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Perspectives on topology of the human m(1)A methylome at single nucleotide resolution

N(1)-methyladenosine was recently reported to be a chemical modification in mRNA. However, while we identified hundreds of m(1)A sites in the human transcriptome in a previous work, others have detected only nine sites in cytosolic and mitochondrial mRNAs. Herein, we provide additional evidence that...

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Detalles Bibliográficos
Autores principales: Xiong, Xushen, Li, Xiaoyu, Wang, Kun, Yi, Chengqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191714/
https://www.ncbi.nlm.nih.gov/pubmed/30131401
http://dx.doi.org/10.1261/rna.067694.118
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author Xiong, Xushen
Li, Xiaoyu
Wang, Kun
Yi, Chengqi
author_facet Xiong, Xushen
Li, Xiaoyu
Wang, Kun
Yi, Chengqi
author_sort Xiong, Xushen
collection PubMed
description N(1)-methyladenosine was recently reported to be a chemical modification in mRNA. However, while we identified hundreds of m(1)A sites in the human transcriptome in a previous work, others have detected only nine sites in cytosolic and mitochondrial mRNAs. Herein, we provide additional evidence that hundreds of m(1)A sites are present in the human transcriptome. Moreover, we show that both the improper bioinformatic tools and the poor quality of sequencing data in a previous study led to the failure in identifying the majority of m(1)A sites. Our analysis hence provides an explanation of the divergence in the prevalence of this newly discovered mRNA mark.
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spelling pubmed-61917142019-11-01 Perspectives on topology of the human m(1)A methylome at single nucleotide resolution Xiong, Xushen Li, Xiaoyu Wang, Kun Yi, Chengqi RNA Divergent Views N(1)-methyladenosine was recently reported to be a chemical modification in mRNA. However, while we identified hundreds of m(1)A sites in the human transcriptome in a previous work, others have detected only nine sites in cytosolic and mitochondrial mRNAs. Herein, we provide additional evidence that hundreds of m(1)A sites are present in the human transcriptome. Moreover, we show that both the improper bioinformatic tools and the poor quality of sequencing data in a previous study led to the failure in identifying the majority of m(1)A sites. Our analysis hence provides an explanation of the divergence in the prevalence of this newly discovered mRNA mark. Cold Spring Harbor Laboratory Press 2018-11 /pmc/articles/PMC6191714/ /pubmed/30131401 http://dx.doi.org/10.1261/rna.067694.118 Text en © 2018 Xiong et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 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 Divergent Views
Xiong, Xushen
Li, Xiaoyu
Wang, Kun
Yi, Chengqi
Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title_full Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title_fullStr Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title_full_unstemmed Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title_short Perspectives on topology of the human m(1)A methylome at single nucleotide resolution
title_sort perspectives on topology of the human m(1)a methylome at single nucleotide resolution
topic Divergent Views
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191714/
https://www.ncbi.nlm.nih.gov/pubmed/30131401
http://dx.doi.org/10.1261/rna.067694.118
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AT wangkun perspectivesontopologyofthehumanm1amethylomeatsinglenucleotideresolution
AT yichengqi perspectivesontopologyofthehumanm1amethylomeatsinglenucleotideresolution