Patent application title: PLANT HEIGHT REGULATORY GENE AND USES THEREOF
Zuhua He (Shanghai, CN)
Shanghai Institutes Of Biological Sciences, Chinese Academy Of Sciences
Yingying Zhang (Shanghai, CN)
Qun Li (Shanghai, CN)
Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences
IPC8 Class: AC12N1582FI
Class name: Multicellular living organisms and unmodified parts thereof and related processes method of using a plant or plant part in a breeding process which includes a step of sexual hybridization
Publication date: 2013-09-19
Patent application number: 20130247242
Provided are a crop height regulatory gene from Arabidopsis thaliana,
expression regulatory sequences thereof and uses thereof. The crop
regulatory gene can be used to regulate the plant height, volume, tiller,
yield, flower organ size, or seed size of crops.
20. A method for increasing flower organ size, seed size, plant height, or plant volume of a crop, comprising reducing the level of an mRNA in the crop, wherein the mRNA is encoded by a polynucleotide selected from the group consisting of: (a) a polynucleotide encoding a polypeptide having the amino acid sequence set forth in SEQ ID NO:3; (b) a polynucleotide encoding a variant of the polypeptide of (a), comprising substitution, deletion, or addition of 1-50 amino acid residues in the amino acid sequence set forth in SEQ ID NO:3; (c) the nucleotide sequence set forth in SEQ ID NO: 2; and (d) the nucleotide sequence set forth in SEQ ID NO: 1; wherein the reducing the level of the mRNA is selected from the group consisting of knocking out any one of the polynucleotide of (a)-(d), expressing an RNAi construct comprising a fragment of any one of the polynucleotide of (a)-(d), expressing an antisense construct comprising a fragment of any one of the polynucleotide of (a)-(d) in an antisense orientation, and any combination thereof.
21. The method of claim 20, wherein the polynucleotide encodes the polypeptide having the amino acid sequence set forth in SEQ ID NO:3.
22. The method of claim 20, wherein the polynucleotide comprises the nucleotide sequence set forth in SEQ ID NO:1.
23. The method of claim 20, wherein said polynucleotide comprises the nucleotide sequence set forth in SEQ ID NO:2.
24. The method of claim 20, wherein the reducing the level of the mRNA is by knocking out any one of the polynucleotide of (a)-(d).
25. The method of claim 20, wherein the reducing the level of the mRNA is by expressing an RNAi construct comprising a fragment of any one of the polynucleotide of (a)-(d).
26. The method of claim 20, wherein the reducing the level of the mRNA is by expressing an antisense construct comprising a fragment of any one of the polynucleotide of (a)-(d) in an antisense orientation.
27. A method of producing a plant, wherein said method comprises the following steps: (1) providing Agrobacterium carrying an RNAi construct comprising a fragment of a polynucleotide selected from the group consisting of: (a) a polynucleotide encoding a polypeptide having the amino acid sequence set forth in SEQ ID NO:3, (b) a polynucleotide encoding a variant of the polypeptide of (a), comprising substitution, deletion, or addition of 1-50 amino acid residues in the amino acid sequence set forth in SEQ ID NO:3, (c) the nucleotide sequence set forth in SEQ ID NO: 2, and (d) the nucleotide sequence set forth in SEQ ID NO: 1, wherein expression of the RNAi construct reduces the level of mRNA encoded by any one of the polynucleotide of (a)-(d), so as to increase flower organ size, seed size, plant height, or plant volume of the plant; (2) contacting a cell, tissue, or organ of the plant with the Agrobacterium described in step (1), to introduce the RNAi construct into the cell, tissue, or organ and allow the RNAi construct to integrate into a chromosome of the cell, tissue, or organ; (3) selecting the cell, tissue, or organ of the plant containing the RNAi construct; and (4) allowing the cell, tissue, or organ of the plant described in step (3) to regenerate a new plant.
28. The method of claim 27, further comprising: crossbreeding the new plant with a non-transgenic plant, thereby obtaining a hybrid offspring containing the polynucleotide.
29. The method of claim 27, wherein the polynucleotide encodes the polypeptide having the amino acid sequence set forth in SEQ ID NO:3.
30. The method of claim 27, wherein the polynucleotide comprises the nucleotide sequence set forth in SEQ ID NO:1.
31. The method of claim 27, wherein said polynucleotide comprises the nucleotide sequence set forth in SEQ ID NO:2.
32. A transgenic plant prepared by the method of claim 27.
33. The transgenic plant of claim 32, wherein the plant is one selected from the group consisting of a Gramineae plant, a Cruciferae plant, and a xylophyta plant.
34. The transgenic plant of claim 32, wherein the plant is selected from the group consisting of soybean, corn (maize), cotton, canola, sugar beet, alfalfa, rice, wheat, barley, rye, sorghum, sugarcane, sunflower, oilseed rape, and vegetables.
FIELD OF THE INVENTION
 The present invention relates to the fields of genetic technology and botany. In particular, the present invention relates to a plant height regulatory gene and uses thereof.
BACKGROUND OF THE INVENTION
 Currently, the investigation for high-yield crop breeding mainly focuses on improving the plant type and panicle traits. Many high-yielding crop varieties have been developed to date due to the progression of cultivar improvement.
 However, one major problem existing in many high-yield crops, such as high-yield rice cultivars (especially, super hybrid rice varieties), is over-height of the plants. The over-height can result in a higher tendency of lodging (beaten flat to ground) and limiting the potential for higher yields. This issue significantly impacts further increases in crop yields and wide adoption of the high-yield varieties.
 Accordingly, it is necessary, in the art, to develop a method for regulating the heights of crop plants, in order to further improve the crop traits and increase the crop yields.
SUMMARY OF THE INVENTION
 The object of the present invention is to provide a plant height regulatory gene and uses thereof.
 In the first aspect, the invention provides isolated plant height regulatory polypeptides, selected from the group consisting of:
 (a) a polypeptide having the amino acid sequence set forth in SEQ ID NO: 3; and
 (b) a polypeptide derived from (a), comprising substitution, deletion, or addition of one or more amino acid residues in the amino acid sequence set forth in SEQ ID NO:3 and having a plant height regulatory function.
 In a preferred embodiment, said polypeptide is the polypeptide having the amino acid sequence set forth in SEQ ID NO: 3.
 In a second aspect, the invention provides isolated polynucleotides each having a nucleotide sequence selected from the group consisting of:
 (a) a polynucleotide encoding the polypeptide described above; and
 (b) a polynucleotide complementary to the polynucleotide of (a).
 In a preferred embodiment, the polynucleotide encodes a polypeptide having the amino acid sequence set forth in SEQ ID NO:3.
 In another preferred embodiment, the sequence of the polynucleotide has the nucleotide sequence set forth in SEQ ID NO: 2; or the nucleotide sequence set forth in SEQ ID NO: 1.
 In a third aspect, the invention provides vectors each comprising a polynucleotide described above.
 In a fourth aspect, the invention provides genetically engineered host cells each comprising a vector described above.
 In a fifth aspect, the invention provides plants each comprising a polynucleotide described above.
 In a sixth aspect, the invention provides methods for producing the plants described above, wherein a method comprises introducing a polynucleotide described above into a plant.
 In a preferred embodiment, a method described above comprises:
 (1) providing Agrobacterium cells carrying an expression vector containing a polynucleotide described above;
 (2) contacting cells, tissues, or organs of a plant with the Agrobacterium cells described in the step (1), to introduce said polynucleotide into the plant cells, and allowing the polynucleotide to integrate into the chromosomes of the plant cells;
 (3) selecting the plant cell, tissue, or organ containing said polynucleotide; and
 (4) allowing the plant cell, tissue, or organ described in the step (3) to regenerate a new plant.
 In a seventh aspect, the invention provides methods for producing a plant. Each method comprises crossbreeding the plant with the introduced polynucleotide with a non-transgenic plant, thereby obtaining hybrid offspring containing said polynucleotide.
 In an eighth aspect, the invention provides methods for producing a polypeptides described above. A method comprises:
 (a) culturing a host cell containing said polynucleotide under a condition suitable for expression;
 (b) isolating said polypeptide from the culture.
 In a ninth aspect, the invention provides uses of a polypeptide or its encoding polynucleotide described above in:
 regulating plant heights, volumes, tillerings, yields, flower organ sizes, or seed sizes of crops; or
 preparing a material for regulating plant heights, volumes, tillerings, yields, flower organ sizes, or seed sizes of crops.
 In a tenth aspect, the invention provides methods for regulating plant heights, volumes, tillerings, yields, flower organ sizes, or seed sizes of crops. A method comprises regulating the expression or activity of a plant height regulatory gene in crops.
 In another preferred embodiment, decreased plant heights and volumes, and increased tillerings and yields can be achieved by enhancement of the expression or activity of the plant height regulatory gene in crops; and increased flower organ sizes, seed sizes, plant heights, or volumes can be achieved by inhibition of the expression or activity of the plant height regulatory gene in crops;
 In an eleventh aspect, the invention provides agonists or antagonists for a plant height regulatory polypeptide described above or its encoding gene.
 In a twelfth aspect, the invention provides promoters for specific expression in plant stems or leaves. A promoter is selected from the group consisting of:
 (1) a polynucleotide having the nucleotide sequence set forth in SEQ ID NO: 13;
 (2) a polynucleotide capable of hybridizing to the polynucleotide sequence described in (1) under stringent conditions, and capable of directing specific expression of a target gene in plant stems or leaves; and
 (3) a polynucleotide having more than 70% (preferably more than 80%, more preferably more than 90%, most preferably more than 95%, such as 98%, 99%) identity with the nucleotide sequence set forth in SEQ ID NO:13 and capable of directing specific expression of a target gene in plant stems or leaves.
 In the thirteenth aspect, the invention relates to uses of said promoters to direct specific expression of a target gene in plant sterns or leaves.
 In the fourteenth aspect, the invention provides constructs, each of which comprising a promoter described above for specific expression in plant sterns or leaves.
 In another preferred embodiment, a construct described above comprises at least one polyclonal site (such as restriction sites), for inserting a target gene, downstream of and operably linked to a promoter for specific expression in plant stems or leaves.
 In another preferred embodiment, said construct is an expression vector.
 In another preferred embodiment, said construct comprises the following elements operably linked to each other: said promoter and a target gene.
 In another preferred embodiment, said target gene is an exogenous gene.
 In another preferred embodiment, said target gene is a structural gene.
 In another preferred embodiment, said target gene can encode a protein with a specific function.
 In another preferred embodiment, said target gene is located less than 2000 bp (preferably less than 1000 bp, more preferably less than 500 bp, most preferably less than 300 bp) downstream of said promoter.
 In light of the description provided herein, other aspects of the invention would be apparent to those skilled in the art.
