Cargando…
Microhomology-mediated end joining is activated in irradiated human cells due to phosphorylation-dependent formation of the XRCC1 repair complex
Microhomology-mediated end joining (MMEJ), an error-prone pathway for DNA double-strand break (DSB) repair, is implicated in genomic rearrangement and oncogenic transformation; however, its contribution to repair of radiation-induced DSBs has not been characterized. We used recircularization of a li...
Autores principales: | Dutta, Arijit, Eckelmann, Bradley, Adhikari, Sanjay, Ahmed, Kazi Mokim, Sengupta, Shiladitya, Pandey, Arvind, Hegde, Pavana M., Tsai, Miaw-Sheue, Tainer, John A., Weinfeld, Michael, Hegde, Muralidhar L., Mitra, Sankar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389627/ https://www.ncbi.nlm.nih.gov/pubmed/27994036 http://dx.doi.org/10.1093/nar/gkw1262 |
Ejemplares similares
-
Regulation of oxidized base damage repair by chromatin assembly factor 1 subunit A
por: Yang, Chunying, et al.
Publicado: (2017) -
PLK1 targets CtIP to promote microhomology-mediated end joining
por: Wang, Hailong, et al.
Publicado: (2018) -
Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions
por: Yu, Amy Marie, et al.
Publicado: (2010) -
A role for human homologous recombination factors in suppressing microhomology-mediated end joining
por: Ahrabi, Sara, et al.
Publicado: (2016) -
An atypical BRCT–BRCT interaction with the XRCC1 scaffold protein compacts human DNA Ligase IIIα within a flexible DNA repair complex
por: Hammel, Michal, et al.
Publicado: (2020)