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利用ISSR标记对中国特有濒危植物岷江柏木进行保护遗传学研究。

A study of conservation genetics in Cupressus chengiana, an endangered endemic of China, using ISSR markers.

作者信息

Hao Bingqing, Li Wang, Linchun Mu, Li Yao, Rui Zhang, Mingxia Tang, Weikai Bao

机构信息

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, P. R. China.

出版信息

Biochem Genet. 2006 Feb;44(1-2):31-45. doi: 10.1007/s10528-006-9011-8. Epub 2006 May 3.

DOI:10.1007/s10528-006-9011-8
PMID:16670947
Abstract

ISSR markers were used to analyze the genetic diversity and genetic structure of eight natural populations of Cupressus chengiana in China. ISSR analysis using 10 primers was carried out on 92 different samples. At the species level, 136 polymorphic loci were detected. The percentage of polymorphic bands (PPB) was 99%. Genetic diversity (He) was 0.3120, effective number of alleles (Ae) was 1.5236, and Shannon's information index (I) was 0.4740. At the population level, PPB = 48%, Ae = 1.2774, He = 0.1631, and I = 0.2452. Genetic differentiation (Gst) detected by Nei's genetic diversity analysis suggested 48% occurred among populations. The partitioning of molecular variance by AMOVA analysis indicated significant genetic differentiation within populations (54%) and among populations (46%; P < 0.0003). The average number of individuals exchanged between populations per generation (Nm) was 0.5436. Samples from the same population clustered in the same population-specific cluster, and two groups of Sichuan and Gansu populations were distinguishable. A significantly positive correlation between genetic and geographic distance was detected (r = 0.6701). Human impacts were considered one of the main factors to cause the rarity of C. chengiana, and conservation strategies are suggested based on the genetic characters and field investigation, e.g., protection of wild populations, reestablishment of germplasm bank, and reintroduction of more genetic diversity.

摘要

利用ISSR标记分析了中国岷江柏木8个天然种群的遗传多样性和遗传结构。使用10条引物对92个不同样本进行了ISSR分析。在物种水平上,检测到136个多态性位点。多态性条带百分比(PPB)为99%。遗传多样性(He)为0.3120,有效等位基因数(Ae)为1.5236,香农信息指数(I)为0.4740。在种群水平上,PPB = 48%,Ae = 1.2774,He = 0.1631,I = 0.2452。通过Nei氏遗传多样性分析检测到的遗传分化(Gst)表明,48%的遗传分化发生在种群之间。AMOVA分析的分子方差划分表明,种群内(54%)和种群间(46%;P < 0.0003)存在显著的遗传分化。每代种群间交换的个体平均数量(Nm)为0.5436。来自同一种群的样本聚集在同一个种群特异性聚类中,四川和甘肃种群的两组样本可区分。检测到遗传距离与地理距离之间存在显著的正相关(r = 0.6701)。人为影响被认为是导致岷江柏木珍稀的主要因素之一,并根据遗传特征和实地调查提出了保护策略,例如保护野生种群、重建种质库以及引入更多遗传多样性进行再引入。

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