Cdc25磷酸酶家族调控细胞周期。

I Nilsson, I Hoffmann
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引用次数: 453

摘要

在高等真核细胞中,细胞周期蛋白依赖性激酶的激活可以通过Cdc25磷酸酶家族成员Cdc25A、Cdc25B和Cdc25C的去磷酸化来实现。Cdc25A在G1/ s相转变中起重要作用。Cdc25B在s期被激活,在细胞质中激活有丝分裂激酶Cdk1/cyclin B。然后活性Cdk1/cyclin B磷酸化并激活Cdc25C,导致正反馈机制并进入有丝分裂。Cdc25A和B是潜在的人类致癌基因。此外,Cdc25是DNA损伤或未复制DNA存在时引起的G2阻滞的主要参与者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cell cycle regulation by the Cdc25 phosphatase family.

Activation of cyclin-dependent kinases in higher eukaryotic cells can be achieved through dephosphorylation by members of the Cdc25 phosphatase family, Cdc25A, Cdc25B and Cdc25C. Cdc25A plays an important role at the G1/S-phase transition. Cdc25B undergoes activation during S-phase and plays a role in activating the mitotic kinase Cdk1/cyclin B in the cytoplasm. Active Cdk1/cyclin B then phosphorylates and activates Cdc25C leading to a positive feedback mechanism and to entry into mitosis. Cdc25A and B are potential human oncogenes. In addition, Cdc25 is a main player of the G2 arrest caused by DNA damage or in the presence of unreplicated DNA.

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