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首页> 外文期刊>Genome Biology and Evolution >Impact of Mutation Rate and Selection at Linked Sites on DNA Variation across the Genomes of Humans and Other Homininae
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Impact of Mutation Rate and Selection at Linked Sites on DNA Variation across the Genomes of Humans and Other Homininae

机译:突变率和选择在人类和其他Hominina的基因组中DNA变异的关联网站的影响

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DNA diversity varies across the genome of many species. Variation in diversity across a genome might arise from regional variation in the mutation rate, variation in the intensity and mode of natural selection, and regional variation in the recombination rate. We show that both noncoding and nonsynonymous diversity are positively correlated to a measure of the mutation rate and the recombination rate and negatively correlated to the density of conserved sequences in 50?kb windows across the genomes of humans and nonhuman homininae. Interestingly, we find that although noncoding diversity is equally affected by these three genomic variables, nonsynonymous diversity is mostly dominated by the density of conserved sequences. The positive correlation between diversity and our measure of the mutation rate seems to be largely a direct consequence of regions with higher mutation rates having more diversity. However, the positive correlation with recombination rate and the negative correlation with the density of conserved sequences suggest that selection at linked sites also affect levels of diversity. This is supported by the observation that the ratio of the number of nonsynonymous to noncoding polymorphisms is negatively correlated to a measure of the effective population size across the genome. We show these patterns persist even when we restrict our analysis to GC-conservative mutations, demonstrating that the patterns are not driven by GC biased gene conversion. In conclusion, our comparative analyses describe how recombination rate, gene density, and mutation rate interact to produce the patterns of DNA diversity that we observe along the hominine genomes.
机译:DNA多样性在许多物种的基因组上变化。在基因组上的多样性变化可能从突变率的区域变异,自然选择的强度和模式的变化以及重组率的区域变化。我们表明,非编码和非同义多样性都与突变率和重组率的量度呈正相关,并且与跨越人类和非人均原始内突的50μlkB窗口中的保守序列的密度负相关。有趣的是,我们发现,尽管非编码的多样性同样受到这三个基因组变量的同样影响,但不合适的多样性主要由保守序列的密度主导。多样性与我们的突变率之间的正相关性似乎主要是具有更高突变率具有更多多样性的区域的直接后果。然而,与重组率的正相关和与保守序列密度的负相关表明,联系地点的选择也影响了多样性的水平。这是通过观察结果来支持,即非偶数与非编码多态性的数量的比率与基因组中有效种群大小的量度负相关。我们展示了这些模式仍然存在,即使我们将分析限制对GC保守突变,表明模式不受GC偏置基因转化的驱动。总之,我们的对比分析描述了复合率,基因密度和突变率如何相互作用,从而产生我们观察沿着同源基因组的DNA多样性。

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