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NCOA4 转录共激活因子抑制 DNA 复制起点的激活。

NCOA4 transcriptional coactivator inhibits activation of DNA replication origins.

机构信息

Istituto di Endocrinologia ed Oncologia Sperimentale del CNR/Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli "Federico II," 80131 Naples, Italy.

Istituto di Biostrutture e Bioimmagini del CNR, 80134 Naples, Italy.

出版信息

Mol Cell. 2014 Jul 3;55(1):123-37. doi: 10.1016/j.molcel.2014.04.031. Epub 2014 Jun 5.

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.

摘要

NCOA4 是核激素受体的转录共激活因子,在人类癌症中发生基因重排。通过结合非洲爪蟾卵提取物和小鼠胚胎成纤维细胞(MEFs)的研究,我们在这里表明,NCOA4 是一种与 minichromosome maintenance 7(MCM7)相互作用的蛋白,能够控制 DNA 复制。非洲爪蟾卵提取物中的耗尽-重建实验表明,NCOA4 通过调节 CMG(CDC45/MCM2-7/GINS)解旋酶来抑制 DNA 复制起始的激活。NCOA4(-/-) MEFs 显示出无计划的起始激活和减少的起始之间的距离;这导致复制应激,如叉停止、叉速度降低和过早衰老的存在所示。总之,我们的发现表明,NCOA4 作为 DNA 复制起始的调节剂发挥作用,有助于防止不适当的 DNA 合成和复制应激。

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