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The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes

Connections between distinct catalytic RNA motifs through networks of mutations that retain catalytic function (neutral networks) were likely central to the evolution of biocatalysis. Despite suggestions that functional RNAs collectively form an interconnected web of neutral networks, little evidenc...

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Detalles Bibliográficos
Autores principales: DasGupta, Saurja, Nykiel, Kamila, Piccirilli, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370743/
https://www.ncbi.nlm.nih.gov/pubmed/34131025
http://dx.doi.org/10.1261/rna.078813.121
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author DasGupta, Saurja
Nykiel, Kamila
Piccirilli, Joseph A.
author_facet DasGupta, Saurja
Nykiel, Kamila
Piccirilli, Joseph A.
author_sort DasGupta, Saurja
collection PubMed
description Connections between distinct catalytic RNA motifs through networks of mutations that retain catalytic function (neutral networks) were likely central to the evolution of biocatalysis. Despite suggestions that functional RNAs collectively form an interconnected web of neutral networks, little evidence has emerged to demonstrate the existence of such intersecting networks in naturally occurring RNAs. Here we show that neutral networks of two naturally occurring, seemingly unrelated endonucleolytic ribozymes, the hammerhead (HH) and hairpin (HP), intersect. Sequences at the intersection of these networks exhibit catalytic functions corresponding to both ribozymes by potentially populating both catalytic folds and enable a smooth crossover between the two. Small and structurally simple endonucleolytic motifs like the HH ribozyme could, through mutational walks along their neutral networks, encounter novel catalytic phenotypes, and structurally flexible, bifunctional sequences at the intersection of these networks could have acted as nodes for evolutionary diversification in an RNA world. Considering the simplicity and small size of the HH ribozyme, we propose that this self-cleaving motif could have been a precursor to other more complex endonucleolytic ribozymes. More generally, our results suggest that RNAs that possess distinct sequences, structures, and catalytic functions, can potentially share evolutionary history through mutational connections in sequence space.
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spelling pubmed-83707432022-09-01 The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes DasGupta, Saurja Nykiel, Kamila Piccirilli, Joseph A. RNA Article Connections between distinct catalytic RNA motifs through networks of mutations that retain catalytic function (neutral networks) were likely central to the evolution of biocatalysis. Despite suggestions that functional RNAs collectively form an interconnected web of neutral networks, little evidence has emerged to demonstrate the existence of such intersecting networks in naturally occurring RNAs. Here we show that neutral networks of two naturally occurring, seemingly unrelated endonucleolytic ribozymes, the hammerhead (HH) and hairpin (HP), intersect. Sequences at the intersection of these networks exhibit catalytic functions corresponding to both ribozymes by potentially populating both catalytic folds and enable a smooth crossover between the two. Small and structurally simple endonucleolytic motifs like the HH ribozyme could, through mutational walks along their neutral networks, encounter novel catalytic phenotypes, and structurally flexible, bifunctional sequences at the intersection of these networks could have acted as nodes for evolutionary diversification in an RNA world. Considering the simplicity and small size of the HH ribozyme, we propose that this self-cleaving motif could have been a precursor to other more complex endonucleolytic ribozymes. More generally, our results suggest that RNAs that possess distinct sequences, structures, and catalytic functions, can potentially share evolutionary history through mutational connections in sequence space. Cold Spring Harbor Laboratory Press 2021-09 /pmc/articles/PMC8370743/ /pubmed/34131025 http://dx.doi.org/10.1261/rna.078813.121 Text en © 2021 DasGupta et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Article
DasGupta, Saurja
Nykiel, Kamila
Piccirilli, Joseph A.
The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title_full The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title_fullStr The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title_full_unstemmed The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title_short The hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
title_sort hammerhead self-cleaving motif as a precursor to complex endonucleolytic ribozymes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370743/
https://www.ncbi.nlm.nih.gov/pubmed/34131025
http://dx.doi.org/10.1261/rna.078813.121
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