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CREB 调节转录共激活因子 2 通过防止 RNA Pol II 与 HIV-1 LTR 结合来抑制 HIV-1 转录。

The CREB Regulated Transcription Coactivator 2 Suppresses HIV-1 Transcription by Preventing RNA Pol II from Binding to HIV-1 LTR.

机构信息

Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical School, Beijing, 100050, China.

Department of Blood Transfusion, The Affiliated Hospital of Qingdao University, Qingdao 266000, China.

出版信息

Virol Sin. 2021 Aug;36(4):796-809. doi: 10.1007/s12250-021-00363-1. Epub 2021 Mar 15.

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.

摘要

CREB 调节的转录共激活因子(CRTCs),包括 CRTC1、CRTC2 和 CRTC3,可增强 CREB 靶向基因的转录。除了响应 cAMP 调节宿主基因表达外,CRTCs 还会增加几种病毒的感染。虽然人类免疫缺陷病毒 1(HIV-1)长末端重复(LTR)启动子含有 cAMP 反应元件,并且 cAMP 途径的激活可促进 HIV-1 转录,但 CRTCs 是否对 HIV-1 转录和 HIV-1 感染有任何影响尚不清楚。在这里,我们报道了 HIV-1 感染可诱导 CRTC2 表达,但 CRTC2 抑制 HIV-1 感染并降低病毒 RNA 表达。机制研究表明,CRTC2 抑制 HIV-1 LTR 的转录并减少 RNA Pol II 在 LTR 上的占据,而与 CREB 无关。重要的是,CRTC2 抑制潜伏 HIV-1 的激活。这些数据表明,在 HIV-1 感染后,细胞增加 CRTC2 的表达,抑制 HIV-1 基因表达,可能在将 HIV-1 驱动进入潜伏期方面发挥作用。

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