PUBLICATION
            Genetic analysis of adenohypophysis formation in zebrafish
- Authors
- Herzog, W., Sonntag, C., Walderich, B., Odenthal, J., Maischein, H.M., and Hammerschmidt, M.
- ID
- ZDB-PUB-040202-1
- Date
- 2004
- Source
- Molecular endocrinology (Baltimore, Md.) 18(5): 1185-1195 (Journal)
- Registered Authors
- Hammerschmidt, Matthias, Herzog, Wiebke, Maischein, Hans-Martin, Odenthal, Joerg, Sonntag, Carmen, Walderich, Brigitte
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Morphogenesis/genetics
- Gene Expression Regulation, Developmental
- Cell Lineage/genetics*
- Zebrafish/genetics
- Zebrafish/metabolism*
- Animals
- Mutation/genetics*
- Cloning, Molecular
- Pituitary Gland, Anterior/growth & development*
- Pituitary Gland, Anterior/metabolism
 
- PubMed
- 14752054 Full text @ Mol. Endocrinol.
            Citation
        
        
            Herzog, W., Sonntag, C., Walderich, B., Odenthal, J., Maischein, H.M., and Hammerschmidt, M. (2004) Genetic analysis of adenohypophysis formation in zebrafish. Molecular endocrinology (Baltimore, Md.). 18(5):1185-1195.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The adenohypophysis consists of at least six different cell types, somatotropes, lactotropes, thyrotropes, melanotropes, corticotropes and gonadotropes. In mouse, cloning of spontaneous mutations and gene targeting has revealed multiple genes required for different steps of adenohypophysis development. Here, we report the results of a systematic search for genes required for adenohypophysis formation and patterning in zebrafish. By screening F3 offspring of ENU-mutagenized founder fish, we isolated eleven mutants with absent or reduced expression of GH, the product of somatotropes, but a normally developing hypothalamus. Of such mutants, eight were further analyzed and mapped. They define four genes essential for different steps of adenohypophysis development. Two of them, lia and pia, affect the entire adenohypophysis, while the other two are required for a subset of adenohypophyseal cell types only. The third gene is zebrafish pit1 and is required for lactotropes, thyrotropes and somatotropes, similar to its mouse orthologue, while the fourth, aal, is required for corticotropes, melanotropes, thyrotropes and somatotropes, but not lactotropes. In conclusion, the isolated zebrafish mutants confirm principles of adenohypophysis development revealed in mouse, thereby demonstrating the high degree of molecular and mechanistic conservation among the different vertebrate species. In addition, they point to thus far unknown features of adenohypophysis development, such as the existence of a new lineage of pituitary cells which partially overlaps with the Pit1 lineage. Positional cloning of the lia, pia and aal genes might reveal novel regulators of vertebrate pituitary development.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    