m6A-Atlas v2.0: updated resources for unraveling the N6-methyladenosine (m6A) epitranscriptome among multiple species

Author:

Liang Zhanmin12,Ye Haokai23,Ma Jiongming123,Wei Zhen24ORCID,Wang Yue56,Zhang Yuxin123,Huang Daiyun26,Song Bowen7ORCID,Meng Jia283ORCID,Rigden Daniel J3,Chen Kunqi1ORCID

Affiliation:

1. Key Laboratory of Ministry of Education for Gastrointestinal Cancer, School of Basic Medical Sciences, Fujian Medical University , Fuzhou , Fujian  350004 , China

2. Department of Biological Sciences, Xi’an Jiaotong-Liverpool University , Suzhou , Jiangsu  215123 , China

3. Institute of Systems, Molecular and Integrative Biology, University of Liverpool , Liverpool L69 7ZB, Liverpool , UK

4. Institute of Life Course and Medical Sciences, University of Liverpool , Liverpool L69 7ZB, UK

5. Department of Mathematical Sciences, Xi’an Jiaotong-Liverpool University , Suzhou , Jiangsu  215123 , China

6. Department of Computer Science, University of Liverpool , Liverpool L69 7ZB, UK

7. Department of Public Health, School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine , Nanjing  210023 , China

8. AI University Research Centre, Xi’an Jiaotong-Liverpool University , Suzhou , Jiangsu  215123 , China

Abstract

Abstract N 6-Methyladenosine (m6A) is one of the most abundant internal chemical modifications on eukaryote mRNA and is involved in numerous essential molecular functions and biological processes. To facilitate the study of this important post-transcriptional modification, we present here m6A-Atlas v2.0, an updated version of m6A-Atlas. It was expanded to include a total of 797 091 reliable m6A sites from 13 high-resolution technologies and two single-cell m6A profiles. Additionally, three methods (exomePeaks2, MACS2 and TRESS) were used to identify >16 million m6A enrichment peaks from 2712 MeRIP-seq experiments covering 651 conditions in 42 species. Quality control results of MeRIP-seq samples were also provided to help users to select reliable peaks. We also estimated the condition-specific quantitative m6A profiles (i.e. differential methylation) under 172 experimental conditions for 19 species. Further, to provide insights into potential functional circuitry, the m6A epitranscriptomics were annotated with various genomic features, interactions with RNA-binding proteins and microRNA, potentially linked splicing events and single nucleotide polymorphisms. The collected m6A sites and their functional annotations can be freely queried and downloaded via a user-friendly graphical interface at: http://rnamd.org/m6a.

Funder

National Natural Science Foundation of China

XJTLU Key Program Special Fund

Scientific Research Foundation for Advanced Talents of Fujian Medical University

Publisher

Oxford University Press (OUP)

Subject

Genetics

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