| Literature DB >> 19793862 |
Alberto Ciccia1, Andrea L Bredemeyer, Mathew E Sowa, Marie-Emilie Terret, Prasad V Jallepalli, J Wade Harper, Stephen J Elledge.
Abstract
The integrity of genomic DNA is continuously challenged by the presence of DNA base lesions or DNA strand breaks. Here we report the identification of a new DNA damage response protein, SMARCAL1 (SWI/SNF-related, matrix associated, actin-dependent regulator of chromatin, subfamily a-like 1), which is a member of the SNF2 family and is mutated in Schimke immunoosseous dysplasia (SIOD). We demonstrate that SMARCAL1 directly interacts with Replication protein A (RPA) and is recruited to sites of DNA damage in an RPA-dependent manner. SMARCAL1-depleted cells display sensitivity to DNA-damaging agents that induce replication fork collapse, and exhibit slower fork recovery and delayed entry into mitosis following S-phase arrest. Furthermore, SIOD patient fibroblasts reconstituted with SMARCAL1 exhibit faster cell cycle progression after S-phase arrest. Thus, the symptoms of SIOD may be caused, at least in part, by defects in the cellular response to DNA replication stress.Entities:
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Year: 2009 PMID: 19793862 PMCID: PMC2764500 DOI: 10.1101/gad.1832309
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361