PUBLICATION
            Transferrin-a modulates hepcidin expression in zebrafish embryos
- Authors
 - Fraenkel, P.G., Gibert, Y., Holzheimer, J.L., Lattanzi, V.J., Burnett, S.F., Dooley, K.A., Wingert, R.A., and Zon, L.I.
 - ID
 - ZDB-PUB-081203-35
 - Date
 - 2009
 - Source
 - Blood 113(12): 2843-2850 (Journal)
 - Registered Authors
 - Dooley, Kim, Fraenkel, Paula, Gibert, Yann, Wingert, Rebecca, Zon, Leonard I.
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Anemia, Hypochromic/chemically induced
 - Anemia, Hypochromic/embryology
 - Anemia, Hypochromic/genetics
 - Sequence Homology, Amino Acid
 - Zebrafish/embryology
 - Hepcidins
 - Humans
 - Erythropoiesis/drug effects
 - Erythropoiesis/genetics
 - Mutation
 - Transferrin/deficiency
 - Transferrin/genetics
 - Transferrin/physiology*
 - Cation Transport Proteins/genetics
 - Amino Acid Sequence
 - Organ Specificity
 - Molecular Sequence Data
 - Gene Expression Regulation, Developmental/drug effects
 - Gene Expression Regulation, Developmental/physiology*
 - Phenylhydrazines/toxicity
 - Sequence Alignment
 - Antimicrobial Cationic Peptides/biosynthesis*
 - Antimicrobial Cationic Peptides/genetics
 - Animals
 - Embryo, Nonmammalian/drug effects
 - Embryo, Nonmammalian/metabolism
 - Zebrafish Proteins/biosynthesis
 - Zebrafish Proteins/deficiency
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/physiology*
 - Gene Knockdown Techniques
 - Iron/metabolism*
 - Iron/pharmacology
 - Receptors, Transferrin/antagonists & inhibitors
 - Receptors, Transferrin/genetics
 - Receptors, Transferrin/physiology
 - Species Specificity
 
 - PubMed
 - 19047682 Full text @ Blood
 
            Citation
        
        
            Fraenkel, P.G., Gibert, Y., Holzheimer, J.L., Lattanzi, V.J., Burnett, S.F., Dooley, K.A., Wingert, R.A., and Zon, L.I. (2009) Transferrin-a modulates hepcidin expression in zebrafish embryos. Blood. 113(12):2843-2850.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The iron regulatory hormone hepcidin is transcriptionally upregulated in response to iron loading, but the mechanisms by which iron levels are sensed are not well understood. Large-scale genetic screens in the zebrafish have resulted in the identification of hypochromic anemia mutants with a range of mutations affecting conserved pathways in iron metabolism and heme synthesis. We hypothesized that transferrin plays a critical role both in iron transport and in regulating hepcidin expression in zebrafish embryos. Here we report the identification and characterization of the zebrafish hypochromic anemia mutant, gavi, which exhibits transferrin-deficiency due to mutations in transferrin-a. Morpholino knockdown of transferrin-a in wild type embryos reproduced the anemia phenotype and decreased somite and terminal gut iron staining, while co-injection of transferrin-a cRNA partially restored these defects. Embryos with transferrin-a or transferrin receptor 2 (TfR2) deficiency exhibited low levels of hepcidin expression, however anemia, in the absence of a defect in the transferrin pathway, failed to impair hepcidin expression. These data indicate that transferrin-a transports iron and that hepcidin expression is regulated by a transferrin-a-dependent pathway in the zebrafish embryo.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping