Hellmann Ines, Prüfer Kay, Ji Hongkai, Zody Michael C, Pääbo Svante, Ptak Susan E
Max-Planck-Institute for Evolutionary Anthropology, D-04103 Leipzig, Germany.
Genome Res. 2005 Sep;15(9):1222-31. doi: 10.1101/gr.3461105.
Levels of diversity vary across the human genome. This variation is caused by two forces: differences in mutation rates and the differential impact of natural selection. Pertinent to the question of the relative importance of these two forces is the observation that both diversity within species and interspecies divergence increase with recombination rates. This suggests that mutation and recombination are either directly coupled or linked through some third factor. Here, we test these possibilities using the recently generated sequence of the chimpanzee genome and new estimates of human diversity. We find that measures of GC and CpG content, simple-repeat structures, as well as the distance from the centromeres and the telomeres predict diversity as well as divergence. After controlling for these factors, large-scale recombination rates measured from pedigrees are still significant predictors of human diversity and human-chimpanzee divergence. Furthermore, the correlation between human diversity and recombination remains significant even after controlling for human-chimpanzee divergence. Two plausible and non-mutually exclusive explanations are, first, that natural selection has shaped the patterns of diversity seen in humans and, second, that recombination rates across the genome have changed since humans and chimpanzees shared a common ancestor, so that current recombination rates are a better predictor of diversity than of divergence. Because there are indications that recombination rates may have changed rapidly during human evolution, we favor the latter explanation.
人类基因组中多样性水平各不相同。这种变异是由两种力量造成的:突变率的差异和自然选择的不同影响。与这两种力量的相对重要性问题相关的是,物种内的多样性和种间差异都随着重组率的增加而增加这一观察结果。这表明突变和重组要么直接相关,要么通过某个第三个因素联系在一起。在这里,我们使用最近生成的黑猩猩基因组序列和对人类多样性的新估计来检验这些可能性。我们发现,GC和CpG含量、简单重复结构的测量值,以及与着丝粒和端粒的距离,都能预测多样性和差异。在控制了这些因素之后,从谱系中测量的大规模重组率仍然是人类多样性和人类与黑猩猩差异的重要预测指标。此外,即使在控制了人类与黑猩猩的差异之后,人类多样性与重组之间的相关性仍然显著。有两种合理且并非相互排斥的解释,第一,自然选择塑造了人类中所见的多样性模式;第二,自从人类和黑猩猩拥有共同祖先以来,全基因组的重组率发生了变化,因此当前的重组率是多样性而非差异的更好预测指标。因为有迹象表明重组率在人类进化过程中可能迅速变化,所以我们倾向于后一种解释。