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微卫星DNA标记分析野生鲤鱼群体的遗传多样性
引用本文:李大宇,康大海,殷倩茜,孙效文,梁利群.微卫星DNA标记分析野生鲤鱼群体的遗传多样性[J].遗传学报,2007,34(11):984-993.
作者姓名:李大宇  康大海  殷倩茜  孙效文  梁利群
作者单位:1. 黑龙江水产研究所北方鱼类生物工程育种重点开放实验室,哈尔滨,150070;大连水产学院生命科学与技术学院,大连,116023
2. 大连水产学院生命科学与技术学院,大连,116023
3. 黑龙江水产研究所北方鱼类生物工程育种重点开放实验室,哈尔滨,150070
基金项目:国家重点基础研究发展计划(973计划);教育部科学技术研究项目
摘    要:利用30个微卫星分子标记对海南鲤(HN)、长江鲤(CY)、月亮湖鲤(YL)、黑龙江鲤(FY)、呼伦湖鲤(ZL)、贝尔湖鲤(BR)6个野生鲤鱼群体的观测杂合度(Ho)、期望杂合度(He)、多态信息含量(PIC)和有效等位基因数(Ae)等进行了遗传检测,根据基因频率计算遗传相似系数和Nei氏标准遗传距离,χ2检验估计Hardy-Weinberg平衡,用近交系数(FST)和基因流(Nm)分析群体的遗传分化及其来源。同时,使用PHYLIP3.63软件绘制基于Nei氏标准遗传距离的UPGMA进化树。6个群体共检测到8,136个扩增片段,长度在125bp~414bp,30个基因座扩增出等位基因数从3~13个不等,共计210个等位基因,平均每个基因座扩增得到7个等位基因。结果显示:(1)6个野鲤群体的多态性指标均适中,多态信息含量依次0.44、0.52、0.53、0.57、0.63和0.64,有效等位基因数1.04~4.72个不等,平均有效等位基因数依次为2.19、2.60、2.42、2.43、2.45和2.33,无偏期望杂合度平均值为0.50、0.59、0.56、0.56、0.57和0.54;(2)遗传相似系数BR与ZL最高(0.8511),BR与HN最低(0.6688),聚类结果与地理分布呈一定相关性。

关 键 词:分子标记  微卫星  群体多样性  鲤鱼
修稿时间:2007-01-11

Microsatellite DNA Marker Analysis of Genetic Diversity in Wild Common Carp (Cyprinus carpio L.) Populations
Dayu Li,Dahai Kang,Qianqian Yin,Xiaowen Sun,Liqun Liang.Microsatellite DNA Marker Analysis of Genetic Diversity in Wild Common Carp (Cyprinus carpio L.) Populations[J].Journal of Genetics and Genomics,2007,34(11):984-993.
Authors:Dayu Li  Dahai Kang  Qianqian Yin  Xiaowen Sun  Liqun Liang
Institution:1. Heilongjiang Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China; 2. College of Aqua-life Science and Technology, Dalian Fisheries University, Dalian 116023, China
Abstract:Thirty microsatellite loci were used for analyzing six wild populations of common carp (Cyprinus carpio L.). Observed (H(o)) and expected (H(e)) heterozygosity values, polymorphic information content (PIC), and number of effective alleles (A(e)) were all detected. Genetic similarity index and genetic distance were computed based on the allele frequency. The Hardy-Weinberg Equilibrium was checked according to the test of chi2. Genetic differentiation and hierarchical partition of genetic diversity were evaluated by F(ST) and N(m). A clustering dendrogram was made based on the results of UPGMA methods using the PHYLIP software package (version 3.63). There were totally 8,136 fragments ranging from 125 bp to 414 bp in length. Three to thirteen alleles were amplified in 30 loci and 210 alleles in all six populations. The average number of alleles in each locus was seven. The result showed that 1) the level of genetic variability was moderate in the six populations. Polymorphic information contents of the six wild common carp populations were 0.44, 0.52, 0.53, 0.57, 0.63, and 0.64 respectively. Effective alleles were from 1.04 to 4.72, the average numbers in each population were 2.19, 2.60, 2.42, 2.43, 2.45, and 2.33. The average expected heterozygosity values were 0.50, 0.59, 0.56, 0.56, 0.57, and 0.54 respectively; 2) the highest genetic similarity index that came from the populations of BR and ZL was 0.8511 and the lowest index was 0.6688, and it came from the populations of BR and HN. There was a correlation between the clustering result and the geographical distribution.
Keywords:molecular marker  microsatellite  population variety  common carp
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