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HLA II类基因中的基因座特异性和群体特异性进化

Locus and population specific evolution in HLA class II genes.

作者信息

Valdes A M, McWeeney S K, Meyer D, Nelson M P, Thomson G

机构信息

Department of Integrative Biology, University of California at Berkeley 94720-3140, USA.

出版信息

Ann Hum Genet. 1999 Jan;63(Pt 1):27-43. doi: 10.1046/j.1469-1809.1999.6310027.x.

Abstract

The population genetics of the HLA class II loci was studied with reference to variation in the frequency of (a) alleles at a locus and (b) amino acids at specific sites. Variation was surveyed at 4 loci (DRB1, DQA1, DQB1, and DPB1) in 22 populations from the Twelfth International Histocompatibility Workshop (Saint-Malo, 1996). Allele and amino acid variation was measured by computing heterozygosity and the effective number of alleles. Substantial variations in polymorphism were observed among the various populations and loci studied. In the majority of the populations, DRB1 has the highest heterozygosity and effective number of alleles. As previously shown, the Amerindian populations have lower levels of allelic diversity when compared to other populations. At the amino acid level, DRB1 antigen recognition sites (ARS) have the highest heterozygosities and effective number of alleles. For the other loci (DPB1, DQA1, and DQB1) for which there is no crystal structure and for which ARS sites were inferred from DRB1, non-ARS sites were often among the sites with highest levels of variation. It is possible that these putative non-ARS sites do play a role in antigen presentation. The homozygosity test for neutrality was applied to allele and amino acid data. Of the four HLA class II loci studied, only DPB1 failed to show evidence of balancing selection. DQB1 and DQA1 depart significantly from neutrality in the largest number of populations. Genetic distances between populations were computed based on frequency of alleles and amino acids at ARS sites.

摘要

参照(a)一个基因座上等位基因的频率变化以及(b)特定位点上氨基酸的频率变化,对HLA II类基因座的群体遗传学进行了研究。在第十二届国际组织相容性研讨会(1996年,圣马洛)的22个群体中,对4个基因座(DRB1、DQA1、DQB1和DPB1)的变异情况进行了调查。通过计算杂合度和有效等位基因数来测量等位基因和氨基酸的变异。在所研究的不同群体和基因座中观察到了多态性的显著差异。在大多数群体中,DRB1具有最高的杂合度和有效等位基因数。如先前所示,与其他群体相比,美洲印第安人群体的等位基因多样性水平较低。在氨基酸水平上,DRB1抗原识别位点(ARS)具有最高的杂合度和有效等位基因数。对于其他没有晶体结构且从DRB1推断出ARS位点的基因座(DPB1、DQA1和DQB1),非ARS位点往往是变异水平最高的位点之一。这些假定的非ARS位点有可能在抗原呈递中发挥作用。对中性的纯合度检验应用于等位基因和氨基酸数据。在所研究的四个HLA II类基因座中,只有DPB1没有显示出平衡选择的证据。在大多数群体中,DQB1和DQA1显著偏离中性。基于ARS位点上等位基因和氨基酸的频率计算群体之间的遗传距离。

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