PUBLICATION
            Using GAL4-Inducible Transgenics to Modulate Rho GTPase Activity in Zebrafish
- Authors
 - Hanovice, N.J., McMains, E., Gross, J.M.
 - ID
 - ZDB-PUB-180801-12
 - Date
 - 2018
 - Source
 - Methods in molecular biology (Clifton, N.J.) 1821: 359-370 (Chapter)
 - Registered Authors
 - Gross, Jeffrey, Hanovice, Nick
 - Keywords
 - Cdc42, GAL4/UAS, Heat shock, Rac1, RhoA, Transgenics, Zebrafish
 - MeSH Terms
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- rho GTP-Binding Proteins*/biosynthesis
 - rho GTP-Binding Proteins*/genetics
 - Embryo, Nonmammalian/embryology*
 - Transcription Factors*/genetics
 - Transcription Factors*/metabolism
 - Gene Expression Regulation, Developmental
 - Zebrafish Proteins*/genetics
 - Zebrafish Proteins*/metabolism
 - Zebrafish*/embryology
 - Zebrafish*/genetics
 - Gene Expression Regulation, Enzymologic
 - Embryonic Development*
 - Animals
 - Animals, Genetically Modified*/embryology
 - Animals, Genetically Modified*/genetics
 - DNA-Binding Proteins*/genetics
 - DNA-Binding Proteins*/metabolism
 
 - PubMed
 - 30062424 Full text @ Meth. Mol. Biol.
 
            Citation
        
        
            Hanovice, N.J., McMains, E., Gross, J.M. (2018) Using GAL4-Inducible Transgenics to Modulate Rho GTPase Activity in Zebrafish. Methods in molecular biology (Clifton, N.J.). 1821:359-370.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Rho GTPases are Ras-family G proteins that regulate many critical cellular functions. Due to their requirement during early embryonic development, investigations into the function of Rho GTPases at a tissue-specific level require inducible and spatially targeted modulation of Rho GTPase activity. Here, we describe the use of ten novel zebrafish transgenics enabling GAL4-specific expression of Rho GTPases to modulate Rho GTPase activity with spatial and temporal control.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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