PUBLICATION
            Segmental homologies among reticulospinal neurons in the hindbrain of the zebrafish larva
- Authors
 - Metcalfe, W.K., Mendelson, B., and Kimmel, C.B.
 - ID
 - ZDB-PUB-961014-770
 - Date
 - 1986
 - Source
 - The Journal of comparative neurology 251: 147-159 (Journal)
 - Registered Authors
 - Kimmel, Charles B., Mendelson, Bruce, Metcalfe, Walt
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Animals
 - Efferent Pathways
 - Larva
 - Cyprinidae/anatomy & histology*
 - Motor Neurons/classification*
 - Spinal Cord/anatomy & histology*
 - Dendrites/classification
 - Zebrafish/anatomy & histology*
 - Zebrafish/growth & development
 - Functional Laterality
 - Rhombencephalon/anatomy & histology*
 - Horseradish Peroxidase
 
 - PubMed
 - 3782495 Full text @ J. Comp. Neurol.
 
            Citation
        
        
            Metcalfe, W.K., Mendelson, B., and Kimmel, C.B. (1986) Segmental homologies among reticulospinal neurons in the hindbrain of the zebrafish larva. The Journal of comparative neurology. 251:147-159.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                We have examined the morphology of identified reticulospinal neurons in larval zebrafish by retrogradely labeling them with horseradish peroxidase. We described the morphology of 27 different types of reticulospinal neurons found in the hindbrain 5 days after fertilization. Nineteen of these types are present as single identified neurons on each side of the brain; the others are present as pairs or small groups of cells. The hindbrain reticulospinal neurons are present in seven bilateral clusters that are spaced periodically along the neuraxis. Each cluster contains two to five different types of reticulospinal neurons. Cells with similar morphological features are found in adjacent clusters. By considering cell position within the cluster and axon pathway, nearly all of the cells can be assigned to one of about seven serially repeated classes. Independent morphological features of the cells support the same classification. We propose that the clusters represent hindbrain segments and that the neurons of the same class that are present in the different clusters are segmental homologues. Assuming that this series evolved by successive duplications and divergence of the primitive segments, we have analyzed the changes that may have occurred during the evolution of each new segment. Changes between ipsilaterally and contralaterally projecting axons may have occurred several times during the evolution of the series. In addition, cells may have been added or deleted.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping