ATR-mediated phosphorylation of DNA polymerase eta is needed for efficient recovery from UV damage.

Abstract:

DNA polymerase eta (poleta) belongs to the Y-family of DNA polymerases and facilitates translesion synthesis past UV damage. We show that, after UV irradiation, poleta becomes phosphorylated at Ser601 by the ataxia-telangiectasia mutated and Rad3-related (ATR) kinase. DNA damage-induced phosphorylation of poleta depends on its physical interaction with Rad18 but is independent of PCNA monoubiquitination. It requires the ubiquitin-binding domain of poleta but not its PCNA-interacting motif. ATR-dependent phosphorylation of poleta is necessary to restore normal survival and postreplication repair after ultraviolet irradiation in xeroderma pigmentosum variant fibroblasts, and is involved in the checkpoint response to UV damage. Taken together, our results provide evidence for a link between DNA damage-induced checkpoint activation and translesion synthesis in mammalian cells.

Polymerases:

Topics:

Nucleotide Analogs / Template Lesions

Status:

new topics/pols set partial results complete validated

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