PUBLICATION
            Maternal induction of ventral fate by zebrafish radar
- Authors
- Sidi, S., Goutel, C., Peyriéras, N., and Rosa, F.M.
- ID
- ZDB-PUB-030304-6
- Date
- 2003
- Source
- Proceedings of the National Academy of Sciences of the United States of America 100(6): 3315-3320 (Journal)
- Registered Authors
- Goutel, Carole, Rosa, Frederic, Sidi, Samuel
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - RNA, Messenger/genetics
- RNA, Messenger/metabolism
- Animals
- Bone Morphogenetic Proteins/genetics*
- Bone Morphogenetic Proteins/physiology*
- Growth Differentiation Factor 6
- Base Sequence
- Zebrafish/embryology*
- Zebrafish/genetics*
- Body Patterning
- In Situ Hybridization
- Mutation
- Female
- Gene Expression Regulation, Developmental
- Zebrafish Proteins*
- Phenotype
- Embryonic Induction
 
- PubMed
- 12601179 Full text @ Proc. Natl. Acad. Sci. USA
            Citation
        
        
            Sidi, S., Goutel, C., Peyriéras, N., and Rosa, F.M. (2003) Maternal induction of ventral fate by zebrafish radar. Proceedings of the National Academy of Sciences of the United States of America. 100(6):3315-3320.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                In vertebrate embryos, maternal determinants are thought to preestablish the dorsoventral axis by locally activating zygotic ventral- and dorsal-specifying genes, e.g., genes encoding bone morphogenetic proteins (BMPs) and BMP inhibitors, respectively. Whereas the canonical Wnt/beta-catenin pathway fulfills this role dorsally, the existence of a reciprocal maternal ventralizing signal remains hypothetical. Maternal noncanonical Wnt/Ca(2+) signaling may promote ventral fates by suppressing Wnt/beta-catenin dorsalizing signals; however, whether any maternal determinant is directly required for the activation of zygotic ventral-specifying genes is unknown. Here, we show that such a function is achieved, in part, in the zebrafish embryo by the maternally encoded transforming growth factor beta (TGF-beta) signaling molecule, Radar. Loss-of-function experiments, together with epistasis analyses, identify maternal Radar as an upstream activator of bmps expression. Maternal induction of bmps by Radar is essential for zebrafish development as its removal results in larval-lethal dorsalized phenotypes. Double-morphant analyses further suggest that Radar functions through the TGF-beta receptor Alk8 to initiate the expression of bmp genes. Our results support the existence of a previously uncharacterized maternal ventralizing pathway. They might further indicate that maternal TGF-beta/Rdr and Wnt/Ca(2+) pathways complementarily specify ventral cell fates, with the former triggering bmps expression and the latter indirectly repressing genes encoding BMP antagonists.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    