PUBLICATION
            Microcystin-induced variations in transcription of GSTs in an omnivorous freshwater fish, goldfish
- Authors
- Li, G., Xie, P., Fu, J., Hao, L., Xiong, Q., and Li, H.
- ID
- ZDB-PUB-080506-10
- Date
- 2008
- Source
- Aquatic toxicology (Amsterdam, Netherlands) 88(1): 75-80 (Journal)
- Registered Authors
- Keywords
- Microcystin, Glutathione S-transferases, Real-time PCR, Goldfish, Carassius auratus L
- MeSH Terms
- 
    
        
        
            
                - Phylogeny
- Gene Expression Regulation, Enzymologic/drug effects*
- Glutathione Transferase/genetics*
- Glutathione Transferase/metabolism
- Time Factors
- Protein Isoforms/genetics
- Cloning, Molecular
- Fresh Water
- Molecular Sequence Data
- Transcription, Genetic/drug effects*
- Goldfish/genetics*
- Microcystins/pharmacology*
- Animals
 
- PubMed
- 18455246 Full text @ Aquat. Toxicol.
            Citation
        
        
            Li, G., Xie, P., Fu, J., Hao, L., Xiong, Q., and Li, H. (2008) Microcystin-induced variations in transcription of GSTs in an omnivorous freshwater fish, goldfish. Aquatic toxicology (Amsterdam, Netherlands). 88(1):75-80.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The glutathione S-transferases are important enzymes in the microcystin-induced detoxication processes. In this experiment, we cloned the full-length cDNA of alpha, pi and theta-class-like glutathione S-transferase genes from goldfish (Carassius auratus L). Their derived amino acid sequences were clustered with other vertebrate alpha, pi and theta-class GSTs in a phylogenetic tree and the goldfish GST sequences have the highest similarity with those from common carp and zebrafish. Goldfish were i.p. injected with microcystins extract at two doses (50 and 200mugkg(-1)BW MC-LR(eq)) and the relative changes of the mRNA abundance in liver, kidney and intestine were analyzed by real-time PCR. The transcription of GST alpha was suppressed in both liver and intestine, but induced in the kidney. Decreased transcription of GST theta was detected in liver, kidney and intestine in the low-dose group. The transcription of GST pi was suppressed in liver and intestine post-injection in both dose groups. These results suggested that the transcription of GST isoforms varied in different ways within an organ and among organs of goldfish exposed to MCs.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    