particularly preferred embodiment of the present invention, the vector comprises a human troponin T promoter as defined above and a nucleic acid sequence encoding a recognition site for micro-RNA 122 as defined above.

[0096] As used herein, "operatively linked" means incorporated into a genetic construct so that expression control sequences effectively control expression of a coding sequence of interest.

[0097] Specific initiation signals may also be required for efficient translation of coding sequences. These signals include the ATG initiation codon and adjacent sequences. Exogenous translational control signals, including the ATG initiation codon, may additionally need to be provided. One of ordinary skill in the art would readily be capable of determining this and providing the necessary signals. It is well known that the initiation codon must be in-frame (or in-phase) with the reading frame of the desired coding sequence to ensure translation of the entire insert. These exogenous translational control signals and initiation codons can be of a variety of origins, both natural and synthetic.

HDAC4-NT and Variants Thereof

[0098] HDAC4-NT not just represses the transcription factor MEF2 in vitro, thus inhibiting cardiomyocyte hypertrophy (Backs et al., 2011, cited supra). The study underlying the present invention surprisingly showed that overexpression of HDAC4 by an adenoviral expression system in vivo (i) prevents myocardial remodeling, and (ii) does not cause intolerable side effects. Given the fact, that similar approaches with other peptides proved non feasible in vivo due to side effects (Czubryt et al. 2003, Proc Natl Acad Sci USA. 100:1711-6), this finding was unexpected and highlights the advantages of HDAC4-NT as a therapeutic means.

[0099] Therefore, in yet another embodiment, the present invention relates to an elongated and or multimerized variant of the N-terminal fragment of histone deacetylase 4 (HDAC4-NT).

[0100] In yet another embodiment, the present invention relates to HDAC4-NT or a variant thereof for use as a medicament.

[0101] In yet another embodiment, the present invention relates to HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0102] All definitions given above for the terms "heart failure", "patient", "treatment" and "prevention" with respect to ABHD5 also apply to embodiments of the invention relating to HDAC4-NT and the variants thereof.

[0103] The term "HDAC4-NT" relates to a polypeptide having an amino acid sequence as defined by one of the sequences SEQ ID NO: 13 (human HDAC4-NT) or 14 (mouse HDAC4-NT) or a variant thereof. Preferably, HDAC4-NT has an amino acid sequence as defined by SEQ ID NO: 13 or a variant thereof.

[0104] "Variants" of HDAC4-NT are preferably N-terminally and/or C-terminally truncated variants, amino acid substitution or deletion variants, multimerized or elongated variants of the sequences defined by SEQ ID NO: 13 or 14. Variants comprise furthermore an amino acid sequence comprising modified amino acid(s), unnatural amino acid(s) or peptidomimetic(s) or further compounds which can mimic a peptide backbone/structure. Preferably, variants are selected from C-terminally truncated variants of SEQ ID NO: 13 or 14; amino acid substitution or deletion variants; variants comprising modified amino acid(s), unnatural amino acid(s) or peptidomimetic(s) or further compounds which can mimic a peptide backbone/structure.

[0105] Deletion variants are, preferably, characterized by C-terminal deletion of up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids. Independently of the presence or absence of C-terminal deletions further preferred deletion variants are characterized by N-terminal deletion of up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids. A preferred deletion variant comprises amino acid positions 2 to 201 of SEQ ID NO: 13 or 14, more preferably of SEQ ID NO: 13. This variant is also referred to as "HDAC4 2-201".

[0106] The term "HDAC4-NT variants" preferably includes proteins which have at least 600, 65%, 70%, 80%, 81%, 82%, 83%, 84%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence similarity, preferably sequence identity over the entire length of the protein according to SEQ ID NO: 13 or 14 or proteins based on SEQ ID NO: 13 or 14 carrying above outlined N- and/or C-terminal deletions using the best sequence alignment and/or over the region of the best sequence alignment, wherein the best sequence alignment is obtainable with art known tools, e.g. Align, using standard settings, preferably EMBOSS::needle, Matrix: Blosum62, Gap Open 10.0, Gap Extend 0.5, with the amino acid sequence set forth in SEQ ID NOs: 13 or 14. It is preferred that when a given HDAC4-NT variant is aligned with a HDAC4-NT according to SEQ ID NO: 13 or 14 that alignment will be over the entire length of the two proteins and, thus, that the alignment score will be determined on this basis.

[0107] Preferably, a deletion variant retains amino acid positions 169 to 185 of SEQ ID NO: 13 as these positions are important for binding of HDAC-NT to MEF2.

[0108] Preferred substitution variants are generated by substituting up to 1, 2, 3, 4, 5, 10, 15, 20, 25 or 30 amino acids against natural amino acids, unnatural amino acids or peptidomimetics.

[0109] Preferably, the amino acids of the wild type protein or a deletion variant thereof are substituted for natural amino acids, more preferably, said substitutions are conservative substitutions.

[0110] A "conservative amino acid substitution" is one in which an amino acid residue is substituted by another amino acid residue having a side chain (R group) with similar chemical properties (e.g., charge or hydrophobicity). In general, a conservative amino acid substitution will not substantially change the functional properties of a protein. In cases, where two or more amino acid sequences differ from each other by conservative substitutions, the number of substitutions may be adjusted upwards to correct for the conservative nature of the substitution. Thus, in the case of conservative amino acid substitutions up to 40, up to 50 or even up to 70 amino acids may be substituted. Examples of groups of amino acids that have side chains with similar chemical properties include

[0111] 1) aliphatic side chains: glycine, alanine, valine, leucine and isoleucine;

[0112] 2) aliphatic-hydroxyl side chains: serine and threonine;

[0113] 3) amide-containing side chains: asparagine and glutamine;

[0114] 4) aromatic side chains: phenylalanine, tyrosine, and tryptophan;

[0115] 5) basic side chains: lysine, arginine, and histidine;

[0116] 6) acidic side chains: aspartate and glutamate, and

[0117] 7) sulfur-containing side chains: cysteine and methionine.

[0118] Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, glutamate-aspartate, and asparagine-glutamine. Alternatively, a conservative replacement is any change having a positive value in the PAM250 log-likelihood matrix disclosed in Gonnet G. H. et al, 1992 "Exhaustive matching of the entire protein sequence database." Science 1992, 256:1443-1445. A "moderately conservative" replacement is any change having a non-negative value in the PAM250 log-likelihood matrix.

[0119] Further preferred variants of HDAC4-NT are elongated variants which comprise additional amino acids at the C-terminus. More preferred are variants which comprise amino acid positions 2 to 202, 1 to 220, 1 to 216, 1 to 212 or 1 to 208 of full-length HDAC4 as defined by SEQ ID NO: 11 (human) or 12 (mouse). Even more preferably, a variant of HDAC4-NT comprises amino acid positions 2 to 202, 1 to 208 or 1 to 220 of SEQ ID NO: 11 or 12. Most preferably, an elongated variant of HDAC4-NT comprises amino acid positions 2 to 202, 1 to 220 or 1 to 208 of SEQ ID NO: 11. It is to be understood that said elongated variants may be modified by amino acid substitutions as set forth above. The variant comprising amino acid positions 2 to 202 is also referred to as HDAC4 2-202.

[0120] In a further preferred embodiment, the variant of HDAC4-NT is a variant generated by multimerization of HDAC4-NT. A multimerized variant of HDAC4-NT is a polypeptide which comprises the amino acid sequence of HDAC4-NT or any of the variants described above not just once but in at least 2, at least 3, at least 4 or at least 5 repeats. Thus, a single polypeptide comprises more than one binding site for MEF2. It is to be understood that a multimerized variant of HDAC4-NT or any of the above-described deletion, elongation or substitution variants thereof may be generated by repeating the same amino acid sequence (homogeneous multimer) or by combining more than one of the aforementioned variants (heterogeneous multimer), thus generating a polypeptide whose repeated sequence motifs are similar but not identical

[0121] In an especially preferred embodiment of the present invention, amino acid positions 1 to 201, 2 to 201, 2 to 202, 1 to 208 or 1 to 220 are multimerized. In one preferred embodiment, the multimerization is homogeneous, i.e. only a sequence comprising amino acid positions 2 to 201, 2 to 202, 1 to 201, 1 to 208 or 1 to 220 is repeated. In another preferred embodiment, the multimerization is heterogeneous, i.e. the multimer comprises a combination of at least two different sequences.

[0122] Any "variant" defined above is, preferably, a functional variant. A functional variant is a variant of the wild type HDAC4-NT as described above which retains its capability to repress myocyte enhancer factor 2 (MEF2). Preferably, the HDAC4-NT variant has at least 50% of the MEF2 repressing ability of HDAC4-NT comprising amino acid positions 1 to 220 of SEQ ID NO: 11 or 12. More preferably at least 60%, 70%, 80%, 90%., 95% or 100%.

[0123] An assay for testing whether a variant of HDAC4-NT is still functional disclosed by Backs et al., 2011 cited supra. Briefly, a reporter gene such as luciferase is coupled to a MEF2-regulated promoter. If this construct is expressed in a cell, the signal generated by the reporter gene is decreased in the presence of repressors of MEF2. Thus, variants of HDAC4-NT can be expressed in the cell and their ability to repress MEF2 can be determined by measuring the signal of the reporter gene relative to the signal in a control experiment with the presence of HDAC4-NT or a variant thereof.

[0124] It is to be understood that the most preferred variant of HDAC4 is not always the variant which has the highest activity as determined by the repression of MEF2 in the assay described above. As excessive repression of MEF2 may have deleterious effects, HDAC4 variants with decreased activity may be preferred as these have a wider therapeutic index, thus decreasing the risk of undesired side effects.

[0125] For this reason, HDAC4 2-201 and 2-202 are equally preferred. HDAC4 2-202 is especially preferred in those cases, where side effects have to be avoided, while HDAC4 2-201,

Nucleic Acid

[0126] In yet another aspect, the present invention relates to a nucleic acid encoding HDAC4-NT or a variant thereof for use as a medicament.

[0127] In yet another aspect, the present invention relates to a nucleic acid encoding HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0128] The term "nucleic acid" refers to a polymeric macromolecule made from nucleotide monomers. Nucleotide monomers are composed of a nucleobase, a five-carbon sugar (such as but not limited to ribose or 2'-deoxyribose), and one to three phosphate groups. Typically, a polynucleotide is formed through phosphodiester bonds between the individual nucleotide monomers. In the context of the present invention preferred nucleic acid molecules include but are not limited to ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). Moreover, the term "polynucleotide" also includes artificial analogs of DNA or RNA, such as peptide nucleic acid (PNA).

[0129] The nucleic acid of the present invention encodes HDAC4-NT or a variant thereof. Since the genetic code is degenerated, i.e. each amino acid is encoded by more than one nucleic acid, each peptide or its variant may be encoded by a multiplicity of different nucleic acid sequences. Preferably, a nucleic acid encoding HDAC4-NT is defined by SEQ ID NO: 17.

Vector

[0130] For an effective treatment of heart failure, the increase of the amount of HDAC4-NT or a variant thereof is advantageous. The administration of HDAC4-NT as peptide may pose practical difficulties. Therefore, the use of expression systems which mediate expression of HDAC4-NT or a variant thereof by the cardiomyocytes of the patient are a solution for the problem underlying the present invention.

[0131] Thus, in yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof.

[0132] In yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof for use as a medicament.

[0133] In yet another embodiment, the present invention relates to a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof for use in the treatment or prevention of heart failure.

[0134] As used herein, the term "vector" refers to at least one nucleic acid or to a mixture of at least one nucleic acid and at least one protein which is capable of introducing the nucleic acid comprised therein into a cell. At least one nucleic acid comprised by the vector consists of or comprises at least one nucleic acid encoding HDAC4-NT or a variant thereof. In addition to the nucleic acid consisting of or comprising the nucleic acid encoding HDAC4-NT or the variant thereof, additional nucleic acids and/or polypeptides may be introduced into the cell. The addition of additional nucleic acids and/or polypeptides is especially preferred if said additional nucleic acids and/or polypeptides are required to introduce the nucleic acid encoding HDAC4-NT or the variant thereof into the cell.

[0135] In the context of the present invention it is preferred that HDAC4-NT or the variant thereof is expressed within the cell upon introduction of the vector or vectors. Examples of suitable vectors include but are not limited to plasmids, cosmids, phages, viruses or artificial chromosomes.

[0136] In preferred embodiments, the vector is selected from the group consisting of plasmids, cosmids, phages, viruses, and artificial chromosomes. More preferably, a vector suitable for practicing the present invention is a phage vector, preferably lambda phage and filamentous phage vectors, or a viral vector.

[0137] Preferred viral vectors are based on naturally occurring vectors, which are modified to be replication incompetent also referred to as non-replicating. Non-replicating viruses require the provision of proteins in trans for replication. Typically those proteins are stably or transiently expressed in a viral producer cell line, thereby allowing replication of the virus. The viral vectors are, thus, preferably infectious and non-replicating. The skilled person is aware of how to render various viruses replication incompetent.

[0138] In a preferred embodiment of the present invention the vector is selected from the group consisting of adenovirus vectors, adeno-associated virus (AAV) vectors (e.g., AAV type 1, type 2, type 5, type 6 and type 9), alphavirus vectors (e.g., Venezuelan equine encephalitis virus (VEE), sindbis virus (SIN), semliki forest virus (SFV), and VEE-SIN chimeras), herpes virus vectors (e.g. vectors derived from cytomegaloviruses, like rhesus cytomegalovirus (RhCMV) (14)), arena virus vectors (e.g. lymphocytic choriomeningitis virus (LCMV) vectors (15)), measles virus vectors, pox virus vectors (e.g., vaccinia virus, modified vaccinia virus Ankara (MVA), NYVAC (derived from the Copenhagen strain of vaccinia), and avipox vectors: canarypox (ALVAC) and fowlpox (FPV) vectors), vesicular stomatitis virus vectors, retrovirus, lentivirus, viral like particles, and bacterial spores.

[0139] An especially preferred vector with HDAC4-NT as insert is given in SEQ ID NO: 18. Also preferred is a vector as defined by SEQ ID NO: 19. Said sequence comprises luciferase instead of a peptide of the present invention. However, the exchange of the luciferase for HDAC4-NT is easily accomplished.

[0140] The most preferred vector is an adenovirus, more preferably adeno associated virus (AAV) type 1, type 6 or type 9. For use in humans, AAV types 1 or 6 are preferred, for use in mice AAV type 9.

[0141] To direct expression of HDAC4-NT or the variant thereof, the nucleic acid encoding it is operationally linked to an internal promoter and/or enhancer that is recognized by the transcriptional machinery of the cell. Suitable promoters may be derived from the genome of mammalian cells (e. g., MHCII promoter, EF1alpha promoter) or from mammalian viruses (e.g., the cytomegalovirus promoter, the spleen focus-forming virus SFFV promoter). Especially preferred are promoters which enable the expression of the above-mentioned gene in cardiomyocytes.

[0142] One preferred promoter is defined by SEQ ID NO: 22. In an especially preferred embodiment, the promoter is a human troponin promoter as this promoter is especially well suited for cardiomyocyte-specific expression of transgenes. Preferably, the human troponin promoter has a nucleic acid sequence as defined by SEQ ID NO: 21.

[0143] In another preferred embodiment, the vector encodes a recognition site for micro-RNA 122 between the promoter and the terminator sequence so that said recognition site becomes part of the transcript produced from this vector. Since micro-RNA 122 is found in many types of cells but not in cardiomyocytes, said recognition site causes breakdown of the mRNA in those types of cells where micro-RNA 122 is present, thus preventing translation of the transcript. Preferably the recognition site for micro-RNA 122 has a nucleic acid sequence as defined by SEQ ID NO: 20.

[0144] In a particularly preferred embodiment of the present invention, the vector comprises a human troponin T promoter as defined above and a nucleic acid sequence encoding a recognition site for micro-RNA 122 as defined above.

[0145] As used herein, "operatively linked" means incorporated into a genetic construct so that expression control sequences effectively control expression of a coding sequence of interest.

[0146] Specific initiation signals may also be required for efficient translation of coding sequences. These signals include the ATG initiation codon and adjacent sequences. Exogenous translational control signals, including the ATG initiation codon, may additionally need to be provided. One of ordinary skill in the art would readily be capable of determining this and providing the necessary signals. It is well known that the initiation codon must be in-frame (or in-phase) with the reading frame of the desired coding sequence to ensure translation of the entire insert. These exogenous translational control signals and initiation codons can be of a variety of origins, both natural and synthetic.

