Vishwakarma Rishi Kishore, Brodolin Konstantin
Institut de Recherche en Infectiologie de Montpellier, CNRS, Université de Montpellier, Montpellier, France.
Front Microbiol. 2020 Jul 29;11:1798. doi: 10.3389/fmicb.2020.01798. eCollection 2020.
Transcription initiation is a key checkpoint and highly regulated step of gene expression. The sigma (σ) subunit of RNA polymerase (RNAP) controls all transcription initiation steps, from recognition of the -10/-35 promoter elements, upon formation of the closed promoter complex (RPc), to stabilization of the open promoter complex (RPo) and stimulation of the primary steps in RNA synthesis. The canonical mechanism to regulate σ activity upon transcription initiation relies on activators that recognize specific DNA motifs and recruit RNAP to promoters. This mini-review describes an emerging group of transcriptional regulators that form a complex with σ or/and RNAP prior to promoter binding, remodel the σ subunit conformation, and thus modify RNAP activity. Such strategy is widely used by bacteriophages to appropriate the host RNAP. Recent findings on RNAP-binding protein A (RbpA) from and Crl from suggest that activator-driven changes in σ conformation can be a widespread regulatory mechanism in bacteria.
转录起始是基因表达的一个关键检查点和受到高度调控的步骤。RNA聚合酶(RNAP)的σ亚基控制着所有转录起始步骤,从识别-10/-35启动子元件、形成封闭启动子复合物(RPc),到开放启动子复合物(RPo)的稳定以及刺激RNA合成的初级步骤。转录起始时调控σ活性的经典机制依赖于激活因子,这些激活因子识别特定的DNA基序并将RNAP招募到启动子。这篇小型综述描述了一类新兴的转录调节因子,它们在启动子结合之前与σ或/和RNAP形成复合物,重塑σ亚基构象,从而改变RNAP活性。这种策略被噬菌体广泛用于利用宿主RNAP。来自[具体来源1]的RNAP结合蛋白A(RbpA)和来自[具体来源2]的Crl的最新研究结果表明,激活因子驱动的σ构象变化可能是细菌中一种广泛存在的调控机制。