Evidence map›Paper›PMID 30979904›Full record

ArticleNature communications2019

TET3 prevents terminal differentiation of adult NSCs by a non-catalytic action at Snrpn.

Raquel Montalbán-Loro, Anna Lozano-Ureña, Mitsuteru Ito, Christel Krueger, Wolf Reik, Anne C Ferguson-Smith, Sacri R Ferrón

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. TET3 protects theiScience · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Epigenetic regulation in adult neural stem cells.Frontiers in cell and developmental biology · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. New Insights into TETs in Psychiatric Disorders.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Sex-specific nicotine sensitization and imprinting of self-administration in rats inform GWAS findings on human addiction phenotypes.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  19. Article
  20. Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

7 authors at 3 institutions in 2 countries.

Raquel Montalbán-LoroERI BiotecMed/Departamento de Biología Celular, Universidad de Valencia, 46100, Valencia, Spain.
Anna Lozano-UreñaERI BiotecMed/Departamento de Biología Celular, Universidad de Valencia, 46100, Valencia, Spain.
Mitsuteru ItoDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.ORCID http://orcid.org/0000-0002-3498-850X
Christel KruegerEpigenetics Programme, The Babraham Institute, Cambridge, CB22 3AT, UK.
Wolf ReikEpigenetics Programme, The Babraham Institute, Cambridge, CB22 3AT, UK.
Anne C Ferguson-SmithDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Sacri R FerrónERI BiotecMed/Departamento de Biología Celular, Universidad de Valencia, 46100, Valencia, Spain. sacramento.rodriguez@uv.es.ORCID http://orcid.org/0000-0003-0854-8575
Universitat de València · ESBabraham Institute · GBUniversity of Cambridge · GB

Funding

Medical Research Council MR/R009791/1Wellcome Trust 210757/Z/18/Z
6 · The paper itself

Abstract

Ten-eleven-translocation (TET) proteins catalyze DNA hydroxylation, playing an important role in demethylation of DNA in mammals. Remarkably, although hydroxymethylation levels are high in the mouse brain, the potential role of TET proteins in adult neurogenesis is unknown. We show here that a non-catalytic action of TET3 is essentially required for the maintenance of the neural stem cell (NSC) pool in the adult subventricular zone (SVZ) niche by preventing premature differentiation of NSCs into non-neurogenic astrocytes. This occurs through direct binding of TET3 to the paternal transcribed allele of the imprinted gene Small nuclear ribonucleoprotein-associated polypeptide N (Snrpn), contributing to transcriptional repression of the gene. The study also identifies BMP2 as an effector of the astrocytic terminal differentiation mediated by SNRPN. Our work describes a novel mechanism of control of an imprinted gene in the regulation of adult neurogenesis through an unconventional role of TET3.

Indexed as

Cell DifferentiationAnimalsAstrocytesBrainCatalysisDioxygenasesDNA-Binding ProteinsLateral VentriclesMiceNeural Stem CellsProto-Oncogene ProteinsRNA, Small InterferingSignal TransductionsnRNP Core ProteinsDioxygenasesDNA-Binding ProteinsProto-Oncogene ProteinsRNA, Small InterferingsnRNP Core ProteinsTet3 protein, mouse

Identifiers

PMID30979904
PMCPMC6461695
OpenAlexW2939033389

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.