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Goldilocks and RNA: where Mg(2+) concentration is just right

Magnesium, the most abundant divalent cation in cells, catalyzes RNA cleavage but also promotes RNA folding. Because folding can protect RNA from cleavage, we predicted a ‘Goldilocks landscape’, with local maximum in RNA lifetime at Mg(2+) concentrations required for folding. Here, we use simulation...

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Autores principales: Guth-Metzler, Rebecca, Mohamed, Ahmad Mohyeldin, Cowan, Elizabeth T, Henning, Ashleigh, Ito, Chieri, Frenkel-Pinter, Moran, Wartell, Roger M, Glass, Jennifer B, Williams, Loren Dean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164553/
https://www.ncbi.nlm.nih.gov/pubmed/36987860
http://dx.doi.org/10.1093/nar/gkad124
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author Guth-Metzler, Rebecca
Mohamed, Ahmad Mohyeldin
Cowan, Elizabeth T
Henning, Ashleigh
Ito, Chieri
Frenkel-Pinter, Moran
Wartell, Roger M
Glass, Jennifer B
Williams, Loren Dean
author_facet Guth-Metzler, Rebecca
Mohamed, Ahmad Mohyeldin
Cowan, Elizabeth T
Henning, Ashleigh
Ito, Chieri
Frenkel-Pinter, Moran
Wartell, Roger M
Glass, Jennifer B
Williams, Loren Dean
author_sort Guth-Metzler, Rebecca
collection PubMed
description Magnesium, the most abundant divalent cation in cells, catalyzes RNA cleavage but also promotes RNA folding. Because folding can protect RNA from cleavage, we predicted a ‘Goldilocks landscape’, with local maximum in RNA lifetime at Mg(2+) concentrations required for folding. Here, we use simulation and experiment to discover an innate and sophisticated mechanism of control of RNA lifetime. By simulation we characterized RNA Goldilocks landscapes and their dependence on cleavage and folding parameters. Experiments with yeast tRNA(Phe) and the Tetrahymena ribozyme P4–P6 domain show that structured RNAs can inhabit Goldilocks peaks. The Goldilocks peaks are tunable by differences in folded and unfolded cleavage rate constants, Mg(2+) binding cooperativity, and Mg(2+) affinity. Different folding and cleavage parameters produce Goldilocks landscapes with a variety of features. Goldilocks behavior allows ultrafine control of RNA chemical lifetime, whereas non-folding RNAs do not display Goldilocks peaks of protection. In sum, the effects of Mg(2+) on RNA persistence are expected to be pleomorphic, both protecting and degrading RNA. In evolutionary context, Goldilocks behavior may have been a selectable trait of RNA in an early Earth environment containing Mg(2+) and other metals.
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spelling pubmed-101645532023-05-08 Goldilocks and RNA: where Mg(2+) concentration is just right Guth-Metzler, Rebecca Mohamed, Ahmad Mohyeldin Cowan, Elizabeth T Henning, Ashleigh Ito, Chieri Frenkel-Pinter, Moran Wartell, Roger M Glass, Jennifer B Williams, Loren Dean Nucleic Acids Res Chemical Biology and Nucleic Acid Chemistry Magnesium, the most abundant divalent cation in cells, catalyzes RNA cleavage but also promotes RNA folding. Because folding can protect RNA from cleavage, we predicted a ‘Goldilocks landscape’, with local maximum in RNA lifetime at Mg(2+) concentrations required for folding. Here, we use simulation and experiment to discover an innate and sophisticated mechanism of control of RNA lifetime. By simulation we characterized RNA Goldilocks landscapes and their dependence on cleavage and folding parameters. Experiments with yeast tRNA(Phe) and the Tetrahymena ribozyme P4–P6 domain show that structured RNAs can inhabit Goldilocks peaks. The Goldilocks peaks are tunable by differences in folded and unfolded cleavage rate constants, Mg(2+) binding cooperativity, and Mg(2+) affinity. Different folding and cleavage parameters produce Goldilocks landscapes with a variety of features. Goldilocks behavior allows ultrafine control of RNA chemical lifetime, whereas non-folding RNAs do not display Goldilocks peaks of protection. In sum, the effects of Mg(2+) on RNA persistence are expected to be pleomorphic, both protecting and degrading RNA. In evolutionary context, Goldilocks behavior may have been a selectable trait of RNA in an early Earth environment containing Mg(2+) and other metals. Oxford University Press 2023-03-29 /pmc/articles/PMC10164553/ /pubmed/36987860 http://dx.doi.org/10.1093/nar/gkad124 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemical Biology and Nucleic Acid Chemistry
Guth-Metzler, Rebecca
Mohamed, Ahmad Mohyeldin
Cowan, Elizabeth T
Henning, Ashleigh
Ito, Chieri
Frenkel-Pinter, Moran
Wartell, Roger M
Glass, Jennifer B
Williams, Loren Dean
Goldilocks and RNA: where Mg(2+) concentration is just right
title Goldilocks and RNA: where Mg(2+) concentration is just right
title_full Goldilocks and RNA: where Mg(2+) concentration is just right
title_fullStr Goldilocks and RNA: where Mg(2+) concentration is just right
title_full_unstemmed Goldilocks and RNA: where Mg(2+) concentration is just right
title_short Goldilocks and RNA: where Mg(2+) concentration is just right
title_sort goldilocks and rna: where mg(2+) concentration is just right
topic Chemical Biology and Nucleic Acid Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164553/
https://www.ncbi.nlm.nih.gov/pubmed/36987860
http://dx.doi.org/10.1093/nar/gkad124
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