PUBLICATION

Control of muscle cell-type specification in the zebrafish embryo by hedgehog signalling

Authors
Lewis, K.E., Currie, P.D., Roy, S., Schauerte, H., Haffter, P., and Ingham, P.W.
ID
ZDB-PUB-991216-1
Date
1999
Source
Developmental Biology   216(2): 469-480 (Journal)
Registered Authors
Currie, Peter D., Haffter, Pascal, Ingham, Philip, Lewis, Katharine E., Roy, Sudipto, Schauerte, Heike
Keywords
Zebrafish; Patched1; Sonic hedgehog; Gli2; U-type mutants; Muscle fibre type; MyoD; Myosin heavy chain; You; You-too; Sonic you; Chameleon; U-boot; gene control; muscle cell; cell type; cell specificity; signal transduction; sonic hedgehog protein
MeSH Terms
  • Mutation
  • RNA, Messenger/metabolism
  • Transcription Factors/metabolism
  • Membrane Proteins/genetics
  • Trans-Activators*
  • Myosins/metabolism
  • In Situ Hybridization
  • Fluorescent Antibody Technique
  • Zebrafish
  • MyoD Protein/genetics
  • Animals
  • Cell Differentiation
  • Receptors, Cell Surface
  • Muscles/embryology*
  • Muscles/metabolism
  • Gene Expression Regulation, Developmental
  • Kruppel-Like Transcription Factors
  • Somites/metabolism
  • Hedgehog Proteins
  • Proteins/metabolism*
  • Signal Transduction*
(all 21)
PubMed
10642786 Full text @ Dev. Biol.
Abstract
The specification of different muscle cell types in the zebrafish embryo requires signals that emanate from the axial mesoderm. In previous studies we and others have shown that overexpression of different members of the Hedgehog protein family can induce the differentiation of two types of slow-twitch muscles, the superficially located slow-twitch fibres and the medially located muscle pioneer cells. Here we have investigated the requirement for Hedgehog signalling in the specification of these distinct muscle cell types in two ways: first, by characterising the effects on target gene expression and muscle cell differentiation of the u-type mutants, members of a phenotypic group previously implicated in Hedgehog signalling, and second, by analysing the effects of overexpression of the Patched1 protein, a negative regulator of Hedgehog signalling. Our results support the idea that most u-type genes are required for Hedgehog signalling and indicate that while such signalling is essential for slow myocyte differentiation, the loss of activity of one signal, Sonic hedgehog, can be partially compensated for by other Hedgehog family proteins.
Genes / Markers
Figures
Figure Gallery (6 images)
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
t4
    Deficiency
    tm15a
      Point Mutation
      tp39
        Point Mutation
        ty97
          Point Mutation
          ty119
            Point Mutation
            1 - 5 of 5
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            Human Disease / Model
            No data available
            Sequence Targeting Reagents
            No data available
            Fish
            Antibodies
            Name Type Antigen Genes Isotypes Host Organism
            Ab1-engmonoclonalIgG1Mouse
            Ab1-smyhcmonoclonal
              IgG2bMouse
              Ab-EB165monoclonal
                IgG1Mouse
                1 - 3 of 3
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                Orthology
                No data available
                Engineered Foreign Genes
                No data available
                Mapping
                No data available