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Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control

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 adjace...

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Autores principales: Scull, Catherine E., Dandpat, Shiba S., Romero, Rosa A., Walter, Nils G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838592/
https://www.ncbi.nlm.nih.gov/pubmed/33521053
http://dx.doi.org/10.3389/fmolb.2020.607158
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author Scull, Catherine E.
Dandpat, Shiba S.
Romero, Rosa A.
Walter, Nils G.
author_facet Scull, Catherine E.
Dandpat, Shiba S.
Romero, Rosa A.
Walter, Nils G.
author_sort Scull, Catherine E.
collection PubMed
description 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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spelling pubmed-78385922021-01-28 Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control Scull, Catherine E. Dandpat, Shiba S. Romero, Rosa A. Walter, Nils G. Front Mol Biosci Molecular Biosciences 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. Frontiers Media S.A. 2021-01-13 /pmc/articles/PMC7838592/ /pubmed/33521053 http://dx.doi.org/10.3389/fmolb.2020.607158 Text en Copyright © 2021 Scull, Dandpat, Romero and Walter. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Scull, Catherine E.
Dandpat, Shiba S.
Romero, Rosa A.
Walter, Nils G.
Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title_full Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title_fullStr Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title_full_unstemmed Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title_short Transcriptional Riboswitches Integrate Timescales for Bacterial Gene Expression Control
title_sort transcriptional riboswitches integrate timescales for bacterial gene expression control
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838592/
https://www.ncbi.nlm.nih.gov/pubmed/33521053
http://dx.doi.org/10.3389/fmolb.2020.607158
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