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细胞周期中的同胞竞争:Cdc2 与 Cdk2

Cell cycle sibling rivalry: Cdc2 vs. Cdk2.

作者信息

Kaldis Philipp, Aleem Eiman

机构信息

National Cancer Institute, Mouse Cancer Genetics Program, Frederick, Maryland, USA.

出版信息

Cell Cycle. 2005 Nov;4(11):1491-4. doi: 10.4161/cc.4.11.2124. Epub 2005 Nov 29.

Abstract

It has been long believed that the cyclin-dependent kinase 2 (Cdk2) binds to cyclin E or cyclin A and exclusively promotes the G1/S phase transition and that Cdc2/cyclin B complexes play a major role in mitosis. We now provide evidence that Cdc2 binds to cyclin E (in addition to cyclin A and B) and is able to promote the G1/S transition. This new concept indicates that both Cdk2 and/or Cdc2 can drive cells through G1/S phase in parallel. In this review we discuss the classic cell cycle model and how results from knockout mice provide new evidence that refute this model. We focus on the roles of Cdc2 and p27 in regulating the mammalian cell cycle and propose a new model for cell cycle regulation that accommodates these novel findings.

摘要

长期以来,人们一直认为细胞周期蛋白依赖性激酶2(Cdk2)与细胞周期蛋白E或细胞周期蛋白A结合,并专门促进G1/S期转换,且Cdc2/细胞周期蛋白B复合物在有丝分裂中起主要作用。我们现在提供证据表明,Cdc2与细胞周期蛋白E结合(除细胞周期蛋白A和B外),并能够促进G1/S转换。这一新概念表明,Cdk2和/或Cdc2都可以并行驱动细胞通过G1/S期。在这篇综述中,我们讨论了经典的细胞周期模型,以及基因敲除小鼠的实验结果如何提供了反驳该模型的新证据。我们重点关注Cdc2和p27在调节哺乳动物细胞周期中的作用,并提出一个适应这些新发现的细胞周期调节新模型。

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