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中国和CIMMYT小麦品种Bx7亚基超量表达基因(Bx7OE)的分子检测
引用本文:任妍,梁丹,张平平,何中虎,陈静,傅体华,夏先春.中国和CIMMYT小麦品种Bx7亚基超量表达基因(Bx7OE)的分子检测[J].作物学报,2009,35(3):403-411.
作者姓名:任妍  梁丹  张平平  何中虎  陈静  傅体华  夏先春
作者单位:1.四川农业大学农学院,四川雅安625014;2.中国农业科学院作物科学研究所国家小麦改良中心/国家农作物基因资源与基因改良重大科学工程,北京100081;3.江苏省农业科学院农业生物技术研究所,江苏南京210014;4.CIMMYT中国办事处,北京100081;5.中国科学院成都生物研究所,四川成都610041
基金项目:国家自然科学基金,引进国际先进农业科学技术计划(948计划)重大国际合作项目,国家高技术研究发展计划(863计划),四川省科技厅育种攻关项目 
摘    要:高分子量谷蛋白亚基Bx7的超量表达对提高小麦面筋强度有重要作用。利用反相高效液相色谱(RP-HPLC)和STS标记检测了163份中国和CIMMYT小麦品种(系)的高分子谷蛋白亚基Bx7超量表达基因(Bx7OE)。结果表明,TaBAC1215C06-F517/R964标记和TaBAC1215C06-F24671/R25515标记可分别在含有Bx7OE基因的材料中扩增出447 bp和844 bp的特异带,在不含Bx7OE基因的材料中无相应目标带,两个STS标记的检测结果完全一致。在163份小麦品种(系)中,11份品种(系)含有Bx7OE基因,占总数的6.7%。RP-HPLC与STS标记检测结果一致。利用这两个STS标记可以方便、快速、准确地检测Bx7OE基因。

关 键 词:普通小麦(Triticum  aestivum  L.)  RP-HPLC  STS标记  分子标记辅助选择  Bx7OE  
收稿时间:2008-06-30

Characterization of Overexpressed Bx7 Gene (Bx7OE) in Chinese and CIMMYT Wheats by STS Markers
REN Yan,LIANG Dan,ZHANG Ping-Ping,HE Zhong-Hu,CHEN Jing,FU Ti-Hua,XIA Xian-Chun.Characterization of Overexpressed Bx7 Gene (Bx7OE) in Chinese and CIMMYT Wheats by STS Markers[J].Acta Agronomica Sinica,2009,35(3):403-411.
Authors:REN Yan  LIANG Dan  ZHANG Ping-Ping  HE Zhong-Hu  CHEN Jing  FU Ti-Hua  XIA Xian-Chun
Institution:1.College of Agronomy,Sichuan Agricultural University,Ya'an 625014,China;2.National Wheat Improvement Center,Institute of Crop Sciences/National key Facility for Crop Gene Resource and Genetic Improvement, Chinese Academy of Agricultural Sciences, Beijing 100081,China;3.Institute of Agricultural Biotechnology, Jiangsu Academy of Agricultural Sciences, Nanjing 210014,China;4.CIMMYT China Office, Beijing 100081,China;5.Institute of Biology,Chinese Academy of Sciences,Chengdu610041,China
Abstract:Over-expression of the high molecular weight glutenin subunit (HMW-GS) Bx7 is highly associated with dough strength of wheat (Triticum aestivum L.) flour. A total of 163 Chinese and CIMMYT wheat cultivars and advanced lines were tested by two STS markers and RP-HPLC to understand the presence of HMW-GS gene Bx7OE The results indicated that the markers TaBAC1215C06-F517/R964 and TaBAC1215C06-F24671/R25515 could amplify a 447 bp and a 844 bp PCR fragments, respectively, in the lines with Bx7OE, whereas no PCR products were detected in the lines without Bx7OE. Of the 163 cultivars and lines, specific PCR fragments were amplified in 11 genotypes by the two markers, indicating the presence of Bx7OE in these lines, with a frequency of 6.7%. The results obtained by RP-HPLC were consistent with those revealed by STS markers. These two STS markers could be used to detect the presence of Bx7OE gene in wheat cultivars.
Keywords:aestivum  L  RP-HPLC  Bx7OE
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