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The SIOD disorder protein SMARCAL1 is an RPA-interacting protein involved in replication fork restart.

Genes & development (2009-10-02)
Alberto Ciccia, 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.

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Sigma-Aldrich
Anticorpo anti fosfo-istone H2A.X (Ser139), colone JBW301, clone JBW301, Upstate®, from mouse
Sigma-Aldrich
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