PUBLICATION
            Molecular characterization and dietary regulation of aminopeptidase N (APN) in the grass carp (Ctenopharyngodon idella)
- Authors
 - Tang, J., Qu, F., Tang, X., Zhao, Q., Wang, Y., Zhou, Y., Feng, J., Lu, S., Hou, D., Liu, Z.
 - ID
 - ZDB-PUB-160202-8
 - Date
 - 2016
 - Source
 - Gene 582(1): 77-84 (Journal)
 - Registered Authors
 - Zhou, Yi
 - Keywords
 - Aminopeptidase N, Ctenopharyngodon idellus, Molecular characteristics, mRNA expression profile
 - MeSH Terms
 - 
    
        
        
            
                
- Animals
 - Gene Expression Regulation
 - CD13 Antigens/biosynthesis
 - CD13 Antigens/genetics
 - CD13 Antigens/metabolism*
 - Diet*
 - Carps/genetics*
 - Carps/metabolism
 - Zebrafish/genetics
 - RNA, Messenger/biosynthesis*
 - RNA, Messenger/genetics
 
 - PubMed
 - 26828613 Full text @ Gene
 
            Citation
        
        
            Tang, J., Qu, F., Tang, X., Zhao, Q., Wang, Y., Zhou, Y., Feng, J., Lu, S., Hou, D., Liu, Z. (2016) Molecular characterization and dietary regulation of aminopeptidase N (APN) in the grass carp (Ctenopharyngodon idella). Gene. 582(1):77-84.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Aminopeptidase N (APN) is a member of the peptidase M1 family and plays an important role in protein digestion. In the present study, an APN gene was cloned from the intestine of Ctenopharyngodon idellus. The full-length cDNA sequence of APN encodes an 892-amino-acid peptide that includes one helix trans-membrane region. Phylogenetic analysis showed that the APN sequence clustered with Danio rerio as its closest neighbor, sharing a sequence similarity of 81.5%. APN mRNA was differentially expressed in different tissues, with a gradient expression from high to low in the tissues of the fore-intestine, hind-intestine, liver, mid-intestine, kidney, muscle, spleen and heart. APN expression in grass carp had a circadian pattern, showing time-dependent higher expression between 06:00 and 18:00 and lower expression between 18:00 and 06:00. In addition, the protein levels and resource in the diet-regulated APN expression suggested that low crude protein (CP) level and fish meal stimulated APN gene expression. Furthermore, the mRNA expression of APN in the intestine was significantly suppressed by high concentrations of glutamine and glutamine dipeptides, respectively. This study may provide valuable knowledge on the regulation of APN expression in teleost, which has potential applications for improving fish dietary formulations.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping