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RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation

N(6)-methyladenosine (m(6)A) is the most prevalent and internal modification that occurs in the messenger RNAs (mRNA) of most eukaryotes, although its functional relevance remained a mystery for decades. This modification is installed by the m(6)A methylation “writers” and can be reversed by demethy...

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Detalles Bibliográficos
Autores principales: Yue, Yanan, Liu, Jianzhao, He, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511210/
https://www.ncbi.nlm.nih.gov/pubmed/26159994
http://dx.doi.org/10.1101/gad.262766.115
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author Yue, Yanan
Liu, Jianzhao
He, Chuan
author_facet Yue, Yanan
Liu, Jianzhao
He, Chuan
author_sort Yue, Yanan
collection PubMed
description N(6)-methyladenosine (m(6)A) is the most prevalent and internal modification that occurs in the messenger RNAs (mRNA) of most eukaryotes, although its functional relevance remained a mystery for decades. This modification is installed by the m(6)A methylation “writers” and can be reversed by demethylases that serve as “erasers.” In this review, we mainly summarize recent progress in the study of the m(6)A mRNA methylation machineries across eukaryotes and discuss their newly uncovered biological functions. The broad roles of m(6)A in regulating cell fates and embryonic development highlight the existence of another layer of epigenetic regulation at the RNA level, where mRNA is subjected to chemical modifications that affect protein expression.
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spelling pubmed-45112102016-01-01 RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation Yue, Yanan Liu, Jianzhao He, Chuan Genes Dev Review N(6)-methyladenosine (m(6)A) is the most prevalent and internal modification that occurs in the messenger RNAs (mRNA) of most eukaryotes, although its functional relevance remained a mystery for decades. This modification is installed by the m(6)A methylation “writers” and can be reversed by demethylases that serve as “erasers.” In this review, we mainly summarize recent progress in the study of the m(6)A mRNA methylation machineries across eukaryotes and discuss their newly uncovered biological functions. The broad roles of m(6)A in regulating cell fates and embryonic development highlight the existence of another layer of epigenetic regulation at the RNA level, where mRNA is subjected to chemical modifications that affect protein expression. Cold Spring Harbor Laboratory Press 2015-07-01 /pmc/articles/PMC4511210/ /pubmed/26159994 http://dx.doi.org/10.1101/gad.262766.115 Text en © 2015 Yue et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six 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/.
spellingShingle Review
Yue, Yanan
Liu, Jianzhao
He, Chuan
RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title_full RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title_fullStr RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title_full_unstemmed RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title_short RNA N(6)-methyladenosine methylation in post-transcriptional gene expression regulation
title_sort rna n(6)-methyladenosine methylation in post-transcriptional gene expression regulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511210/
https://www.ncbi.nlm.nih.gov/pubmed/26159994
http://dx.doi.org/10.1101/gad.262766.115
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