BRIEF DESCRIPTION OF THE DRAWINGS
 FIG. 1 shows a top view of a wild-type (Wt) Arabidopsis plant and an ELb (Eui-like b) over-expressing transgenic Arabidopsis (ELb-OE) plant. An ELa (Eui-like a) over-expressing transgenic Arabidopsis (ELa-OE) plant and a rice OsEui over-expressional transgenic Arabidopsis (OsEui-OE) plant act as controls.
 FIG. 2 shows a comparison of growth profiles between a wild-type (WT) Arabidopsis plant and ELb RNAi/ela Arabidopsis plants.
 FIG. 3 shows a comparison of growth profiles of flower organs and seeds between Elb RNAi/ela Arabidopsis plants and a wild-type (WT) Arabidopsis plant.
 FIG. 4 shows tissue-specific expression of a reporter gene GUS initiated by the ELb promoter. The arrows indicate the regions displaying blue color.
 FIG. 5 shows a comparison of growth profiles between a wild-type rice (TP309) plant and Elb over-expressing rice (ELb-OE) plants.
 FIG. 6 shows statistical analysis of plant heights of a wild type rice (TP309) plant and Elb over-expressing rice (ELb-OE) plants.
 FIG. 7 shows statistical analysis of effective tillering numbers of a wild-type rice (TP309) plant and Elb over-expressing rice (ELb-OE) plants.
 FIG. 8 shows a comparison of grain weights from a single plant between a wild-type rice (TP309) plant and Elb over-expressing rice (ELb-OE) plants.
 By extensive researches, the inventors discovered an ELb gene useful for regulating plant heights, volumes, tillerings, yields, flower organ sizes, and seed sizes in crops. It is possible to decrease the plant heights and volumes and increase effective tillering numbers and yields of crops by increasing the expression of this gene. It is also possible to increase flower organ sizes and seed sizes by decreasing the expression of this gene. The present invention is based on these findings.
 As used herein, the term "crop" or "crops" include, but are not limited to: Gramineae, Cruciferae, and xylophyta, and the like. More preferably, the Gramineae includes, but is not limited to: rice, wheat, barley, maize, sorghum, and the like; or the Cruciferae includes, but is not limited to: Arabidopsis.
 As used herein, "isolated" refers to material isolated from its original environments (original environments are natural environments for natural material). For example, natural polynucleotides and polypeptides in living cells are non-isolated or non-purified, but polynucleotides and polypeptides are isolated or purified when separated from other materials which commonly accompany them in natural states.
 As used herein, "an isolated plant height regulatory polypeptide," "an isolated ELb protein", or "an isolated ELb polypeptide" refers to an ELb protein substantially free from other proteins, lipids, saccharides, or other materials which accompany ELb protein in natural states. Those skilled in the art are capable of purifying ELb protein using standard protein purification techniques. A substantially pure polypeptide forms a single main band in a non-reduction polyacrylamide gel.
 As used herein, the term "contain," "having," or "comprise" includes the meaning of "including," "mainly composed of," "substantially composed of," and "composed of"; "mainly composed of," "substantially composed of" and "composed of" are specific terms of "contain," "having," or "comprise."
 ELb Polypeptide and Uses Thereof
 Polypeptides of the invention can be recombinant polypeptides, natural polypeptides, or synthetic polypeptides, preferably recombinant polypeptides. Polypeptides of the invention can be purified natural products, or chemically synthesized products, or products derived from prokaryotic or eukaryotic hosts (such as bacterial, yeast, higher plant, insect, and mammalian cells) using recombinant techniques. Polypeptides of the invention can be glycosylated or non-glycosylated, depending on the host cells used for recombinant production. Polypeptides of the invention may or may not comprise a methionine residue at the initiating site.
 The invention further includes fragments, derivatives, and analogues of ELb proteins. As used herein, the term "fragment", "derivative", and "analogue" refer to a polypeptide that retains substantially the same biological functions or activities as ELb polypeptides of the invention. The fragments, derivatives, and analogues of the invention can be (i) a polypeptides with one or more conservative or non-conservative amino acid residues (preferably conservative residue) substituted, said substituted residues may or may not be encoded by genetic codes, or (ii) a polypeptides with substituent group(s) in one or more amino acid residues, or (iii) a polypeptide derived from a mature polypeptide coupled to another compound (such as compound capable of extending the half life of a polypeptide, e.g. polyethylene glycol), or (iv) a polypeptide derived from said polypeptide coupled to an additional amino acid sequence (e.g. a leading sequence, a secretion sequence, a sequence used to purify said polypeptide, a proteinogen sequence, or a fusion protein). As defined herein, these fragments, derivatives, and analogues are well known to those skilled in the art.
 In the invention, the term "ELb protein" means the polypeptide set forth in SEQ ID NO: 3 having the activity of ELb protein. This term also includes variants of the polypeptide of SEQ ID NO: 3 having the same function as ELb protein. These variants include (but are not limited to) deletion, insert, and/or substitution of several (generally 1-50, preferably 1-30, more preferably 1-20, most preferably 1-10, still more preferably 1-8 or 1-5) amino acids, as well as addition of one or more (generally less than 20, preferably less than 10, more preferably less than 5) amino acids to the C-terminal and/or N-terminal. For example, functions of proteins typically are not changed by substitution of one amino acid with another amino acid having the same or similar property. As another example, functions of proteins typically are not changed by addition of one or several amino acids to C-terminal and/or N-terminal as well. This term, ELb protein, also includes active fragments and derivatives of ELb protein.
 The variants of a polypeptide include: homologous sequences, conservative variants, allelic variants, natural mutants, induced mutants, proteins encoded by a DNA sequence that hybrids to an ELb-protein encoding DNA sequence under high or low stringent conditions, and polypeptides or proteins obtained using antibodies against the ELb protein. The invention also provides other polypeptides, such as fused proteins comprising ELb protein or a fragment thereof. In addition to almost full-length polypeptide, the invention further comprises soluble fragments of ELb protein. These fragments generally comprise at least about 20 contiguous amino acids, typically at least about 30 contiguous amino acids, preferably at least about 50 contiguous amino acids, more preferably at least about 80 contiguous amino acids, most preferably at least about 100 contiguous amino acids in the sequence of ELb protein.
 The invention further provides analogues of ELb proteins or polypeptides. The difference between these analogues and the native ELb protein could be the difference in amino acid sequence, the difference in modification patterns not resulting in any sequence change, or both. These polypeptides include natural or induced genetic variants. The induced variants can be obtained by various techniques, such as random mutagenesis by exposure to radiation or mutagen, as well as site-directed mutagenesis or other known molecular biology techniques. These analogues also include the analogues containing a residue (e.g. D-amino acid) different from the natural L-amino acid residues, and analogues containing a non-naturally occurring or synthetic amino acid (e.g. β, γ-amino acid). It should be understood that the polypeptides of the invention are not limited to the representative polypeptides described above.
 The modified (generally not resulting in primary structure change) forms include: chemically derived form, such as acetylated or carboxylated form, of a peptide in vivo or in vitro. The modifications also include glycosylation. The modified forms also include a sequence containing a phosphorylated amino acid (e.g. phosphotyrosine, phosphoserine, phosphothreonine), or a polypeptide modified to enhance resistance to proteolysis or optimize solubility.
 In the present invention, "a conservative variant polypeptide of ELb protein" refers to the polypeptides containing up to 20, preferably at most 10, more preferably at most 5, most preferably at most 3 amino acids substituted by other amino acids with similar or comparable properties in comparison with the amino acid sequence set forth in SEQ ID NO:3. Preferably, these conservative variant peptides are produced by substitution of amino acids according to table 1.
TABLE-US-00001 TABLE 1 Amino acid residue Representative substitution Preferred substitution Ala (A) Val; Leu; Ile Val Arg (R) Lys; Gln; Asn Lys Asn (N) Gln; His; Lys; Arg Gln Asp (D) Glu Glu Cys (C) Ser Ser Gln (Q) Asn Asn Glu (E) Asp Asp Gly (G) Pro; Ala Ala His (H) Asn; Gln; Lys; Arg Arg Ile (I) Leu; Val; Met; Ala; Phe Leu Leu (L) Ile; Val; Met; Ala; Phe Ile Lys (K) Arg; Gln; Asn Arg Met (M) Leu; Phe; Ile Leu Phe (F) Leu; Val; Ile; Ala; Tyr Leu Pro (P) Ala Ala Ser (S) Thr Thr Thr (T) Ser Ser Trp (W) Tyr; Phe Tyr Tyr (Y) Trp; Phe; Thr; Ser Phe Val (V) Ile; Leu; Met; Phe; Ala Leu
 The invention further provides polynucleotide sequences encoding the ELb proteins of the invention or conservative variant polypeptides thereof.
 Polynucleotides of the invention can be DNA or RNA. DNA includes cDNA, genomic DNA, or artificial synthetic DNA. DNA can be single-stranded or double-stranded. DNA can be a coding strand or a non-coding strand. The coding region sequence encoding a mature polypeptide can be the same as the coding region sequence set forth in SEQ ID NO: 2 or a degenerate variant thereof. As used herein, "degenerate variant" means a polynucleotide sequence encoding a protein with the sequence set forth in SEQ ID NO: 3, but differing from the coding the region sequence set forth in SEQ ID NO:2.
 Polynucleotides encoding a mature polypeptide set forth in SEQ ID NO:3 include: a coding sequence only encoding a mature polypeptide; a sequence encoding a mature polypeptide and various additional coding sequences; a sequence encoding a mature polypeptide (and any additional coding sequence) and non-coding sequence.
 The term "a polynucleotide encoding a polypeptide" refers to a polynucleotide encoding the polypeptide, or a polynucleotide further containing additional coding and/or non-coding sequences.
 The invention also relates to variants of the above polynucleotides, encoding polypeptides with the same amino acid sequences as described herein or fragments, analogues, and derivatives thereof. The variants of the polynucleotides can be naturally occurring allelic variants or non-naturally occurring variants. These nucleotide variants include substitution variants, deletion variants, and insertion variants. As known in the art, an allelic variant is an alternative of a polynucleotide, which can include one or more substituted, deleted, or inserted nucleotides, which do not result in substantial function changes in the polypeptide encoded by the variant.
 The invention also relates to polynucleotides which hybrid to the sequences described above and having at least 50%, preferably at least 70%, more preferably at least 80% identity with the sequences described above. The invention particularly relates to polynucleotides hybridizing to the polynucleotides described herein under stringent conditions. In the invention, "stringent conditions" refer to (1) hybridization and wash under lower ionic strength and higher temperature, such as 0.2×SSC, 0.1% SDS, 60° C.; or (2) hybridization in the presence of a denaturant, such as 50% (v/v) formamide, 0.1% bovine serum/0.1% Ficoll, 42° C., etc; or (3) hybridization occurring only between two sequences having at least 80%, preferably at least 90%, more preferably more than 95% identity. Moreover, the biological functions and activities of polypeptides encoded by the hybridizable polynucleotides are the same as those of the mature polypeptide set forth in SEQ ID NO:3.
