PUBLICATION
            Effects of decreased muscle activity on developing axial musculature in nicb107 mutant zebrafish (Danio rerio)
- Authors
 - van der Meulen, T., Schipper, H., van Leeuwen, J.L., and Kranenbarg, S.
 - ID
 - ZDB-PUB-050920-12
 - Date
 - 2005
 - Source
 - The Journal of experimental biology 208(19): 3675-3687 (Journal)
 - Registered Authors
 - Schipper, Henk, van der Meulen, Talitha, van Leeuwen, Johan
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Receptors, Nicotinic/genetics*
 - Microscopy, Electron
 - Embryo, Nonmammalian/embryology*
 - Zebrafish/embryology*
 - Zebrafish/genetics
 - Muscle, Skeletal/embryology*
 - Muscle, Skeletal/physiology
 - Muscle, Skeletal/ultrastructure
 - Muscle Fibers, Skeletal/ultrastructure
 - Polymerase Chain Reaction
 - Mutation/genetics
 - Peptide Fragments/genetics*
 - Animals
 - Body Patterning/genetics
 - Body Patterning/physiology*
 - Gene Expression Regulation, Developmental*
 
 - PubMed
 - 16169945 Full text @ J. Exp. Biol.
 
            Citation
        
        
            van der Meulen, T., Schipper, H., van Leeuwen, J.L., and Kranenbarg, S. (2005) Effects of decreased muscle activity on developing axial musculature in nicb107 mutant zebrafish (Danio rerio). The Journal of experimental biology. 208(19):3675-3687.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The present paper discusses the effects of decreased muscle activity (DMA) on embryonic development in the zebrafish. Wild-type zebrafish embryos become mobile around 18 h post-fertilisation, long before the axial musculature is fully differentiated. As a model for DMA, the nic(b107) mutant was used. In nic(b107) mutant embryos, muscle fibres are mechanically intact and able to contract, but neuronal signalling is defective and the fibres are not activated, rendering the embryos immobile. Despite the immobility, distinguished slow and fast muscle fibres developed at the correct location in the axial muscles, helical muscle fibre arrangements were detected and sarcomere architecture was generated. However, in nic(b107) mutant embryos the notochord is flatter and the cross-sectional body shape more rounded, also affecting muscle fibre orientation. The stacking of sarcomeres and myofibril arrangement show a less regular pattern. Finally, expression levels of several genes were changed. Together, these changes in expression indicate that muscle growth is not impeded and energy metabolism is not changed by the decrease in muscle activity but that the composition of muscle is altered. In addition, skin stiffness is affected. In conclusion, the lack of muscle fibre activity did not prevent the basal muscle components developing but influenced further organisation and differentiation of these components.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping