Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences.

Investigative genetics Pub Date : 2014-09-24 eCollection Date: 2014-01-01 DOI:10.1186/2041-2223-5-13
Sebastian Lippold, Hongyang Xu, Albert Ko, Mingkun Li, Gabriel Renaud, Anne Butthof, Roland Schröder, Mark Stoneking
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引用次数: 147

Abstract

Background: 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.

Results: 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.

Conclusions: 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.

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人类父系和母系的人口统计学历史:来自高分辨率Y染色体和mtDNA序列的见解。
背景:比较母系遗传的线粒体DNA (mtDNA)和父系遗传的非重组Y染色体(NRY)变异,为性别偏倚过程(如迁移、居住模式等)对人类遗传变异的影响提供了重要的见解。然而,这种比较受到通常用于测定mtDNA和NRY变异的不同分子方法的限制(例如,对mtDNA控制区的高可变片段进行测序与对NRY的snp和/或STR位点进行基因分型)。在这里,我们报告了一种简单的捕获阵列方法,以丰富Illumina测序文库,获得约500 kb的NRY序列,我们使用该文库从CEPH人类基因组多样性小组(HGDP)的51个人群中的623名男性中生成NRY序列。我们还获得了来自同一个体的完整mtDNA基因组序列,使我们能够在没有任何确定偏差的情况下比较母亲和父亲的历史。结果:在NRY序列中鉴定出2228个snp,在mtDNA序列中鉴定出2163个snp。我们的研究结果证实了一个有争议的论断,即在全球范围内,人类种群之间的NRY基因差异比mtDNA基因差异更大,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变异模式存在实质性的区域差异。结论:NRY和mtDNA序列为人类种群的父系和母系历史提供了新的见解,我们在这里介绍的方法应该广泛适用于进一步的此类研究。
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