首页> 美国卫生研究院文献>Journal of Virology >Note: CXCR4 and CCR5 Genetic Polymorphisms in Long-Term Nonprogressive Human Immunodeficiency Virus Infection: Lack of Association with Mutations other than CCR5-Δ32
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Note: CXCR4 and CCR5 Genetic Polymorphisms in Long-Term Nonprogressive Human Immunodeficiency Virus Infection: Lack of Association with Mutations other than CCR5-Δ32

机译:注意:长期非进行性人类免疫缺陷病毒感染中的CXCR4和CCR5遗传多态性:与CCR5-Δ32以外的其他突变缺乏关联

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摘要

Polymorphisms in the coding sequences of CCR5 and CXCR4 were studied in a group of human immunodeficiency virus (HIV)-infected long-term nonprogressors. Two different point mutations were found in the CXCR4 coding sequence. One of these CXCR4 mutations was silent, and each was unique to two nonprogressors. The well-described 32-bp deletion within the CCR5 coding sequence (CCR5-Δ32) was found in 4 of 13 nonprogressors, and 12 different point mutations were found scattered over the CCR5 coding sequence from 8 nonprogressors. Most of the mutations created either silent or conservative changes in the predicted amino acid sequence: only one of these mutations was found in more than a single nonprogressor. All nonsilent mutations were tested in an HIV envelope-dependent fusion assay, and all functioned comparably to wild-type controls. Polymorphisms in the CXCR4 and CCR5 coding sequences other than CCR5-Δ32 do not appear to play a dominant mechanistic role in nonprogression among HIV-infected individuals.
机译:在一组感染人类免疫缺陷病毒(HIV)的长期非进展者中研究了CCR5和CXCR4编码序列的多态性。在CXCR4编码序列中发现了两个不同的点突变。这些CXCR4突变之一是沉默的,每个突变对于两个非进行者都是唯一的。在13个非进行者中的4个中发现了CCR5编码序列(CCR5-Δ32)中众所周知的32 bp缺失,在8个非进行者的CCR5编码序列中发现了12个不同的点突变。大多数突变会在预测的氨基酸序列中产生沉默或保守的变化:在一个以上的非渐进基因中仅发现了这些突变之一。所有非沉默突变均在HIV包膜依赖性融合试验中进行了测试,并且所有功能均与野生型对照相当。除了CCR5-Δ32以外,CXCR4和CCR5编码序列中的多态性似乎并未在HIV感染者的非进展中起主导作用。

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