生物技术进展 ›› 2019, Vol. 9 ›› Issue (3): 303-308.DOI: 10.19586/j.2095-2341.2018.0134

• 技术与方法 • 上一篇    下一篇

棉花线粒体基因cRT-PCR改良及其在寻找CMS相关基因中的应用

王裴林,周利利,梁成真,孟志刚,郭三堆*,张锐*   

  1. 中国农业科学院生物技术研究所, 北京 100081
  • 收稿日期:2018-12-10 出版日期:2019-05-25 发布日期:2019-03-01
  • 通讯作者: 郭三堆,研究员,研究方向为植物基因工程。E-mail:guosandui@caas.cn;张锐,研究员,博士,研究方向为植物分子生物学与基因工程。E-mail:zhangrui@caas.cn
  • 作者简介:王裴林,硕士研究生,研究方向为植物分子生物学与基因工程。E-mail:123695298@qq.com。
  • 基金资助:
    国家自然科学基金项目(31771850);国家新品种培育转基因重大专项(2016ZX08009003-003-004)资助。

Improvement of Cotton Mitochondrial Gene cRT-PCR and its Application in Searching for CMS Related Genes

WANG Peilin, ZHOU Lili, LIANG Chengzhen, MENG Zhigang, GUO Sandui, ZHANG Rui   

  1. Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China
  • Received:2018-12-10 Online:2019-05-25 Published:2019-03-01

摘要: 植物线粒体是含有遗传物质的细胞器,为细胞生命活动提供必需的能量。农业生产中,线粒体基因的变异容易导致细胞质雄性不育,为作物杂交育种提供了高效的杂交母本。然而,植物线粒体基因组结构复杂,不同类型的细胞质雄性不育的发生往往由特异的基因突变所导致,为雄性不育基因的克隆带来了较大的困难。针对棉花线粒体基因的特性,改进了cRT-PCR技术,RNA连接酶将线粒体mRNA的5′和3′末端连接环化后,应用随机引物进行反转录,在保证与特异引物获得相同的完整线粒体基因转录本的基础上,实现了同时对所有线粒体编码基因的cRT-PCR,方便对线粒体编码基因的结构进行全局分析,并且通过改良方法对棉花CMS基因进行探索,从而快速找到异常因素,为线粒体功能基因组分析提供了新的方法。

关键词: 棉花, 线粒体, 环式RT-PCR, 细胞质雄性不育

Abstract: Plant mitochondria is a type of organelles containing genetic material,which provides necessary energy for cells. In agricultural production, genovariation of mitochondrial gene may lead to cytoplasmic male sterility, providing a convenient female parent for hybird breeding. Despite successful utilization of CMS and restoration of fertility (Rf) in breeding programs, the underlying mechanisms of these processes remain elusive because the mitochondrial genome structure is complex, and occurrence of different types of CMS is often caused by specific mutations consequently limiting gene cloning. This study summarized the techniques to improve cRT-PCR technology and present detailed characteristics mitochondrial gene involved in CMS. After RNA ligase cyclizes the 5′ and 3′ ends of mitochondrial mRNA, random primers were used for reverse transcription to ensure the same integrity as specific primers. Based on the mitochondrial gene transcript, cRT-PCR was performed on all mitochondrial coding genes, which provided insight of structure of mitochondrial coding genes. Therefore, we used this system to explore cotton CMS genes, thus quickly figuring out abnormal factors and providing a new method for mitochondrial functional genomic analysis.

Key words: cotton, mitochondrial, cRT-PCR, CMS