PUBLICATION
            Polysialyltransferase expression is linked to neuronal migration in the developing and adult zebrafish
- Authors
- Rieger, S., Volkmann, K., and Köster, R.W.
- ID
- ZDB-PUB-071227-12
- Date
- 2008
- Source
- Developmental Dynamics : an official publication of the American Association of Anatomists 237(1): 276-285 (Journal)
- Registered Authors
- Köster, Reinhard W., Rieger, Sandra, Volkmann, Katrin
- Keywords
- polysialyltransferase, PSA-NCAM, cell adhesion, zebrafish, cerebellum, neuronal migration, bio-imaging
- MeSH Terms
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                - Neural Cell Adhesion Molecules/genetics
- Neural Cell Adhesion Molecules/metabolism
- Neural Cell Adhesion Molecules/physiology
- Reverse Transcriptase Polymerase Chain Reaction
- Brain/embryology
- Brain/growth & development
- Brain/metabolism
- Central Nervous System/embryology
- Central Nervous System/growth & development
- Central Nervous System/metabolism
- Sialyltransferases/genetics*
- Sialyltransferases/metabolism
- Animals
- Cerebellum/embryology
- Cerebellum/growth & development
- Cerebellum/metabolism
- Immunohistochemistry
- Cell Adhesion/genetics
- Cell Adhesion/physiology
- Gene Expression Regulation, Developmental
- Cell Movement/genetics*
- Cell Movement/physiology
- Sialic Acids/metabolism
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- Zebrafish Proteins/physiology
- Neurons/cytology
- Neurons/enzymology
- Neurons/metabolism*
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/growth & development
 
- PubMed
- 18095350 Full text @ Dev. Dyn.
            Citation
        
        
            Rieger, S., Volkmann, K., and Köster, R.W. (2008) Polysialyltransferase expression is linked to neuronal migration in the developing and adult zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 237(1):276-285.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Modulation of cell-cell adhesion is crucial for regulating neuronal migration and maintenance of structural plasticity in the embryonic and mature brain. Such modulation can be obtained by the enzymatic attachment of polysialic acid (PSA) to the neural cell adhesion molecule (NCAM) by means of the polysialyltransferases STX and PST. Thus, differential expression of STX and PST is likely to be responsible for varying functions of PSA-NCAM during neuronal differentiation, maintenance, plasticity, and regeneration. We have isolated the zebrafish homologues of STX (St8sia2) and PST (St8sia4) and demonstrate that their expression in the embryonic and adult nervous system is often confined to regions of neuronal migration. Moreover, in the adult cerebellum, the complementary expression pattern of both polysialyltransferases suggests a function in regulating cerebellar neuronal plasticity. Enzymatic removal of PSA in the embryonic cerebellum results in impaired neuronal migration, suggesting that PSA-NCAM is a key regulator of motility for cerebellar neuronal progenitors.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    