Pharmaceutical Compositions

[0147] In a preferred embodiment of the present invention, the peptides, nucleic acids or vectors of the present invention are part of a pharmaceutical composition. These embodiments relate to all parts of the invention, i.e. to ABHD5 and the variants thereof as well as HDAC4-NT and the variants thereof.

[0148] The term "composition" refers to the combination of a vector, nucleic acid or peptide of the present invention and at least one further compound selected from the group consisting of pharmaceutically acceptable carriers and pharmaceutical excipients.

[0149] "Pharmaceutically acceptable" means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans.

[0150] The term "carrier", as used herein, refers to a pharmacologically inactive substance such as but not limited to a diluent, excipient, or vehicle with which the therapeutically active ingredient is administered. Such pharmaceutical carriers can be liquid or solid. Liquid carrier include but are not limited to sterile liquids, such as saline solutions in water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions. A saline solution is a preferred carrier when the pharmaceutical composition is administered intravenously or intranasally by a nebulizer.

[0151] Suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like.

[0152] Examples of suitable pharmaceutical carriers are described in "Remington's Pharmaceutical Sciences" by E. W. Martin.

Test System

[0153] In yet another embodiment, the present invention relates to a method for identifying a compound which modulates the activity and/or localization of ABHD5 or a variant thereof comprising the steps of

[0154] a) contacting a test system comprising ABHD5 or a variant thereof with a candidate compound;

[0155] b) determining whether the candidate compound modulates the activity and/or localization of ABHD5 or the variant thereof;

[0156] c) identifying the compound as a compound which modulating the activity of ABHD5 or the variant thereof based on the comparison of the activity and/or localization of ABHD5 or the variant thereof in the test system comprising the candidate compound and the activity of ABHD5 or the variant thereof determined in a control in step b).

[0157] It is preferred to use the variant of ABHD5 whose activity is to be determined in the test system. However, if it is expected that two variants of ABHD5 will show the same response to the candidate compound, it is also possible to use only one of these variants and to extrapolate to the effect of said compound on the other candidate compound. Similarly, if wild-type ABHD5 and a variant thereof can be expected to show the same response, it may be possible--and thus also preferred--to use a test system comprising wild type ABHD5 to test the modulation of the variant and vice versa.

[0158] A test system is a composition of reagents comprising ABHD5 or a variant thereof, wherein said ABHD5 generates a signal which allows the differentiation between a test compound which modulates the activity of ABHD5 and a test compound which does not.

[0159] If localization of ABHD5 is used as an indicator of its activity, the test system is, preferably, a cell expressing ABHD5 or a variant thereof, more preferably a cardiomyocyte.

[0160] If the enzymatic activity of ABHD5 is to be analyzed, the test system is, preferably a cell as described above. However, due to their simplicity, cell free systems are more preferred.

[0161] Preferably, the modulation of the activity of ABHD5 is determined by comparing a test system to which the test compound is added and an otherwise identical test system without the test compound.

[0162] Preferably, the activity determined with the test system is the ability of ABHD5 to mediate cleavage of HDAC4 or a variant of HDAC4 which does not bind to MEF2 into a fragment which binds to MEF2. Preferably, said fragment is HDAC4-NT as described further above in the present application.

[0163] Preferably, the modulation of the activity of ABHD5 is an increase of its activity. Said increase may be caused by increased affinity of ABHD5 for HDAC4 or by an increased turnover number. The cleavage of HDAC4 may be determined as explained in the examples section.

[0164] Moreover, the activity of ABHD5 or a variant thereof may be influenced by its binding affinity to lipid droplets as set forth above. Thus, the localization of ABHD5 may be used as an indicator of its activity. The less ABHD is bound to lipid droplets, the higher its activity.

[0165] We further claim potential tests were the link to HDAC4 or the proteolytic activity of abhd5 are directly or indirectly tested. This could be achieved by

[0166] The subcellular localization (bound to LD, vs homogenous expression in the cytosol/nucleus) of ABHD4 may be analyzed by expressing GFP- or RFP or other fluophor-tagged ABHD5 in cell-based assays (high-content screening).

[0167] Protein-protein interaction assays (e.g. alpha screen, FRET assays, mammalian two hybrid screen) to test the binding between ABHD5 and perilipin or between ABHD5 and HDAC4.

[0168] The test compound may be any peptide or small molecule. A peptide as referred to in this embodiment comprises at least 2, more preferably at least 3 even more preferably at least 4 and most preferably at least 5 amino acids linked by peptide bonds. Preferably, said amino acids are amino acids found in nature, more preferably proteinogenic amino acids. However, it is also preferred to use peptides comprising at least one amino acid having a residue not found in nature.

[0169] A small molecule is, preferably, an organic molecule having a molecular weight of not more than 2000 Da, more preferably not more than 1600 Da, even more preferably not more than 1200 Da and, most preferably, not more than 800 Da.

[0170] Since the proteolytic cleavage of HDAC4 mediated by ABHD5 generates an N-terminal fragment (HDAC4-NT) which is useful for the treatment or prevention of heart failure, the identification of modulators which increase the activity of ABHD5, preferably in cell based systems and more preferably in vivo, is of great clinical importance. Hence, the test system of the invention is a valuable tool for the discovery of novel pharmaceutical compounds useful for the treatment or prevention of heart failure.

[0171] In yet another embodiment, the present invention relates to the use of ABHD5 for identifying a compound which suppresses myocardial remodeling.

TABLE-US-00001 TABLE 1 Overview over the sequences disclosed by the present application SEQ Sequence ID NO. 1 Human ABHD5 polypeptide 2 Orangutan ABHD 5 polypeptide 3 Mouse ABHD5 polypeptide 4 Rat ABHD5 polypeptide 5 Pig ABHD 5 polypeptide 6 Human ABHD5 nucleic acid 7 Orangutan ABHD 5 nucleic acid 8 Mouse ABHD5 nucleic acid 9 Rat ABHD5 nucleic acid 10 Pig ABHD5 nucleic acid 11 Human HDAC4 polypeptide 12 Mouse HDAC4 polypeptide 13 Human HDAC4-NT polypeptide 14 Mouse HDAC4-NT polypeptide 15 Human HDAC4 nucleic acid 16 Mouse HDAC4 nucleic acid 17 Human HDAC4-NT nucleic acid 18 Expression vector encoding human HDAC4-NT 19 Expression vector for cardiomyocyte-specific expression of transgenes, encodes luciferase as transgen 20 Recognition site of micro-RNA 122 21 Human troponin T promoter sequence 22 CMVMLC260-Promoter sequence

BRIEF DESCRIPTION OF THE FIGURES

[0172] FIG. 1: Principle of invention and improvement of current technologies. AAV-9 is an example as an use in vivo. (A) gain of function of the protease abhd5 to increase the quantity of cardioprotective HDAC4-NT. (B) Gene transfer of HDAC4-NT, optimized HDAC4-NT or HDAC4-NT related constructs via adeno associated virus (AAV). NT: N-terminus; abhd5: 1-acylglycerol-3-phosphate O-acyltransferase;

[0173] FIG. 2: HDAC4 aa 2-201 were cloned into an AAV-9 virus (NT). NT was applied to animals 6 weeks before TAC surgery (indicated as a lines in the timecourse of echos, A). Controls received Luciferase cloned into AAV-9 (LUC). In consecutive echos, fs decreased after TAC surgery whereas NT treated animals were protected from reduced function, n=5, **p<0.01. Arrow indicates timepoint of echo in figure (B). Heartweight/Bodyweight ratio was normalized (n=5; **p<0.01) (C)

[0174] FIG. 3: In part, dyregulated genes were normalized, such as myh6 (A) and nppb (D). Myh7 (B) and nppa (C) were not normalized by NT-treatment (n=5). Values indicate relative expression level normalized to WT sham group; .+-.SEM *p<0.05.

[0175] FIG. 4: Validation experiment of the siRNA-screen confirmed results from the siRNA screen. Co-expression of flag tagged HDAC4 with myc tagged PKA leads to a cleavage of HDAC4 (first three lanes). The cleavage is not longer present when abhd5 is knocked down by using different siRNA in the last three lanes (siRNAs labeled with 1-3). Quantification of the western blots confirmed the results (p<0.05).

[0176] FIG. 5: To proof the results from our loss of function approach, we overexpressed abhd5 in cardiomyocytes (last three lanes). Overexpressed flag tagged HDAC4 was cleaved whenever gfp tagged abhd5 was coexpressed. IB: immunoblot; Ad: adenovirus construct.

[0177] FIG. 6: Overexpression of abhd5 rescues FCS induced MEF2 luciferase activity. Neonatal rat ventricular cardiomyocytes were treated with 10% FCS for 24 h. HDAC4 alone was not able to inhibit this activation, whereas coexpression of abhd5 was able to blunt the MEF2 activation back on a basic value. This effect was not seen when cells were treated with a EGFP tagged control virus. MEF2-Luc: myosin enhancer factor 2 luciferase construct; FCS: fetal bovine serum; Ad: Adenovirus; #p<0.05 treatment vs. no treatment; $p<0.05 Ad-abhd5 treated vs. cells treated with FCS 10%.

[0178] FIG. 7: Cardiomyocyte hypertrophy was significant reduced when abhd5 was expressed. A FCS induced hypertrophy was completely blunted whereas EGFP control virus did not show any beneficial effects on cardiomyocytes. NRVM: neonatal rat ventricular myocytes; FCS: felta bovine serum; #p<0.05 cell size of groups as indicated compared to control group without FCS; $p<0.05 cell size of abhd5 treated group compared to FCS treated group.

[0179] FIG. 8: (A) Overexpression of ABHD5 leads to proteolysis of HDAC4. Flag tagged HDAC4 was overexpressed in neonatal rat cardiomycytes with ABHD5, Western blot was performed with an antibody, recognizing Flag. Successful overexpression of ABHD5-GFP was confirmed with a western blot, detecting GFP. (B) HDAC4 and ABHD5 were cloned into a plasmid bearing constitutively active promoter (pNOP) and Galactose inducible promoter (pGAL) respectively. By overexpression either together or with backbone vector in Saccharomyces cerevisiae we found cleavage of HDAC4, confirmed by westernblot analysis. This experiment confirms that ABHD5 cleaves HDAC4 directly without the recruitment of factors only present in mammalian cells. (C) By co-treatment of mice with insulin and a beta receptor agonist (ISO) we found an increase of ABHD5 expression and consequently an increase of endogenous HDAC4 proteolysis. We show here exemplary western blots, performed with antibodies recognizing endogenous N-terminal HDAC4 and endogenous ABHD5. Westernblot against GAPDH confirmed equally protein loading.

[0180] FIG. 9: (A) The transcription factor myocyte enhancer factor 2 (MEF2) is sufficiently repressed by overexpression of ABHD5. MEF2-luciferase reporter was overexpressed in neonatal rat cardiomyocytes and stimulated with either endothelin-1 (ET-1) or (B) fetal calf serum (FCS) for 24 h. Co-expression of HDAC4 and ABHD5 leads to a cleavage of HDAC4 and consequently to a repression of MEF2 luciferase activity. Equally expression of HDAC4, ABHD5 and equally protein loading was confirmed by westernblot analysis as indicated. Values are shown as mean.+-.SEM; n>3/group; **p<0.05.

[0181] FIG. 10: ABHD5 counteracts cardiomyocyte hypertrophy in vitro. We stimulated neonatal rat cardiomyocyte with the prohypertorphic agents endothelin-1 (ET-1) and fetal calf serum (FCS) for 24 h as indicated. By adenoviral overexpression of ABHD5, hypertrophic response was blunted. (B) Cardiomyocyte size was quantified by counting 3 fields of view (>100 cardiomyocytes per field). Values are sown as mean.+-.SEM; **p<0.05.

[0182] FIG. 11: Transgenic overexpression of ABHD5 in vivo protects from cardiac hypertrophy and heart failure. We generated transgenic animals, overexpressing ABHD5 under the control of the .alpha.MHC promoter. 3 weeks after induction of pathological cardiac remodeling by transaortic constriction (TAC), we found less hypertrophy indicated by a reduction of heartweight/bodyweight ratio (HW/BW) and heartweight/tibia length ratio (HW/TL). Left ventricular function was improved in transgenic animals, shown as ejection fraction and fractional shortening. Classical pathological genes, such as atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) were less induced in ABHD5 transgenic animals. Values are shown as mean.+-.SEM; *p<0.05; **p<0.01; ***p<0.001.

[0183] FIG. 12: HDAC4-NT reverses pathological induction of metabolic genes. We measured 4 weeks after induction of pathological cardiac remodeling by transaortic constriction (TAC) the enzymatic activity of key enzymes of the glycolysis. Pathological induction of glycolytic enzymes was reversed when HDAC4 was overexpressed by using the previous described novel AAV-construct. We show here a hierarchical clustering of enzymatic activity of key enzymes as indicated. Color key shows difference from the mean.

[0184] FIG. 13: HDAC4 2-202 inhibits MEF2 luciferase activity as well. To test whether different mutations of HDAC4 lead to inhibition of MEF2, we overexpressed HDAC4 2-202 by using an adenovirus system in neonatal rat cardiomyocytes and treated them with the prohypertrophic agent fetal calf serum (FCS). By overexpression of either HDAC4 2-201 or 2-202 endogenous MEF2 activity was sufficient inhibited. We found HDAC4 2-202 was less efficient compared to HDAC4 2-201 in inhibiting MEF2 luciferase activity. In case of pharmacological interventions, this could be an eligible aim since transient or moderate inhibition of MEF2 might be more useful in the clinical setting. Therefore, we claim HDAC4 and HDAC4 mutants as potential therapeutic tools for inhibition of MEF2 and consecutive pathological hypertrophy or pathological cardiac remodeling.

[0185] FIG. 14: HDAC4 aa 2-201 were cloned into an AAV-9 virus (NT). NT was applied to animals 6 weeks before TAC surgery. Controls received Luciferase cloned into AAV-9 (LUC). Expression analysis of hearts revealed a specific pattern of genes that was completely normalized in animals that received AAV-NT. These genes are listed beside the heatmap. All of these genes were upregulated in TAC (p<0.0001) and normalized as compared to the AAV-LUC treated sham group (+20%).

[0186] FIG. 15: Forced treadmill running was performed twice a day during a 4 week running training program. Shown is the total distance that WT and HDAC4-KO mice run during the entire training program within 4 weeks (A) and the daily distance until exhaustion (B). AAV-NT expression in HDAC4 KO animals was able to rescue the phenotype of reduced exercise performance. Values are shown as mean+SEM (HDAC4-KO and WT n=8; AAV-NT n=3). Echocardiography was performed directly after exercise and revealed a reduced fractional shortening in HDAC4-KO animals, values are shown as mean+SEM (n=8/group; *p<0.05). Westernblot against N-terminal HDAC4 shows and increased HDAC4-NT production after 2 weeks of exercise (D). GAPDH is shown as a loading control.

[0187] The following examples are merely intended to illustrate the invention. They shall not limit the scope of the claims in any way.

EXAMPLES

[0188] Materials and Methods

[0189] Transthoracic echocardiography. Echocardiography was performed using a Sonos 5500 with a S12 transducer (12 MHz). The echocardiographer was blinded with respect to the treatment group. Mice were shaved and left ventricular parasternal short-axis views were obtained in M-mode imaging at the papillary muscle level. Three consecutive beats were used for measurements of left ventricular end-diastolic internal diameter (LVEDD) and left ventricular end-systolic internal diameter (LVESD). Fractional shortening (FS) was calculated as FS %=[(LVEDD-LVESD)/LVEDD].times.100%.

[0190] Generation of an adeno associated virus (HDAC4-AAV). HDAC4 aa2-201 was cloned into a double-stranded AAV-vector downstream of a CMV-enhanced short (260 bp) myosin light chain promoter (CMVenh/MLC260). AAV9 vectors were produced with the three plasmid transfection method.

[0191] RNA analysis. Total RNA was isolated from ventricular tissue using TRIzol (Invitrogen, Germany). Total RNA was digested with DNase, and cDNA synthesis from 500 ng of RNA was carried out using a SuperScript first-strand synthesis system for RT-PCR (Invitrogen). Quantitative real-time PCR (qPCR) was performed with Universal ProbeLibrary (Roche) by using TaqMan Universal PCR Mastermix (Applied Biosystems) and detection on a 7500 Fast Cycler (Applied Biosystems) as described previously [1].

