Genetic variation in wild and hatchery population of Catla catla (Hamilton, 1822) analyzed through mtDNA cytochrome b region

IF 1.1 4区生物学 Q4 GENETICS & HEREDITY

Mitochondrial Dna Part a Pub Date : 2018-01-02 DOI:10.1080/24701394.2016.1253072

B. Behera, S. Kunal, V. Baisvar, D. Meena, D. Panda, S. Pakrashi, P. Paria, P. Das, D. Debnath, P. Parida, B. Das, J. Jena

引用次数: 7

Abstract

Abstract Catla (Catla catla) is a one of the most harvested Indian major carps and is widely cultured fish species in Indian subcontinent. In the present study, genetic variability between hatchery and wild stocks of Catla was surveyed using sequence data of mitochondrial DNA of partial 307 bp of cytochrome b region. A total of 174 Catla individuals were examined from three different river basins and hatcheries. Significant genetic heterogeneity was observed for the sequence data (FST = 0.308, p ≤ 0.001). However, analysis of molecular variance (AMOVA) resulted in insignificant genetic differentiation among the samples of three rivers and culture zones (FCT = −0.10, p = 0.44). The result suggested a significant genetic variation within different riverine system, low genetic differentiation among samples from river basins and a lack of genetic variation in hatchery populations.

查看原文本刊更多论文

利用mtDNA细胞色素b区分析了Catla Catla (Hamilton, 1822)野生种群和孵化场种群的遗传变异

鲶鱼(Catla Catla)是印度次大陆上收获最多的主要鲤鱼之一，是印度次大陆上广泛养殖的鱼类。利用细胞色素b区部分307bp的线粒体DNA序列数据，对孵化场和野生种群间的遗传变异进行了研究。在三个不同的河流流域和孵化场共检测了174只卡特拉个体。序列数据存在显著的遗传异质性(FST = 0.308, p≤0.001)。然而，分子方差分析(AMOVA)结果显示，三河和养殖区样品的遗传分化不显著(FCT = - 0.10, p = 0.44)。结果表明，不同水系间遗传差异较大，不同流域间遗传分化程度较低，孵化场种群间遗传差异不大。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Mitochondrial Dna Part a Biochemistry, Genetics and Molecular Biology-Genetics

CiteScore

3.00

自引率

0.00%

发文量

期刊介绍： Mitochondrial DNA Part A publishes original high-quality manuscripts on physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism, and/or interactions. Manuscripts on cytosolic and extracellular mtDNA, and on dysfunction caused by alterations in mtDNA integrity as well as methodological papers detailing novel approaches for mtDNA manipulation in vitro and in vivo are welcome. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The Journal also considers manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences, as well as papers that discuss the utility of mitochondrial DNA information in medical studies and in human evolutionary biology.