首页 | 本学科首页   官方微博 | 高级检索  
     检索      

黄瓜抗病基因同源序列的表达分析
引用本文:许春梅,秦智伟,丁国华,周秀艳.黄瓜抗病基因同源序列的表达分析[J].东北农业大学学报,2010,41(4).
作者姓名:许春梅  秦智伟  丁国华  周秀艳
作者单位:1. 东北农业大学园艺学院,哈尔滨,150030
2. 哈尔滨师范大学生命科学与技术学院,哈尔滨,150025
基金项目:哈尔滨市科技创新人才研究专项资金项目 
摘    要:对黄瓜抗霜霉病品种东农129进行霜霉菌诱导,以稳定表达的18S RNA基因做对照,用RT-PCR半定量的方法分析黄瓜抗病基因同源序列(RGAs)的表达情况。结果表明,霜霉菌能诱导RGA基因的表达,经霜霉菌诱导后多数RGA基因相对表达量增强。说明了RGA基因的表达情况和霜霉菌密切相关。用半定量RT-PCR研究RGA基因的表达具有操作简单,特异性高,可靠性强的优点。

关 键 词:黄瓜  RGAs  cDNA  表达

Expression analysis of resistance gene analogs in cucumber
XU Chunmei,QIN Zhiwei,DING Guohua,ZHOU Xiuyan.Expression analysis of resistance gene analogs in cucumber[J].Journal of Northeast Agricultural University,2010,41(4).
Authors:XU Chunmei  QIN Zhiwei  DING Guohua  ZHOU Xiuyan
Abstract:Downy mildew resistance of cucumber Dongnong129 was induced with P.cubensis by using 18S gene of stable expression as the control.The experiment used RT-PCR semi-quantitative method to analyze the expression of cucumber resistance gene analogs(RGAs).The results showed that the P.cubensis could induce the expression of RGA gene.The relative expression of the majority of RGA gene enhanced after inducement. lt illuminated that the gene expression of RGA was closely related with the P.cubensis.The method of semi-quantitative RT-PCR was simple,high specificity and reliability so as to study the RGA gene expression.
Keywords:RGAs  cDNA  cucumber  RGAs  cDNA  expression
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号