 The invention also relates to polynucleotide fragments hybridizing to the sequences described above. As used herein, a "polynucleotide fragment" comprises at least 15, preferably at least 30, more preferably at least 50, most preferably at least 100 or more nucleotides in length. The polynucleotide fragments can be used with nucleic acid amplification techniques (e.g. PCR) to determine and/or isolate polynucleotides encoding ELb protein.
 It should be understood that in accordance with embodiments of the invention, ELb gene is preferably derived from Arabidopsis. However, embodiments of the invention also include other genes which have high homology (for example, more than 60%, such as 70%, 80%, 85%, 90%, 95%, even 98% sequence identity) with the Arabidopsis ELb gene and are derived from other plants. The alignment methods and means for determining sequence identity or homology (such as BLAST) are well known in the art.
 The full length nucleotide sequences encoding ELb protein of the invention, or fragments thereof can be produced using PCR amplification, recombinant technology, or chemical synthesis. For PCR amplification, the primers can be designed according to the related nucleotide sequences, especially the sequences of open reading frames, disclosed, and commercially available cDNA library or cDNA library made by routine methods known to those skilled in the art can be used as templates. Using these primers and libraries, PCR amplification can be carried out to obtain the desired sequences. When the sequences are long, it is usually necessary to perform PCR twice or multiple times, and then ligate the amplified fragments in a correct order.
 Once a desired sequence is obtained, a large amount of the desired sequence can be obtained by recombinant techniques. Usually, the desired sequence is cloned into a vector, and the vector is introduced into cells, and then the desired sequences are isolated from propagated host cells by routine methods.
 In addition, the desired sequences, especially shorter fragments can be produced by chemical synthesis. In general, multiple small fragments may be first synthesized, and then ligated together to produce a long fragment.
 Currently, it is possible to obtain a DNA sequence encoding a protein of the present invention (or fragment or derivative thereof) exclusively by chemical synthesis. Then, this DNA can be introduced into various existing DNA molecules (e.g. vectors) and cells known in the art. In addition, some mutations can be introduced into a protein of the present invention by chemical synthesis as well.
 The invention also relates to vectors containing polynucleotides of the invention, host cells resulted from genetic engineering using these vectors or ELb protein-encoding sequences, as well as methods for preparing polypeptides of the invention by recombinant techniques.
 Using conventional DNA recombinant techniques (Science, 1984; 224:1431), polynucleotide sequences of the invention can be used to express or produce recombinant ELb proteins. This typically comprises the following steps:
 (1) transforming or transducing suitable host cells with a polynucleotide (or its variants) encoding ELb protein, or a recombinant expression vector containing said polynucleotide;
 (2) culturing the host cells in an appropriate medium;
 (3) isolating and purifying the protein from the medium or cells.
 In the invention, the polynucleotide sequence encoding ELb protein can be inserted into a recombinant expression vector. The term "recombinant expression vector" means bacterial plasmid, phage, yeast plasmid, plant cell virus, mammalian cell virus, or other vectors. Altogether, any plasmid and vector can be used provided that they are capable of replicating and stabilizing in the host. An important feature of the expression vector is having a replication origin, a promoter, a maker gene, and a translation control element.
 An expression vector containing an ELb protein-encoding DNA sequence and appropriate transcription/translation control signals can be constructed using methods well known to those skilled in the art. These methods include in vitro recombinant DNA techniques, DNA synthesis techniques, in vivo recombinant techniques, and the like. Said DNA sequence can be effectively linked to an appropriate promoter in the expression vector in order to direct mRNA synthesis. An expression vector may also comprise a ribosome binding site as a translation initiation site and a transcription terminator.
 In addition, an expression vector preferably comprises one or more selectable marker genes, such as dihydrofolate reductase, neomycin resistance, or green fluorescent protein (GFP) useful in eukaryotic cell culture, or kanamycin resistance or ampicillin resistance useful in E. coli culture, to provide phenotypes useful in selecting the transformed host cells.
 A vector containing an appropriate DNA sequence described above and an appropriate promoter or control sequence described above can be used to transform suitable host cells for expression of the proteins.
 The host cells can be prokaryotic cells, such as bacterial cells; or lower eukaryotic cells, such as yeast cells; or higher eukaryotic cells, such as plant cells. Representative examples are E. coli, Streptomyces, Agrobacterium; fungal cells, e.g., yeast; plant cells, and the like.
 An inserted enhancer sequence in a vector will enhance transcription when a polynucleotide of the invention is expressed in higher eukaryotic cells. An enhancer, a DNA cis-acting factor, generally comprises about 10-300 base pairs, and acts on the promoter to enhance gene transcription.
 Those having ordinary skill in the art would understand how to select appropriate vectors, promoters, enhancers, and host cells.
 Transformation of host cells with recombinant DNA can be carried out using routine techniques well known to one skilled in the art. For prokaryotic hosts, such as E. coli, the competent cells capable of absorbing DNA can be obtained by harvesting cells after exponential growth phase and treating the cells with CaCl2. These preparation methods are well known in the art. Another method uses MgCl2 treatment. Transformation can also be carried out by electroporation, if necessary. For eukaryotic hosts, one can use any suitable DNA transfection methods, e.g. calcium phosphate coprecipitation, routine mechanical methods such as microinjection, electroporation, liposome-encapsulation, and the like. The plant cells can be transformed using methods like Agrobacterium transformation or gene gun transformation, and other techniques such as leaf dish method, transformation of immature rice embryo, and so on. The transformed plant cells, tissues, or organs are allowed to regenerate new plants by conventional methods, to obtain plants with changed traits.
 The resulting transformants can be grown routinely to express the polypeptide encoded by the genes of the invention. The culture medium can be selected from various conventional media, depending on the host cells used. The culture is performed under conditions suitable for host cell growth. The selected promoter may be induced using an appropriate method (e.g. temperature changes or chemical inducements) when host cells are grown to an appropriate density, and then the cells are cultured for an additional period.
 The recombinant polypeptides described above can be expressed intracellularly or on cell membrane, or secreted by cells. If necessary, the recombinant proteins can be isolated and purified by various isolation methods taking advantage of their physical, chemical, and other properties. These methods are well known to those skilled in the art. The examples of such methods include, without limitation, conventional renaturation treatments, treatments with protein precipitant (salting out), centrifuge, breaking bacteria by osmosis, ultratreatment, ultracentrifugation, molecular sieve chromatography (gel filtration), adsorption chromatography, ion exchange chromatography, high-performance liquid chromatography (HPLC), and other liquid chromatography, and combination thereof.
 The recombinant ELb proteins can be used to, for example, screen for antibodies, polypeptides, or other ligands capable of enhancing or inhibiting ELb protein functions. Screening a polypeptide library with expressed recombinant ELb protein can be used to search for valuable polypeptide molecules that inhibit or stimulate ELb protein functions.
 A portion or the whole polynucleotides of the invention can be immobilized on a microarray or DNA chip ("gene chip") as probes for analysis of differential gene expression in the tissues. The transcripts of ELb protein can be detected by in vitro amplification using RNA-polymerase chain reaction (RT-PCR) and specific primers for ELb protein.
 The invention also relates to methods for crop improvement, comprising regulation of the expression or activity of ELb gene or a homologous gene thereof in the plants. Whether enhancing or inhibiting ELb expression or activity would depend on the plant traits to be improved. The need for decreased plant heights and volumes, or increased plant tillering and yields can be met by increasing ELb expression or activity in crops; alternatively, the need for increased flower organ sizes, seed sizes, plant heights, or volumes can be met by inhibiting the expression or activity of plant height regulatory genes in crops.
 Methods for increasing expression of ELb gene or a homologous gene thereof are well known in the art. For example, an expression construct containing an ELb-encoding gene may be introduced into a plant to overexpress ELb; or enhancement of expression of ELb gene or a homologous gene thereof can be driven by a strong promoter; or the expression of ELb gene can be enhanced by an enhancer (e.g. the first intron of rice waxy gene, the first intron of Actin gene, etc.). Strong promotors suitable for these methods include, but are not limited to: 35S promoter, Ubi promotors of rice and maize, etc.
 Methods for inhibition of expression of ELb gene or a homologous gene thereof are well known in the art. For example, inhibition can be accomplished by RNA interference (RNAi) or gene silencing (knock-out) techniques.
 As a preferable embodiment of the invention, a method for obtaining a plant with high expression of ELb comprises the following steps:
 (1) providing Agrobacterium cells carrying an expression vector containing DNA coding sequence of ELb protein;
 (2) contacting cells, tissues, or organs of the plant with the Agrobacterium cells described in step (I), to introduce said DNA coding sequence of ELb protein into the plant cells, tissues or organs and allow them to integrate into the chromosomes of the plant cells;
 (3) selecting the plant cells, tissues or organs containing said DNA coding sequence of ELb protein; and
 (4) allowing the plant cells, tissues or organs described in step (3) to regenerate a new plant.
 Any appropriate routine means, including reagent, temperature, pressure, etc. can be used to practice this method.
 The present invention further relates to agonists or antagonists of ELb protein or coding gene thereof. The agonists or antagonists can regulate ELb activity or expression, therefore can be used to regulate plant heights, volumes, tillerings, yields, flower organ sizes, or seed sizes, and the like, in crops by their effects on ELb functions, in order to achieve the goal for traits improvement.
 An ELb antagonist refers to an agent capable of decreasing ELb activity and stability, down-regulating ELb expression, decreasing ELb effective acting time, or inhibiting ELb transcription or translation. These agents can be used, according to the present invention, as useful agents for increasing flower organ sizes, seed sizes, plant heights, or volumes of crops.
 An ELb agonist refers to an agent capable of increasing ELb activity, maintaining ELb stability, promoting ELb expression, increasing ELb effective acting time, or promoting ELb transcription or translation. These agents can be used, in accordance with the present invention, as useful agents for decreasing plant heights and volumes, and increasing tillerings and yields of crops.
 In one embodiment, the invention relates to an ELb gene having a genomic sequence as set forth in SEQ ID NO:1, wherein the open reading frame (ORF) is located in regions 61-353, 1363-1585, 1690-1943, 2028-2414, 2559-2979, and the full length cDNA (SEQ ID NO:1) has 1578 bp encoding a protein comprising 525 amino acids (SEQ ID NO:3). The ELb gene provides a new means for improvement of plant heights, volumes, yields, tillerings, and etc. of crops, and has therefore a promising prospect.
 The Promoter for Specific Expression in Plant Stems or Leaves, and Directing Gene Expression
 As used herein, the "promoter" or "promoter region" means a nucleotide sequence usually located upstream (5') of the coding sequence of a target gene, which initiates polynucleotide sequence transcription into mRNA. In general, a promoter or promoter region can provide a recognition site for RNA polymerases and other factors necessary for correct initiation of transcription. Herein, the promoter or promoter region includes a promoter variant, i.e., a naturally occurring allelic variant or a non-naturally occurring variant, including a substitution variant, a deletion variant, and an insertion variant.
