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细胞周期蛋白依赖性激酶对DNA复制程序的调控:新发现与展望

Regulation of the program of DNA replication by CDK: new findings and perspectives.

作者信息

Singh Balveer, Wu Pei-Yun Jenny

机构信息

CNRS, Institute of Genetics and Development of Rennes, University of Rennes, UMR 6290, 2 avenue du Pr. Léon Bernard, 35043, Rennes, France.

出版信息

Curr Genet. 2019 Feb;65(1):79-85. doi: 10.1007/s00294-018-0860-6. Epub 2018 Jun 20.

Abstract

Progression through the cell cycle is driven by the activities of the cyclin-dependent kinase (CDK) family of enzymes, which establish an ordered passage through the cell cycle phases. CDK activity is crucial for the cellular transitions from G1 to S and G2 to M, which are highly controlled to promote the faithful duplication of the genetic material and the transmission of the genome into daughter cells, respectively. While oscillations in CDK activity are essential for cell division, how its specific dynamics may shape cellular processes remains an open question. Recently, we have investigated the potential role of CDK in establishing the profile of replication initiation along the chromosomes, also referred to as the replication program. Our results demonstrated that the timing and level of CDK activity at G1/S provide two critical and independent inputs that modulate the pattern of origin usage. In this review, we will present the conclusions of our study and discuss the implications of our findings for cellular function and physiology.

摘要

细胞周期的进程由细胞周期蛋白依赖性激酶(CDK)家族酶的活性驱动,这些酶在细胞周期各阶段建立有序的进程。CDK活性对于细胞从G1期到S期以及从G2期到M期的转变至关重要,这两个转变受到高度控制,分别促进遗传物质的忠实复制和基因组向子细胞的传递。虽然CDK活性的振荡对于细胞分裂至关重要,但其特定动态如何塑造细胞过程仍是一个悬而未决的问题。最近,我们研究了CDK在建立沿染色体的复制起始图谱(也称为复制程序)中的潜在作用。我们的结果表明,G1/S期CDK活性的时间和水平提供了两个关键且独立的输入,可调节起始位点的使用模式。在这篇综述中,我们将展示我们研究的结论,并讨论我们的发现对细胞功能和生理学的影响。

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