基于AFLP标记的韩国扁桃群体遗传多样性和结构分析

IF 1.8 Q2 FORESTRY
Ji-young Ahn, Jei-Wan Lee, Hyo-In Lim, K. Hong
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引用次数: 2

摘要

摘要采用7对引物-限制性内切酶组合,对带有AFLP标记的扁桃群体的遗传多样性、遗传分化和遗传结构进行了研究。有效等位基因平均值(A e)、多态位点百分率(%P)、Shannon多样性指数(I)和期望杂合度(H e)分别为1.38、81.4、0.357和0.223%。贝叶斯方法得到的期望杂合度(Hj)为0.256。与李属和其他具有相似生活史的物种相比,白杨属的遗传多样性水平较低。近似贝叶斯方法得到的近交系数(F IS)为0.767。这一数值低于既有性繁殖又无性繁殖的乌尔mus davidiana。但与其他有性繁殖的树种(Carpinus laxiflora)、黄柏(Phellodendron amurense)和伪西波槭(Acer pseudosieboldianum)相比,该值较大。AMOVA法的遗传分化值为0.245 (ΦST),贝叶斯法的遗传分化值为0.278 (θII)。与其他李属植物和具有相似生活史的李属植物相比,其遗传分化水平较高。根据UPGMA和贝叶斯聚类,将11个居群划分为2个遗传群。然而,根据地理分布,发现一些群体存在弱遗传结构。这是由于森林演替、适应当地环境变化的无性繁殖策略以及人口干扰导致的种群破碎化导致的基因流动逐渐减少等原因造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic diversity and structure of Prunus padus populations in South Korea based on AFLP markers
Abstract We applied seven pairs of primer-restriction enzyme combinations to investigate the genetic diversity, genetic differentiation, and genetic structure of Prunus padus populations with AFLP markers. The values obtained for average of effective alleles (A e), percentage of polymorphic loci (%P), Shannon’s diversity index (I), and expected heterozygosity (H e) were 1.38, 81.4, 0.357, and 0.223%, respectively. The expected heterozygosity (Hj) obtained by using a Bayesian method was 0.256. The level of genetic diversity obtained for P. padus was low compared to that of Prunus species and other species with a similar life history. The inbreeding coefficient (F IS) from the approximated Bayesian method was 0.767. This value was lower than that obtained for Ulmus davidiana, which undergoes both sexual and asexual reproduction. However, the value obtained was larger than that for other species that undergo sexual reproduction, such as, Carpinus laxiflora, Phellodendron amurense, and Acer pseudosieboldianum. The value of genetic differentiation was 0.245 from AMOVA (ΦST) and 0.278 from Bayesian method (θII). The obtained level of genetic differentiation was large compared to that of other Prunus species plants and other species with a similar life history. According to UPGMA and Bayesian clustering, 11 populations were divided into two genetic groups. However, some populations were detected as weak genetic structures according to the geographical distribution. It was occurred by forest succession, asexual propagation strategies to adapt local environmental change, and gene flow being gradually decreased due to population fragmentation by demographic disturbances.
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来源期刊
CiteScore
3.30
自引率
5.30%
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0
审稿时长
21 weeks
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