基于mtDNA控制区的陕西秦岭青鲑科短爪菌种群系统地理结构研究

Mitochondrial Dna Pub Date : 2015-08-01 Epub Date: 2014-01-10 DOI:10.3109/19401736.2013.865168
Haixia Liu, Yang Li, Xiaolin Liu, Dongmei Xiong, Lixin Wang, Guiwei Zou, Qiwei Wei
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引用次数: 16

摘要

秦岭短蛸(Brachymystax lenok tsinlingensis)是一种分布于中国秦岭山区的濒危淡水鱼。本研究通过mtDNA控制区(D-loop)的比较研究,分析了TB、YX、LX和ZZ 4个种群53个个体的自然种群结构和遗传多样性。序列分析显示了三个不同的结构域和两个控制区的特征序列。单倍型和核苷酸多样性分别为9和0.0023。遗传结构分析表明,该品种具有较高的遗传多样性(h = 0.6060±0.1499)。AMOVA分析表明,总变异的26.02%来自个体群体,73.98%来自4个地理群体内的变异,表明4个地理群体之间的遗传分化程度较低。中性进化和错配分布的检验表明,这些种群在历史上没有发生过扩张。高遗传多样性和低遗传分化将为该物种的保护和开发利用提供新的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phylogeographic structure of Brachymystax lenok tsinlingensis (Salmonidae) populations in the Qinling Mountains, Shaanxi, based on mtDNA control region.

Brachymystax lenok tsinlingensis is an endangered freshwater fish and distributed in mountains steams of Qinling Mountains, China. In this study, a comparative study of the mtDNA control region (D-loop) was performed to analyze its natural population structure and the genetic diversity of 53 individuals from four locations (TB, YX, LX and ZZ populations). Sequence analysis revealed three different domains and two feature sequences of the control region. The estimated haplotype and nucleotide diversity were 9 and 0.0023, respectively. Genetic structure analysis showed a high-level genetic diversity of B. lenok tisnlingensis (h = 0.6060 ± 0.1499). The AMOVA analysis indicated that 26.02% of total variation came from individual populations, and 73.98% from variation within the four geographic populations, which showed low genetic differentiation between the four geographic groups. Test of neutral evolution and mismatch distribution indicated that no historical expansion occurred in these populations. The high genetic diversity and low genetic differentiation would provide new information for conservation and exploitation of this species.

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来源期刊
Mitochondrial Dna
Mitochondrial Dna 生物-遗传学
自引率
0.00%
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0
审稿时长
2.4 months
期刊介绍: Previously published under the title DNA Sequence (Vols 1-19.3), Mitochondrial DNA accepts original high-quality reports based on mapping, sequencing and analysis of mitochondrial DNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The editorial board will also consider manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences.
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