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Genetic variation of the MHC class II DRB genes in the Japanese weasel, Mustela itatsi, endemic to Japan, compared with the Siberian weasel, Mustela sibirica

机译:与日本西伯利亚鼬鼠,鼬鼬相比,日本鼬鼠Mustela itatsi中MHC II类DRB基因的遗传变异

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摘要

Major histocompatibility complex (MHC) genes encode proteins that play a critical role in vertebrate immune system and are highly polymorphic. To further understand the molecular evolution of the MHC genes, we compared MHC class II DRB genes between the Japanese weasel (Mustela itatsi), a species endemic to Japan, and the Siberian weasel (Mustela sibirica), a closely related species on the continent. We sequenced a 242-bp region of DRB exon 2, which encodes antigen-binding sites (ABS), and found 24 alleles from 31 M. itatsi individuals and 17 alleles from 21 M. sibirica individuals, including broadly distributed, species-specific and/or geographically restricted alleles. Our results suggest that pathogen-driven balancing selection have acted to maintain the diversity in the DRB genes. For predicted ABS, nonsynonymous substitutions exceeded synonymous substitutions, also indicating positive selection, which was not seen at non-ABS. In a Bayesian phylogenetic tree, two M. sibirica DRB alleles were basal to the rest of the sequences from mustelid species and may represent ancestral alleles. Trans-species polymorphism was evident between many mustelid DRB alleles, especially between M. itatsi and M. sibirica. These two Mustela species divided about 1.7 million years ago, but still share many MHC alleles, indicative of their close phylogenetic relationship.
机译:主要的组织相容性复合体(MHC)基因编码在脊椎动物免疫系统中起关键作用且高度多态的蛋白质。为了进一步了解MHC基因的分子进化,我们比较了日本特有物种黄鼬(Mustela itatsi)和大陆上密切相关的西伯利亚鼬鼬(Mustela sibirica)之间的MHC II类DRB基因。我们对DRB外显子2的242 bp区域进行了测序,该区域编码抗原结合位点(ABS),发现来自31 M. itatsi个体的24个等位基因和来自21 M. sibirica个体的17个等位基因,包括分布广泛的物种特异性/或受地理位置限制的等位基因。我们的结果表明,病原体驱动的平衡选择已起到维持DRB基因多样性的作用。对于预测的ABS,非同义替换超过了同义替换,也表明存在正选择,这在非ABS上看不到。在贝叶斯系统发育树中,两个西伯利亚白屈菜DRB等位基因是芥菜种其余序列的基础,可能代表祖先等位基因。在许多鼬类DRB等位基因之间,特别是在M. itatsi和M. sibirica之间,明显存在跨物种多态性。这两个鼬物种大约在170万年前分裂,但仍共享许多MHC等位基因,表明它们之间有着密切的系统发育关系。

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