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The SIOD disorder protein SMARCAL1 is an RPA-interacting protein involved in replication fork restart.
Ciccia, Alberto; Bredemeyer, Andrea L; Sowa, Mathew E; Terret, Marie-Emilie; Jallepalli, Prasad V; Harper, J Wade; Elledge, Stephen J.
Afiliación
  • Ciccia A; Howard Hughes Medical Institute and Department of Genetics, Harvard Medical School, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Genes Dev ; 23(20): 2415-25, 2009 Oct 15.
Article en En | MEDLINE | ID: mdl-19793862
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / ADN Helicasas / Proteína de Replicación A Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / ADN Helicasas / Proteína de Replicación A Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2009 Tipo del documento: Article País de afiliación: Estados Unidos