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Título

Non-Canonical CRL4A/4BCDT2 Interacts with RAD18 to Modulate Post Replication Repair and Cell Survival

AutorSertic, Sarah; Evolvi, Claudio; Tumini, Emanuela ; Plevani, Paolo; Muzi-Falconi, Marco; Rotondo, Giuseppe
Fecha de publicación29-mar-2013
EditorPublic Library of Science
CitaciónPLoS ONE 8(3): e60000 (2013)
ResumenThe Cullin-4CDT2 E3 ubiquitin ligase plays an essential role in DNA replication origin licensing directing degradation of several licensing factors at the G1/S transition in order to prevent DNA re-replication. Recently a RAD18-independent role of Cullin-4CDT2 in PCNA monoubiquitylation has been proposed. In an effort to better understand the function of Cullin-4CDT2 E3 ubiquitin ligase in mammalian Post-Replication Repair during an unperturbed S-phase, we show that down-regulation of Cullin-4CDT2 leads to two distinguishable independent phenotypes in human cells that unveil at least two independent roles of Cullin-4CDT2 in S-phase. Apart from the re-replication preventing activity, we identified a non-canonical Cullin-4CDT2 complex, containing both CUL4A and CUL4B, associated to the COP9 signalosome, that controls a RAD18-dependent damage avoidance pathway essential during an unperturbed S-phase. Indeed, we show that the non-canonical Cullin-4A/4BCDT2 complex binds to RAD18 and it is required to modulate RAD18 protein levels onto chromatin and the consequent dynamics of PCNA monoubiquitylation during a normal S-phase. This function prevents replication stress, ATR hyper-signaling and, ultimately, apoptosis. A very similar PRR regulatory mechanism has been recently described for Spartan. Our findings uncover a finely regulated process in mammalian cells involving Post-Replication Repair factors, COP9 signalosome and a non-canonical Cullin4-based E3 ligase which is essential to tolerate spontaneous damage and for cell survival during physiological DNA replication. © 2013 Sertic et al.
Versión del editorhttp://dx.doi.org/10.1371/journal.pone.0060000
URIhttp://hdl.handle.net/10261/123156
DOI10.1371/journal.pone.0060000
Identificadoresdoi: 10.1371/journal.pone.0060000
issn: 1932-6203
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