Cargando…
HIV Vpr Modulates the Host DNA Damage Response at Two Independent Steps to Damage DNA and Repress Double-Strand DNA Break Repair
The DNA damage response (DDR) is a signaling cascade that is vital to ensuring the fidelity of the host genome in the presence of genotoxic stress. Growing evidence has emphasized the importance of both activation and repression of the host DDR by diverse DNA and RNA viruses. Previous work has shown...
Autores principales: | Li, Donna, Lopez, Andrew, Sandoval, Carina, Nichols Doyle, Randilea, Fregoso, Oliver I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407082/ https://www.ncbi.nlm.nih.gov/pubmed/32753492 http://dx.doi.org/10.1128/mBio.00940-20 |
Ejemplares similares
-
HIV-1 Vpr-induced DNA damage activates NF-κB independent of cell cycle arrest and CRL4A(DCAF1) engagement
por: Sandoval, Carina, et al.
Publicado: (2023) -
Activation of the DNA Damage Response Is a Conserved Function of HIV-1 and HIV-2 Vpr That Is Independent of SLX4 Recruitment
por: Fregoso, Oliver I., et al.
Publicado: (2016) -
Removal of heat-sensitive clustered damaged DNA sites is independent of double-strand break repair
por: Abramenkovs, Andris, et al.
Publicado: (2018) -
SMCHD1 accumulates at DNA damage sites and facilitates the repair of DNA double-strand breaks
por: Coker, Heather, et al.
Publicado: (2014) -
Early Chk1 Phosphorylation Is Driven by Temozolomide-Induced, DNA Double Strand Break- and Mismatch Repair-Independent DNA Damage
por: Ito, Motokazu, et al.
Publicado: (2013)