CN1817900A

CN1817900A - Transcription factor for regulating plant fallen, its coding gene and use

Info

Publication number: CN1817900A
Application number: CN 200610059834
Authority: CN
Inventors: 孙传清; 林中伟; 朱作峰; 谭禄宾; 付永彩
Original assignee: China Agricultural University
Current assignee: China Agricultural University
Priority date: 2006-03-15
Filing date: 2006-03-15
Publication date: 2006-08-16
Anticipated expiration: 2026-03-15
Also published as: CN100372868C

Abstract

本发明公开了一个调控植物落粒性的转录因子及其编码基因与应用，其目的是提供一个调控植物落粒性的转录因子及其编码基因与其在调控植物落粒性中的应用。该转录因子具有下述氨基酸残基序列之一：1)序列表中的SEQ ID №：1或SEQ ID №：5；2)将序列表中SEQ ID №：1或SEQ ID №：5的氨基酸残基序列经过一至十个氨基酸残基的取代、缺失或添加且具有调控植物落粒性的蛋白质。该转录因子及其编码基因对于落粒分子机制的研究，以及培育落粒性提高的水稻、草坪草及其它作物新品种具有重要的理论及实际意义。本发明在农业领域具有广阔的应用和市场前景。The invention discloses a transcription factor regulating plant shattering, its encoding gene and application thereof, and aims to provide a transcription factor regulating plant shattering, its encoding gene and its application in regulating plant shattering. The transcription factor has one of the following amino acid residue sequences: 1) SEQ ID No.: 1 or SEQ ID No.: 5 in the sequence listing; 2) the amino acid of SEQ ID No.: 1 or SEQ ID No.: 5 in the sequence listing The residue sequence undergoes one to ten amino acid residue substitutions, deletions or additions and has a protein that regulates plant shattering. The transcription factor and its coding gene have important theoretical and practical significance for the study of the molecular mechanism of shattering and the cultivation of new varieties of rice, turfgrass and other crops with improved shattering performance. The invention has broad application and market prospects in the agricultural field.

Description

The transcription factor of a regulating plant fallen and encoding gene thereof and application

Technical field

The present invention relates to transcription factor and the encoding gene and the application of regulating plant fallen shape, particularly relate to transcription factor and encoding gene and its application in the regulating plant fallen shape that derives from the regulating plant fallen of paddy rice.

Background technology

The natural seed holding of wild-rice is that it is different from one of most important characteristic of cultivated rice.In wild-rice, when seed was ripe, seed can fall immediately, so just can avoid being eaten up by some animalcules (particularly birds), thereby provide assurance for the normal procreation of wild-rice.In the domestication process, this shattering habit of wild-rice is selected have been fallen, and the mankind just can gather in the crops rice grain easily like this, have reduced production loss.In cultivated rice, long-grained nonglutinous rice and long-grained nonglutinous rice exist evident difference on seed holding, and generally speaking, japonica rice is than the difficult shattering of long-grained nonglutinous rice; The extremely difficult shattering of some japonica rice bring very big inconvenience to results, and some long-grained nonglutinous rice is easy to shattering, causes the very big loss on the output again.Therefore, how regulating and control seed holding, to obtain the moderate kind of seed holding be an important problem.Simultaneously, good shattering gene can be applied to some easy shattering crops, as the lawn crop, thus the harvest yield of raising seed.

Coming off of seed generally can be divided into for two steps: one, the differentiation of abscission zone cell; Two, the come off startup of signal and separating of abscission zone cell.The signal that comes off comprises a variety of: grow signal (as pollination), ambient signal (as drought, waterlogging, high temperature, low temperature etc.) and biology are coerced signal (as the infringement of sick worm) etc.Plant hormone plays an important role in the conduction of the signal that comes off.Result of study to the abscission zone tissues of many plants shows that ethene is the push agent that comes off, and growth hormone is inhibitor, and ethene is the primary hormone that guarantees that plant comes off and in time comes off.The seed holding of paddy rice is inseparable with the growth of absciss layer, and absciss layer is formed at the base portion of lemma, is made up of the cell that a group is tiny.Before absciss layer appears at heading stage, the diameter of the cell of absciss layer reaches maximum (Jin when heading stage, I., Inouye, J. (1981) .On the degreeof grain shedding of Japonica-Indica hybrid rice bred in Korea.Jpn.J.CropSci.50,181-185.).The absciss layer of bennet occurs early in the long-grained nonglutinous rice, obviously.At present, with method modern molecular biology the seed holding of paddy rice is discovered that the seed holding of paddy rice is by a plurality of Gene Handling (Kennard by traditional, W.C., Phillips, R.L., Porter, R.A. (2002) .Genetic dissectionof seed shattering, agronomic, and color traits in American wild rice (Zizaniapalustris var.interior L.) with a comparative map.Theor.Appl.Genet.105,1075-1086.; Thomson, M.J., Tai; T.H., McClum, A.M.; Lai; X.H., Hinga, M.E.; Lobos; K.B., Xu, Y.; Martinez; C.P., McCouch, S.R. (2003) .Mappingquantitative trait loci for yield; yield components and morphological traitsin an advanced backcross population between Oryza rufipogon and Oryza sativacultiar Jefferson.Theor.Appl.Genet.107; 479-493.), wherein, be positioned at the 1st karyomit(e) and the 4th chromosomal two shattering genes play main effect (Cai; H.W.; Morishima, H. (2000) .Genomic regions affecting seed shattering and seed dormancy in rice.Theor.Appl.Genet.100,840-846.).These two genes all are dominant genes, shattering gene on the 1st karyomit(e) has been proved the division of control paddy rice absciss layer cell, the first step (the Oba that i.e. control comes off, S., Sumi, N., Fujimoto, F., Yasue, T. (1995) .Association between grain shattering habitand formation of abscission layer controlled by grain shattering gene sh-2in rice (Oryza sativa L.) .Jpn.J.Crop Sci.64,607-615.; Watanabe, K., Oba, S., Horiuchi, T. (2003) .Allelic test of rice shattering genes sh1 and sh2in an F sub (2) population derived from the cross between Momigaredatsu andDee-Geo-Woo-Gen (Oryza sativa L.) SABRAO J.Breed.Genet.35,57-64.); The inventor thinks that after deliberation the function of the shattering gene on No. 4 karyomit(e) is second step that control comes off, and promptly controls the separation of absciss layer cell.

Summary of the invention

The transcription factor that the purpose of this invention is to provide a regulating plant fallen.

The transcription factor of regulating plant fallen provided by the present invention, name are called SHATTERING1 (being called for short SHA1), derive from Yunnan Yuanjiang River wild-rice (O.rufipogon Griff.), have one of following amino acid residue sequences:

1) the SEQ ID № in the sequence table: 1 or SEQ ID №: 5;

2) with SEQ ID № in the sequence table: 1 or SEQ ID №: 5 amino acid residue sequence is through replacement, disappearance or the interpolation of one to ten amino-acid residue and have the protein of regulating plant fallen.

SEQ ID № in the sequence table: 1 and SEQ ID №: 5 are made up of 390 amino-acid residues, from aminoterminal (N end) 59-139 amino acids residue is Myb DNA-binding structural domain, is proline rich zone (proline_rich region) from aminoterminal 215-274 amino acids residue.

