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Molecular mapping of quantitative trait loci for kernel morphology traits in a non-1BL.1RS x 1BL.1RS wheat cross

机译:非1BL.1RS x 1BL.1RS小麦杂交种籽粒形态性状的数量性状基因座的分子作图

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The improvement of kernel morphology traits is an important goal in common wheat (Triticum aestivum L.) breeding programs because of their close relationship with grain yield and milling quality. The aim of this study was to map quantitative trait loci (QTL) for kernel morphology traits using 240 recombinant inbred lines derived from a cross between the non-1BL. 1RS translocation cv. PH 82-2 and the 1BL. 1RS translocation cv. Neixiang 188, grown in six environments in China. Inclusive composite interval mapping identified 71 main-effect QTL on 16 chromosomes for seven kernel morphology traits measured by digital imaging, viz. kernel length, width, perimeter, area, shape factor, factor form-density and width/length ratio. Each of these loci explained from 2.6 to 28.2% of the phenotypic variation. Eight QTL clusters conferring the largest effects on kernel weight and kernel morphology traits were detected on chromosomes 1BL. 1RS (2), 2A, 4A, 4B, 6B, 6D and 7A. Fourteen epistatic QTL were identified for all kernel morphology traits except kernel width/length ratio, involving 24 main-effect QTL distributed on 13 chromosomes, and explaining 2.5-8.3% of the phenotypic variance. Five loci, viz. Sec-1 on 1BL. 1RS, Glu-B1 on 1BL, Xcfe53 on 2A, Xwmc238 on 4B, and Xbarc174 on 7A, were detected consistently across environments, and their linked DNA markers may be used for marker-assisted selection in breeding for improved wheat kernel traits and grain yield.
机译:籽粒形态性状的改善是普通小麦(Triticum aestivum L.)育种计划的重要目标,因为它们与谷物产量和制粉质量密切相关。这项研究的目的是使用来源于非1BL杂交的240个重组自交系,绘制定量性状位点(QTL)来绘制内核形态性状。 1RS易位简历。 PH 82-2和1BL。 1RS易位简历。内乡188号在中国的六个环境中生长。包容性复合区间作图确定了16个染色体上的71个主要效应QTL,用于通过数字成像测得的7个核心形态特征。籽粒的长度,宽度,周长,面积,形状系数,系数形式密度和宽度/长度比。这些位点中的每个位点解释了表型变异的2.6%至28.2%。在1BL染色体上检测到八个对籽粒重量和籽粒形态性状影响最大的QTL簇。 1RS(2),2A,4A,4B,6B,6D和7A。除果粒宽/长比外,针对所有果粒形态性状鉴定了14个上位QTL,涉及分布在13个染色体上的24个主要效应QTL,解释了2.5-8.3%的表型变异。五个座位,即。 1BL的Sec-1。在整个环境中均检测到1RS,1BL上的Glu-B1、2A上的Xcfe53、4B上的Xwmc238和7A上的Xbarc174,它们的相关DNA标记可用于标记辅助选择,从而提高小麦籽粒性状和籽粒产量。

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