Scull Catherine E, Dandpat Shiba S, Romero Rosa A, Walter Nils G
Department of Chemistry, Single Molecule Analysis Group and Center for RNA Biomedicine, University of Michigan, Ann Arbor, MI, United States.
Front Mol Biosci. 2021 Jan 13;7:607158. doi: 10.3389/fmolb.2020.607158. eCollection 2020.
Transcriptional riboswitches involve RNA aptamers that are typically found in the 5' untranslated regions (UTRs) of bacterial mRNAs and form alternative secondary structures upon binding to cognate ligands. Alteration of the riboswitch's secondary structure results in perturbations of an adjacent expression platform that controls transcription elongation and termination, thus turning downstream gene expression "on" or "off." Riboswitch ligands are typically small metabolites, divalent cations, anions, signaling molecules, or other RNAs, and can be part of larger signaling cascades. The interconnectedness of ligand binding, RNA folding, RNA transcription, and gene expression empowers riboswitches to integrate cellular processes and environmental conditions across multiple timescales. For a successful response to an environmental cue that may determine a bacterium's chance of survival, a coordinated coupling of timescales from microseconds to minutes must be achieved. This review focuses on recent advances in our understanding of how riboswitches affect such critical gene expression control across time.
转录核糖开关涉及RNA适体,这些适体通常存在于细菌mRNA的5'非翻译区(UTR)中,并在与同源配体结合时形成不同的二级结构。核糖开关二级结构的改变会导致相邻表达平台受到干扰,该平台控制转录延伸和终止,从而开启或关闭下游基因表达。核糖开关配体通常是小分子代谢物、二价阳离子、阴离子、信号分子或其他RNA,并且可以是更大信号级联的一部分。配体结合、RNA折叠、RNA转录和基因表达之间的相互联系使核糖开关能够在多个时间尺度上整合细胞过程和环境条件。为了成功应对可能决定细菌生存几率的环境信号,必须实现从微秒到分钟的时间尺度的协调耦合。本综述重点关注我们对核糖开关如何随时间影响这种关键基因表达控制的理解的最新进展。