The gene of the transcription factor of code book invention regulating plant fallen (SHATTERING1 is called for short SHA1), its cDNA is one of following nucleotide sequence:

1) SEQ ID № in the sequence table: 8 or SEQ ID №: 9 dna sequence dna;

2) SEQ ID № in the code sequence tabulation: 1 or SEQ ID №: 5 dna sequence dna;

3) under the rigorous condition of height can with SEQ ID № in the sequence table: the nucleotide sequence of 8 or SEQ ID №: the 9 dna sequence dnas hybridization that limit.

The rigorous condition of described height be 0.1 * SSPE (or 0.1 * SSC), in the solution of 0.1%SDS, hybridization and wash film under 65 ℃ of conditions.

SEQ ID № in the sequence table: 8 by 1173 based compositions, its encoding sequence is from 5 ' end 1-1173 bit base, coding has SEQ ID № in the sequence table: the protein of 1 amino acid residue sequence, from 5 ' end 175-417 bit base coding Myb DNA-binding structural domain, from 5 ' end 643-822 bit base coding proline rich zone; SEQ ID № in the sequence table: 9 by 1173 based compositions, its encoding sequence is from 5 ' end 1-1173 bit base, coding has SEQ ID № in the sequence table: the protein of 5 amino acid residue sequence, from 5 ' end 175-417 bit base coding Myb DNA-binding structural domain, from 5 ' end 643-822 bit base coding proline rich zone.

Its genomic gene is one of following nucleotide sequence:

1) SEQ ID № in the sequence table: 6 or SEQ ID №: 7 dna sequence dna;

2) under the rigorous condition of height can with SEQ ID № in the sequence table: the nucleotide sequence of 6 or SEQ ID №: the 7 dna sequence dnas hybridization that limit.

SEQ ID № in the sequence table: 6 by 2037 based compositions, from 5 ' end 1-835 bit base is first exon of this genomic gene, from 5 ' end 836-1699 bit base is first intron of this genomic gene, from 5 ' end 1700-2037 bit base is second exon of this genomic gene, from 5 ' end 1-3 bit base is the initiator codon ATG of this genomic gene, is the terminator codon TGA of this genomic gene from 5 ' end 2035-2037 bit base; SEQ ID № in the sequence table: 7 by 2036 based compositions, from 5 ' end 1-835 bit base is first exon of this genomic gene, from 5 ' end 836-1699 bit base is first intron of this genomic gene, from 5 ' end 1700-2036 bit base is second exon of this genomic gene, from 5 ' end 1-3 bit base is the initiator codon ATG of this genomic gene, is the terminator codon TGA of this genomic gene from 5 ' end 2034-2036 bit base.

Contain expression carrier of the present invention, transgenic cell line and host bacterium and all belong to protection scope of the present invention.

Arbitrary segmental primer is to also within protection scope of the present invention among the amplification SHATTERING1.

Another object of the present invention provides a kind of method of regulating plant fallen.

The method of regulating plant fallen provided by the present invention is that plant fallen obtains regulation and control with the gene SHATTERING1 importing plant tissue or the cell of described coding regulating plant fallen transcription factor.

The gene SHATTERING1 of described coding regulating plant fallen transcription factor can import explant by the plant expression vector that contains SHATTERING1; The carrier that sets out that is used to make up described plant expression vector can be any one double base agrobacterium vector or can be used for carrier of plant micropellet bombardment etc., as pBI121, pBin19, pCAMBIA2301, pCAMBIA1301, pCAMBIA1300 or other plant expression vector of deriving.

When using SHATTERING1 to make up plant expression vector, before its transcription initiation Nucleotide, can add any enhancement type, composing type, organizing specific type or inducible promoter, as cauliflower mosaic virus (CAMV) 35S promoter, general living plain gene Ubiquitin promotor (pUbi) etc., they can use separately or be used in combination with other plant promoter; In addition, when using gene constructed plant expression vector of the present invention, also can use enhanser, comprise translational enhancer or transcriptional enhancer, these enhanser zones can be ATG initiator codon or neighboring region initiator codon etc., but must be identical with the reading frame of encoding sequence, to guarantee the correct translation of whole sequence.The source of described translation control signal and initiator codon is widely, can be natural, also can be synthetic.Translation initiation region can be from transcription initiation zone or structure gene.

For the ease of transgenic plant cells or plant being identified and screening, can process used plant expression vector, can produce the enzyme of colour-change or the gene of luminophor (gus gene, GFP gene, luciferase genes etc.) as adding the coding that in plant, to express, have the antibiotic marker thing (gentamicin marker, kantlex marker etc.) of resistance or anti-chemical reagent marker gene (as anti-weedkiller gene) etc.From the security consideration of transgenic plant, can not add any selected marker, directly with adverse circumstance screening transformed plant.

Carry the present invention encode the regulating plant fallen transcription factor gene SHATTERING1 plant expression vector can Ti-plasmids, Ri plasmid, plant viral vector, directly DNA conversion, microinjection, electricity be led, conventional biological method transformed plant cells or tissue such as agriculture bacillus mediated by using, and the plant transformed cell or tissue is cultivated into plant.Be can be plants such as turfgrass, paddy rice, wheat, soybean, tobacco, corn, rape, Chinese sorghum, cotton, clover, grape or tomato by the plant transformed host.

The invention provides the transcription factor and the encoding gene thereof of a regulating plant fallen.This transcription factor and encoding gene thereof are for the shattering Molecular Study, and paddy rice, turfgrass and other crop new variety that the cultivation seed holding improves have important theory and practical significance.The present invention has wide application and market outlook at agriculture field.

The present invention will be further described below in conjunction with specific embodiment.

Description of drawings

Fig. 1 is the come off structure of section of BC3F4-100-5 under the scanning electron microscope and special blue or green seed

Fig. 2 is BC3F4-100-5 and special blue or green phenotype

Fig. 3 is BC3F4-100-5 and special blue or green shattering rate comparative result

Fig. 4 is the genotype synoptic diagram of BC3F4-39-2 and BC3F4-100-5

Fig. 5 is the Fine Mapping figure of SHA1

Fig. 6 is the BLAST analytical results of SHA1 amino acid residue sequence

Fig. 7 is the polymorphism analysis result of SHA1 in common wild-rice, four long-grained nonglutinous rices and four japonica rice

Fig. 8 is the expression pattern analytical results of filling stage Yunnan Yuanjiang River wild-rice SHA1

Fig. 9 be pollinated the back same day, the 5th day and the 10th day Yunnan Yuanjiang River wild-rice SHA1 the expression pattern analytical results

Embodiment

Method therefor is ordinary method if no special instructions among the following embodiment, and it is synthetic that the primer and probe are given birth to the worker by Shanghai.

The acquisition of embodiment 1, wild-rice shattering gene SHATTERING1

At first making up one is donor with Yunnan Yuanjiang River common wild-rice, the special green grass or young crops of long-grained nonglutinous rice is acceptor, and contain the F2 shattering segregating population of 383 individual plants, the individuality of nature shattering is 293: 90 with the ratio of shattering individuality not, meet 3: 1 ratio, show that this shattering proterties is controlled by single-gene, with this single-gene called after SHATTERING1 (being called for short SHA1); Then select 1 shattering strain and special green grass or young crops to backcross and made up a high generation backcross population (called after BC3), in order accurately to describe this shattering proterties, the shattering rate of BC3F4-100-5 strain system and special blue or green (phenotype is seen Fig. 2) wherein, the result as shown in Figure 3, special blue or green shattering rate has reduced nearly 95 times than BC3F4-100-5, in order to disclose the reason on the huge histology of both shattering rate differences, now the absciss layer tissue to both has carried out scanning electron microscopic observation, (A and A1 are BC3F4-100-5, and B and B1 are special blue or green) as shown in Figure 1.In pollination back 14 days, the seed of BC3F4-100-5 just begins to come off, special blue or green seed then needs the people just can come off for applying external force, come off and the people finds that BC3F4-100-5 and special green grass or young crops all can produce absciss layer after applying the seed section that external force comes off by observation of nature, the former wants big the strength ratio of different is special blue or green absciss layer cell walls, when applying external force garland stalk, sterile glume can be shut down in the lump together with bennet, the variation that shows the absciss layer cell walls is the huge reasons of both shattering rate differences.

