PARP1 promotes nucleotide excision repair through DDB2 stabilization and recruitment of ALC1

A Pines, MG Vrouwe, Jurgen Marteijn, D Typas, MS Luijsterburg, Medine Cansoy, P Hensbergen, A Deelder, A (Anton) de Groot, S Matsumoto, K Sugasawa, N Thoma, Wim Vermeulen, H Vrieling, L Mullenders

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The WD40-repeat protein DDB2 is essential for efficient recognition and subsequent removal of ultraviolet (UV)-induced DNA lesions by nucleotide excision repair (NER). However, how DDB2 promotes NER in chromatin is poorly understood. Here, we identify poly(ADP-ribose) polymerase 1 (PARP1) as a novel DDB2-associated factor. We demonstrate that DDB2 facilitated poly(ADP-ribosyl)ation of UV-damaged chromatin through the activity of PARP1, resulting in the recruitment of the chromatin-remodeling enzyme ALC1. Depletion of ALC1 rendered cells sensitive to UV and impaired repair of UV-induced DNA lesions. Additionally, DDB2 itself was targeted by poly(ADP-ribosyl)ation, resulting in increased protein stability and a prolonged chromatin retention time. Our in vitro and in vivo data support a model in which poly(ADP-ribosyl)ation of DDB2 suppresses DDB2 ubiquitylation and outline a molecular mechanism for PARP1-mediated regulation of NER through DDB2 stabilization and recruitment of the chromatin remodeler ALC1.
Original languageUndefined/Unknown
Pages (from-to)235-249
Number of pages15
JournalJournal of Cell Biology
Volume199
Issue number2
DOIs
Publication statusPublished - 2012

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