利用m13尾SSR标记和序列分析对栽培型和野生型花生的遗传多样性进行了评价。

Noelle A Barkley, Rob E Dean, Roy N Pittman, Ming L Wang, Corley C Holbrook, Gary A Pederson
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引用次数: 62

摘要

利用31个带M13尾的基因组SSR标记,对花生迷你核心材料的遗传多样性进行了评价。m13 -尾法对栽培和野生材料的鉴别效果良好。共检测到477个等位基因,平均每个位点15.4个等位基因。多态信息含量(PIC)均值为0.687。栽培花生(arachhis hypogaea L.)小核共产生312个等位基因,平均每个位点10.1个等位基因。通过构建邻居连接树来确定该数据集的种间和种内关系。在这个数据集中,几乎所有的花生资料都被划分为亚种和植物变种,如亚种。Hypogaea的变体。尖形藻变种尖形藻和小尖形藻。与具有相同分类的其他种属聚类,进一步支持了其现有分类。对其中一个SSR标记的等位基因进行了测序,结果表明,该重复基序在跨物种转移时是保守的。本研究对花生迷你核的多样性和系统发育关系进行了研究,这是以前没有报道过的。
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Genetic diversity of cultivated and wild-type peanuts evaluated with M13-tailed SSR markers and sequencing.

Thirty-one genomic SSR markers with a M13 tail attached were used to assess the genetic diversity of the peanut mini core collection. The M13-tailed method was effective in discriminating almost all the cultivated and wild accessions. A total of 477 alleles were detected with an average of 15.4 alleles per locus. The mean polymorphic information content (PIC) score was 0.687. The cultivated peanut (Arachis hypogaea L.) mini core produced a total of 312 alleles with an average of 10.1 alleles per locus. A neighbour-joining tree was constructed to determine the interspecific and intraspecific relationships in this data set. Almost all the peanut accessions in this data set classified into subspecies and botanical varieties such as subsp. hypogaea var. hypogaea, subsp. fastigiata var. fastigiata, and subsp. fastigiata var. vulgaris clustered with other accessions with the same classification, which lends further support to their current taxonomy. Alleles were sequenced from one of the SSR markers used in this study, which demonstrated that the repeat motif is conserved when transferring the marker across species borders. This study allowed the examination of the diversity and phylogenetic relationships in the peanut mini core which has not been previously reported.

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