PUBLICATION
            Med14 cooperates with brg1 in the differentiation of skeletogenic neural crest
- Authors
- Lou, X., Burrows, J.T., Scott, I.C.
- ID
- ZDB-PUB-151111-3
- Date
- 2015
- Source
- BMC Developmental Biology 15: 41 (Journal)
- Registered Authors
- Burrows, Jeff, Lou, Xin, Scott, Ian
- Keywords
- Neural crest, Mediator complex, BAF complex, Brg1, Craniofacial defect, Med14, Jaw development
- MeSH Terms
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                - Embryo, Nonmammalian/embryology
- Cells, Cultured
- Neural Crest/cytology*
- Cell Differentiation/genetics
- Cell Proliferation
- Osteogenesis/genetics*
- Osteogenesis/physiology
- Gene Regulatory Networks/genetics
- Zebrafish/embryology*
- Jaw Abnormalities/genetics
- Maxillofacial Development/genetics*
- Maxillofacial Development/physiology
- Gene Expression Regulation, Developmental
- Animals
- Jaw/embryology
- Adaptor Proteins, Signal Transducing/genetics*
- Adaptor Proteins, Signal Transducing/metabolism
- Cell Movement
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- Mediator Complex/genetics*
- Mediator Complex/metabolism
 
- PubMed
- 26553192 Full text @ BMC Dev. Biol.
            Citation
        
        
            Lou, X., Burrows, J.T., Scott, I.C. (2015) Med14 cooperates with brg1 in the differentiation of skeletogenic neural crest. BMC Developmental Biology. 15:41.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
Background An intricate gene regulatory network drives neural crest migration and differentiation. How epigenetic regulators contribute to this process is just starting to be understood.
Results We found that mutation of med14 or brg1 in zebrafish embryos resulted in a cluster of neural crest cell-related defects. In med14 or brg1 mutants, neural crest cells that form the jaw skeleton were specified normally and migrated to target sites. However, defects in their subsequent terminal differentiation were evident. Transplantation experiments demonstrated that med14 and brg1 are required directly in neural crest cells. Analysis of med14; brg1 double mutant embryos suggested the existence of a strong genetic interaction between members of the Mediator and BAF complexes.
Conclusions These results suggest a critical role for Mediator and BAF complex function in neural crest development, and may also clarify the nature of defects in some craniofacial abnormalities.
            
    
                
                    
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                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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