PUBLICATION
            Differential requirement for ptf1a in endocrine and exocrine lineages of developing zebrafish pancreas
- Authors
- Lin, J.W., Biankin, A.V., Horb, M.E., Ghosh, B., Prasad, N.B., Yee, N.S., Pack, M.A., and Leach, S.D.
- ID
- ZDB-PUB-040609-2
- Date
- 2004
- Source
- Developmental Biology 270(2): 474-486 (Journal)
- Registered Authors
- Leach, Steven D., Pack, Michael, Yee, Nelson S.
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Sequence Alignment
- Homeodomain Proteins*
- Fluorescent Antibody Technique
- Zebrafish/embryology*
- Zebrafish/metabolism
- In Situ Hybridization
- DNA Primers
- Cell Lineage/physiology
- Insulin/metabolism
- Animals
- Base Sequence
- DNA, Complementary/genetics
- Helix-Loop-Helix Motifs/genetics
- Amino Acid Sequence
- Morphogenesis
- Trans-Activators/metabolism
- Transcription Factors/genetics*
- Transcription Factors/metabolism*
- Histological Techniques
- Sequence Analysis, DNA
- Gene Expression Regulation, Developmental*
- Cell Differentiation/physiology*
- Molecular Sequence Data
- Pancreas/cytology
- Pancreas/embryology*
- Pancreas/metabolism
 
- PubMed
- 15183727 Full text @ Dev. Biol.
            Citation
        
        
            Lin, J.W., Biankin, A.V., Horb, M.E., Ghosh, B., Prasad, N.B., Yee, N.S., Pack, M.A., and Leach, S.D. (2004) Differential requirement for ptf1a in endocrine and exocrine lineages of developing zebrafish pancreas. Developmental Biology. 270(2):474-486.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Mammalian studies have implicated important roles for the basic helix-loop-helix transcription factor Ptf1a-p48 in the development of both exocrine and endocrine pancreas. We have cloned the Ptf1a-p48 ortholog in Danio rerio. Early zebrafish ptf1a expression is observed in developing hindbrain and in endodermal pancreatic precursors. Analysis of ptf1a and insulin expression reveals a population of exocrine precursors that, throughout early development, are temporally and spatially segregated from endocrine elements. Morpholino-mediated knockdown of ptf1a confirms early divergence of these endocrine and exocrine lineages. Ptf1a morphants lack differentiated exocrine pancreas, but maintain normal differentiation and organization of the principal islet. In addition to the exocrine phenotype, ptf1a knockdown also reduces the prevalence of a small population of anterior endocrine cells normally found outside the principal islet. Together, these findings suggest the presence of distinct ptf1a-dependent and ptf1a-independent precursor populations in developing zebrafish pancreas.
            
    
        
        
    
    
    
                
                    
                        Errata / Notes
                    
                    
                
                
            
        
        
    
        
            
            Erratum in: Dev Biol. 2004 Oct 15;274(2):490.The publisher regrets that Figs. 1–8 were not published in color in the printed issue, as intended.
                
                    
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                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    