Zheng Zhi, Ma Jian, Stiller Jiri, Zhao Qiang, Feng Qi, Choulet Frédéric, Feuillet Catherine, Zheng You-Liang, Wei Yuming, Han Bin, Yan Guijun, Manners John M, Liu Chunji
CSIRO Agriculture, 306 Carmody Road, St Lucia, QLD, 4067, Australia.
School of Plant Biology, Faculty of Science and The UWA Institute of Agriculture, The University of Western Australia, Perth, WA, 6009, Australia.
BMC Genomics. 2015 Oct 23;16:850. doi: 10.1186/s12864-015-2105-0.
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 F10 lines were generated and exploited to assess markers selected from the existing linkage map and generated from sequences of the 3B pseudomolecule.
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.
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.
镰刀菌冠腐病(FCR)是全球半干旱地区主要的谷类病害。在已报道的各种数量性状基因座(QTL)中,位于3B染色体臂上的那个基因座(Qcrs.cpi - 3B)具有最大效应,且能在不同遗传背景中持续检测到。在先前的一项研究中获得了该基因座的九组近等基因系(NILs)。为了鉴定可可靠用于标记Qcrs.cpi - 3B基因座的分子标记,构建并利用了一个由774个F10株系组成的NIL衍生群体,以评估从现有连锁图谱中选择的以及从3B假分子序列产生的分子标记。
这是关于在小麦中精细定位赋予FCR抗性的QTL的首次报道。通过使用NILs和NIL衍生群体进行三轮连锁图谱构建,将Qcrs.cpi - 3B基因座定位到一个0.7厘摩的区间,该区间覆盖约1.5兆碱基的物理距离。开发了七个与该基因座共分离的分子标记。基于3B假分子,该区间总共包含63个基因编码序列,其中六个已知编码抗病蛋白。该区间的几个基因是早期研究中检测到的对FCR感染有响应的基因。
Qcrs.cpi - 3B基因座的准确定位以及与其共分离的分子标记的开发,应有助于将这个赋予FCR抗性的大效应QTL纳入育种计划,以及克隆该QTL的相关基因。