Artículo
The ubiquitin E3/E4 ligase, UBE4A, fine-tunes protein ubiquitylation and accumulation at sites of DNA damage facilitating double-strand break repair
Autor/es | Soria Bretones, Isabel
Baranes Bachar, Keren Huertas Sánchez, Pablo Levy Barda, Adva Oehler, Judith |
Departamento | Universidad de Sevilla. Departamento de Genética |
Fecha de publicación | 2018 |
Fecha de depósito | 2019-03-20 |
Publicado en |
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Resumen | Double-strand breaks (DSBs) are critical DNA lesions that robustly activate the elaborate DNA
damage response (DDR) network. We identified a critical player in DDR fine-tuning - the E3/E4
ubiquitin ligase, UBE4A. UBE4A’s ... Double-strand breaks (DSBs) are critical DNA lesions that robustly activate the elaborate DNA damage response (DDR) network. We identified a critical player in DDR fine-tuning - the E3/E4 ubiquitin ligase, UBE4A. UBE4A’s recruitment to sites of DNA damage is dependent on primary E3 ligases in the DDR and promotes enhancement and sustainment of K48- and K63-linked ubiquitin chains at these sites. This step is required for timely recruitment of the RAP80 and BRCA1 proteins and proper organization of RAP80- and BRCA1-associated protein complexes at DSB sites. This pathway is essential for optimal end-resection at DSBs, and its abrogation leads to up-regulation of the highly mutagenic alternative end-joining repair at the expense of error-free homologous recombination repair. Our data uncover a critical regulatory level in the DSB response and underscore the importance of fine-tuning of the complex DDR network for accurate and balanced execution of DSB repair |
Cita | Soria Bretones, I., Baranes Bachar, K., Huertas Sánchez, P., Levy Barda, A. y Oehler, J. (2018). The ubiquitin E3/E4 ligase, UBE4A, fine-tunes protein ubiquitylation and accumulation at sites of DNA damage facilitating double-strand break repair. Molecular Cell, 69 (5), 866-878. |
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