PUBLICATION
            Structural characteristics of zebrafish orthologs of adaptor molecules that associate with transmembrane immune receptors
- Authors
 - Yoder, J.A., Orcutt, T.M., Traver, D., and Litman, G.W.
 - ID
 - ZDB-PUB-070907-4
 - Date
 - 2007
 - Source
 - Gene 401(1-2): 154-164 (Journal)
 - Registered Authors
 - Litman, Gary W., Orcutt, Timothy, Traver, David, Yoder, Jeff
 - Keywords
 - DAP10; DAP12; FcRγ; CD3ζ
 - MeSH Terms
 - 
    
        
        
            
                
- Gene Expression Regulation, Developmental
 - Receptors, KIR
 - Phylogeny
 - Sequence Homology, Amino Acid
 - Zebrafish/embryology*
 - Zebrafish/genetics
 - Embryo, Nonmammalian
 - Animals
 - Molecular Sequence Data
 - Cloning, Molecular
 - Receptors, IgG/immunology
 - CD3 Complex/genetics
 - CD3 Complex/metabolism
 - Receptors, Immunologic/chemistry*
 - Receptors, Immunologic/genetics
 - Receptors, Immunologic/metabolism*
 - Cell Lineage
 - Killer Cells, Natural/immunology
 - Cell Membrane/immunology
 - Cell Membrane/metabolism
 - Amino Acid Sequence
 - Genome
 - Protein Structure, Tertiary
 - DNA, Complementary
 - Zebrafish Proteins
 - Adaptor Proteins, Signal Transducing/chemistry*
 - Adaptor Proteins, Signal Transducing/genetics
 - Adaptor Proteins, Signal Transducing/metabolism*
 
 - PubMed
 - 17719728 Full text @ Gene
 
            Citation
        
        
            Yoder, J.A., Orcutt, T.M., Traver, D., and Litman, G.W. (2007) Structural characteristics of zebrafish orthologs of adaptor molecules that associate with transmembrane immune receptors. Gene. 401(1-2):154-164.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Transmembrane bound receptors comprised of extracellular immunoglobulin (Ig) or lectin domains play integral roles in a large number of immune functions including inhibitory and activating responses. The function of many of the activating receptors requires a physical interaction with an adaptor protein possessing a cytoplasmic regulatory motif. The partnering of an activating receptor with an adaptor protein relies on complementary charged residues in the two transmembrane domains. The mammalian natural killer (NK) and Fc receptors (FcR) represent two of many receptor families, which possess activating receptors that partner with adaptor proteins for signaling. Zebrafish represent a powerful experimental model for understanding developmental regulation at early stages of embryogenesis and for efficiently generating transgenic animals. In an effort to understand developmental aspects of immune receptor function, we have accessed the partially annotated zebrafish genome to identify six different adaptor molecules: Dap10, Dap12, Cd3zeta, Cd3zeta-like, FcRgamma and FcRgamma-like that are homologous to those effecting immune function in mammals. Their genomic organizations have been characterized, cDNA transcripts have been recovered, phylogenetic relationships have been defined and their cell lineage-specific expression patterns have been established.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping