PUBLICATION

Zebrafish foxd3 is selectively required for neural crest specification, migration and survival

Authors
Stewart, R.A., Arduini, B.L., Berghmans, S., George, R.E., Kanki, J.P., Henion, P.D., and Look, A.T.
ID
ZDB-PUB-060306-12
Date
2006
Source
Developmental Biology   292(1): 174-188 (Journal)
Registered Authors
Arduini, Brigitte, George, Rani, Henion, Paul, Kanki, John, Look, A. Thomas, Stewart, Rodney A.
Keywords
Neural crest, foxd3, Sympathetic, sox10, snai1b, Survival, Migration, Specification, Zebrafish
MeSH Terms
  • Animals
  • Cell Lineage/genetics
  • Cell Lineage/physiology
  • Cell Movement/genetics
  • Cell Movement/physiology*
  • Cell Survival/genetics
  • Cell Survival/physiology
  • Female
  • Forkhead Transcription Factors/deficiency
  • Forkhead Transcription Factors/genetics
  • Forkhead Transcription Factors/physiology*
  • Neural Crest/cytology*
  • Neural Crest/embryology*
  • Neural Crest/physiology
  • Sympathetic Nervous System/cytology
  • Sympathetic Nervous System/physiology
  • Transcription Factors/biosynthesis
  • Transcription Factors/physiology
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish/physiology
  • Zebrafish Proteins/deficiency
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
(all 24)
PubMed
16499899 Full text @ Dev. Biol.
Abstract
The vertebrate neural crest is a pluripotent cell population that generates a large variety of cell types, including peripheral neurons, cartilage and pigment cells. Mechanisms that control the patterning of the neural crest toward specific cell fates remain only partially understood. Zebrafish homozygous for the sympathetic mutation 1 (sym1) have defects in a subset of neural crest derivatives, such as peripheral neurons, glia and cartilage, but retain normal numbers of melanocytes. The sym1 mutation is a nucleotide deletion that disrupts the forkhead DNA-binding domain of the foxd3 gene, which encodes a conserved winged-helix transcription factor. We show that sym1 mutants have normal numbers of premigratory neural crest cells, but these cells express reduced levels of snai1b and sox10, implicating foxd3 as an essential regulator of these transcription factors in the premigratory neural crest. The onset of neural crest migration is also delayed in sym1 mutants, and there is a reduction in the number of migratory trunk neural crest cells, particularly along the medial migration pathway. TUNEL analysis revealed aberrant apoptosis localized to the hindbrain neural crest at the 15-somite stage, indicating a critical role for foxd3 in the survival of a subpopulation of neural crest cells. These results show that foxd3 selectively specifies premigratory neural crest cells for a neuronal, glial or cartilage fate, by inducing the expression of lineage-associated transcription factors in these cells and regulating their subsequent migration.
Genes / Markers
Marker Marker Type Name
aox5GENEaldehyde oxidase 5
ascl1aGENEachaete-scute family bHLH transcription factor 1a
col2a1aGENEcollagen, type II, alpha 1a
crestinGENEcrestin
dctGENEdopachrome tautomerase
dlx2aGENEdistal-less homeobox 2a
ednrbaGENEendothelin receptor Ba
elavl3GENEELAV like neuron-specific RNA binding protein 3
foxd3GENEforkhead box D3
mitfaGENEmelanocyte inducing transcription factor a
1 - 10 of 22
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Figures
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
zdf10
    Small Deletion
    1 - 1 of 1
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    Human Disease / Model
    No data available
    Sequence Targeting Reagents
    Target Reagent Reagent Type
    foxd3MO3-foxd3MRPHLNO
    1 - 1 of 1
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    Fish
    1 - 2 of 2
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    Antibodies
    No data available
    Orthology
    No data available
    Engineered Foreign Genes
    No data available
    Mapping
    Entity Type Entity Symbol Location
    zdf10Chr: 6 Details
    SSLPz10183Chr: 6 Details
    1 - 2 of 2
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