PUBLICATION
            casanova encodes a novel Sox-related protein necessary and sufficient for early endoderm formation in zebrafish
- Authors
- Kikuchi, Y., Agathon, A., Alexander, J., Thisse, C., Waldron, S., Yelon, D., Thisse, B., and Stainier, D.Y.
- ID
- ZDB-PUB-010706-3
- Date
- 2001
- Source
- Genes & Development 15(12): 1493-1505 (Journal)
- Registered Authors
- Agathon, Antoine, Alexander, Jon, Kikuchi, Yutaka, Stainier, Didier, Thisse, Bernard, Thisse, Christine, Waldron, Steve, Yelon, Deborah
- Keywords
- sox; gut endoderm; Nodal; bonnie and clyde; faust; casanova
- MeSH Terms
- 
    
        
        
            
                - Transforming Growth Factor beta/genetics
- Zebrafish Proteins*
- Molecular Sequence Data
- SOX Transcription Factors
- Amino Acid Sequence
- Signal Transduction/physiology*
- Proteins/genetics
- Zebrafish
- GATA5 Transcription Factor
- SOXF Transcription Factors
- Transcription Factors/classification
- Transcription Factors/genetics
- Transcription Factors/metabolism*
- Mesoderm/cytology
- Mesoderm/physiology
- Endoderm/physiology*
- Gene Expression Regulation, Developmental
- Animals
- Cell Differentiation
- High Mobility Group Proteins/classification
- High Mobility Group Proteins/genetics
- High Mobility Group Proteins/metabolism*
- Homeodomain Proteins/metabolism
- Sequence Homology, Amino Acid
- Intracellular Signaling Peptides and Proteins
- Nodal Signaling Ligands
- DNA-Binding Proteins/metabolism
- Humans
 
- PubMed
- 11410530 Full text @ Genes & Dev.
            Citation
        
        
            Kikuchi, Y., Agathon, A., Alexander, J., Thisse, C., Waldron, S., Yelon, D., Thisse, B., and Stainier, D.Y. (2001) casanova encodes a novel Sox-related protein necessary and sufficient for early endoderm formation in zebrafish. Genes & Development. 15(12):1493-1505.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Early endoderm formation in zebrafish requires at least three loci that function downstream of Nodal signaling but upstream of the early endodermal marker sox17: bonnie and clyde (bon), faust (fau), and casanova (cas). cas mutants show the most severe phenotype as they do not form any gut tissue and lack all sox17 expression. Activation of the Nodal signaling pathway or overexpression of Bon or Fau/Gata5 fails to restore any sox17 expression in cas mutants, demonstrating that cas plays a central role in endoderm formation. Here we show that cas encodes a novel member of the Sox family of transcription factors. Initial cas expression appears in the dorsal yolk syncytial layer (YSL) in the early blastula, and is independent of Nodal signaling. In contrast, endodermal expression of cas, which begins in the late blastula, is regulated by Nodal signaling. Cas is a potent inducer of sox17 expression in wild-type embryos as well as in bon and fau/gata5 mutants. Cas is also a potent inducer of sox17 expression in MZoep mutants, which cannot respond to Nodal signaling. In addition, ectopic expression of cas in presumptive mesodermal cells leads to their transfating into endoderm. Altogether, these data indicate that Cas is the principal transcriptional effector of Nodal signaling during zebrafish endoderm formation.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    