Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA.
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri, USA
J Bacteriol. 2021 Mar 23;203(8). doi: 10.1128/JB.00512-20.
The fitness of an individual bacterial cell is highly dependent upon the temporal tuning of gene expression levels when subjected to different environmental cues. Kinetic regulation of transcription initiation is a key step in modulating the levels of transcribed genes to promote bacterial survival. The initiation phase encompasses the binding of RNA polymerase (RNAP) to promoter DNA and a series of coupled protein-DNA conformational changes prior to entry into processive elongation. The time required to complete the initiation phase can vary by orders of magnitude and is ultimately dictated by the DNA sequence of the promoter. In this review, we aim to provide the required background to understand how promoter sequence motifs may affect initiation kinetics during promoter recognition and binding, subsequent conformational changes which lead to DNA opening around the transcription start site, and promoter escape. By calculating the steady-state flux of RNA production as a function of these effects, we illustrate that the presence/absence of a consensus promoter motif cannot be used in isolation to make conclusions regarding promoter strength. Instead, the entire series of linked, sequence-dependent structural transitions must be considered holistically. Finally, we describe how individual transcription factors take advantage of the broad distribution of sequence-dependent basal kinetics to either increase or decrease RNA flux.
个体细菌细胞的适应性高度依赖于其在受到不同环境线索刺激时对基因表达水平的时间调谐。转录起始的动力学调控是调节转录基因水平以促进细菌生存的关键步骤。起始阶段包括 RNA 聚合酶 (RNAP) 与启动子 DNA 的结合,以及在进入连续延伸之前一系列偶联的蛋白-DNA 构象变化。完成起始阶段所需的时间可能相差几个数量级,最终由启动子的 DNA 序列决定。在这篇综述中,我们旨在提供必要的背景知识,以了解启动子序列基序如何在启动子识别和结合过程中影响起始动力学,随后导致转录起始位点周围 DNA 开放和启动子逃逸的构象变化。通过将 RNA 产生的稳态通量作为这些效应的函数进行计算,我们说明仅通过存在/不存在共识启动子基序,不能孤立地得出启动子强度的结论。相反,必须整体考虑整个序列依赖性结构转变系列。最后,我们描述了单个转录因子如何利用广泛分布的序列依赖性基础动力学来增加或减少 RNA 通量。