For separating SHATTERING1, at first select BC3F4-39-2, these two shattering systems of BC3F4-100-5, two tie up to that all performance is consistent on shattering rate and other proterties, and the infiltration fragment (genotype is seen Fig. 4) that the Yuanjiang River common wild-rice is all arranged on the 4th chromosomal long arm end, therefore this fragment infers that SHA1 is on No. 4 karyomit(e) between RM348 and the RM131 between RM348 and RM131.For further this gene of location, existing is male parent with BC3F4-100-5, and special green grass or young crops be female parent, makes up a F2 colony that approximately comprises 15,000 individualities, therefrom selects 3089 to show as not that the individuality of shattering is used for locating.Because the polymorphism of RM348 and RM131 is relatively poor, near these two marks, find two good mark SP33 and RM1113 of polymorphism to be used for the location respectively, the labeled analysis result shows this two marks and SHA1 close linkage, and it is stuck between these two marks.Then we are positioned SHA1 again to develop three mark 19E according to this BAC cloned sequence of OSJNBa0043A12 then between RM6441 and the RM1113,19K, and 19Q, and this gene is compressed in the scope of about 50Kb.In order to continue this gene of Fine Mapping, utilize 19Q (forward primer F:5 '-AGACGTGAATGTACGGTAAC-3 '; Reverse primer R:5 '-CTTGAGGGATACAACCTTAC-3 ') with RM1113 (forward primer F:5 '-CGAAAGGTCGGCATCTTTC-3 '; Reverse primer R:5 '-ATGGCAATGATACGG AGGAG-3 '), from the Yuanjiang River common wild-rice BAC library that makes up, screens one and covered the BAC clone of this section from 19Q to RM1113, called after B-17-14-10 as probe.After with the Shot-gun method B-17-14-10 being checked order again, two mark P1 (forward primer F:5 '-GTGTGTGGTGTGAATGATCG-3 ' have been developed; Reverse primer R:5 '-CACCCGAGAAGAAAAAACGC-3 ') and P2 (forward primer F:5 '-CCCAGGTTGGGTCTTATCTG-3 '; Reverse primer R:5 '-AAGTGCAGCCATGGCTTTCC-3 '), the SHA1 Fine Mapping is in the scope of 5.5Kb the most at last, and it accurately sees Fig. 5 in the location.After to this section note, only find an open reading frame (ORF), has the SEQ ID № in the sequence table: 8 nucleotide sequence, by 1173 based compositions, coding has SEQ ID №: the protein of 1 amino acid residue sequence, SEQ ID № in the sequence table: 1 is made up of 390 amino-acid residues, with this albumen called after SHATTERING1 (being called for short SHA1).This new albumen has a MybDNA-binding structural domain and a proline rich zone (proline_rich region), lays respectively between aminoterminal 59-139 amino acids residue and between aminoterminal 215-274 amino acids residue.This proteic amino acid residue sequence is carried out the BLAST analysis, and (amino acid residue sequence of YD2-65, IRGC100204, YD2-0225 and special blue or green (Teqing) middle corresponding protein is respectively the SEQ ID № in the sequence table: 2,3,4,5), analytical results as shown in Figure 6, an expressing protein in this new albumen and the Arabidopis thaliana (sequence number: Atlg31310) height homology.In order to confirm whether this predicted gene is goal gene, now relatively 18 pleomorphism sites have been found behind the full length sequence of this supposition gene in four common wild-rices (rufipogon), four long-grained nonglutinous rices (indica) and four japonica rice (japonica), wherein only there is a mononucleotide (SNP1) pleomorphism site can cause the variation of amino-acid residue, and can with wild-type and mutant this etc. the site distinguished, see as the figure A among Fig. 7.Confirm after the sequence of continuation comparison 15 wild-rices, 23 long-grained nonglutinous rices and 19 these SNP1 regions of japonica rice that SNP1 sites such as mutant complete and this wild-rice wild-type and cultivated rice are consistent, be that wild-type is G, mutant is T, analytical results is seen the figure B among Fig. 7, proves absolutely that this gene is exactly a goal gene.By comparing genomic dna and the cDNA of SHA1, the genomic gene of wild-type rice SHA1 has SEQ ID № in the sequence table: 6 nucleotide sequence, the genomic gene of cultivated rice SHA1 has SEQ ID № in the sequence table: 7 nucleotide sequence, SEQ ID № in the sequence table: 6 by 2037 based compositions, from 5 ' end 1-835 bit base is first exon of this genomic gene, from 5 ' end 836-1699 bit base is first intron of this genomic gene, from 5 ' end 1700-2037 bit base is second exon of this genomic gene, from 5 ' end 1-3 bit base is the initiator codon ATG of this genomic gene, is the terminator codon TGA of this genomic gene from 5 ' end 2035-2037 bit base; SEQ ID № in the sequence table: 7 by 2036 based compositions, from 5 ' end 1-835 bit base is first exon of this genomic gene, from 5 ' end 836-1699 bit base is first intron of this genomic gene, from 5 ' end 1700-2036 bit base is second exon of this genomic gene, from 5 ' end 1-3 bit base is the initiator codon ATG of this genomic gene, from 5 ' end 2034-2036 bit base is the terminator codon TGA of this genomic gene, SNP1 (AAG → AAT, from 5 ' end 235-237 bit base) be positioned on first exon, cause in Myb DNA-binding structural domain, having taken place by the variation of Methionin (K) to aspartic acid (N), the cDNA of cultivated rice SHA1 has the SEQ ID № in the sequence table: 9 nucleotide sequence, by 1173 based compositions, coding has a SEQ ID № in the sequence table: the protein of 5 amino acid residue sequence, the SEQ ID № in the sequence table: 5 are made up of 390 amino-acid residues.

The expression pattern analysis of embodiment 2, SHA1

Respectively in the watery stage, the same day, the 5th day, the 10th day are extracted the RNA of Yunnan Yuanjiang River wild-rice leaf, stem, root in the pollination back, analyze SHA1 expression in tassel, leaf, stem, root with the RT-PCR method, the primer is SP (forward primer F:5 '-CAGAACCAGTGCAATGACAAGTGGGACAAC-3 '; Reverse primer R:5 '-ATAATCCGATGCCTCGATCCATGCATCTCC-3 '), with ACTIN is contrast, (swimming lane P is bennet (having absciss layer) to the detected result of filling stage as shown in Figure 8, swimming lane R is a root, swimming lane C is a cane, and swimming lane FL is a boot leaf), in the watery stage, SHA1 is high expression level in bennet (having absciss layer), and expresses hardly in leaf, stem, root; (W is the Yuanjiang River wild-rice to the detected result on the same day, the 5th day and the 10th day as shown in Figure 9 after the pollination, M is special blue or green), in the growth course of rice grain, pollination back the 5th day, the expression amount of SHA1 in bennet reaches the highest, and all very low at the expression amount of the pollination same day and the 10th day SHA1 in pollination back.Above-mentioned expression pattern is consistent on wild-type and mutant plant.The observations of the scanning electron microscope in 1 can confirm that SHA1 is a transcription factor that control shattering absciss layer cell walls is grown in conjunction with the embodiments.

