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Adenosine methylation as a molecular imprint defining the fate of RNA

Multiple lines of evidence suggest the RNA modification N (6)‐methyladonsine (m(6)A), which is installed in the nucleus cotranscriptionally and, thereafter, serves as a reversible chemical imprint that influences several steps of mRNA metabolism. This includes but is not limited to RNA folding, spli...

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Autores principales: Knuckles, Philip, Bühler, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175371/
https://www.ncbi.nlm.nih.gov/pubmed/29782652
http://dx.doi.org/10.1002/1873-3468.13107
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author Knuckles, Philip
Bühler, Marc
author_facet Knuckles, Philip
Bühler, Marc
author_sort Knuckles, Philip
collection PubMed
description Multiple lines of evidence suggest the RNA modification N (6)‐methyladonsine (m(6)A), which is installed in the nucleus cotranscriptionally and, thereafter, serves as a reversible chemical imprint that influences several steps of mRNA metabolism. This includes but is not limited to RNA folding, splicing, stability, transport and translation. In this Review we focus on the current view of the nuclear installation of m(6)A as well as the molecular players involved, the so called m(6)A writers. We also explore the effector proteins, or m(6)A readers, that decode the imprint in different cellular contexts and compartments, and ultimately, the way the modification influences the lifecycle of an RNA molecule. The wide evolutionary conservation of m(6)A and its critical role in physiology and disease warrants further studies into this burgeoning and exciting field.
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spelling pubmed-61753712018-10-19 Adenosine methylation as a molecular imprint defining the fate of RNA Knuckles, Philip Bühler, Marc FEBS Lett Review Articles Multiple lines of evidence suggest the RNA modification N (6)‐methyladonsine (m(6)A), which is installed in the nucleus cotranscriptionally and, thereafter, serves as a reversible chemical imprint that influences several steps of mRNA metabolism. This includes but is not limited to RNA folding, splicing, stability, transport and translation. In this Review we focus on the current view of the nuclear installation of m(6)A as well as the molecular players involved, the so called m(6)A writers. We also explore the effector proteins, or m(6)A readers, that decode the imprint in different cellular contexts and compartments, and ultimately, the way the modification influences the lifecycle of an RNA molecule. The wide evolutionary conservation of m(6)A and its critical role in physiology and disease warrants further studies into this burgeoning and exciting field. John Wiley and Sons Inc. 2018-05-31 2018-09 /pmc/articles/PMC6175371/ /pubmed/29782652 http://dx.doi.org/10.1002/1873-3468.13107 Text en © 2018 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Knuckles, Philip
Bühler, Marc
Adenosine methylation as a molecular imprint defining the fate of RNA
title Adenosine methylation as a molecular imprint defining the fate of RNA
title_full Adenosine methylation as a molecular imprint defining the fate of RNA
title_fullStr Adenosine methylation as a molecular imprint defining the fate of RNA
title_full_unstemmed Adenosine methylation as a molecular imprint defining the fate of RNA
title_short Adenosine methylation as a molecular imprint defining the fate of RNA
title_sort adenosine methylation as a molecular imprint defining the fate of rna
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175371/
https://www.ncbi.nlm.nih.gov/pubmed/29782652
http://dx.doi.org/10.1002/1873-3468.13107
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