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Regulation of the bacterial cell cycle by an integrated genetic circuit

机译:集成遗传电路调节细菌细胞周期

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How bacteria regulate cell cycle progression at a molecular level is a fundamental but poorly understood problem. In Caulobacter crescentus, two-component signal transduction proteins are crucial for cell cycle regulation, but the connectivity of regulators involved has remained elusive and key factors are unidentified. Here we identify ChpT, an essential histidine phosphotransferase that controls the activity of CtrA, the master cell cycle regulator. We show that the essential histidine kinase CckA initiates two phosphorelays, each requiring ChpT, which lead to the phosphorylation and stabilization of CtrA. Downregulation of CckA activity therefore results in the dephosphorylation and degradation of CtrA, which in turn allow the initiation of DNA replication. Furthermore, we show that CtrA triggers its own destruction by promoting cell division and inducing synthesis of the essential regulator DivK, which feeds back to downregulate CckA immediately before S phase. Our results define a single integrated circuit whose components and connectivity can account for the cell cycle oscillations of CtrA in Caulobacter.
机译:细菌如何在分子水平上调节细胞周期进程是一个基本的但尚不清楚的问题。在新月形杆菌中,两组分信号转导蛋白对于细胞周期调控至关重要,但所涉及的调控因子之间的连通性仍然难以捉摸,关键因素尚不清楚。在这里,我们确定了ChpT,这是一种必需的组氨酸磷酸转移酶,可控制主细胞周期调节剂CtrA的活性。我们表明,必要的组氨酸激酶CckA会引发两个磷酸化,每个都需要ChpT,从而导致CtrA的磷酸化和稳定化。因此,CckA活性的下调导致CtrA的去磷酸化和降解,进而允许DNA复制的启动。此外,我们显示CtrA通过促进细胞分裂并诱导必需调节剂DivK的合成来触发自身的破坏,后者在S期之前回馈以下调CckA。我们的结果定义了一个集成电路,其组件和连通性可解释杆状细菌中CtrA的细胞周期振荡。

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