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首页> 外文期刊>Plant Molecular Biology Reporter >Fine Mapping of qHD4-1, a QTL Controlling the Heading Date, to a 20.7-kb DNA Fragment in Rice (Oryza sativa L.)
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Fine Mapping of qHD4-1, a QTL Controlling the Heading Date, to a 20.7-kb DNA Fragment in Rice (Oryza sativa L.)

机译:qHD4-1(控制抽穗期的QTL)与水稻(Oryza sativa L.)中一个20.7-kb DNA片段的精细映射

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摘要

A library consisting of 1,123 single-segment substitution lines (SSSLs) in the same genetic background of an elite rice variety Huajingxian74 (HJX74) was evaluated for heading date. From this library, the SSSL W05-1-11-5-16-2-5 with the substituted interval of PSM103—RM348-OSR15-PSM382-RM131-RM127—RM280 was found having a gene, which stably performed extreme late heading date which performed stable and late heading in the different environments of Shandong, Guangdong, and Hainan. To map the gene governing heading date, the SSSL W05-1-11-5-16-2-5 was crossed with the recipient HJX74 to develop an F2 segregating population. The distribution of late and early heading plants in this population fitted a segregation ratio of 3:1, indicating the late heading was controlled by a dominant gene. The gene locus for heading date was tentatively designated as qHD4-1. Using a random sample of 460 individuals from the F2 segregation population, the qHD4-1 locus was mapped between two SSR markers RM3335 and RM17572, with genetic distances of 0.1 and 0.2 cM, respectively. For fine mapping of qHD4-1, a large F2:3 segregating population of 3,000 individuals were developed from F2 plants heterozygous in the RM3335-RM17572 region. Recombinants analyses further mapped qHD4-1 to an interval of 20.7-kb-bounded WB05 and the WB06. Sequence analysis of this 20.7-kb region revealed that it contains three open reading frames (ORFs), encoding wall-associated receptor kinase-like 5, putative F-box domain containing protein, and putative arogenate/prephenate dehydratase. Of them, ORF1, predicting to encode serine/threonine kinase, is considered the most likely as the candidate gene. The genetic and physical map of the qHD4-1 locus will be very useful in molecular cloning of the qHD4-1gene.
机译:评价了在优良稻米品种华粳先74(HJX74)的相同遗传背景下由1,123条单链替换系(SSSL)组成的文库。从该文库中,发现间隔为PSM103-RM348-OSR15-PSM382-RM131-RM127-RM280的SSSL W05-1-11-5-16-2-5具有稳定执行极端迟交日期的基因在山东,广东和海南的不同环境中表现稳定且迟滞。为了确定基因控制的起始日期,将SSSL W05-1-11-5-16-2-5与受体HJX74杂交,形成F 2 隔离种群。该种群中晚抽穗和早抽穗植物的分布符合3:1的隔离比,这表明晚抽穗由一个显性基因控制。暂定日期的基因座暂定为qHD4-1。使用来自F 2 隔离种群的460个个体的随机样本,将qHD4-1基因座定位在两个SSR标记RM3335和RM17572之间,遗传距离分别为0.1和0.2 cM。为了对qHD4-1进行精细定位,从RM3335-RM17572区域杂合的F 2 植物中形成了3,000个大的F 2:3 隔离种群。重组子进一步分析了将qHD4-1映射到以20.7kb为界的WB05和WB06的间隔。对这个20.7kb区域的序列分析显示,它包含三个开放阅读框(ORF),它们编码与壁相关的受体激酶样5,推定的F-box结构域蛋白和推定的Arnateate / prephenate脱水酶。其中,预测编码丝氨酸/苏氨酸激酶的ORF1被认为最有可能成为候选基因。 qHD4-1基因座的遗传和物理图谱在qHD4-1基因的分子克隆中将非常有用。

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