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大西洋鲱(Clupea harengus)种群结构的微卫星DNA分析,并与等位酶和线粒体DNA限制性片段长度多态性分析进行直接比较。

Microsatellite DNA analysis of population structure in Atlantic herring (Clupea harengus), with direct comparison to allozyme and mtDNA RFLP analyses.

作者信息

Shaw P W, Turan C, Wright J M, O'Connell M, Carvalho G R

机构信息

Molecular Ecology & Fisheries Genetics Laboratory, Department of Biological Sciences, University of Hull, Hull HU6 7RX, U.K.

出版信息

Heredity (Edinb). 1999 Oct;83 ( Pt 4):490-9. doi: 10.1038/sj.hdy.6885860.

Abstract

Previous attempts to test for small-scale stock structuring within Atlantic herring (Clupea harengus L.) with molecular markers have been hampered by uninformative levels of genetic variation. Here we report the first application of microsatellite DNA markers to investigate population subdivision in Atlantic herring from Norwegian waters and the Barents Sea, and also examine microsatellite differentiation between C. harengus and Pacific herring (C. pallasi). Results from four microsatellite loci indicate high, and informative, variation compared to molecular markers used previously: number of alleles per locus=18-41; mean expected heterozygosity within samples=0.90-0.93. Significant genetic differences were detected between almost all samples representing postulated Icelandic summer-spawner, Norwegian spring-spawner and Norwegian fjord stocks, using Fisher's exact test, FST and RST values. Levels of allele frequency differentiation between Atlantic and Pacific herring overlapped the range seen among Atlantic herring samples, indicating that microsatellites are poor indicators of the degree of species differentiation. Comparison with allozyme and mitochondrial DNA restriction fragment length polymorphism (RFLP) datasets from the same samples suggests that microsatellites may detect structuring at a finer scale, but are less informative at larger scales of divergence.

摘要

以往利用分子标记检测大西洋鲱(Clupea harengus L.)小规模种群结构的尝试,因遗传变异信息不足而受阻。在此,我们报告首次应用微卫星DNA标记来研究挪威海域和巴伦支海大西洋鲱的种群细分情况,并检验大西洋鲱与太平洋鲱(C. pallasi)之间的微卫星分化。来自四个微卫星位点的结果表明,与先前使用的分子标记相比,其变异程度高且信息丰富:每个位点的等位基因数 = 18 - 41;样本内的平均期望杂合度 = 0.90 - 0.93。使用费希尔精确检验、FST和RST值,在几乎所有代表假定的冰岛夏季产卵群体、挪威春季产卵群体和挪威峡湾种群的样本之间检测到显著的遗传差异。大西洋鲱和太平洋鲱之间的等位基因频率分化水平与大西洋鲱样本之间的分化范围重叠,这表明微卫星对于物种分化程度来说是较差的指标。与来自相同样本的同工酶和线粒体DNA限制性片段长度多态性(RFLP)数据集的比较表明,微卫星可能在更精细的尺度上检测到种群结构,但在更大的分化尺度上信息量较少。

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