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人类族群中的多态性混合分型

Polymorphic admixture typing in human ethnic populations.

作者信息

Dean M, Stephens J C, Winkler C, Lomb D A, Ramsburg M, Boaze R, Stewart C, Charbonneau L, Goldman D, Albaugh B J

机构信息

Laboratory of Viral Carcinogenesis, National Cancer Institute, Frederick, MD 21702-1201.

出版信息

Am J Hum Genet. 1994 Oct;55(4):788-808.

PMID:7942857
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1918306/
Abstract

A panel of 257 RFLP loci was selected on the basis of high heterozygosity in Caucasian DNA surveys and equivalent spacing throughout the human genome. Probes from each locus were used in a Southern blot survey of allele frequency distribution for four human ethnic groups: Caucasian, African American, Asian (Chinese), and American Indian (Cheyenne). Nearly all RFLP loci were polymorphic in each group, albeit with a broad range of differing allele frequencies (delta). The distribution of frequency differences (delta values) was used for three purposes: (1) to provide estimates for genetic distance (differentiation) among these ethnic groups, (2) to revisit with a large data set the proportion of human genetic variation attributable to differentiation within ethnic groups, and (3) to identify loci with high delta values between recently admixed populations of use in mapping by admixture linkage disequilibrium (MALD). Although most markers display significant allele frequency differences between ethnic groups, the overall genetic distances between ethnic groups were small (.066-.098), and < 10% of the measured overall molecular genetic diversity in these human samples can be attributed to "racial" differentiation. The median delta values for pairwise comparisons between groups fell between .15 and .20, permitting identification of highly informative RFLP loci for MALD disease association studies.

摘要

根据高加索人DNA调查中的高杂合性以及整个人类基因组中的等间距,选择了一组257个RFLP位点。来自每个位点的探针用于对四个人类种族群体(高加索人、非裔美国人、亚洲人(中国人)和美洲印第安人(夏延人))的等位基因频率分布进行Southern印迹调查。几乎所有RFLP位点在每个群体中都是多态性的,尽管等位基因频率(δ)差异很大。频率差异(δ值)的分布用于三个目的:(1)估计这些种族群体之间的遗传距离(分化);(2)用一个大数据集重新审视人类遗传变异中可归因于种族群体内部分化的比例;(3)识别在通过混合连锁不平衡(MALD)进行定位的近期混合群体之间具有高δ值的位点。尽管大多数标记在种族群体之间显示出显著的等位基因频率差异,但种族群体之间的总体遗传距离很小(0.066 - 0.098),并且这些人类样本中测量到的总体分子遗传多样性的不到10%可归因于“种族”分化。群体间两两比较的中位δ值在0.15和0.20之间,这使得能够识别出用于MALD疾病关联研究的高信息含量RFLP位点。