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UV-Induced Mutagenesis in Escherichia coli SOS Response: A Quantitative Model

机译:紫外线诱导的大肠杆菌SOS反应诱变:定量模型。

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摘要

Escherichia coli bacteria respond to DNA damage by a highly orchestrated series of events known as the SOS response, regulated by transcription factors, protein–protein binding, and active protein degradation. We present a dynamical model of the UV-induced SOS response, incorporating mutagenesis by the error-prone polymerase, Pol V. In our model, mutagenesis depends on a combination of two key processes: damage counting by the replication forks and a long-term memory associated with the accumulation of UmuD′. Together, these provide a tight regulation of mutagenesis, resulting, we show, in a “digital” turn-on and turn-off of Pol V. Our model provides a compact view of the topology and design of the SOS network, pinpointing the specific functional role of each of the regulatory processes. In particular, we suggest that the recently observed second peak in the activity of promoters in the SOS regulon (Friedman et al., 2005, PLoS Biology 3(7): e238) is the result of positive feedback from Pol V to RecA filaments.
机译:大肠杆菌细菌通过一系列高度协调的事件来响应DNA损伤,这些事件被称为SOS响应,受转录因子,蛋白质-蛋白质结合和活性蛋白质降解的调节。我们提供了一个紫外线诱导的SOS响应的动力学模型,并结合了易错聚合酶Pol V的诱变作用。在我们的模型中,诱变取决于两个关键过程的组合:复制叉造成的破坏计数和长期的与UmuD'的积累有关的记忆。在一起,它们提供了严格的诱变调节,因此,我们证明了Pol V的“数字”开启和关闭。我们的模型提供了SOS网络的拓扑结构和设计的紧凑视图,指出了具体的每个监管流程的功能角色。特别是,我们建议最近观察到的SOS调节子中启动子活性的第二个峰(Friedman等,2005,PLoS Biology 3(7):e238)是从Pol V到RecA细丝的正反馈的结果。

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