International Crops Research Institute for the Semi-Arid Tropics, Hyderabad, Andhra Pradesh, India.
Theor Appl Genet. 2013 Aug;126(8):2051-64. doi: 10.1007/s00122-013-2117-6. Epub 2013 May 25.
Selection and use of genetically diverse genotypes are key factors in any crop breeding program to develop cultivars with a broad genetic base. Molecular markers play a major role in selecting diverse genotypes. In the present study, a reference set representing a wide range of sorghum genetic diversity was screened with 40 EST-SSR markers to validate both the use of these markers for genetic structure analyses and the population structure of this set. Grouping of accessions is identical in distance-based and model-based clustering methods. Genotypes were grouped primarily based on race within the geographic origins. Accessions derived from the African continent contributed 88.6 % of alleles confirming the African origin of sorghum. In total, 360 alleles were detected in the reference set with an average of 9 alleles per marker. The average PIC value was 0.5230 with a range of 0.1379-0.9483. Sub-race, guinea margaritiferum (Gma) from West Africa formed a separate cluster in close proximity to wild accessions suggesting that the Gma group represents an independent domestication event. Guineas from India and Western Africa formed two distinct clusters. Accessions belongs to the kafir race formed the most homogeneous group as observed in earlier studies. This analysis suggests that the EST-SSR markers used in the present study have greater discriminating power than the genomic SSRs. Genetic variance within the subpopulations was very high (71.7 %) suggesting that the germplasm lines included in the set are more diverse. Thus, this reference set representing the global germplasm is an ideal material for the breeding community, serving as a community resource for trait-specific allele mining as well as genome-wide association mapping.
选择和利用具有广泛遗传基础的基因型是任何作物育种计划开发品种的关键因素。分子标记在选择多样化基因型方面发挥着重要作用。本研究利用 40 个 EST-SSR 标记对代表广泛的高粱遗传多样性的参考群体进行了筛选,以验证这些标记在遗传结构分析中的应用以及该群体的群体结构。基于距离和基于模型的聚类方法的分组是相同的。基因型主要基于起源地的品种进行分组。来自非洲大陆的材料贡献了 88.6%的等位基因,证实了高粱的非洲起源。在参考群体中总共检测到 360 个等位基因,每个标记平均 9 个等位基因。平均 PIC 值为 0.5230,范围为 0.1379-0.9483。来自西非的几内亚珍珠粟亚种(Gma)与野生材料密切相关,形成了一个单独的聚类,表明 Gma 群体代表了一个独立的驯化事件。来自印度和西非的几内亚形成了两个不同的聚类。属于卡菲尔品种的材料形成了与早期研究中观察到的最相似的聚类。该分析表明,本研究中使用的 EST-SSR 标记比基因组 SSR 标记具有更高的区分能力。亚种群内的遗传方差非常高(71.7%),表明该群体中包含的种质系更加多样化。因此,这个代表全球种质资源的参考群体是育种社区的理想材料,可作为特定性状等位基因挖掘以及全基因组关联图谱的社区资源。