PUBLICATION
            Identification of ephrin-A3 and novel genes specific to the midbrain-MHB in embryonic zebrafish by ordered differential display
- Authors
 - Hirate, Y., Mieda, M., Harada, T., Yamasu, K., and Okamoto, H.
 - ID
 - ZDB-PUB-010912-18
 - Date
 - 2001
 - Source
 - Mechanisms of Development 107(1-2): 83-96 (Journal)
 - Registered Authors
 - Harada, Tae, Hirate, Yoshikazu, Mieda, Michihiro, Okamoto, Hitoshi, Yamasu, Kyo
 - Keywords
 - zebrafish; Islet-3; ordered differential display; midbrain/hindbrain boundary; ephrin-A3; midbrain signaling
 - MeSH Terms
 - 
    
        
        
            
                
- In Situ Hybridization
 - Sequence Alignment
 - Ephrin-A3
 - Zebrafish/embryology*
 - Zebrafish/genetics
 - Zebrafish/metabolism
 - Mesencephalon/embryology*
 - Mesencephalon/metabolism
 - Amino Acid Sequence
 - Embryo, Nonmammalian/metabolism
 - Gene Expression Profiling
 - Nerve Tissue Proteins*
 - Humans
 - Gene Expression Regulation, Developmental
 - Transcription Factors
 - Rhombencephalon/embryology*
 - Rhombencephalon/metabolism
 - Homeodomain Proteins/genetics
 - Homeodomain Proteins/metabolism
 - LIM-Homeodomain Proteins
 - Cloning, Molecular
 - DNA, Complementary
 - Animals
 - Molecular Sequence Data
 - Membrane Proteins/chemistry
 - Membrane Proteins/genetics*
 
 - PubMed
 - 11520665 Full text @ Mech. Dev.
 
            Citation
        
        
            Hirate, Y., Mieda, M., Harada, T., Yamasu, K., and Okamoto, H. (2001) Identification of ephrin-A3 and novel genes specific to the midbrain-MHB in embryonic zebrafish by ordered differential display. Mechanisms of Development. 107(1-2):83-96.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Development of the tectum and the cerebellum is induced by a reciprocal inductive signaling between their respective primordia, the midbrain and the midbrain/hindbrain boundary (MHB). We set out to identify molecules that function in and downstream of this reciprocal signaling. Overexpression of LIM domain of the transcription factor Islet-3 (LIM(Isl-3)) leads to inhibition of this reciprocal signaling and to resultant defects in tectal and cerebellar development. We therefore searched for genes that may be either up- or down-regulated by overexpression of LIM(Isl-3) by comparing the gene expression profiles in the midbrain and the MHB of normal embryos and embryos in which Islet-3 function was repressed, using a combination of ordered differential display and whole-mount in situ hybridization. Among genes identified in this search, two cDNA fragments encoded Wnt1 and FGF8, which are already known to be essential for the reciprocal signaling between the midbrain and the MHB, confirming the effectiveness of our strategy. We identified four other partial cDNA clones that were specifically expressed around the MHB, ten cDNAs specifically expressed in the tectum, and three cDNAs expressed in neural crest cells including those derived from the midbrain level. The ephrin-A3 gene was specifically expressed in posterior tectum in a gradient that decreased anteriorly. Although ephrin-A2 and ephrin-A5 have been reported to be expressed in the corresponding region in mouse embryos, the superior/inferior colliculi, mouse ephrin-A3 is not expressed prominently in this region, suggesting that the role of ephrin-A3 in brain development may have been altered in the process of brain evolution.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping