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Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture

Compensatory mutations in RNA are generally regarded as those that maintain base pairing, and their identification forms the basis of phylogenetic predictions of RNA secondary structure. However, other types of compensatory mutations can provide higher-order structural and evolutionary information....

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Autores principales: Lacroix-Labonté, Julie, Girard, Nicolas, Lemieux, Sébastien, Legault, Pascale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299992/
https://www.ncbi.nlm.nih.gov/pubmed/22086962
http://dx.doi.org/10.1093/nar/gkr1018
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author Lacroix-Labonté, Julie
Girard, Nicolas
Lemieux, Sébastien
Legault, Pascale
author_facet Lacroix-Labonté, Julie
Girard, Nicolas
Lemieux, Sébastien
Legault, Pascale
author_sort Lacroix-Labonté, Julie
collection PubMed
description Compensatory mutations in RNA are generally regarded as those that maintain base pairing, and their identification forms the basis of phylogenetic predictions of RNA secondary structure. However, other types of compensatory mutations can provide higher-order structural and evolutionary information. Here, we present a helix-length compensation study for investigating structure–function relationships in RNA. The approach is demonstrated for stem-loop I and stem-loop V of the Neurospora VS ribozyme, which form a kissing–loop interaction important for substrate recognition. To rapidly characterize the substrate specificity (k(cat)/K(M)) of several substrate/ribozyme pairs, a procedure was established for simultaneous kinetic characterization of multiple substrates. Several active substrate/ribozyme pairs were identified, indicating the presence of limited substrate promiscuity for stem Ib variants and helix-length compensation between stems Ib and V. 3D models of the I/V interaction were generated that are compatible with the kinetic data. These models further illustrate the adaptability of the VS ribozyme architecture for substrate cleavage and provide global structural information on the I/V kissing–loop interaction. By exploring higher-order compensatory mutations in RNA our approach brings a deeper understanding of the adaptability of RNA structure, while opening new avenues for RNA research.
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spelling pubmed-32999922012-03-13 Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture Lacroix-Labonté, Julie Girard, Nicolas Lemieux, Sébastien Legault, Pascale Nucleic Acids Res Structural Biology Compensatory mutations in RNA are generally regarded as those that maintain base pairing, and their identification forms the basis of phylogenetic predictions of RNA secondary structure. However, other types of compensatory mutations can provide higher-order structural and evolutionary information. Here, we present a helix-length compensation study for investigating structure–function relationships in RNA. The approach is demonstrated for stem-loop I and stem-loop V of the Neurospora VS ribozyme, which form a kissing–loop interaction important for substrate recognition. To rapidly characterize the substrate specificity (k(cat)/K(M)) of several substrate/ribozyme pairs, a procedure was established for simultaneous kinetic characterization of multiple substrates. Several active substrate/ribozyme pairs were identified, indicating the presence of limited substrate promiscuity for stem Ib variants and helix-length compensation between stems Ib and V. 3D models of the I/V interaction were generated that are compatible with the kinetic data. These models further illustrate the adaptability of the VS ribozyme architecture for substrate cleavage and provide global structural information on the I/V kissing–loop interaction. By exploring higher-order compensatory mutations in RNA our approach brings a deeper understanding of the adaptability of RNA structure, while opening new avenues for RNA research. Oxford University Press 2012-03 2011-11-15 /pmc/articles/PMC3299992/ /pubmed/22086962 http://dx.doi.org/10.1093/nar/gkr1018 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Structural Biology
Lacroix-Labonté, Julie
Girard, Nicolas
Lemieux, Sébastien
Legault, Pascale
Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title_full Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title_fullStr Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title_full_unstemmed Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title_short Helix-length compensation studies reveal the adaptability of the VS ribozyme architecture
title_sort helix-length compensation studies reveal the adaptability of the vs ribozyme architecture
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299992/
https://www.ncbi.nlm.nih.gov/pubmed/22086962
http://dx.doi.org/10.1093/nar/gkr1018
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