PUBLICATION
            Glutathione S-transferase protein expression in different life stages of zebrafish (Danio rerio)
- Authors
 - Tierbach, A., Groh, K.J., Schönenberger, R., Schirmer, K., Suter, M.J.
 - ID
 - ZDB-PUB-180124-8
 - Date
 - 2018
 - Source
 - Toxicological sciences : an official journal of the Society of Toxicology 162(2): 702-712 (Journal)
 - Registered Authors
 - Keywords
 - GST, biotransformation, mass spectrometry, multiple reaction monitoring, targeted proteomics
 - MeSH Terms
 - 
    
        
        
            
                
- Sex Factors
 - Life Cycle Stages/genetics*
 - Zebrafish/genetics
 - Zebrafish/growth & development*
 - Biotransformation
 - Cytosol/enzymology
 - Proteomics
 - Amino Acid Sequence
 - Isoenzymes
 - Glutathione Transferase/genetics*
 - Liver/enzymology
 - Organ Specificity
 - Animals
 - Female
 - Male
 
 - PubMed
 - 29361160 Full text @ Toxicol. Sci.
 
            Citation
        
        
            Tierbach, A., Groh, K.J., Schönenberger, R., Schirmer, K., Suter, M.J. (2018) Glutathione S-transferase protein expression in different life stages of zebrafish (Danio rerio). Toxicological sciences : an official journal of the Society of Toxicology. 162(2):702-712.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Zebrafish is a widely used animal model in biomedical sciences and toxicology. Although evidence for the presence of phase I and phase II xenobiotic defense mechanisms in zebrafish exists on the transcriptional and enzyme activity level, little is known about the protein expression of xenobiotic metabolizing enzymes. Given the important role of glutathione S-transferases (GSTs) in phase II biotransformation, we analyzed cytosolic GST proteins in zebrafish early life stages and different organs of adult male and female fish, using a targeted proteomics approach. The established Multiple Reaction Monitoring-based assays enable the measurement of the relative abundance of specific GST isoenzymes and GST classes in zebrafish through a combination of proteotypic peptides and peptides shared within the same class.GSTs of the classes alpha, mu, pi and rho are expressed in zebrafish embryo as early as 4 hours post fertilization (hpf). The majority of GST enzymes are present at 72 hpf followed by a continuous increase in expression thereafter. In adult zebrafish, GST expression is organ dependent, with most of the GST classes showing the highest expression in the liver.The expression of a wide range of cytosolic GST isoenzymes and classes in zebrafish early life stages and adulthood supports the use of zebrafish as a model organism in chemical-related investigations.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping