PUBLICATION
            Systematic identification of seven ribosomal protein genes in bighead carp and their expression in response to microcystin-LR
- Authors
 - Cai, Y., Zhang, C., Hao, L., Chen, J., Xie, P., Chen, Z.
 - ID
 - ZDB-PUB-160311-6
 - Date
 - 2016
 - Source
 - The Journal of Toxicological Sciences 41: 293-302 (Journal)
 - Registered Authors
 - Chen, Jun
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Gene Expression/drug effects*
 - Species Specificity
 - Carps/genetics*
 - Carps/metabolism*
 - Protein Conformation
 - Amino Acid Sequence
 - Tissue Distribution
 - Evolution, Molecular
 - Zebrafish
 - Ribosomal Proteins/chemistry
 - Ribosomal Proteins/genetics*
 - Ribosomal Proteins/isolation & purification*
 - Ribosomal Proteins/metabolism
 - Animals
 - Microcystins/toxicity*
 - Time Factors
 - Brain/metabolism
 - Humans
 
 - PubMed
 - 26961614 Full text @ J. Toxicol. Sci.
 
            Citation
        
        
            Cai, Y., Zhang, C., Hao, L., Chen, J., Xie, P., Chen, Z. (2016) Systematic identification of seven ribosomal protein genes in bighead carp and their expression in response to microcystin-LR. The Journal of Toxicological Sciences. 41:293-302.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Microcystin-LR (MCLR) is one of the most toxic cyanotoxins produced in algal blooms. The toxic effects of MCLR on the expression of some organelles genes (mitochondrion, endoplasmic reticulum, and cytoskeleton etc) have been widely investigated, but little is known how it impacts on the expression of ribosomal genes. In this study we identified seven ribosomal protein genes RPS6, RPS12, RPS24, RPS27a, RPL12, RPL27 and RPL29 in bighead carp (Aristichthys nobilis), whose expression was regulated by MCLR. The amino acid sequences of those 7 genes shared more than 90% identity with corresponding sequences from zebrafish, and were well conserved throughout evolution. The 3D structure prediction showed that the structures of these ribosomal proteins were conserved, but had species specificity. Q-PCR analysis revealed that expression of seven genes changed dramatically at 3 hr, then went back to a moderate change- level at 24 hr in almost all tested tissues (liver, kidney, intestine, heart, spleen and gill) post MCLR injection, but in brain expression of the seven genes stayed same as the normal level. This study will help us to know not only about the evolution and functions of ribosomal proteins in anti-MCLR response in bighead carp, but also about the MCLR toxicity and its impact on aquaculture and human health.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping