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茶叶科学 ›› 2021, Vol. 41 ›› Issue (6): 777-788.

• 研究报告 • 上一篇    下一篇

信阳10号叶绿体基因组及其系统进化

闫明慧1, 刘柯2, 王满2, 吕颖1, 张倩1   

  1. 1.信阳师范学院生命科学学院/河南省茶树生物学重点实验室,河南 信阳 464000;
    2.信阳师范学院国教学院,河南 信阳 464000
  • 收稿日期:2021-06-16 修回日期:2021-07-26 出版日期:2021-12-15 发布日期:2021-12-09
  • 作者简介:闫明慧,女,讲师,主要从事植物系统进化研究,yanminghui8899@163.com
  • 基金资助:
    国家自然科学基金(31800276)、河南省高等学校重点科研项目(19A180029)、信阳师范学院“南湖学者奖励计划”青年项目

Complete Chloroplast Genome of Camellia sinensis cv. Xinyang 10 and Its Phylogenetic Evolution

YAN Minghui1, LIU Ke2, WANG Man2, LYU Ying1, ZHANG Qian1   

  1. 1. College of Life Science, Xinyang Normal University/Henan Key Laboratory of Tea Plant Biology, Xinyang 464000, China;
    2. College of International Education, Xinyang Normal University, Xinyang 464000, China
  • Received:2021-06-16 Revised:2021-07-26 Online:2021-12-15 Published:2021-12-09

摘要: 信阳10号是适制信阳毛尖的国家级良种,然而其起源以及与其他茶树品种之间的进化关系尚不清晰。利用MGI2000平台对信阳10号进行测序,组装获得了信阳10号的完整叶绿体基因组并对其结构进行分析,同时,为探究信阳10号与其他茶树的进化关系,构建了46个物种的叶绿体基因组系统发育树。结果表明:(1)信阳10号叶绿体基因组大小为157 041 bp,包括2个反向重复区(IR,26 078 bp),1个大单拷贝区(LSC,86 594 bp)和1个小单拷贝区(SSC,18 291 bp);共注释得到叶绿体基因113个,包括79个蛋白质编码基因,30个tRNA基因和4个rRNA基因。(2)在信阳10号的叶绿体基因组中共检测到了74个SSR位点,大部分SSR由A/T组成。(3)贝叶斯法构建的系统进化关系树显示,信阳10号与福建铁罗汉关系最近,并且两者的叶绿体基因组完全相同,推测可能来源于相同母本;信阳10号与韩国茶Chamnok和Sangmok、福建白鸡冠、云南德宏茶也有较近的亲缘关系。研究结果为进一步探究茶树起源与演化以及分子育种提供了基础。

关键词: 茶树, 信阳10号, 叶绿体基因组, 系统发育分析

Abstract: Camellia sinensis cv. Xinyang 10 is a national excellent cultivar suitable for producing Xinyangmaojian. However, its origin and evolutionary relationship with other tea cultivars are still unknown. This study obtained the complete chloroplast genome of C. sinensis cv. Xinyang 10 by using MGI2000 sequencing platform, and then analyzed the chloroplast genome structure. A chloroplast genome phylogenetic analysis of 46 species was also conducted to infer the position of C. sinensis cv. Xinyang 10. The results show that: (1) the chloroplast genome of Xinyang 10 is 157 041 bp in length, including a pair of inverted repeat regions (IR, 26 078 bp), a large single-copy region (LSC, 86 594 bp) and a small single-copy region (SSC, 18 291 bp). A total of 113 genes are annotated, including 79 protein-coding genes, 30 tRNA genes, and 4 rRNA genes. (2) 74 SSR loci were detected in the chloroplast genome of Xinyang 10, most of the SSRs were composed of A/T. (3) The cluster analysis using Bayesian method shows that Xinyang 10 had the closest genetic relationship with C. sinensis cv. Tieluohan. Both cultivars may share the same female parent as their chloroplast genomes were identical. Xinyang 10 also had a close relationship with two Korean tea (Chamnok and Sangmok), Baijiguan and C. sinensis var. Dehungensis. The results provided a basis for further research on the origin and evolution of tea and molecular breeding.

Key words: Camellia sinensis, C. sinensis cv. Xinyang 10, chloroplast genome, phylogentic analysis

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