Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo
Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo
The Notch ligands Dll1 and Dll3 are coexpressed in the presomitic mesoderm of mouse embryos. Despite their coexpression, mutations in Dll1 and Dll3 cause strikingly different defects. To determine if there is any functional equivalence, we replaced Dll1 with Dll3 in mice. Dll3 does not compensate for Dll1; DLL1 activates Notch in Drosophila wing discs, but DLL3 does not. We do not observe evidence for antagonism between DLL1 and DLL3, or repression of Notch activity in mice or Drosophila. In vitro analyses show that differences in various domains of DLL1 and DLL3 individually contribute to their biochemical nonequivalence. In contrast to endogenous DLL1 located on the surface of presomitic mesoderm cells, we find endogenous DLL3 predominantly in the Golgi apparatus. Our data demonstrate distinct in vivo functions for DLL1 and DLL3. They suggest that DLL3 does not antagonize DLL1 in the presomitic mesoderm and warrant further analyses of potential physiological functions of DLL3 in the Golgi network.
- UNSW Sydney Australia
- Hannover Medical School Germany
- Hochschule Hannover Germany
- University of Oxford United Kingdom
- Victor Chang Cardiac Research Institute Australia
Receptors, Notch, Recombinant Fusion Proteins, Calcium-Binding Proteins, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Embryo, Mammalian, Ligands, Cell Line, Protein Structure, Tertiary, Animals, Genetically Modified, Mice, Drosophila melanogaster, Phenotype, Somites, Animals, Intercellular Signaling Peptides and Proteins, Protein Isoforms, Tissue Distribution, Research Articles, Body Patterning, Signal Transduction
Receptors, Notch, Recombinant Fusion Proteins, Calcium-Binding Proteins, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Embryo, Mammalian, Ligands, Cell Line, Protein Structure, Tertiary, Animals, Genetically Modified, Mice, Drosophila melanogaster, Phenotype, Somites, Animals, Intercellular Signaling Peptides and Proteins, Protein Isoforms, Tissue Distribution, Research Articles, Body Patterning, Signal Transduction
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