Schroeder Kari B, Jakobsson Mattias, Crawford Michael H, Schurr Theodore G, Boca Simina M, Conrad Donald F, Tito Raul Y, Osipova Ludmilla P, Tarskaia Larissa A, Zhadanov Sergey I, Wall Jeffrey D, Pritchard Jonathan K, Malhi Ripan S, Smith David G, Rosenberg Noah A
Department of Anthropology, University of California, Davis, CA, USA.
Mol Biol Evol. 2009 May;26(5):995-1016. doi: 10.1093/molbev/msp024. Epub 2009 Feb 12.
Recently, the observation of a high-frequency private allele, the 9-repeat allele at microsatellite D9S1120, in all sampled Native American and Western Beringian populations has been interpreted as evidence that all modern Native Americans descend primarily from a single founding population. However, this inference assumed that all copies of the 9-repeat allele were identical by descent and that the geographic distribution of this allele had not been influenced by natural selection. To investigate whether these assumptions are satisfied, we genotyped 34 single nucleotide polymorphisms across approximately 500 kilobases (kb) around D9S1120 in 21 Native American and Western Beringian populations and 54 other worldwide populations. All chromosomes with the 9-repeat allele share the same haplotypic background in the vicinity of D9S1120, suggesting that all sampled copies of the 9-repeat allele are identical by descent. Ninety-one percent of these chromosomes share the same 76.26 kb haplotype, which we call the "American Modal Haplotype" (AMH). Three observations lead us to conclude that the high frequency and widespread distribution of the 9-repeat allele are unlikely to be the result of positive selection: 1) aside from its association with the 9-repeat allele, the AMH does not have a high frequency in the Americas, 2) the AMH is not unusually long for its frequency compared with other haplotypes in the Americas, and 3) in Latin American mestizo populations, the proportion of Native American ancestry at D9S1120 is not unusual compared with that observed at other genomewide microsatellites. Using a new method for estimating the time to the most recent common ancestor (MRCA) of all sampled copies of an allele on the basis of an estimate of the length of the genealogy descended from the MRCA, we calculate the mean time to the MRCA of the 9-repeat allele to be between 7,325 and 39,900 years, depending on the demographic model used. The results support the hypothesis that all modern Native Americans and Western Beringians trace a large portion of their ancestry to a single founding population that may have been isolated from other Asian populations prior to expanding into the Americas.
最近,在所有抽样的美洲原住民和白令海峡西部人群中观察到一个高频私有等位基因,即微卫星D9S1120处的9重复等位基因,这被解释为所有现代美洲原住民主要源自单一奠基人群的证据。然而,这一推断假定9重复等位基因的所有拷贝都是同源的,并且该等位基因的地理分布未受自然选择的影响。为了研究这些假设是否成立,我们对21个美洲原住民和白令海峡西部人群以及54个其他全球人群中D9S1120周围约500千碱基(kb)范围内的34个单核苷酸多态性进行了基因分型。所有携带9重复等位基因的染色体在D9S1120附近共享相同的单倍型背景,这表明9重复等位基因的所有抽样拷贝都是同源的。这些染色体中有91%共享相同的76.26 kb单倍型,我们将其称为“美洲模式单倍型”(AMH)。三项观察结果使我们得出结论,9重复等位基因的高频和广泛分布不太可能是正选择的结果:1)除了与9重复等位基因相关外,AMH在美洲的频率并不高;2)与美洲的其他单倍型相比,AMH的长度与其频率相比并无异常;3)在拉丁美洲混血人群中,D9S1120处美洲原住民血统的比例与在全基因组其他微卫星处观察到的比例并无异常。使用一种基于从最近共同祖先(MRCA)衍生的谱系长度估计来估计等位基因所有抽样拷贝的最近共同祖先时间(MRCA)的新方法,我们计算出9重复等位基因的MRCA平均时间在7325年至39900年之间,具体取决于所使用的人口模型。结果支持了这样一种假设,即所有现代美洲原住民和白令海峡西部人群的大部分血统都可追溯到一个单一的奠基人群,该人群在扩展到美洲之前可能已与其他亚洲人群隔离。