PUBLICATION
            The paired domain-containing nuclear factor pax[b] is expressed in specific commissural interneurons in zebrafish embryos
- Authors
- Mikkola, I., Fjose, A., Kuwada, J.Y., Wilson, S., Guddal, P.H., and Krauss, S.
- ID
- ZDB-PUB-961014-781
- Date
- 1992
- Source
- Journal of neurobiology 23: 933-946 (Journal)
- Registered Authors
- Fjose, Anders, Krauss, Stefan, Kuwada, John, Wilson, Steve
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Embryo, Nonmammalian/metabolism*
- Gene Expression/physiology*
- Cell Nucleus/metabolism
- Cell Nucleus/ultrastructure
- Immunohistochemistry
- 3,3'-Diaminobenzidine
- Genes, Homeobox
- Mesencephalon/anatomy & histology
- Mesencephalon/metabolism
- Animals
- Spinal Cord/anatomy & histology
- Spinal Cord/metabolism
- DNA/immunology
- DNA/metabolism
- Terminology as Topic
- Zebrafish/metabolism*
- Interneurons/metabolism*
- Transcription, Genetic
- Brain/anatomy & histology
- Brain/metabolism
 
- PubMed
- 1361000 Full text @ J. Neurobiol.
            Citation
        
        
            Mikkola, I., Fjose, A., Kuwada, J.Y., Wilson, S., Guddal, P.H., and Krauss, S. (1992) The paired domain-containing nuclear factor pax[b] is expressed in specific commissural interneurons in zebrafish embryos. Journal of neurobiology. 23:933-946.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The zebrafish paired box (Pax) genes are expressed in the early neural tube and are thought to be transcription factors that regulate the differentiation of cells in the central nervous system (CNS). The protein product of one of these Pax genes, pax[b], is detectable as a nuclear antigen in all the regions of the embryo that transcribe the gene including the posterior midbrain, the nephritic primordium, the Wolffian duct, the optic stalk, and, in specific neurons, in the hindbrain and spinal cord. The timing and pattern of axonal outgrowth by the early pax[b]-positive neurons suggest that they are the commissural secondary ascending (CoSA) interneurons in the spinal cord; the primary commissural interneurons (MiD2c and MiD3c) in hindbrain rhombomeres mi2 and mi3; and a previously unclassified set of commissural interneurons that we termed the commissural caudalrhombomere ascending (CoCaA) interneurons in the caudal hindbrain. In contrast, the Mauthner interneurons do not express pax[b] early in development. Shortly after the appearance of the first pax[b]-positive interneurons, additional nuclei adjacent to the first pax[b]-positive interneurons become pax[b] positive. This pattern of expression suggests that the pax[b] protein may be involved in determining the identity of specific commissural interneurons.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    