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裂殖酵母中 cdc2 对 S 期和有丝分裂控制的定量模型。

A quantitative model for the cdc2 control of S phase and mitosis in fission yeast.

作者信息

Stern B, Nurse P

机构信息

Cell Cycle Laboratory, Imperial Cancer Research Fund, London, UK.

出版信息

Trends Genet. 1996 Sep;12(9):345-50.

PMID:8855663
Abstract

In this article we consider the role of the cyclin-dependent protein kinase cdc2 in regulating progression through the fission yeast cell cycle. The onset of mitosis is governed by cdc2 in partnership with the B-type cyclin, cdc13. Recent evidence shows that the cdc2-cdc13 complex can also control the onset of S phase and, in addition, ensures that there is only one S phase per cell cycle. This leads us to propose a novel quantitative model in which different levels of cdc2 activity regulate cell-cycle progression: S phase is initiated when protein kinase activity increases from a very low to a moderate level; maintenance of this moderate level prevents re-initiation of S phase, and a further increase of activity to a high level initiates mitosis. Inactivation of the kinase activity at the end of mitosis resets the cell for a new cell cycle.

摘要

在本文中,我们探讨了细胞周期蛋白依赖性蛋白激酶cdc2在调控裂殖酵母细胞周期进程中的作用。有丝分裂的起始由cdc2与B型细胞周期蛋白cdc13协同控制。最近的证据表明,cdc2-cdc13复合物还能控制S期的起始,此外,还能确保每个细胞周期仅发生一次S期。这使我们提出了一个新的定量模型,其中不同水平的cdc2活性调控细胞周期进程:当蛋白激酶活性从极低水平增加到中等水平时,S期开始;维持这种中等水平可防止S期重新起始,而活性进一步升高到高水平则启动有丝分裂。有丝分裂结束时激酶活性的失活使细胞为新的细胞周期做好准备。

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