[0192] Transverse aortic constriction. TAC to a 27 gauge stenosis was performed in 9-10 week-old male black six mice (charles river), mice as described previously [2]. AAV vectors were intravenously injected into the tail vein of male adult mice as 150-200 sL bolus using a sterile syringe and 29-gauge needle. Animals were euthanized by cervical dislocation. Organs were dissected and rapidly frozen in liquid nitrogen.

[0193] Western blotting. Proteins from heart tissue and cultured cardiomyocytes were isolated, and Western blot analysis was performed according to protocols described previously [1]. Primary antibodies used were anti-flag (santa cruz), anit-myc (santa cruz), anti-gfp (abcam). Primary antibody incubation was followed by corresponding horseradish peroxidase (HRP)-conjugated secondary anti-mouse and anti-rabbit antibodies and ECL detection. Relative protein levels were detected by densitometry using the Image J program.

[0194] Histology. Hematoxylin and cosin (H&E) and Masson's trichrome stainings were performed as previously described [3]. Cardiomyocyte size was assessed on H&E-stained sections by using Image J software (http://rsb.info.nih.gov/ij/). More than 200 randomly chosen cardiomyocytes from each group were analyzed to measure cross-sectional cardiomyocyte area. To quantify cardiac fibrosis, 20 trichrome-stained sections (magnification 20.times.) from the left ventricle were randomly selected, and morphometric analysis by using Image J was performed. Photographs were acquired with an Olympus SZH zoom stereo dissection scope with an Optronics DEI-750 CCD digital camera. All data were analyzed by a single observer blinded to the mouse genotypes.

[0195] Results:

[0196] Overexpression of N-terminal HDAC4 via an adeno associated virus (AAV) In mice is cardioprotective. HDAC4-NT is able to inhibit the transcription factor myocyte enhancer factor 2 (MEF2). [4] MEF2 is thought to be involved in pathological cardiac remodeling. [5] We therefore hypothesized that HDAC4-NT could have beneficial and cardioprotective effects in vivo. By cloning HDAC4-NT into a cardiotrophic AAV substrain (AAV9) under the control of a cardiomyocyte specific promoter (CMVenh-MLC260), we were able to transduce cardiomyocytes in vivo via a single tail vein injection. Mice were injected 4 weeks before they were exposed to transthoracic aortic constriction (TAC)-surgery as a model for cardiac stress and the development of heart failure. By doing so, animals that were treated with AAV-HDAC4-NT showed reduced cardiac hypertrophy, improved cardiac function and normalized gene regulation from genes that are known to play an important role in pathological cardiac remodeling (FIG. 2). Cardiac fibrosis that was developed by control-mice was diminished when animals were treated with HDAC4-NT.

[0197] We further aimed to investigate the endogenous role of HDAC4-NT. In wildtype animals, HDAC4-NT production is increased after physiological exercise. We generated conditional HDAC4-knockout animals, lacking HDAC4 in cardiomyocytes only and exposed these animals to running exercise. HDAC4-KO animals showed a reduced exercise tolerance with a reduced left ventricular function after running exercise. Reduced exercise performance was rescued when HDAC4-KO were treated with AAV-HDAC4-NT, indicating that HDAC4-NT is crucial for sustained cardiac function after cardiac stress (FIG. 15). By further carefully characterization of the animals we did not found any harmful effects or any side effects that were linked to AAV-HDAC4-NT treatment.

[0198] Abhd5 is a critical HDAC4 protease. To get insides about the upstream regulation of HDAC4 cleavage, we performed a siRNA-screen with a set of potential serine-proteases. By doing so, we identified a protein called 1-acylglycerol-3-phosphate O-acyltransferase (abhd5) playing a crucial role in PKA induced HDAC4 cleavage. HDAC4 cleavage was not longer present when abhd5 was knocked down by different siRNAs even when PKA was co-expressed with HDAC4 (FIG. 4). Abhd5 is characterized by typical structural features that can be found predominantly in serine proteases. However, it was not shown before, that abhd5 can indeed act as a protease. By adenoviral overexpression in neonatal rat ventricular myocytes (NRVMs) of abhd5 we were able to achieve HDAC4 cleavage without additional PKA activation or expression (FIG. 5).

[0199] Abhd5 overexpression leads to MEF2 inhibition and is cleavage dependent. By using a MEF2-luciferase assay, we found that abhd5 is able to completely normalize MEF2 activity induced by fetal calf serum (FCS), which is commonly used to induce cardiomyocyte hypertrophy. EGFP control virus did not show any beneficial effects in this system (FIG. 6)

[0200] Abhd5 Inhibits cardiomyocyte hypertrophy in vitro. We next hypothesized, that abhd5 induced HDAC4-NT is able to inhibit cardiomyocyte hypertrophy in vitro. Indeed, abhd5 was able to inhibit FCS induced cardiomyocyte hypertrophy. This effect was independent from a control virus with EGFP. (FIG. 7)

DISCUSSION

[0201] We found that HDAC4-NT is cardioprotective in mice and thus could serve as a potential pharmacological tool for the treatment of heart failure in human. This was surprising because earlier approaches to protect the heart by overexpression of a class II HDAC failed [6]. These earlier approaches used transgenic expression of full length HDACs and specific mutations of phosphosites to render HDACs signal-resistant and to force them to localize to the nucleus. However, class II HDAC mutant overexpression showed dramatic harmful effects by inducing mitochondrial dysfunction and apoptosis. In this work we provide two novel ways to circumvent harmful effects. First, we use the AAV system which allowed us to closely titrate the dosage of HDAC expression. The AAV system was already used in clinical trials (SERCA gene therapy). Second, by using an partial HDAC4 peptide we specifically seem to prevent the disease process of the heart and not essential functions such as mitochondrial function or cell survival. As a proof of concept, by expressing HDAC4 1-201 via AAVs, we show here for the first time, that this concept is a new promising therapeutic approach. Given the previous experience with the overexpression of putatively protective proteins in the same animal model, this was not expected.

[0202] Upstream Regulation could Serve as an Additional Tool:

[0203] With the identification of a critical PKA dependent protease (abhd5) we have identified the upstream signaling molecule that induced cardioprotective HDAC4 proteolysis. Abhd5 was not described as a protease and the involvement in potential cardioprotective pathways is new. Under normal conditions, abhd5 is bound to lipid droplets (LDs) and is involved in the regulation of lipolysis.

[0204] 1. Backs, J., et al., CaM kinase U selectively signals to histone deacetylase 4 during cardiomyocyte hypertrophy. J Clin Invest, 2006. 116(7): p. 1853-64.

[0205] 2. Backs, J., et al., The delta isoform of CaM kinase H is required for pathological cardiac hypertrophy and remodeling after pressure overload. Proc Natl Acad Sci USA, 2009. 106(7): p. 2342-7.

[0206] 3. Song, K., et al., The transcriptional coactivator CAMTA2 stimulates cardiac growth by opposing class II histone deacetylases. Cell, 2006. 125(3): p. 453-66.

[0207] 4. Sun, Q., et al., Role of myocyte enhancing factor 2B in epithelial myofibroblast transition of human gingival keratinocytes. Exp Biol Mod (Maywood), 2012. 237(2): p. 178-85.

[0208] 5. Kim, Y., et al., The MEF2D transcription factor mediates stress-dependent cardiac remodeling in mice. J Clin Invest, 2008. 118(1): p. 124-32.

[0209] 6. Czubryt, M. P., et al., Regulation of peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1 alpha) and mitochondrial function by MEF2 and HDAC5. Proc Natl Acad Sci USA, 2003. 100(4): p. 1711-6.

