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首页> 外文期刊>Genes and immunity. >Worldwide genetic variation at the 3' untranslated region of the HLA-G gene: balancing selection influencing genetic diversity.
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Worldwide genetic variation at the 3' untranslated region of the HLA-G gene: balancing selection influencing genetic diversity.

机译:HLA-G基因3'非翻译区的全球遗传变异:平衡影响遗传多样性的选择。

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摘要

The HLA-G (human leukocyte antigen-G) molecule plays a pivotal role in immune tolerance by inhibiting different cell subsets involved in both innate and adaptive immunity. Besides its primary function in maintaining the maternal-fetal tolerance, HLA-G has been involved in a wide range of pathological conditions where it can be either favorable or detrimental to the patient, depending on the nature of the pathology. Although several studies have demonstrated the utmost importance of the 3' untranslated region (3'UTR) in the HLA-G expression profile, limited data exist on the sequence variability of this gene region in human populations. In this study, we characterized the genetic diversity and haplotype structure of the HLA-G 3'UTR by resequencing 444 individuals from three sub-Saharan African populations and retrieving data from the 1000 Genomes project and the literature. A total of 1936 individuals representing 21 worldwide populations were combined and jointly analyzed. Our data revealed a high level of nucleotide diversity, an excess of intermediate frequency variants and an extremely low population differentiation, strongly supporting a history of balancing selection at this locus. The 14-bp insertion/deletion polymorphism was further pointed out as the likely target of selection, emphasizing its potential role in the post-transcriptional regulation of HLA-G expression.
机译:HLA-G(人类白细胞抗原-G)分子通过抑制参与先天性和适应性免疫的不同细胞亚群,在免疫耐受中起关键作用。 HLA-G除了具有维持母胎耐受性的主要功能外,还涉及多种病理状况,根据病理性质,它对患者可能是有利还是有害的。尽管一些研究表明3'非翻译区(3'UTR)在HLA-G表达谱中具有最重要的意义,但是有关该基因区在人群中的序列变异性的数据有限。在这项研究中,我们通过对来自三个撒哈拉以南非洲人口的444个人进行重新测序,并从1000个基因组计划和文献中检索数据,表征了HLA-G 3'UTR的遗传多样性和单倍型结构。总共对1936个代表21个全球人口的个体进行了合并和联合分析。我们的数据揭示了高水平的核苷酸多样性,过多的中频变体和极低的群体分化,有力地支持了该基因座平衡选择的历史。进一步指出了14 bp插入/缺失多态性是可能的选择靶标,强调了其在HLA-G表达的转录后调控中的潜在作用。

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