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Genome-Wide Genetic Dissection of Supernumerary Spikelet and Related Traits in Common Wheat

机译:普通小麦小穗小穗的全基因组遗传解剖及相关性状

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Branched spike or supernumerary spikelet (SS) is a naturally occurring variant in wheat and holds great potential for increasing the number of grains per spike, and ultimately, increasing wheat yield. However, detailed knowledge of the molecular basis of spike branching in common wheat is lacking. In the present study, a recombinant inbred line (RIL) population derived from the cross of an SS accession and an elite non-SS line was developed and evaluated over four to six environments for seven SS-related traits to identify the genetic basis of SS in wheat. A framework linkage map was generated using 939 diversity arrays technology (DArT) markers. Composite interval mapping (CIM) identified a total of seven consistent quantitative trait loci (QTL) located on five chromosomes (2D, 5B, 6A, 6B, and 7B), suggesting a polygenic inheritance of SS. The phenotypic variation explained (PVE) by individual QTL ranged from 3.3 to 37.3%. The QTL located on 2D (QSS.ndsu-2D) and 7B (QSS.ndsu-7B.2) have major effects (PVE 15%), while the remaining five QTL (QSS.ndsu-5B, QSS.ndsu-6A, QSS.ndsu-6B.1, QSS.ndsu-6B.2, QSS.ndsu-7B.1) have minor effects (PVE 15%). Comparison of the genomic locations of the QTL suggested that QSS.ndsu-2D was located in the same regions on 2DS, where QTL for several traits have been reported. However, the remaining six QTL for SS are reported for the first time. Multiple interval mapping (MIM) showed that all seven QTL are involved in epistatic interaction. The major genomic regions controlling these SS-related traits may prove invaluable for wheat improvement and could also be the target for future studies aimed at cloning these genes.
机译:分支穗或超小穗(SS)是小麦中的天然变异,具有增加每个穗粒数并最终提高小麦产量的巨大潜力。但是,缺乏对普通小麦穗分枝的分子基础的详细了解。在本研究中,开发了从SS品种和优良非SS系杂交得到的重组近交系(RIL)群体,并在4至6个环境中对七个SS相关性状进行了评估,以鉴定SS的遗传基础。在小麦中。使用939分集阵列技术(DArT)标记生成框架链接图。复合间隔图谱(CIM)确定了位于五个染色体(2D,5B,6A,6B和7B)上的总共七个一致的定量性状基因座(QTL),表明SS的多基因遗传。单个QTL解释的表型变异(PVE)为3.3%至37.3%。位于2D(QSS.ndsu-2D)和7B(QSS.ndsu-7B.2)上的QTL具有重大影响(PVE> 15%),而其余五个QTL(QSS.ndsu-5B,QSS.ndsu-6A) ,QSS.ndsu-6B.1,QSS.ndsu-6B.2,QSS.ndsu-7B.1)的影响较小(PVE <15%)。比较QTL的基因组位置表明,QSS.ndsu-2D位于2DS的相同区域,其中已报道了多个性状的QTL。但是,第一次报告了SS的其余六个QTL。多重区间作图(MIM)显示,所有七个QTL均参与上位相互作用。控制这些与SS相关性状的主要基因组区域可能对小麦改良无价之宝,并且也可能是旨在克隆这些基因的未来研究的目标。

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