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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
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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. |
format | Online Article Text |
id | pubmed-6191714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
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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