Sequence CWU 1

1

221349PRTHomo sapiensSOURCE1..349/mol_type="protein" /organism="Homo sapiens" 1Met Ala Ala Glu Glu Glu Glu Val Asp Ser Ala Asp Thr Gly Glu Arg1 5 10 15Ser Gly Trp Leu Thr Gly Trp Leu Pro Thr Trp Cys Pro Thr Ser Ile 20 25 30Ser His Leu Lys Glu Ala Glu Glu Lys Met Leu Lys Cys Val Pro Cys 35 40 45Thr Tyr Lys Lys Glu Pro Val Arg Ile Ser Asn Gly Asn Lys Ile Trp 50 55 60Thr Leu Lys Phe Ser His Asn Ile Ser Asn Lys Thr Pro Leu Val Leu65 70 75 80Leu His Gly Phe Gly Gly Gly Leu Gly Leu Trp Ala Leu Asn Phe Gly 85 90 95Asp Leu Cys Thr Asn Arg Pro Val Tyr Ala Phe Asp Leu Leu Gly Phe 100 105 110Gly Arg Ser Ser Arg Pro Arg Phe Asp Ser Asp Ala Glu Glu Val Glu 115 120 125Asn Gln Phe Val Glu Ser Ile Glu Glu Trp Arg Cys Ala Leu Gly Leu 130 135 140Asp Lys Met Ile Leu Leu Gly His Asn Leu Gly Gly Phe Leu Ala Ala145 150 155 160Ala Tyr Ser Leu Lys Tyr Pro Ser Arg Val Asn His Leu Ile Leu Val 165 170 175Glu Pro Trp Gly Phe Pro Glu Arg Pro Asp Leu Ala Asp Gln Asp Arg 180 185 190Pro Ile Pro Val Trp Ile Arg Ala Leu Gly Ala Ala Leu Thr Pro Phe 195 200 205Asn Pro Leu Ala Gly Leu Arg Ile Ala Gly Pro Phe Gly Leu Ser Leu 210 215 220Val Gln Arg Leu Arg Pro Asp Phe Lys Arg Lys Tyr Ser Ser Met Phe225 230 235 240Glu Asp Asp Thr Val Thr Glu Tyr Ile Tyr His Cys Asn Val Gln Thr 245 250 255Pro Ser Gly Glu Thr Ala Phe Lys Asn Met Thr Ile Pro Tyr Gly Trp 260 265 270Ala Lys Arg Pro Met Leu Gln Arg Ile Gly Lys Met His Pro Asp Ile 275 280 285Pro Val Ser Val Ile Phe Gly Ala Arg Ser Cys Ile Asp Gly Asn Ser 290 295 300Gly Thr Ser Ile Gln Ser Leu Arg Pro His Ser Tyr Val Lys Thr Ile305 310 315 320Ala Ile Leu Gly Ala Gly His Tyr Val Tyr Ala Asp Gln Pro Glu Glu 325 330 335Phe Asn Gln Lys Val Lys Glu Ile Cys Asp Thr Val Asp 340 3452349PRTPongo abeliiSOURCE1..349/mol_type="protein" /organism="Pongo abelii" 2Met Ala Ala Glu Glu Glu Glu Val Asp Ser Ala Asp Thr Gly Glu Arg1 5 10 15Ser Gly Trp Leu Thr Gly Trp Leu Pro Thr Trp Cys Pro Thr Ser Thr 20 25 30Ser His Leu Lys Glu Ala Glu Glu Lys Met Leu Lys Cys Val Pro Cys 35 40 45Thr Tyr Lys Lys Glu Pro Val His Ile Ser Asn Gly Asn Lys Ile Trp 50 55 60Thr Leu Lys Phe Ser His Asn Ile Ser Asn Lys Thr Pro Leu Val Leu65 70 75 80Leu His Gly Phe Gly Gly Gly Leu Gly Leu Trp Ala Leu Asn Phe Gly 85 90 95Asp Leu Cys Thr Asn Arg Pro Val Tyr Ala Phe Asp Leu Leu Gly Phe 100 105 110Gly Arg Ser Ser Arg Pro Arg Phe Asp Ser Asp Ala Glu Glu Val Glu 115 120 125Asn Gln Phe Val Glu Ser Ile Glu Glu Trp Arg Cys Ala Leu Gly Leu 130 135 140Asp Lys Met Ile Leu Leu Gly His Asn Leu Gly Gly Phe Leu Ala Ala145 150 155 160Ala Tyr Ser Leu Lys Tyr Pro Ser Arg Val Asn His Leu Ile Leu Val 165 170 175Glu Pro Trp Gly Phe Pro Glu Arg Pro Asp Leu Ala Asp Gln Asp Arg 180 185 190Pro Ile Pro Val Trp Ile Arg Ala Leu Gly Ala Ala Leu Thr Pro Phe 195 200 205Asn Pro Leu Ala Gly Leu Arg Ile Ala Gly Pro Phe Gly Leu Ser Leu 210 215 220Val Gln Arg Leu Arg Pro Asp Phe Lys Arg Lys Tyr Ser Ser Met Phe225 230 235 240Glu Asp Asp Thr Val Thr Glu Tyr Ile Tyr His Cys Asn Val Gln Thr 245 250 255Pro Ser Gly Glu Thr Ala Phe Lys Asn Met Thr Ile Pro Tyr Gly Trp 260 265 270Ala Lys Arg Pro Met Leu Gln Arg Ile Gly Lys Met His Pro Asp Ile 275 280 285Pro Val Ser Val Ile Phe Gly Ala Arg Ser Cys Ile Asp Gly Asn Ser 290 295 300Gly Thr Ser Ile Gln Ser Leu Arg Pro His Ser Tyr Val Lys Thr Ile305 310 315 320Ala Ile Leu Gly Ala Gly His Tyr Val Tyr Ala Asp Gln Pro Glu Glu 325 330 335Phe Asn Gln Lys Val Lys Glu Ile Cys Asp Thr Val Asp 340 3453351PRTMus musculusSOURCE1..351/mol_type="protein" /organism="Mus musculus" 3Met Lys Ala Met Ala Ala Glu Glu Glu Val Asp Ser Ala Asp Ala Gly1 5 10 15Gly Gly Ser Gly Trp Leu Thr Gly Trp Leu Pro Thr Trp Cys Pro Thr 20 25 30Ser Thr Ser His Leu Lys Glu Ala Glu Glu Lys Met Leu Lys Cys Val 35 40 45Pro Cys Thr Tyr Lys Lys Glu Pro Val Arg Ile Ser Asn Gly Asn Arg 50 55 60Ile Trp Thr Leu Met Phe Ser His Asn Ile Ser Ser Lys Thr Pro Leu65 70 75 80Val Leu Leu His Gly Phe Gly Gly Gly Leu Gly Leu Trp Ala Leu Asn 85 90 95Phe Glu Asp Leu Ser Thr Asp Arg Pro Val Tyr Ala Phe Asp Leu Leu 100 105 110Gly Phe Gly Arg Ser Ser Arg Pro Arg Phe Asp Ser Asp Ala Glu Glu 115 120 125Val Glu Asn Gln Phe Val Glu Ser Ile Glu Glu Trp Arg Cys Ala Leu 130 135 140Arg Leu Asp Lys Met Ile Leu Leu Gly His Asn Leu Gly Gly Phe Leu145 150 155 160Ala Ala Ala Tyr Ser Leu Lys Tyr Pro Ser Arg Val Ser His Leu Ile 165 170 175Leu Val Glu Pro Trp Gly Phe Pro Glu Arg Pro Asp Leu Ala Asp Gln 180 185 190Glu Arg Pro Ile Pro Val Trp Ile Arg Ala Leu Gly Ala Ala Leu Thr 195 200 205Pro Phe Asn Pro Leu Ala Gly Leu Arg Ile Ala Gly Pro Phe Gly Leu 210 215 220Ser Leu Val Gln Arg Leu Arg Pro Asp Phe Lys Arg Lys Tyr Ser Ser225 230 235 240Met Phe Glu Asp Asp Thr Val Thr Glu Tyr Ile Tyr His Cys Asn Val 245 250 255Gln Thr Pro Ser Gly Glu Thr Ala Phe Lys Asn Met Thr Ile Pro Tyr 260 265 270Gly Trp Ala Lys Arg Pro Met Leu Gln Arg Ile Gly Gly Leu His Pro 275 280 285Asp Ile Pro Val Ser Val Ile Phe Gly Ala Arg Ser Cys Ile Asp Gly 290 295 300Asn Ser Gly Thr Ser Ile Gln Ser Leu Arg Pro Lys Ser Tyr Val Lys305 310 315 320Thr Ile Ala Ile Leu Gly Ala Gly His Tyr Val Tyr Ala Asp Gln Pro 325 330 335Glu Glu Phe Asn Gln Lys Val Lys Glu Ile Cys His Thr Val Asp 340 345 3504351PRTRattus norvegicusSOURCE1..351/mol_type="protein" /organism="Rattus norvegicus" 4Met Lys Ala Met Ala Ala Glu Glu Glu Val Asp Ser Ala Asp Ala Gly1 5 10 15Gly Gly Ser Gly Trp Leu Thr Gly Trp Leu Pro Thr Trp Cys Pro Thr 20 25 30Ser Thr Ser His Leu Lys Glu Ala Glu Glu Lys Met Leu Lys Cys Val 35 40 45Pro Cys Thr Tyr Lys Lys Glu Pro Val Arg Ile Ser Asn Gly Asn Ser 50 55 60Ile Trp Thr Leu Met Phe Ser His Asn Met Ser Ser Lys Thr Pro Leu65 70 75 80Val Leu Leu His Gly Phe Gly Gly Gly Leu Gly Leu Trp Ala Leu Asn 85 90 95Phe Glu Asp Leu Ser Thr Asp Arg Pro Val Tyr Ala Phe Asp Leu Leu 100 105 110Gly Phe Gly Arg Ser Ser Arg Pro Arg Phe Asp Ser Asp Ala Glu Glu 115 120 125Val Glu Asn Gln Phe Val Glu Ser Ile Glu Glu Trp Arg Cys Ala Leu 130 135 140Arg Leu Asp Lys Met Ile Leu Leu Gly His Asn Leu Gly Gly Phe Leu145 150 155 160Ala Ala Ala Tyr Ser Leu Lys Tyr Pro Ser Arg Val Ser His Leu Ile 165 170 175Leu Val Glu Pro Trp Gly Phe Pro Glu Arg Pro Asp Leu Ala Asp Gln 180 185 190Glu Arg Pro Ile Pro Val Trp Ile Arg Ala Leu Gly Ala Ala Leu Thr 195 200 205Pro Phe Asn Pro Leu Ala Gly Leu Arg Ile Ala Gly Pro Phe Gly Leu 210 215 220Ser Leu Val Gln Arg Leu Arg Pro Asp Phe Lys Arg Lys Tyr Ser Ser225 230 235 240Met Phe Glu Asp Asp Thr Val Thr Glu Tyr Ile Tyr His Cys Asn Val 245 250 255Gln Thr Pro Ser Gly Glu Thr Ala Phe Lys Asn Met Thr Ile Pro Tyr 260 265 270Gly Trp Ala Lys Arg Pro Met Leu Gln Arg Ile Gly Gly Leu His Pro 275 280 285Asp Ile Pro Val Ser Val Ile Phe Gly Ala Arg Ser Cys Ile Asp Gly 290 295 300Asn Ser Gly Thr Ser Ile Gln Ser Leu Arg Pro Lys Ser Tyr Val Lys305 310 315 320Thr Ile Ala Ile Leu Gly Ala Gly His Tyr Val Tyr Ala Asp Gln Pro 325 330 335Glu Glu Phe Asn Gln Lys Val Lys Glu Ile Cys His Thr Val Asp 340 345 3505349PRTSus scrofaSOURCE1..349/mol_type="protein" /organism="Sus scrofa" 5Met Ala Ala Glu Glu Glu Glu Met Asp Ser Thr Asp Ala Cys Glu Arg1 5 10 15Ser Gly Trp Leu Thr Gly Trp Leu Pro Thr Trp Cys Pro Thr Ser Thr 20 25 30Ser His Leu Lys Glu Ala Glu Glu Lys Ile Leu Lys Cys Val Pro Cys 35 40 45Ile Tyr Lys Lys Gly Pro Val Arg Ile Ser Asn Gly Asn Lys Ile Trp 50 55 60Thr Leu Lys Leu Ser His Asn Ile Ser Asn Lys Ile Pro Leu Val Leu65 70 75 80Leu His Gly Phe Gly Gly Gly Leu Gly Leu Trp Ala Leu Asn Phe Gly 85 90 95Asp Leu Cys Thr Asn Arg Pro Val Tyr Ala Phe Asp Leu Leu Gly Phe 100 105 110Gly Arg Ser Ser Arg Pro Arg Phe Asp Thr Asp Ala Glu Glu Val Glu 115 120 125Asn Gln Phe Val Glu Ser Ile Glu Glu Trp Arg Cys Ala Leu Gly Leu 130 135 140Asp Lys Val Ile Leu Leu Gly His Asn Leu Gly Gly Phe Leu Ala Ala145 150 155 160Ala Tyr Ser Leu Lys Tyr Pro Ser Arg Val Ser His Leu Ile Leu Val 165 170 175Glu Pro Trp Gly Phe Pro Glu Arg Pro Asp Leu Ala Asp Gln Glu Arg 180 185 190Pro Ile Pro Val Trp Ile Arg Ala Leu Gly Ala Ala Leu Thr Pro Phe 195 200 205Asn Pro Leu Ala Gly Leu Arg Ile Ala Gly Pro Phe Gly Leu Ser Leu 210 215 220Val Gln Arg Leu Arg Pro Asp Phe Lys Arg Lys Tyr Ser Ser Met Phe225 230 235 240Glu Asp Asp Thr Val Thr Glu Tyr Ile Tyr His Cys Asn Val Gln Thr 245 250 255Pro Ser Gly Glu Thr Ala Phe Lys Asn Met Thr Ile Pro Tyr Gly Trp 260 265 270Ala Lys Arg Pro Met Leu His Arg Ile Gly Lys Met Asn Pro Asp Ile 275 280 285Pro Val Ser Val Ile Tyr Gly Ala Arg Ser Cys Ile Asp Gly Asn Ser 290 295 300Gly Thr Ser Ile Gln Ser Leu Arg Pro His Ser Tyr Val Lys Thr Ile305 310 315 320Ala Ile Leu Gly Ala Gly His Tyr Val Tyr Ala Asp Gln Pro Glu Asp 325 330 335Phe Asn Leu Lys Val Lys Glu Ile Cys Asp Thr Val Asp 340 34561328DNAHomo sapienssource1..1328/mol_type="DNA" /organism="Homo sapiens" 6gcggctatgg cggcggagga ggaggaggtg gactctgccg acaccggaga gaggtcagga 60tggctaactg gttggctccc cacatggtgc cctacgtcta tatcacacct taaagaagct 120gaagagaaga tgttaaaatg tgtgccttgc acatacaaaa aagaacctgt tcgtatatct 180aatggaaata aaatatggac actgaagttc tctcataata tttcaaataa gactccactt 240gtccttctcc atggttttgg aggaggtctt gggctctggg cactgaattt tggagatctt 300tgcaccaaca gacctgtcta tgcttttgac ctattgggtt ttggacgaag tagtagaccc 360aggtttgaca gtgatgcaga agaagtggag aatcagtttg tggaatccat tgaagagtgg 420agatgtgccc taggattgga caaaatgatc ttgcttgggc acaacctagg tggattcttg 480gctgctgctt actcgctgaa gtacccatca agggttaatc atctcatttt agtggagcct 540tggggtttcc ctgaacgacc agaccttgct gatcaagaca gaccaattcc agtttggatc 600agagccttgg gagcagcatt gactcccttt aaccctttag ctggcctaag gattgcagga 660ccctttggtt taagtctagt gcagcgttta aggcctgatt tcaaacgaaa gtattcttca 720atgttcgaag acgatactgt gacagaatac atctaccact gtaatgtgca gactccaagt 780ggtgagacag cttcaaagaa tatgactatt ccttatggat gggcaaaaag gccaatgctc 840cagcgaattg gtaaaatgca ccctgacatt ccagtttcag tgatctttgg cgcccgatcc 900tgcatagatg gcaattctgg caccagcatc cagtccttac gaccacattc atatgtgaag 960acaatagcta ttcttggggc aggacattat gtatatgcag atcaaccaga agaattcaac 1020cagaaagtaa aggagatctg cgacactgtg gactgaacac actgaagctc tgatgggaaa 1080acctggtgac tgatatagtt gttcagcaat aattcatagt ctgtgatgaa gagtagtgaa 1140tacaacacac aaccaggcag ccttcttgac tatactttgc acatgttttc tttaggaatt 1200cactcacaca tttaaaccag ttagtgcctt ctagaagaat ggctttcctt tctcctacac 1260aaaattgaaa tatacaagtc tctaaatata atacctttaa ataaaaggtt atttgtccct 1320ctgaaaaa 132873276DNAPongo abeliisource1..3276/mol_type="DNA" /organism="Pongo abelii" 7ccagtcggcc tgtcagccgg ctttgagata agtccaggcg cttgcgcggc ggcggctatg 60gcggcggagg aggaggaggt ggactctgcc gacaccggag agaggtcagg gtggctaact 120ggttggcttc ccacatggtg ccctacgtct acatcacacc ttaaagaagc tgaagagaag 180atgttaaaat gtgtgccttg cacatacaaa aaagaacctg ttcatatatc taatggaaat 240aaaatatgga cactgaagtt ctctcataat atttcaaata agactccact tgtccttctc 300catggttttg gaggaggtct tgggctctgg gcactgaatt ttggagatct ttgcaccaac 360agacctgtct atgcttttga cctattgggt tttggacgaa gtagtagacc caggtttgac 420agtgacgcag aagaagtgga gaatcagttt gtggaatcca ttgaagagtg gagatgtgcc 480ctaggattgg acaaaatgat cttgcttggg cacaacctag gtggattctt ggctgctgct 540tactcactga agtacccatc aagggttaat catctcattt tagtggagcc ttggggtttc 600cctgaacgac cagaccttgc tgatcaagac agaccaattc cagtttggat cagagccttg 660ggagcagcat tgactccctt taacccttta gctggcctaa ggattgcagg accctttggt 720ttaagtctag tgcagcgttt aaggcctgat ttcaaacgaa agtattcttc aatgttcgaa 780gacgatactg tgacagaata catctaccac tgtaatgtgc agactccaag tggtgagaca 840gctttcaaga atatgactat tccttatgga tgggcaaaaa ggccaatgct ccagcgaatt 900ggtaaaatgc accctgacat tccagtttca gtgatctttg gcgcccgatc ctgcatagat 960ggcaattctg gcaccagcat ccagtcctta cgaccacatt catatgtgaa gacaatagct 1020attcttgggg caggacatta tgtatatgca gatcaaccag aagaattcaa ccagaaagta 1080aaggagatct gcgacactgt ggactgaaca cactgaagct ctgatgggaa aacctggtga 1140ctgatacagt tgttcagcaa taattcatag tctgtgatga agagtaatga atacaacata 1200gaaccaggca gccttcttga ctatactttt gcacatgttt tctttaggaa ttcgctcgca 1260catttaaacc agttagtgcc ttctagaaga atggctttcc tttctcctac acaaaattga 1320aatatacaag tctctaaatt taataccttt aaataaaagg ttatttgtcc ctctgatgta 1380ctgaaaaact aatttttcag ctgaaaattt tttaatctaa ctttgctagt tatttttgta 1440ttgcaatcta tattgccaat ttaggaagtg atttctgagt ctcttacact gtaaaggtgc 1500actttatttt ctttgtcttc cccatcatgt atttattgtg tcttgataac tgatattaat 1560ctaaattcaa tgtgttttta tgtaaaaatt tgtcagttgt ttagaatatt tcactttgtt 1620tttgaaacgg agtgacaagg cagatttttg gttaaaggac gggagttgat cactatcatt 1680actttttcta gtttacctct tttttatatt taaggctgct aagccatgtt cagcatttta 1740aatgtggtct atcctgacat acacagtgta taacaaccta actccttgga acctcttatg 1800tgtggtataa ttctacactt ccaaggaaca cgacttcagt gattcaggta ctgaaaagcc 1860ttagctaaaa ggctgttgtt tccccctttc atactgttct tttccatgac ccaggatgca 1920gcaaatgaaa cagatttctt ctcttaaggg gatattaaga ctgttacttc ctagtaagcc 1980aagtaatacc atatttttat taacatctaa cttttgtaga tgggtgctaa aattgcatac 2040gttttaacca ctaaaataga aaaacaagtg gtgctattat gtctcatggc accagaaatg 2100agctagcact tgggtttgtt gttgttgttt attaagagta ttgtgttaat taaatcatta 2160catacttgaa gttatattac aaaaattcta gaaggttggt tgaactattt ttttaggaac 2220taccatcaag tgtagcattt tcttgcagtt ttaaaatgag gaaagcttct ttgaaactgt 2280gaaatgctcc atgtggtaac tggctgctga gaaaaccctt caccaaaaaa ataaataaaa 2340attgaatagg attgtcatca agaaggcatc tgtcgctaac gttgcttgtc taggagaaag 2400gtagctatgt aaataaaaac agtgaactag agcaaatagt ggtttaatgg ttttgttatt 2460gcatttttaa aatggttaat tagggaattt gtagttgtta ggaaatgtaa ggttgtgtca 2520ctgttgatta actgccagaa agactgaatg ttctattttc

