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HLA supertype variation across populations: new insights into the role of natural selection in the evolution of HLA-A and HLA-B polymorphisms

机译:人群中HLA超型变异:自然选择在HLA-A和HLA-B多态性进化中的作用的新见解

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摘要

Supertypes are groups of human leukocyte antigen (HLA) alleles which bind overlapping sets of peptides due to sharing specific residues at the anchor positions—the B and F pockets—of the peptide-binding region (PBR). HLA alleles within the same supertype are expected to be functionally similar, while those from different supertypes are expected to be functionally distinct, presenting different sets of peptides. In this study, we applied the supertype classification to the HLA-A and HLA-B data of 55 worldwide populations in order to investigate the effect of natural selection on supertype rather than allelic variation at these loci. We compared the nucleotide diversity of the B and F pockets with that of the other PBR regions through a resampling procedure and compared the patterns of within-population heterozygosity (He) and between-population differentiation (GST) observed when using the supertype definition to those estimated when using randomized groups of alleles. At HLA-A, low levels of variation are observed at B and F pockets and randomized He and GST do not differ from the observed data. By contrast, HLA-B concentrates most of the differences between supertypes, the B pocket showing a particularly high level of variation. Moreover, at HLA-B, the reassignment of alleles into random groups does not reproduce the patterns of population differentiation observed with supertypes. We thus conclude that differently from HLA-A, for which supertype and allelic variation show similar patterns of nucleotide diversity within and between populations, HLA-B has likely evolved through specific adaptations of its B pocket to local pathogens.Electronic supplementary materialThe online version of this article (doi:10.1007/s00251-015-0875-9) contains supplementary material, which is available to authorized users.
机译:超型是人类白细胞抗原(HLA)等位基因的组,它们由于在肽结合区(PBR)的锚点位置(B和F口袋)共享特定残基而结合了重叠的肽组。预期同一超型中的HLA等位基因在功能上相似,而不同超型中的HLA等位基因在功能上不同,呈现出不同的肽组。在这项研究中,我们将超型分类应用于全球55个人群的HLA-A和HLA-B数据,以研究自然选择对这些位点上超型而非等位基因变异的影响。我们通过重采样程序将B和F口袋的核苷酸多样性与其他PBR区域的核苷酸多样性进行了比较,并比较了使用超型定义时观察到的种群内杂合性(He)和种群间分化(GST)的模式使用随机等位基因组时估计。在HLA-A处,在B和F凹处观察到低水平的变化,随机He和GST与观察到的数据没有差异。相比之下,HLA-B集中了超型之间的大多数差异,B口袋显示出特别高的变异水平。此外,在HLA-B,将等位基因重新分配到随机组中不会重现超型观察到的种群分化模式。因此,我们得出结论,与HLA-A不同,HLA-A的超型和等位基因变异显示出种群内和种群之间核苷酸多样性的相似模式,HLA-B可能是通过B口袋对当地病原体的特定适应而进化的。本文(doi:10.1007 / s00251-015-0875-9)包含补充材料,授权用户可以使用。

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