 As used herein, "tissue-specific promoter" or "organ-specific promoter" means that gene expression usually occurs only in certain specified organs or tissues under the control of these promoters.
 As used herein, "operably linked" means the functional spatial arrangement of two or more nucleic acid regions or nucleic acid sequences. For example, a promoter region is located in at specified position relative to the nucleic acid sequence of a target gene, so that the transcription of the nucleic acid sequence is under control of the promoter region, accordingly, the promoter region can be "operably linked" to the nucleic acid sequence.
 Generally, a promoter is considered tissue-specific or organ-specific if the mRNA expression in a tissue or organ is at least 2 times, preferably at least 5 times, more preferably at least 10 times, more preferably at least 25 times, more preferably at least 50 times, still more preferably at least 100 times, most preferably at least 1000 times higher than in other tissues or organs.
 The invention relates to a promoter selected from the group consisting of:
 (1) a polynucleotide having nucleotide sequence set forth in SEQ ID NO:13; or
 (2) a polynucleotide hybridizing to the polynucleotide sequence described in (1) under a stringent condition and directing specific expression of a target gene in plant stems or leaves.
 In the invention, a "stringent condition" refers to (1) hybridization and wash under lower ionic strength and higher temperature, such as 0.2×SSC, 0.1% SDS, and 60° C.; or (2) hybridization in the presence of a denaturant, such as 50% (v/v) formamide, 0.1% bovine serum/0.1% Ficoll, and 42° C., etc; or (3) hybridization occurring only between two sequences having at least 80%, preferably at least 90%, more preferably more than 95% identity. Moreover, the hybridizable polynucleotide can direct specific expression of a target gene in plant stems or leaves.
 Polynucleotide hybridization is a technique well known to those skilled in the art, and hybridization profile for a pair of specified polynucleotides indicates their similarity or identity. Therefore, the invention further relates to a polynucleotide hybridizing to the nucleotide sequence set forth in SEQ ID NO: 13 and having at least 50%, preferably at least 60%, more preferably at least 70%, still more preferably at least 80%, even still more preferably at least 85%, more preferably at least 90% (e.g., 95%, 96%, 97%, 98%, or 99%) identity with the nucleotide sequence set forth in SEQ ID NO: 13.
 A promoter of the invention is specific for plant tissue or organ, in particular, for plant stems or leaves. In some embodiments of the invention, the inventors have discovered that ELb gene or GUS gene can be specifically expressed in plant stems and leaves, but substantially not expressed in other tissues or organs, under the control of a promoter of the invention.
 A promoter of the invention can be operably linked to a target gene which can be exogenous (heterogenous) to the promoter. The target gene is usually an nucleotide sequence (preferably a structural nucleotide sequence), and preferably encodes a protein with a specified function, such as certain proteins regulating growth of plant stems and leaves, in particular, the proteins associated with plant heights, in accordance with embodiments of the invention.
 A promoter of the invention can also be operably linked to an improved target gene which is exogenous (heterogenous) to the promoter. The target gene may be improved to have various desirable properties, such as enhanced expression, altered post-translational modification (e.g. phosphorylation site), transport of translation product out of the cell, improved stability, insertion or deletion of a cellular signal, and so on.
 In addition, the promoter and target gene can be designed to down-regulate a specified gene, which is usually achieved by linking the promoter to the target gene sequence, and initiating the sequence in a reverse direction and in an antisense manner. Those skilled in the art are familiar with the antisense techniques. Any nucleotide sequences can be regulated in this way.
 Any promoter and target gene sequence described above can be included in a construct, in particular, a recombinant vector.
 A recombinant vector usually comprises an operably linked (generally 5'→3') promoter for initiating transcription of a target gene and the target gene. If necessary, a recombinant vector can further comprise a 3' transcription terminator, a 3' polyadenylation signal, other non-translational nucleotide sequences, a transporting or targeting nucleotide sequence, a resistance selection marker, an enhancer, or an operon.
 In general, a target gene is located less than 2000 bp (preferably less than 1000 bp, more preferably less than 500 bp, most preferably less than 300 bp) downstream of the promoter for specific expression in plant stems or leaves.
 In addition to a promoter of the invention, the recombinant vector can further comprise one or more other promoters, such as tissue-specific, constitutive, or inducible promoters.
 A vector containing an appropriate promoter described above and a target gene can be used to transform suitable host cells for protein expression.
 The advantages of the invention are:
 (1). providing a new isolated plant height regulatory gene which is capable of regulating plant heights, volumes, tillerings, yields, flower organ sizes, or seed sizes of crops; therefore, they can be used to improve crop cultivars.
 (2). a regulatory gene of the invention may be transformed into crops to decrease plant heights, which can be useful in breeding for dwarf plant types, because moderately decreased plant heights and increased effective tillering numbers are ideotypes of high-yield breeding. For example, different expression levels in Gramineae crops could be used to decrease the plant heights to different extents to increase effective tillering numbers and yields.
 (3) a promoter of the plant height regulatory gene is isolated for the first time, which directs specifically expression in plant stems or leaves, and can be used to regulate specific expression of a target gene in plant stems or leaves.
 The invention is now further described in more detail in combination of the following examples. It should be understood that these examples are provided only for illustration without limiting the scope of the invention. The assays which are not particularly described in the following examples can be performed according to conventional procedures, as described in Sambrook et al, Molecular Cloning: Laboratory Manual (Cold Spring Harbor Laboratory Press, New York, 2001) or PCR primer: Laboratory Manual (Carl W. Dieffenbach and Gabriela S. Devksler eds., Cold Spring Harbor Laboratory Press, 1995), or as recommend by the manufacturers.
 1.1 Plant Materials
 Arabidopsis thaliana, the ecotype is Columbia (Col-0).
 T-DNA inserted mutant: ELa (SALK016089)
 Rice cultiva: Taipei 309 (Oryza sativa L. ssp Japonica. cv Taipei309, TP309).
 1.2 Bacterium Strains and Plasmid Vectors
 Agrobacterium tumefaciens: GV3101 (see, Narasimhulu, S. B, et al, Gelvin. 1996. Early transcription of Agrobacterium t-DNA genes in tobacco and maize. Plant Cell 8:873-886), EHA105 (see, Hood, E. E. et al, 1993, New Agrobacterium helper plasmids for gene transfer to plants. Transgen. Res. 2:208-218).
 Plasmid vectors:
 pBluescript SK (pSK): purchased from Invitrogen Inc.
 pCambia1300S: pCambia1300RS, purchased from CAMBIA.
 pBI101.1: purchased from Invitrogen Inc.
 pGEM-T Easy vector: purchased from Promega Inc.
 RNAi vector 1300RS: available from Arkansas State University, USA.
 1.3 Reagents and Enzymes
 T4 DNA ligase, various restrictive endonucleases, and Taq DNA polymerase are purchased from MBI Ferment, TaKaRa, New England Biolabs, or Promega. A Recovery kit for DNA fragment in gel was purchased from Omega Inc. The Reverse Transcription System was purchased from GIBCOBRL. The molecular weight markers of nucleic acids are MBI products. The pGEM-Teasy vector was purchased from Promega Inc. (Madison, USA). The (α-32P)dCTP was purchased from YaHui Bioengineering Inc. (Beijing, China). A reverse transcription kit using SuperScript First-Strand Synthesis System for RT-PCR (#11904-018, Invitrogen) was used. Other conventional chemical reagents are analytically pure products imported or made in China. Various deoxynucleotide primers were synthesized by Sangon Inc, Shanghai, China. DNA sequences were determined by JiKang Inc., Shanghai; or Invitrogen Inc., Shanghai. Sequence analysis was completed using Genedoc, DNAStar software, and etc.
 1. Arabidopsis thaliana Cultivation and Transformation
 For sterile cultivation of Arabidopsis thaliana, the seeds were superficially (by 70% ethanol for 30 sec, then washed 4× with sterile water) and internally (by 7% sodium hypochlorite for 10 min, then washed 3× with sterile water) sterilized, and then sowed on 1/2 MS (1/2 Murashige and Skoog basal medium, 0.8% agar, pH 5.8) solid medium, placed at 4° C. for 72 hr, and subsequently transferred to 22° C. One week later, the seedlings were transplanted in artificial soil (vermiculite: black soil: pearlite=3:1:0.5) soaked by nutrient solution (HuaWuQue 3 g/10 L, YongTong Chemical Ltd, Shanghai, China), and subsequently transferred to an artificial climatic chamber with a diurnal cycle of 14/10 (L/D).
 For Arabidopsis thaliana transformation, the plants aged 4-5 weeks in a favorable growth status (cutting off main scape 1 week before transformation, to promote developing more lateral scapes and more flowers, thereby increasing the transformation efficiency) were treated by sprinkle. The Agrobacterium tumefaciens cells containing the transgenic vectors were grown to OD600˜2.0 at 28° C., and then centrifuged at 4,000 rpm for 10 min, the pellet were resuspended in freshly prepared transformation solution (1/2 MS liquid medium containing 5% sucrose and 0.02% Silwet L-77), and grown to a final concentration as OD600˜0.6-0.8. The pollinated flowers and fruits were removed before transformation, and then the soil was allowed to absorb sufficient water. During transformation, the suspension of bacteria was sprinkled on the Arabidopsis thaliana plants until a few drops of the suspension dropped off from the leaves. The plants were covered by black bags to maintain humidity overnight in the dark. 24 hr later, the plants were transferred to normal conditions. 7 days later, the transformation was repeated once according to the procedure described above. The plants were collected and mixed in a paper bag after the seeds became mature. The collected plants were placed in a dessicator for 7 days, and then threshed. The sterilized seeds of T1 generation were sowed on 1/2×MS medium containing 50 μg/ml Kan or hygromycin, placed at 4° C. for 72 hr, and then placed under normal light condition.
 2. The Gene Transformation of Callus of Mature Rice Embryo Mediated by Agrobacterium tumefaciens
 (1) Inducing Callus of Mature Rice Embryo
 The seeds of rice 307T were hulled, then soaked with 70% ethanol for 1 min, and with 20% (v/v) sodium hypochlorite for 20-30 min, with continuous shaking. The seeds were rinsed with sterile water for 5-6 times. After suck-dried by sterile filter paper, the rice seeds were sowed on MSD medium and grown at 26° C. in the dark to induce callus. One week later, the endosperm, plumule, and radicle were removed to obtain callus, and the resulted callus were passaged on MSD in the dark. They were passaged every 2-3 weeks. For the callus of TP309 seeds, the medium used was NBD.
 (2) Preparing the Bacteria Suspension Useful for Transformation
 In morning of day 1: a small part of the bacteria stored at -70° C. was inoculated in 5 ml YEB (Rif 20 mg/L+Kan 50 mg/L) liquid medium, and cultured with shaking at 28° C. overnight.