aacatttctc ccctacaaaa 2580gaatagacaa attatactga agcatgatat aaacatcttc ccaatgaaca atttgtctca 2640cttgtcagat taactaggtt agtgcaggaa gcaacatgag cgccaagatg tgttgtctga 2700tttctctacc ttaagaacaa taatagtctt tttagttagt attttggatg gccaggtttc 2760aaacctgtat gtggtacaaa taatttgggt aatatttttg tatttttgtt ttacacactg 2820tccaatctca attatccttt gctgggagaa tgacaggttt cacttatata ggaaggtttt 2880tgcacaggaa atttggtccc agcccttgga aggaagaagt tccttggttt acttagtgaa 2940tggagtttct ggccacagat gtgccaagtg attcaagaaa gatatacctg aatatcaagt 3000gataatttat tttcctacag actgaatttg ctttatttga aagatgttgt aactcttttt 3060aaagttagat tttaccctga ggtatagtat atgtaatttt gtgaagattg agctagaagg 3120gaagttcaca atcctcacat ttaaaaaaat gtagtgtgtg ctaaatgttt tcttaaaaat 3180ctattacagc atttgatctt tgttatgcac agtgtacttt tattttacag aataaatttt 3240cctgtgatag tcacaacaaa aaaaaaaaaa aaaaaa 327683148DNAMus musculussource1..3148/mol_type="DNA" /organism="Mus musculus" 8gccgctggga cgccgagcct gcggtggcgc ggccgcgccc tcggatcgtc ccagcgggcg 60gacgacgcat gcgcgggcgg tgcggtctta agggcggccg cggcccgggg ccgcccagtc 120ggcctgtcag ccggcttcga ggtgtgtccc tgcgcttgcg cggcggcggt gatgaaagcg 180atggcggcgg aggaggaggt ggactcggca gacgccggtg gagggtcagg atggctgaca 240gggtggcttc ctacctggtg tcccacatct acatcacacc ttaaagaagc tgaagagaaa 300atgttaaaat gtgtcccctg cacttacaag aaagagcctg tgcgcatatc caatggaaac 360agaatatgga cgctgatgtt ctctcacaac atttctagta agacgccact tgtcctcctt 420catggttttg gaggaggtct tggactttgg gccctgaatt ttgaagatct aagcaccgat 480aggcctgtct atgcctttga cctattgggc ttcggaagaa gtagtagacc taggtttgac 540agtgatgcgg aagaagtgga gaatcagttt gtggaatcca ttgaagagtg gagatgtgcc 600ctcaggttgg acaaaatgat cttgcttgga cacaacctgg gagggttctt ggctgccgct 660tactcactga agtacccatc aagggttagt cacctcattt tagtagagcc atggggtttt 720cctgagcgac cagatcttgc tgatcaagag agaccaattc cagtttggat cagggcccta 780ggggcagcat tgactccctt taaccccttg gctggcctca ggattgcagg accttttggg 840ttaagtctag tgcagcgttt gaggcctgat ttcaagcgga agtactcctc tatgtttgaa 900gatgacacgg tgacagagta catctaccac tgtaatgtac aaaccccaag tggtgagaca 960gctttcaaaa acatgacgat tccttatggg tgggccaaac ggccaatgct tcagcggata 1020ggtggcttgc atcctgacat tccagtttca gtgatctttg gagcccgatc ctgcatagat 1080ggcaactctg gaaccagcat ccagtcactg cgaccgaagt cctacgtgaa gacaattgcc 1140atcctcgggg cggggcatta tgtgtatgca gatcagccag aagaattcaa ccagaaagtc 1200aaggagatct gccacacagt agactgagca cacagaacca tgcagcaccc gtgacgggtg 1260ccgttcatga gcaatcccca cagcccgagg acccccgcag tctcctggac tggactctgc 1320agctttccac atttaaacca accagtgcct tctagaagaa tggctttcct ttctcctaca 1380cagaattaaa atataggaga gtctcccaat ttaataatcg ccttaaataa aggttgtcct 1440tctgatgtac tgaaaaattg tgatttttca gctgagactt ttctcaattt cacctaactg 1500cttgttaggt gtttggtgtt gcagtccgta tgccagtgta cctagtccat atgccagtgt 1560acctagtcca tatgccagtg tacctagcga cttctgggcc tgtggtgtta ggtgttggga 1620agctgcactt tattttcctt gcatgtattt actgtctcta acaactaaca tagttaaccc 1680aagtattttt atgtaaaaag atttcaattt agaatacttc atttttgaga tggagtttag 1740aatatttcat tttgaaatgg aacgaaaggg ttaggttttg atgtaaaaga caggagtcaa 1800tcactagcgt taactttcct tgttttcctg ttttatgatc aaggccgtgt ttcagcattt 1860taaatgtgtt ccatggtgac atagtgctta cagcaacgca gttcctgggg cccttctgtg 1920tgtaatctac agggttctat gagaacatat gcatagactc agccattcaa gtgctgagta 1980gcccgaacct gaaacctgtc ccctttcctt ccagtattcc caggacccag gatctaggtc 2040ccctcacttg cagggatgtt aacactgttg cctatcggga aaccaagtcc cactgtgttc 2100tcatgagcaa ccagcttaca tggtgcttaa actggattgc attttaccac taacatttaa 2160aactatgtgg tgctgttacg tctcatggcg ccagaaatga gatagaactt gtggttattt 2220ttattgaata ttatgttaat ctaaccactt atatacttga agtaaaatta tgaaaaaaat 2280ctattatgtt gtttgaactg tttggcagaa accaccattg gatttataac tttctgacag 2340tgttaaagtg agagacaatt tgaaactatg aaaaagctcc atggaatagc tggatgctga 2400gaaagccttc tgtctagaga acagagaaca aagagcattg ttaccaacat tgtttgtcca 2460ggagaaaagc agattacaca aataaaacct cgacctcaca aatcacgact cgatgacttg 2520agctattaca tttttagtga ctagtcagga aatttttttg aaaatataaa attatatcac 2580atgtaattaa ctgccagcaa gattagctcc atactttagg agaccgtgaa aatcatattg 2640aagcgggaca aagcagcctc ccagcgaccc tttatctgac tcatttaacg cattaggtta 2700gtgcaaggag ccaccgtgag accaaaagtg cttgttctca ccaccttgag aataaaaata 2760gcctttttcc ccctttatag ttagtgttgt gggtggccag atccacactt gagagtggta 2820gaacatttgt gcaggactct tacttggcag tcaccagcct cagtcttttg ttcaccaaag 2880aaaaaaaatt ctgcacaaga aaccggtctg cccaaagaaa ctgacttccc cactgagctg 2940ctttgcttta ctggaaacct gtgaagcttc ctaaacatta aaatttccat ggtgtgtgca 3000gtgattgttg taaaggttga agtagtaaag tttataatct gcaaattctt gagaacagtg 3060gttgctaaac atctttcttg taaacgatct cttaactatc attggtcttt gctaagttat 3120tttacagaat aaactcgaca gtgctagc 314891108DNARattus norvegicussource1..1108/mol_type="DNA" /organism="Rattus norvegicus" 9cggcttcgag gtgccttcct gcgcttgcgc ggcggcagtg atgaaagcga tggcggcgga 60ggaggaggtg gactcggcag acgccggtgg agggtcagga tggctgacag ggtggcttcc 120tacctggtgt cccacgtcta catcacacct taaagaagct gaagagaaaa tgctaaaatg 180tgtcccctgc acttacaaga aagaacctgt gcgcatatcc aatggaaaca gcatatggac 240actgatgttc tcgcacaaca tgtctagtaa gacaccactt gtcctcctgc atggttttgg 300aggaggtctt ggactttggg ccctgaattt tgaagatcta agcactgata ggcctgtcta 360tgcctttgac ctattgggct ttggaagaag tagtagacct aggtttgaca gtgacgcgga 420agaagtggag aatcagtttg tggaatccat tgaagagtgg agatgtgccc tcaggttgga 480caaaatgatc ttgcttggac acaacctggg agggttcttg gctgctgcct actcactgaa 540gtacccgtca agggtcagtc acctcatttt agtagaacca tggggttttc ctgagcgacc 600agatcttgct gatcaagaga gaccaattcc agtttggatc agagccttag gggcagcatt 660gactcccttt aaccccttgg ctggcctcag gattgcagga ccttttgggt tgagtctagt 720gcagcgcctg aggccggact tcaagcggaa gtactcctct atgtttgaag atgacacggt 780gacagagtac atctaccact gtaatgtaca aaccccaagt ggtgagacag ctttcaaaaa 840catgacgatt ccttacgggt gggccaagcg gcccatgctc cagcgcatag gtggcttgca 900ccctgacatt ccagtttcag tcatcttcgg cgcccggtcc tgcatagatg gcaactctgg 960caccagcatc cagtcactgc gacccaagtc atacgtgaag acaattgcta tcctcggggc 1020agggcattat gtgtatgcag accagccaga ggagttcaac cagaaagtca aggagatctg 1080ccacacagta gactgagcac acggaacc 1108101353DNASus scrofasource1..1353/mol_type="DNA" /organism="Sus scrofa" 10attgcgcgcg gctatggcag cagaggagga ggagatggac tccacggatg cctgtgagag 60gtctggatgg ctaactggtt ggcttcccac atggtgccct acatcgacgt cacaccttaa 120agaagctgaa gagaaaattt taaaatgtgt cccctgcata tacaaaaaag gacctgttcg 180tatatctaat ggaaataaaa tatggacact gaagctctct cataatattt caaataagat 240tccccttgtc ctccttcatg gttttggagg aggtctcgga ctttgggcac tgaattttgg 300agatctttgc accaatagac ccgtctatgc ttttgacctg ctgggctttg gacgaagtag 360tagacccaga tttgacactg atgcagaaga agtggagaat cagtttgtgg aatccattga 420agagtggaga tgtgccttag gattggacaa agtgatcttg ctgggacaca acctgggtgg 480gttcctagct gctgcttact cactgaagta cccctcaagg gttagtcatc tcattttagt 540tgaaccttgg ggttttcctg agcgaccaga ccttgctgat caagagagac caattccagt 600ttggatcaga gccttgggag cggcattgac tcccttcaac cctttagctg gtctcaggat 660tgcaggaccc tttggtttaa gtctagtaca gcgtttaagg cctgatttca aacggaagta 720ttcttcaatg tttgaagatg atactgtgac agaatatatc taccactgta atgttcagac 780tcccagtggt gagactgcat tcaaaaatat gactatccct tatggatggg caaaaaggcc 840aatgctccat cggattggta aaatgaaccc tgacattcca gtttcggtga tctacggagc 900ccgatcctgc atagatggca attctggcac cagcatccag tcattacgac cacattcata 960cgtgaagaca atagccattc ttggagcagg acattatgtg tatgcagatc aaccagaaga 1020cttcaaccta aaagtaaagg agatctgtga cactgtggac tgagtgcaat gcagatgaca 1080taggaagccc gatggctgat ccagttcctc agcaataatc cccagtctgc aatgaagagt 1140aaggaatcca gcatgagaac caggcactct tcctgcctgt actttgcaca tgttttcttt 1200atgaagctac tcacacattt aaaccagttg gtgccttcta gacgattggc tttcctttct 1260cctacacaaa atcaaaatat acaagaccct ccaaatctaa tagctttaat aaaaggttat 1320ttgtccctct gctgtaaaaa aaaaaaaaaa aaa 1353111084PRTHomo sapiensSOURCE1..1084/mol_type="protein" /organism="Homo sapiens" 11Met Ser Ser Gln Ser His Pro Asp Gly Leu Ser Gly Arg Asp Gln Pro1 5 10 15Val Glu Leu Leu Asn Pro Ala Arg Val Asn His Met Pro Ser Thr Val 20 25 30Asp Val Ala Thr Ala Leu Pro Leu Gln Val Ala Pro Ser Ala Val Pro 35 40 45Met Asp Leu Arg Leu Asp His Gln Phe Ser Leu Pro Val Ala Glu Pro 50 55 60Ala Leu Arg Glu Gln Gln Leu Gln Gln Glu Leu Leu Ala Leu Lys Gln65 70 75 80Lys Gln Gln Ile Gln Arg Gln Ile Leu Ile Ala Glu Phe Gln Arg Gln 85 90 95His Glu Gln Leu Ser Arg Gln His Glu Ala Gln Leu His Glu His Ile 100 105 110Lys Gln Gln Gln Glu Met Leu Ala Met Lys His Gln Gln Glu Leu Leu 115 120 125Glu His Gln Arg Lys Leu Glu Arg His Arg Gln Glu Gln Glu Leu Glu 130 135 140Lys Gln His Arg Glu Gln Lys Leu Gln Gln Leu Lys Asn Lys Glu Lys145 150 155 160Gly Lys Glu Ser Ala Val Ala Ser Thr Glu Val Lys Met Lys Leu Gln 165 170 175Glu Phe Val Leu Asn Lys Lys Lys Ala Leu Ala His Arg Asn Leu Asn 180 185 190His Cys Ile Ser Ser Asp Pro Arg Tyr Trp Tyr Gly Lys Thr Gln His 195 200 205Ser Ser Leu Asp Gln Ser Ser Pro Pro Gln Ser Gly Val Ser Thr Ser 210 215 220Tyr Asn His Pro Val Leu Gly Met Tyr Asp Ala Lys Asp Asp Phe Pro225 230 235 240Leu Arg Lys Thr Ala Ser Glu Pro Asn Leu Lys Leu Arg Ser Arg Leu 245 250 255Lys Gln Lys Val Ala Glu Arg Arg Ser Ser Pro Leu Leu Arg Arg Lys 260 265 270Asp Gly Pro Val Val Thr Ala Leu Lys Lys Arg Pro Leu Asp Val Thr 275 280 285Asp Ser Ala Cys Ser Ser Ala Pro Gly Ser Gly Pro Ser Ser Pro Asn 290 295 300Asn Ser Ser Gly Ser Val Ser Ala Glu Asn Gly Ile Ala Pro Ala Val305 310 315 320Pro Ser Ile Pro Ala Glu Thr Ser Leu Ala His Arg Leu Val Ala Arg 325 330 335Glu Gly Ser Ala Ala Pro Leu Pro Leu Tyr Thr Ser Pro Ser Leu Pro 340 345 350Asn Ile Thr Leu Gly Leu Pro Ala Thr Gly Pro Ser Ala Gly Thr Ala 355 360 365Gly Gln Gln Asp Thr Glu Arg Leu Thr Leu Pro Ala Leu Gln Gln Arg 370 375 380Leu Ser Leu Phe Pro Gly Thr His Leu Thr Pro Tyr Leu Ser Thr Ser385 390 395 400Pro Leu Glu Arg Asp Gly Gly Ala Ala His Ser Pro Leu Leu Gln His 405 410 415Met Val Leu Leu Glu Gln Pro Pro Ala Gln Ala Pro Leu Val Thr Gly 420 425 430Leu Gly Ala Leu Pro Leu His Ala Gln Ser Leu Val Gly Ala Asp Arg 435 440 445Val Ser Pro Ser Ile His Lys Leu Arg Gln His Arg Pro Leu Gly Arg 450 455 460Thr Gln Ser Ala Pro Leu Pro Gln Asn Ala Gln Ala Leu Gln His Leu465 470 475 480Val Ile Gln Gln Gln His Gln Gln Phe Leu Glu Lys His Lys Gln Gln 485 490 495Phe Gln Gln Gln Gln Leu Gln Met Asn Lys Ile Ile Pro Lys Pro Ser 500 505 510Glu Pro Ala Arg Gln Pro Glu Ser His Pro Glu Glu Thr Glu Glu Glu 515 520 525Leu Arg Glu His Gln Ala Leu Leu Asp Glu Pro Tyr Leu Asp Arg Leu 530 535 540Pro Gly Gln Lys Glu Ala His Ala Gln Ala Gly Val Gln Val Lys Gln545 550 555 560Glu Pro Ile Glu Ser Asp Glu Glu Glu Ala Glu Pro Pro Arg Glu Val 565 570 575Glu Pro Gly Gln Arg Gln Pro Ser Glu Gln Glu Leu Leu Phe Arg Gln 580 585 590Gln Ala Leu Leu Leu Glu Gln Gln Arg Ile His Gln Leu Arg Asn Tyr 595 600 605Gln Ala Ser Met Glu Ala Ala Gly Ile Pro Val Ser Phe Gly Gly His 610 615 620Arg Pro Leu Ser Arg Ala Gln Ser Ser Pro Ala Ser Ala Thr Phe Pro625 630 635 640Val Ser Val Gln Glu Pro Pro Thr Lys Pro Arg Phe Thr Thr Gly Leu 645 650 655Val Tyr Asp Thr Leu Met Leu Lys His Gln Cys Thr Cys Gly Ser Ser 660 665 670Ser Ser His Pro Glu His Ala Gly Arg Ile Gln Ser Ile Trp Ser Arg 675 680 685Leu Gln Glu Thr Gly Leu Arg Gly Lys Cys Glu Cys Ile Arg Gly Arg 690 695 700Lys Ala Thr Leu Glu Glu Leu Gln Thr Val His Ser Glu Ala His Thr705 710 715 720Leu Leu Tyr Gly Thr Asn Pro Leu Asn Arg Gln Lys Leu Asp Ser Lys 725 730 735Lys Leu Leu Gly Ser Leu Ala Ser Val Phe Val Arg Leu Pro Cys Gly 740 745 750Gly Val Gly Val Asp Ser Asp Thr Ile Trp Asn Glu Val His Ser Ala 755 760 765Gly Ala Ala Arg Leu Ala Val Gly Cys Val Val Glu Leu Val Phe Lys 770 775 780Val Ala Thr Gly Glu Leu Lys Asn Gly Phe Ala Val Val Arg Pro Pro785 790 795 800Gly His His Ala Glu Glu Ser Thr Pro Met Gly Phe Cys Tyr Phe Asn 805 810 815Ser Val Ala Val Ala Ala Lys Leu Leu Gln Gln Arg Leu Ser Val Ser 820 825 830Lys Ile Leu Ile Val Asp Trp Asp Val His His Gly Asn Gly Thr Gln 835 840 845Gln Ala Phe Tyr Ser Asp Pro Ser Val Leu Tyr Met Ser Leu His Arg 850 855 860Tyr Asp Asp Gly Asn Phe Phe Pro Gly Ser Gly Ala Pro Asp Glu Val865 870 875 880Gly Thr Gly Pro Gly Val Gly Phe Asn Val Asn Met Ala Phe Thr Gly 885 890 895Gly Leu Asp Pro Pro Met Gly Asp Ala Glu Tyr Leu Ala Ala Phe Arg 900 905 910Thr Val Val Met Pro Ile Ala Ser Glu Phe Ala Pro Asp Val Val Leu 915 920 925Val Ser Ser Gly Phe Asp Ala Val Glu Gly His Pro Thr Pro Leu Gly 930 935 940Gly Tyr Asn Leu Ser Ala Arg Cys Phe Gly Tyr Leu Thr Lys Gln Leu945 950 955 960Met Gly Leu Ala Gly Gly Arg Ile Val Leu Ala Leu Glu Gly Gly His 965 970 975Asp Leu Thr Ala Ile Cys Asp Ala Ser Glu Ala Cys Val Ser Ala Leu 980 985 990Leu Gly Asn Glu Leu Asp Pro Leu Pro Glu Lys Val Leu Gln Gln Arg 995 1000 1005Pro Asn Ala Asn Ala Val Arg Ser Met Glu Lys Val Met Glu Ile His 1010 1015 1020Ser Lys Tyr Trp Arg Cys Leu Gln Arg Thr Thr Ser Thr Ala Gly Arg1025 1030 1035 1040Ser Leu Ile Glu Ala Gln Thr Cys Glu Asn Glu Glu Ala Glu Thr Val 1045 1050 1055Thr Ala Met Ala Ser Leu Ser Val Gly Val Lys Pro Ala Glu Lys Arg 1060 1065 1070Pro Asp Glu Glu Pro Met Glu Glu Glu Pro Pro Leu 1075 1080121081PRTMus musculusSOURCE1..1081/mol_type="protein" /organism="Mus musculus" 12Met Ser Ser Gln Ser His Pro Asp Gly Leu Ser Gly Arg Asp Gln Pro1 5 10 15Val Glu Leu Leu Asn Pro Ala Arg Val Asn His Met Pro Ser Thr Val 20 25 30Asp Val Ala Thr Ala Leu Pro Leu Gln Val Ala Pro Thr Ala Val Pro 35 40 45Met Asp Leu Arg Leu Asp His Gln Phe Ser Leu Pro Leu Glu Pro Ala 50 55 60Leu Arg Glu Gln Gln Leu Gln Gln Glu Leu Leu Ala Leu Lys Gln Lys65 70 75 80Gln Gln Ile Gln Arg Gln Ile Leu Ile Ala Glu Phe Gln Arg Gln His 85 90 95Glu Gln Leu Ser Arg Gln His Glu Ala Gln Leu His Glu His Ile Lys 100 105 110Gln Gln Gln Glu Met Leu Ala Met Lys His Gln Gln Glu Leu Leu Glu 115 120 125His Gln Arg Lys Leu Glu Arg His Arg Gln Glu Gln Glu Leu Glu Lys 130 135 140Gln His Arg Glu Gln Lys Leu Gln Gln Leu Lys Asn Lys Glu Lys Gly145 150 155 160Lys Glu Ser Ala Val Ala Ser Thr Glu Val Lys Met Lys Leu Gln Glu 165 170 175Phe Val Leu Asn Lys Lys Lys Ala Leu Ala His Arg Asn Leu Asn His 180 185 190Cys Ile Ser Ser Asp Pro Arg Tyr Trp Tyr Gly Lys Thr Gln His Ser 195 200 205Ser Leu Asp Gln Ser Ser Pro Pro Gln Ser Gly Val Ser Ala Ser Tyr 210 215 220Asn His Pro Val Leu Gly Met Tyr Asp Ala Lys Asp Asp Phe Pro Leu225 230 235 240Arg Lys Thr Ala Ser Glu Pro Asn Leu Lys Leu Arg Ser Arg Leu Lys 245 250 255Gln Lys Val Ala Glu Arg Arg Ser Ser Pro Leu Leu Arg

