PUBLICATION
            Wnt4 is not sufficient to induce lobuloalveolar mammary development
- Authors
- Kim, Y.C., Clark, R.J., Pelegri, F., and Alexander, C.M.
- ID
- ZDB-PUB-091120-4
- Date
- 2009
- Source
- BMC Developmental Biology 9: 55 (Journal)
- Registered Authors
- Pelegri, Francisco
- Keywords
- none
- MeSH Terms
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                - Blotting, Southern
- Wnt4 Protein
- Luciferases/genetics
- Luciferases/metabolism
- Blotting, Western
- Gene Expression Regulation, Developmental/drug effects
- Gene Expression Regulation, Developmental/genetics
- Mice
- Animals
- Doxycycline/pharmacology
- Mice, Mutant Strains
- Tetracyclines/pharmacology
- Pregnancy
- Male
- Mice, Transgenic
- Polymerase Chain Reaction
- Wnt Proteins/genetics
- Wnt Proteins/metabolism
- Wnt Proteins/physiology*
- Female
- Mammary Glands, Animal/growth & development*
- Mammary Glands, Animal/metabolism*
 
- PubMed
- 19878558 Full text @ BMC Dev. Biol.
            Citation
        
        
            Kim, Y.C., Clark, R.J., Pelegri, F., and Alexander, C.M. (2009) Wnt4 is not sufficient to induce lobuloalveolar mammary development. BMC Developmental Biology. 9:55.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                BACKGROUND: Brisken et al (2000) showed that Wnt4 null mammary glands were deficient in early lobuloalveolar mammary outgrowth during pregnancy, and implicated Wnt4 as an effector for the progesterone-induced mammary growth program. Though ectopic Wnt1 signaling is known to be mitogenic and oncogenic, no endogenously expressed Wnt ligands have ever been directly implicated in mammary growth and morphogenesis. Therefore, we generated conditional transgenic mice to test whether Wnt4 can stimulate mammary epithelial cell growth. RESULTS: We found that despite pregnancy-associated expression levels of Wnt4, mammary glands did not display the side-branching typical of early pregnancy. Control experiments designed to test the Wnt4 construct in zebrafish reproduced other studies that demonstrated Wnt4-specific phenotypes distinct from Wnt1-induced phenotypes. Indeed, using qPCR-based array analyses, we found that a specific transcriptional target of Wnt4, namely Wnt16, was induced in Wnt4-expressing transgenic glands, to levels equivalent to that of early pregnant glands. CONCLUSION: Taken together, we propose that Wnt4 is necessary, but not sufficient, to induce side-branch development.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    