实验技术

利用四引物扩增受阻突变体系PCR技术检测水稻光温敏核不育基因p/tms12-1

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  • 嘉兴市农业科学研究院, 浙江 嘉兴 314016;

收稿日期: 2014-01-09

  修回日期: 2014-02-21

  网络出版日期: 2014-07-10

基金资助

嘉兴市科技计划资助项目(2013BY26006, 2012AZ2021,2013BZ26002)。

Detection of Gene p/tms121  for Photoperiod and ThermoSensitive Genic Male Sterility by TetraPrimer Amplication Refractory Mutation System PCR in Rice

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  • Jiaxing Academy of Agricultural Sciences, Jiaxing 314016, China; 

Received date: 2014-01-09

  Revised date: 2014-02-21

  Online published: 2014-07-10

摘要

根据p/tms121基因存在的单核苷酸变异,利用四引物扩增受阻突变体系PCR(Tetraprimer ARMSPCR)的方法设计特异引物,对11个两系不育系水稻品种(或品系)以及2个常规稻品系进行扩增。根据其PCR产物带型,可以准确鉴定光温敏核不育基因p/tms121的基因型,其检测结果与通过CAPS标记检测的结果完全一致。该方法成本低、简单、可靠,可用于p/tms121基因的鉴定和分子标记辅助育种。

本文引用格式

李军* ,李白,高荣村 . 利用四引物扩增受阻突变体系PCR技术检测水稻光温敏核不育基因p/tms12-1[J]. 中国水稻科学, 2014 , 28(4) : 442 -446 . DOI: 10.3969/j.issn.1001-7216.2014.04.014

Abstract

Specific primers were designed for tetraprimer amplification refractory mutation system PCR (ARMSPCR) method according to the single nucleodide mutation in gene p/tms121.  Eleven twoline sterile lines and two normal varieties were analyzed by this method. The results could clearly distinguish the genotype of p/tms121,  which was completely consistent with the result of CAPs markerbased analysis. Therefore, as a lowcost, simple and reliable technique, this method could be widely used to the p/tms121  detection and molecular markerassisted breeding in rice.

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