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首页> 外文期刊>American Journal of Plant Sciences >Molecular Diversity Analysis of Some Chilli (Capsicum spp.) Genotypes Using SSR Markers
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Molecular Diversity Analysis of Some Chilli (Capsicum spp.) Genotypes Using SSR Markers

机译:利用SSR标记分析某些辣椒( Capsicum spp。)基因型的分子多样性

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Chilli belongs to the genus style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;">Capsicum style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> which possesses enormous wealth of genetic diversity. Extent of genetic diversity determines the success level of crop improvement programme. Simple sequence repeats (SSRs) are the most widely used marker system for molecular diversity analysis especially in cultivated species. The aim of our present study was to assess the molecular genetic diversity of 20 local chilli genotypes of Bangladesh using SSR markers. Genomic DNA was extracted from young leaves and PCR reactions were performed. Eleven SSR primers were used in PCR amplification. Total 10 alleles were detected for the five polymorphic SSR loci, with a mean of 2.00 alleles per primer. Gene diversity ranged from 0.333 to 1.00 with an average of 0.567. Polymorphic Information Content (PIC) values of the SSR primers ranged from 0.255 to 0.500 with an average value of 0.371. The similarity index matrix ranged from 0.00 to 1.000. It was highest in several germplasms style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;">viz style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;">. style="font-family:Verdana;"> style="font-family:Verdana;"> style="font-family:Verdana;"> Pop-2 vs Pop-18; Pop-3 vs Pop-5 vs Pop-19 vs Pop-20 and the lowest in the germplasm Pop-8 vs Pop-18. Dendrogram based on Nei’s genetic distance using Unweighted Pair Group Method of Arithmetic Means (UPGMA) indicated the segregation of 20 chilli genotypes into two main clusters. The SSR markers showed genetic variability in the studied pepper genotypes and they are powerful tools for estimating molecular diversity of chilli. The findings of the present study have potential applications in future breeding programme for the genetic improvement of chilli.
机译:辣椒属于 style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;“>辣椒 style =” font-family:Verdana;“> style =” font-family:Verdana;“ > style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”>具有丰富的遗传多样性。基因多样性的程度决定了作物改良计划的成功水平。简单序列重复(SSR)是用于分子多样性分析的最广泛使用的标记系统,尤其是在栽培物种中。我们本研究的目的是使用SSR标记评估孟加拉国20个当地辣椒基因型的分子遗传多样性。从幼叶中提取基因组DNA,并进行PCR反应。在PCR扩增中使用了11种SSR引物。共检测到五个多态性SSR基因座的10个等位基因,每个引物平均2.00个等位基因。基因多样性范围从0.333到1.00,平均为0.567。 SSR引物的多态信息含量(PIC)值介于0.255至0.500之间,平均值为0.371。相似度指标矩阵的范围是0.00到1.000。 style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font -family:Verdana;“> style =” font-family:Verdana;“> style =” font-family :Verdana;“> style =” font-family:Verdana;“> viz style =” font-family:Verdana;“ > style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”>。 style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> style =“ font-family:Verdana;”> Pop- 2对Pop-18; Pop-3 vs Pop-5 vs Pop-19 vs Pop-20在种质中Pop-8 vs Pop-18最低。基于Nei遗传距离的树状图,使用算术平均非加权对组法(UPGMA)表明,将20个辣椒基因型分离为两个主要簇。 SSR标记显示了所研究的辣椒基因型的遗传变异性,并且它们是估算辣椒分子多样性的有力工具。本研究结果可为辣椒的遗传改良在今后的育种程序中应用。

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