| Literature DB >> 24910095 |
Roberto Bellelli1, Maria Domenica Castellone1, Teresa Guida1, Roberto Limongello1, Nina Alayne Dathan2, Francesco Merolla1, Anna Maria Cirafici1, Andrea Affuso3, Hisao Masai4, Vincenzo Costanzo5, Domenico Grieco1, Alfredo Fusco1, Massimo Santoro6, Francesca Carlomagno7.
Abstract
NCOA4 is a transcriptional coactivator of nuclear hormone receptors that undergoes gene rearrangement in human cancer. By combining studies in Xenopus laevis egg extracts and mouse embryonic fibroblasts (MEFs), we show here that NCOA4 is a minichromosome maintenance 7 (MCM7)-interacting protein that is able to control DNA replication. Depletion-reconstitution experiments in Xenopus laevis egg extracts indicate that NCOA4 acts as an inhibitor of DNA replication origin activation by regulating CMG (CDC45/MCM2-7/GINS) helicase. NCOA4(-/-) MEFs display unscheduled origin activation and reduced interorigin distance; this results in replication stress, as shown by the presence of fork stalling, reduction of fork speed, and premature senescence. Together, our findings indicate that NCOA4 acts as a regulator of DNA replication origins that helps prevent inappropriate DNA synthesis and replication stress.Entities:
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Year: 2014 PMID: 24910095 DOI: 10.1016/j.molcel.2014.04.031
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970