首页> 外文期刊>Genetic Resources and Crop Evolution >Genetic diversity of wild soybean (Glycine soja Sieb. et Zucc.) and Japanese cultivated soybeans [G. max (L.) Merr.] based on microsatellite (SSR) analysis and the selection of a core collection
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Genetic diversity of wild soybean (Glycine soja Sieb. et Zucc.) and Japanese cultivated soybeans [G. max (L.) Merr.] based on microsatellite (SSR) analysis and the selection of a core collection

机译:野生大豆(Glycine soja Sieb。et Zucc。)和日本栽培大豆的遗传多样性。最大(L.)Merr。]基于微卫星(SSR)分析和核心收藏的选择

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摘要

Wild soybeans, Glycine soja, are a source of genetic variation to improve soybeans. To improve the efficiency evaluation of conserved germplasm a core or mini-core collection approach that maximizes allelic diversity in a proportion of the whole collection has frequently been advocated. The genetic diversity of a wild soybean collection (1,305 accessions) plus Japanese cultivated soybeans (53 accessions) were analyzed at 20 SSR marker loci. Higher levels of allelic diversity were found in wild soybeans (28 alleles per locus) than Japanese cultivated soybean (five alleles per locus). The genetic distance between wild soybeans from different regions reflected their proximity. Accessions from Russia consisted of a diverse array of alleles resulting in accessions being spread further apart in a PCA plot than accessions from other regions. Accessions of wild soybean from Korea included many rare alleles and thus had a high representation in the core collection. The two core collections developed here, traditional and mini, consisted of 192 accessions with 97% of the allelic diversity (14% of the whole collection) and 53 accessions with 62.4% of the allelic diversity (5% of the whole collection), respectively.
机译:野生大豆甘氨酸大豆是遗传改良大豆的来源。为了提高对保守种质的效率评估,人们经常提倡采用核心或微型核心收集方法,该方法在整个收集物中的比例最大化等位基因多样性。在20个SSR标记位点分析了野生大豆(1,305份)和日本栽培的大豆(53份)的遗传多样性。与日本栽培大豆(每个位点五个等位基因)相比,野生大豆(每个位点28个等位基因)的等位基因多样性水平更高。来自不同地区的野生大豆之间的遗传距离反映了它们的接近性。来自俄罗斯的种质由各种各样的等位基因组成,导致这些种质在PCA图中的分布比其他地区的种质传播得更远。韩国野生大豆的种质包括许多稀有等位基因,因此在核心品种中具有很高的代表性。在此开发的两个核心集合,传统的和迷你的,分别由192个等位基因多样性的97%(占整个集合的14%)和53个等位基因多样性的62.4%(占整个集合的5%)组成。 。

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