Arg Lys Asp 260 265 270Gly Pro Val Ala Thr Ala Leu Lys Lys Arg Pro Leu Asp Val Thr Asp 275 280 285Ser Ala Cys Ser Ser Ala Pro Gly Ser Gly Pro Ser Ser Pro Asn Ser 290 295 300Ser Ser Gly Asn Val Ser Thr Glu Asn Gly Ile Ala Pro Thr Val Pro305 310 315 320Ser Ala Pro Ala Glu Thr Ser Leu Ala His Arg Leu Val Thr Arg Glu 325 330 335Gly Ser Val Ala Pro Leu Pro Leu Tyr Thr Ser Pro Ser Leu Pro Asn 340 345 350Ile Thr Leu Gly Leu Pro Ala Thr Gly Pro Ala Ala Gly Ala Ala Gly 355 360 365Gln Gln Asp Ala Glu Arg Leu Ala Leu Pro Ala Leu Gln Gln Arg Ile 370 375 380Leu Phe Pro Gly Thr His Leu Thr Pro Tyr Leu Ser Thr Ser Pro Leu385 390 395 400Glu Arg Asp Gly Ala Ala Ala His Asn Pro Leu Leu Gln His Met Val 405 410 415Leu Leu Glu Gln Pro Pro Thr Gln Thr Pro Leu Val Thr Gly Leu Gly 420 425 430Ala Leu Pro Leu His Ser Gln Ser Leu Val Gly Ala Asp Arg Val Ser 435 440 445Pro Ser Ile His Lys Leu Arg Gln His Arg Pro Leu Gly Arg Thr Gln 450 455 460Ser Ala Pro Leu Pro Gln Asn Ala Gln Ala Leu Gln His Leu Val Ile465 470 475 480Gln Gln Gln His Gln Gln Phe Leu Glu Lys His Lys Gln Gln Phe Gln 485 490 495Gln Gln Gln Leu His Leu Ser Lys Ile Ile Ser Lys Pro Ser Glu Pro 500 505 510Pro Arg Gln Pro Glu Ser His Pro Glu Glu Thr Glu Glu Glu Leu Arg 515 520 525Glu His Gln Ala Leu Leu Asp Glu Pro Tyr Leu Asp Arg Leu Pro Gly 530 535 540Gln Lys Glu Pro Ser Leu Ala Gly Val Gln Val Lys Gln Glu Pro Ile545 550 555 560Glu Ser Glu Glu Glu Glu Ala Glu Ala Thr Arg Glu Thr Glu Pro Gly 565 570 575Gln Arg Pro Ala Thr Glu Gln Glu Leu Leu Phe Arg Gln Gln Ala Leu 580 585 590Leu Leu Glu Gln Gln Arg Ile His Gln Leu Arg Asn Tyr Gln Ala Ser 595 600 605Met Glu Ala Ala Gly Ile Pro Val Ser Phe Gly Ser His Arg Pro Leu 610 615 620Ser Arg Ala Gln Ser Ser Pro Ala Ser Ala Thr Phe Pro Met Ser Val625 630 635 640Gln Glu Pro Pro Thr Lys Pro Arg Phe Thr Thr Gly Leu Val Tyr Asp 645 650 655Thr Leu Met Leu Lys His Gln Cys Thr Cys Gly Asn Thr Asn Ser His 660 665 670Pro Glu His Ala Gly Arg Ile Gln Ser Ile Trp Ser Arg Leu Gln Glu 675 680 685Thr Gly Leu Arg Gly Lys Cys Glu Cys Ile Arg Gly Arg Lys Ala Thr 690 695 700Leu Glu Glu Leu Gln Thr Val His Ser Glu Ala His Thr Leu Leu Tyr705 710 715 720Gly Thr Asn Pro Leu Asn Arg Gln Lys Leu Asp Ser Lys Lys Leu Leu 725 730 735Gly Ser Leu Thr Ser Val Phe Val Arg Leu Pro Cys Gly Gly Val Gly 740 745 750Val Asp Ser Asp Thr Ile Trp Asn Glu Val His Ser Ser Gly Ala Ala 755 760 765Arg Leu Ala Val Gly Cys Val Val Glu Leu Val Phe Lys Val Ala Thr 770 775 780Gly Glu Leu Lys Asn Gly Phe Ala Val Val Arg Pro Pro Gly His His785 790 795 800Ala Glu Glu Ser Thr Pro Met Gly Phe Cys Tyr Phe Asn Ser Val Ala 805 810 815Val Ala Ala Lys Leu Leu Gln Gln Arg Leu Asn Val Ser Lys Ile Leu 820 825 830Ile Val Asp Trp Asp Val His His Gly Asn Gly Thr Gln Gln Ala Phe 835 840 845Tyr Asn Asp Pro Asn Val Leu Tyr Met Ser Leu His Arg Tyr Asp Asp 850 855 860Gly Asn Phe Phe Pro Gly Ser Gly Ala Pro Asp Glu Val Gly Thr Gly865 870 875 880Pro Gly Val Gly Phe Asn Val Asn Met Ala Phe Thr Gly Gly Leu Glu 885 890 895Pro Pro Met Gly Asp Ala Glu Tyr Leu Ala Ala Phe Arg Thr Val Val 900 905 910Met Pro Ile Ala Asn Glu Phe Ala Pro Asp Val Val Leu Val Ser Ser 915 920 925Gly Phe Asp Ala Val Glu Gly His Pro Thr Pro Leu Gly Gly Tyr Asn 930 935 940Leu Ser Ala Lys Cys Phe Gly Tyr Leu Thr Lys Gln Leu Met Gly Leu945 950 955 960Ala Gly Gly Arg Leu Val Leu Ala Leu Glu Gly Gly His Asp Leu Thr 965 970 975Ala Ile Cys Asp Ala Ser Glu Ala Cys Val Ser Ala Leu Leu Gly Asn 980 985 990Glu Leu Glu Pro Leu Pro Glu Lys Val Leu His Gln Arg Pro Asn Ala 995 1000 1005Asn Ala Val His Ser Met Glu Lys Val Met Asp Ile His Ser Lys Tyr 1010 1015 1020Trp Arg Cys Leu Gln Arg Leu Ser Ser Thr Val Gly His Ser Leu Ile1025 1030 1035 1040Glu Ala Gln Lys Cys Glu Lys Glu Glu Ala Glu Thr Val Thr Ala Met 1045 1050 1055Ala Ser Leu Ser Val Gly Val Lys Pro Ala Glu Lys Arg Ser Glu Glu 1060 1065 1070Glu Pro Met Glu Glu Glu Pro Pro Leu 1075 108013201PRTHomo sapiensSOURCE1..201/mol_type="protein" /organism="Homo sapiens" 13Met Ser Ser Gln Ser His Pro Asp Gly Leu Ser Gly Arg Asp Gln Pro1 5 10 15Val Glu Leu Leu Asn Pro Ala Arg Val Asn His Met Pro Ser Thr Val 20 25 30Asp Val Ala Thr Ala Leu Pro Leu Gln Val Ala Pro Ser Ala Val Pro 35 40 45Met Asp Leu Arg Leu Asp His Gln Phe Ser Leu Pro Val Ala Glu Pro 50 55 60Ala Leu Arg Glu Gln Gln Leu Gln Gln Glu Leu Leu Ala Leu Lys Gln65 70 75 80Lys Gln Gln Ile Gln Arg Gln Ile Leu Ile Ala Glu Phe Gln Arg Gln 85 90 95His Glu Gln Leu Ser Arg Gln His Glu Ala Gln Leu His Glu His Ile 100 105 110Lys Gln Gln Gln Glu Met Leu Ala Met Lys His Gln Gln Glu Leu Leu 115 120 125Glu His Gln Arg Lys Leu Glu Arg His Arg Gln Glu Gln Glu Leu Glu 130 135 140Lys Gln His Arg Glu Gln Lys Leu Gln Gln Leu Lys Asn Lys Glu Lys145 150 155 160Gly Lys Glu Ser Ala Val Ala Ser Thr Glu Val Lys Met Lys Leu Gln 165 170 175Glu Phe Val Leu Asn Lys Lys Lys Ala Leu Ala His Arg Asn Leu Asn 180 185 190His Cys Ile Ser Ser Asp Pro Arg Tyr 195 20014201PRTMus musculusSOURCE1..201/mol_type="protein" /organism="Mus musculus" 14Met Ser Ser Gln Ser His Pro Asp Gly Leu Ser Gly Arg Asp Gln Pro1 5 10 15Val Glu Leu Leu Asn Pro Ala Arg Val Asn His Met Pro Ser Thr Val 20 25 30Asp Val Ala Thr Ala Leu Pro Leu Gln Val Ala Pro Thr Ala Val Pro 35 40 45Met Asp Leu Arg Leu Asp His Gln Phe Ser Leu Pro Leu Glu Pro Ala 50 55 60Leu Arg Glu Gln Gln Leu Gln Gln Glu Leu Leu Ala Leu Lys Gln Lys65 70 75 80Gln Gln Ile Gln Arg Gln Ile Leu Ile Ala Glu Phe Gln Arg Gln His 85 90 95Glu Gln Leu Ser Arg Gln His Glu Ala Gln Leu His Glu His Ile Lys 100 105 110Gln Gln Gln Glu Met Leu Ala Met Lys His Gln Gln Glu Leu Leu Glu 115 120 125His Gln Arg Lys Leu Glu Arg His Arg Gln Glu Gln Glu Leu Glu Lys 130 135 140Gln His Arg Glu Gln Lys Leu Gln Gln Leu Lys Asn Lys Glu Lys Gly145 150 155 160Lys Glu Ser Ala Val Ala Ser Thr Glu Val Lys Met Lys Leu Gln Glu 165 170 175Phe Val Leu Asn Lys Lys Lys Ala Leu Ala His Arg Asn Leu Asn His 180 185 190Cys Ile Ser Ser Asp Pro Arg Tyr Trp 195 200153255DNAHomo sapienssource1..3255/mol_type="DNA" /organism="Homo sapiens" 15atgagctccc aaagccatcc agatggactt tctggccgag accagccagt ggagctgctg 60aatcctgccc gcgtgaacca catgcccagc acggtggatg tggccacggc gctgcctctg 120caagtggccc cctcggcagt gcccatggac ctgcgcctgg accaccagtt ctcactgcct 180gtggcagagc cggccctgcg ggagcagcag ctgcagcagg agctcctggc gctcaagcag 240aagcagcaga tccagaggca gatcctcatc gctgagttcc agaggcagca cgagcagctc 300tcccggcagc acgaggcgca gctccacgag cacatcaagc aacaacagga gatgctggcc 360atgaagcacc agcaggagct gctggaacac cagcggaagc tggagaggca ccgccaggag 420caggagctgg agaagcagca ccgggagcag aagctgcagc agctcaagaa caaggagaag 480ggcaaagaga gtgccgtggc cagcacagaa gtgaagatga agttacaaga atttgtcctc 540aataaaaaga aggcgctggc ccaccggaat ctgaaccact gcatttccag cgaccctcgc 600tactggtacg ggaaaacgca gcacagttcc cttgaccaga gttctccacc ccagagcgga 660gtgtcgacct cctataacca cccggtcctg ggaatgtacg acgccaaaga tgacttccct 720cttaggaaaa cagcttctga accgaatctg aaattacggt ccaggctaaa gcagaaagtg 780gccgaaagac ggagcagccc cctgttacgc aggaaagacg ggccagtggt cactgctcta 840aaaaagcgtc cgttggatgt cacagactcc gcgtgcagca gcgccccagg ctccggaccc 900agctcaccca acaacagctc cgggagcgtc agcgcggaga acggtatcgc gcccgccgtc 960cccagcatcc cggcggagac gagtttggcg cacagacttg tggcacgaga aggctcggcc 1020gctccacttc ccctctacac atcgccatcc ttgcccaaca tcacgctggg cctgcctgcc 1080accggcccct ctgcgggcac ggcgggccag caggacaccg agagactcac ccttcccgcc 1140ctccagcaga ggctctccct tttccccggc acccacctca ctccctacct gagcacctcg 1200cccttggagc gggacggagg ggcagcgcac agccctcttc tgcagcacat ggtcttactg 1260gagcagccac cggcacaagc acccctcgtc acaggcctgg gagcactgcc cctccacgca 1320cagtccttgg ttggtgcaga ccgggtgtcc ccctccatcc acaagctgcg gcagcaccgc 1380ccactggggc ggacccagtc ggccccgctg ccccagaacg cccaggctct gcagcacctg 1440gtcatccagc agcagcatca gcagtttctg gagaaacaca agcagcagtt ccagcagcag 1500caactgcaga tgaacaagat catccccaag ccaagcgagc cagcccggca gccggagagc 1560cacccggagg agacggagga ggagctccgt gagcaccagg ctctgctgga cgagccctac 1620ctggaccggc tgccggggca gaaggaggcg cacgcacagg ccggcgtgca ggtgaagcag 1680gagcccattg agagcgatga ggaagaggca gagcccccac gggaggtgga gccgggccag 1740cgccagccca gtgagcagga gctgctcttc agacagcaag ccctcctgct ggagcagcag 1800cggatccacc agctgaggaa ctaccaggcg tccatggagg ccgccggcat ccccgtgtcc 1860ttcggcggcc acaggcctct gtcccgggcg cagtcctcac ccgcgtctgc caccttcccc 1920gtgtctgtgc aggagccccc caccaagccg aggttcacga caggcctcgt gtatgacacg 1980ctgatgctga agcaccagtg cacctgcggg agtagcagca gccaccccga gcacgccggg 2040aggatccaga gcatctggtc ccgcctgcag gagacgggcc tccggggcaa atgcgagtgc 2100atccgcggac gcaaggccac cctggaggag ctacagacgg tgcactcgga agcccacacc 2160ctcctgtatg gcacgaaccc cctcaaccgg cagaaactgg acagtaagaa acttctaggc 2220tcgctcgcct ccgtgttcgt ccggctccct tgcggtggtg ttggggtgga cagtgacacc 2280atatggaacg aggtgcactc ggcgggggca gcccgcctgg ctgtgggctg cgtggtagag 2340ctggtcttca aggtggccac aggggagctg aagaatggct ttgctgtggt ccgcccccct 2400ggacaccatg cggaggagag cacgcccatg ggcttttgct acttcaactc cgtggccgtg 2460gcagccaagc ttctgcagca gaggttgagc gtgagcaaga tcctcatcgt ggactgggac 2520gtgcaccatg gaaacgggac ccagcaggct ttctacagcg accctagcgt cctgtacatg 2580tccctccacc gctacgacga tgggaacttc ttcccaggca gcggggctcc tgatgaggtg 2640ggcacagggc ccggcgtggg tttcaacgtc aacatggctt tcaccggcgg cctggacccc 2700cccatgggag acgctgagta cttggcggcc ttcagaacgg tggtcatgcc gatcgccagc 2760gagtttgccc cggatgtggt gctggtgtca tcaggcttcg atgccgtgga gggccacccc 2820acccctcttg ggggctacaa cctctccgcc agatgcttcg ggtacctgac gaagcagctg 2880atgggcctgg ctggcggccg gattgtcctg gccctcgagg gaggccacga cctgaccgcc 2940atttgcgacg cctcggaagc atgtgtttct gccttgctgg gaaacgagct tgatcctctc 3000ccagaaaagg ttttacagca aagacccaat gcaaacgctg tccgttccat ggagaaagtc 3060atggagatcc acagcaagta ctggcgctgc ctgcagcgca caacctccac agcggggcgt 3120tctctgatcg aggctcagac ttgcgagaac gaagaagccg agacggtcac cgccatggcc 3180tcgctgtccg tgggcgtgaa gcccgccgaa aagagaccag atgaggagcc catggaagag 3240gagccgcccc tgtag 3255163246DNAMus musculussource1..3246/mol_type="DNA" /organism="Mus musculus" 16atgagctccc aaagccatcc agatggactt tctggccgag accagcctgt ggagctgctg 60aatcctgccc gtgtgaacca catgcccagc acggtggacg tggctacagc gctgcctctg 120caagtggccc ctacagcagt acccatggac ctgcgcttgg accaccagtt ctcactgccc 180ttggaacctg cattgcggga gcagcaactg cagcaggaac tcctagcact gaaacagaag 240cagcagatcc agcggcagat actcattgca gagttccagc gtcaacatga gcagttgtcc 300cgacagcatg aggcacagtt gcatgaacat atcaagcagc agcaggagat gctggccatg 360aagcaccagc aggagctgct ggagcaccag cggaaactgg agcggcaccg gcaagagcag 420gagctggaga agcagcaccg tgagcagaag ctgcagcagc tcaagaacaa ggagaagggc 480aaagagagtg ctgtggcgag cacagaggtg aagatgaagc tgcaggagtt tgttctcaac 540aagaagaagg ctctagccca ccggaacctg aaccactgca tttccagcga tccccgctac 600tggtatggga agacacagca cagctccctt gaccagagct ctccacccca gagtggggtg 660tcagcctcct acaaccaccc cgtcttggga atgtacgacg ccaaagatga cttccctctt 720aggaaaacag cttctgaacc taacctgaaa ttacgctcaa ggcttaagca gaaagtagct 780gagagacgga gcagccccct gttgcgcagg aaagatggcc ctgtggccac tgctctaaaa 840aagcgacccc tggatgttac agactccgca tgcagcagcg cccctggctc cggtcccagc 900tctccaaata gcagctctgg caacgtcagc actgagaatg gcatcgcacc cactgtgccc 960agcgctccag ctgagacgag cttggcacac agacttgtga ctcgagaagg ctcagtcgcc 1020ccacttcctc tctacacgtc accatcctta cccaacatca ccttgggact tcctgccact 1080ggccctgccg ctggtgcggc aggtcagcag gatgctgaga ggcttgctct cccagctctc 1140cagcagcgga tcttgttccc tgggacccac ctcaccccgt acctgagcac ctcgcccctg 1200gagagggacg gtgcagcagc tcacaacccc ctcctgcagc acatggtcct gctggagcag 1260ccacccaccc agacacccct tgtcacaggc ctgggggcgc tgcccctcca ctcacagtcc 1320ctggttggtg cggacagggt gtccccatcc attcacaagc tgcggcagca ccgccctctg 1380gggcgcacgc agtcagcacc cctgccgcag aacgcacagg ccctgcagca cctggtgatc 1440cagcagcagc accagcagtt cctggagaag cacaagcaac agttccagca gcagcagctg 1500cacctcagca agataatctc caaacctagt gagccacctc ggcagcctga gagccaccca 1560gaggagacag aggaggagct ccgtgagcac caggccttgc tggatgagcc ctacctagat 1620cggctacctg ggcagaagga gccctccctg gctggtgtgc aggtgaagca ggagcccatt 1680gagagtgagg aggaagaagc ggaggccact cgagagacag agcccggcca gcgcccagcc 1740actgagcagg agctgctctt cagacagcaa gccctcctac tggagcagca gaggatccac 1800cagttaagaa actaccaggc atctatggag gctgctggca tccctgtgtc atttggcagc 1860cacagacctc tgtctcgggc acagtcctcc ccagcatctg ccaccttccc catgtcagtc 1920caggagcccc ccaccaagcc aaggttcacc acaggtcttg tgtatgacac actgatgttg 1980aagcatcagt gcacctgtgg gaacaccaac agccacccgg agcatgctgg gaggatccag 2040agcatctggt cccgcctgca ggagactgga ctccgtggca agtgtgagtg catccgtgga 2100cgcaaggcca cattggagga gctgcagaca gtgcactcgg aggcccacac actcctctac 2160ggcacaaatc ctctcaacag acagaaactg gacagtaaga aacttctagg ctcgctgacc 2220tcagtgttcg tcaggcttcc ttgtggtggt gttggggtgg atagcgacac catatggaat 2280gaggtgcact cgtctggggc agcccgcctg gctgtaggct gtgtagtgga gctggtcttc 2340aaggtggcca cgggagagct aaagaatggc tttgctgtgg ttcgtccccc aggacaccat 2400gccgaggaga gcacacccat gggtttctgc tactttaact ccgtggcagt tgcagccaaa 2460cttctccagc agaggctgaa tgtgagcaag atcctcattg tagactggga tgtacatcat 2520gggaatggga cccagcaggc cttctacaat gaccccaatg ttctctacat gtccctgcac 2580cgctatgacg atgggaactt cttcccagga agtggagcac cagatgaggt gggcacaggg 2640ccaggcgtgg gtttcaatgt caacatggct ttcacgggtg gcctcgaacc ccccatggga 2700gacgctgagt acttggcagc cttcagaacg gtggttatgc ctatcgcaaa tgagtttgcc 2760ccagatgtgg tactggtgtc atcgggcttc gatgctgtgg agggccaccc cacacctctt 2820ggagggtaca atctctctgc caaatgtttt gggtacttga caaaacagct gatgggctta 2880gctggtggcc ggcttgtgct ggcccttgag ggaggccatg acctgacagc catctgtgat 2940gcttctgaag cctgcgtgtc tgctctgctg ggaaacgagc ttgagcctct gccagaaaag 3000gttctacatc agagacccaa tgccaatgct gtccactcca tggagaaagt gatggacatc 3060cacagcaagt actggcgctg cctgcagcgt ctgtcctcca cggtggggca ctctctgatt 3120gaggcgcaaa agtgtgagaa ggaagaagct gagacagtca ccgccatggc ctcgctgtct 3180gtaggcgtca aacctgctga gaagagatct gaggaggagc ccatggagga ggaaccacca 3240ctgtag 324617603DNAHomo sapienssource1..603/mol_type="DNA" /organism="Homo sapiens" 17atgagctccc aaagccatcc agatggactt tctggccgag accagccagt ggagctgctg 60aatcctgccc gcgtgaacca catgcccagc acggtggatg tggccacggc gctgcctctg 120caagtggccc cctcggcagt gcccatggac ctgcgcctgg accaccagtt ctcactgcct 180gtggcagagc cggccctgcg ggagcagcag ctgcagcagg agctcctggc gctcaagcag 240aagcagcaga tccagaggca gatcctcatc gctgagttcc agaggcagca cgagcagctc 300tcccggcagc acgaggcgca gctccacgag cacatcaagc aacaacagga gatgctggcc 360atgaagcacc agcaggagct gctggaacac cagcggaagc tggagaggca ccgccaggag 420caggagctgg agaagcagca ccgggagcag aagctgcagc agctcaagaa caaggagaag 480ggcaaagaga gtgccgtggc cagcacagaa gtgaagatga agttacaaga atttgtcctc 540aataaaaaga aggcgctggc ccaccggaat ctgaaccact gcatttccag cgaccctcgc 600tac

