Miyashiro Tim, Goulian Mark
Department of Physics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16305-10. doi: 10.1073/pnas.0700025104. Epub 2007 Oct 1.
In Escherichia coli, Salmonella, and related bacteria, the PhoQ-PhoP system regulates the expression of a large collection of genes in response to conditions of low magnesium or to the presence of certain antimicrobial peptides. We measured transcription of four PhoP-regulated promoters in E. coli that have significantly different PhoP-binding sites. Surprisingly, three promoters show identical responses to magnesium concentrations that range over four orders of magnitude. By analyzing and testing a simple model of transcriptional regulation, we find an explanation for this puzzle and show that these promoters are indeed differentially regulated at sufficiently high levels of stimulus. We then use this analysis to infer an effective level of phosphorylated PhoP as a function of magnesium stimulus. Our results demonstrate that differential regulation generally depends on the strength of the stimulus and highlight how quantitative analysis of stimulus-response curves can be used to infer properties of cell regulatory circuits that cannot be easily obtained from in vitro measurements.
在大肠杆菌、沙门氏菌及相关细菌中,PhoQ - PhoP系统会根据低镁条件或某些抗菌肽的存在来调节大量基因的表达。我们测量了大肠杆菌中四个受PhoP调控的启动子的转录情况,这些启动子具有显著不同的PhoP结合位点。令人惊讶的是,三个启动子对跨越四个数量级的镁浓度显示出相同的反应。通过分析和测试一个简单的转录调控模型,我们找到了这个谜题的解释,并表明这些启动子在足够高的刺激水平下确实受到差异调控。然后,我们利用这一分析来推断磷酸化PhoP的有效水平作为镁刺激的函数。我们的结果表明,差异调控通常取决于刺激的强度,并突出了如何通过对刺激 - 反应曲线的定量分析来推断难以从体外测量中轻易获得的细胞调节回路的特性。