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

被引:171
作者
Ciccia, Alberto [1 ,2 ]
Bredemeyer, Andrea L. [1 ,2 ]
Sowa, Mathew E. [3 ]
Terret, Marie-Emilie [4 ]
Jallepalli, Prasad V. [4 ]
Harper, J. Wade [3 ]
Elledge, Stephen J. [1 ,2 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Dept Genet, Div Genet,Sch Med, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Howard Hughes Med Inst, Sch Med, Boston, MA 02115 USA
[3] Harvard Univ, Dept Pathol, Sch Med, Boston, MA 02115 USA
[4] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10065 USA
关键词
HARP; DNA replication; DNA double-strand breaks; DNA replication stress; IMMUNO-OSSEOUS DYSPLASIA; CHROMATIN-REMODELING COMPLEX; DNA-REPLICATION; REPAIR; DAMAGE; IDENTIFICATION; RECOGNITION; ACTIVATION; CHECKPOINT; STABILITY;
D O I
10.1101/gad.1832309
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:2415 / 2425
页数:11
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