Institute of Technology, University of Tartu, 50411 Tartu, Estonia.
Mol Biol Cell. 2019 Jan 15;30(2):169-172. doi: 10.1091/mbc.E18-05-0272.
Eukaryotic cell division has been studied thoroughly and is understood in great mechanistic detail. Paradoxically, however, we lack an understanding of its core control process, in which the master regulator of the cell cycle, cyclin-dependent kinase (CDK), temporally coordinates an array of complex molecular events. The core elements of the CDK control system are conserved in eukaryotic cells, which contain multiple cyclin-CDK forms that have poorly defined and partially overlapping responsibilities in the cell cycle. However, a single CDK can drive all events of cell division in both mammalian and yeast cells, and in fission yeast a single mitotic cyclin can drive the cell cycle without major problems. But how can the same CDK induce different events when activated at different times during the cell cycle? This question, which has bewildered cell cycle researchers for decades, now has a sufficiently clear mechanistic answer. This Perspective aims to provide a synthesis of recent data to facilitate a better understanding of this central cellular control system.
真核细胞的分裂过程已经得到了深入的研究,其机制细节也得到了很好的理解。然而,具有讽刺意味的是,我们仍然缺乏对其核心控制过程的理解,在这个过程中,细胞周期的主要调节因子细胞周期蛋白依赖性激酶(CDK)在时间上协调了一系列复杂的分子事件。CDK 控制系统的核心要素在真核细胞中是保守的,真核细胞中含有多种细胞周期蛋白-CDK 形式,它们在细胞周期中的职责定义不明确且部分重叠。然而,在哺乳动物和酵母细胞中,单个 CDK 可以驱动所有的细胞分裂事件,在裂殖酵母中,单个有丝分裂周期蛋白可以在没有重大问题的情况下驱动细胞周期。但是,当 CDK 在细胞周期的不同时间被激活时,它如何能诱导不同的事件呢?这个问题已经困扰了细胞周期研究人员几十年,现在已经有了一个足够清晰的机制答案。本观点旨在综合最近的数据,以促进对这个核心细胞控制系统的更好理解。