Department of Genetics, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.
Genome Biol. 2009;10(12):R141. doi: 10.1186/gb-2009-10-12-r141. Epub 2009 Dec 22.
Accurate, high-throughput genotyping allows the fine characterization of genetic ancestry. Here we applied recently developed statistical and computational techniques to the question of African ancestry in African Americans by using data on more than 450,000 single-nucleotide polymorphisms (SNPs) genotyped in 94 Africans of diverse geographic origins included in the HGDP, as well as 136 African Americans and 38 European Americans participating in the Atherosclerotic Disease Vascular Function and Genetic Epidemiology (ADVANCE) study. To focus on African ancestry, we reduced the data to include only those genotypes in each African American determined statistically to be African in origin.
From cluster analysis, we found that all the African Americans are admixed in their African components of ancestry, with the majority contributions being from West and West-Central Africa, and only modest variation in these African-ancestry proportions among individuals. Furthermore, by principal components analysis, we found little evidence of genetic structure within the African component of ancestry in African Americans.
These results are consistent with historic mating patterns among African Americans that are largely uncorrelated to African ancestral origins, and they cast doubt on the general utility of mtDNA or Y-chromosome markers alone to delineate the full African ancestry of African Americans. Our results also indicate that the genetic architecture of African Americans is distinct from that of Africans, and that the greatest source of potential genetic stratification bias in case-control studies of African Americans derives from the proportion of European ancestry.
准确、高通量的基因分型可实现遗传起源的精细特征描述。在这里,我们应用了最近开发的统计和计算技术,通过对来自 HGDP 的 94 名具有不同地理起源的非洲人以及 136 名非裔美国人和 38 名欧洲裔美国人的超过 450,000 个单核苷酸多态性 (SNP) 进行基因分型的数据,来研究非裔美国人的非洲血统问题。为了专注于非洲血统,我们将数据简化为仅包括那些在统计学上确定为非洲起源的非裔美国人的基因型。
从聚类分析中,我们发现所有的非裔美国人在其非洲血统中都有混合,其中大部分来自西非和中非,而且个体之间这些非洲血统比例的变化不大。此外,通过主成分分析,我们发现非裔美国人的非洲血统中几乎没有遗传结构的证据。
这些结果与非裔美国人之间的历史交配模式一致,这些模式与非洲祖先的起源基本无关,这使得单凭线粒体 DNA 或 Y 染色体标记来描绘非裔美国人的完整非洲血统的普遍适用性受到质疑。我们的结果还表明,非裔美国人的遗传结构与非洲人不同,并且在非裔美国人病例对照研究中潜在遗传分层偏差的最大来源源自欧洲血统的比例。