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Diversifying Selection Underlies the Origin of Allozyme Polymorphism at the Phosphoglucose Isomerase Locus in Tigriopus californicus

机译:多样化的选择奠定了加州灰熊磷酸葡萄糖异构酶基因座上同工酶多态性的起源

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摘要

The marine copepod Tigriopus californicus lives in intertidal rock pools along the Pacific coast, where it exhibits strong, temporally stable population genetic structure. Previous allozyme surveys have found high frequency private alleles among neighboring subpopulations, indicating that there is limited genetic exchange between populations. Here we evaluate the factors responsible for the diversification and maintenance of alleles at the phosphoglucose isomerase (Pgi) locus by evaluating patterns of nucleotide variation underlying previously identified allozyme polymorphism. Copepods were sampled from eleven sites throughout California and Baja California, revealing deep genetic structure among populations as well as genetic variability within populations. Evidence of recombination is limited to the sample from Pescadero and there is no support for linkage disequilibrium across the Pgi locus. Neutrality tests and codon-based models of substitution suggest the action of natural selection due to elevated non-synonymous substitutions at a small number of sites in Pgi. Two sites are identified as the charge-changing residues underlying allozyme polymorphisms in T. californicus. A reanalysis of allozyme variation at several focal populations, spanning a period of 26 years and over 200 generations, shows that Pgi alleles are maintained without notable frequency changes. Our data suggest that diversifying selection accounted for the origin of Pgi allozymes, while McDonald-Kreitman tests and the temporal stability of private allozyme alleles suggests that balancing selection may be involved in the maintenance of amino acid polymorphisms within populations.
机译:海洋co足类Tigriopus californicus生活在太平洋沿岸的潮间带岩石池中,那里展现出强大的,暂时稳定的种群遗传结构。先前的同工酶调查发现,在邻近的亚群之间存在高频私人等位基因,表明种群之间的遗传交换有限。在这里,我们通过评估先前确定的同工酶多态性背后的核苷酸变异模式,来评估负责在磷酸葡萄糖异构酶(Pgi)基因座等位基因的多样化和维持的因素。从整个加利福尼亚和下加利福尼亚州的11个地点取样了pe足类动物,揭示了种群之间的深层遗传结构以及种群内的遗传变异性。重组的证据仅限于Pescadero的样品,并且不支持整个Pgi基因座的连锁不平衡。中性测试和基于密码子的替换模型表明,由于Pgi少数位置上非同义替换的增多,自然选择的作用。在加州棉铃虫的同工酶多态性下,两个位点被确定为电荷改变残基。在长达26年的200多个世代中,对多个焦点人群的同工酶变异进行了重新分析,结果表明,维持Pgi等位基因没有明显的频率变化。我们的数据表明,多样化选择是造成Pgi等位酶起源的原因,而McDonald-Kreitman测试和私人等位基因等位基因的时间稳定性表明,平衡选择可能与种群内氨基酸多态性的维持有关。

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