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The ribosome epitranscriptome: inert—or a platform for functional plasticity?
A universal property of all rRNAs explored to date is the prevalence of post-transcriptional (“epitranscriptional”) modifications, which expand the chemical and topological properties of the four standard nucleosides. Are these modifications an inert, constitutive part of the ribosome? Or could they...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522695/ https://www.ncbi.nlm.nih.gov/pubmed/34312287 http://dx.doi.org/10.1261/rna.078859.121 |
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author | Georgeson, Joseph Schwartz, Schraga |
author_facet | Georgeson, Joseph Schwartz, Schraga |
author_sort | Georgeson, Joseph |
collection | PubMed |
description | A universal property of all rRNAs explored to date is the prevalence of post-transcriptional (“epitranscriptional”) modifications, which expand the chemical and topological properties of the four standard nucleosides. Are these modifications an inert, constitutive part of the ribosome? Or could they, in part, also regulate the structure or function of the ribosome? In this review, we summarize emerging evidence that rRNA modifications are more heterogeneous than previously thought, and that they can also vary from one condition to another, such as in the context of a cellular response or a developmental trajectory. We discuss the implications of these results and key open questions on the path toward connecting such heterogeneity with function. |
format | Online Article Text |
id | pubmed-8522695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85226952021-11-01 The ribosome epitranscriptome: inert—or a platform for functional plasticity? Georgeson, Joseph Schwartz, Schraga RNA Mini-Review A universal property of all rRNAs explored to date is the prevalence of post-transcriptional (“epitranscriptional”) modifications, which expand the chemical and topological properties of the four standard nucleosides. Are these modifications an inert, constitutive part of the ribosome? Or could they, in part, also regulate the structure or function of the ribosome? In this review, we summarize emerging evidence that rRNA modifications are more heterogeneous than previously thought, and that they can also vary from one condition to another, such as in the context of a cellular response or a developmental trajectory. We discuss the implications of these results and key open questions on the path toward connecting such heterogeneity with function. Cold Spring Harbor Laboratory Press 2021-11 /pmc/articles/PMC8522695/ /pubmed/34312287 http://dx.doi.org/10.1261/rna.078859.121 Text en © 2021 Georgeson and Schwartz; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article, published in RNA, 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 | Mini-Review Georgeson, Joseph Schwartz, Schraga The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title | The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title_full | The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title_fullStr | The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title_full_unstemmed | The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title_short | The ribosome epitranscriptome: inert—or a platform for functional plasticity? |
title_sort | ribosome epitranscriptome: inert—or a platform for functional plasticity? |
topic | Mini-Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522695/ https://www.ncbi.nlm.nih.gov/pubmed/34312287 http://dx.doi.org/10.1261/rna.078859.121 |
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