PUBLICATION

Conservation of intracellular Wnt signaling components in dorsal-ventral axis formation in zebrafish

Authors
Sumoy, L., Kiefer, J., and Kimelman, D.
ID
ZDB-PUB-990218-5
Date
1999
Source
Development genes and evolution   209: 48-58 (Journal)
Registered Authors
Kimelman, David, Sumoy, Lauro
Keywords
glycogen synthase kinase-3 binding; protein dorso-ventral axis;; zebrafish; Wnt signaling; T cell factor
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Blotting, Northern
  • Body Patterning*
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Carrier Proteins/isolation & purification
  • Cell Communication/genetics
  • Conserved Sequence
  • Cytoskeletal Proteins/pharmacology
  • Gene Expression
  • Gene Expression Regulation, Developmental
  • Genes, Reporter
  • Glycogen Synthase Kinase 3
  • Glycogen Synthase Kinases
  • In Situ Hybridization
  • Microinjections
  • Mitogens
  • Molecular Sequence Data
  • Proto-Oncogene Proteins/genetics*
  • Trans-Activators*
  • Transcription Factors
  • Wnt Proteins
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish Proteins*
  • beta Catenin
PubMed
9914418 Full text @ Dev. Genes Evol.
Abstract
The mechanism of early dorso-ventral axis specification in zebrafish embryos is not well understood. While beta-catenin has been clearly implicated as a determinant of the axis, the factors upstream and downstream of beta-catenin in this system are not defined. Unlike in Xenopus, where a sperm-induced cortical rotation is used to localize beta-catenin on the future dorsal side of the embryo, zebrafish do not have an obviously similar morphogenetic movement. Recently, a GSK-3 (Glycogen Synthase Kinase-3) binding protein (GBP) was identified as a novel member of the Wnt pathway required for maternal dorsal axis formation in Xenopus. GBP stabilizes beta-catenin levels by inhibiting GSK-3 and potentially provides a link between cortical rotation and beta-catenin regulation. Since zebrafish may use a different mechanism for regulating beta-catenin, we asked whether zebrafish also express a maternal GBP. We report the isolation of the zebrafish GBP gene and show that it is maternally expressed and is present as mRNA ubiquitously throughout early embryonic development. Over-expression of zebrafish GBP in frogs and fish leads to hyper-dorsalized phenotypes, similar to the effects resulting from over-expression of beta-catenin, indicating that components upstream of beta-catenin are conserved between amphibians and teleosts. We also examined whether Tcf (T cell factor) functions in zebrafish embryos. As in frogs, ectopic expression of a dominant negative form of XTcf-3 ventralizes zebrafish embryos. In addition, ectopic beta-catenin expression activates the promoter of the Tcf-dependent gene siamois, indicating that the step immediately downstream of beta-catenin is also conserved between fish and frogs.
Genes / Markers
Figures
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Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes