PUBLICATION
            In Vivo Analysis of Ifn-γ1 and Ifn-γ2 Signaling in Zebrafish
- Authors
- Aggad, D., Stein, C., Sieger, D., Mazel, M., Boudinot, P., Herbomel, P., Levraud, J.P., Lutfalla, G., and Leptin, M.
- ID
- ZDB-PUB-101108-32
- Date
- 2010
- Source
- Journal of immunology (Baltimore, Md. : 1950) 185(11): 6774-6782 (Journal)
- Registered Authors
- Herbomel, Philippe, Levraud, Jean-Pierre, Lutfalla, Georges, Sieger, Dirk, Stein, Cornelia
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Protein-Tyrosine Kinases/physiology
- Isoenzymes/physiology
- Larva/immunology
- Larva/metabolism
- Molecular Sequence Data
- Receptors, Interferon/biosynthesis
- Receptors, Interferon/physiology
- Intracellular Fluid/enzymology
- Intracellular Fluid/immunology
- Intracellular Fluid/metabolism
- Animals
- Zebrafish Proteins/biosynthesis
- Zebrafish Proteins/metabolism
- Zebrafish Proteins/physiology*
- Signal Transduction/immunology*
- Interferon-gamma/biosynthesis
- Interferon-gamma/metabolism
- Interferon-gamma/physiology*
- Zebrafish/immunology*
- Zebrafish/metabolism
 
- PubMed
- 21048110 Full text @ J. Immunol.
            Citation
        
        
            Aggad, D., Stein, C., Sieger, D., Mazel, M., Boudinot, P., Herbomel, P., Levraud, J.P., Lutfalla, G., and Leptin, M. (2010) In Vivo Analysis of Ifn-γ1 and Ifn-γ2 Signaling in Zebrafish. Journal of immunology (Baltimore, Md. : 1950). 185(11):6774-6782.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The zebrafish genome contains a large number of genes encoding potential cytokine receptor genes as judged by homology to mammalian receptors. The sequences are too divergent to allow unambiguous assignments of all receptors to specific cytokines, and only a few have been assigned functions by functional studies. Among receptors for class II helical cytokines-i.e., IFNs that include virus-induced Ifns (Ifn-φ) and type II Ifns (Ifn-γ), together with Il-10 and its related cytokines (Il-20, Il-22, and Il-26)-only the Ifn-φ-specific complexes have been functionally identified, whereas the receptors for the two Ifn-γ (Ifn-γ1 and Ifn-γ2) are unknown. In this work, we identify conditions in which Ifn-γ1 and Ifn-γ2 (also called IFNG or IFN-γ and IFN-gammarel) are induced in fish larvae and adults. We use morpholino-mediated loss-of-function analysis to screen candidate receptors and identify the components of their receptor complexes. We find that Ifn-γ1 and Ifn-γ2 bind to different receptor complexes. The receptor complex for Ifn-γ2 includes cytokine receptor family B (Crfb)6 together with Crfb13 and Crfb17, whereas the receptor complex for Ifn-γ1 does not include Crfb6 or Crfb13 but includes Crfb17. We also show that of the two Jak2 paralogues present in the zebrafish Jak2a but not Jak2b is involved in the intracellular transmission of the Ifn-γ signal. These results shed new light on the evolution of the Ifn-γ signaling in fish and tetrapods and contribute toward an integrated view of the innate immune regulation in vertebrates.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    