PUBLICATION
            Early Developmental Expression of Two Insulins in Zebrafish (Danio rerio)
- Authors
 - Papasani, M.R, Robison, B.D., Hardy, R.W., and Hill, R.A.
 - ID
 - ZDB-PUB-060724-22
 - Date
 - 2006
 - Source
 - Physiological Genomics 27(1): 79-85 (Journal)
 - Registered Authors
 - Keywords
 - insulin, gene duplication, polymerase chain reaction
 - MeSH Terms
 - 
    
        
        
            
                
- Chromosome Mapping
 - Animals
 - Insulin/genetics*
 - Insulin/metabolism
 - Base Sequence
 - Cloning, Molecular
 - Zebrafish/embryology*
 - Zebrafish/genetics
 - Zebrafish/metabolism
 - Molecular Sequence Data
 - RNA, Messenger/analysis
 - In Situ Hybridization
 - Zebrafish Proteins/genetics*
 - Zebrafish Proteins/metabolism
 - Amino Acid Sequence
 - Gene Expression
 - Sequence Alignment
 
 - PubMed
 - 16849636 Full text @ Physiol. Genomics
 
            Citation
        
        
            Papasani, M.R, Robison, B.D., Hardy, R.W., and Hill, R.A. (2006) Early Developmental Expression of Two Insulins in Zebrafish (Danio rerio). Physiological Genomics. 27(1):79-85.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                In the present study, we have cloned a second insulin gene in zebrafish, and studied temporal and spatial expression of two zebrafish insulin genes. Zebrafish insulin a (insa) and insulin b (insb) mRNAs are derived from two different DNA contigs on chromosome 5 and chromosome 14 respectively, representing two different insulin genes. Real time PCR studies suggest that insa is a maternal and also a post-zygotic transcript. insa was observed at 1 hpf, and was rapidly degraded by 6 and 12 hpf, but was induced at 24 hpf (i.e. after pancreas formation). The expression levels at 24 hpf were approximately 220-fold higher than at 6 hpf and were significantly different from earlier time points. At 72 hpf (at the time of hatching), zebrafish insa mRNA levels tended to be higher than at 24 hpf and were approximately 727-fold higher compared to 6 hpf. This further increase in insa expression may be one of the many rapid physiological changes associated with hatching. insb expression was observed from1hpf and was significantly decreased from 12 hpf onwards. Its expression levels at 12 hpf and 24 hpf were approximately 2-fold, and 6-fold lower respectively, compared to its expression at 6 hpf. insb expression levels at 48 hpf were significantly lower than at 24 hpf, but not different from 72 hpf. Its expression levels at 72 hpf were approximately 61-fold lower than at 6 hpf. In situ hybridization studies showed insb expression in proliferating blastomeres at 3 hpf and 4 hpf. At later time points insb expression was restricted to the brain and pancreas (24 and 48 hpf). insa expression was observed in the pancreas at 24 and 48 hpf. The expression of insb in blastomeres and the head, suggest that insb could be acting as a pro-growth, survival and neuro-trophic factor during development. Pancreatic insa and insb may both be involved in the regulation of glucose homeostatsis as in mammals.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping