Atkinson Quentin D, Gray Russell D, Drummond Alexei J
Institute of Cognitive and Evolutionary Anthropology, University of Oxford, 58A Banbury Rd, Oxford, OX2 6QS, United Kingdom.
Mol Biol Evol. 2008 Feb;25(2):468-74. doi: 10.1093/molbev/msm277. Epub 2007 Dec 18.
The relative timing and size of regional human population growth following our expansion from Africa remain unknown. Human mitochondrial DNA (mtDNA) diversity carries a legacy of our population history. Given a set of sequences, we can use coalescent theory to estimate past population size through time and draw inferences about human population history. However, recent work has challenged the validity of using mtDNA diversity to infer species population sizes. Here we use Bayesian coalescent inference methods, together with a global data set of 357 human mtDNA coding-region sequences, to infer human population sizes through time across 8 major geographic regions. Our estimates of relative population sizes show remarkable concordance with the contemporary regional distribution of humans across Africa, Eurasia, and the Americas, indicating that mtDNA diversity is a good predictor of population size in humans. Plots of population size through time show slow growth in sub-Saharan Africa beginning 143-193 kya, followed by a rapid expansion into Eurasia after the emergence of the first non-African mtDNA lineages 50-70 kya. Outside Africa, the earliest and fastest growth is inferred in Southern Asia approximately 52 kya, followed by a succession of growth phases in Northern and Central Asia (approximately 49 kya), Australia (approximately 48 kya), Europe (approximately 42 kya), the Middle East and North Africa (approximately 40 kya), New Guinea (approximately 39 kya), the Americas (approximately 18 kya), and a second expansion in Europe (approximately 10-15 kya). Comparisons of relative regional population sizes through time suggest that between approximately 45 and 20 kya most of humanity lived in Southern Asia. These findings not only support the use of mtDNA data for estimating human population size but also provide a unique picture of human prehistory and demonstrate the importance of Southern Asia to our recent evolutionary past.
自我们从非洲扩张以来,各地区人类人口增长的相对时间和规模仍然未知。人类线粒体DNA(mtDNA)多样性承载着我们人口历史的印记。给定一组序列,我们可以使用溯祖理论来估计过去不同时间的人口规模,并推断人类人口历史。然而,最近的研究对利用mtDNA多样性推断物种人口规模的有效性提出了质疑。在此,我们使用贝叶斯溯祖推断方法,结合一个包含357条人类mtDNA编码区序列的全球数据集,来推断8个主要地理区域随时间变化的人类人口规模。我们对相对人口规模的估计与当今人类在非洲、欧亚大陆和美洲的区域分布显著一致,这表明mtDNA多样性是人类人口规模的良好预测指标。随时间变化的人口规模图显示,撒哈拉以南非洲在14.3 - 19.3万年前开始缓慢增长,随后在5 - 7万年前第一批非非洲mtDNA谱系出现后迅速扩张到欧亚大陆。在非洲以外地区,最早且最快的增长推断发生在约5.2万年前的南亚,随后是中亚和北亚(约4.9万年前)、澳大利亚(约4.8万年前)、欧洲(约4.2万年前)、中东和北非(约4.0万年前)、新几内亚(约3.9万年前)、美洲(约1.8万年前)相继出现增长阶段,欧洲在约1.0 - 1.5万年前出现第二次扩张。对不同时间相对区域人口规模的比较表明,在约4.5 - 2.0万年前,大部分人类生活在南亚。这些发现不仅支持利用mtDNA数据估计人类人口规模,还提供了一幅独特的人类史前史图景,并证明了南亚在我们近代进化史上的重要性。