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美洲原住民的血型 O 等位基因:对美洲人群迁徙的影响。

Blood group O alleles in Native Americans: implications in the peopling of the Americas.

机构信息

Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM), Mexico City, México.

出版信息

Am J Phys Anthropol. 2010 May;142(1):85-94. doi: 10.1002/ajpa.21204.

DOI:10.1002/ajpa.21204
PMID:19862808
Abstract

All major ABO blood alleles are found in most populations worldwide, whereas the majority of Native Americans are nearly exclusively in the O group. O allele molecular characterization could aid in elucidating the possible causes of group O predominance in Native American populations. In this work, we studied exon 6 and 7 sequence diversity in 180 O blood group individuals from four different Mesoamerican populations. Additionally, a comparative analysis of genetic diversity and population structure including South American populations was performed. Results revealed no significant differences among Mesoamerican and South American groups, but showed significant differences within population groups attributable to previously detected differences in genetic drift and founder effects throughout the American continent. Interestingly, in all American populations, the same set of haplotypes O(1), O(1v), and O(1v(G542A)) was present, suggesting the following: (1) that they constitute the main genetic pool of the founding population of the Americas and (2) that they derive from the same ancestral source, partially supporting the single founding population hypothesis. In addition, the consistent and restricted presence of the G542A mutation in Native Americans compared to worldwide populations allows it to be employed as an Ancestry informative marker (AIM). Present knowledge of the peopling of the Americas allows the prediction of the way in which the G542A mutation could have emerged in Beringia, probably during the differentiation process of Asian lineages that gave rise to the founding population of the continent.

摘要

所有主要的 ABO 血型等位基因在世界上大多数人群中都有发现,而大多数美洲原住民几乎完全属于 O 组。O 等位基因的分子特征可以帮助阐明 O 组在美洲原住民人群中占优势的可能原因。在这项工作中,我们研究了来自四个中美洲人群的 180 名 O 血型个体的外显子 6 和 7 序列多样性。此外,还对包括南美洲人群在内的遗传多样性和群体结构进行了比较分析。结果表明,中美洲和南美洲群体之间没有显著差异,但在群体内部存在显著差异,这归因于整个美洲大陆上先前检测到的遗传漂变和奠基者效应的差异。有趣的是,在所有美洲人群中,都存在相同的单倍型 O(1)、O(1v)和 O(1v(G542A)),这表明:(1) 它们构成了美洲创始人群的主要遗传库;(2) 它们来自同一祖先来源,部分支持单一创始人群假说。此外,与全球人群相比,G542A 突变在美洲原住民中的一致且受限存在,使其可作为一个祖先信息标记 (AIM)。目前对美洲人口的了解可以预测 G542A 突变是如何在白令海峡出现的,可能是在导致该大陆创始人群的亚洲谱系分化过程中出现的。

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