 In morning of day 2: 1-2 ml of YEB medium containing the bacteria were collected and transferred into 25-50 ml AB (20 mg/L Rif+50 mg/L Kan) liquid medium, and then grown at 28° C. for about 4 hr until OD600˜0.5.
 (3) Co-Culture
 In the afternoon of day 2: after detection of OD600 value, the bacteria suspension was centrifuged at 5,000 rpm for 15 min, the pellet was resuspended in AAM (containing AS 100) and cultured until OD600=0.4-0.6. The bacteria suspension was poured into a triangular flask containing rice callus, and the callus was soaked for 20 min with occasional shaking; after the bacteria suspension was suck-dried by sterile filter paper (or a pipette), the soaked callus were transferred on NBD (AS100) medium containing 2.5% Phytagel with a layer of sterile filter paper thereon, and were co-cultured for 2-3 days, and then, to each dish 1 ml AAM (+AS100) medium was added to sufficiently moisten the sterile filter paper.
 (4) Screening
 After suck-dried by sterile filter paper (another filter paper), the callus were transferred on screening medium containing hygromycin (Hyg) to screen resistant callus. The callus was cultured in dark for about 30 days, during which the screening medium was exchanged once.
 The screening media used are:
 the medium for the first screening containing 0.26% Phytagel MS+Timentin 100 mg/L+Hyg 30 mg/L;
 the medium for the second screening containing 0.26% Phytagel NBD+Timentin 100 mg/L+Hyg 50 mg/L;
 the medium for the third screening containing 0.26% Phytagel MS+Timentin 100 mg/L+Hyg 50 mg/L.
 (5) Predifferentiation
 The screened rice callus was transferred to a predifferentiation medium and grown for 10 days.
 Predifferentiation medium: containing 0.45% Phytagel MS+BAP 2 mg/L+NAA 1 mg/L+ABA 5 mg/L Hyg 50 mg/L, pH 5.7, without 2,4-dichlorophenoxyacetic acid (2,4-D).
 (6) Differentiation
 The predifferentiated rice callus was transferred to a differentiation medium and cultivated to differentiate into a young plant (light, 15-30 days).
 Differentiation medium: containing 0.45% Phytagel NB+BAP 3 mg/L+NAA 0.5 mg/L, pH 5.7, without 2,4-D.
 (7) Rooting
 The green young plant was transferred to a rooting medium for rooting.
 Rooting medium: containing 0.45% Phytagel 1/2 MS+Hyg 50 mg/L, pH 5.7, without 2,4-D.
 3. Vector Construction
 p35S::ELb Vector Construction
 cDNA coding region sequence of ELb protein was amplified by RT-PCR. The steps are as follows: total RNA of Arabidopsis thaliana plant was extracted by RNeasy Plant Mini kit (Qiagen) according to the instruction provided by the manufacturer, and then the resulted total RNA was reverse transcribed to produce ELb cDNA with M-MLV reverse transcriptase (Promega). The cDNA coding region sequence of ELb protein was amplified by a PCR reaction using Takara perobest DNA polymerase and the above cDNA used as templates. The primers used are:
TABLE-US-00002 Upstream primer (SEQ ID NO: 7): 5'-TGAGGATCCAAATAAAATAAAAAG-3' (underlined: BamHI site); Downstream primer (SEQ ID NO: 8): 5'-AAAGTCGACCACACACAAAGCAAA-3' (underlined: ClaI site).
 PCR condition: 94° C. for 3 min; 35 cycles of 94° C. for 30 sec, 58° C. for 30 sec, and 72° C. for 2 min; 72° C. for 10 min. The product was stored at 16° C.
 PCR product was recovered and digested by both BamH1 and ClaI. The product was recovered, and then ligated to pSK vector which had also been digested and recovered as supra. The resulted vector was used to transform DH5α cells. The correct clone confirmed by restriction cleavage was selected for sequencing. For the clone with correct sequence confirmed by sequencing, the ELb cDNA coding region was cleaved by BamHI/ClaI and ligated into a double expression vector pCambia1300S cleaved by BamHI/ClaI, and transformed into DH5α cells to obtain transgenic clones. After extraction, the correct plasmid confirmed by restriction cleavage was transformed into Agrobacterium tumefaciens GV3101 and EHA105 cells. The plasmid was extracted from the Agrobacterium tumefaciens cells and re-transformed into DH5α cells. The plasmid was extracted from DH5α and cleaved by the restriction enzymes to verify the Agrobacterium tumefaciens cells transformed with the correct plasmid. The transgenic Arabidopsis thaliana plants were obtained by transformation of the Arabidopsis thaliana cells by sprinkle method, and the transgenic rice plants were obtained by Agrobacterium tumefaciens mediated genetic transformation of callus of mature rice embryo.
 pELb Promoter::GUS Vector Construction
 The upstream and downstream primers were designed based on the sequences (GeneID: 832559) available from GenBank, and the primers were within the range of 1.4 kb upstream of the translation initiation site of ELb gene. The genomic DNA extracted from a young plant (aged 7 days) of wild-typed Arabidopsis thaliana Columbia was used as template to perform PCR. Said primers are as follows:
TABLE-US-00003 Upstream primer (SEQ ID NO: 9): 5'-CTGCTGCAGACTCTATTTCCA-3' (underlined: PstI site); Downstream primer (SEQ ID NO: 10): 5'-TTCAGGATCCTTTACTTTTTATTTT-3' (underlined: BamHI site);
 Amplification condition: 94° C. for 3 min; 35 cycles of 94° C. for 30 sec, 58° C. for 30 sec, 72° C. for 2 min; 72° C. for 10 min. The product was stored at 16° C.
 PCR product was cleaved by PstI/BamHI enzymes, and then ligated into the corresponding PstI/BamHI site in a pSK vector. The correct clone confirmed by restriction cleavage was selected for sequencing. For the clone with correct sequence confirmed by sequencing, the ELb promoter region (as set forth in SEQ ID NO:13) was cleaved by PstI/BamHI and ligated to a double expression vector pBI101.1 cleaved by PstI/BamHI, and transformed into E. coli. DH5α cells. After extraction, the correct plasmid confirmed by restriction cleavage was transformed into Agrobacterium tumefaciens GV3101 cells. The plasmid was extracted from the Agrobacterium tumefaciens cells and re-transformed into DH5α cells. The plasmid was extracted from DH5α and cleaved by the restriction enzymes to verify the Agrobacterium tumefaciens cells transformed with the correct plasmid. Meanwhile, the pBI101.1 vectors were transformed into GV3101 cells as negative and positive controls, respectively.
 ELb Transgenic RNAi Plant Construction Under Background of ELa T-DNA Insertion Mutant
 The transgenic clone was constructed using RNAi vector 1300RS as follows: The genomic DNA of a young plant (aged 7 days) of wild-typed Arabidopsis thaliana Columbia was used as template to perform PCR to amplify a sequence of about 500 bp in the fourth exon of ELb gene. Said primers are as following:
TABLE-US-00004 Upstream primer (SEQ ID NO: 11): 5'-AATGGTACCACAAGAAACAA-3' (underlined: KpnI site); Downstream primer (SEQ ID NO: 12): 5'-TCTAGATTTGAGCTGAAAAAA-3' (underlined: XbaI site).
 Amplification condition: 94° C. for 3 min; 35 cycles of 94° C. for 30 sec, 50° C. for 30 sec, 72° C. for 30 sec; 72° C. for 10 min. The product was stored at 16° C.
 PCR product was cleaved by KpnI/XbaI enzymes, and then ligated into the corresponding KpnI/XbaI site of pSK vector. The correct clone confirmed by restriction cleavage was selected for sequencing. For the clone with correct sequence confirmed by sequencing, the ELb partial fragment was cleaved by KpnI/XbaI and ligated to a double expression vector 1300RS cleaved by KpnI/XbaI, and transformed into E. coli. DH5α cells. After extraction, the correct plasmid confirmed by restriction cleavage was transformed into Agrobacterium tumefaciens GV3101 cells. The plasmid was extracted from the Agrobacterium tumefaciens cells and re-transformed into DH5α cells. The plasmid was extracted from DH5α and cleaved by the restriction enzymes to verify the Agrobacterium tumefaciens cells transformed with the correct plasmid.
 The ELa T-DNA insertion mutant was transformed by sprinkle method to obtain the ELb RNAi transgenic plant (ELb RNAi/eLa) of Arabidopsis thaliana under the background of ELa T-DNA insertion mutant.
Cloning of ELb Gene
 The inventor discovered 2 p450 monooxyganase genes, i.e., 714A1 and 714A2 by searching the genomic sequences of Arabidopsis thaliana and performing bioinformatic research. They were initially predicted to involve in plant growth and development under the control of gibberellin, and designated as ELa (or AtEui1a) and ELb (or AtEui1b) by the inventor.
 The genomic DNA sequence of ELb gene coding region was set forth in SEQ ID NO:1; the cDNA sequence of ELb gene encoding region was set forth in SEQ ID NO:2; the ELb protein sequence was set forth in SEQ ID NO:3. The genomic sequence of ELa gene coding region was set forth in SEQ ID NO:4; the cDNA sequence of ELa gene coding region was set forth in SEQ ID NO:5; the ELa protein sequence was set forth in SEQ ID NO:6.
Decreased Plant Height and Volume in the Transgenic Arabidopsis thaliana Plants Overexpressing ELb Gene
 In this example, the inventor prepared transgenic Arabidopsis thaliana plants that overexpressed ELb, ELa, or OsEui, respectively. The wild-type (WT) plant, a transgenic plant overexpressing Arabidopsis ELa (ELa-OE), and a transgenic plant overexpressing rice OsEui were used as controls.
 The growth profiles were observed after 4 weeks of growth, and the results are shown in FIG. 1. As shown in the figure, the wild type Arabidopsis thaliana plant was the largest, the ELb over-expressing plant were substantially smaller than the wild type plant, and the ELa over-expressing plant and the OsEui overexpressing plant were the smallest.
 After 7 weeks of growth, the inventor determined the plant height of wild type plant, and plants overexpressing ELb, ELa, and rice OsEui, and the average plant height values were 26.2 cm, 14.2 cm, 9.63 cm, and 3.7 cm, respectively. Therefore, the plant height of the transgenic Arabidopsis thaliana plant overexpressing ELb was dramatically lower than the wild type plant.
ELb RNAi or Knock-Out Mutantion Increase Plant Height and Volume
 In this example, the inventors prepared, starting with a plant variant that is an ELa T-DNA insertion mutant, ELb RNAi transgenic Arabidopsis thaliana plants (ELb RNAi/eLa) and Arabidopsis thaliana variant plants with ELb gene knocked out. After 10 days of growth of both plants, the effects of ELb RNAi or knock-out mutations on plant heights and volumes were observed, and compared with a wild type plant cultivated under the same condition as control.
 The growth profiles of the ELb RNAi/eLa plants and the wild type plant were shown in FIG. 2. In comparison with the wild type plant, the leaf areas, plant heights, and volumes of the ELb RNAi/eLa plants were dramatically increased.