Sequence table

<160>9

<210>1

<211>390

<212>PRT

＜213〉Yunnan Yuanjiang River wild-rice (O.rufipogon Griff.)

<400>1

Met?Ser?Gly?Ser?Ser?Ala?Asp?Pro?Ser?Pro?Ser?Ala?Ser?Thr?Ala?Gly

1 5 10 15

Ala?Ala?Val?Ser?Pro?Leu?Ala?Leu?Leu?Arg?Ala?His?Gly?His?Gly?His

20 25 30

Gly?His?Leu?Thr?Ala?Thr?Pro?Pro?Ser?Gly?Ala?Thr?Gly?Pro?Ala?Pro

35 40 45

Pro?Pro?Pro?Ser?Pro?Ala?Ser?Gly?Ser?Ala?Pro?Arg?Asp?Tyr?Arg?Lys

50 55 60

Gly?Asn?Trp?Thr?Leu?His?Glu?Thr?Leu?Ile?Leu?Ile?Thr?Ala?Lys?Arg

65 70 75 80

Leu?Asp?Asp?Asp?Arg?Arg?Ala?Gly?Val?Gly?Gly?Ala?Ala?Ala?Gly?Gly

85 90 95

Gly?Gly?Ala?Gly?Ser?Pro?Pro?Thr?Pro?Arg?Ser?Ala?Glu?Gln?Arg?Trp

100 105 110

Lys?Trp?Val?Glu?Asn?Tyr?Cys?Trp?Lys?Asn?Gly?Cys?Leu?Arg?Ser?Gln

115 120 125

Asn?Gln?Cys?Asn?Asp?Lys?Trp?Asp?Asn?Leu?Leu?Arg?Asp?Tyr?Lys?Lys

130 135 140

Val?Arg?Asp?Tyr?Glu?Ser?Arg?Val?Ala?Ala?Ala?Ala?Ala?Thr?Gly?Gly

145 150 155 160

Ala?Ala?Ala?Ala?Asn?Ser?Ala?Pro?Leu?Pro?Ser?Tyr?Trp?Thr?Met?Glu

165 170 175

Arg?His?Glu?Arg?Lys?Asp?Cys?Asn?Leu?Pro?Thr?Asn?Leu?Ala?Pro?Glu

180 185 190

Val?Tyr?Asp?Ala?Leu?Ser?Glu?Val?Leu?Ser?Arg?Arg?Ala?Ala?Arg?Arg

195 200 205

Gly?Gly?Ala?Thr?Ile?Ala?Pro?Thr?Pro?Pro?Pro?Pro?Pro?Leu?Ala?Leu

210 215 220

Pro?Leu?Pro?Pro?Pro?Pro?Pro?Pro?Ser?Pro?Pro?Lys?Pro?Leu?Val?Ala

225 230 235 240

Gln?Gln?Gln?His?His?His?His?Gly?His?His?His?His?Pro?Pro?Pro?Pro

245 250 255

Gln?Pro?Pro?Pro?Ser?Ser?Leu?Gln?Leu?Pro?Pro?Ala?Val?Val?Ala?Pro

260 265 270

Pro?Pro?Ala?Ser?Val?Ser?Ala?Glu?Glu?Glu?Met?Ser?Gly?Ser?Ser?Glu

275 280 285

Ser?Gly?Glu?Glu?Glu?Glu?Gly?Ser?Gly?Gly?Glu?Pro?Glu?Ala?Lys?Arg

290 295 300

Arg?Arg?Leu?Ser?Arg?Leu?Gly?Ser?Ser?Val?Val?Arg?Ser?Ala?Thr?Val

305 310 315 320

Val?Ala?Arg?Thr?Leu?Val?Ala?Cys?Glu?Glu?Lys?Arg?Glu?Arg?Arg?His

325 330 335

Arg?Glu?Leu?Leu?Gln?Leu?Glu?Glu?Arg?Arg?Leu?Arg?Leu?Glu?Glu?Glu

340 345 350

Arg?Thr?Glu?Val?Arg?Arg?Gln?Gly?Phe?Ala?Gly?Leu?Ile?Ala?Ala?Val

355 360 365

Asn?Ser?Leu?Ser?Ser?Ala?Ile?His?Ala?Leu?Val?Ser?Asp?His?Arg?Ser

370 375 380

Gly?Asp?Ser?Ser?Gly?Arg

385 390

<210>2

<211>390

<212>PRT

＜213〉Jiangxi Dongxiang Wild Rice (O.rufipogon Griff.)

