Beyond 2/3 and 1/3: The Complex Signatures of Sex-Biased Admixture on the X Chromosome

被引:53
作者
Goldberg, Amy [1 ]
Rosenberg, Noah A. [1 ]
机构
[1] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
admixture; African-American genetics; mechanistic model; sex bias; X chromosome; GENOME-WIDE PATTERNS; POPULATION-STRUCTURE; GENETIC ANCESTRY; AFRICAN-AMERICANS; DIVERSE SYSTEMS; PROPORTIONS; HISTORIES; MIGRATION; SELECTION; DYNAMICS;
D O I
10.1534/genetics.115.178509
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Sex-biased demography, in which parameters governing migration and population size differ between females and males, has been studied through comparisons of X chromosomes, which are inherited sex-specifically, and autosomes, which are not. A common form of sex bias in humans is sex-biased admixture, in which at least one of the source populations differs in its proportions of females and males contributing to an admixed population. Studies of sex-biased admixture often examine the mean ancestry for markers on the X chromosome in relation to the autosomes. A simple framework noting that in a population with equally many females and males, two-thirds of X chromosomes appear in females, suggests that the mean X-chromosomal admixture fraction is a linear combination of female and male admixture parameters, with coefficients 2/3 and 1/3, respectively. Extending a mechanistic admixture model to accommodate the X chromosome, we demonstrate that this prediction is not generally true in admixture models, although it holds in the limit for an admixture process occurring as a single event. For a model with constant ongoing admixture, we determine the mean X-chromosomal admixture, comparing admixture on female and male X chromosomes to corresponding autosomal values. Surprisingly, in reanalyzing African-American genetic data to estimate sex-specific contributions from African and European sources, we find that the range of contributions compatible with the excess African ancestry on the X chromosome compared to autosomes has a wide spread, permitting scenarios either without male-biased contributions from Europe or without female-biased contributions from Africa.
引用
收藏
页码:263 / 279
页数:17
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