植物学报 ›› 2025, Vol. 60 ›› Issue (2): 218-234.DOI: 10.11983/CBB24098  cstr: 32102.14.CBB24098

• 研究报告 • 上一篇    下一篇

基于形态学性状和SSR标记的辣椒种质资源遗传多样性分析(长英文摘要

杨志刚1,*,(), 张鹏程1,, 常海文1, 康立茹1, 左毅2, 向浩鑫2, 韩凤英1   

  1. 1内蒙古自治区农牧业科学院蔬菜花卉研究所, 呼和浩特 010031
    2中国科学院植物研究所, 植物分子生理学重点实验室, 北京 100093
  • 收稿日期:2024-06-28 接受日期:2025-01-20 出版日期:2025-03-10 发布日期:2025-01-21
  • 通讯作者: 杨志刚
  • 作者简介:第一联系人:

    †共同第一作者

  • 基金资助:
    内蒙古“揭榜挂帅”项目(2022JBGS0028);内蒙古自然科学基金(2019BS03031);内蒙古科技计划(2021GG0382)

Genetic Diversity Analysis of Pepper Germplasms Based on Morphological Traits and SSR Markers

Zhigang Yang1,*,(), Pengcheng Zhang1,, Haiwen Chang1, Liru Kang1, Yi Zuo2, Haoxin Xiang2, Fengying Han1   

  1. 1Vegetable and Flower Research Institute, Inner Mongolia Academy of Agricultural and Animal Husbandry Sciences, Hohhot 010031, China
    2Key Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China
  • Received:2024-06-28 Accepted:2025-01-20 Online:2025-03-10 Published:2025-01-21
  • Contact: Zhigang Yang
  • About author:First author contact:

    †These authors contributed equally to this paper

摘要: 分析了146份辣椒(Capsicum spp.)种质资源的形态学性状, 同时利用简单重复序列(SSR)标记分析了其遗传多样性和群体遗传结构。形态学性状多样性分析结果表明, 质量性状和数量性状的变异系数分别为8.22%-267.58%与14.35%- 72.51%, Shannon多样性指数分别为0.04-1.91与1.58-2.02, 说明辣椒种质资源多样性丰富。利用SSR标记从22对引物中检测出102个等位基因, 平均每对引物检测出4.636个等位基因, 有效等位基因变异范围为1.191-5.311, Shannon多样性指数为0.345-2.056, 多态性信息含量(PIC)为0.153-0.795, 146份辣椒种质资源平均遗传距离为0.429。基于表型和分子标记的聚类分析分别将辣椒种质资源分为6类和7类, 但2种聚类结果相关性较弱(r=0.396 7)。群体遗传结构分析将辣椒种质遗传结构分为2组, 不同组之间界限明显。研究阐明了146份辣椒种质资源的遗传多样性和群体遗传结构, 为后续种质鉴定及新品种选育奠定了理论基础。

关键词: 辣椒, 形态学性状, 分子标记, 遗传多样性

Abstract: INTRODUCTION Genetic diversity is the natural attribute of organisms formed in the long-term evolution process, which refers to the sum of all genetic variations of different individuals within a species or a group. Pepper (Capsicumspp.), a popular vegetable crop in China, is cultivated extensively with a substantial annual yield. Nevertheless, the widespread adoption of commercial pepper varieties has led to a gradual reduction in its genetic diversity, resulting in an increasing homogenization of germplasm resources. Given that germplasm forms the foundation for crop genetic improvement, maintaining rich genetic diversity is crucial for effective breeding. RATIONALE On the other hand, morphological markers serve as a fundamental approach for investigating plant phenotypic diversity, as they allow researchers to evaluate the variations in marked samples through the observation of plant agronomic traits. On the other hand, molecular markers, particularly SSR (simple sequence repeat) markers, have gained widespread application in the breeding of new crop varieties and related fields due to their accuracy and reliability. This study focused on analyzing the diversity of 146 pepper germplasms in Inner Mongolia by employing both morphological traits and SSR markers. RESULTS We assessed 34 morphological traits of 146 pepper germplasms and evaluated their genetic diversity using 22 pairs of SSR primers. Our analysis revealed a high degree of diversity in the traits of these pepper lines. The results of phenotypic trait diversity analysis showed that the coefficient of variation of quality traits and quantitative traits ranged from 8.22% to 267.58% and 14.35% to 72.51%, respectively, and the Shannon-Wiener diversity index ranged from 0.04 to 1.91 and 1.58 to 2.02, respectively. The genetic diversity of pepper germplasm resources was rich. A total of 102 alleles were detected by 22 pairs of SSR fluorescent molecular markers, with an average of 4.636 alleles per pair of primers. The effective allelic variation ranged from 1.191 to 5.311, the Shannon-Wiener diversity index ranged from 0.345 to 2.056, and the polymorphic information content (PIC) ranged from 0.153 to 0.795. The average genetic distance of 146 pepper germplasm resources was 0.429. Phenotypic value clustering and principal component analysis categorized the 146 accessions into six distinct groups, while the analysis of the SSR marker data divided them into seven groups. Population genetic structure analysis further delineated the 146 pepper germplasms into two main groups. Most of these germplasms were high-generation breeding lines with high homozygosity. However, gene introgression was observed within Group1 and Group2. CONCLUSION This study is the systematic analysis of the morphological characteristics, genetic diversity and population structure of 146 pepper germplasms, particularly by utilizing SSR fluorescent molecular markers. The high diversity in both morphological traits and genetic markers of these pepper germplasm resources indicated significant genetic diffe- rences in them. Consequently, this study provides a better understanding of the germplasm diversity and population genetic structure of these 146 pepper germplasms, establishing a theoretical foundation for future variety breeding efforts. Genetic diversity analysis of 146 pepper germplasms. 146 pepper germplasms were categorized into six groups based on phenotypic markers and seven groups based on molecular markers, but the correlation between these clusters was weak (r=0.3967). Population genetic structure analysis further divided the germplasms into two distinct groups.

Key words: pepper, morphological traits, molecular markers, genetic diversity