Lippold Sebastian, Xu Hongyang, Ko Albert, Li Mingkun, Renaud Gabriel, Butthof Anne, Schröder Roland, Stoneking Mark
Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, Leipzig D04103, Germany.
Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, Leipzig D04103, Germany ; Department of Computational Genetics, CAS-MPG Partner Institute for Computational Biology, Shanghai 200031, China.
Investig Genet. 2014 Sep 24;5:13. doi: 10.1186/2041-2223-5-13. eCollection 2014.
Comparisons of maternally-inherited mitochondrial DNA (mtDNA) and paternally-inherited non-recombining Y chromosome (NRY) variation have provided important insights into the impact of sex-biased processes (such as migration, residence pattern, and so on) on human genetic variation. However, such comparisons have been limited by the different molecular methods typically used to assay mtDNA and NRY variation (for example, sequencing hypervariable segments of the control region for mtDNA vs. genotyping SNPs and/or STR loci for the NRY). Here, we report a simple capture array method to enrich Illumina sequencing libraries for approximately 500 kb of NRY sequence, which we use to generate NRY sequences from 623 males from 51 populations in the CEPH Human Genome Diversity Panel (HGDP). We also obtained complete mtDNA genome sequences from the same individuals, allowing us to compare maternal and paternal histories free of any ascertainment bias.
We identified 2,228 SNPs in the NRY sequences and 2,163 SNPs in the mtDNA sequences. Our results confirm the controversial assertion that genetic differences between human populations on a global scale are bigger for the NRY than for mtDNA, although the differences are not as large as previously suggested. More importantly, we find substantial regional variation in patterns of mtDNA versus NRY variation. Model-based simulations indicate very small ancestral effective population sizes (<100) for the out-of-Africa migration as well as for many human populations. We also find that the ratio of female effective population size to male effective population size (Nf/Nm) has been greater than one throughout the history of modern humans, and has recently increased due to faster growth in Nf than Nm.
The NRY and mtDNA sequences provide new insights into the paternal and maternal histories of human populations, and the methods we introduce here should be widely applicable for further such studies.
对母系遗传的线粒体DNA(mtDNA)和父系遗传的非重组Y染色体(NRY)变异的比较,为性别偏向过程(如迁移、居住模式等)对人类遗传变异的影响提供了重要见解。然而,此类比较受到通常用于检测mtDNA和NRY变异的不同分子方法的限制(例如,对mtDNA控制区的高变段进行测序,而对NRY进行单核苷酸多态性(SNP)和/或短串联重复序列(STR)位点的基因分型)。在此,我们报告一种简单的捕获阵列方法,用于富集Illumina测序文库中约500 kb的NRY序列,我们用该方法从CEPH人类基因组多样性研究小组(HGDP)的51个群体的623名男性中生成NRY序列。我们还从相同个体中获得了完整的mtDNA基因组序列,从而使我们能够比较母系和父系历史,而不存在任何样本确定偏差。
我们在NRY序列中鉴定出2228个SNP,在mtDNA序列中鉴定出2163个SNP。我们的结果证实了一个有争议的观点,即全球范围内人类群体之间的遗传差异在NRY上比在mtDNA上更大,尽管差异没有之前认为的那么大。更重要的是,我们发现mtDNA与NRY变异模式存在显著的区域差异。基于模型的模拟表明,走出非洲的迁移以及许多人类群体的祖先有效群体大小非常小(<100)。我们还发现,在现代人类历史中,女性有效群体大小与男性有效群体大小的比率(Nf/Nm)一直大于1,并且最近由于Nf比Nm增长更快而有所增加。
NRY和mtDNA序列为人类群体的父系和母系历史提供了新的见解,我们在此介绍的方法应广泛适用于进一步的此类研究。