 Moreover, in comparison with the wild type plant, the leaf areas, plant heights, and volumes of ELb knock-out mutants (in the background of ELa T-DNA insertion) were also dramatically increased.
 Accordingly, it can be concluded that decreased or silenced ELb expression leads to increased plant heights and volumes, i.e., ELb is a gene associated with decreased plant heights and volumes.
ELb RNAi/Ela or Knock-Out Mutantion Increase Flower Organ Sizes and Seed Sizes
 In this example, the inventor observed the growth profiles for flower organ and seed of the ELb RNAi/eLa Arabidopsis thaliana plants or the ELb knock-out Arabidopsis thaliana plants (generated in Example 3), and compare with the flower organs and seeds of a wild type Arabidopsis thaliana plant as controls.
 The growth profiles for flower organs and seeds of the ELb RNAi/eLa Arabidopsis thaliana plants and a wild type Arabidopsis thaliana plant were shown in FIG. 3. The flower organs and seeds of the ELb RNAi/eLa Arabidopsis thaliana plant were significantly larger than those of the wild type plant.
 Moreover, the flower organs and seeds of ELb knock-out mutant were also substantially larger than those of the wild type plant.
 Accordingly, it can be concluded that decreased or silenced ELb expression leads to increased flower organ sizes and seed sizes of the plants, i.e., ELb is a gene associated with decreased flower organ sizes and seed sizes.
The Tissue-Specific Expression of GUS Reporter Gene Initiated by ELb Promoter
 In this example, the inventor constructed a p ELb promoter::GUS vector that could be transformed into Agrobacterium tumefaciens cells to prepare transgenic Arabidopsis thaliana plants. The expression of GUS reporter gene in the plants was observed by a conventional assay for detection of GUS reporter gene.
 The result was shown in FIG. 4. The GUS reporter gene was expressed in the eugonic sites of plant stems and leaves, but essentially not expressed in roots. Therefore, ELb gene is a tissue-specific gene.
Decreased Plant Height of ELb Over-Expressing Transgenic Rice
 In this example, the inventor prepared ELb over-expressing transgenic rice plants (ELb-OE) and observed the effect of ELb over-expression on rice plants. The wild-type rice plant TP309 cultivated in the same growth condition was used as control.
 After 110 days of growth, the growth profiles of the plants were shown in FIG. 5. It could be seen that the plant heights of ELb over-expressing transgenic rice plants were dramatically lower than the wild type plant. FIG. 6 is a statistical histogram showing the plant heights of the ELb over-expressing plants and the wild type plant.
Increased Effective Tillering Number and Yield of ELb Over-Expressing Transgenic Rice
 In this example, the inventor detected the tillering number and yield of ELb over-expressing transgenic rice plants (ELb-OE) and the wild-type rice plant TP309 in order to demonstrate the effect of ELb over-expression on tillering and yield of the rice plants.
 The effective tillers were counted after the cultivated plants tasseled, and the statistical results were shown in FIG. 7. The tillering number of the wild type plant was about 10, whereas the tillering numbers of ELb over-expressing plants were about 20-22. It can be concluded that ELb over-expression can dramatically increase the effective tillering numbers of the plants.
 The yields of the ELb over-expressing plants and the wild type plant were analyzed after maturation of the plants. The results were shown in FIG. 8. It can be concluded that the grain weights of a single plant for ELb over-expressing transgenic rice plants were dramatically increased.
The Function of ELb Variants
 The ELb cDNA coding region in p358::ELb vector was substituted by a coding sequence that encodes a protein having a sequence similar to SEQ ID NO:3, and the only difference is Leu at position 522 of the sequence as compared to Ile at the same position of the wild type ELb protein. This vector was transformed into Agrobacterium tumefaciens cells as described above to prepare the transgenic plants. The result showed that the plant heights of the transgenic plants were lower than the wild type plant.
 All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety as if each individual publication, patent, or patent application were individually indicated to be incorporated by reference. In addition, it is understood that various modifications or changes can be made by the persons skilled in the art in light of the content described herein, and these equivalents should also be included within the scope defined by the following claims in the application.
1313040DNAArabidopsis thaliana 1aagaagtgaa gatgcaaata aaataaaaag taaaagatcc tgaatagaca aaaagttaaa 60atggagagtt tggttgttca tacggtaaat gcaatttggt gcatagttat tgtcggaatc 120ttcagcgtag gttatcatgt gtatggaaga gcggtggtgg agcagtggag gatgcggagg 180agtttaaagt tgcaaggcgt gaagggtcct ccaccgtcga tctttaacgg caatgtgtcg 240gagatgcaac ggattcagtc ggaggctaaa cactgttccg gcgataacat catttctcat 300gactattctt cttctctatt tcctcatttc gatcactggc gaaaacaata cggtttgttt 360tttaaatctc gtttagtaca aaatgcatac atataacaat atcaaaaaat tcatttaaat 420cgtaaactag aacaacattt ataaatctat taactacata tgaagtttca tttacacagt 480ttttaagttt atgggtttga tattcgagcc atatcatcgc attaaaaaca aaaaaatccc 540aaatgcacta gtggttaaaa gattaaaaaa aatatattgt tttttgatag agttcaaact 600ttttcattat gatttcaatt atcttggctt ctcatacatt ttaaataata aatccttcaa 660tttttatgga ttttagaggt acttatcatt tcaacttagg ttttgaatgg atcttgtggt 720tagtgcggac taatccgtca gcggtgtaat ccatattatt tttggggcgg acaacaaagc 780gctgtggatt tagtctaaag acaatccaca gttagtgtgt agtgtttttt ttttgttttt 840ttttagtccc aatattaaaa actataattt atgaatggta aataaaaagc gatccggttt 900gtaaatgtta ttattcgttt ggaccgctgt aaccattcaa aagtttctca aaaaaaactt 960atacattttt attagaaaat tattgttcaa aagttaatgt tcttcatagt agggtccatc 1020ccacttaaaa ggcattgaac gtttcacttg cattcacaaa aagacagctt tgcaagcttt 1080ttctcagtta acgttacacg aagaaaaatc cattaccaga tagaagaaaa tatcccatca 1140aagacaacac atatatagaa taaaaatgta gaaacgtctg catataggtt attctaaatt 1200aattagagaa atatgatcca cgcacatatt tacttaattg aattcaatac aaataaaagt 1260tgtgcatgag catgatgatt gtgatttggg cgtggctgaa cttgaaccaa gtttgatatt 1320ggtttggagt aatttttttt taatacaaaa cggtaatgaa ggaaggattt acacatactc 1380aacggggtta aagcagcacc tttacataaa ccacccggaa atggtgaagg agcttagcca 1440aaccaacaca cttaaccttg gtagaatcac tcacatcacc aaacgcctta accccattct 1500cggcaatggc atcatcacct ctaatgggcc tcattgggcc catcaacgtc gtatcattgc 1560ctatgagttt acccacgaca aaatcaaggt tctattcaca ttgcgaacta attaaagata 1620tggatgtaga aatcttaata tatatattga tttgaaatat tgttgtgatt gcctgattgg 1680tgaatggtga agggaatggt tggtttaatg gtggaatctg ccatgccaat gttgaacaaa 1740tgggaagaga tggtgaaaag aggaggagaa atgggttgtg acataagagt ggacgaagac 1800cttaaggatg tctcagctga tgtcatcgct aaggcttgct ttgggagctc tttttcaaaa 1860ggcaaagcaa tattctctat gattagggat cttttaaccg ccattactaa acgaagcgtc 1920ctcttcagat tcaatggctt cacgtaagtt tcgatatatt tattttttct acttcttcca 1980tgcaaaacta tttctctata taatatagtt gagtatacgg tggcaagtga tatggtgttt 2040ggaagtaaga agcatggtga tgtggatatt gatgcgcttg agatggaatt agaatcttct 2100atatgggaaa cggttaagga gagggaaatt gaatgtaagg atactcacaa gaaggatcta 2160atgcagttga tactcgaggg agcgatgcga agctgcgatg gtaacttgtg ggacaagtca 2220gcctatagac ggtttgtggt ggacaattgc aagagcatct atttcgccgg acatgattca 2280accgcagtct cagtgtcttg gtgccttatg ctcctcgctc tcaatcctag ttggcaggtt 2340aaaattcgcg atgaaatctt gagttcttgc aagaatggca ttcccgacgc agaatcaatt 2400cctaatctca aaacggtaat cttttattta taatcataaa gaaaacgtta gagaatttta 2460cattgaatga atttatacac aaaatcagtg tataaatgta gcttatttta aaaatctaac 2520aacattttat tgttaatata