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A Spatial Control for Correct Timing of Gene Expression during the Escherichia coli Cell Cycle

机译:大肠杆菌细胞周期中基因表达的正确时机的空间控制。

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摘要

Temporal transcriptions of genes are achieved by different mechanisms such as dynamic interaction of activator and repressor proteins with promoters, and accumulation and/or degradation of key regulators as a function of cell cycle. We find that the TorR protein localizes to the old poles of the Escherichia coli cells, forming a functional focus. The TorR focus co-localizes with the nucleoid in a cell-cycle-dependent manner, and consequently regulates transcription of a number of genes. Formation of one TorR focus at the old poles of cells requires interaction with the MreB and DnaK proteins, and ATP, suggesting that TorR delivery requires cytoskeleton organization and ATP. Further, absence of the protein–protein interactions and ATP leads to loss in function of TorR as a transcription factor. We propose a mechanism for timing of cell-cycle-dependent gene transcription, where a transcription factor interacts with its target genes during a specific period of the cell cycle by limiting its own spatial distribution.
机译:基因的暂时转录是通过不同的机制实现的,例如激活剂和阻遏蛋白与启动子的动态相互作用,以及关键调节剂根据细胞周期的积累和/或降解。我们发现,TorR蛋白位于大肠杆菌细胞的旧极,形成功能焦点。 TorR焦点以依赖细胞周期的方式与核苷共定位,并因此调节许多基因的转录。在老细胞两极形成一个TorR聚焦点需要与MreB和DnaK蛋白以及ATP相互作用,这表明TorR的传递需要细胞骨架的组织和ATP。此外,缺乏蛋白质间相互作用和ATP会导致TorR作为转录因子的功能丧失。我们提出了一种细胞周期依赖性基因转录时机的机制,其中转录因子通过限制其自身的空间分布在细胞周期的特定时期与其靶基因相互作用。

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