| Literature DB >> 33723808 |
Ling Ma1, Shumin Chen2, Zhen Wang3, Saisai Guo1, Jianyuan Zhao1, Dongrong Yi1, Quanjie Li1, Zhenlong Liu3, Fei Guo4, Xiaoyu Li1, Pingping Jia5, Jiwei Ding6,7, Chen Liang3, Shan Cen8,9,10.
Abstract
The CREB-regulated transcriptional co-activators (CRTCs), including CRTC1, CRTC2 and CRTC3, enhance transcription of CREB-targeted genes. In addition to regulating host gene expression in response to cAMP, CRTCs also increase the infection of several viruses. While human immunodeficiency virus type 1 (HIV-1) long terminal repeat (LTR) promoter harbors a cAMP response element and activation of the cAMP pathway promotes HIV-1 transcription, it remains unknown whether CRTCs have any effect on HIV-1 transcription and HIV-1 infection. Here, we reported that CRTC2 expression was induced by HIV-1 infection, but CRTC2 suppressed HIV-1 infection and diminished viral RNA expression. Mechanistic studies revealed that CRTC2 inhibited transcription from HIV-1 LTR and diminished RNA Pol II occupancy at the LTR independent of its association with CREB. Importantly, CRTC2 inhibits the activation of latent HIV-1. Together, these data suggest that in response to HIV-1 infection, cells increase the expression of CRTC2 which inhibits HIV-1 gene expression and may play a role in driving HIV-1 into latency.Entities:
Keywords: CREB regulated transcription coactivator 2 (CRTC2); Human immunodeficiency virus (HIV); Infection; Latency; Long terminal repeat (LTR); RNA polymerase II (RNA Pol II); Viral transcription; Virology
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Year: 2021 PMID: 33723808 PMCID: PMC8379306 DOI: 10.1007/s12250-021-00363-1
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327