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The CREB Regulated Transcription Coactivator 2 Suppresses HIV-1 Transcription by Preventing RNA Pol II from Binding to HIV-1 LTR
Author(s) -
Ling Ma,
Shumin Chen,
Zhen Wang,
Saisai Guo,
Jianyuan Zhao,
Dongrong Yi,
Quanjie Li,
Zhenlong Liu,
Fei Guo,
Xiaoyu Li,
Pingping Jia,
Jiwei Ding,
Chen Liang,
Shan Cen
Publication year - 2021
Publication title -
virologica sinica
Language(s) - English
Resource type - Journals
eISSN - 1995-820X
pISSN - 1674-0769
DOI - 10.1007/s12250-021-00363-1
Subject(s) - creb , transcription (linguistics) , response element , biology , coactivator , transcription factor , gene expression , microbiology and biotechnology , virology , gene , promoter , genetics , linguistics , philosophy
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.

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