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三个连锁基因座的选择、搭便车及不平衡分析及其在HLA数据中的应用

Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data.

作者信息

Robinson W P, Cambon-Thomsen A, Borot N, Klitz W, Thomson G

机构信息

Department of Integrative Biology, University of California, Berkeley 94720.

出版信息

Genetics. 1991 Nov;129(3):931-48. doi: 10.1093/genetics/129.3.931.

Abstract

The HLA system has been extensively studied from an evolutionary perspective. Although it is clear that selection has acted on the genes in the HLA complex, the nature of this selection has yet to be fully clarified. A study of constrained disequilibrium values is presented that is applicable to HLA and other less polymorphic systems with three or more linked loci, with the purpose of identifying selection events. The method uses the fact that three locus systems impose additional constraints on the range of possible disequilibrium values for any pair of loci. We have thus examined the behavior of the normalized pairwise disequilibrium measures using two locus (D'), and also three locus (D"), constraints on pairwise disequilibria in a three locus system when one of the three loci is under positive selection. The difference between these measures, delta = magnitude of D' - magnitude of D", has a distribution for the two unselected loci differing from that for the selected locus with either of the unselected loci (the hallmark is a high positive value of delta for the two unselected loci). An examination of genetic drift indicates that positive delta values are unlikely to be found in human populations in the absence of selection when recombination is greater than about 0.1%. This measure can thus provide insight into which allele of several linked loci might have been subject to selection. Application of this method to HLA haplotypes from a large French population study (Provinces Francaise) identifies selected alleles on particular haplotypes. Application of a complementary method, disequilibrium pattern analysis also confirms the action of selection on these haplotypes.

摘要

从进化的角度对人类白细胞抗原(HLA)系统进行了广泛研究。尽管很明显选择作用于HLA复合体中的基因,但这种选择的本质尚未完全阐明。本文提出了一种适用于HLA和其他具有三个或更多连锁基因座的低多态性系统的受限不平衡值研究,目的是识别选择事件。该方法利用了三个基因座系统对任何一对基因座的可能不平衡值范围施加额外限制这一事实。因此,我们研究了在一个三位点系统中,当三个基因座之一受到正选择时,使用两位点(D')和三位点(D")对两位点不平衡进行约束的标准化两位点不平衡度量的行为。这些度量之间的差异,δ = D'的大小 - D"的大小,对于两个未选择的基因座与选择的基因座和任何一个未选择的基因座具有不同的分布(特征是两个未选择的基因座的δ值为高正值)。对遗传漂变的研究表明,当重组大于约0.1%时,在没有选择的情况下,人类群体中不太可能出现正的δ值。因此,这种度量可以深入了解几个连锁基因座中的哪个等位基因可能受到了选择。将该方法应用于一项大型法国人群研究(法国省份)的HLA单倍型,可识别特定单倍型上的选择等位基因。应用一种补充方法,不平衡模式分析也证实了对这些单倍型的选择作用。

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