PUBLICATION
            Zebrafish smad7 is regulated by Smad3 and BMP signals
- Authors
- Pogoda, H.M. and Meyer, D.
- ID
- ZDB-PUB-020716-15
- Date
- 2002
- Source
- Developmental Dynamics : an official publication of the American Association of Anatomists 224(3): 334-349 (Journal)
- Registered Authors
- Meyer, Dirk, Pogoda, Hans-Martin
- Keywords
- Smad3b; Smad3; Smad7; antiSmad; zebrafish; TGF-b; VMP; nodal; antivin; foxH1; schmalspur (sur); one-eyed pinhead (oep); swirl (swr); snail-house (snh); dino (din)
- MeSH Terms
- 
    
        
        
            
                - Signal Transduction
- Sequence Homology, Amino Acid
- Cloning, Molecular
- Gene Expression Regulation, Developmental*
- Trans-Activators/biosynthesis*
- Trans-Activators/genetics
- Amino Acid Sequence
- Smad7 Protein
- Plasmids/metabolism
- Zebrafish
- Bone Morphogenetic Proteins/biosynthesis
- Bone Morphogenetic Proteins/genetics*
- Zebrafish Proteins
- DNA-Binding Proteins/biosynthesis*
- DNA-Binding Proteins/genetics
- RNA, Messenger/metabolism
- Nodal Protein
- Models, Biological
- Ligands
- Cytoplasm/metabolism
- DNA Mutational Analysis
- In Situ Hybridization
- Smad3 Protein
- Molecular Sequence Data
- Phylogeny
- Transforming Growth Factor beta/biosynthesis
- Transforming Growth Factor beta/metabolism
- Time Factors
- Animals
 
- PubMed
- 12112463 Full text @ Dev. Dyn.
            Citation
        
        
            Pogoda, H.M. and Meyer, D. (2002) Zebrafish smad7 is regulated by Smad3 and BMP signals. Developmental Dynamics : an official publication of the American Association of Anatomists. 224(3):334-349.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Growth factors of the TGF-beta superfamily such as BMPs and Nodals are important signaling factors during all stages of animal development. Smad proteins, the cytoplasmic mediators of most TGF-beta signals in vertebrates, play central roles not only for transmission but also in controlling inductive TGF-beta signals by feedback regulation. Here, we describe cloning, expression pattern, transcriptional regulation, and functional properties of two novel zebrafish Smad proteins: the TGF-beta agonist Smad3b, and the anti-Smad Smad7. We show that zebrafish Smad3b, in contrast to the related zebrafish Smad2, can induce mesoderm independently of TGF-beta signaling. Although mammalian Smad3 was shown to inhibit expression of the organizer-specific genes goosecoid, zebrafish smad3b activates organizer genes such as goosecoid. Furthermore, we show that Smad3 and BMP signals activate smad7. Because Smad7 blocks distinct TGF-beta signals in early zebrafish development, our data provide hints for new roles of smad3 genes in the regulation and modulation of TGF-beta signals. In summary, our analyses point out differences of Smad3b and Smad2 functions in zebrafish and provide the first link of smad3 and smad7 function in context of vertebrate development.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    