Markham B E, Harper J E, Mount D W
Mol Gen Genet. 1985;198(2):207-12. doi: 10.1007/BF00382997.
The products of the lexA and recA genes play central roles in the regulation of the Escherichia coli SOS response. We have measured the rate of mRNA synthesis from each gene at intervals following various inducing treatments in order to obtain a more precise timing of the induction process. Further, we provide quantitative evidence for kinetics of decay from fully induced levels of mRNA synthesis to basal levels as the cells shut down the SOS response which are in agreement with previously published data on the expression of specific SOS functions. The induction kinetics of lexA and recA gene expression are parallel except for nalidixic acid (NAL) treatment, with the actual levels of lexA mRNA synthesis being about 10-fold lower than that of recA. Reestablishment of repression from RecA commenced over 30 min earlier than from lexA. These results are fully consistent with the model that the functions result from the increased gene expression.
lexA和recA基因的产物在大肠杆菌SOS反应的调控中起核心作用。我们在各种诱导处理后的不同时间间隔测量了每个基因的mRNA合成速率,以便更精确地确定诱导过程的时间。此外,我们提供了定量证据,证明随着细胞关闭SOS反应,mRNA合成从完全诱导水平衰减到基础水平的动力学,这与先前发表的关于特定SOS功能表达的数据一致。除了萘啶酸(NAL)处理外,lexA和recA基因表达的诱导动力学是平行的,lexA mRNA合成的实际水平比recA低约10倍。RecA介导的阻遏重建比lexA早30多分钟开始。这些结果与基因表达增加导致功能的模型完全一致。