江淮地区夏大豆新品系SSR和PAV分子标记多样性分析
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  • 英文篇名:Diversity Analysis of SSR and PAV Molecular Marker in New Breeding Lines of Summer Soybean from Changjiang and Huaihe
  • 作者:滕康开 ; 郭呈宇 ; 张吉顺 ; 孔杰杰 ; 赵团结
  • 英文作者:Teng Kangkai;Guo Chengyu;Zhang Jishun;Kong Jiejie;Zhao Tuanjie;Soybean Research Institute, National Center for Soybean Improvement, Key Laboratory for Biology and Genetic Improvement of Soybean (General),Ministry of Agriculture, National Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University;Suzhou Vocational Technical College;
  • 关键词:大豆 ; 新品系 ; 分子标记 ; 遗传多样性 ; 亲缘关系
  • 英文关键词:Soybean;;New breeding line;;Molecular marker;;Genetic diversity;;Genetic relationship
  • 中文刊名:FZZW
  • 英文刊名:Molecular Plant Breeding
  • 机构:南京农业大学大豆研究所国家大豆改良中心农业部大豆生物学与遗传育种重点实验室(综合)作物遗传与种质创新国家重点实验室;宿州职业技术学院;
  • 出版日期:2018-03-02 10:41
  • 出版单位:分子植物育种
  • 年:2018
  • 期:v.16
  • 基金:国家重点研发计划课题(2016YFD0100201);; 国家自然科学基金(31571691);; 江苏省现代作物生产协同创新中心项目(JCIC-MCP)共同资助
  • 语种:中文;
  • 页:FZZW201815024
  • 页数:11
  • CN:15
  • ISSN:46-1068/S
  • 分类号:165-175
摘要
大豆新品系已成为杂交育种中最主要亲本类型,本研究对系谱明确、适合江淮地区种植的296份大豆新品系进行SSR和PAV标记分析,以揭示其遗传关系,促进其育种利用。结果 93个SSR标记共检测到417个等位变异,平均每个位点等位变异数为4.48,变幅为2~15,PIC值为0.46;227对PAV标记每个位点平均等位变异数为2.10,变幅2~4,PIC值为0.22;基于SSR标记所计算的多样性指标数值均高于PAV标记所得。根据核心亲本划分的4个亚群间分子标记遗传多样性值相近,但都存在一些特有和特缺等位变异。基于SSR和PAV标记遗传距离的聚类分析分别可将供试材料分为12和10类,其中4个大类均可与4个核心亲本亚群对应,还发现一些系谱相同/相近的品系被聚在不同类群。两类分子标记都可用于揭示供试材料的遗传背景,利用所有320个标记可将296份新品系分为8类。
        New breeding line of soybean has been the most important parent types in hybrid breeding program. In the present study, SSR and PAV marker analysis was conducted to reveal the genetic diversity of 296 new lines of soybean with clear pedigree which was suitable for further plantation in Changjiang and Huaihe region and promote its breeding and utilization. Total 417 allele variations were identified by 93 SSR markers, and the average allele number(AN) per locus was 4.48, ranged from 2~15. The polymorphism information content(PIC) was0.46. The average allele number per locus of 227 PAV markers was 2.10, ranged from 2~4, and the PIC was 0.22.The diversity index values determined based on SSR markers were all higher than those by PAV markers. Genetic diversity values of molecular marker of four subpopulations divided from different core parents were similar, butthey all had several specifically existent and specifically deficient alleles. These test materials could be clustered into 12 and 10 groups based on genetic distances of SSR and PAV markers respectively. Among them, four major groups could correspond to the four subpopulations of the core parents. Some lines of same or similar pedigree were clustered in different groups. Both SSR and PAV markers could be utilized to reveal the genetic background of test materials. All 296 new lines could be clustered into 8 groups based on all 320 markers.
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