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Genetic diversity analysis and DNA fingerprinting of elite genetic stocks of tomato using SSR markers

机译:利用SSR标记对番茄优良遗传种质的遗传多样性分析和DNA指纹图谱。

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Thirty genetic stocks of tomato (Solanum lycopersicum L.) were subjected to genetic diversity analysis and DNA fingerprinting using SSR markers. The stocks included male sterile lines (both pollen abortive and functional types); non-ripening mutants;disease (leaf curl virus, late blight and early blight) and nematode resistant lines; temperature stress (both low and high); and salt tolerant lines. Of the 25 primers used, 21 showed polymorphism and amplified 60 alleles with an average of 2.86 allelesper locus. Of these alleles, 21 were polymorphic and the rest were monomorphic. The PIC values for 21 primers obtained varied from 0.06 for SSR128 to 0.68 for SSR565, with an average PIC value to be 0.43. The greater number of repeat units and longer SSRs tend to have higher PIC values. Based on the PIC values and number of alleles amplified, the primer SSR565 was found to be more informative in the present set of genotypes. Similarity coefficient between any two genotypes estimated based on DNA amplification by SSR primers varied from 0.18 to 0.94. The lowest similarity coefficient (0.18) observed between genotypes belonging to the cultivated species lycopersicum and the wild species pimpinellifolium confirmed their differentiation at the species level. Many of the cultivated types were found to have fairly narrow genetic base. UPGMA revealed that SSR markers were helpful in differentiating the genotypes on the basis of horticultural and genetic factors. However, grouping of the 30 genetic stocks was independent of their geographic distribution. Based on the DNA fingerprints, it was possible to differentiate 23 of the 30 genotypes screened.
机译:使用SSR标记对30株番茄(Solanum lycopersicum L.)的遗传种群进行了遗传多样性分析和DNA指纹分析。种群中包括雄性不育系(花粉败育型和功能型);非成熟突变体;疾病(叶卷曲病毒,晚疫病和早疫病)和线虫抗性品系;温度应力(低和高);和耐盐品系。在使用的25个引物中,有21个表现出多态性并扩增了60个等位基因,平均每个位点为2.86个等位基因。在这些等位基因中,有21个为多态性,其余为单态性。获得的21个引物的PIC值从SSR128的0.06到SSR565的0.68不等,平均PIC值为0.43。重复单元数量越多,SSR越长,其PIC值就越高。根据PIC值和扩增的等位基因数量,发现引物SSR565在当前的基因型中更具参考价值。根据SSR引物的DNA扩增估计的任何两种基因型之间的相似系数在0.18至0.94之间。在属于栽培品种lycopersicum的基因型和野生物种pimpinellifolium的基因型之间观察到的最低相似系数(0.18)证实了它们在物种水平上的分化。发现许多栽培类型具有相当狭窄的遗传基础。 UPGMA发现,SSR标记有助于根据园艺和遗传因素区分基因型。但是,这30个遗传种群的分组与它们的地理分布无关。根据DNA指纹图谱,可以区分所筛选的30个基因型中的23个。

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