Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Mol Syst Biol. 2013 Apr 16;9:658. doi: 10.1038/msb.2013.14.
Gene expression is regulated by specific transcriptional circuits but also by the global expression machinery as a function of growth. Simultaneous specific and global regulation thus constitutes an additional--but often neglected--layer of complexity in gene expression. Here, we develop an experimental-computational approach to dissect specific and global regulation in the bacterium Escherichia coli. By using fluorescent promoter reporters, we show that global regulation is growth rate dependent not only during steady state but also during dynamic changes in growth rate and can be quantified through two promoter-specific parameters. By applying our approach to arginine biosynthesis, we obtain a quantitative understanding of both specific and global regulation that allows accurate prediction of the temporal response to simultaneous perturbations in arginine availability and growth rate. We thereby uncover two principles of joint regulation: (i) specific regulation by repression dominates the transcriptional response during metabolic steady states, largely repressing the biosynthesis genes even when biosynthesis is required and (ii) global regulation sets the maximum promoter activity that is exploited during the transition between steady states.
基因表达受特定转录回路调控,但也受生长的全局表达机制调控。因此,特定和全局调控的同时发生构成了基因表达中一个额外的——但往往被忽视的——复杂性层次。在这里,我们开发了一种实验计算方法来剖析细菌大肠杆菌中的特定和全局调控。通过使用荧光启动子报告基因,我们表明全局调控不仅在稳态期间,而且在生长速率的动态变化期间都依赖于生长速率,并且可以通过两个启动子特异性参数进行量化。通过将我们的方法应用于精氨酸生物合成,我们获得了对特定和全局调控的定量理解,这允许对精氨酸可用性和生长速率同时受到干扰时的时间响应进行准确预测。我们因此揭示了联合调控的两个原则:(i)在代谢稳态期间,抑制的特异性调控占主导地位,即使需要生物合成时,也会抑制生物合成基因;(ii)全局调控设定了在稳态之间过渡期间利用的最大启动子活性。