棉花重组自交系铃重性状的QTL定位
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  • 英文篇名:QTL Mapping of Boll Weight Trait Based on Recombinant Inbred Lines in Gossypium hirsutum L.
  • 作者:曲朝阳 ; 贾晓昀 ; 马启峰 ; 王寒涛 ; 魏恒玲 ; 范术丽
  • 英文作者:Qu Zhaoyang;Jia Xiaoyun;Ma Qifeng;Wang Hantao;Wei Hengling;Fan Shuli;Institute of Cotton Research of Chinese Academy of Agricultural Sciences/State Key Laboratory of Cotton Biology;Institute of Cereal and Oil Crops,Hebei Academy of Agriculture and Forestry Science;
  • 关键词:棉花 ; 重组自交系 ; 铃重 ; QTL
  • 英文关键词:cotton;;recombinant inbred lines;;boll weight;;QTL
  • 中文刊名:MHXB
  • 英文刊名:Cotton Science
  • 机构:中国农业科学院棉花研究所/棉花生物学国家重点实验室;河北省农林科学院粮油作物研究所;
  • 出版日期:2019-01-15
  • 出版单位:棉花学报
  • 年:2019
  • 期:v.31
  • 基金:国家自然科学基金(31701474);; 棉花生物学国家重点实验室自主课题(CB2017C05)
  • 语种:中文;
  • 页:MHXB201901002
  • 页数:11
  • CN:01
  • ISSN:41-1163/S
  • 分类号:16-26
摘要
【目的】铃重是构成棉花产量的基本因子之一。本研究旨在定位铃重QTL(Quantitative trait loci),为分析铃重遗传组成提供参考。【方法】以中棉所36和海陆渐渗系G2005组配的137个RILs (Recombinant inbred lines)家系为作图群体,利用RAD-seq(Restriction-site associated DNA sequencing)技术及SSR(Simple sequence repeat)标记,构建遗传连锁图谱,并对5个环境下的铃重进行QTL分析。【结果】构建了包含26个连锁群、6 434个标记、总长为4 071.98 cM、标记间平均距离为0.63 cM的遗传图谱。采用WinQTLCart 2.5软件的复合区间作图法进行QTL定位,共得到32个铃重QTL,分布于15条染色体,单个位点解释的表型变异率为4.46%~15.84%;qBW-A4-1、qBW-A4-2、qBW-A5-2、qBW-D9-1和qBW-D9-2能够在2个环境中检测到,解释5.07%~15.84%的表型变异率。【结论】本研究定位的主效QTL可用于分析铃重遗传机理。
        [Objective] The aim of this study was to explore the quantitative trait locus(QTL) related to the boll weight.[Method]A single seed descended population of 137 recombinant inbred lines(RILs) was developed from the cross of upland cotton(Gossypium hirsutum L.) CCRI 36 and G2005,an introgression inbred line introgressed from G.barbadense.Using restriction-site associated DNA sequencing(RAD-seq),a genetic linkage map composed of 6 434 makers,including 6 295 single nucleotide polymorphisms(SNP) and 139 simple sequence repeat(SSR) markers,was developed from the RILs population.[Result] This map spanned 4 071.98 cM with an average distance of 0.63 cM between adjacent markers.QTL mapping was performed by using boll weight data of five environments through Win QTLCart 2.5 software.Thirty-two QTL,with 4.46%-15.84%explained phenotypic variation related boll weight,were detected and found distributing on 15 chromosomes.qBW-A4-1,qBW-A4-2,qBW-A5-2,qBW-D9-1,and qBW-D9-2 were detected in two environments,which explained 5.07%-15.84% of the phenotypic variation.[Conclusion] Major QTLs detected in this study will provide an important reference for analysis of the genetic mechanism of boll weight.
引文
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