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FTO, RNA epigenetics and epilepsy

Several recent landmark papers describing N(6)-methyladenosine (m(6)A) RNA modifications have provided valuable new insights as to the importance of m(6)A in the RNA transcriptome and in furthering the understanding of RNA epigenetics. One endogenous enzyme responsible for demethylating RNA m(6)A, F...

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Detalles Bibliográficos
Autores principales: Rowles, Joie, Wong, Morgan, Powers, Ryan, Olsen, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469450/
https://www.ncbi.nlm.nih.gov/pubmed/22948233
http://dx.doi.org/10.4161/epi.21977
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author Rowles, Joie
Wong, Morgan
Powers, Ryan
Olsen, Mark
author_facet Rowles, Joie
Wong, Morgan
Powers, Ryan
Olsen, Mark
author_sort Rowles, Joie
collection PubMed
description Several recent landmark papers describing N(6)-methyladenosine (m(6)A) RNA modifications have provided valuable new insights as to the importance of m(6)A in the RNA transcriptome and in furthering the understanding of RNA epigenetics. One endogenous enzyme responsible for demethylating RNA m(6)A, FTO, is highly expressed in the CNS and is likely involved in mRNA metabolism, splicing or other nuclear RNA processing events. microRNAs (miRNAs), a family of small, non-coding transcripts that bind to target mRNAs and inhibit subsequent translation, are highly expressed in the CNS and are associated with several neurological disorders, including epilepsy. miRNAs frequently bind to recognition sequences in the 3′UTR, a region that is also enriched for m(6)A. Certain specific miRNAs are upregulated by neuronal activity and are coupled to epileptogenesis; these miRNAs contain a consensus m(6)A site that if methylated could possibly regulate miRNA processing or function. This commentary highlights aspects from recent papers to propose a functional association between FTO, RNA epigenetics and epilepsy.
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spelling pubmed-34694502012-10-23 FTO, RNA epigenetics and epilepsy Rowles, Joie Wong, Morgan Powers, Ryan Olsen, Mark Epigenetics Point of View Several recent landmark papers describing N(6)-methyladenosine (m(6)A) RNA modifications have provided valuable new insights as to the importance of m(6)A in the RNA transcriptome and in furthering the understanding of RNA epigenetics. One endogenous enzyme responsible for demethylating RNA m(6)A, FTO, is highly expressed in the CNS and is likely involved in mRNA metabolism, splicing or other nuclear RNA processing events. microRNAs (miRNAs), a family of small, non-coding transcripts that bind to target mRNAs and inhibit subsequent translation, are highly expressed in the CNS and are associated with several neurological disorders, including epilepsy. miRNAs frequently bind to recognition sequences in the 3′UTR, a region that is also enriched for m(6)A. Certain specific miRNAs are upregulated by neuronal activity and are coupled to epileptogenesis; these miRNAs contain a consensus m(6)A site that if methylated could possibly regulate miRNA processing or function. This commentary highlights aspects from recent papers to propose a functional association between FTO, RNA epigenetics and epilepsy. Landes Bioscience 2012-10-01 /pmc/articles/PMC3469450/ /pubmed/22948233 http://dx.doi.org/10.4161/epi.21977 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Point of View
Rowles, Joie
Wong, Morgan
Powers, Ryan
Olsen, Mark
FTO, RNA epigenetics and epilepsy
title FTO, RNA epigenetics and epilepsy
title_full FTO, RNA epigenetics and epilepsy
title_fullStr FTO, RNA epigenetics and epilepsy
title_full_unstemmed FTO, RNA epigenetics and epilepsy
title_short FTO, RNA epigenetics and epilepsy
title_sort fto, rna epigenetics and epilepsy
topic Point of View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469450/
https://www.ncbi.nlm.nih.gov/pubmed/22948233
http://dx.doi.org/10.4161/epi.21977
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