<400>2

Met?Ser?Gly?Ser?Ser?Ala?Asp?Pro?Ser?Pro?Ser?Ala?Ser?Thr?Ala?Gly

1 5 10 15

Ala?Ala?Val?Ser?Pro?Leu?Ala?Leu?Leu?Arg?Ala?His?Gly?His?Gly?His

20 25 30

Gly?His?Leu?Thr?Ala?Thr?Pro?Pro?Ser?Gly?Ala?Thr?Gly?Pro?Ala?Pro

35 40 45

Pro?Pro?Pro?Ser?Pro?Ala?Ser?Gly?Ser?Ala?Pro?Arg?Asp?Tyr?Arg?Lys

50 55 60

Gly?Asn?Trp?Thr?Leu?His?Glu?Thr?Leu?Ile?Leu?Ile?Thr?Ala?Lys?Arg

65 70 75 80

Leu?Asp?Asp?Asp?Arg?Arg?Ala?Gly?Val?Gly?Gly?Ala?Ala?Ala?Gly?Gly

85 90 95

Gly?Gly?Ala?Gly?Ser?Pro?Pro?Thr?Pro?Arg?Ser?Ala?Glu?Gln?Arg?Trp

100 105 110

Lys?Trp?Val?Glu?Asn?Tyr?Cys?Trp?Lys?Asn?Gly?Cys?Leu?Arg?Ser?Gln

115 120 125

Asn?Gln?Cys?Asn?Asp?Lys?Trp?Asp?Asn?Leu?Leu?Arg?Asp?Tyr?Lys?Lys

130 135 140

Val?Arg?Asp?Tyr?Glu?Ser?Arg?Val?Ala?Ala?Ala?Ala?Ala?Thr?Gly?Gly

145 150 155 160

Ala?Ala?Ala?Ala?Asn?Ser?Ala?Pro?Leu?Pro?Ser?Tyr?Trp?Thr?Met?Glu

165 170 175

Arg?His?Glu?Arg?Lys?Asp?Cys?Asn?Leu?Pro?Thr?Asn?Leu?Ala?Pro?Glu

180 185 190

Val?Tyr?Asp?Ala?Leu?Ser?Glu?Val?Leu?Ser?Arg?Arg?Ala?Ala?Arg?Arg

195 200 205

Gly?Gly?Ala?Thr?Ile?Ala?Pro?Thr?Pro?Pro?Pro?Pro?Pro?Leu?Ala?Leu

210 215 220

Pro?Leu?Pro?Pro?Pro?Pro?Pro?Pro?Ser?Pro?Pro?Lys?Pro?Leu?Val?Ala

225 230 235 240

Gln?Gln?Gln?His?His?His?His?Gly?His?His?His?His?Pro?Pro?Pro?Pro

245 250 255

Gln?Pro?Pro?Pro?Ser?Ser?Leu?Gln?Leu?Pro?Pro?Ala?Val?Val?Ala?Pro

260 265 270

Pro?Pro?Ala?Ser?Val?Ser?Ala?Glu?Glu?Glu?Met?Ser?Gly?Ser?Ser?Glu

275 280 285

Ser?Gly?Glu?Glu?Glu?Glu?Gly?Ser?Gly?Gly?Glu?Pro?Glu?Ala?Lys?Arg

290 295 300

Arg?Arg?Leu?Ser?Arg?Leu?Gly?Ser?Ser?Val?Val?Arg?Ser?Ala?Thr?Val

305 310 315 320

Val?Ala?Arg?Thr?Leu?Val?Ala?Cys?Glu?Glu?Lys?Arg?Glu?Arg?Arg?His

325 330 335

Arg?Glu?Leu?Leu?Gln?Leu?Glu?Glu?Arg?Arg?Leu?Arg?Leu?Glu?Glu?Glu

340 345 350

Arg?Thr?Glu?Val?Arg?Arg?Gln?Gly?Phe?Ala?Gly?Leu?Ile?Ala?Ala?Val

355 360 365

Asn?Ser?Leu?Ser?Ser?Ala?Ile?His?Ala?Leu?Val?Ser?Asp?His?Arg?Ser

370 375 380

Gly?Asp?Ser?Ser?Gly?Arg

385 390

<210>3

<211>391

<212>PRT

＜213〉India's wild-rice (O.rufipogon Griff)

