中国农业科技导报 ›› 2022, Vol. 24 ›› Issue (4): 38-51.DOI: 10.13304/j.nykjdb.2021.0521

• 生物技术 生命科学 • 上一篇    下一篇

苦荞全基因组SSR位点挖掘及遗传多样性分析

左茜茜1,2(), 宋英杰1,2, 马心妍2, 杨云卉1,2, 王轶菲1,2, 郭泽光2, 朱雄智2, 刘越1,2()   

  1. 1.中央民族大学民族地区生态环境国家民委重点实验室, 北京 100081
    2.中央民族大学生命与环境科学学院, 北京 100081
  • 收稿日期:2021-06-26 接受日期:2021-11-30 出版日期:2022-04-15 发布日期:2022-04-19
  • 通讯作者: 刘越
  • 作者简介:左茜茜 E-mail: 609517510@qq.com
  • 基金资助:
    生态环境部生物多样性调查评估项目(2019HJ2096001006);国家自然科学基金项目(81274185);国家民委中青年英才项目(2016-03-01);中央民族大学一流大学一流学科建设项目

Mining SSR Loci and Analysis the Genetic Diversity of Tartary Buckwheat Based on the Whole Genome Sequence

Xixi ZUO1,2(), Yingjie SONG1,2, Xinyan MA2, Yunhui YANG1,2, Yifei WANG1,2, Zeguang GUO2, Xiongzhi ZHU2, Yue LIU1,2()   

  1. 1.Key Laboratory of Ecology and Environment in Minority Areas of National Ethnic Affairs Commission,Minzu University of China,Beijing 100081,China
    2.College of Life and Environmental Sciences,Minzu University of China,Beijing 100081
  • Received:2021-06-26 Accepted:2021-11-30 Online:2022-04-15 Published:2022-04-19
  • Contact: Yue LIU

摘要:

苦荞是一种重要的杂粮作物。利用GenBank数据库中苦荞的8条染色体基因组序列进行SSR标记挖掘,并基于Primer 3.0设计SSR引物,筛选多态性高的引物进行遗传多样性评价。共检测到51 485个SSR 位点,平均发生频率为114.07 Mb-1,二核苷酸重复型最多(78.20%),其次为三核苷酸重复型(17.76%)。苦荞SSR中包含361种类型重复基元,具有碱基偏好性,优势基元为AT/TA (69.60%)、AAT/TTA (2.49 %)和AGA/TCT(2.10 %)。序列长度变化范围为12~228 bp,长度12~20 bp的占比57.93 %,长度大于20 bp 的占比42.07 %。SSR位点分布在每条染色体上的数量和种类特征较为一致,不同染色体能检出的SSR种类具有特异性。根据不同类型SSR位点设计并合成156对引物,筛选出17对多态性较高的引物用于遗传多样性分析,发现42份苦荞地方品种资源具有较高的多样性,美姑县的黑苦荞遗传多样性最高,布拖县的样品多数聚为同一分支,多样性显著低于美姑县和昭觉县的品种,西南种质库保存的野生苦荞与其他栽培品种明显分离。通过大量SSR的挖掘特别是染色体特异性SSR位点的挖掘,对苦荞种质资源的鉴定分析以及苦荞分子标记辅助育种有重要意义;遗传多样性检测也显示了SSR分子标记的可用性,以及黑苦荞的遗传多样性水平,对苦荞遗传多样性保护研究提供了新的途径。

关键词: 苦荞, 染色体, 简单重复序列(SSR), 遗传多样性

Abstract:

Tartary buckwheat (Fagopyrum tataricum) is an important minor crop. In this study, molecular markers of the simple sequence repeat (SSR) were mined from 8 chromosomes sequence of tartary buckwheat in GenBank database. SSR primers were designed by primer 3.0 software and those with high polymorphism were employed to evaluate the genetic diversity. A total of 51 485 SSR loci were screened with average frequency of 114.07 Mb-1. Among these SSR motifs, dinucleotide repeat was the main type accounting for 78.20%, followed by trinucleotide repeat (17.76%). There were 361 types of repeat motifs, while AT/AT (69.60 %), AAT/TTA (2.49%) and AGA/TCT (2.10%) were the main repeat types. The SSRs length ranged from 12 to 228 bp, and the ratio of SSRs with length ranging from 12 to 20 bp was 57.93%, the ratio with length above 20 bp was 42.07%. It was found that the SSR types detected were specific to the chromosomes. Based on the type of SSR loci, 156 pairs of primers were designed and 17 pairs of primers were screened with high polymorphism to analyze the genetic diversity of the 42 local varieties of tartary buckwheat. The diversity of black tartary buckwheat samples in Meigu County was the highest. The diversity of samples in Butuo County was significantly lower than that in the other two counties. It was of great significance to identify and analyze tartary buckwheat germplasm resources and molecular marker-assisted breeding through a large number of SSR mining, especially the chromosome specific SSR loci mining. In this study, a large number of SSRs were mined, especially the chromosomal specific SSR sites were mined, which was of great significance for the identification and analysis of tartary buckwheat germplasm resources and the molecular marker-assisted breeding of tartary buckwheat. Genetic diversity analysis also revealed the availability of SSR markers and the level of genetic diversity of tartary buckwheat, which provided a new approach for the study of the conservation of genetic diversity of tartary buckwheat.

Key words: Fagopyrum tataricum, chromosome, simple repeat sequence (SSR), genetic diversity

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