| Literature DB >> 30197295 |
Jiangbo Wei1, Fange Liu1, Zhike Lu2, Qili Fei1, Yuxi Ai1, P Cody He1, Hailing Shi1, Xiaolong Cui1, Rui Su3, Arne Klungland4, Guifang Jia5, Jianjun Chen3, Chuan He6.
Abstract
FTO, the first RNA demethylase discovered, mediates the demethylation of internal N6-methyladenosine (m6A) and N6, 2-O-dimethyladenosine (m6Am) at the +1 position from the 5' cap in mRNA. Here we demonstrate that the cellular distribution of FTO is distinct among different cell lines, affecting the access of FTO to different RNA substrates. We find that FTO binds multiple RNA species, including mRNA, snRNA, and tRNA, and can demethylate internal m6A and cap m6Am in mRNA, internal m6A in U6 RNA, internal and cap m6Am in snRNAs, and N1-methyladenosine (m1A) in tRNA. FTO-mediated demethylation has a greater effect on the transcript levels of mRNAs possessing internal m6A than the ones with cap m6Am in the tested cells. We also show that FTO can directly repress translation by catalyzing m1A tRNA demethylation. Collectively, FTO-mediated RNA demethylation occurs to m6A and m6Am in mRNA and snRNA as well as m1A in tRNA.Entities:
Keywords: FTO; cap m(6)A(m); cytoplasmic demethylation; m(6)A; nuclear m(6)A demethylation; snRNA demethylation; tRNA m(1)A demethylation; translation regulation
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Year: 2018 PMID: 30197295 PMCID: PMC6151148 DOI: 10.1016/j.molcel.2018.08.011
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970