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一个水稻长芒基因AWN-2的定位与克隆 被引量:9

Mapping and Cloning of AWN-2 Controlling Long Awn in Rice
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摘要 本研究在以广西普通野生稻DP30为供体,籼稻品种9311为受体构建的染色体片段代换系中,筛选鉴定出1份稳定遗传的具有长芒表型的染色体片段代换系。利用该代换系与轮回亲本9311构建了BC5F2分离群体,对控制长芒表型的基因进行了遗传分析,发现该群体中长芒与短芒的单株分离比符合3:1的比例,表明该长芒性状受一对显性核基因控制。采用图位克隆法,将目的基因精细定位于水稻第4染色体分子标记M7和M8之间的12.14 kb范围内,该区域只有一个候选基因即LOC_Os04g43840,测序分析发现与栽培稻日本晴、9311相比,CSSL5的LOC_Os04g43840基因在5'UTR区有29个碱基的缺失和2个碱基的置换,因此,推测LOC_Os04g43840可能为该长芒候选基因。 In this study, one accession of Guangxi common wild rice(Oryza rufipogon Griff.) were used as donor parent, and an indica rice varieties 9311 was used as receptor parent, a set of rice chromosome segment substitution lines(CSSLs) had been established, from which we characterized a long awn line CSSL5. In the BC5F2 segregating population derived from the cross between CSSL5 and 9311, the ratio of long awn plants to short awn plants showed 3:1 frequency distribution, suggesting that the long awn phenotype was controlled by a pair of dominant nuclear genes. Using the method of map-based cloning, we located this gene to a 12.14 kb region between markers M7 and M8 on chromosome 4, including only one predicted gene, which was LOC_Os04g43840.Comparison of the coding sequences of the predicted gene in CSSL5, Nipponbare and 9311, we revealed 29 bp deletions and 2 bp mutations of LOC_Os04g43840 in CSSL5. Therefore, we speculate LOC_Os04g43840 is the candidate gene.
出处 《基因组学与应用生物学》 CAS CSCD 北大核心 2016年第4期949-956,共8页 Genomics and Applied Biology
基金 国家自然科学基金项目(31460278) 广西自然科学基金项目(2013GXNSFBA019059 14GXNSFAA118104)共同资助
关键词 水稻 长芒 基因定位 克隆 Rice Long awn Gene mapping Cloning
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