PUBLICATION
            Redundant Roles for Sox7 and Sox18 in Arteriovenous Specification in Zebrafish
- Authors
- Herpers, R., van de Kamp, E., Duckers, H.J., and Schulte-Merker, S.
- ID
- ZDB-PUB-071125-30
- Date
- 2008
- Source
- Circulation research 102(1): 12-15 (Journal)
- Registered Authors
- Herpers, Robert, Schulte-Merker, Stefan
- Keywords
- zebrafish, sox7, sox18, AV-differentiation, hypotrichosis–lymphedema–telangiectasia, hereditary hemorrhagic telangiectasia
- MeSH Terms
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                - Veins/abnormalities
- Veins/embryology
- Veins/growth & development
- Transcription Factors/analysis
- Transcription Factors/physiology
- Blood Vessels/abnormalities
- Blood Vessels/embryology
- Blood Vessels/growth & development*
- Arteries/abnormalities
- Arteries/embryology
- Arteries/growth & development
- Zebrafish Proteins/physiology
- Zebrafish
- High Mobility Group Proteins/analysis
- High Mobility Group Proteins/physiology*
- Animals
- DNA-Binding Proteins/analysis
- DNA-Binding Proteins/physiology
- Aorta/growth & development
- SOXF Transcription Factors
- Embryonic Induction*
 
- PubMed
- 18032732 Full text @ Circ. Res.
            Citation
        
        
            Herpers, R., van de Kamp, E., Duckers, H.J., and Schulte-Merker, S. (2008) Redundant Roles for Sox7 and Sox18 in Arteriovenous Specification in Zebrafish. Circulation research. 102(1):12-15.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The specification of arteries and veins is an essential process in establishing and maintaining a functional blood vessel system. Incorrect arteriovenous specification disrupts embryonic development but has also been diagnosed in human syndromes such as hypotrichosis-lymphedema-telangiectasia, characterized by defects in blood and lymphatic vessels and associated with mutations in SOX18. Here we characterize the role of sox7 and sox18 during zebrafish vasculogenesis. Sox7 and sox18 are specifically expressed in the developing vasculature, and simultaneous loss of their function results in a severe loss of the arterial identity of the presumptive aorta which instead expresses venous markers, followed by dramatic arteriovenous shunt formations. Our study identifies members of the Sox family as key factors in specifying arteriovenous identity and will help to better understand Hypotrichosis-lymphedema-telangiectasia and other diseases.
            
    
        
        
    
    
    
                
                    
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                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    