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Genetic Diversity of Wild Soybeans from Some Regions of Southern China Based on SSR and SRAP Markers

机译:基于SSR和SRAP标记的华南部分地区野生大豆遗传多样性

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There are rich annual wild soybean (Glycine soja) resources in Southern China, which are the progenitor of cultivated soybean. To evaluate the genetic diversity and differentiation of G. soja in Southern China, we analyzed allelic profiles of 141 annual wild soybean accessions from Southern China and 8 core wild soybean accessions fromNorthern Chinaby using 41 simple sequence repeat (SSR) markers and 18 Sequence-related amplified polymorphism (SRAP) primer combinations. The 41 SSR markers produced a total of 421 alleles (10.27 per locus) with a mean of gene diversity of 0.825 (Simpson index) and 1.987 (Shannon-weaver index). The 18 SRAP primer combinations detected a total of 90 polymorphism bands (5 per primer combination) with a mean of gene diversity of 0.918 (Shannon-weaver index). SSR and SRAP markers detected 43 and 5 rare alleles in 149 wild soybeans, respectively. The wild soybeans from Fujian province showed the highest genetic diversity with Shannon-weaver index of 1.837 (by SSR) and 0.803 (by SRAP), and the highest allelic richness with an average of 8.8 alleles per locus and the most number of rare alleles of 0.68 per locus based on SSR data. An analysis of Molecular Variance (AMOVA) analysis showed that significant variance did exist amongHunan,Fujian, Guangxi andNorthern Chinasubpopulations based on SSR and SRAP data. The unweighted pair-group method of the arithmetic average (UPGMA) cluster analysis indicated that the wild soybeans fromFujianprovince occurred in different clusters based on both SSR and SRAP data. The above results indicated thatFujianprovince could be the major center of genetic diversity for annual wild soybean inSouthern China. In addition, Mantle test showed there was a weak positive linear correlation (r = 0.25) between SSR and SRAP analysis in the study.
机译:中国南方每年都有丰富的野生大豆(甘氨酸大豆)资源,是栽培大豆的祖先。为了评估华南大豆的遗传多样性和分化,我们使用41个简单序列重复(SSR)标记和18个与序列相关的标记,分析了华南地区141个年度野生大豆种质和华北地区8个核心野生大豆种质的等位基因谱。扩增多态性(SRAP)引物组合。 41个SSR标记共产生421个等位基因(每个位点10.27),平均基因多样性为0.825(辛普森指数)和1.987(香农-韦弗指数)。 18个SRAP引物组合检测到总共90个多态性条带(每个引物组合5个),平​​均基因多样性为0.918(Shannon-weaver指数)。 SSR和SRAP标记分别在149个野生大豆中检测到43个和5个稀有等位基因。福建野生大豆遗传多样性最高,Shannon-weaver指数分别为1.837(SRAP)和0.803(SRAP),等位基因丰富度最高,平均每个基因座为8.8个等位基因,稀有等位基因数量最多。基于SSR数据的每个基因座0.68。分子变异分析(AMOVA)分析表明,基于SSR和SRAP数据,湖南,福建,广西和中国北方亚人群之间确实存在显着差异。算术平均(UPGMA)聚类分析的非加权成对组方法表明,基于SSR和SRAP数据,来自福建省的野生大豆出现在不同的聚类中。以上结果表明,福建省可能是中国南方一年生野生大豆遗传多样性的主要中心。此外,Mantle测试表明,研究中SSR和SRAP分析之间存在弱的线性正相关(r = 0.25)。

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