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细胞周期检验点调控因子达百万。

Cell cycle checkpoint regulators reach a zillion.

机构信息

Department of Biology, University of Virginia, Charlottesville, VA, USA.

出版信息

Cell Cycle. 2013 May 15;12(10):1501-9. doi: 10.4161/cc.24637. Epub 2013 Apr 17.

Abstract

Entry into mitosis is regulated by a checkpoint at the boundary between the G2 and M phases of the cell cycle (G2/M). In many organisms, this checkpoint surveys DNA damage and cell size and is controlled by both the activation of mitotic cyclin-dependent kinases (Cdks) and the inhibition of an opposing phosphatase, protein phosphatase 2A (PP2A). Misregulation of mitotic entry can often lead to oncogenesis or cell death. Recent research has focused on discovering the signaling pathways that feed into the core checkpoint control mechanisms dependent on Cdk and PP2A. Herein, we review the conserved mechanisms of the G2/M transition, including recently discovered upstream signaling pathways that link cell growth and DNA replication to cell cycle progression. Critical consideration of the human, frog and yeast models of mitotic entry frame unresolved and emerging questions in this field, providing a prediction of signaling molecules and pathways yet to be discovered.

摘要

有丝分裂的进入是由细胞周期的 G2 和 M 期之间的边界处的一个检查点(G2/M)调控的。在许多生物中,这个检查点检测 DNA 损伤和细胞大小,并且受到有丝分裂周期蛋白依赖性激酶(Cdk)的激活和对向磷酸酶蛋白磷酸酶 2A(PP2A)的抑制的控制。有丝分裂进入的失调通常会导致肿瘤发生或细胞死亡。最近的研究集中在发现信号通路,这些信号通路可以将核心检查点控制机制与 Cdk 和 PP2A 联系起来。在此,我们综述了 G2/M 转换的保守机制,包括最近发现的将细胞生长和 DNA 复制与细胞周期进程联系起来的上游信号通路。对人类、青蛙和酵母有丝分裂进入模型的批判性考虑,为该领域尚未解决和新出现的问题提供了预测,预测了尚未发现的信号分子和通路。

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