PUBLICATION

Fascin1-Dependent Filopodia are Required for Directional Migration of a Subset of Neural Crest Cells

Authors
Boer, E.F., Howell, E.D., Schilling, T.F., Jette, C.A., Stewart, R.A.
ID
ZDB-PUB-150122-3
Date
2015
Source
PLoS Genetics   11: e1004946 (Journal)
Registered Authors
Jette, Cicely A., Schilling, Tom, Stewart, Rodney A.
Keywords
Embryos, Cell migration, Neuron migration, Zebrafish, Neurons, Ganglia, Cartilage, Cancer cell migration
MeSH Terms
  • Animals
  • Body Patterning/genetics
  • Cell Movement/genetics
  • Epithelial-Mesenchymal Transition/genetics
  • Gene Expression Regulation, Developmental
  • Microfilament Proteins/genetics*
  • Mutation
  • Neural Crest/cytology
  • Neural Crest/growth & development*
  • Pseudopodia/genetics*
  • Signal Transduction
  • Zebrafish/genetics
  • Zebrafish/growth & development*
  • Zebrafish Proteins/biosynthesis
  • Zebrafish Proteins/genetics*
(all 15)
PubMed
25607881 Full text @ PLoS Genet.
Abstract
Directional migration of neural crest (NC) cells is essential for patterning the vertebrate embryo, including the craniofacial skeleton. Extensive filopodial protrusions in NC cells are thought to sense chemo-attractive/repulsive signals that provide directionality. To test this hypothesis, we generated null mutations in zebrafish fascin1a (fscn1a), which encodes an actin-bundling protein required for filopodia formation. Homozygous fscn1a zygotic null mutants have normal NC filopodia due to unexpected stability of maternal Fscn1a protein throughout NC development and into juvenile stages. In contrast, maternal/zygotic fscn1a null mutant embryos (fscn1a MZ) have severe loss of NC filopodia. However, only a subset of NC streams display migration defects, associated with selective loss of craniofacial elements and peripheral neurons. We also show that fscn1a-dependent NC migration functions through cxcr4a/cxcl12b chemokine signaling to ensure the fidelity of directional cell migration. These data show that fscn1a-dependent filopodia are required in a subset of NC cells to promote cell migration and NC derivative formation, and that perdurance of long-lived maternal proteins can mask essential zygotic gene functions during NC development.
Genes / Markers
Figures
Figure Gallery (15 images) / 2
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
ir937TgTransgenic Insertion
    sb2TgTransgenic Insertion
      vu234TgTransgenic Insertion
        w37TgTransgenic Insertion
          zd1011
            Small Deletion
            zd1012
              Small Deletion
              zd1013
                Indel
                zdf15TgTransgenic Insertion
                  1 - 8 of 8
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                  Human Disease / Model
                  No data available
                  Sequence Targeting Reagents
                  Target Reagent Reagent Type
                  cxcr4aMO2-cxcr4aMRPHLNO
                  foxd3MO3-foxd3MRPHLNO
                  fscn1aTALEN1-fscn1aTALEN
                  tfap2aMO4-tfap2aMRPHLNO
                  1 - 4 of 4
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                  Fish
                  Antibodies
                  No data available
                  Orthology
                  Engineered Foreign Genes
                  Marker Marker Type Name
                  EGFPEFGEGFP
                  GFPEFGGFP
                  mRFPEFGmRFP
                  RFPEFGRFP
                  1 - 4 of 4
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                  Mapping