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铜鱼线粒体控制区的序列变异和遗传多样性
引用本文:袁娟,张其中,李飞,朱成科,罗芬.铜鱼线粒体控制区的序列变异和遗传多样性[J].水生生物学报,2010,34(1):9.
作者姓名:袁娟  张其中  李飞  朱成科  罗芬
作者单位:1. 西南大学生命科学学院,水产科学重庆市市级重点实验室,三峡库区生态环境教育部重点实验室,重庆,400715
2. 西南大学生命科学学院,水产科学重庆市市级重点实验室,三峡库区生态环境教育部重点实验室,重庆,400715;暨南大学水生生物研究所,广州,510632
3. 西南大学生命科学学院,水产科学重庆市市级重点实验室,三峡库区生态环境教育部重点实验室,重庆,400715;第三军医大学中心实验室,重庆,400038
4. 宁德高等师范专科学院生物系,宁德,352100
基金项目:重庆市重大科技攻关项,三峡库区生态环境教育部重点实验室基金 
摘    要:采用PCR和DNA测序技术研究长江中上游野生铜鱼的遗传多样性和群体遗传学特征,从9个采样点共获得100尾铜鱼,用于分析的线粒体DNA控制区的片段序列为946bp。在100个序列中,共检测出变异位点47个(其中增添/缺失位点8个),单倍型41种。9个地理群体的平均单倍型多样性(Hd)和平均核苷酸多样性(Pi)分别为0.9257±0.0162和0.004178±0.002337,表现出较贫乏的遗传多样性。群体间的分化指数(FST值)、平均基因流(Nm)、分子方差分析(AMOVA)和平均K2-P遗传距离均表明9个铜鱼地理群体间存在广泛的基因交流,未明显发生群体遗传分化。另外,共享单倍型比例较高,约为34%(14/41)。单倍型的UPGMA分子系统树和简约网络图显示单倍型的聚类与地理分群没有相关性。上述结果表明9个铜鱼地理群体属于同一种群。

关 键 词:枯草芽孢杆菌B115  抗菌物质  分离纯化  理化特性  铜鱼  线粒体控制区  遗传多样性

MtDNA CONTROL REGION SEQUENCE VARIATION AND GENETIC DIVERSITY OF COREIUS HETERODON(BLEEKER) IN THE UPPER AND MIDDLE SECTIONS OF THE YANGTZE RIVER
YUAN Juan,ZHANG Qi-Zhong,LI Fei,ZHU Cheng-Ke,LUO Fen.MtDNA CONTROL REGION SEQUENCE VARIATION AND GENETIC DIVERSITY OF COREIUS HETERODON(BLEEKER) IN THE UPPER AND MIDDLE SECTIONS OF THE YANGTZE RIVER[J].Acta Hydrobiologica Sinica,2010,34(1):9.
Authors:YUAN Juan  ZHANG Qi-Zhong  LI Fei  ZHU Cheng-Ke  LUO Fen
Institution:YUAN Juan1,ZHANG Qi-Zhong1,2,LI Fei1,3,ZHU Cheng-Ke1 , LUO Fen4(1.Key laboratory Eco-environments in Three Gorges Reservoir Region(Ministry of Education),Key laboratory of Aquatic science of Chongqing,School of Life Sciences,Southwest University,Chongqing 400715,China,2.Hydrobiology Institute of Jinan University,Guangzhou 510632,3.Central Laboratory of Third Military Medical University,Chongqing 400038,4.Biology Department,Ningde Teachers College,Fujian 352100,China)
Abstract:Brass gudgeon (Coreius heterodon) is an endemic species in China, and mainly distributes in the upper and middle sections of the Yangtze River. The fish population has been greatly decreased these years due to various factors, such as destruction of spawning condition, water pollution, over exploitation and so on. In order to protect the fish population, it is necessary to study genetic diversity of the fish population. The fish specimens were collected from 9 sampling locations in the upper and middle sections of the Yangtze River, i. e., Hechuan (HC), Mudong (MD), Fuling (FL), Wanzhou (WZ), Wushan (WS), Sandouping (SDP), Yichang (YC), Yueyang (YY) and Jinkou (JK). The specimen number was in Tab. 1. The mitochondrial D-loop region (control region) of the fish was amplified by polymerase chain reaction (PCR) technology and sequenced with ABI 3730 sequencer. 100 sequences were analyzed using some softwares, viz., Clustal X 1.83, MEGA 3.1, DnaSP 4.50.3 and Arlequin v3.01. The results were as follows: Every specimen sequence was 946 bp for genetic diversity analysis of the fish. Both 47 mutations of nucleotide acids including 8 inserting or deleting ones and 41 haplotypes were found in the 100 sequences. About 34% of the 41 haplotypes presented at least in two or more geographic groups and every one of 27 haplotypes just appeared in single one of the 9 groups. The UPGMA tree and the Parsimony network of 41 haplotypes showed that the clustering of haplotypes did not correspond to every geographic group of the fish. Genetic structure analysis showed a low level genetic diversity of C. heterodon (Hd=0.9257±0.0162, Pi=0.004178±0.002337). The AMOVA analysis indicated that 99.66% of the total variation in D-loop region sequence came from nucleotide acid mutations of the fish individuals in the 9 geographic populations, and just 0.34% from variation between the 9 geographic populations, which showed little genetic differentiation between the 9 geographic groups. Meanwhile, average Kimura 2-parameter distances (Tab. 6), the FST value (Tab. 4) and Nm value (20.84) also revealed little genetic differentiation between the 9 geographic groups. All the data mentioned above indicated that the 9 geographic groups belonged to single nature population.
Keywords:Coreius heterodon (Bleeker)  Mitochondrial DNA D-loop region  Genetic diversity
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