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Fine mapping of a large-effect QTL conferring Fusarium crown rot resistance on the long arm of chromosome 3B in hexaploid wheat

机译:六倍体小麦的3B染色体长臂上赋予镰刀菌冠腐病抗性的QTL的精细定位

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Background Fusarium crown rot (FCR) is a major cereal disease in semi-arid areas worldwide. Of the various QTL reported, the one on chromosome arm 3BL (Qcrs.cpi-3B) has the largest effect that can be consistently detected in different genetic backgrounds. Nine sets of near isogenic lines (NILs) for this locus were made available in a previous study. To identify markers that could be reliably used in tagging the Qcrs.cpi-3B locus, a NIL-derived population consisting of 774?F 10 lines were generated and exploited to assess markers selected from the existing linkage map and generated from sequences of the 3B pseudomolecule. Results This is the first report on fine mapping a QTL conferring FCR resistance in wheat. By three rounds of linkage mapping using the NILs and the NIL-derived population, the Qcrs.cpi-3B locus was mapped to an interval of 0.7?cM covering a physical distance of about 1.5?Mb. Seven markers co-segregating with the locus were developed. This interval contains a total of 63 gene-coding sequences based on the 3B pseudomolecule, and six of them were known to encode disease resistance proteins. Several of the genes in this interval were among those responsive to FCR infection detected in an earlier study. Conclusions The accurate localization of the Qcrs.cpi-3B locus and the development of the markers co-segregating with it should facilitate the incorporation of this large-effect QTL conferring FCR resistance into breeding programs as well as the cloning of the gene(s) underlying the QTL.
机译:背景镰刀菌冠腐病(FCR)是全球半干旱地区的一种主要谷物疾病。在报道的各种QTL中,染色体臂3BL(Qcrs.cpi-3B)上的一个具有最大的影响,可以在不同的遗传背景下一致地检测到。在先前的研究中提供了用于该基因座的九套近等基因系(NIL)。为了鉴定可以可靠地用于标记Qcrs.cpi-3B基因座的标记物,产生了由774?F 10 系组成的NIL群体,并利用其评估了从现有连锁图中选择的标记物并从3B假分子的序列生成。结果这是关于精细绘制赋予小麦FCR抗性的QTL的首次报道。通过使用NIL和NIL衍生种群的三轮连锁作图,将Qcrs.cpi-3B基因座映射到0.7?cM的间隔,覆盖了约1.5?Mb的物理距离。与基因座共分离的七个标记被开发出来。该间隔总共包含基于3B假分子的63个基因编码序列,其中六个已知编码抗病蛋白。在较早的一项研究中,在此间隔中的几个基因属于对FCR感染有反应的基因。结论Qcrs.cpi-3B基因座的准确定位和与之共分离的标记的开发应有助于将这种赋予FCR抗性的大效应QTL纳入育种程序,并克隆基因。基本的QTL。

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