PUBLICATION
            Zebrafish wnt8 and wnt8b share a common activity but are involved in distinct developmental pathways
- Authors
- Kelly, G.M., Greenstein, P., Erezyilmaz, D.F., and Moon, R.T.
- ID
- ZDB-PUB-961014-544
- Date
- 1995
- Source
- Development (Cambridge, England) 121: 1787-1799 (Journal)
- Registered Authors
- Kelly, Greg, Moon, Randall T.
- Keywords
- Danio rerio, wnt, krox20, gsc, pax, snail1, spadetail, cyclops, mesoderm induction, pattern formation
- MeSH Terms
- 
    
        
        
            
                - Molecular Sequence Data
- Animals
- Sequence Alignment
- Zebrafish/embryology
- Zebrafish/genetics*
- Gene Expression
- DNA Primers
- Base Sequence
- Proteins/genetics*
- Amino Acid Sequence
- Female
- Xenopus
- Embryonic Induction/genetics*
- Phenotype
- Polymerase Chain Reaction
- Cytoskeletal Proteins
- In Situ Hybridization
- Wnt Proteins
- Zebrafish Proteins*
- Morphogenesis
- Mesoderm/physiology*
 
- PubMed
- 7600994 Full text @ Development
            Citation
        
        
            Kelly, G.M., Greenstein, P., Erezyilmaz, D.F., and Moon, R.T. (1995) Zebrafish wnt8 and wnt8b share a common activity but are involved in distinct developmental pathways. Development (Cambridge, England). 121:1787-1799.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The specification of the vertebrate body plan is dependent on numerous signaling molecules, including members of the Wnt family. We have identified two zebrafish wnt8 paralogs related to Xwnt-8B and Xwnt-8, respectively. A RT-PCR assay demonstrated that wnt8 is expressed maternally, with transcripts detected throughout embryogenesis, whereas wnt8b transcripts were first detected during late gastrulation. The wnt8 transcripts at 50% epiboly are spatially restricted to those cells at the blastoderm margin, overlying gsc-expressing cells in the axial hypoblast. During late gastrulation, wnt8 was no longer detected in the marginal cells at the dorsal midline and by mid-segmentation, transcripts were found in the presumptive tail bud. In contrast, wnt8b expression is spatially restricted to prospective neuroepithelium, and later to neural-specific structures. Overexpression of both wnts results in two major phenotypes: radialized embryos and embryos with anterior defects. These phenotypes were preceded by significant changes in the spatial expression patterns of gsc and ntl transcripts, reminiscent of activities of Xwnt-8 in Xenopus, and consistent with a role for wnt8 in the specification or patterning of mesoderm.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    