PUBLICATION
            Neuronal and neuroendocrine expression of lim3, a LIM class homeobox gene, is altered in mutant zebrafish with axial signaling defects
- Authors
- Glasgow, E., Karavanov, A.A., and Dawid, I.B.
- ID
- ZDB-PUB-980205-18
- Date
- 1997
- Source
- Developmental Biology 192: 405-419 (Journal)
- Registered Authors
- Dawid, Igor B., Glasgow, Eric
- Keywords
- pituitary, pineal, spinal cord, development, transcription factors
- MeSH Terms
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                - Sequence Alignment
- Nerve Tissue Proteins/biosynthesis*
- Nerve Tissue Proteins/genetics
- Molecular Sequence Data
- Animals
- Rhombencephalon/embryology
- Rhombencephalon/metabolism
- Neurosecretory Systems/metabolism*
- Zebrafish Proteins*
- Spinal Cord/embryology
- Spinal Cord/metabolism
- Gene Expression Regulation, Developmental*
- Head/embryology
- Homeodomain Proteins/biosynthesis*
- Homeodomain Proteins/genetics
- Tail/embryology
- Pituitary Gland/embryology
- Pituitary Gland/metabolism
- RNA, Messenger/biosynthesis
- Neurons/metabolism*
- Cell Lineage
- Sequence Homology, Amino Acid
- Abnormalities, Multiple/genetics
- Central Nervous System/abnormalities
- Central Nervous System/embryology
- Central Nervous System/metabolism
- LIM-Homeodomain Proteins
- Transcription Factors
- Genes, Homeobox*
- Amino Acid Sequence
- Zebrafish/embryology*
- Zebrafish/genetics
 
- PubMed
- 9441677 Full text @ Dev. Biol.
            Citation
        
        
            Glasgow, E., Karavanov, A.A., and Dawid, I.B. (1997) Neuronal and neuroendocrine expression of lim3, a LIM class homeobox gene, is altered in mutant zebrafish with axial signaling defects. Developmental Biology. 192:405-419.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                LIM class homeobox genes code for a family of transcriptional regulators that encode important determinants of cell lineage and cell type specificity. The lim3 gene from the zebrafish, Danio rerio, is highly conserved in sequence and expression pattern compared to its homologs in other vertebrates. In this paper we report immunocytochemical analysis of Lim3 protein expression in the pituitary, pineal, hindbrain, and spinal cord of the embryo, revealing an asymmetrical, lateral and late program of pituitary development in zebrafish, distinct from the pattern in other vertebrates. We studied Lim3 expression in no tail, floating head, and cyclops mutant embryos, all of which have midline defects, with special reference to spinal cord differentiation where Lim3 marks mostly motoneurons. cyclops embryos showed essentially normal Lim3 expression in the hindbrain and spinal cord despite the absence of the floor plate, while no tail mutant embryos, which lack a differentiated notochord, displayed an excess of Lim3-expressing cells in a generally normal pattern. In contrast, Lim3-positive cells largely disappeared from the posterior spinal cord in floating head mutants, except in patches that correlated with remnants of apparent floor plate cells. These results support the view that either notochord or floor plate signaling can specify Lim3-positive motoneurons in the spinal cord.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    