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Conflicting selection pressures on T-cell epitopes in HIV-1 subtype B

机译:HIV-1 B亚型T细胞表位上的选择压力冲突

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摘要

Analysis of population-level polymorphism in eight coding genes of human immunodeficiency virus type 1 (HIV-1) subtype B revealed evidence not only of past purifying selection, but also of abundant slightly deleterious nonsynonymous variants subject to ongoing purifying selection. Both CD4 and CTL epitopes showed an excess of nonsynonymous variants that were singletons (occurring in just one sequence) in our dataset. Overall, median gene diversities at polymorphic nonsynonymous sites were highest at sites located in neither CD4 nor CTL epitopes, while polymorphic nonsynonymous sites in CD4 epitopes revealed the lowest median gene diversity. Our results support the hypothesis that there is an evolutionary conflict between immune escape and functional constraint on epitopes recognized by host T-cells, and suggest that amino acid sequences of CD4 epitopes are subject to particularly strong functional constraint
机译:分析人类免疫缺陷病毒1型(HIV-1)B亚型的8个编码基因的种群水平多态性,不仅显示了过去纯化选择的证据,而且还显示了仍在进行纯化选择的大量轻微有害的非同义词变体的证据。 CD4和CTL表位都显示出过多的非同义变体,在我们的数据集中是单例(仅在一个序列中出现)。总体而言,多态性非同义位点的中位基因多样性最高位于既不位于CD4抗原表位也不位于CTL表位的位点,而CD4表位中的多态性非同义位点揭示最低的中位基因多样性。我们的结果支持以下假设:免疫逃逸与宿主T细胞识别的表位上的功能限制之间存在进化冲突,并表明CD4表位的氨基酸序列受到特别强的功能限制

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