Evidence map›Paper›PMID 23228892›Full record

ArticleDevelopmental biology2013

A novel FoxD3 gene trap line reveals neural crest precursor movement and a role for FoxD3 in their specification.

Tatiana Hochgreb-Hägele, Marianne E Bronner

Abstract read
In one paragraph

Article in Developmental biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Advancing Knock-In Approaches for Robust Genome Editing in Zebrafish.bioRxiv : the preprint server for biology · 2025
    Article
  4. From neural crest migration to the onset of gangliogenesis.Current topics in developmental biology · 2025
    Review
  5. Review
  6. Article
  7. The Polycomb group geneFrontiers in neuroscience · 2022
    Article
  8. Article
  9. Glutamate Signaling via the AMPAR Subunit GluR4 Regulates Oligodendrocyte Progenitor Cell Migration in the Developing Spinal Cord.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  10. Article
  11. The Cranial Neural Crest in a Multiomics Era.Frontiers in physiology · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Tatiana Hochgreb-HägeleDivision of Biology, California Institute of Technology, 1200 E. California Blvd., MC139-74, Pasadena, CA 91125, USA. hochgreb@caltech.edu
Marianne E Bronner
California Institute of Technology · US

Funding

Transcriptional Casualty in Embryonic Morphogenesis: from the Specifications GRNP01HD037105 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI DAVIDSON, ERIC H · 1999 to 2018
$27.1M
Center for in Toto Genomic Analysis of Vertebrate DevelopmentP50HG004071 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI FRASER, SCOTT E · 2006 to 2011
$18.4M
NHGRI NIH HHS HG004071NHGRI NIH HHS P50 HG004071NICHD NIH HHS HD037105NICHD NIH HHS P01 HD037105
6 · The paper itself

Abstract

Neural crest cells migrate extensively and contribute to diverse derivatives, including the craniofacial skeleton, peripheral neurons and glia, and pigment cells. Although several transgenic lines label neural crest subpopulations, few are suited for studying early events in neural crest development. Here, we present a zebrafish gene/protein trap line gt(foxd3-citrine)(ct110a) that expresses a Citrine fusion protein with FoxD3, a transcription factor expressed in premigratory and migrating neural crest cells. In this novel line, citrine expression exactly parallels endogenous foxd3 expression. High-resolution time-lapse imaging reveals the dynamic phases of precursor and migratory neural crest cell movements from the neural keel stage to times of active cell migration. In addition, Cre-recombination produces a variant line FoxD3-mCherry-pA whose homozygosis generates a FoxD3 mutant. Taking advantage of the endogenously regulated expression of FoxD3-mCherry fusion protein, we directly assess early effects of FoxD3 loss-of-function on specification and morphogenesis of dorsal root ganglia, craniofacial skeleton and melanophores. These novel lines provide new insights and useful new tools for studying specification, migration and differentiation of neural crest cells.

Indexed as

AnimalsAnimals, Genetically ModifiedCell MovementCells, CulturedForkhead Transcription FactorsGene Expression RegulationGenetic TechniquesHomozygoteIn Situ HybridizationMicroscopy, ConfocalMicroscopy, FluorescenceModels, GeneticNeural CrestRecombinant Fusion ProteinsRecombination, GeneticTime FactorsForkhead Transcription Factorsfoxd3 protein, zebrafishRecombinant Fusion ProteinsTranscription FactorsZebrafish Proteins

Identifiers

PMID23228892
PMCPMC3553214
OpenAlexW1966987683

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.