Abstract

N6-methyladenosine (m6A) is the most prevalent and reversible internal modification in mammalian messenger and non-coding RNAs. We report here that human METTL14 catalyzes m6A RNA methylation. Together with METTL3, the only previously known m6A methyltransferase, these two proteins form a stable heterodimer core complex of METTL3-14 that functions in cellular m6A deposition on mammalian nuclear RNAs. WTAP, a mammalian splicing factor, can interact with this complex and affect this methylation.

Keywords

RNA methylationMethylationMethyltransferaseRNA splicingRNACell biologyN6-MethyladenosineBiologyNon-coding RNAFive-prime capBiochemistryChemistryGene

MeSH Terms

AdenosineAnimalsBase SequenceBinding SitesCell NucleusEnzyme StabilityHeLa CellsHumansMethylationMethyltransferasesModelsMolecularMultienzyme ComplexesRNA

Affiliated Institutions

Related Publications

Publication Info

Year
2013
Type
article
Volume
10
Issue
2
Pages
93-95
Citations
3388
Access
Closed

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Citation Metrics

3388
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194
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2871
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Cite This

Jianzhao Liu, Yanan Yue, Dali Han et al. (2013). A METTL3–METTL14 complex mediates mammalian nuclear RNA N6-adenosine methylation. Nature Chemical Biology , 10 (2) , 93-95. https://doi.org/10.1038/nchembio.1432

Identifiers

DOI
10.1038/nchembio.1432
PMID
24316715
PMCID
PMC3911877

Data Quality

Data completeness: 86%