| Autor: |
Shaliny Ramachandran, Dania Haddad, Conglei Li, Michael X. Le, Alexanda K. Ling, Clare C. So, Rajeev M. Nepal, Jennifer L. Gommerman, Kefei Yu, Troy Ketela, Jason Moffat, Alberto Martin |
| Jazyk: |
angličtina |
| Rok vydání: |
2016 |
| Předmět: |
|
| Zdroj: |
Cell Reports, Vol 15, Iss 7, Pp 1554-1565 (2016) |
| Druh dokumentu: |
article |
| ISSN: |
2211-1247 |
| DOI: |
10.1016/j.celrep.2016.04.041 |
| Popis: |
Summary: Class switch recombination (CSR) requires activation-induced deaminase (AID) to instigate double-stranded DNA breaks at the immunoglobulin locus. DNA breaks activate the DNA damage response (DDR) by inducing phosphorylation of histone H2AX followed by non-homologous end joining (NHEJ) repair. We carried out a genome-wide screen to identify CSR factors. We found that Usp22, Eny2, and Atxn7, members of the Spt-Ada-Gcn5-acetyltransferase (SAGA) deubiquitination module, are required for deubiquitination of H2BK120ub following DNA damage, are critical for CSR, and function downstream of AID. The SAGA deubiquitinase activity was required for optimal irradiation-induced γH2AX formation, and failure to remove H2BK120ub inhibits ATM- and DNAPK-induced γH2AX formation. Consistent with this effect, these proteins were found to function upstream of various double-stranded DNA repair pathways. This report demonstrates that deubiquitination of histone H2B impacts the early stages of the DDR and is required for the DNA repair phase of CSR. : Activation-induced deaminase induces class switch recombination by inducing DNA breaks at the immunoglobulin locus. Ramachandran et al. showed that the SAGA deubiquitination module is critical for this process. They showed that this complex is required for optimal γH2AX formation and functions upstream of various double-stranded DNA repair pathways. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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