PUBLICATION
            miR-451 protects against erythroid oxidant stress by repressing 14-3-3ζ
- Authors
 - Yu, D., Dos Santos, C.O., Zhao, G., Jiang, J., Amigo, J.D., Khandros, E., Dore, L.C., Yao, Y., D'Souza, J., Zhang, Z., Ghaffari, S., Choi, J., Friend, S., Tong, W., Orange, J.S., Paw, B.H., and Weiss, M.J.
 - ID
 - ZDB-PUB-100806-15
 - Date
 - 2010
 - Source
 - Genes & Development 24(15): 1620-1633 (Journal)
 - Registered Authors
 - Amigo, Julio, Paw, Barry
 - Keywords
 - MicroRNA, erythropoiesis, FoxO3, hemolytic anemia
 - MeSH Terms
 - 
    
        
        
            
                
- Erythroid Cells/enzymology
 - Erythroid Cells/metabolism*
 - Mice
 - Gene Expression Regulation, Developmental*
 - Base Sequence
 - Zebrafish/genetics
 - Zebrafish/metabolism
 - Oxidative Stress*
 - 14-3-3 Proteins/genetics
 - 14-3-3 Proteins/metabolism*
 - Gene Knockdown Techniques
 - Catalase/metabolism
 - Sequence Alignment
 - Forkhead Transcription Factors/metabolism
 - MicroRNAs/genetics
 - MicroRNAs/metabolism*
 - Sequence Deletion/genetics
 - Active Transport, Cell Nucleus
 - Animals
 - Mice, Knockout
 
 - PubMed
 - 20679398 Full text @ Genes & Dev.
 
            Citation
        
        
            Yu, D., Dos Santos, C.O., Zhao, G., Jiang, J., Amigo, J.D., Khandros, E., Dore, L.C., Yao, Y., D'Souza, J., Zhang, Z., Ghaffari, S., Choi, J., Friend, S., Tong, W., Orange, J.S., Paw, B.H., and Weiss, M.J. (2010) miR-451 protects against erythroid oxidant stress by repressing 14-3-3ζ. Genes & Development. 24(15):1620-1633.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The bicistronic microRNA (miRNA) locus miR-144/451 is highly expressed during erythrocyte development, although its physiological roles are poorly understood. We show that miR-144/451 ablation in mice causes mild erythrocyte instability and increased susceptibility to damage after exposure to oxidant drugs. This phenotype is deeply conserved, as miR-451 depletion synergizes with oxidant stress to cause profound anemia in zebrafish embryos. At least some protective activities of miR-451 stem from its ability to directly suppress production of 14-3-3zeta, a phospho-serine/threonine-binding protein that inhibits nuclear accumulation of transcription factor FoxO3, a positive regulator of erythroid anti-oxidant genes. Thus, in miR-144/451(-/-) erythroblasts, 14-3-3zeta accumulates, causing partial relocalization of FoxO3 from nucleus to cytoplasm with dampening of its transcriptional program, including anti-oxidant-encoding genes Cat and Gpx1. Supporting this mechanism, overexpression of 14-3-3zeta in erythroid cells and fibroblasts inhibits nuclear localization and activity of FoxO3. Moreover, shRNA suppression of 14-3-3zeta protects miR-144/451(-/-) erythrocytes against peroxide-induced destruction, and restores catalase activity. Our findings define a novel miRNA-regulated pathway that protects erythrocytes against oxidant stress, and, more generally, illustrate how a miRNA can influence gene expression by altering the activity of a key transcription factor.
            
    
        
        
    
    
    
                
                    
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                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping