MOLECULAR CHARACTERISTICS AND FUNCTIONS OF THE SMYD3 GENE IN ANTIVIRAL IMMUNITY IN SINIPERCA CHUATSI

Interferon regulatory factor 3 and 7 (IRF3 and IRF7), which serve as key transcription factors in IFN activation, are tightly regulated to fulfill normal physiological functions. In this study, we found that SMYD3 (SET and MYND domain containing 3), a lysine methylase, exerts a negative regulatory effect on antiviral innate immunity in <italic>Siniperca chuatsi</italic>. Firstly, amino acid sequence alignment, protein structure prediction, and phylogenetic analysis indicated that the <italic>SMYD3</italic> gene in <italic>Siniperca chuatsi</italic> exhibits high evolutionary conservation. Furthermore, overexpression of <italic>Sc</italic>-SMYD3 significantly suppressed antiviral gene expression upon <italic>Siniperca chuatsi</italic> Rhabdovirus (SCRV) infection. Mechanistically, SMYD3 interacts with the key transcription factors IRF3 and IRF7 and inhibits the activity to activate interferon promoter and interferon-sensitive response element (ISRE) reporters. Finally, using zebrafish as a model, we found that <italic>smyd3</italic>-deficient zebrafish exhibited enhanced resistance to SCRV infection compared to wild-type zebrafish. Our results reveal a novel function of the lysine methyltransferase SMYD3 during SCRV infection and identify <italic>SMYD3</italic> as a potential target for breeding new <italic>Siniperca chuatsi</italic> strains with anti-SCRV ability.