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CCR5基因32碱基对缺失的全球分布情况。

Global distribution of the CCR5 gene 32-basepair deletion.

作者信息

Martinson J J, Chapman N H, Rees D C, Liu Y T, Clegg J B

机构信息

MRC Molecular Haematology Unit, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

Nat Genet. 1997 May;16(1):100-3. doi: 10.1038/ng0597-100.

Abstract

A mutant allele of the beta-chemokine receptor gene CCR5 bearing a 32-basepair (bp) deletion (denoted delta ccr5) which prevents cell invasion by the primary transmitting strain of HIV-1 has recently been characterized. Homozygotes for the mutation are resistant to infection, even after repeated high-risk exposures, but this resistance appears not to be total, as isolated cases of HIV-positive deletion homozygotes are now emerging. The consequence of the heterozygous state is not clear, but it may delay the progression to AIDS in infected individuals. A gene frequency of approximately 10% was found for delta ccr5 in populations of European descent, but no mutant alleles were reported in indigenous non-European populations. As the total number of non-European samples surveyed was small in comparison with the Europeans the global distribution of this mutation is far from clear. We have devised a rapid PCR assay for delta ccr5 and used it to screen 3,342 individuals from a globally-distributed range of populations. We find that delta ccr5 is not confined to people of European descent but is found at frequencies of 2-5% throughout Europe, the Middle East and the Indian subcontinent (Fig. 1). Isolated occurrences are seen elsewhere throughout the world, but these most likely represent recent European gene flow into the indigenous populations. The inter-population differences in delta ccr5 frequency may influence the pattern of HIV transmission and so will need to be incorporated into future predictions of HIV levels.

摘要

β趋化因子受体基因CCR5的一个突变等位基因带有一个32个碱基对(bp)的缺失(记为Δccr5),该缺失可阻止HIV-1主要传播株对细胞的侵袭,最近已得到鉴定。该突变的纯合子即使在反复高风险暴露后仍对感染具有抗性,但这种抗性似乎并非完全有效,因为现在已出现HIV阳性缺失纯合子的个别病例。杂合状态的后果尚不清楚,但它可能会延缓受感染个体发展为艾滋病的进程。在欧洲裔人群中发现Δccr5的基因频率约为10%,但在非欧洲本土人群中未报告有突变等位基因。由于与欧洲人相比,所调查的非欧洲样本总数较少,这种突变的全球分布情况远未明确。我们设计了一种针对Δccr5的快速聚合酶链反应(PCR)检测方法,并用于对来自全球分布的一系列人群的3342人进行筛查。我们发现Δccr5并不局限于欧洲裔人群,而是在欧洲、中东和印度次大陆各地以2%至5%的频率出现(图1)。在世界其他地方也有个别出现的情况,但这些很可能代表了近期欧洲基因流入本土人群。Δccr5频率的人群间差异可能会影响HIV传播模式,因此需要纳入未来对HIV水平的预测中。

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