Evidence map›Paper›PMID 25527292›Full record

ArticleThe EMBO journal2015

Tox: a multifunctional transcription factor and novel regulator of mammalian corticogenesis.

Benedetta Artegiani, Antonio M de Jesus Domingues, Sara Bragado Alonso, Elisabeth Brandl, Simone Massalini, Andreas Dahl, Federico Calegari

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.6field-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

39 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Novel Insights into Emx2 and Dmrta2 Cooperation during Cortex Development and Evidence for Dmrta2 Function in the Choroid Plexus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  7. Article
  8. TOX, through a glass, darkly.Frontiers in immunology · 2025
    Review
  9. Aryl Hydrocarbon Receptor (AHR) Suppresses Arsenic (AsInternational journal of biological sciences · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Midbrain Dopaminergic Neuron Development at the Single Cell Level:Frontiers in cell and developmental biology · 2020
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Benedetta ArtegianiDFG-Research Center for Regenerative Therapies, Cluster of Excellence, TU-Dresden, Dresden, Germany.
Antonio M de Jesus DominguesDeep Sequencing Group-SFB655, Biotechnology Center, TU-Dresden, Dresden, Germany.
Sara Bragado AlonsoDFG-Research Center for Regenerative Therapies, Cluster of Excellence, TU-Dresden, Dresden, Germany.
Elisabeth BrandlDFG-Research Center for Regenerative Therapies, Cluster of Excellence, TU-Dresden, Dresden, Germany.
Simone MassaliniDFG-Research Center for Regenerative Therapies, Cluster of Excellence, TU-Dresden, Dresden, Germany.
Andreas DahlDeep Sequencing Group-SFB655, Biotechnology Center, TU-Dresden, Dresden, Germany.
Federico CalegariDFG-Research Center for Regenerative Therapies, Cluster of Excellence, TU-Dresden, Dresden, Germany federico.calegari@crt-dresden.de.
TU Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major efforts are invested to characterize the factors controlling the proliferation of neural stem cells. During mammalian corticogenesis, our group has identified a small pool of genes that are transiently downregulated in the switch of neural stem cells to neurogenic division and reinduced in newborn neurons. Among these switch genes, we found Tox, a transcription factor with hitherto uncharacterized roles in the nervous system. Here, we investigated the role of Tox in corticogenesis by characterizing its expression at the tissue, cellular and temporal level. We found that Tox is regulated by calcineurin/Nfat signalling. Moreover, we combined DNA adenine methyltransferase identification (DamID) with deep sequencing to characterize the chromatin binding properties of Tox including its motif and downstream transcriptional targets including Sox2, Tbr2, Prox1 and other key factors. Finally, we manipulated Tox in the developing brain and validated its multiple roles in promoting neural stem cell proliferation and neurite outgrowth of newborn neurons. Our data provide a valuable resource to study the role of Tox in other tissues and highlight a novel key player in brain development.

Indexed as

AnimalsCalcineurinCell ProliferationCerebral CortexGene Expression Regulation, DevelopmentalHomeodomain ProteinsMiceNeural Stem CellsNeuronsNFATC Transcription FactorsProspero-Related Homeobox 1 ProteinSignal TransductionSite-Specific DNA-Methyltransferase (Adenine-Specific)SOXB1 Transcription FactorsT-Box Domain ProteinsTumor Suppressor ProteinsCalcineurinEomes protein, mouseHomeodomain ProteinsNFATC Transcription FactorsProspero-Related Homeobox 1 ProteinRhox8 protein, mouseSite-Specific DNA-Methyltransferase (Adenine-Specific)Sox2 protein, mouseSOXB1 Transcription FactorsT-Box Domain ProteinsTumor Suppressor Proteinsbrain developmentDamID sequencingHMG‐box transcription factorsneural stem cellsTox

Identifiers

PMID25527292
PMCPMC4388598
OpenAlexW2167075602

What OpenQuestion holds

Textmetadata
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.