Unprecedented tunability of riboswitch structure and regulatory function by sub-millimolar variations in physiological Mg2+

Kaley Allyn McCluskey, Julien Boudreault, Patrick St-Pierre, Cibran Perez Gonzalez, Adrien Chauvier, Adrien Rizzi, Pascale B Beauregard, Daniel A Lafontaine, Juan Carlos Penedo-Esteiro

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)
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Abstract

Riboswitches are cis-acting regulatory RNA biosensors that rival the efficiency of those found in proteins. At the heart of their regulatory function is the formation of a highly specific aptamer–ligand complex. Understanding how these RNAs recognize the ligand to regulate gene expression at physiological concentrations of Mg2+ ions and ligand is critical given their broad impact on bacterial gene expression and their potential as antibiotic targets. In this work, we used single-molecule FRET and biochemical techniques to demonstrate that Mg2+ ions act as fine-tuning elements of the amino acid-sensing lysC aptamer's ligand-free structure in the mesophile Bacillus subtilis. Mg2+ interactions with the aptamer produce encounter complexes with strikingly different sensitivities to the ligand in different, yet equally accessible, physiological ionic conditions. Our results demonstrate that the aptamer adapts its structure and folding landscape on a Mg2+-tunable scale to efficiently respond to changes in intracellular lysine of more than two orders of magnitude. The remarkable tunability of the lysC aptamer by sub-millimolar variations in the physiological concentration of Mg2+ ions suggests that some single-aptamer riboswitches have exploited the coupling of cellular levels of ligand and divalent metal ions to tightly control gene expression.
Original languageEnglish
Pages (from-to)6478–6487
Number of pages10
JournalNucleic Acids Research
Volume47
Issue number12
Early online date2 May 2019
DOIs
Publication statusPublished - 9 Jul 2019

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