tataaatgtt ataaaatagg tgacaatggt aatacaagaa 2580acaatgagac tatacccacc agcaccaatc gtgggaagag aagcatccaa agacataaga 2640cttggagacc ttgtggtgcc aaaaggagtg tgcatttgga cactcattcc tgccttacac 2700cgagaccccg agatctgggg accagacgca aacgacttca agccagagag gtttagtgag 2760ggaatctcta aggcttgcaa ataccctcag tcatacatcc catttggcct tggaccaaga 2820acatgcgtag gcaaaaactt tggtatgatg gaagtgaaag tgcttgtttc acttattgtc 2880tcaaagttca gttttactct ttccccgact tatcagcact ctccaagcca taaactcctt 2940gtagagcctc aacatggtgt tgtcattagg gttgtttgac tgtgttacgt gatccgtaga 3000cttttataat gatttaattt gctttgtgtg ttcgaatttc 304021578DNAArabidopsis thaliana 2atggagagtt tggttgttca tacggtaaat gcaatttggt gcatagttat tgtcggaatc 60ttcagcgtag gttatcatgt gtatggaaga gcggtggtgg agcagtggag gatgcggagg 120agtttaaagt tgcaaggcgt gaagggtcct ccaccgtcga tctttaacgg caatgtgtcg 180gagatgcaac ggattcagtc ggaggctaaa cactgttccg gcgataacat catttctcat 240gactattctt cttctctatt tcctcatttc gatcactggc gaaaacaata cggaaggatt 300tacacatact caacggggtt aaagcagcac ctttacataa accacccgga aatggtgaag 360gagcttagcc aaaccaacac acttaacctt ggtagaatca ctcacatcac caaacgcctt 420aaccccattc tcggcaatgg catcatcacc tctaatgggc ctcattgggc ccatcaacgt 480cgtatcattg cctatgagtt tacccacgac aaaatcaagg gaatggttgg tttaatggtg 540gaatctgcca tgccaatgtt gaacaaatgg gaagagatgg tgaaaagagg aggagaaatg 600ggttgtgaca taagagtgga cgaagacctt aaggatgtct cagctgatgt catcgctaag 660gcttgctttg ggagctcttt ttcaaaaggc aaagcaatat tctctatgat tagggatctt 720ttaaccgcca ttactaaacg aagcgtcctc ttcagattca atggcttcac tgatatggtg 780tttggaagta agaagcatgg tgatgtggat attgatgcgc ttgagatgga attagaatct 840tctatatggg aaacggttaa ggagagggaa attgaatgta aggatactca caagaaggat 900ctaatgcagt tgatactcga gggagcgatg cgaagctgcg atggtaactt gtgggacaag 960tcagcctata gacggtttgt ggtggacaat tgcaagagca tctatttcgc cggacatgat 1020tcaaccgcag tctcagtgtc ttggtgcctt atgctcctcg ctctcaatcc tagttggcag 1080gttaaaattc gcgatgaaat cttgagttct tgcaagaatg gcattcccga cgcagaatca 1140attcctaatc tcaaaacggt gacaatggta atacaagaaa caatgagact atacccacca 1200gcaccaatcg tgggaagaga agcatccaaa gacataagac ttggagacct tgtggtgcca 1260aaaggagtgt gcatttggac actcattcct gccttacacc gagaccccga gatctgggga 1320ccagacgcaa acgacttcaa gccagagagg tttagtgagg gaatctctaa ggcttgcaaa 1380taccctcagt catacatccc atttggcctt ggaccaagaa catgcgtagg caaaaacttt 1440ggtatgatgg aagtgaaagt gcttgtttca cttattgtct caaagttcag ttttactctt 1500tccccgactt atcagcactc tccaagccat aaactccttg tagagcctca acatggtgtt 1560gtcattaggg ttgtttga 15783525PRTArabidopsis thaliana 3Met Glu Ser Leu Val Val His Thr Val Asn Ala Ile Trp Cys Ile Val 1 5 10 15 Ile Val Gly Ile Phe Ser Val Gly Tyr His Val Tyr Gly Arg Ala Val 20 25 30 Val Glu Gln Trp Arg Met Arg Arg Ser Leu Lys Leu Gln Gly Val Lys 35 40 45 Gly Pro Pro Pro Ser Ile Phe Asn Gly Asn Val Ser Glu Met Gln Arg 50 55 60 Ile Gln Ser Glu Ala Lys His Cys Ser Gly Asp Asn Ile Ile Ser His 65 70 75 80 Asp Tyr Ser Ser Ser Leu Phe Pro His Phe Asp His Trp Arg Lys Gln 85 90 95 Tyr Gly Arg Ile Tyr Thr Tyr Ser Thr Gly Leu Lys Gln His Leu Tyr 100 105 110 Ile Asn His Pro Glu Met Val Lys Glu Leu Ser Gln Thr Asn Thr Leu 115 120 125 Asn Leu Gly Arg Ile Thr His Ile Thr Lys Arg Leu Asn Pro Ile Leu 130 135 140 Gly Asn Gly Ile Ile Thr Ser Asn Gly Pro His Trp Ala His Gln Arg 145 150 155 160 Arg Ile Ile Ala Tyr Glu Phe Thr His Asp Lys Ile Lys Gly Met Val 165 170 175 Gly Leu Met Val Glu Ser Ala Met Pro Met Leu Asn Lys Trp Glu Glu 180 185 190 Met Val Lys Arg Gly Gly Glu Met Gly Cys Asp Ile Arg Val Asp Glu 195 200 205 Asp Leu Lys Asp Val Ser Ala Asp Val Ile Ala Lys Ala Cys Phe Gly 210 215 220 Ser Ser Phe Ser Lys Gly Lys Ala Ile Phe Ser Met Ile Arg Asp Leu 225 230 235 240 Leu Thr Ala Ile Thr Lys Arg Ser Val Leu Phe Arg Phe Asn Gly Phe 245 250 255 Thr Asp Met Val Phe Gly Ser Lys Lys His Gly Asp Val Asp Ile Asp 260 265 270 Ala Leu Glu Met Glu Leu Glu Ser Ser Ile Trp Glu Thr Val Lys Glu 275 280 285 Arg Glu Ile Glu Cys Lys Asp Thr His Lys Lys Asp Leu Met Gln Leu 290 295 300 Ile Leu Glu Gly Ala Met Arg Ser Cys Asp Gly Asn Leu Trp Asp Lys 305 310 315 320 Ser Ala Tyr Arg Arg Phe Val Val Asp Asn Cys Lys Ser Ile Tyr Phe 325 330 335 Ala Gly His Asp Ser Thr Ala Val Ser Val Ser Trp Cys Leu Met Leu 340 345 350 Leu Ala Leu Asn Pro Ser Trp Gln Val Lys Ile Arg Asp Glu Ile Leu 355 360 365 Ser Ser Cys Lys Asn Gly Ile Pro Asp Ala Glu Ser Ile Pro Asn Leu 370 375 380 Lys Thr Val Thr Met Val Ile Gln Glu Thr Met Arg Leu Tyr Pro Pro 385 390 395 400 Ala Pro Ile Val Gly Arg Glu Ala Ser Lys Asp Ile Arg Leu Gly Asp 405 410 415 Leu Val Val Pro Lys Gly Val Cys Ile Trp Thr Leu Ile Pro Ala Leu 420 425 430 His Arg Asp Pro Glu Ile Trp Gly Pro Asp Ala Asn Asp Phe Lys Pro 435 440 445 Glu Arg Phe Ser Glu Gly Ile Ser Lys Ala Cys Lys Tyr Pro Gln Ser 450 455 460 Tyr Ile Pro Phe Gly Leu Gly Pro Arg Thr Cys Val Gly Lys Asn Phe 465 470 475 480 Gly Met Met Glu Val Lys Val Leu Val Ser Leu Ile Val Ser Lys Phe 485 490 495 Ser Phe Thr Leu Ser Pro Thr Tyr Gln His Ser Pro Ser His Lys Leu 500 505 510 Leu Val Glu Pro Gln His Gly Val Val Ile Arg Val Val 515 520 525 42778DNAArabidopsis thaliana 4agtgctcgac tatacatata gccaaagaag agcagaaaaa tcaaagtcgt gagttcagaa 60gctataacaa aatttctaag aaaaagaaag ataagaaaat ggagaatttt atggtagaga 120tggccaagac catttcgtgg atagttgtaa taggagtgtt aggtttaggg attcgtgttt 180acggtaaagt gatggcggag caatggagga tgcggaggaa gctgacgatg cagggcgtga 240agggtcctcc gccgtcgcta tttcgtggaa acgtgccgga gatgcaaaaa atccagtcac 300aaataatgag taactctaaa cactactccg gtgataatat catcgcccat gactacactt 360cttctctctt tccatatctc gaccactggc gaaaacaata cggtaagctt tcaataatct 420gataatttca acaatttttg agactcttaa ttttgggatc tgtggcaaat gtttttttgt 480caacaaagta gatacgcctc tgaatttgaa taatgatagc acacaaggca gattagtcct 540ttgttggtcg ttttgagtta gacgaatcca tttttcggac cgatgatgat gcagacaaaa 600caaacatata tcttcattaa atcttgtaaa tagttaacga aagtactata tcattacaca 660cacatacaaa agacactagt taacatgcat acgtgaattt atatattcat aatacatgcg 720tgaattttaa ttcatacata tgtgaatact gattgacagc taagtcgtat atataatata 780tgtgtgtaac gtatgcatgg attgacatga cacctaatga caactaacgc cgcagaattt 840aaaatttatg aaaagccaat aaggttttgt acgatcgggt ctacttgatc caaaagttag 900gagctgatca attatatgat aactcctcaa tgattcattt tgattccctt ttttttatag 960taataaatcg taagatatat tttaaattta gttttaaaat accaaagtag ttgtcgcttc 1020gctagtggat cgtttaatag tttatgatcg gtcatattga ttgagaggaa atcttaagtt 1080tttgattttc accgttttct aagttggttt tgagcattta ttgtatattt attttgtatg 1140agtaatttat tgaaaaaaat tgatatgttc agggagagtg tacacgtatt cgacgggggt 1200gaagcaacac ttgtacatga accacccgga gttggtgaaa gaacttaacc aagccaacac 1260tcttaacctt ggcaaagtct cttacgtcac caaacgcctt aaatccattc ttggccgtgg 1320tgttatcacc tctaatgggc ctcattgggc ccatcaacgt cgtatcattg cacctgagtt 1380tttcctcgac aaagtcaagg gaatggtggg attggtggtg gaatcagcga tgccaatgct 1440gagtaaatgg gaagagatga tgaaaagaga aggagaaatg gtgtgtgaca taattgtaga 1500cgaagaccta agagctgcct ctgctgacgt tatctctaga gcttgctttg ggagctcttt 1560ctccaaaggc aaagagatct tctctaagct tagatgtctt caaaaggcca tcactcacaa 1620caacatcctc ttcagcctca atggcttcac gtaagtgaat tcaaaagtca tttctatctc 1680tatatatatt ttattaaggc agtgtcatgt aatggtgtta aattttgtgg ttgcaagtga 1740tgttgtgttc gggactaaga agcatgggaa cgggaagatt gatgagctag agagacacat 1800tgagtctttg atatgggaaa ccgttaaaga aagagaaagg gaatgtgtgg gagatcacaa 1860gaaggatcta atgcagttga tactagaagg ggccaggagt agttgtgatg gcaacttgga 1920ggacaagaca caatcttaca aaagtttcgt ggtggacaat tgcaagagca tctattttgc 1980cgggcatgag accagtgcgg ttgctgtctc ttggtgtctt atgctcctcg ctctcaaccc 2040ttcttggcaa actcgtatcc gcgatgaagt ctttcttcat tgcaagaacg gtatacctga 2100cgcagactct atttccaacc tcaaaacggt aatttacaag ttacaacctt gcctctcatg 2160tcaagttcct taaactctct taaaccaaaa aaaaaaatgt tccttggact ccaagtatga 2220ctattttcat aacctaacat cacttgaata aaaatatagg tgacaatggt tatccaggaa 