PUBLICATION
            pigk mutation underlies macho behavior and affects Rohon-Beard cell excitability
- Authors
 - Carmean, V., Yonkers, M.A., Tellez, M.B., Willer, J.R., Willer, G.B., Gregg, R.G., Geisler, R., Neuhauss, S.C., Ribera, A.B.
 - ID
 - ZDB-PUB-150703-15
 - Date
 - 2015
 - Source
 - Journal of neurophysiology 114(2): 1146-57 (Journal)
 - Registered Authors
 - Geisler, Robert, Neuhauss, Stephan, Ribera, Angie, Willer, Greg, Willer, Jason, Yonkers, Marc
 - Keywords
 - GPI-AP, Nav, PigK, Rohon-Beard Cells, touch response
 - MeSH Terms
 - 
    
        
        
            
                
- Polymerase Chain Reaction
 - Animals, Genetically Modified
 - Sodium/metabolism
 - Gene Knockdown Techniques
 - Mutation
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/metabolism*
 - Action Potentials/physiology
 - Sensory Receptor Cells/physiology*
 - Animals
 - Genotyping Techniques
 - Phenotype
 - Cell Adhesion Molecules/genetics
 - Cell Adhesion Molecules/metabolism*
 - Patch-Clamp Techniques
 - Zebrafish
 - RNA, Messenger/metabolism
 - Touch Perception/genetics
 - Touch Perception/physiology*
 
 - PubMed
 - 26133798 Full text @ J. Neurophysiol.
 
            Citation
        
        
            Carmean, V., Yonkers, M.A., Tellez, M.B., Willer, J.R., Willer, G.B., Gregg, R.G., Geisler, R., Neuhauss, S.C., Ribera, A.B. (2015) pigk mutation underlies macho behavior and affects Rohon-Beard cell excitability. Journal of neurophysiology. 114(2):1146-57.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The study of touch-evoked behavior allows investigation of both the cells and circuits that generate a response to tactile stimulation. We investigate a touch-insensitive zebrafish mutant, macho (maco), previously shown to have reduced sodium current amplitude and lack of action potential firing in sensory neurons. In the genomes of mutant but not wild type embryos, we identify a mutation in the pigk gene. The encoded protein, PigK, functions in attachment of glycophosphatidylinositol anchors to precursor proteins. In wild type embryos, pigk mRNA is present at times when mutant embryos display behavioral phenotypes. Consistent with the predicted loss of function induced by the mutation, knock-down of PigK phenocopies maco touch insensitivity and leads to reduced sodium current amplitudes in sensory neurons. We further test whether the genetic defect in pigk underlies the maco phenotype by overexpressing wild-type pigk in mutant embryos. We find that ubiquitous expression of wild type pigk rescues the touch response in maco mutants. In addition, for maco mutants, expression of wild type pigk restricted to sensory neurons rescues sodium current amplitudes and action potential firing in sensory neurons. However, expression of wild type pigk limited to sensory cells of mutant embryos does not allow rescue of the behavioral touch response. Our results demonstrate an essential role for pigk in generation of the touch response beyond that required for maintenance of proper INa density and action potential firing in sensory neurons.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping