CpG站点
生物
锌指
病毒学
基因
慢病毒
人类免疫缺陷病毒(HIV)
遗传学
病毒性疾病
DNA甲基化
基因表达
转录因子
作者
Dorota Kmiec,Rayhane Nchioua,Scott Sherrill-Mix,Christina M. Stürzel,Elena Heusinger,Elisabeth Braun,Marcos V. P. Gondim,Dominik Hotter,Konstantin M. J. Sparrer,Beatrice H. Hahn,Daniel Sauter,Frank Kirchhoff
出处
期刊:MBio
[American Society for Microbiology]
日期:2020-01-14
卷期号:11 (1)
被引量:33
标识
DOI:10.1128/mbio.02903-19
摘要
Evasion of the zinc-finger antiviral protein (ZAP) may drive CpG dinucleotide suppression in HIV-1 and many other viral pathogens but the viral determinants of ZAP sensitivity are poorly defined. Here, we examined CpG suppression and ZAP sensitivity in a large number of primate lentiviruses and demonstrate that their genomic frequency of CpGs varies substantially and does not correlate with ZAP sensitivity. We further show that the number of CpG residues in a defined region at the 5′ end of the env gene together with structural features plays a key role in HIV-1 susceptibility to ZAP and correlates with differences in clinical progression rates in HIV-1-infected individuals. Our identification of a specific part of env as a major determinant of HIV-1 susceptibility to ZAP restriction provides a basis for future studies of the underlying inhibitory mechanisms and their potential relevance in the pathogenesis of AIDS.
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