PUBLICATION
            Disruption of zebrafish cyclin G-associated kinase (GAK) function impairs the expression of Notch-dependent genes during neurogenesis and causes defects in neuronal development
- Authors
 - Bai, T., Seebald, J.L., Kim, K.E., Ding, H.M., Szeto, D.P., and Chang, H.C.
 - ID
 - ZDB-PUB-100126-1
 - Date
 - 2010
 - Source
 - BMC Developmental Biology 10: 7 (Journal)
 - Registered Authors
 - Szeto, Daniel P.
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Auxilins/genetics
 - Zebrafish Proteins/metabolism*
 - Brain/embryology
 - Brain/metabolism
 - Humans
 - Gene Expression
 - Clathrin/metabolism
 - Cell Death
 - Amino Acid Sequence
 - Homeodomain Proteins/metabolism
 - Protein Serine-Threonine Kinases/metabolism*
 - Neurogenesis*
 - Zebrafish/embryology*
 - Zebrafish/metabolism
 - Animals
 - Molecular Sequence Data
 
 - PubMed
 - 20082716 Full text @ BMC Dev. Biol.
 
            Citation
        
        
            Bai, T., Seebald, J.L., Kim, K.E., Ding, H.M., Szeto, D.P., and Chang, H.C. (2010) Disruption of zebrafish cyclin G-associated kinase (GAK) function impairs the expression of Notch-dependent genes during neurogenesis and causes defects in neuronal development. BMC Developmental Biology. 10:7.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                BACKGROUND: The J-domain-containing protein auxilin, a critical regulator in clathrin-mediated transport, has been implicated in Drosophila Notch signaling. To ask if this role of auxilin is conserved and whether auxilin has additional roles in development, we have investigated the functions of auxilin orthologs in zebrafish. RESULTS: Like mammals, zebrafish has two distinct auxilin-like molecules, auxilin and cyclin G-associated kinase (GAK), differing in their domain structures and expression patterns. Both zebrafish auxilin and GAK can functionally substitute for the Drosophila auxilin, suggesting that they have overlapping molecular functions. Still, they are not completely redundant, as morpholino-mediated knockdown of the ubiquitously expressed GAK alone can increase the specification of neuronal cells, a known Notch-dependent process, and decrease the expression of Her4, a Notch target gene. Furthermore, inhibition of GAK function caused an elevated level of apoptosis in neural tissues, resulting in severe degeneration of neural structures. CONCLUSION: In support of the notion that endocytosis plays important roles in Notch signaling, inhibition of zebrafish GAK function affects embryonic neuronal cell specification and Her4 expression. In addition, our analysis suggests that zebrafish GAK has at least two functions during the development of neural tissues: an early Notch-dependent role in neuronal patterning and a late role in maintaining the survival of neural cells.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping