PUBLICATION
            Direct lysine dimethylation of IRF3 by the methyltransferase SMYD3 attenuates antiviral innate immunity
- Authors
 - Wang, Z., Chen, X., Zhu, C., Fan, S., Tang, J., Deng, H., Sun, X., Liu, X., Xiao, W.
 - ID
 - ZDB-PUB-250116-1
 - Date
 - 2025
 - Source
 - Proceedings of the National Academy of Sciences of the United States of America 122: e2320644122e2320644122 (Journal)
 - Registered Authors
 - Xiao, Wuhan
 - Keywords
 - IRF3, SMYD3, innate immunity, methylation
 - MeSH Terms
 - 
    
        
        
            
                
- Interferon Regulatory Factor-3*/metabolism
 - Immunity, Innate*
 - Histone-Lysine N-Methyltransferase*/genetics
 - Histone-Lysine N-Methyltransferase*/metabolism
 - Interferon Type I/immunology
 - Interferon Type I/metabolism
 - Phosphorylation
 - Signal Transduction/immunology
 - HEK293 Cells
 - Zebrafish*/immunology
 - Mice
 - Mice, Knockout
 - Animals
 - Humans
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/immunology
 - Zebrafish Proteins/metabolism
 - Lysine*/metabolism
 - Methylation
 
 - PubMed
 - 39813248 Full text @ Proc. Natl. Acad. Sci. USA
 
            Citation
        
        
            Wang, Z., Chen, X., Zhu, C., Fan, S., Tang, J., Deng, H., Sun, X., Liu, X., Xiao, W. (2025) Direct lysine dimethylation of IRF3 by the methyltransferase SMYD3 attenuates antiviral innate immunity. Proceedings of the National Academy of Sciences of the United States of America. 122:e2320644122e2320644122.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Interferon regulatory factor 3 (IRF3) is the key transcription factor in the type I IFN signaling pathway, whose activation is regulated by multiple posttranslational modifications. Here, we identify SMYD3, a lysine methyltransferase, as a negative regulator of IRF3. SMYD3 interacts with IRF3 and catalyzes the dimethylation of IRF3 at lysine 39. This modification reduces IRF3 phosphorylation, dimerization, and subsequent nuclear translocation, leading to the inhibition of downstream type I interferon production. In addition, Smyd3-deficient mice are more resistant to RNA and DNA viral infections. Zebrafish lacking smyd3 or treated with the inhibitor BCI121 are also more resistant to viral infection. Our findings reveal a role for SMYD3 in the regulation of antiviral innate immunity and provide insight into a specific modulation of IRF3 that affects its activation.
            
    
        
        
    
    
    
                
                    
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