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RNA 2′-O-Methylation (Nm) Modification in Human Diseases

Nm (2′-O-methylation) is one of the most common modifications in the RNA world. It has the potential to influence the RNA molecules in multiple ways, such as structure, stability, and interactions, and to play a role in various cellular processes from epigenetic gene regulation, through translation...

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Detalles Bibliográficos
Autores principales: Dimitrova, Dilyana G., Teysset, Laure, Carré, Clément
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409641/
https://www.ncbi.nlm.nih.gov/pubmed/30764532
http://dx.doi.org/10.3390/genes10020117
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author Dimitrova, Dilyana G.
Teysset, Laure
Carré, Clément
author_facet Dimitrova, Dilyana G.
Teysset, Laure
Carré, Clément
author_sort Dimitrova, Dilyana G.
collection PubMed
description Nm (2′-O-methylation) is one of the most common modifications in the RNA world. It has the potential to influence the RNA molecules in multiple ways, such as structure, stability, and interactions, and to play a role in various cellular processes from epigenetic gene regulation, through translation to self versus non-self recognition. Yet, building scientific knowledge on the Nm matter has been hampered for a long time by the challenges in detecting and mapping this modification. Today, with the latest advancements in the area, more and more Nm sites are discovered on RNAs (tRNA, rRNA, mRNA, and small non-coding RNA) and linked to normal or pathological conditions. This review aims to synthesize the Nm-associated human diseases known to date and to tackle potential indirect links to some other biological defects.
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spelling pubmed-64096412019-03-26 RNA 2′-O-Methylation (Nm) Modification in Human Diseases Dimitrova, Dilyana G. Teysset, Laure Carré, Clément Genes (Basel) Review Nm (2′-O-methylation) is one of the most common modifications in the RNA world. It has the potential to influence the RNA molecules in multiple ways, such as structure, stability, and interactions, and to play a role in various cellular processes from epigenetic gene regulation, through translation to self versus non-self recognition. Yet, building scientific knowledge on the Nm matter has been hampered for a long time by the challenges in detecting and mapping this modification. Today, with the latest advancements in the area, more and more Nm sites are discovered on RNAs (tRNA, rRNA, mRNA, and small non-coding RNA) and linked to normal or pathological conditions. This review aims to synthesize the Nm-associated human diseases known to date and to tackle potential indirect links to some other biological defects. MDPI 2019-02-05 /pmc/articles/PMC6409641/ /pubmed/30764532 http://dx.doi.org/10.3390/genes10020117 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dimitrova, Dilyana G.
Teysset, Laure
Carré, Clément
RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title_full RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title_fullStr RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title_full_unstemmed RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title_short RNA 2′-O-Methylation (Nm) Modification in Human Diseases
title_sort rna 2′-o-methylation (nm) modification in human diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409641/
https://www.ncbi.nlm.nih.gov/pubmed/30764532
http://dx.doi.org/10.3390/genes10020117
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