Evidence map›Paper›PMID 20460180›Full record

ArticleDevelopmental biology2010

Interplay between Foxd3 and Mitf regulates cell fate plasticity in the zebrafish neural crest.

Kevin Curran, James A Lister, Gary R Kunkel, Andrew Prendergast, David M Parichy, David W Raible

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 174 citations in OpenAlex.

  1. Pooled it
  2. Control Strategies in Guanine Biocrystallization.Angewandte Chemie (International ed. in English) · 2026
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  5. Long-term evolutionary persistence of a cryptic color polymorphism in frogs.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. Mgat4b-mediated selectiveProceedings of the National Academy of Sciences of the United States of America · 2025
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  9. Agouti and BMP signaling drive a naturally occurring fate conversion of melanophores to leucophores in zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
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  20. Review

37 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

6 authors at 3 institutions in 1 country.

Kevin CurranDepartment of Biology, University of Washington, Seattle, WA 98195-7420, USA.
James A Lister
Gary R Kunkel
Andrew Prendergast
David M Parichy
David W Raible
University of Washington · USTexas A&M University · USVirginia Commonwealth University · US

Funding

INTERDISCIPLINARY TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007183 · NICHD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2015
$5.7M
Genetic Regulation of Neural Crest NeurocongenesisR01NS057220 · NINDS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 2007 to 2011
$1.3M
Cell Fate Regulation by Transcriptional RepressionR01NS045246 · NINDS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 2003 to 2006
$984k
NICHD NIH HHS T32 HD007183NINDS NIH HHS R01 NS045246NINDS NIH HHS R01 NS057220
6 · The paper itself

Abstract

Pigment cells of the zebrafish, Danio rerio, offer an exceptionally tractable system for studying the genetic and cellular bases of cell fate decisions. In the zebrafish, neural crest cells generate three types of pigment cells during embryogenesis: yellow xanthophores, iridescent iridophores and black melanophores. In this study, we present evidence for a model whereby melanophores and iridophores descend from a common precursor whose fate is regulated by an interplay between the transcription factors Mitf and Foxd3. Loss of mitfa, a key regulator of melanophore development, resulted in supernumerary ectopic iridophores while loss of foxd3, a mitfa repressor, resulted in fewer iridophores. Double mutants showed a restoration of iridophores, suggesting that one of Foxd3's roles is to suppress mitfa to promote iridophore development. Foxd3 co-localized with pnp4a, a novel marker of early iridophore development, and was necessary for its expression. A considerable overlap was found between iridoblast and melanoblast markers but not xanthoblast markers, which resolved as cells began to differentiate. Cell lineage analyses using the photoconvertible marker, EosFP, revealed that both melanophores and iridophores develop from a mitfa+ precursor. Taken together, our data reveal a Foxd3/mitfa transcriptional switch that governs whether a bi-potent pigment precursor will attain either an iridophore or a melanophore fate.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAnimals, Genetically ModifiedCell LineageForkhead Transcription FactorsMelanocytesMicrophthalmia-Associated Transcription FactorMicroscopy, FluorescenceModels, BiologicalModels, GeneticMutationNeural CrestPhylogenyPigmentationZebrafishZebrafish ProteinsForkhead Transcription Factorsfoxd3 protein, zebrafishMicrophthalmia-Associated Transcription FactorZebrafish Proteins

Identifiers

PMID20460180
PMCPMC2909359
OpenAlexW2040365962

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.