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两种方法定位5个地点大豆蛋白质含量QTL

QTL analysis of soybean protein content using two methods in 5 different environments

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【作者】 单大鹏刘春燕蒋洪蔚董晓慧陈庆山胡国华

【Author】 SHAN Da-peng1,2,3,LIU Chun-yan1,JIANG Hong-wei1, DONG Xiao-hui3,CHEN Qing-shan1,2*,HU Guo-hua1,2*(1.The Crop Research and Breeding Center of Land-Reclamation,Harbin 150090,China; 2.Northeast Agricultural University,Harbin 150030,China; 3.Suihua Branch of Heilongjiang Academy of Agricultural Sciences,Suihua 152052,China)

【机构】 黑龙江省农垦科研育种中心东北农业大学黑龙江省农科院绥化分院

【摘要】 利用CIM和MIM法,对大豆Charleston×东农594的154个重组自交系在5个不同地点进行蛋白质含量测定和QTL定位分析。共检测到25个QTL,分别位于A1、B1、C2、D1a、D1b、E、J、L和N连锁群上。用CIM法定位了20个与蛋白质含量相关的QTL,用MIM法定位了9个与蛋白质含量相关的QTL。在C2连锁群上多次定位的ProC2-4,标记区间为Sat092-Satt460,与前人找到的QTL位点一致。

【Abstract】 Two mapping methods,composite interval mapping(CIM) and multiple interval mapping(MIM),were employed to detect quantitative trait loci(QTL) of soybean protein content using 154 recombination inbred lines(RIL) population derived from a cross between Charleston and Dongnong 594 in five different locations.As a result,25 QTLs for protein content were mapped in linkage group A1,B1,C2,D1a,D1b,E,J,L,and N.In total,20 QTLs for protein content were detected by CIM,and 9 QTLs detected by MIM.Among the QTLs,ProC2-4 was mapped multiple times between Sat092 and Satt460 on C2 linkage group,referred as a main effect QTL for soybean protein content.

【基金】 转基因专项大豆导入系构建及有利隐蔽基因挖掘(2009ZX08009-013B);农业部“引进国际先进农业科学技术”(2006G01);国家863计划(2006AA10Z1F4)
  • 【文献出处】 中国油料作物学报 ,Chinese Journal of Oil Crop Sciences , 编辑部邮箱 ,2011年01期
  • 【分类号】S565.1
  • 【被引频次】13
  • 【下载频次】310
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