PUBLICATION
            Regulation of hypocretin (OREXIN) expression in embryonic zebrafish
- Authors
- Faraco, J.H., Appelbaum, L., Marin, W., Gaus, S.E., Mourrain, P., and Mignot, E.
- ID
- ZDB-PUB-060731-12
- Date
- 2006
- Source
- The Journal of biological chemistry 281(40): 29753-29761 (Journal)
- Registered Authors
- Mourrain, Philippe
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Humans
- Promoter Regions, Genetic
- Zebrafish/embryology*
- Zebrafish/genetics*
- Intracellular Signaling Peptides and Proteins/genetics*
- Animals
- Gene Expression Regulation, Developmental/physiology*
- Orexins
- Molecular Sequence Data
- Amino Acid Sequence
- Neuropeptides/biosynthesis*
- Neuropeptides/genetics*
 
- PubMed
- 16867991 Full text @ J. Biol. Chem.
            Citation
        
        
            Faraco, J.H., Appelbaum, L., Marin, W., Gaus, S.E., Mourrain, P., and Mignot, E. (2006) Regulation of hypocretin (OREXIN) expression in embryonic zebrafish. The Journal of biological chemistry. 281(40):29753-29761.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Hypocretins/orexins (HCRT) are neuropeptides involved in the regulation of sleep and energy balance in mammals. Conservation of gene sequence, hypothalamic localization of cell bodies, and projection patterns in adult zebrafish suggest that the architecture and function of the hypocretin system are conserved in fish. We report on the complete genomic structure of the zebrafish and Tetraodon hypocretin genes and the complete predicted hypocretin protein sequences from 5 teleosts. Using whole-mount in situ hybridization, we have traced the development of hypocretin cells in zebrafish from onset of expression at 22hpf through the first week of development. Promoter elements of similar size from zebrafish and Tetraodon were capable of driving efficient and specific expression of EGFP in developing zebrafish embryos, thus defining a minimal promoter region able to accurately mimic the native hypocretin pattern. This EGFP expression also revealed a complex pattern of projections within the hypothalamus, to the midbrain, and to the spinal cord. To further analyze the promoter, a series of deletion and substitution constructs were injected into embryos, and resulting promoter activity was monitored in the first week of development. A critical region of 250 base pairs was identified containing a core 13 base pair element essential for hypocretin expression.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    