Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control

被引:37
|
作者
Scull, Catherine E.
Dandpat, Shiba S.
Romero, Rosa A.
Walter, Nils G. [1 ]
机构
[1] Univ Michigan, Dept Chem, Single Mol Anal Grp, Ann Arbor, MI 48109 USA
关键词
RNA polymerase; RNA folding; riboswitch control of gene expression; transcription; structural dynamics; RNA-POLYMERASE-I; SINGLE-MOLECULE FRET; LIGAND-BINDING; ELONGATION; MECHANISMS; ARCHITECTURE; MODULATION; TRANSPORT; RIBOZYMES; DYNAMICS;
D O I
10.3389/fmolb.2020.607158
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:10
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