PUBLICATION
            Morphogenesis of prechordal plate and notochord requires intact Eph/Ephrin B signaling
- Authors
 - Chan, J., Mably, J.D., Serluca, F.C., Chen, J.-N., Goldstein, N.B., Thomas, M.C., Cleary, J.A., Brennan, C., Fishman, M.C., and Roberts, T.M.
 - ID
 - ZDB-PUB-010514-1
 - Date
 - 2001
 - Source
 - Developmental Biology 234(2): 470-482 (Journal)
 - Registered Authors
 - Brennan, Caroline, Chan, Joanne, Chen, Jau-Nian, Fishman, Mark C., Mably, John, Roberts, Thomas M., Serluca, Fabrizio, Thomas, Matthew
 - Keywords
 - Eph; ephrin B; zebrafish; gastrulation; prechordal plate; notochord; morphogenesis; cell movement
 - MeSH Terms
 - 
    
        
        
            
                
- Embryonic Structures/embryology*
 - Tissue Distribution
 - Body Patterning
 - Cell Movement
 - Gastrula
 - Signal Transduction
 - Morphogenesis
 - Nervous System/embryology
 - Notochord/embryology*
 - Ectoderm
 - Sequence Homology, Amino Acid
 - Receptor Protein-Tyrosine Kinases/metabolism*
 - Molecular Sequence Data
 - Sequence Analysis, DNA
 - Animals
 - Membrane Proteins/genetics*
 - Membrane Proteins/metabolism*
 - Zebrafish
 - Amino Acid Sequence
 
 - PubMed
 - 11397014 Full text @ Dev. Biol.
 
            Citation
        
        
            Chan, J., Mably, J.D., Serluca, F.C., Chen, J.-N., Goldstein, N.B., Thomas, M.C., Cleary, J.A., Brennan, C., Fishman, M.C., and Roberts, T.M. (2001) Morphogenesis of prechordal plate and notochord requires intact Eph/Ephrin B signaling. Developmental Biology. 234(2):470-482.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Eph receptors and their ligands, the ephrins, mediate cell-to-cell signals implicated in the regulation of cell migration processes during development. We report the molecular cloning and tissue distribution of zebrafish transmembrane ephrins that represent all known members of the mammalian class B ephrin family. The degree of homology among predicted ephrin B sequences suggests that, similar to their mammalian counterparts, zebrafish B-ephrins can also bind promiscuously to several Eph receptors. The dynamic expression patterns for each zebrafish B-ephrin support the idea that these ligands are confined to interact with their receptors at the borders of their complementary expression domains. Zebrafish B-ephrins are expressed as early as 30% epiboly and during gastrula stages: in the germ ring, shield, prechordal plate, and notochord. Ectopic overexpression of dominant-negative soluble ephrin B constructs yields reproducible defects in the morphology of the notochord and prechordal plate by the end of gastrulation. Notably disruption of Eph/ephrin B signaling does not completely destroy structures examined, suggesting that cell fate specification is not altered. Thus abnormal morphogenesis of the prechordal plate and the notochord is likely a consequence of a cell movement defect. Our observations suggest Eph/ephrin B signaling plays an essential role in regulating cell movements during gastrulation.
            
    
        
        
    
    
    
                
                    
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