Department of Human Genetics, Eccles Institute of Human Genetics, University of Utah, 15 North 2030 East, Salt Lake City, UT 84112, USA.
Genome Biol. 2010;11(11):R113. doi: 10.1186/gb-2010-11-11-r113. Epub 2010 Nov 24.
Genetic studies of populations from the Indian subcontinent are of great interest because of India's large population size, complex demographic history, and unique social structure. Despite recent large-scale efforts in discovering human genetic variation, India's vast reservoir of genetic diversity remains largely unexplored.
To analyze an unbiased sample of genetic diversity in India and to investigate human migration history in Eurasia, we resequenced one 100-kb ENCODE region in 92 samples collected from three castes and one tribal group from the state of Andhra Pradesh in south India. Analyses of the four Indian populations, along with eight HapMap populations (692 samples), showed that 30% of all SNPs in the south Indian populations are not seen in HapMap populations. Several Indian populations, such as the Yadava, Mala/Madiga, and Irula, have nucleotide diversity levels as high as those of HapMap African populations. Using unbiased allele-frequency spectra, we investigated the expansion of human populations into Eurasia. The divergence time estimates among the major population groups suggest that Eurasian populations in this study diverged from Africans during the same time frame (approximately 90 to 110 thousand years ago). The divergence among different Eurasian populations occurred more than 40,000 years after their divergence with Africans.
Our results show that Indian populations harbor large amounts of genetic variation that have not been surveyed adequately by public SNP discovery efforts. Our data also support a delayed expansion hypothesis in which an ancestral Eurasian founding population remained isolated long after the out-of-Africa diaspora, before expanding throughout Eurasia.
对来自印度次大陆的人群进行遗传研究很有意义,因为印度拥有庞大的人口规模、复杂的人口历史和独特的社会结构。尽管最近在发现人类遗传变异方面做出了大规模的努力,但印度丰富的遗传多样性仍在很大程度上未被探索。
为了分析印度遗传多样性的无偏样本,并研究欧亚大陆人类迁移历史,我们对来自印度安得拉邦的三个种姓和一个部落群体的 92 个样本中的一个 100kb 的 ENCODE 区域进行了重测序。对这四个印度人群的分析,以及对 8 个 HapMap 人群(692 个样本)的分析表明,在南印度人群中,30%的 SNP 没有在 HapMap 人群中出现。一些印度人群,如雅达瓦人、马拉/马达加斯加人和伊鲁拉人,其核苷酸多样性水平与 HapMap 非洲人群一样高。利用无偏等位基因频率谱,我们研究了人类种群向欧亚大陆的扩张。主要人群群体之间的分歧时间估计表明,本研究中的欧亚人群与非洲人群在同一时间框架内(约 9 万至 11 万年前)发生分歧。不同欧亚人群之间的分歧发生在他们与非洲人分歧之后的 4 万多年。
我们的结果表明,印度人群蕴藏着大量的遗传变异,这些变异尚未被公共 SNP 发现工作充分调查。我们的数据还支持一种延迟扩张假说,即一个祖先的欧亚大陆创始人群在走出非洲的大迁徙之后很久就一直保持孤立,然后才在整个欧亚大陆扩张。