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双色囊翼蝠主要组织相容性复合体II类基因DRB1的非中性进化

Non-neutral evolution of the major histocompatibility complex class II gene DRB1 in the sac-winged bat Saccopteryx bilineata.

作者信息

Mayer F, Brunner A

机构信息

Department of Zoology, University of Erlangen, Erlangen, Germany.

出版信息

Heredity (Edinb). 2007 Sep;99(3):257-64. doi: 10.1038/sj.hdy.6800989. Epub 2007 May 23.

DOI:10.1038/sj.hdy.6800989
PMID:17519971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7094720/
Abstract

The immune genes of the major histocompatibility complex (MHC) are classical examples for high levels of genetic diversity and non-neutral evolution. This is particularly true for the regions containing the antigen-binding sites as, for instance, in the exon 2 of the MHC class II gene DRB. We surveyed, for the first time in the order Chiroptera, the genetic diversity within this exon in the sac-winged bat Saccopteryx bilineata. We detected 11 alleles among 85 bats, of which 79 were sampled in one population. Pairwise comparisons revealed that interallelic sequence differences ranged between 3 and 22%, although nucleotide substitutions were not evenly distributed along the exon sequence. This was most probably the result of intragenic recombination. High levels of sequence divergence and significantly more nonsynonymous than synonymous substitutions (d(N)/d(S)>1) suggest long-term balancing selection. Thus, the data are consistent with the hypothesis that recombination gives rise to new alleles at the DRB locus of the sac-winged bat, and these are maintained in the population through balancing selection. In this respect, the sac-winged bat closely resembles other mammalian species.

摘要

主要组织相容性复合体(MHC)的免疫基因是遗传多样性高和非中性进化的经典例子。对于包含抗原结合位点的区域来说尤其如此,例如在MHC II类基因DRB的外显子2中。我们首次在翼手目动物中调查了双色囊翼蝠这个外显子内的遗传多样性。我们在85只蝙蝠中检测到11个等位基因,其中79只是在一个种群中采样的。成对比较显示,等位基因间的序列差异在3%到22%之间,尽管核苷酸替换并非沿外显子序列均匀分布。这很可能是基因内重组的结果。高水平的序列分歧以及非同义替换显著多于同义替换(d(N)/d(S)>1)表明存在长期的平衡选择。因此,这些数据与以下假设一致:重组在囊翼蝠的DRB位点产生新的等位基因,并且这些等位基因通过平衡选择在种群中得以维持。在这方面,囊翼蝠与其他哺乳动物物种非常相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/f8e4c5c710ab/41437_2007_Article_BF6800989_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/ee0aecd1dd6b/41437_2007_Article_BF6800989_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/598600422ed6/41437_2007_Article_BF6800989_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/8897a21308b4/41437_2007_Article_BF6800989_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/f8e4c5c710ab/41437_2007_Article_BF6800989_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/ee0aecd1dd6b/41437_2007_Article_BF6800989_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/598600422ed6/41437_2007_Article_BF6800989_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/8897a21308b4/41437_2007_Article_BF6800989_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1de/7094720/f8e4c5c710ab/41437_2007_Article_BF6800989_Fig4_HTML.jpg

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