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Polymorphism, haplotype composition, and selection in the Mhc-DRB of wild baboons.

机译:野生狒狒的Mhc-DRB中的多态性,单倍型组成和选择。

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摘要

General patterns of organization in the major histocompatibility complex (MHC) have been successfully explained by the model of birth-and-death evolution, but understanding why certain MHC genes are maintained together into specific haplotypes remains challenging. The haplotype configurations of the functionally important class II DR region have been described in few primates and display important interspecific variability with respect to the extent of allelic variation, the number of loci and/or combinations of loci present. Understanding the evolutionary mechanisms driving such variation is conditional upon characterizing haplotypes in new species and identifying the selective pressures acting on haplotypes. This study explores the variability of haplotype configurations in the Mhc-DRB region (exon 2) for the first time in wild non-human primates, chacma baboons (Papio ursinus). Paur-DRB haplotypes were characterized through segregation studies and linkage disequilibrium. 23 Paur-DRB sequences and 15haplotype configurations were identified in 199 animals. The Paur-DRB exon 2 is shown to be subjected to intense positive selection and frequent recombination. An approach recently developed for human vaccine studies was used to classify Paur-DRB sequences into supertypes, based on the physico-chemical properties of amino acids that are positively selected, thus most probably involved in antigen recognition. Sequences grouped into the same supertype (thus presumably sharing antigen-binding affinities) are non-randomly distributed within haplotypes, leading to an increased individual diversity of supertypes. Our results suggest that selection favoring haplotypes with complementary sets of DRB supertypes shapes functionally tuned haplotypes in this natural baboon population.
机译:主要的组织相容性复合体(MHC)的组织一般模式已通过生与死进化模型成功地进行了解释,但是了解为什么某些MHC基因保持在一起形成特定的单倍型仍然具有挑战性。已经在少数灵长类动物中描述了功能重要的II类DR区的单倍型构型,并且在等位基因变异程度,基因座数量和/或基因座组合方面表现出重要的种间变异性。了解驱动这种变异的进化机制的条件是表征新物种的单倍型并确定作用于单倍型的选择性压力。这项研究首次探索了在野生非人类灵长类动物chacma狒狒(Papio ursinus)中,Mhc-DRB区(第2外显子)的单倍型构型的变异性。通过分离研究和连锁不平衡来表征Paur-DRB单倍型。在199只动物中鉴定出23个Paur-DRB序列和15个单倍型构型。显示Paur-DRB外显子2受到强烈的阳性选择和频繁的重组。基于积极选择的氨基酸的理化特性,最近使用了一种为人类疫苗研究开发的方法,将Paur-DRB序列分类为超型,因此很可能涉及抗原识别。分组为同一超型的序列(因此大概具有抗原结合亲和力)在单倍型内非随机分布,从而导致超型的个体多样性增加。我们的研究结果表明,在这种自然狒狒种群中,偏爱单倍型与DRB超型的互补集的选择会影响功能调整的单倍型。

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