PUBLICATION

Analysis of a zebrafish VEGF receptor mutant reveals specific disruption of angiogenesis

Authors
Habeck, H., Odenthal, J., Walderich, B., Maischein, H.-M., Tübingen 2000 screen consortium, and Schulte-Merker, S.
ID
ZDB-PUB-020820-7
Date
2002
Source
Current biology : CB   12(16): 1405-1412 (Journal)
Registered Authors
Habeck, Hinrich, Maischein, Hans-Martin, Odenthal, Joerg, Schulte-Merker, Stefan
Keywords
none
MeSH Terms
  • Alleles
  • Animals
  • Blood Vessels/physiology
  • Chromosome Mapping
  • Cloning, Molecular
  • DNA-Binding Proteins/genetics
  • DNA-Binding Proteins/metabolism
  • Embryo, Nonmammalian/physiology
  • Endothelial Growth Factors/genetics
  • Endothelial Growth Factors/metabolism
  • In Situ Hybridization
  • Intercellular Signaling Peptides and Proteins/genetics
  • Intercellular Signaling Peptides and Proteins/metabolism
  • Larva/anatomy & histology
  • Larva/physiology
  • Lymphokines/genetics
  • Lymphokines/metabolism
  • Molecular Sequence Data
  • Neovascularization, Physiologic/genetics*
  • Neovascularization, Physiologic/physiology
  • Phenotype
  • Proto-Oncogene Protein c-fli-1
  • Proto-Oncogene Proteins*
  • Receptors, Vascular Endothelial Growth Factor/genetics*
  • Receptors, Vascular Endothelial Growth Factor/metabolism
  • Trans-Activators/genetics
  • Trans-Activators/metabolism
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor Receptor-2/genetics*
  • Vascular Endothelial Growth Factor Receptor-2/metabolism
  • Vascular Endothelial Growth Factors
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/physiology*
PubMed
12194822 Full text @ Curr. Biol.
Abstract
Blood vessels form either by the assembly and differentiation of mesodermal precursor cells (vasculogenesis) or by sprouting from preexisting vessels (angiogenesis). Endothelial-specific receptor tyrosine kinases and their ligands are known to be essential for these processes. Targeted disruption of vascular endothelial growth factor (VEGF) or its receptor kdr (flk1, VEGFR2) in mouse embryos results in a severe reduction of all blood vessels, while the complete loss of flt1 (VEGFR1) leads to an increased number of hemangioblasts and a disorganized vasculature. In a large-scale forward genetic screen, we identified two allelic zebrafish mutants in which the sprouting of blood vessels is specifically disrupted without affecting the assembly and differentiation of angioblasts. Molecular cloning revealed nonsense mutations in flk1. Analysis of mRNA expression in flk1 mutant embryos showed that flk1 expression was severely downregulated, while the expression of other genes (scl, gata1, and fli1) involved in vasculogenesis or hematopoiesis was unchanged. Overexpression of vegf(121+165) led to the formation of additional vessels only in sibling larvae, not in flk1 mutants. We demonstrate that flk1 is not required for proper vasculogenesis and hematopoiesis in zebrafish embryos. However, the disruption of flk1 impairs the formation or function of vessels generated by sprouting angiogenesis.
Genes / Markers
Figures
Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes