Evidence map›Paper›PMID 28977517›Full record

ArticleNucleic acids research2017

N6-methyladenosine demethylase FTO targets pre-mRNAs and regulates alternative splicing and 3'-end processing.

Marek Bartosovic, Helena Covelo Molares, Pavlina Gregorova, Dominika Hrossova, Grzegorz Kudla, Stepanka Vanacova

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 301 papers.

0numbers the graph read from it
0cells of the map it votes in
301citing papers in PubMed
14.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

301 citing papers in PubMed, 452 citations in OpenAlex.

  1. Article
  2. Emerging roles of mJournal of assisted reproduction and genetics · 2026
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  6. Methylation marks breast cancer metastasis: The roles of mThe Journal of biological chemistry · 2026
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  9. RNA mCell biology and toxicology · 2026
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  10. Review
  11. Targeting intracellular mRNA mJournal of advanced research · 2026
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  12. NBiomolecules · 2026
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. The RNA NCell death & disease · 2025
    Article
  18. Article
  19. FTO depletion does not alter mbioRxiv : the preprint server for biology · 2025
    Article
  20. Article

241 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Marek BartosovicCEITEC-Central European Institute of Technology, Masaryk University, Brno 62500, Czech Republic.
Helena Covelo MolaresCEITEC-Central European Institute of Technology, Masaryk University, Brno 62500, Czech Republic.
Pavlina GregorovaCEITEC-Central European Institute of Technology, Masaryk University, Brno 62500, Czech Republic.
Dominika HrossovaCEITEC-Central European Institute of Technology, Masaryk University, Brno 62500, Czech Republic.
Grzegorz KudlaMRC Human Genetics Unit MRC IGMM, University of Edinburgh Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
Stepanka VanacovaCEITEC-Central European Institute of Technology, Masaryk University, Brno 62500, Czech Republic.
Central European Institute of Technology · CZWestern General Hospital · GB

Funding

Medical Research Council MC_UU_12018/23
6 · The paper itself

Abstract

N6-methyladenosine (m6A) is the most abundant base modification found in messenger RNAs (mRNAs). The discovery of FTO as the first m6A mRNA demethylase established the concept of reversible RNA modification. Here, we present a comprehensive transcriptome-wide analysis of RNA demethylation and uncover FTO as a potent regulator of nuclear mRNA processing events such as alternative splicing and 3΄ end mRNA processing. We show that FTO binds preferentially to pre-mRNAs in intronic regions, in the proximity of alternatively spliced (AS) exons and poly(A) sites. FTO knockout (KO) results in substantial changes in pre-mRNA splicing with prevalence of exon skipping events. The alternative splicing effects of FTO KO anti-correlate with METTL3 knockdown suggesting the involvement of m6A. Besides, deletion of intronic region that contains m6A-linked DRACH motifs partially rescues the FTO KO phenotype in a reporter system. All together, we demonstrate that the splicing effects of FTO are dependent on the catalytic activity in vivo and are mediated by m6A. Our results reveal for the first time the dynamic connection between FTO RNA binding and demethylation activity that influences several mRNA processing events.

Indexed as

Alternative Splicing3' Untranslated RegionsAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOExonsGene Expression ProfilingHEK293 CellsHumansIntronsMethyltransferasesMutagenesis, Site-DirectedMutationPoly AProtein BindingRNA Precursors3' Untranslated RegionsAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOMethyltransferasesMETTL3 protein, humanN-methyladenosinePoly ARNA Precursors

Identifiers

PMID28977517
PMCPMC5737695
OpenAlexW2750801274

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.