2280acgttgaggc tatacccacc agcagcattc gtgtcgagag aagcccttga ggacacaaaa 2340ctcggaaacc tcgtggtgcc aaagggagtg tgcatctgga cgttgatccc tacattgcac 2400agagaccctg agatatgggg agctgacgca aatgaattca atccagaaag atttagcgaa 2460ggagtctcta aagcctgcaa acaccctcag tcattcgtcc catttggctt agggacaagg 2520ttgtgtttag gaaagaattt tggtatgatg gagctcaagg ttcttgtctc acttattgtg 2580tcaaggttta gctttactct ctctcccaca tatcaacact ctccggtgtt tagaatgctt 2640gtagagcctc aacatggtgt tgtcattaga gttctgagac aataagatat gtcgttagct 2700tatggtttta gttttaatcc tgtgtaataa taagatatta ttacactata gtactataat 2760agtattttct ttggtatc 277851599DNAArabidopsis thaliana 5atggagaatt ttatggtaga gatggccaag accatttcgt ggatagttgt aataggagtg 60ttaggtttag ggattcgtgt ttacggtaaa gtgatggcgg agcaatggag gatgcggagg 120aagctgacga tgcagggcgt gaagggtcct ccgccgtcgc tatttcgtgg aaacgtgccg 180gagatgcaaa aaatccagtc acaaataatg agtaactcta aacactactc cggtgataat 240atcatcgccc atgactacac ttcttctctc tttccatatc tcgaccactg gcgaaaacaa 300tacgggagag tgtacacgta ttcgacgggg gtgaagcaac acttgtacat gaaccacccg 360gagttggtga aagaacttaa ccaagccaac actcttaacc ttggcaaagt ctcttacgtc 420accaaacgcc ttaaatccat tcttggccgt ggtgttatca cctctaatgg gcctcattgg 480gcccatcaac gtcgtatcat tgcacctgag tttttcctcg acaaagtcaa gggaatggtg 540ggattggtgg tggaatcagc gatgccaatg ctgagtaaat gggaagagat gatgaaaaga 600gaaggagaaa tggtgtgtga cataattgta gacgaagacc taagagctgc ctctgctgac 660gttatctcta gagcttgctt tgggagctct ttctccaaag gcaaagagat cttctctaag 720cttagatgtc ttcaaaaggc catcactcac aacaacatcc tcttcagcct caatggcttc 780actgatgttg tgttcgggac taagaagcat gggaacggga agattgatga gctagagaga 840cacattgagt ctttgatatg ggaaaccgtt aaagaaagag aaagggaatg tgtgggagat 900cacaagaagg atctaatgca gttgatacta gaaggggcca ggagtagttg tgatggcaac 960ttggaggaca agacacaatc ttacaaaagt ttcgtggtgg acaattgcaa gagcatctat 1020tttgccgggc atgagaccag tgcggttgct gtctcttggt gtcttatgct cctcgctctc 1080aacccttctt ggcaaactcg tatccgcgat gaagtctttc ttcattgcaa gaacggtata 1140cctgacgcag actctatttc caacctcaaa acggtgacaa tggttatcca ggaaacgttg 1200aggctatacc caccagcagc attcgtgtcg agagaagccc ttgaggacac aaaactcgga 1260aacctcgtgg tgccaaaggg agtgtgcatc tggacgttga tccctacatt gcacagagac 1320cctgagatat ggggagctga cgcaaatgaa ttcaatccag aaagatttag cgaaggagtc 1380tctaaagcct gcaaacaccc tcagtcattc gtcccatttg gcttagggac aaggttgtgt 1440ttaggaaaga attttggtat gatggagctc aaggttcttg tctcacttat tgtgtcaagg 1500tttagcttta ctctctctcc cacatatcaa cactctccgg tgtttagaat gcttgtagag 1560cctcaacatg gtgttgtcat tagagttctg agacaataa 15996532PRTArabidopsis thaliana 6Met Glu Asn Phe Met Val Glu Met Ala Lys Thr Ile Ser Trp Ile Val 1 5 10 15 Val Ile Gly Val Leu Gly Leu Gly Ile Arg Val Tyr Gly Lys Val Met 20 25 30 Ala Glu Gln Trp Arg Met Arg Arg Lys Leu Thr Met Gln Gly Val Lys 35 40 45 Gly Pro Pro Pro Ser Leu Phe Arg Gly Asn Val Pro Glu Met Gln Lys 50 55 60 Ile Gln Ser Gln Ile Met Ser Asn Ser Lys His Tyr Ser Gly Asp Asn 65 70 75 80 Ile Ile Ala His Asp Tyr Thr Ser Ser Leu Phe Pro Tyr Leu Asp His 85 90 95 Trp Arg Lys Gln Tyr Gly Arg Val Tyr Thr Tyr Ser Thr Gly Val Lys 100 105 110 Gln His Leu Tyr Met Asn His Pro Glu Leu Val Lys Glu Leu Asn Gln 115 120 125 Ala Asn Thr Leu Asn Leu Gly Lys Val Ser Tyr Val Thr Lys Arg Leu 130 135 140 Lys Ser Ile Leu Gly Arg Gly Val Ile Thr Ser Asn Gly Pro His Trp 145 150 155 160 Ala His Gln Arg Arg Ile Ile Ala Pro Glu Phe Phe Leu Asp Lys Val 165 170 175 Lys Gly Met Val Gly Leu Val Val Glu Ser Ala Met Pro Met Leu Ser 180 185 190 Lys Trp Glu Glu Met Met Lys Arg Glu Gly Glu Met Val Cys Asp Ile 195 200 205 Ile Val Asp Glu Asp Leu Arg Ala Ala Ser Ala Asp Val Ile Ser Arg 210 215 220 Ala Cys Phe Gly Ser Ser Phe Ser Lys Gly Lys Glu Ile Phe Ser Lys 225 230 235 240 Leu Arg Cys Leu Gln Lys Ala Ile Thr His Asn Asn Ile Leu Phe Ser 245 250 255 Leu Asn Gly Phe Thr Asp Val Val Phe Gly Thr Lys Lys His Gly Asn 260 265 270 Gly Lys Ile Asp Glu Leu Glu Arg His Ile Glu Ser Leu Ile Trp Glu 275 280 285 Thr Val Lys Glu Arg Glu Arg Glu Cys Val Gly Asp His Lys Lys Asp 290 295 300 Leu Met Gln Leu Ile Leu Glu Gly Ala Arg Ser Ser Cys Asp Gly Asn 305 310 315 320 Leu Glu Asp Lys Thr Gln Ser Tyr Lys Ser Phe Val Val Asp Asn Cys 325 330 335 Lys Ser Ile Tyr Phe Ala Gly His Glu Thr Ser Ala Val Ala Val Ser 340 345 350 Trp Cys Leu Met Leu Leu Ala Leu Asn Pro Ser Trp Gln Thr
Arg Ile 355 360 365 Arg Asp Glu Val Phe Leu His Cys Lys Asn Gly Ile Pro Asp Ala Asp 370 375 380 Ser Ile Ser Asn Leu Lys Thr Val Thr Met Val Ile Gln Glu Thr Leu 385 390 395 400 Arg Leu Tyr Pro Pro Ala Ala Phe Val Ser Arg Glu Ala Leu Glu Asp 405 410 415 Thr Lys Leu Gly Asn Leu Val Val Pro Lys Gly Val Cys Ile Trp Thr 420 425 430 Leu Ile Pro Thr Leu His Arg Asp Pro Glu Ile Trp Gly Ala Asp Ala 435 440 445 Asn Glu Phe Asn Pro Glu Arg Phe Ser Glu Gly Val Ser Lys Ala Cys 450 455 460 Lys His Pro Gln Ser Phe Val Pro Phe Gly Leu Gly Thr Arg Leu Cys 465 470 475 480 Leu Gly Lys Asn Phe Gly Met Met Glu Leu Lys Val Leu Val Ser Leu 485 490 495 Ile Val Ser Arg Phe Ser Phe Thr Leu Ser Pro Thr Tyr Gln His Ser 500 505 510 Pro Val Phe Arg Met Leu Val Glu Pro Gln His Gly Val Val Ile Arg 515 520 525 Val Leu Arg Gln 530 724DNAartifitial sequencemisc_featureprimer 7tgaggatcca aataaaataa aaag 24824DNAartifitial sequencemisc_featureprimer 8aaagtcgacc acacacaaag caaa 24921DNAartificial sequencemisc_featureprimer 9ctgctgcaga ctctatttcc a 211025DNAartificial sequencemisc_featureprimer 10ttcaggatcc tttacttttt atttt 251120DNAartificial sequencemisc_featureprimer 11aatggtacca caagaaacaa 201221DNAartificial sequencemisc_featureprimer 12tctagatttg agctgaaaaa a 21131491DNAArabidopsis thaliana 13ctgacgcaga ctctatttcc aacctcaaaa cggtaattta caagttacaa ccttgcctct 60catgtcaagt tccttaaact ctcttaaacc aaaaaaaaaa atgttccttg gactccaagt 120atgactattt tcataaccta acatcacttg aataaaaata taggtgacaa tggttatcca 180ggaaacgttg aggctatacc caccagcagc attcgtgtcg agagaagccc ttgaggacac 240aaaactcgga aacctcgtgg tgccaaaggg agtgtgcatc tggacgttga tccctacatt 300gcacagagac cctgagatat ggggagctga cgcaaatgaa ttcaatccag aaagatttag 360cgaaggagtc tctaaagcct gcaaacaccc tcagtcattc gtcccatttg gcttagggac 420aaggttgtgt ttaggaaaga attttggtat gatggagctc aaggttcttg tctcacttat 480tgtgtcaagg tttagcttta ctctctctcc cacatatcaa cactctccgg tgtttagaat 540gcttgtagag cctcaacatg gtgttgtcat tagagttctg agacaataag atatgtcgtt 600agcttatggt tttagtttta atcctgtgta ataataagat attattacac tatagtacta 660taatagtatt ttctttggta tctttttttt tttgttctgt atatacagat ttaccaatag 720tcatcgaaaa aaatcagttg tctactaaaa gtaactagct agcttgtaac ttattcattc 780gaaaaagaaa ttaaaaaact attcgtaact agcatgttat taaaagccta taaaacaaat 840cattaaaatt aacaaatcgt tgtagtttaa attactaacc ttaattttat tataatttat 900gtataaatac actctactgt ctctacctac ttatttgata gggtgttttt ttttgtcttt 960ccttaaatat agttatggat cttgaatcta cttagatttg taatgctttt aatcattttt 1020tacactatta gactattagt actagatatt tagagtaaat aacttggatt tgctaaaatc 1080atgaatactg attgatgaat gtttgagatc tacattgttt ctaagaaaac cgagattatt 1140ccatagcttt gtttaggtcg tgttaagttt tcaaatataa gtccaagaac aattggacag 1200ccaaggtcgt gctaaaagta tgtgggcttt tcaagcgtaa actgaaccgg gagtcccagg 1260attgttccct gctgtgtaat atatttaata tttaataaaa taataaatat ctgcattttt 1320attgtttcgt tagtctaatt gaacttattt gttcaaagta gttatgattt aataaactaa 1380aattttggac ttatttgttc aaaaggaatc tggttgacta taatatggtt caagaagtga 1440agatgcaaat aaaataaaaa gtaaaagatc ctgaatagac aaaaagttaa a 1491
Patent applications by Qun Li, Shanghai CN
Patent applications by Yingying Zhang, Shanghai CN
Patent applications by Zuhua He, Shanghai CN
Patent applications in class METHOD OF USING A PLANT OR PLANT PART IN A BREEDING PROCESS WHICH INCLUDES A STEP OF SEXUAL HYBRIDIZATION
Patent applications in all subclasses METHOD OF USING A PLANT OR PLANT PART IN A BREEDING PROCESS WHICH INCLUDES A STEP OF SEXUAL HYBRIDIZATION