Cargando…
A requirement for STAG2 in replication fork progression creates a targetable synthetic lethality in cohesin-mutant cancers
Cohesin is a multiprotein ring that is responsible for cohesion of sister chromatids and formation of DNA loops to regulate gene expression. Genomic analyses have identified that the cohesin subunit STAG2 is frequently inactivated by mutations in cancer. However, the reason STAG2 mutations are selec...
Autores principales: | Mondal, Gourish, Stevers, Meredith, Goode, Benjamin, Ashworth, Alan, Solomon, David A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459917/ https://www.ncbi.nlm.nih.gov/pubmed/30975996 http://dx.doi.org/10.1038/s41467-019-09659-z |
Ejemplares similares
-
Synthetic Lethality of Cohesins with PARPs and Replication Fork Mediators
por: McLellan, Jessica L., et al.
Publicado: (2012) -
STAG1 vulnerabilities for exploiting cohesin synthetic lethality in STAG2-deficient cancers
por: van der Lelij, Petra, et al.
Publicado: (2020) -
Synthetic lethality between the cohesin subunits STAG1 and STAG2 in diverse cancer contexts
por: van der Lelij, Petra, et al.
Publicado: (2017) -
Different NIPBL requirements of cohesin-STAG1 and cohesin-STAG2
por: Alonso-Gil, Dácil, et al.
Publicado: (2023) -
Cohesin acetylation speeds the replication fork
por: Terret, Marie-Emilie, et al.
Publicado: (2009)