<400>3

Met?Ser?Gly?Ser?Ser?Ala?Asp?Pro?Ser?Pro?Ser?Ala?Ser?Thr?Ala?Gly

1 5 10 15

Ala?Ala?Val?Ser?Pro?Leu?Ala?Leu?Leu?Arg?Ala?His?Gly?His?Gly?His

20 25 30

Gly?His?Leu?Thr?Ala?Thr?Pro?Pro?Ser?Gly?Ala?Thr?Gly?Pro?Ala?Pro

35 40 45

Pro?Pro?Pro?Ser?Pro?Ala?Ser?Gly?Ser?Ala?Pro?Arg?Asp?Tyr?Arg?Lys

50 55 60

Gly?Asn?Trp?Thr?Leu?His?Glu?Thr?Leu?Ile?Leu?Ile?Thr?Ala?Lys?Arg

65 70 75 80

Leu?Asp?Asp?Asp?Arg?Arg?Ala?Gly?Val?Gly?Gly?Ala?Ala?Ala?Gly?Gly

85 90 95

Gly?Gly?Ala?Gly?Ser?Pro?Pro?Thr?Pro?Arg?Ser?Ala?Glu?Gln?Arg?Trp

100 105 110

Lys?Trp?Val?Glu?Asn?Tyr?Cys?Trp?Lys?Asn?Gly?Cys?Leu?Arg?Ser?Gln

115 120 125

Asn?Gln?Cys?Asn?Asp?Lys?Trp?Asp?Asn?Leu?Leu?Arg?Asp?Tyr?Lys?Lys

130 135 140

Val?Arg?Asp?Tyr?Glu?Ser?Arg?Val?Ala?Ala?Ala?Ala?Ala?Thr?Gly?Gly

145 150 155 160

Ala?Ala?Ala?Ala?Asn?Ser?Ala?Pro?Leu?Pro?Ser?Tyr?Trp?Thr?Met?Glu

165 170 175

Arg?His?Glu?Arg?Lys?Asp?Cys?Asn?Leu?Pro?Thr?Asn?Leu?Ala?Pro?Glu

180 185 190

Val?Tyr?Asp?Ala?Leu?Ser?Glu?Val?Leu?Ser?Arg?Arg?Ala?Ala?Arg?Arg

195 200 205

Gly?Gly?Ala?Thr?Ile?Ala?Pro?Thr?Pro?Pro?Pro?Pro?Pro?Leu?Ala?Leu

210 215 220

Pro?Leu?Pro?Pro?Pro?Pro?Pro?Pro?Pro?Ser?Pro?Pro?Lys?Pro?Leu?Val

225 230 235 240

Ala?Gln?Gln?Gln?His?His?His?His?Gly?His?His?His?His?Pro?Pro?Pro

245 250 255

Pro?Gln?Pro?Pro?Pro?Ser?Ser?Leu?Gln?Leu?Pro?Pro?Ala?Val?Val?Ala

260 265 270

Pro?Pro?Pro?Ala?Ser?Val?Ser?Ala?Glu?Glu?Glu?Met?Ser?Gly?Ser?Ser

275 280 285

Glu?Ser?Gly?Glu?Glu?Glu?Glu?Gly?Ser?Gly?Gly?Glu?Pro?Glu?Ala?Lys

290 295 300

Arg?Arg?Arg?Leu?Ser?Arg?Leu?Gly?Ser?Ser?Val?Val?Arg?Ser?Ala?Thr

305 310 315 320

Val?Val?Ala?Arg?Thr?Leu?Val?Ala?Cys?Glu?Glu?Lys?Arg?Glu?Arg?Arg

325 330 335

His?Arg?Glu?Leu?Leu?Gln?Leu?Glu?Glu?Arg?Arg?Leu?Arg?Leu?Glu?Glu

340 345 350

Glu?Arg?Thr?Glu?Val?Arg?Arg?Gln?Gly?Phe?Ala?Gly?Leu?Ile?Ala?Ala

355 360 365

Val?Asn?Ser?Leu?Ser?Ser?Ala?Ile?His?Ala?Leu?Val?Ser?Asp?His?Arg

370 375 380

Ser?Gly?Asp?Ser?Ser?Gly?Arg

385 390

<210>4

<211>390

<212>PRT

＜213〉the beautiful osmanthus wild-rice (O.rufipogon Griff) in Guangxi

<400>4

Met?Ser?Gly?Ser?Ser?Ala?Asp?Pro?Ser?Pro?Ser?Ala?Ser?Thr?Ala?Gly

1 5 10 15

Ala?Ala?Val?Ser?Pro?Leu?Ala?Leu?Leu?Arg?Ala?His?Gly?His?Gly?His

20 25 30

Gly?His?Leu?Thr?Ala?Thr?Pro?Pro?Ser?Gly?Ala?Thr?Gly?Pro?Ala?Pro

35 40 45

Pro?Pro?Pro?Ser?Pro?Ala?Ser?Gly?Ser?Ala?Pro?Arg?Asp?Tyr?Arg?Lys

50 55 60

Gly?Asn?Trp?Thr?Leu?His?Glu?Thr?Leu?Ile?Leu?Ile?Thr?Ala?Lys?Arg

65 70 75 80

Leu?Asp?Asp?Asp?Arg?Arg?Ala?Gly?Val?Gly?Gly?Ala?Ala?Ala?Gly?Gly

85 90 95

Gly?Gly?Ala?Gly?Ser?Pro?Pro?Thr?Pro?Arg?Ser?Ala?Glu?Gln?Arg?Trp

100 105 110

Lys?Trp?Val?Glu?Asn?Tyr?Cys?Trp?Lys?Asn?Gly?Cys?Leu?Arg?Ser?Gln

115 120 125

Asn?Gln?Cys?Asn?Asp?Lys?Trp?Asp?Asn?Leu?Leu?Arg?Asp?Tyr?Lys?Lys

130 135 140

Val?Arg?Asp?Tyr?Glu?Ser?Arg?Val?Ala?Ala?Ala?Ala?Ala?Thr?Gly?Gly

145 150 155 160

Ala?Ala?Ala?Ala?Asn?Ser?Ala?Pro?Leu?Pro?Ser?Tyr?Trp?Thr?Met?Glu

165 170 175

Arg?His?Glu?Arg?Lys?Asp?Cys?Asn?Leu?Pro?Thr?Asn?Leu?Ala?Pro?Glu

180 185 190

Val?Tyr?Asp?Ala?Leu?Ser?Glu?Val?Leu?Ser?Arg?Arg?Ala?Ala?Arg?Arg

195 200 205

Gly?Gly?Ala?Thr?Ile?Ala?Pro?Thr?Pro?Pro?Pro?Pro?Pro?Leu?Ala?Leu

210 215 220

Pro?Pro?Pro?Pro?Pro?Pro?Pro?Pro?Ser?Pro?Pro?Lys?Pro?Leu?Val?Ala

225 230 235 240

Gln?Gln?Gln?His?His?His?His?Gly?His?His?His?His?Pro?Pro?Pro?Pro

245 250 255

Gln?Pro?Pro?Pro?Ser?Ser?Leu?Gln?Leu?Pro?Pro?Ala?Val?Val?Ala?Pro

260 265 270

Pro?Pro?Ala?Ser?Val?Ser?Ala?Glu?Glu?Glu?Met?Ser?Gly?Ser?Ser?Glu

275 280 285

Ser?Gly?Glu?Glu?Glu?Glu?Gly?Ser?Gly?Gly?Glu?Pro?Glu?Ala?Lys?Arg

290 295 300

Arg?Arg?Leu?Ser?Arg?Leu?Gly?Ser?Ser?Val?Val?Arg?Ser?Ala?Thr?Val

305 310 315 320

Val?Ala?Arg?Thr?Leu?Val?Ala?Cys?Glu?Glu?Lys?Arg?Glu?Arg?Arg?His

325 330 335

Arg?Glu?Leu?Leu?Gln?Leu?Glu?Glu?Arg?Arg?Leu?Arg?Leu?Glu?Glu?Glu

340 345 350

Arg?Thr?Glu?Val?Arg?Arg?Gln?Gly?Phe?Ala?Gly?Leu?Ile?Ala?Ala?Val

355 360 365

Asn?Ser?Leu?Ser?Ser?Ala?Ile?His?Ala?Leu?Val?Ser?Asp?His?Arg?Ser

370 375 380

Gly?Asp?Ser?Ser?Gly?Arg

385 390

<210>5

<211>390

<212>PRT

＜213〉special blue or green (O.sativa ssp.Indica)

<400>5

Met?Ser?Gly?Ser?Ser?Ala?Asp?Pro?Ser?Pro?Ser?Ala?Ser?Thr?Ala?Gly

1 5 10 15

Ala?Ala?Val?Ser?Pro?Leu?Ala?Leu?Leu?Arg?Ala?His?Gly?His?Gly?His

20 25 30

Gly?His?Leu?Thr?Ala?Thr?Pro?Pro?Ser?Gly?Ala?Thr?Gly?Pro?Ala?Pro

35 40 45

Pro?Pro?Pro?Ser?Pro?Ala?Ser?Gly?Ser?Ala?Pro?Arg?Asp?Tyr?Arg?Lys

50 55 60

Gly?Asn?Trp?Thr?Leu?His?Glu?Thr?Leu?Ile?Leu?Ile?Thr?Ala?Asn?Arg

65 70 75 80

Leu?Asp?Asp?Asp?Arg?Arg?Ala?Gly?Val?Gly?Gly?Ala?Ala?Ala?Gly?Gly

85 90 95

Gly?Gly?Ala?Gly?Ser?Pro?Pro?Thr?Pro?Arg?Ser?Ala?Glu?Gln?Arg?Trp

100 105 110

Lys?Trp?Val?Glu?Asn?Tyr?Cys?Trp?Lys?Asn?Gly?Cys?Leu?Arg?Ser?Gln

115 120 125

Asn?Gln?Cys?Asn?Asp?Lys?Trp?Asp?Asn?Leu?Leu?Arg?Asp?Tyr?Lys?Lys

130 135 140

Val?Arg?Asp?Tyr?Glu?Ser?Arg?Val?Ala?Ala?Ala?Ala?Ala?Thr?Gly?Gly

145 150 155 160

Ala?Ala?Ala?Ala?Asn?Ser?Ala?Pro?Leu?Pro?Ser?Tyr?Trp?Thr?Met?Glu

165 170 175

Arg?His?Glu?Arg?Lys?Asp?Cys?Asn?Leu?Pro?Thr?Asn?Leu?Ala?Pro?Glu

180 185 190

Val?Tyr?Asp?Ala?Leu?Ser?Glu?Val?Leu?Ser?Arg?Arg?Ala?Ala?Arg?Arg

195 200 205

Gly?Gly?Ala?Thr?Ile?Ala?Pro?Thr?Pro?Pro?Pro?Pro?Pro?Leu?Ala?Leu

210 215 220

Pro?Leu?Pro?Pro?Pro?Pro?Pro?Pro?Ser?Pro?Pro?Lys?Pro?Leu?Val?Ala

225 230 235 240

Gln?Gln?Gln?His?His?His?His?Gly?His?His?His?His?Pro?Pro?Pro?Pro

245 250 255

Gln?Pro?Pro?Pro?Ser?Ser?Leu?Gln?Leu?Pro?Pro?Ala?Val?Val?Ala?Pro

260 265 270

Pro?Pro?Ala?Ser?Val?Ser?Ala?Glu?Glu?Glu?Met?Ser?Gly?Ser?Ser?Glu

275 280 285

Ser?Gly?Glu?Glu?Glu?Glu?Gly?Ser?Gly?Gly?Glu?Pro?Glu?Ala?Lys?Arg

290 295 300

Arg?Arg?Leu?Ser?Arg?Leu?Gly?Ser?Ser?Val?Val?Arg?Ser?Ala?Thr?Val

305 310 315 320

Val?Ala?Arg?Thr?Leu?Val?Ala?Cys?Glu?Glu?Lys?Arg?Glu?Arg?Arg?His

325 330 335

Arg?Glu?Leu?Leu?Gln?Leu?Glu?Glu?Arg?Arg?Leu?Arg?Leu?Glu?Glu?Glu

340 345 350

Arg?Thr?Glu?Val?Arg?Arg?Gln?Gly?Phe?Ala?Gly?Leu?Ile?Ala?Ala?Val

355 360 365

Asn?Ser?Leu?Ser?Ser?Ala?Ile?His?Ala?Leu?Val?Ser?Asp?His?Arg?Ser

370 375 380

Gly?Asp?Ser?Ser?Gly?Arg

385 390

<210>6

<211>2037

<212>DNA

＜213〉Yunnan Yuanjiang River wild-rice (O.rufipogon Griff.)

