Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY 14850, USA.
Proc Natl Acad Sci U S A. 2010 May 11;107 Suppl 2(Suppl 2):8954-61. doi: 10.1073/pnas.0914618107. Epub 2010 May 5.
Hispanic/Latino populations possess a complex genetic structure that reflects recent admixture among and potentially ancient substructure within Native American, European, and West African source populations. Here, we quantify genome-wide patterns of SNP and haplotype variation among 100 individuals with ancestry from Ecuador, Colombia, Puerto Rico, and the Dominican Republic genotyped on the Illumina 610-Quad arrays and 112 Mexicans genotyped on Affymetrix 500K platform. Intersecting these data with previously collected high-density SNP data from 4,305 individuals, we use principal component analysis and clustering methods FRAPPE and STRUCTURE to investigate genome-wide patterns of African, European, and Native American population structure within and among Hispanic/Latino populations. Comparing autosomal, X and Y chromosome, and mtDNA variation, we find evidence of a significant sex bias in admixture proportions consistent with disproportionate contribution of European male and Native American female ancestry to present-day populations. We also find that patterns of linkage-disequilibria in admixed Hispanic/Latino populations are largely affected by the admixture dynamics of the populations, with faster decay of LD in populations of higher African ancestry. Finally, using the locus-specific ancestry inference method LAMP, we reconstruct fine-scale chromosomal patterns of admixture. We document moderate power to differentiate among potential subcontinental source populations within the Native American, European, and African segments of the admixed Hispanic/Latino genomes. Our results suggest future genome-wide association scans in Hispanic/Latino populations may require correction for local genomic ancestry at a subcontinental scale when associating differences in the genome with disease risk, progression, and drug efficacy, as well as for admixture mapping.
西班牙裔/拉丁裔人群具有复杂的遗传结构,反映了美洲原住民、欧洲和西非来源人群之间的近期混合,以及潜在的古老亚结构。在这里,我们对来自厄瓜多尔、哥伦比亚、波多黎各和多米尼加共和国的 100 个人进行了全基因组 SNP 和单倍型变异的量化分析,这些人是用 Illumina 610-Quad 芯片和 Affymetrix 500K 平台对 112 名墨西哥人进行了基因分型。将这些数据与先前从 4305 个人收集的高密度 SNP 数据相交,我们使用主成分分析和聚类方法 FRAPPE 和 STRUCTURE 来研究西班牙裔/拉丁裔人群内部和之间的非洲、欧洲和美洲原住民人口结构的全基因组模式。比较常染色体、X 和 Y 染色体以及 mtDNA 变异,我们发现有证据表明混合比例存在显著的性别偏差,这与欧洲男性和美洲原住民女性祖先对现代人群的不成比例的贡献一致。我们还发现,混合西班牙裔/拉丁裔人群中的连锁不平衡模式主要受到人群混合动态的影响,具有较高非洲祖先的人群中 LD 的衰减速度更快。最后,使用基于位点的祖先推断方法 LAMP,我们重建了混合西班牙裔/拉丁裔人群中混合的精细染色体模式。我们记录了在混合西班牙裔/拉丁裔基因组的美洲原住民、欧洲和非洲部分内区分潜在的次大陆来源人群的适度能力。我们的研究结果表明,在与疾病风险、进展和药物疗效相关的全基因组关联扫描中,未来可能需要在次大陆范围内对西班牙裔/拉丁裔人群的全基因组进行校正,以纠正局部基因组祖先,同时还需要进行混合映射。