Cargando…
Interplay between H3K36me3, methyltransferase SETD2, and mismatch recognition protein MutSα facilitates processing of oxidative DNA damage in human cells
Oxidative DNA damage contributes to aging and the pathogenesis of numerous human diseases including cancer. 8-hydroxyguanine (8-oxoG) is the major product of oxidative DNA lesions. Although OGG1-mediated base excision repair is the primary mechanism for 8-oxoG removal, DNA mismatch repair has also b...
Autores principales: | Guo, Sida, Fang, Jun, Xu, Weizhi, Ortega, Janice, Liu, Chang-Yi, Gu, Liya, Chang, Zhijie, Li, Guo-Min |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241034/ https://www.ncbi.nlm.nih.gov/pubmed/35667440 http://dx.doi.org/10.1016/j.jbc.2022.102102 |
Ejemplares similares
-
Mispair-bound human MutS–MutL complex triggers DNA incisions and activates mismatch repair
por: Ortega, Janice, et al.
Publicado: (2021) -
SETD2-H3K36ME3: an important bridge between the environment and tumors
por: He, Jiahui, et al.
Publicado: (2023) -
Molecular basis for oncohistone H3 recognition by SETD2 methyltransferase
por: Yang, Shuang, et al.
Publicado: (2016) -
Regulation of SETD2 stability is important for the fidelity of H3K36me3 deposition
por: Bhattacharya, Saikat, et al.
Publicado: (2020) -
HDAC3 deacetylates the DNA mismatch repair factor MutSβ to stimulate triplet repeat expansions
por: Williams, Gregory M., et al.
Publicado: (2020)