PUBLICATION
            Differential regulation of Period 2 and Period 3 expression during development of the zebrafish circadian clock
- Authors
- Delaunay, F., Thisse, C., Thisse, B., and Laudet, V.
- ID
- ZDB-PUB-030716-18
- Date
- 2003
- Source
- Gene expression patterns : GEP 3(3): 319-324 (Journal)
- Registered Authors
- Delaunay, Franck, Laudet, Vincent, Thisse, Bernard, Thisse, Christine
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Gene Expression Regulation, Developmental/physiology*
- Eye Proteins/biosynthesis
- Eye Proteins/genetics*
- Transcription Factors
- Conserved Sequence
- Gene Expression Profiling
- Zebrafish Proteins
- Amino Acid Sequence
- Molecular Sequence Data
- Nuclear Proteins/biosynthesis
- Nuclear Proteins/genetics*
- Animals
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/physiology
- Circadian Rhythm/genetics*
- Circadian Rhythm/physiology
- Period Circadian Proteins
- Phylogeny
 
- PubMed
- 12799078 Full text @ Gene Expr. Patterns
            Citation
        
        
            Delaunay, F., Thisse, C., Thisse, B., and Laudet, V. (2003) Differential regulation of Period 2 and Period 3 expression during development of the zebrafish circadian clock. Gene expression patterns : GEP. 3(3):319-324.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Circadian ( approximately 24h) clocks are endogenous time-keeping systems that drive the daily biological rhythms observed in most living organisms. The oscillation is generated by a transcriptional/translational autoregulatory feedback loop that is reset by external time cues such as the light/dark cycle and which in turn controls rhythms in physiology and behavior through downstream clock-controlled genes (Nature 417 (2002) 329). Genetic and biochemical analysis of Drosophila and mammalian clock genes has provided a comprehensive model for the molecular oscillator that generates these rhythms, but the ontogeny of this oscillator remains poorly understood. A circadian oscillator involving the clock genes Per3 and Rev-erbalpha was identified during early development in zebrafish (Science 289 (2000) 297). Here, we report the isolation of zebrafish Per2 and show the presence of a Per2 maternal mRNA in early embryos as for Per3. However, Per2 rhythmic expression occurs late during embryogenesis as compared to that of Per3. Furthermore, our data indicate that Per2 is not required during embryogenesis for the rhythmicity of physiological outputs such as melatonin synthesis. In addition, Per2 but not Per3 is constitutively expressed in the developing olfactory bulb and pituitary. This differential spatio-temporal expression patterns suggest specific roles for Per2 and Per3 in the establishment of the embryonic circadian system.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    