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转录调节因子的细胞类型特异性磷酸化和蛋白水解控制细菌细胞周期中从G1期到S期的转变。

Cell type-specific phosphorylation and proteolysis of a transcriptional regulator controls the G1-to-S transition in a bacterial cell cycle.

作者信息

Domian I J, Quon K C, Shapiro L

机构信息

Department of Developmental Biology, Stanford University School of Medicine, California 94305, USA.

出版信息

Cell. 1997 Aug 8;90(3):415-24. doi: 10.1016/s0092-8674(00)80502-4.

Abstract

The global transcriptional regulator CtrA controls multiple events in the Caulobacter cell cycle, including the initiation of DNA replication, DNA methylation, cell division, and flagellar biogenesis. CtrA is a member of the response regulator family of two component signal transduction systems and is activated by phosphorylation. We report here that this phosphorylation signal enters the cell cycle at mid S phase. In addition, CtrA function is modulated by temporally and spatially controlled proteolysis. When an active CtrA protein is present at the wrong time in the cell cycle, owing to expression of a mutant CtrA derivative that is active in the absence of phosphorylation and is not turned over during the cell cycle, the G1-to-S transition is blocked and the cell cycle aborts. Thus, both phosphorylation and proteolysis are critical determinants of bacterial cell cycle control in a manner that is analogous to the control of the eukaryotic cell cycle.

摘要

全局转录调节因子CtrA控制着柄杆菌细胞周期中的多个事件,包括DNA复制的起始、DNA甲基化、细胞分裂和鞭毛生物合成。CtrA是双组分信号转导系统中应答调节因子家族的成员,通过磷酸化被激活。我们在此报告,这种磷酸化信号在S期中期进入细胞周期。此外,CtrA的功能受到时间和空间控制的蛋白水解作用的调节。当活性CtrA蛋白在细胞周期的错误时间出现时,由于一种突变CtrA衍生物的表达,该衍生物在没有磷酸化的情况下具有活性且在细胞周期中不会被降解,G1期到S期的转变被阻断,细胞周期中止。因此,磷酸化和蛋白水解都是细菌细胞周期控制的关键决定因素,其方式类似于真核细胞周期的控制。

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