PUBLICATION

Zebrafish sparse corresponds to an orthologue of c-kit and is required for the morphogenesis of a subpopulation of melanocytes, but is not essential for hematopoiesis or primordial germ cell development

Authors
Parichy, D.M., Rawls, J.F., Pratt, S.J., Whitfield, T.T., and Johnson, S.L.
ID
ZDB-PUB-990830-7
Date
1999
Source
Development (Cambridge, England)   126(15): 3425-3436 (Journal)
Registered Authors
Johnson, Stephen L., Parichy, David M., Pratt, Stephen J., Rawls, John F., Whitfield, Tanya T.
Keywords
neural crest; melanocyte; c-kit; Danio rerio; hematopoiesis; primordial germ cell; apoptosis; cell migration
MeSH Terms
  • Germ Cells/growth & development
  • Base Sequence
  • DNA, Complementary/genetics
  • Neural Crest/cytology
  • Proto-Oncogene Proteins c-kit/genetics*
  • Phylogeny
  • Species Specificity
  • Mice
  • Melanocytes/cytology*
  • DNA Primers/genetics
  • Hematopoiesis/genetics
  • Zebrafish/embryology*
  • Zebrafish/genetics*
  • Biological Evolution
  • Male
  • Female
  • Animals
(all 17)
PubMed
10393121 Full text @ Development
Abstract
The relative roles of the Kit receptor in promoting the migration and survival of amniote melanocytes are unresolved. We show that, in the zebrafish, Danio rerio, the pigment pattern mutation sparse corresponds to an orthologue of c-kit. This finding allows us to further elucidate morphogenetic roles for this c-kit-related gene in melanocyte morphogenesis. Our analyses of zebrafish melanocyte development demonstrate that the c-kit orthologue identified in this study is required both for normal migration and for survival of embryonic melanocytes. We also find that, in contrast to mouse, the zebrafish c-kit gene that we have identified is not essential for hematopoiesis or primordial germ cell development. These unexpected differences may reflect evolutionary divergence in c-kit functions following gene duplication events in teleosts.
Genes / Markers
Figures
Figure Gallery (4 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b4
    Insertion
    b5
      Small Deletion
      b465
        Deficiency
        j1e1
          Point Mutation
          j1e15
            Unknown
            j1e41
              Point Mutation
              j1e56
                Point Mutation
                j1g2
                  Deficiency
                  1 - 8 of 8
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                  Human Disease / Model
                  No data available
                  Sequence Targeting Reagents
                  No data available
                  Fish
                  Antibodies
                  No data available
                  Orthology
                  No data available
                  Engineered Foreign Genes
                  No data available
                  Mapping
                  No data available