603184959DNAArtificial Sequencesource1..4959/mol_type="DNA" /note="Vector encoding human HDAC4-NT" /organism="Artificial Sequence" 18gggggggggg gggggggggg ccactccctc tctgcgcgct cgctcgctca ctgaggccgg 60gcgaccaaag gtcgcccgac gcccgggctt tgcccgggcg gcctcagtga gcgagcgagc 120gcgcagagag ggagtggcca actccatcac taggggttcc tagatctgaa ttcggtaccg 180cggtggcggc cgcttcgagc tcgcccgaca ttgattattg actagttatt aatagtaatc 240aattacgggg tcattagttc atagcccata tatggagttc cgcgttacat aacttacggt 300aaatggcccg cctggctgac cgcccaacga cccccgccca ttgacgtcaa taatgacgta 360tgttcccata gtaacgccaa tagggacttt ccattgacgt caatgggtgg agtatttacg 420gtaaactgcc cacttggcag tacatcaagt gtatcatatg ccaagtacgc cccctattga 480cgtcaatgac ggtaaatggc ccgcctggca ttatgcccag tacatgacct tatgggactt 540tcctacttgg cagtacatct acgtattagt catcgctatt accatggtga tgcggttttg 600gcagtacatc aatgggcgtg gatagcggtt tgactcacgg ggatttccaa gtctccaccc 660cattgacgtc aatgggagtt tgttttggca ccaaaatcaa cgggactttc caaaatgtcg 720taacaactcc gccccatgcg gccgctctag gacccagagc acagagcatc gttcccaggc 780caggccccag ccactgtctc tttaaccttg aaggcatttt tgggtctcac gtgtccaccc 840aggcgggtgt cggactttga acggctctta cttcagaaga acggcatggg gtgggggggc 900ttaggtggcc tctgcctcac ctacaactgc caaaagtggt catggggtta tttttaaccc 960cagggaagag gtatttattg ttccacagca ggggccggcc agcaggctcc ttgaattctg 1020cagtcgacgg taccgcggcc gcccccaatt cgagctcgcc cggggatccg ccaccatgag 1080ctcccaaagc catccagatg gactttctgg ccgagaccag ccagtggagc tgctgaatcc 1140tgcccgcgtg aaccacatgc ccagcacggt ggatgtggcc acggcgctgc ctctgcaagt 1200ggccccctcg gcagtgccca tggacctgcg cctggaccac cagttctcac tgcctgtggc 1260agagccggcc ctgcgggagc agcagctgca gcaggagctc ctggcgctca agcagaagca 1320gcagatccag aggcagatcc tcatcgctga gttccagagg cagcacgagc agctctcccg 1380gcagcacgag gcgcagctcc acgagcacat caagcaacaa caggagatgc tggccatgaa 1440gcaccagcag gagctgctgg aacaccagcg gaagctggag aggcaccgcc aggagcagga 1500gctggagaag cagcaccggg agcagaagct gcagcagctc aagaacaagg agaagggcaa 1560agagagtgcc gtggccagca cagaagtgaa gatgaagtta caagaatttg tcctcaataa 1620aaagaaggcg ctggcccacc ggaatctgaa ccactgcatt tccagcgacc ctcgctacta 1680gtctagagtc ggggcggccg gccgcttcga gcagacatga taagatacat tgatgagttt 1740ggacaaacca caactagaat gcagtgaaaa aaatgcttta tttgtgaaat ttgtgatgct 1800attgctttat ttgtaaccat tataagctgc aataaacaag ttaacaacaa caattgcatt 1860cattttatgt ttcaggttca gggggaggtg tgggaggttt tttaaagcaa gtaaaacctc 1920tacaaatgtg gtaaaatcga taactgggga gagatctagg aacccctagt gatggagttg 1980gccactccct ctctgcgcgc tcgctcgctc actgaggccg cccgggcaaa gcccgggcgt 2040cgggcgacct ttggtcgccc ggcctcagtg agcgagcgag cgcgcagaga gggagtggcc 2100cccccccccc cccccccctg cagcccagct gcattaatga atcggccaac gcgcggggag 2160aggcggtttg cgtattgggc gctcttccgc ttcctcgctc actgactcgc tgcgctcggt 2220cgttcggctg cggcgagcgg tatcagctca ctcaaaggcg gtaatacggt tatccacaga 2280atcaggggat aacgcaggaa agaacatgtg agcaaaaggc cagcaaaagg ccaggaaccg 2340taaaaaggcc gcgttgctgg cgtttttcca taggctccgc ccccctgacg agcatcacaa 2400aaatcgacgc tcaagtcaga ggtggcgaaa cccgacagga ctataaagat accaggcgtt 2460tccccctgga agctccctcg tgcgctctcc tgttccgacc ctgccgctta ccggatacct 2520gtccgccttt ctcccttcgg gaagcgtggc gctttctcaa tgctcacgct gtaggtatct 2580cagttcggtg taggtcgttc gctccaagct gggctgtgtg cacgaacccc ccgttcagcc 2640cgaccgctgc gccttatccg gtaactatcg tcttgagtcc aacccggtaa gacacgactt 2700atcgccactg gcagcagcca ctggtaacag gattagcaga gcgaggtatg taggcggtgc 2760tacagagttc ttgaagtggt ggcctaacta cggctacact agaaggacag tatttggtat 2820ctgcgctctg ctgaagccag ttaccttcgg aaaaagagtt ggtagctctt gatccggcaa 2880acaaaccacc gctggtagcg gtggtttttt tgtttgcaag cagcagatta cgcgcagaaa 2940aaaaggatct caagaagatc ctttgatctt ttctacgggg tctgacgctc agtggaacga 3000aaactcacgt taagggattt tggtcatgag attatcaaaa aggatcttca cctagatcct 3060tttaaattaa aaatgaagtt ttaaatcaat ctaaagtata tatgagtaaa cttggtctga 3120cagttaccaa tgcttaatca gtgaggcacc tatctcagcg atctgtctat ttcgttcatc 3180catagttgcc tgactccccg tcgtgtagat aactacgata cgggagggct taccatctgg 3240ccccagtgct gcaatgatac cgcgagaccc acgctcaccg gctccagatt tatcagcaat 3300aaaccagcca gccggaaggg ccgagcgcag aagtggtcct gcaactttat ccgcctccat 3360ccagtctatt aattgttgcc gggaagctag agtaagtagt tcgccagtta atagtttgcg 3420caacgttgtt gccattgcta caggcatcgt ggtgtcacgc tcgtcgtttg gtatggcttc 3480attcagctcc ggttcccaac gatcaaggcg agttacatga tcccccatgt tgtgcaaaaa 3540agcggttagc tccttcggtc ctccgatcgt tgtcagaagt aagttggccg cagtgttatc 3600actcatggtt atggcagcac tgcataattc tcttactgtc atgccatccg taagatgctt 3660ttctgtgact ggtgagtact caaccaagtc attctgagaa tagtgtatgc ggcgaccgag 3720ttgctcttgc ccggcgtcaa tacgggataa taccgcgcca catagcagaa ctttaaaagt 3780gctcatcatt ggaaaacgtt cttcggggcg aaaactctca aggatcttac cgctgttgag 3840atccagttcg atgtaaccca ctcgtgcacc caactgatct tcagcatctt ttactttcac 3900cagcgtttct gggtgagcaa aaacaggaag gcaaaatgcc gcaaaaaagg gaataagggc 3960gacacggaaa tgttgaatac tcatactctt cctttttcaa tattattgaa gcatttatca 4020gggttattgt ctcatgagcg gatacatatt tgaatgtatt tagaaaaata aacaaatagg 4080ggttccgcgc acatttcccc gaaaagtgcc acctgacgtc taagaaacca ttattatcat 4140gacattaacc tataaaaata ggcgtatcac gaggcccttt cgtctcgcgc gtttcggtga 4200tgacggtgaa aacctctgac acatgcagct cccggagacg gtcacagctt gtctgtaagc 4260ggatgccggg agcagacaag cccgtcaggg cgcgtcagcg ggtgttggcg ggtgtcgggg 4320ctggcttaac tatgcggcat cagagcagat tgtactgaga gtgcaccata tgcggtgtga 4380aataccgcac agatgcgtaa ggagaaaata ccgcatcagg aaattgtaaa cgttaatatt 4440ttgttaaaat tcgcgttaaa tttttgttaa atcagctcat tttttaacca ataggccgaa 4500atcggcaaaa tcccttataa atcaaaagaa tagaccgaga tagggttgag tgttgttcca 4560gtttggaaca agagtccact attaaagaac gtggactcca acgtcaaagg gcgaaaaacc 4620gtctatcagg gcgatggccc actacgtgaa ccatcaccct aatcaagttt tttggggtcg 4680aggtgccgta aagcactaaa tcggaaccct aaagggagcc cccgatttag agcttgacgg 4740ggaaagccgg cgaacgtggc gagaaaggaa gggaagaaag cgaaaggagc gggcgctagg 4800gcgctggcaa gtgtagcggt cacgctgcgc gtaaccacca cacccgccgc gcttaatgcg 4860ccgctacagg gcgcgtcgcg ccattcgcca ttcaggctac gcaactgttg ggaagggcga 4920tcggtgcggg cctcttcgct attacgccag ctggctgca 4959195932DNAArtificial Sequencesource1..5932/mol_type="DNA" /note="Vector for cardiomyocyte-specific expression of transgenes " /organism="Artificial Sequence" 19ctgcgcgctc gctcgctcac tgaggccgcc cgggcaaagc ccgggcgtcg ggcgaccttt 60ggtcgcccgg cctcagtgag cgagcgagcg cgcagagagg gagtggaatt cacgcgtctc 120agtccattag gagccagtag cctggaagat gtctttaccc ccagcatcag ttcaagtgga 180gcagcacata actcttgccc tctgccttcc aagattctgg tgctgagact tatggagtgt 240cttggaggtt gccttctgcc ccccaaccct gctcccagct ggccctccca ggcctgggtt 300gctggcctct gctttatcag gattctcaag agggacagct ggtttatgtt gcatgactgt 360tccctgcata tctgctctgg ttttaaatag cttatctgag cagctggagg accacatggg 420cttatatggc gtggggtaca tgttcctgta gccttgtccc tggcacctgc caaaatagca 480gccaacaccc cccaccccca ccgccatccc cctgccccac ccgtcccctg tcgcacattc 540ctccctccgc agggctggct caccaggccc cagcccacat gcctgcttaa agccctctcc 600atcctctgcc tcacccagtc ccaagcttta ttgcggtagt ttatcacagt taaattgcta 660acgcagtcag tgcttctgac acaacagtct cgaacttaag ctgcagaagt tggtcgtgag 720gcactgggca ggtaagtatc aaggttacaa gacaggttta aggagaccaa tagaaactgg 780gcttgtcgag acagagaaga ctcttgcgtt tctgataggc acctattggt cttactgaca 840tccactttgc ctttctctcc acaggtgtcc actcccagtt caattacagc tcttaaggct 900agagtactta atacgactca ctataggcta gcctcgacgg taccgcgggc ccgggatccg 960ccaccatggc ttccaaggtg tacgaccccg agcaacgcaa acgcatgatc actgggcctc 1020agtggtgggc tcgctgcaag caaatgaacg tgctggactc cttcatcaac tactatgatt 1080ccgagaagca cgccgagaac gccgtgattt ttctgcatgg taacgctgcc tccagctacc 1140tgtggaggca cgtcgtgcct cacatcgagc ccgtggctag atgcatcatc cctgatctga 1200tcggaatggg taagtccggc aagagcggga atggctcata tcgcctcctg gatcactaca 1260agtacctcac cgcttggttc gagctgctga accttccaaa gaaaatcatc tttgtgggcc 1320acgactgggg ggcttgtctg gcctttcact actcctacga gcaccaagac aagatcaagg 1380ccatcgtcca tgctgagagt gtcgtggacg tgatcgagtc ctgggacgag tggcctgaca 1440tcgaggagga tatcgccctg atcaagagcg aagagggcga gaaaatggtg cttgagaata 1500acttcttcgt cgagaccatg ctcccaagca agatcatgcg gaaactggag cctgaggagt 1560tcgctgccta cctggagcca ttcaaggaga agggcgaggt tagacggcct accctctcct 1620ggcctcgcga gatccctctc gttaagggag gcaagcccga cgtcgtccag attgtccgca 1680actacaacgc ctaccttcgg gccagcgacg atctgcctaa gatgttcatc gagtccgacc 1740ctgggttctt ttccaacgct attgtcgagg gagctaagaa gttccctaac accgagttcg 1800tgaaggtgaa gggcctccac ttcagccagg aggacgctcc agatgaaatg ggtaagtaca 1860tcaagagctt cgtggagcgc gtgctgaaga acgagcagta atgtacaagt aaagcggccg 1920cgactctaga tcataatcag ccataccaca tttgtagagg ttttacttgc tttaaaaaac 1980ctcccacacc tccccctgaa cctgaaacat aaaatgaatg caattgttgt tgttaacttg 2040tttattgcag cttataatgg ttacaaataa agcaatagca tcacaaattt cacaaataaa 2100gcattttttt cactgcattc tagttgtggt ttgtccaaac tcatcaatgt atcttaaggc 2160gggaattgat ctaggaaccc ctagtgatgg agttggccac tccctctctg cgcgctcgct 2220cgctcactga ggccgcccgg gcaaagcccg ggcgtcgggc gacctttggt cgcccggcct 2280cagtgagcga gcgagcgcgc agagagggag tggccaaccc cccccccccc cccccggcga 2340ttctcttgtt tgctccagac tctcaggcaa tgacctgata gcctttgtag agacctctca 2400aaaatagcta ccctctccgg catgaattta tcagctagaa cggttgaata tcatattgat 2460ggtgatttga ctgtctccgg cctttctcac ccgtttgaat ctttacctac acattactca 2520ggcattgcat ttaaaatata tgagggttct aaaaattttt atccttgcgt tgaaataaag 2580gcttctcccg caaaagtatt acagggtcat aatgtttttg gtacaaccga tttagcttta 2640tgctctgagg ctttattgct taattttgct aattctttgc cttgcctgta tgatttattg 2700gatgttggaa tcgcctgatg cggtattttc tccttacgca tctgtgcggt atttcacacc 2760gcatatggtg cactctcagt acaatctgct ctgatgccgc atagttaagc cagccccgac 2820acccgccaac acccgctgac gcgccctgac gggcttgtct gctcccggca tccgcttaca 2880gacaagctgt gaccgtctcc gggagctgca tgtgtcagag gttttcaccg tcatcaccga 2940aacgcgcgag acgaaagggc ctcgtgatac gcctattttt ataggttaat gtcatgataa 3000taatggtttc ttagacgtca ggtggcactt ttcggggaaa tgtgcgcgga acccctattt 3060gtttattttt ctaaatacat tcaaatatgt atccgctcat gagacaataa ccctgataaa 3120tgcttcaata atattgaaaa aggaagagta tgagtattca acatttccgt gtcgccctta 3180ttcccttttt tgcggcattt tgccttcctg tttttgctca cccagaaacg ctggtgaaag 3240taaaagatgc tgaagatcag ttgggtgcac gagtgggtta catcgaactg gatctcaaca 3300gcggtaagat ccttgagagt tttcgccccg aagaacgttt tccaatgatg agcactttta 3360aagttctgct atgtggcgcg gtattatccc gtattgacgc cgggcaagag caactcggtc 3420gccgcataca ctattctcag aatgacttgg ttgagtactc accagtcaca gaaaagcatc 3480ttacggatgg catgacagta agagaattat gcagtgctgc cataaccatg agtgataaca 3540ctgcggccaa cttacttctg acaacgatcg gaggaccgaa ggagctaacc gcttttttgc 3600acaacatggg ggatcatgta actcgccttg atcgttggga accggagctg aatgaagcca 3660taccaaacga cgagcgtgac accacgatgc ctgtagcaat ggcaacaacg ttgcgcaaac 3720tattaactgg cgaactactt actctagctt cccggcaaca attaatagac tggatggagg 3780cggataaagt tgcaggacca cttctgcgct cggcccttcc ggctggctgg tttattgctg 3840ataaatctgg agccggtgag cgtgggtctc gcggtatcat tgcagcactg gggccagatg 3900gtaagccctc ccgtatcgta gttatctaca cgacggggag tcaggcaact atggatgaac 3960gaaatagaca gatcgctgag ataggtgcct cactgattaa gcattggtaa ctgtcagacc 4020aagtttactc atatatactt tagattgatt taaaacttca tttttaattt aaaaggatct 4080aggtgaagat cctttttgat aatctcatga ccaaaatccc ttaacgtgag ttttcgttcc 4140actgagcgtc agaccccgta gaaaagatca aaggatcttc ttgagatcct ttttttctgc 4200gcgtaatctg ctgcttgcaa acaaaaaaac caccgctacc agcggtggtt tgtttgccgg 4260atcaagagct accaactctt tttccgaagg taactggctt cagcagagcg cagataccaa 4320atactgttct tctagtgtag ccgtagttag gccaccactt caagaactct gtagcaccgc 4380ctacatacct cgctctgcta atcctgttac cagtggctgc tgccagtggc gataagtcgt 4440gtcttaccgg gttggactca agacgatagt taccggataa ggcgcagcgg tcgggctgaa 4500cggggggttc gtgcacacag cccagcttgg agcgaacgac ctacaccgaa ctgagatacc 4560tacagcgtga gctatgagaa agcgccacgc ttcccgaagg gagaaaggcg gacaggtatc 4620cggtaagcgg cagggtcgga acaggagagc gcacgaggga gcttccaggg ggaaacgcct 4680ggtatcttta tagtcctgtc gggtttcgcc acctctgact tgagcgtcga tttttgtgat 4740gctcgtcagg ggggcggagc ctatggaaaa acgccagcaa cgcggccttt ttacggttcc 4800tggccttttg ctggcctttt gctcacatgt tctttcctgc gttatcccct gattctgtgg 4860ataaccgtat taccgccttt gagtgagctg ataccgctcg ccgcagccga acgaccgagc 4920gcagcgagtc agtgagcgag gaagcggaag agcgcccaat acgcaaaccg cctctccccg 4980cgcgttggcc gattcattaa tgcagctggc gtaatagcga agaggcccgc accgatcgcc 5040cttcccaaca gttgcgcagc ctgaatggcg aatggcgatt ccgttgcaat ggctggcggt 5100aatattgttc tggatattac cagcaaggcc gatagtttga gttcttctac tcaggcaagt 5160gatgttatta ctaatcaaag aagtattgcg acaacggtta atttgcgtga tggacagact 5220cttttactcg gtggcctcac tgattataaa aacacttctc aggattctgg cgtaccgttc 5280ctgtctaaaa tccctttaat cggcctcctg tttagctccc gctctgattc taacgaggaa 5340agcacgttat acgtgctcgt caaagcaacc atagtacgcg ccctgtagcg gcgcattaag 5400cgcggcgggt gtggtggtta cgcgcagcgt gaccgctaca cttgccagcg ccctagcgcc 5460cgctcctttc gctttcttcc cttcctttct cgccacgttc gccggctttc cccgtcaagc 5520tctaaatcgg gggctccctt tagggttccg atttagtgct ttacggcacc tcgaccccaa 5580aaaacttgat tagggtgatg gttcacgtag tgggccatcg ccctgataga cggtttttcg 5640ccctttgacg ttggagtcca cgttctttaa tagtggactc ttgttccaaa ctggaacaac 5700actcaaccct atctcggtct attcttttga tttataaggg attttgccga tttcggccta 5760ttggttaaaa aatgagctga tttaacaaaa atttaacgcg aattttaaca aaatattaac 5820gcttacaatt taaatatttg cttatacaat cttcctgttt ttggggcttt tctgattatc 5880aaccggggta catatgattg acatgctagt tttacgatta ccgttcatcg cc 593220107DNAArtificial Sequencesource1..107/mol_type="DNA" /note="recognition site for micro RNA 122" /organism="Artificial Sequence" 20gtaatctaga tcgcgaacaa acaccattgt cacactccag tatacacaaa caccattgtc 60acactccaga tatcacaaac accattgtca cactccaagg cctggct 10721544DNAArtificial Sequencesource1..544/mol_type="DNA" /note="Sequence of the human troponin T promoter" /organism="Artificial Sequence" 21ctcagtccat taggagccag tagcctggaa gatgtcttta cccccagcat cagttcaagt 60ggagcagcac ataactcttg ccctctgcct tccaagattc tggtgctgag acttatggag 120tgtcttggag gttgccttct gccccccaac cctgctccca gctggccctc ccaggcctgg 180gttgctggcc tctgctttat caggattctc aagagggaca gctggtttat gttgcatgac 240tgttccctgc atatctgctc tggttttaaa tagcttatct gagcagctgg aggaccacat 300gggcttatat ggcgtggggt acatgttcct gtagccttgt ccctggcacc tgccaaaata 360gcagccaaca ccccccaccc ccaccgccat ccccctgccc cacccgtccc ctgtcgcaca 420ttcctccctc cgcagggctg gctcaccagg ccccagccca catgcctgct taaagccctc 480tccatcctct gcctcaccca gtcccaagct ttattgcggt agtttatcac agttaaattg 540ctaa 54422828DNAArtificial Sequencesource1..828/mol_type="DNA" /note="CMVMLC260 Promoter" /organism="Artificial Sequence" 22gcggccgctt cgagctcgcc cgacattgat tattgactag ttattaatag taatcaatta 60cggggtcatt agttcatagc ccatatatgg agttccgcgt tacataactt acggtaaatg 120gcccgcctgg ctgaccgccc aacgaccccc gcccattgac gtcaataatg acgtatgttc 180ccatagtaac gccaataggg actttccatt gacgtcaatg ggtggagtat ttacggtaaa 240ctgcccactt ggcagtacat caagtgtatc atatgccaag tacgccccct attgacgtca 300atgacggtaa atggcccgcc tggcattatg cccagtacat gaccttatgg gactttccta 360cttggcagta catctacgta ttagtcatcg ctattaccat ggtgatgcgg ttttggcagt 420acatcaatgg gcgtggatag cggtttgact cacggggatt tccaagtctc caccccattg 480acgtcaatgg gagtttgttt tggcaccaaa atcaacggga ctttccaaaa tgtcgtaaca 540actccgcccc atgcggccgc tctaggaccc agagcacaga gcatcgttcc caggccaggc 600cccagccact gtctctttaa ccttgaaggc atttttgggt ctcacgtgtc cacccaggcg 660ggtgtcggac tttgaacggc tcttacttca gaagaacggc atggggtggg ggggcttagg 720tggcctctgc ctcacctaca actgccaaaa gtggtcatgg ggttattttt aaccccaggg 780aagaggtatt tattgttcca cagcaggggc cggccagcag gctccttg 828

