Cargando…
UHRF1 Suppresses HIV-1 Transcription and Promotes HIV-1 Latency by Competing with p-TEFb for Ubiquitination-Proteasomal Degradation of Tat
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 age...
Autores principales: | Liang, Taizhen, Zhang, Qiao, Wu, Ziyao, Chen, Pei, Huang, Yifan, Liu, Shuwen, Li, Lin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406157/ https://www.ncbi.nlm.nih.gov/pubmed/34465029 http://dx.doi.org/10.1128/mBio.01625-21 |
Ejemplares similares
-
Tat competes with HEXIM1 to increase the active pool of P-TEFb for HIV-1 transcription
por: Barboric, Matjaz, et al.
Publicado: (2007) -
Crystal structure of HIV-1 Tat complexed with human P-TEFb
por: Tahirov, Tahir H., et al.
Publicado: (2010) -
Controlling Cellular P-TEFb Activity by the HIV-1 Transcriptional Transactivator Tat
por: Muniz, Lisa, et al.
Publicado: (2010) -
HIV-1 Tat Recruits HDM2 E3 Ligase To Target IRF-1 for Ubiquitination and Proteasomal Degradation
por: Remoli, Anna Lisa, et al.
Publicado: (2016) -
A Novel Bromodomain Inhibitor Reverses HIV-1 Latency through Specific Binding with BRD4 to Promote Tat and P-TEFb Association
por: Huang, Huachao, et al.
Publicado: (2017)