<400>6

atgtcgggct?cctctgccga?cccctcgcca?tccgcctcga?ccgcgggggc?ggcggtctcg 60

ccgctcgcgc?tgctccgcgc?gcacggccac?ggccacgggc?acctgactgc?tacgccgccg 120

tcgggggcga?cggggccggc?gccgccgccg?ccgtcgccgg?cgtcggggtc?ggcgccgcgg 180

gactaccgca?aggggaactg?gacgctgcac?gagacgctca?tcctcatcac?cgccaagcgt 240

ctggacgacg?accgccgcgc?cggcgttggg?ggcgcggcgg?ctggtggcgg?cggcgccggg 300

tcgccgccga?cgccgaggtc?ggcggagcag?cggtggaagt?gggtggagaa?ctactgctgg 360

aagaacggct?gcctccgcag?ccagaaccag?tgcaatgaca?agtgggacaa?cctcctccgc 420

gactacaaga?aggtccgcga?ctacgagtcc?cgcgtcgccg?ccgccgccgc?caccggcggc 480

gcggccgccg?ccaactccgc?ccccctcccg?tcgtactgga?cgatggagcg?gcacgagcgc 540

aaggactgca?acctccccac?caacctggcg?ccggaggtct?acgacgcgct?ctccgaggtg 600

ctctcccgcc?gcgcggcgcg?acgcggcggc?gccacgatcg?cgcccacccc?gccgccacca 660

ccgctcgcgc?tgccgctgcc?gccgccgccg?ccgccctcgc?cgccgaagcc?tctcgtcgcg 720

cagcagcagc?accaccatca?cggccatcac?caccacccac?ctcctcctca?gccgccgccg 780

tcgtcgctgc?agctccctcc?ggcggtcgtg?gctccgccgc?cggcgtccgt?ttccggtaat 840

ggtcggtgcg?cgcaccgtac?acttaatact?catagtagct?gttacatccc?ctcccctcca 900

aaccatttac?tactgttctc?tcacactgat?atgtggggcc?cacctcgcag?cgagctgagc 960

tccgccacta?tacgttatta?aaagcccgcg?ttatgattgg?gctagttacg?ttgatgagtt 1020

gagctggtcg?taattattta?ctaccgctac?atttttttta?cctttttacc?gtggggttcg 1080

ggagagggtg?gtcgcggtaa?taataatgtc?ctcaactcag?gggttgggag?aataaagctg 1140

cgtgcagtgt?ggtgcagttc?atgcatggga?aaggtgatgc?gaatccggat?attttatggg 1200

ggtttaattg?aaagatttac?tccacgacga?tactaccctc?tactcctgcc?atgctgcaag 1260

catgcgtaat?gcgttacatt?gcgaaatcac?tcgctttgaa?agaaaaaaaa?gcctgaaact 1320

ttggagaaaa?aaaaagcacc?ttttgttttc?tcctcgtgca?tgcatgccgc?gctgcgtatc 1380

ttgaactact?ttggactttt?gtatcgatca?acaaaactat?acctatatta?gcagtaatta 1440

atactacatt?tgtagatatc?ctttgaccgt?tctatcttat?ttttgataat?taaaaaaatt 1500

agttacattt?aaaaatgcta?tttatatttt?attatctaat?aacaataagt?gtattagtta 1560

aatattaaac?gttggatatg?aatagtttaa?aacgttggat?atgaatagtt?taaaactgta 1620

ttgttttggg?gcggagtgag?taattgattg?atcgattaat?taagtggttg?actaatgtgt 1680

gtgtgattta?tttgtgtagc?ggaggaggag?atgtcggggt?cgtcggagtc?gggggaggag 1740

gaggaggggt?cgggcgggga?gccggaggcg?aagcggcggc?ggctgagccg?gctggggtcg 1800

agcgtggtga?ggagcgcgac?ggtggtggcg?aggacgctgg?tggcgtgcga?ggagaagcgg 1860

gagcgccggc?accgggagct?gctgcagctg?gaggagcggc?ggctgcgcct?cgaggaggag 1920

cgcaccgagg?tccgccgcca?gggcttcgcc?ggcctcatcg?ccgccgtcaa?cagcctctcc 1980

tccgccatcc?acgccctcgt?ctccgaccac?cgcagcggcg?actcctccgg?ccgatga 2037

<210>7

<211>2036

<212>DNA

＜213〉special blue or green (O.sativa ssp.indica)

<400>7

atgtcgggct?cctctgccga?cccctcgcca?tccgcctcga?ccgcgggggc?ggcggtctcg 60

ccgctcgcgc?tgctccgcgc?gcacggccac?ggccacgggc?acctgactgc?tacgccgccg 120

tcgggggcga?cggggccggc?gccgccgccg?ccgtcgccgg?cgtcggggtc?ggcgccgcgg 180

gactaccgca?aggggaactg?gacgctgcac?gagacgctca?tcctcatcac?cgccaatcgt 240

ctggacgacg?accgccgcgc?cggcgttggg?ggcgcggcgg?ctggtggcgg?cggcgccggg 300

tcgccgccga?cgccgaggtc?ggcggagcag?cggtggaagt?gggtggagaa?ctactgctgg 360

aagaacggct?gcctccgcag?ccagaaccag?tgcaatgaca?agtgggacaa?cctcctccgc 420

gactacaaga?aggtccgcga?ctacgagtcc?cgcgtcgccg?ccgccgccgc?caccggcggc 480

gcggccgccg?ccaactccgc?ccccctcccg?tcgtactgga?cgatggagcg?gcacgagcgc 540

aaggactgca?acctccccac?caacctggcg?ccggaggtct?acgacgcgct?ctccgaggtg 600

ctctcccgcc?gcgcggcgcg?acgcggcggc?gccacgatcg?cgcccacccc?gccgccacca 660

ccgctcgcgc?tgccgctgcc?gccgccgccg?ccgccctcgc?cgccgaagcc?tctcgtcgcg 720

cagcagcagc?accaccatca?cggccatcac?caccacccac?ctcctcctca?gccgccgccg 780

tcgtcgctgc?agctccctcc?ggcggtcgtg?gctccgccgc?cggcgtccgt?ttccggtaat 840

ggtcggtgcg?cgcaccgtac?acttaatact?catagtagct?gttacatccc?ctcccctcca 900

aaccatttac?tactgttctc?tcacactgat?atgtgggccc?acctcgcagc?gagctgagct 960

ccgccactat?acgttattaa?aagcccgcgt?tatgattggg?ctagttacgt?tgttgagttg 1020

agctggtcgt?aattatttac?taccgctaca?ttttttttac?ctttttaccg?tggggttcgg 1080

gagagggtgg?tcgcggtaat?aataatgtcc?tcaactcagg?ggttgggaga?ataaagctgc 1140

gtgcagtgtg?gtgcagttca?tgcatgggaa?aggtgatgcg?aatccggata?ttttatgggg 1200

gtttaattga?aagatttact?ccacgacgat?actaccctct?actcctgcca?tgctgcaagc 1260

atgcgtaatg?cgttacattg?cgaaatcact?cgctttgaat?gaaaaaaaag?cctgaaactt 1320

tggagaaaaa?aaaagcacct?tttgttttct?cctcgtgcat?gcatgccgcg?ctgcgtatct 1380

tgaactactt?tggacttttg?tatcgatcaa?caaaactata?cctatattag?cagtaattaa 1440

tactacattt?gtagatatcc?tttgaccgtt?ctatcttatt?tttgataatt?aaaaaaatta 1500

gttacattta?aaaatgctat?ttatatttta?ttatctaata?acaataagtg?tattagttaa 1560

atattaaacg?ttggatatga?atagtttaaa?acgttggata?tgaatagttt?aaaactgtat 1620

tgttttgggg?cggagtgagt?aattgattga?tcgattaatt?aagtggttga?ctaatgtgtg 1680

tgtgatttat?ttgtgtagcg?gaggaggaga?tgtcggggtc?gtcggagtcg?ggggaggagg 1740

aggaggggtc?gggcggggag?ccggaggcga?agcggcggcg?gctgagccgg?ctggggtcga 1800

gcgtggtgag?gagcgcgacg?gtggtggcga?ggacgctggt?ggcgtgcgag?gagaagcggg 1860

agcgccggca?ccgggagctg?ctgcagctgg?aggagcggcg?gctgcgcctc?gaggaggagc 1920

gcaccgaggt?ccgccgccag?ggcttcgccg?gcctcatcgc?cgccgtcaac?agcctctcct 1980

ccgccatcca?cgccctcgtc?tccgaccacc?gcagcggcga?ctcctccggc?cgatga 2036

<210>8

<211>1173

<212>cDNA

＜213〉Yunnan Yuanjiang River wild-rice (O.rufipogon Griff.)

