Evidence map›Paper›PMID 28658625›Full record

ArticleCell reports2017

In Vivo Regulation of the Zebrafish Endoderm Progenitor Niche by T-Box Transcription Factors.

Andrew C Nelson, Stephen J Cutty, Saule N Gasiunas, Isabella Deplae, Derek L Stemple, Fiona C Wardle

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  6. Context-dependent TGFβ family signalling in cell fate regulation.Nature reviews. Molecular cell biology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Fgf-driven Tbx protein activities directly induceDevelopment (Cambridge, England) · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Bloody Zebrafish: Novel Methods in Normal and Malignant Hematopoiesis.Frontiers in cell and developmental biology · 2018
    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

6 authors at 2 institutions in 1 country.

Andrew C NelsonRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK; Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK; School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK. Electronic address: a.nelson.1@warwick.ac.uk.
Stephen J CuttyRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Saule N GasiunasRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Isabella DeplaeRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK.
Derek L StempleWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Fiona C WardleRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, UK. Electronic address: fiona.wardle@kcl.ac.uk.
King's College London · GBWellcome Sanger Institute · GB

Funding

Medical Research Council G0700213Wellcome Trust 102811
6 · The paper itself

Abstract

T-box transcription factors T/Brachyury homolog A (Ta) and Tbx16 are essential for correct mesoderm development in zebrafish. The downstream transcriptional networks guiding their functional activities are poorly understood. Additionally, important contributions elsewhere are likely masked due to redundancy. Here, we exploit functional genomic strategies to identify Ta and Tbx16 targets in early embryogenesis. Surprisingly, we discovered they not only activate mesodermal gene expression but also redundantly regulate key endodermal determinants, leading to substantial loss of endoderm in double mutants. To further explore the gene regulatory networks (GRNs) governing endoderm formation, we identified targets of Ta/Tbx16-regulated homeodomain transcription factor Mixl1, which is absolutely required in zebrafish for endoderm formation. Interestingly, we find many endodermal determinants coordinately regulated through common genomic occupancy by Mixl1, Eomesa, Smad2, Nanog, Mxtx2, and Pou5f3. Collectively, these findings augment the endoderm GRN and reveal a panel of target genes underlying the Ta, Tbx16, and Mixl1 mutant phenotypes.

Indexed as

AnimalsCell DifferentiationEndodermTranscription FactorsZebrafishTranscription FactorsChIP-seqendodermredundancyT-boxtranscription

Identifiers

PMID28658625
PMCPMC5494305
OpenAlexW2724521833

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.