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Elevated ATPase Activity of KaiC Applies a Circadian Checkpoint on Cell Division in Synechococcus elongatus

机译:KaiC的ATPase活性升高适用于延长突触球菌细胞分裂的昼夜节律检查点

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摘要

A circadian clock coordinates physiology and behavior in diverse groups of living organisms. Another major cyclic cellular event, the cell cycle, is regulated by the circadian clock in the few cases where linkage of these cycles has been studied. In the cyanobacterium Synechococcus elongatus, the circadian clock gates cell division by an unknown mechanism. Using timelapse microscopy, we confirm the gating of cell division in the wild-type and demonstrate the regulation of cytokinesis by key clock components. Specifically, a state of the oscillator protein KaiC that is associated with elevated ATPase activity closes the gate by acting through a known clock output pathway to inhibit FtsZ ring formation at the division site. An activity that stimulates KaiC phosphorylation independently of the KaiA protein was also uncovered. We propose a model that separates the functions of KaiC ATPase and phosphorylation in cell division gating and other circadian behaviors.
机译:昼夜节律时钟协调各种生物体的生理和行为。在一些研究了这些循环之间的联系的情况下,另一个主要的循环细胞事件,即细胞周期受昼夜节律调节。在蓝藻Synchococcus elongatus中,生物钟通过未知机制控制细胞分裂。使用延时摄影显微镜,我们确认了野生型中细胞分裂的门控,并证明了关键时钟成分对胞质分裂的调节。具体而言,与增加的ATPase活性相关的振荡器蛋白KaiC的状态通过通过已知的时钟输出途径来抑制分裂位点的FtsZ环形成而关闭了门。还没有发现独立于KaiA蛋白刺激KaiC磷酸化的活性。我们提出了一个模型,该模型在细胞分裂门控和其他昼夜节律行为中分离了KaiC ATPase和磷酸化的功能。

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