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首页> 外文期刊>Molecular Biology Reports >Population genetic structure and phylogeography of cyprinid fish, Labeo dero (Hamilton, 1822) inferred from allozyme and microsatellite DNA marker analysis
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Population genetic structure and phylogeography of cyprinid fish, Labeo dero (Hamilton, 1822) inferred from allozyme and microsatellite DNA marker analysis

机译:从异源酶和微卫星DNA标记分析推断出塞浦路斯鲤科鱼类Labeo dero(汉密尔顿,1822年)的种群遗传结构和系统地理学

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摘要

We examined population structure of Labeo dero (Hamilton, 1822) from different riverine locations in India using 10 polymorphic allozyme and eight microsatellite loci. For analysis, 591 different tissue samples were obtained from commercial catches covering a wide geographic range. Allozyme variability (An = 1.28–1.43, Ho = 0.029–0.071) was much lower than for microsatellites (An = 4.625–6.125, Ho = 0.538–0.633). Existence of rare alleles was found at three allozyme (MDH-2*, GPI* and PGDH*) and at two microsatellite loci (R-3* and MFW-15*). Deviation from Hardy–Weinberg equilibrium (P < 0.05, after the critical probability levels were adjusted for sequential Bonferroni adjustment) could be detected at three loci (EST-1*, -2* and XDH*) whereas, after correction for null alleles, two microsatellite loci (MFW-1*,-15*) deviated from HWE in the river Yamuna. Fst for all the samples combined over all allozyme loci was found to be 0.059 suggesting that 5.9% of the total variation was due to genetic differentiation while microsatellite analysis yielded 0.019 which was concordant to mean Rst (0.02). Hierarchical partition of genetic diversity (AMOVA) showed that greater variability (approx. 95%) was due to within population component than between geographical regions. Based on distribution of genetic differentiation detected by both markers, at least five different genetic stocks of L. dero across its natural distribution could be identified. These results are useful for the evaluation and conservation of L. dero in natural water bodies.
机译:我们使用10个多态同工酶和8个微卫星基因座,研究了印度不同河流地区的Labeo dero(汉密尔顿,1822年)的种群结构。为了进行分析,从覆盖广泛地理范围的商业捕获物中获得了591种不同的组织样本。同工酶变异性(An = 1.28–1.43,Ho = 0.029–0.071)远低于微卫星(An = 4.625–6.125,Ho = 0.538–0.633)。在三个同工酶(MDH-2 *,GPI *和PGDH *)和两个微卫星基因座(R-3 *和MFW-15 *)处发现了稀有等位基因的存在。在三个位点(EST-1 *,-2 *和XDH *)可以检测到与Hardy-Weinberg平衡的偏差(P <0.05,在对关键概率水平进行了连续Bonferroni调整之后),而在校正了无效等位基因之后,在亚穆纳河上从HWE偏离的两个微卫星基因座(MFW-1 *,-15 *)。发现所有样本中所有同工酶基因座的组合的Fst为0.059,表明总变异的5.9%是由于遗传分化,而微卫星分析得出的0.019与平均值Rst(0.02)相一致。遗传多样性的分层划分(AMOVA)显示,与地理区域之间的差异相比,归因于人口内部的差异更大(大约95%)。基于两种标记物检测到的遗传分化的分布,可以确定德罗氏乳杆菌在其自然分布中至少有五种不同的遗传种群。这些结果对于天然水体中德氏乳杆菌的评估和保护是有用的。

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