Wang Hantao, Huang Cong, Guo Huanle, Li Ximei, Zhao Wenxia, Dai Baosheng, Yan Zhenhua, Lin Zhongxu
National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University. Wuhan 430070, Hubei, China.
PLoS One. 2015 Jun 25;10(6):e0130742. doi: 10.1371/journal.pone.0130742. eCollection 2015.
A population of 178 recombinant inbred lines (RILs) was developed using a single seed descendant from a cross between G. hirsutum. acc DH962 and G. hirsutum. cv Jimian5, was used to construct a genetic map and to map QTL for fiber and yield traits. A total of 644 polymorphic loci were used to construct a final genetic map, containing 616 loci and spanning 2016.44 cM, with an average of 3.27 cM between adjacent markers. Statistical analysis revealed that segregation distortion in the intraspecific population was more serious than that in the interspecific population. The RIL population and the two parents were phenotyped under 8 environments (two locations, six years), revealing a total of 134 QTL, including 64 for fiber qualities and 70 for yield components, independently detected in seven environments, explaining 4.40-15.28% of phenotypic variation (PV). Among the 134 QTL, 9 common QTL were detected in more than one environment, and 22 QTL and 19 new QTL were detected in combined analysis (E9). A total of 26 QTL hotspot regions were observed on 13 chromosomes and 2 larger linkage groups, and some QTL clusters related to fiber qualities or yield components were also observed. The results obtained in the present study suggested that to map accurate QTL in crops with larger plant types, such as cotton, phenotyping under multiple environments is necessary to effectively apply the obtained results in molecular marker-assisted selection breeding and QTL cloning.
以陆地棉品种DH962和陆地棉品种冀棉5号杂交产生的单粒传后代构建了一个由178个重组自交系(RIL)组成的群体,用于构建遗传图谱并定位纤维和产量性状的QTL。共使用644个多态性位点构建了最终的遗传图谱,该图谱包含616个位点,跨度为2016.44 cM,相邻标记间平均距离为3.27 cM。统计分析表明,种内群体的分离畸变比种间群体更严重。在8种环境(两个地点,6年)下对RIL群体和两个亲本进行了表型分析,共检测到134个QTL,其中包括64个纤维品质QTL和70个产量构成因素QTL,在7种环境中独立检测到,解释了4.40%-15.28%的表型变异(PV)。在这134个QTL中,有9个共同QTL在多个环境中被检测到,在联合分析(E9)中检测到22个QTL和19个新QTL。在13条染色体和2个较大的连锁群上共观察到26个QTL热点区域,还观察到一些与纤维品质或产量构成因素相关的QTL簇。本研究结果表明,对于棉花等植株较大的作物,要准确定位QTL,在多个环境下进行表型分析对于在分子标记辅助选择育种和QTL克隆中有效应用所获结果是必要的。