Krishna Sandeep, Maslov Sergei, Sneppen Kim
Niels Bohr Institute, University of Copenhagen, Copenhagen, Denmark.
PLoS Comput Biol. 2007 Mar 16;3(3):e41. doi: 10.1371/journal.pcbi.0030041. Epub 2007 Jan 16.
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.
大肠杆菌通过一系列高度协调的事件对DNA损伤做出反应,这些事件被称为SOS反应,由转录因子、蛋白质-蛋白质结合和活性蛋白质降解调节。我们提出了一个紫外线诱导的SOS反应的动力学模型,该模型纳入了易出错的聚合酶Pol V介导的诱变作用。在我们的模型中,诱变作用取决于两个关键过程的组合:复制叉对损伤的计数以及与UmuD'积累相关的长期记忆。我们表明,这些共同对诱变作用进行了严格调控,导致Pol V出现“数字式”的开启和关闭。我们的模型提供了SOS网络拓扑结构和设计的简洁视图,明确了每个调节过程的具体功能作用。特别是,我们认为最近在SOS调控子中观察到的启动子活性的第二个峰值(Friedman等人,2005年,《公共科学图书馆·生物学》3(7): e238)是Pol V对RecA细丝产生正反馈的结果。