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小麦背景中来自华山新麦草的抗条锈病基因的遗传学分析和分子标记

Genetic Analysis and Molecular Markers of a Novel Stripe Rust Resistance Gene YrHua in Wheat Originated from Psathyrostachys huashanica Keng

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【作者】 曹张军王献平王美南曹双河井金学商鸿生李振岐张相岐

【Author】 CAO Zhang-Jun~1,2,3,WANG Xian-Ping~2,WANG Mei-Nan~1,CAO Shuang-He~2, JING Jin-Xue~1,SHANG Hong-Sheng~1,LI Zhen-Qi~1,ZHANG Xiang-Qi~2,① (1.College of Plant Protection,Northwest Sci-Tech University of Agriculture and Forestry,Yangling 712100,China; 2.The State Key Laboratory of Plant Cell and Chromosome Engineering,Institute of Genetics and Developmental Biology,Chinese Academy of Sciences,Beijing 100101,China; 3.College of Chemistry and chemical engineering,Donghua University,Shanghai 200051,China)

【机构】 西北农林科技大学植物保护学院中国科学院遗传与发育生物学研究所植物细胞与染色体工程国家重点实验室中国科学院遗传与发育生物学研究所植物细胞与染色体工程国家重点实验室 杨凌712100北京100101东华大学化学与化工学院上海200051北京100101杨凌712100

【摘要】 H9020175是一个通过杂交和回交选育的普通小麦华山新麦草易位系,接种鉴定表明其对条锈病具有优良抗性。遗传学分析证明易位系H9020175的抗条锈性是由单基因控制的显性性状,抗性基因来自于华山新麦草,暂定名为YrHua。为了标记这个来自华山新麦草的抗条锈病基因,利用H9020175与感病小麦品种铭贤169杂交,建立了F2分离群体。应用81对AFLP引物对119个经条锈菌生理小种CY30接种鉴定的F2单株进行了分析,结果得到两个与YrHua基因连锁的AFLP标记PM14(301)和PM42(249),遗传距离分别为5.4cM和2.7cM,并分别位于目标基因的两侧。将标记片段克隆、测序后,根据序列信息和酶切位点多态性设计特异性引物,将AFLP标记PM14(301)转换成了简单的PCR标记。研究结果为标记辅助育种提供了分子选择工具,同时也为进一步精细定位和图位克隆YrHua基因奠定了基础。

【Abstract】 The H9020-17-5,a common wheat-Psathyrostachys huashanica Keng translocation line,possesses excellent resistance to wheat stripe rust.Genetic analysis of F2 and BC1 populations derived from H9020-17-5 × Mingxian169 indicated that resistance to stripe rust in H9020-17-5 was a dominant character controlling by single gene originated from Ps.huashanica.This resistance gene originated from Ps.huashanica was first reported in the present study and named as YrHua .In order to map the resistance gene YrHua,AFLP approach was employed to analyze the 119 individuals of H9020-17-5 × Mingxian169 F2 population which were inoculated by stripe rust isolate CY30.As a result,two markers,PM14(301) and PM42(249) were found to be linked to the resistance gene YrHua,and the genetic distances between the markers and target gene were 5.4 cM and 2.7 cM,respectively.For the convenience of marker-assisted selection in wheat breeding,one of the two AFLP markers was converted to PCR marker using a pair of special primers based on the DNA sequence of PM14(301) and the polymorphism of restriction site.Our research results provided a useful tool for marker-assisted selection and laid a foundation of fine mapping and map based cloning of YrHua gene.

【基金】 国家自然科学基金(编号:30070495);国家十五科技攻关(编号:2004BA525B06);国家“863”计划(编号:2003AA207080);植物细胞与染色体工程国家重点实验室开放课题资助~~
  • 【文献出处】 遗传学报 ,Acta Genetica Sinica , 编辑部邮箱 ,2005年07期
  • 【分类号】S512.1
  • 【被引频次】79
  • 【下载频次】452
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