中国农业科学 ›› 2026, Vol. 59 ›› Issue (3): 637-654.doi: 10.3864/j.issn.0578-1752.2026.03.012

• 园艺 • 上一篇    下一篇

基于BSA-Seq和蛋白组学筛选辣椒核雄性不育基因

裴红霞1(), 汪露瑶2(), 蒋雅苹2, 李生梅3(), 高晶霞1()   

  1. 1 宁夏农林科学院园艺研究所,银川 750002
    2 浙江大学海南研究院,海南三亚 572024
    3 新疆农业职业技术大学,新疆昌吉 831100
  • 收稿日期:2025-07-11 接受日期:2025-09-05 出版日期:2026-02-01 发布日期:2026-01-31
  • 通信作者:
    李生梅,E-mail:
    高晶霞,E-mail:
  • 联系方式: 裴红霞,E-mail:810444147@qq.com。汪露瑶,E-mail:2171100066@zju.edu.cn。裴红霞和汪露瑶为同等贡献作者。
  • 基金资助:
    国家自然科学基金(32560739); 宁夏农林科学院科技创新先导-科技攻关项目(NKYG-25-18); 宁夏自然基金(2023AAC03424); 领军人才项目(2023GKLRLX09)

Identification of Nuclear Male Sterility Genes in Pepper Based on BSA-Seq and Proteomics

PEI HongXia1(), WANG LuYao2(), JIANG YaPing2, LI ShengMei3(), GAO JingXia1()   

  1. 1 Institute of Horticulture, Ningxia Academy of Agriculture and Forestry Sciences, Yinchuan 750002
    2 Hainan Institute of Zhejiang University, Sanya 572024, Hainan
    3 Xinjiang Agricultural Vocational and Technical University, Changji 831100, Xinjiang
  • Received:2025-07-11 Accepted:2025-09-05 Published:2026-02-01 Online:2026-01-31

摘要:

【目的】辣椒雄性不育系是实现辣椒杂种优势和开展辣椒遗传育种的主要方式之一,研究辣椒核雄性不育基因的精确定位,为后续基因克隆、功能验证、分子机制解析和新种质创制提供相关基因资源,为创制辣椒雄性不育系奠定基础。【方法】以田间发现的自然雄性不育突变体pby-1与野生型PBY-1为亲本进行杂交,获得F1后代,并自交至F2代,选取F₂群体中表现不育与正常个体各30株,构建2个极端池。通过混池测序(bulked segregant analysis sequencing,BSA-Seq)分析,鉴定雄性不育候选区间,挖掘区间内候选基因,并进行GO(Gene Ontology)和KEGG(Kyoto Encyclopedia of Genes and Genomes)富集分析。进一步将候选基因与亲本pby-1和PBY-1不同发育时期的差异表达蛋白进行联合分析,缩小辣椒核雄性不育相关候选基因的范围。运用实时荧光定量PCR技术检测候选基因在辣椒花器官中的表达水平,验证候选基因调控辣椒雄性不育的潜力。【结果】通过BSA-Seq测序分析,在Chr.07染色体上鉴定到12个与雄性不育相关联的区域,总长度约70.02 Mb,包含343个候选基因,与已知msc-1msc-2msc-3不育基因区间无重叠。GO富集和KEGG富集分析结果表明,碳水化合物代谢、脂质运输代谢和植物激素信号传导等途径与辣椒雄性不育性密切相关。结合蛋白组学数据综合分析,筛选到12个候选基因(Capana07g000676Capana07g000956Capana07g000979Capana07g000993Capana07g001228Capana07g001239Capana07g001241Capana07g001254Capana07g001294Capana07g001295Capana07g001312Capana07g001315),经qRT-PCR检测,Capana07g000676Capana07g000979Capana07g000993Capana07g001228Capana07g001241Capana07g001294为雄性不育关键候选基因。【结论】结合BSA-Seq与蛋白质组学,在辣椒第7染色体上定位到核雄性不育功能区段,并筛选出6个核心候选基因。

关键词: 辣椒, 核雄性不育, BSA-Seq, 蛋白组学, 多组学联合分析

Abstract:

【Objective】Male-sterile lines constitute a principal means of exploiting heterosis and advancing genetic breeding in pepper (Capsicum annuum L.). Fine mapping of the Genic male sterility (GMS) genes can provide relevant gene resources for subsequent gene cloning, functional verification, molecular mechanism analysis, and creation of new germplasm, laying the foundation for the development of nuclear male sterile lines in pepper. 【Method】A natural GMS mutant pby-1 and its wild type PBY-1 were used as parents for hybridization to obtain F1 progeny, which were then self-pollinated to F2 generation. Thirty plants showing sterile and normal phenotypes were selected from the F2 population to construct two extreme pools. Through bulked segregant analysis sequencing (BSA-Seq), candidate regions associated with male sterility were identified, and candidate genes within the regions were mined. GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) enrichment analyses were conducted. Further, the candidate genes were jointly analyzed with the differentially expressed proteins of the parents pby-1 and PBY-1 at different developmental stages to narrow down the range of candidate genes related to nuclear male sterility in pepper. The expression levels of the candidate genes in pepper flower organs were detected by real-time fluorescence quantitative PCR to verify their potential in regulating male sterility in pepper. 【Result】Through BSA-Seq sequencing analysis, 12 regions associated with male sterility were identified on chromosome Chr.07, with a total length of approximately 70.02 Mb, containing 343 candidate genes, which did not overlap with the known ms-1, ms-2, and ms-3 sterility gene regions. The results of GO enrichment and KEGG enrichment analysis indicated that carbohydrate metabolism, lipid transport metabolism, and plant hormone signal transduction pathways were closely related to male sterility in pepper. Through comprehensive analysis combining proteomics data, 12 candidate genes (Capana07g000676, Capana07g000956, Capana07g000979, Capana07g000993, Capana07g001228, Capana07g001239, Capana07g001241, Capana07g001254, Capana07g001294, Capana07g001295, Capana07g001312, and Capana07g001315) were screened. Through qRT-PCR detection, Capana07g000676, Capana07g000979, Capana07g000993, Capana07g001228, Capana07g001241, and Capana07g001294 were identified as key candidate genes for male sterility. 【Conclusion】By combining BSA-Seq with proteomics, the functional region of nuclear male sterility was located on chromosome 7 of the pepper, and six core candidate genes were screened.

Key words: Capsicum spp., genic male sterility, BSA-Seq, proteomics, integrated multi-omics analysis