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Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method

Studies of chemical modifications on RNA have ushered in the field of epitranscriptomics. N(6)-Methyladenosine (m(6)A) is the most typical RNA modification and is indispensable for basic biological processes. This study presents a chemical pulldown method (m(6)A-ORL-Seq) for transcriptome-wide profi...

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Autores principales: Xie, Yalun, Han, Shaoqing, Li, Qiming, Fang, Zhentian, Yang, Wei, Wei, Qi, Wang, Yafen, Zhou, Yu, Weng, Xiaocheng, Zhou, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600483/
https://www.ncbi.nlm.nih.gov/pubmed/36349098
http://dx.doi.org/10.1039/d2sc03181g
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author Xie, Yalun
Han, Shaoqing
Li, Qiming
Fang, Zhentian
Yang, Wei
Wei, Qi
Wang, Yafen
Zhou, Yu
Weng, Xiaocheng
Zhou, Xiang
author_facet Xie, Yalun
Han, Shaoqing
Li, Qiming
Fang, Zhentian
Yang, Wei
Wei, Qi
Wang, Yafen
Zhou, Yu
Weng, Xiaocheng
Zhou, Xiang
author_sort Xie, Yalun
collection PubMed
description Studies of chemical modifications on RNA have ushered in the field of epitranscriptomics. N(6)-Methyladenosine (m(6)A) is the most typical RNA modification and is indispensable for basic biological processes. This study presents a chemical pulldown method (m(6)A-ORL-Seq) for transcriptome-wide profiling of m(6)A. Moreover, chemical labeling results in a specific reverse transcription (RT) truncation signature. This study has identified four thousand high-confidence m(6)A sites at single-base resolution in the human transcriptome. Unlike previously reported methods based on m(6)A-antibody or m(6)A-sensitive enzymes, the antibody/enzyme-free chemical method provides a new perspective for single-base m(6)A detection at the transcriptome level.
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spelling pubmed-96004832022-11-07 Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method Xie, Yalun Han, Shaoqing Li, Qiming Fang, Zhentian Yang, Wei Wei, Qi Wang, Yafen Zhou, Yu Weng, Xiaocheng Zhou, Xiang Chem Sci Chemistry Studies of chemical modifications on RNA have ushered in the field of epitranscriptomics. N(6)-Methyladenosine (m(6)A) is the most typical RNA modification and is indispensable for basic biological processes. This study presents a chemical pulldown method (m(6)A-ORL-Seq) for transcriptome-wide profiling of m(6)A. Moreover, chemical labeling results in a specific reverse transcription (RT) truncation signature. This study has identified four thousand high-confidence m(6)A sites at single-base resolution in the human transcriptome. Unlike previously reported methods based on m(6)A-antibody or m(6)A-sensitive enzymes, the antibody/enzyme-free chemical method provides a new perspective for single-base m(6)A detection at the transcriptome level. The Royal Society of Chemistry 2022-10-05 /pmc/articles/PMC9600483/ /pubmed/36349098 http://dx.doi.org/10.1039/d2sc03181g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Xie, Yalun
Han, Shaoqing
Li, Qiming
Fang, Zhentian
Yang, Wei
Wei, Qi
Wang, Yafen
Zhou, Yu
Weng, Xiaocheng
Zhou, Xiang
Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title_full Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title_fullStr Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title_full_unstemmed Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title_short Transcriptome-wide profiling of N(6)-methyladenosine via a selective chemical labeling method
title_sort transcriptome-wide profiling of n(6)-methyladenosine via a selective chemical labeling method
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600483/
https://www.ncbi.nlm.nih.gov/pubmed/36349098
http://dx.doi.org/10.1039/d2sc03181g
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