Riboswitch regulation mechanisms: RNA, metabolites and regulatory proteins

Riboswitches are RNA sensors that have been shown to modulate the expression of downstream genes by altering their structure upon metabolite binding. Riboswitches are unique among cellular regulators in that metabolite detection is strictly performed using RNA interactions with the sensed metabolite...

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Veröffentlicht in:Biochimica et biophysica acta. Gene regulatory mechanisms 2020-03, Vol.1863 (3), p.194501-194501, Article 194501
Hauptverfasser: Bédard, Anne-Sophie Vézina, Hien, Elsa D.M., Lafontaine, Daniel A.
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Sprache:eng
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Zusammenfassung:Riboswitches are RNA sensors that have been shown to modulate the expression of downstream genes by altering their structure upon metabolite binding. Riboswitches are unique among cellular regulators in that metabolite detection is strictly performed using RNA interactions with the sensed metabolite and in which no regulatory protein is needed to mediate the interaction. However, recent studies have shed light on riboswitch control mechanisms relying on protein regulators to harness metabolite binding for the mediation of gene expression, thereby increasing the range of cellular factors involved in riboswitch regulation. The interaction between riboswitches and proteins adds another level of evolutionary pressure as riboswitches must maintain key residues for metabolite detection, structural switching and protein binding sites. Here, we review regulatory mechanisms involving Escherichia coli riboswitches that have recently been shown to rely on regulatory proteins. We also discuss the implication of such protein-based riboswitch regulatory mechanisms for genetic regulation. •Riboswitch are metabolite-sensing RNA regulators that modulate gene expression.•RNA conformational change is at the heart of riboswitch regulation mechanisms.•Recent works have shown the implication of proteins in the genetic regulation.•Regulatory proteins are mainly involved in providing additional levels of regulation.
ISSN:1874-9399
1876-4320
DOI:10.1016/j.bbagrm.2020.194501