期刊
MBIO
卷 12, 期 4, 页码 -出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/mBio.01625-21
关键词
HIV-1 latency; UHRF1; Tat; p-TEFb; RING finger
类别
资金
- Natural Science Foundation of China [82073896, 81673481]
- Natural Science Foundation of Guangdong Province [2018B030312010]
- National Science and Technology Major Project [2018ZX10301101]
- Guangdong Basic and Applied Basic Research Foundation [2019A1515010061, 2021A1515011096]
- Guangzhou Science and Technology Basic and Applied Basic Research Foundation [202102080108]
- Opening Project of Zhejiang Provincial Preponderant and Characteristic Subject of Key University (Traditional Chinese Pharmacology) at Zhejiang Chinese Medical University [ZYAOXZD2019001]
HIV-1 latency is influenced by host factors and viral proteins, with UHRF1 playing a crucial role in modulating Tat stability. By disrupting the Tat/cyclin T1/CDK9 complex, UHRF1 suppresses HIV-1 transcription and maintains latency. This study provides new insights into controlling Tat expression through host-pathogen interaction for modulating HIV-1 latency, suggesting potential therapeutic strategies for HIV-1 patients.
HIV-1 remains incurable due to viral reservoirs, which lead to durably latent HIV infection. Identifying novel host factors and deciphering the molecular mechanisms involved in the establishment and maintenance of latency are critical to discover new targets for the development of novel anti-HIV agents. Here, we show that ubiquitin-like with PHD and RING finger domain 1 (UHRF1) modulates HIV-1 5' long terminal repeat (LTR)-driven transcription of the viral genome as a novel HIV-1 restriction factor. Correspondingly, UHRF1 depletion reversed the latency of HIV-1 pro viruses. Mechanistically, UHRF1 competed with positive transcription factor b (p-TEFb) for the binding to the cysteine-rich motifs of HIV-1 Tat via its TTD, PHD, and RING finger domains. Furthermore, UHRF1 mediated K48-linked ubiquitination and proteasomal degradation of Tat in RING-dependent ways, leading to the disruption of Tat/cyclin T1/CDK9 complex and consequential impediment of transcription elongation. In summary, our findings revealed that UHRF1 is an important mediator of HIV-1 latency by controlling Tat-mediated transcriptional activation, providing novel insights on host-pathogen interaction for modulating HIV-1 latency, beneficial for the development of anti-AIDS therapies. IMPORTANCE HIV-1 latency is systematically modulated by host factors and viral proteins. In our work, we identified a critical role of host factor ubiquitin-like with PHD and RING finger domain 1 (UHRF1) in HIV-1 latency via the modulation of the viral protein Tat stability. By disrupting the Tat/cyclin T1/CDK9 complex, UHRF1 promotes the suppression of HIV-1 transcription and maintenance of HIV-1 latency. Our findings provide novel insights in controlling Tat expression via host-pathogen interaction for modulating HIV-1 latency. Based on our results, modulating UHRF1 expression or activity by specific inhibitors is a potential therapeutic strategy for latency reversal in HIV-1 patients.
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