Evidence map›Paper›PMID 23891001›Full record

ArticleCell reports2013

FOXO3 shares common targets with ASCL1 genome-wide and inhibits ASCL1-dependent neurogenesis.

Ashley E Webb, Elizabeth A Pollina, Thomas Vierbuchen, Noelia Urbán, Duygu Ucar, Dena S Leeman, Ben Martynoga, Madhavi Sewak, Thomas A Rando, François Guillemot and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Epigenetic Insights into Autism Spectrum Disorder: DNA Methylation Levels ofClinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Article
  11. Article
  12. Article
  13. Long-Term Epigenetic Regulation ofInternational journal of molecular sciences · 2024
    Article
  14. Forkhead box O proteins: steering the course of stem cell fate.Cell regeneration (London, England) · 2024
    Review
  15. Article
  16. FoxO3 Modulates Circadian Rhythms in Neural Stem Cells.International journal of molecular sciences · 2023
    Article
  17. Review
  18. Review
  19. Article
  20. FOXOs: masters of the equilibrium.The FEBS journal · 2022
    Review

44 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

12 authors at 1 institution in 1 country.

Ashley E WebbDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Elizabeth A Pollina
Thomas Vierbuchen
Noelia Urbán
Duygu Ucar
Dena S Leeman
Ben Martynoga
Madhavi Sewak
Thomas A Rando
François Guillemot
Marius Wernig
Anne Brunet
Stanford University · US

Funding

Wnt signaling in muscle stem cell agingP01AG036695 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Matteo Pellegrini · 2011 to 2026
$29.3M
Leveraging innovative technologies in basic and clinical cancer researchT32CA009302 · NCI · STANFORD UNIVERSITY · PI LAURA D ATTARDI, Aaron M Newman · 1985 to 2026
$19.1M
Induced neuronal cells: A novel tool to study neuropsychiatric diseasesR01MH092931 · NIMH · STANFORD UNIVERSITY · PI Thomas C. Sudhof, Marius Wernig · 2010 to 2026
$9.7M
Notch Signaling and Satellite Cell ActivationR37AG023806 · NIA · STANFORD UNIVERSITY · PI RANDO, THOMAS A. · 2010 to 2019
$2.9M
Forkhead transcription factors in the stress responseR01AG026648 · NIA · STANFORD UNIVERSITY · PI BRUNET, ANNE · 2005 to 2009
$1.5M
Broad H3K4me3 Domains: A Discovery Tool for Regulators of Neural Stem Cell AgingF31AG043232 · NIA · STANFORD UNIVERSITY · PI POLLINA, ELIZABETH A · 2012 to 2014
$116k
Medical Research Council MC_U117570528Medical Research Council U117570528NCI NIH HHS 5T32 CA09302NCI NIH HHS T32 CA009302NIA NIH HHS F31 AG043232NIA NIH HHS P01 AG036695NIA NIH HHS R01 AG026648NIA NIH HHS R37 AG023806NIMH NIH HHS R01 MH092931
6 · The paper itself

Abstract

FOXO transcription factors are central regulators of longevity from worms to humans. FOXO3, the FOXO isoform associated with exceptional human longevity, preserves adult neural stem cell pools. Here, we identify FOXO3 direct targets genome-wide in primary cultures of adult neural progenitor cells (NPCs). Interestingly, FOXO3-bound sites are enriched for motifs for bHLH transcription factors, and FOXO3 shares common targets with the proneuronal bHLH transcription factor ASCL1/MASH1 in NPCs. Analysis of the chromatin landscape reveals that FOXO3 and ASCL1 are particularly enriched at the enhancers of genes involved in neurogenic pathways. Intriguingly, FOXO3 inhibits ASCL1-dependent neurogenesis in NPCs and direct neuronal conversion in fibroblasts. FOXO3 also restrains neurogenesis in vivo. Our study identifies a genome-wide interaction between the prolongevity transcription factor FOXO3 and the cell-fate determinant ASCL1 and raises the possibility that FOXO3's ability to restrain ASCL1-dependent neurogenesis may help preserve the neural stem cell pool.

Indexed as

Adult Stem CellsAnimalsBinding SitesCell DifferentiationCell Growth ProcessesForkhead Box Protein O3Forkhead Transcription FactorsGenomeMiceNeural Stem CellsNeurogenesisForkhead Box Protein O3Forkhead Transcription FactorsFOXO3 protein, humanFoxO3 protein, mouse

Identifiers

PMID23891001
PMCPMC3838667
OpenAlexW2030484015

What OpenQuestion holds

Textmetadata
LicenceTDM
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.