Evidence map›Paper›PMID 39300486›Full record

ArticleGenome biology2024

Recruitment of the m

Syed Nabeel-Shah, Shuye Pu, Giovanni L Burke, Nujhat Ahmed, Ulrich Braunschweig, Shaghayegh Farhangmehr, Hyunmin Lee, Mingkun Wu, Zuyao Ni, Hua Tang and 5 more

Abstract read
In one paragraph

Article in Genome biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. RNA modifications and their role in gene expression.Frontiers in molecular biosciences · 2025
    Review
  11. The RNA Revolution in the Central Molecular Biology Dogma Evolution.International journal of molecular sciences · 2024
    Review
  12. An Overview of Current Detection Methods for RNA Methylation.International journal of molecular sciences · 2024
    Review
  13. FTO in health and disease.Frontiers in cell and developmental biology · 2024
    Review
  14. Article
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

15 authors.

Syed Nabeel-ShahDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.ORCID http://orcid.org/0000-0002-4239-7443
Shuye PuDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Giovanni L BurkeDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Nujhat AhmedDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Ulrich BraunschweigDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Shaghayegh FarhangmehrDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Hyunmin LeeDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Mingkun WuDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Zuyao NiDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Hua TangDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Guoqing ZhongDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Edyta MarconDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Zhaolei ZhangDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Benjamin J BlencoweDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada.
Jack F GreenblattDonnelly Centre, University of Toronto, Toronto, M5S 3E1, Canada. jack.greenblatt@utoronto.ca.ORCID http://orcid.org/0000-0003-1762-2861

Funding

CIHR FDN-154338
6 · The paper itself

Abstract

backgroundN6-methyladenosine (m6A), the most abundant internal modification on eukaryotic mRNA, and N6, 2'-O-dimethyladenosine (m6Am), are epitranscriptomic marks that function in multiple aspects of posttranscriptional regulation. Fat mass and obesity-associated protein (FTO) can remove both m

resultsHere, we demonstrate that ZBTB48, a C2H2-zinc finger protein that functions in telomere maintenance, associates with FTO and binds both mRNA and the telomere-associated regulatory RNA TERRA to regulate the functional interactions of FTO with target transcripts. Specifically, depletion of ZBTB48 affects targeting of FTO to sites of m6A/m6Am modification, changes cellular m6A/m6Am levels and, consequently, alters decay rates of target RNAs. ZBTB48 ablation also accelerates growth of HCT-116 colorectal cancer cells and modulates FTO-dependent regulation of Metastasis-associated protein 1 (MTA1) transcripts by controlling the binding to MTA1 mRNA of the m6A reader IGF2BP2.

conclusionsOur findings thus uncover a previously unknown mechanism of posttranscriptional regulation in which ZBTB48 co-ordinates RNA-binding of the m6A/m6Am demethylase FTO to control expression of its target RNAs.

Indexed as

AdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTODNA-Binding ProteinsHCT116 CellsHumansRNA, MessengerTelomereTranscription FactorsZinc FingersAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTODNA-Binding ProteinsFTO protein, humanN-methyladenosineRNA, MessengerTranscription FactorsZBTB48 protein, humanFTOICLIPM6A/m6AmMRNA modificationRNA-bindingTelomeresTERRATZAPZBTB48

Identifiers

PMID39300486
PMCPMC11414060

What Socratic 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 Socratic graph.