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普通小麦-华山新麦草易位系H9015-17抗条锈病基因的标记定位
引用本文:马东方,方正武,李 强,尹军良,王文凯,王保通.普通小麦-华山新麦草易位系H9015-17抗条锈病基因的标记定位[J].植物病理学报,2015,45(5):501-508.
作者姓名:马东方  方正武  李 强  尹军良  王文凯  王保通
作者单位:湿地生态与农业利用教育部工程研究中心/长江大学农学院, 荆州 434025;
西北农林科技大学/旱区作物逆境生物学国家重点实验室, 杨凌 712100;
湖北省农业科学院粮食作物研究所/粮食作物种质创新与遗传改良重点实验室, 武汉 430064
基金项目:国家自然科学基金项目(31501620);湖北省粮食作物种质创新与遗传改良重点实验室开放课题(2014lzjj06);主要粮食作物产业化湖北省协同创新中心资助项目
摘    要:采用我国当前流行的小麦条锈菌小种和重要致病类型,在常温条件下对普通小麦-华山新麦草易位系H9015-17进行苗期抗条锈性鉴定,并用当前主要流行小种CYR32对H9015-17与铭贤169的杂交后代及其双亲进行抗条锈性遗传分析,以揭示H9015-17抗条锈性遗传基础。结果显示,H9015-17对小麦条锈菌小种CYR31、CYR32、CYR33和致病类型Su11-4、Su11-7、V26、Su11-11均有良好的抗病性,对当前主要流行小种CYR32的抗病性由1对显性基因控制,暂命名为Yr Hua1。采用分子标记定位技术,筛选到5个与抗病基因Yr Hua1连锁的RGAP标记(M1、M2、M3、M4和M5)和1个SSR标记(Xgwm292),这些标记与抗病基因Yr Hua1的遗传距离分别为17.3、15.7、13.1、3.3、2.9和11.2,并将基因Yr Hua1定位在小麦染色体5DL上。研究结果将为分子标记辅助选择改良小麦抗条锈性提供宝贵的种质材料,建议在抗病育种加以利用。

关 键 词:H9015-17    华山新麦草    抗条锈病基因    遗传分析    分子标记  

Molecular mapping of a stripe rust resistance gene of wheat translocation line H9015-17 derived from Psathyrostachys huashanica Keng
MA Dong-fang,FANG Zheng-wu,LI Qiang,YIN Jun-liang,WANG Wen-kai,WANG Bao-tong.Molecular mapping of a stripe rust resistance gene of wheat translocation line H9015-17 derived from Psathyrostachys huashanica Keng[J].Acta Phytopathologica Sinica,2015,45(5):501-508.
Authors:MA Dong-fang  FANG Zheng-wu  LI Qiang  YIN Jun-liang  WANG Wen-kai  WANG Bao-tong
Institution:Engineering Research Center of Ecology and Agricultural Use of Wetland Ministry of Education/College of Agriculture, Yangtze University, Jingzhou 434025,China;
State Key Laboratory of Crop Stress Biology for Arid Areas, Northwest A&F University, Yangling 712100, China;
Hubei Academy of Agriculture Science/Hubei Key Laboratory of Food Crop Germplasm and Genetic Improvement, Wuhan 430064, China
Abstract:To reveal the wheat stripe rust resistance mechanism of H9015-17, it was inoculated with seven prevalent races or strains of Puccinia striiforms f. sp. tritici (Pst) distributed widely in China, H9015-17, susceptible cultivar Mingxian169 and their progeny plants of cross combinations were tested with races CYR32. The methods of resistance gene-analog polymorphism (RGAP) and simple sequence repeat (SSR) markers were used to map the resistance gene(s) in its wheat genome. The results showed that H9015-17 expressed higher level disease resistance to seven races or strains of Pst. Genetic analysis showed that resistance gene of H9015-17 to CYR32 was controlled by one dominant gene, temporarily designated as YrHua1. The RGAP markers including M1, M2, M3, M4, M5 and SSR marker Xgwm292 were tightly linked to the gene YrHua1 and their genetic distance to YrHua1 were 17.3, 15.7, 13.1, 3.3, 2.9 and 11.2 cM, respectively. The gene was mapped to the long arm of chromosome 5D by SSR marker. Our research results provided a useful germplasm for marker-assisted selection used in wheat resistance breeding against stripe rust.
Keywords:H9015-17  Psathynrostachys huashanica  stripe rust resistance gene  genetic analysis  molecular marker  
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