<400>8

atgtcgggct?cctctgccga?cccctcgcca?tccgcctcga?ccgcgggggc?ggcggtctcg 60

ccgctcgcgc?tgctccgcgc?gcacggccac?ggccacgggc?acctgactgc?tacgccgccg 120

tcgggggcga?cggggccggc?gccgccgccg?ccgtcgccgg?cgtcggggtc?ggcgccgcgg 180

gactaccgca?aggggaactg?gacgctgcac?gagacgctca?tcctcatcac?cgccaagcgt 240

ctggacgacg?accgccgcgc?cggcgttggg?ggcgcggcgg?ctggtggcgg?cggcgccggg 300

tcgccgccga?cgccgaggtc?ggcggagcag?cggtggaagt?gggtggagaa?ctactgctgg 360

aagaacggct?gcctccgcag?ccagaaccag?tgcaatgaca?agtgggacaa?cctcctccgc 420

gactacaaga?aggtccgcga?ctacgagtcc?cgcgtcgccg?ccgccgccgc?caccggcggc 480

gcggccgccg?ccaactccgc?ccccctcccg?tcgtactgga?cgatggagcg?gcacgagcgc 540

aaggactgca?acctccccac?caacctggcg?ccggaggtct?acgacgcgct?ctccgaggtg 600

ctctcccgcc?gcgcggcgcg?acgcggcggc?gccacgatcg?cgcccacccc?gccgccacca 660

ccgctcgcgc?tgccgctgcc?gccgccgccg?ccgccctcgc?cgccgaagcc?tctcgtcgcg 720

cagcagcagc?accaccatca?cggccatcac?caccacccac?ctcctcctca?gccgccgccg 780

tcgtcgctgc?agctccctcc?ggcggtcgtg?gctccgccgc?cggcgtccgt?ttccgcggag 840

gaggagatgt?cggggtcgtc?ggagtcgggg?gaggaggagg?aggggtcggg?cggggagccg 900

gaggcgaagc?ggcggcggct?gagccggctg?gggtcgagcg?tggtgaggag?cgcgacggtg 960

gtggcgagga?cgctggtggc?gtgcgaggag?aagcgggagc?gccggcaccg?ggagctgctg 1020

cagctggagg?agcggcggct?gcgcctcgag?gaggagcgca?ccgaggtccg?ccgccagggc 1080

ttcgccggcc?tcatcgccgc?cgtcaacagc?ctctcctccg?ccatccacgc?cctcgtctcc 1140

gaccaccgca?gcggcgactc?ctccggccga?tga 1173

<210>9

<211>1173

<212>cDNA

＜213〉special blue or green (O.sativa ssp.indica)

<400>9

atgtcgggct?cctctgccga?cccctcgcca?tccgcctcga?ccgcgggggc?ggcggtctcg 60

ccgctcgcgc?tgctccgcgc?gcacggccac?ggccacgggc?acctgactgc?tacgccgccg 120

tcgggggcga?cggggccggc?gccgccgccg?ccgtcgccgg?cgtcggggtc?ggcgccgcgg 180

gactaccgca?aggggaactg?gacgctgcac?gagacgctca?tcctcatcac?cgccaatcgt 240

ctggacgacg?accgccgcgc?cggcgttggg?ggcgcggcgg?ctggtggcgg?cggcgccggg 300

tcgccgccga?cgccgaggtc?ggcggagcag?cggtggaagt?gggtggagaa?ctactgctgg 360

aagaacggct?gcctccgcag?ccagaaccag?tgcaatgaca?agtgggacaa?cctcctccgc 420

gactacaaga?aggtccgcga?ctacgagtcc?cgcgtcgccg?ccgccgccgc?caccggcggc 480

gcggccgccg?ccaactccgc?ccccctcccg?tcgtactgga?cgatggagcg?gcacgagcgc 540

aaggactgca?acctccccac?caacctggcg?ccggaggtct?acgacgcgct?ctccgaggtg 600

ctctcccgcc?gcgcggcgcg?acgcggcggc?gccacgatcg?cgcccacccc?gccgccacca 660

ccgctcgcgc?tgccgctgcc?gccgccgccg?ccgccctcgc?cgccgaagcc?tctcgtcgcg 720

cagcagcagc?accaccatca?cggccatcac?caccacccac?ctcctcctca?gccgccgccg 780

tcgtcgctgc?agctccctcc?ggcggtcgtg?gctccgccgc?cggcgtccgt?ttccgcggag 840

gaggagatgt?cggggtcgtc?ggagtcgggg?gaggaggagg?aggggtcggg?cggggagccg 900

gaggcgaagc?ggcggcggct?gagccggctg?gggtcgagcg?tggtgaggag?cgcgacggtg 960

gtggcgagga?cgctggtggc?gtgcgaggag?aagcgggagc?gccggcaccg?ggagctgctg 1020

cagctggagg?agcggcggct?gcgcctcgag?gaggagcgca?ccgaggtccg?ccgccagggc 1080

ttcgccggcc?tcatcgccgc?cgtcaacagc?ctctcctccg?ccatccacgc?cctcgtctcc 1140

gaccaccgca?gcggcgactc?ctccggccga?tga 1173

Claims

1, the transcription factor of regulating plant fallen has one of following amino acid residue sequences:

1) the SEQ ID № in the sequence table: 1 or SEQ ID №: 5;

2, transcription factor according to claim 1 is characterized in that: described transcription factor has SEQ ID № in the sequence table: 1 or SEQ ID №: 5 amino acid residue sequence.

3, the gene of the transcription factor of the described regulating plant fallen of coding claim 1, its cDNA is one of following nucleotide sequence:

1) SEQ ID № in the sequence table: 8 or SEQ ID №: 9 dna sequence dna;

4, gene according to claim 3 is characterized in that: described cDNA has SEQ ID № in the sequence table: 8 or SEQ ID №: 9 dna sequence dna.

5, the gene of the transcription factor of the described regulating plant fallen of coding claim 1, its genomic gene is one of following nucleotide sequence:

1) SEQ ID № in the sequence table: 6 or SEQ ID №: 7 dna sequence dna;

6, contain claim 3 or 4 or 5 described expression carrier, transgenic cell line and host bacterium.

7, a kind of method of regulating plant fallen is gene transfered plant tissue or the cell with the transcription factor of the described coding regulating plant fallen of claim 3, and plant fallen obtains regulation and control.

8, method according to claim 7 is characterized in that: the gene of the transcription factor of described coding regulating plant fallen imports explant by the plant expression vector that contains described gene; The carrier that sets out that is used to make up described plant expression vector is pBI121, pBin19, pCAMBIA2301, pCAMBIA1301 or pCAMBIA1300.

9, method according to claim 7 is characterized in that: described is turfgrass, paddy rice, wheat, soybean, tobacco, corn, rape, Chinese sorghum, cotton, clover, barley, grape or tomato by the plant transformed host.