Orientation-dependent regulation of integrated HIV-1 expression by host gene transcriptional readthrough

被引:175
作者
Han, Yefei [1 ,2 ]
Lin, Yijie B. [1 ]
An, Wenfeng [3 ]
Xu, Jie [1 ]
Yang, Hung-Chih [1 ]
O'Connell, Karen [1 ]
Dordai, Dominic [3 ]
Boeke, Jef D. [3 ]
Siliciano, Janet D. [1 ]
Siliciano, Robert F. [1 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Program Biochem Cell & Mol Biol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
关键词
D O I
10.1016/j.chom.2008.06.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Integrated HIV-1 genomes are found within actively transcribed host genes in latently infected CD4(+) T cells. Readthrough transcription of the host gene might therefore suppress HIV-1 gene expression and promote the latent infection that allows viral persistence in patients on therapy. To address the effect of host gene readthrough, we used homologous recombination to insert HIV-1 genomes in either orientation into an identical position within an intron of an actively transcribed host gene, hypoxanthine-guanine phosphoribosyltransferase (HPRT). Constructs were engineered to permit or block readthrough transcription of HPRT. Readthrough transcription inhibited HIV-1 gene expression for convergently orientated provirus but enhanced HIV-1 gene expression when HIV-1 was in the same orientation as the host gene. Orientation had a >10-fold effect on HIV-1 gene expression. Due to the nature of HIV-1 integration sites in vivo, this orientation-dependent regulation can influence the vast majority of infected cells and adds complexity to the maintenance of latency.
引用
收藏
页码:134 / 146
页数:13
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