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PMID: 28624569 Published · ppublish English Journal Article Review

Readers, writers and erasers of N6-methylated adenosine modification.

Current opinion in structural biology ·Vol. 47 ·2017-00-00 ·Pages 67-76

Wu B, Li L, Huang Y, Ma J, Min J

Abstract

N6-methyladenosine (m6A) as the most prevalent internal modification in mammalian RNAs has been increasingly realized as an important reversible mark that participates in various biological processes and cancer pathogenesis. In this review, we discuss the catalytic mechanisms of MT-A70 domain family proteins for mediating adenosine N6-methylation, the removal of this RNA mark by members of ALKB homologue domain family proteins, and the recognition of these m6A-modified RNAs by YTH domain family proteins. Our discussions focus on the recent advances in our understandings of the structural and functional properties of N6-methyladenosine methyltransferases, demethylases and reader proteins. Overall, we aim to mechanistically explain the reversible and dynamic nature of this unique RNA internal modification that contributes to the complexity of RNA-mediated gene regulation, and inspire new studies in epitranscriptomics.

MeSH Terms
Adenosine/analogs & derivatives,chemistry,metabolism Methylation Methyltransferases/chemistry,metabolism Models, Molecular Molecular Conformation Multiprotein Complexes Protein Binding RNA/chemistry,metabolism Structure-Activity Relationship
Chemicals
Multiprotein Complexes RNA N-methyladenosine Methyltransferases Adenosine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wu Baixing
State Key Laboratory of Genetic Engineering, Collaborative Innovation Centre of Genetics and Development, Department of Biochemistry, Institute of Plant Biology, School of Life Sciences, Fudan University, Shanghai 200438, China.
Li Li
Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, Canada; Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
Huang Ying
State Key Laboratory of Molecular Biology, National Center for Protein Science Shanghai, Shanghai Science Research Center, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 333 Haike Road, Shanghai 201203, China. Electronic address: huangy@sibcb.ac.cn.
Ma Jinbiao
State Key Laboratory of Genetic Engineering, Collaborative Innovation Centre of Genetics and Development, Department of Biochemistry, Institute of Plant Biology, School of Life Sciences, Fudan University, Shanghai 200438, China. Electronic address: majb@fudan.edu.cn.
Min Jinrong
Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, Canada; Department of Physiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada. Electronic address: jr.min@utoronto.ca.
Article Info
Journal
Current opinion in structural biology
Abbr.
Curr Opin Struct Biol
ISSN
1879-033X
Published
2017-00-00
Epub
2017-00-16
Pages
67-76
Language
English
Region
England
NLM ID
9107784
Subset
IM
Grants
Wellcome Trust · United Kingdom
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