Claims

1.-17. (canceled)

18. An elongated and/or multimerized variant of the N-terminal fragment of histone deacetylase 4 (HDAC4-NT).

19. The variant of HDAC4-NT of claim 18, which has at least 80% sequence identity over the entire length of the protein according to SEQ ID NO:13 or 14.

20. The variant of HDAC4-NT of claim 18, which is an elongation variant comprising the amino acid positions 2 to 202, 1 to 220, 1 to 216, 1 to 212 or 1 to 208 of human HDAC4 as defined by SEQ NO: 11.

21. The variant of HDAC4-NT of claim 18, wherein the variant is a multimerization variant comprising at least 2, at least 3, at least 4, or at least 5 repeats of HDAC4-NT.

22. A vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof.

23. The vector of claim 22, selected from the group consisting of plasmids, cosmids, phages, viruses and artificial chromosomes.

24. The vector of claim 22, selected from the group consisting of adenovirus vectors, adeno-associated virus (AAV) vectors, alphavirus vectors, herpes virus vectors, arena virus vectors, measles virus vectors, pox virus vectors, NYVAC, avipox vectors, vesicular stomatitis virus vectors, retrovirus vectors, lentivirus vectors, viral like particles, and bacterial spores.

25. The vector of claim 24, which is an AAV vector.

26. The vector of claim 25, selected from the group consisting of AAV type 6, type 1, type 5, type 9 and type 2.

27. The vector of claim 22 wherein HDAC4-NT or the variant thereof is expressed under control of the human troponin promoter and a recognition site for micro-RNA 122 between the promoter and the terminator sequence so that said recognition site becomes part of the transcript produced from this vector.

28. A method of treating of preventing heart failure, the method comprising administering an effective amount of a nucleic acid encoding HDAC4-NT or a variant thereof or a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof, to a patient.

29. A method of treating myocardial remodeling during heart failure, the method comprising administering an effective amount of a nucleic acid encoding HDAC4-NT or a variant thereof or a vector comprising a nucleic acid encoding HDAC4-NT or a variant thereof, to a patient.