Tripartite Motif Containing Protein 56 (TRIM56)
RNF109; RING finger protein 109; E3 ubiquitin-protein ligase TRIM56
The innate immune system detects pathogen- and host-derived double-stranded DNA exposed to the cytosol and induces type I interferon (IFN) and other cytokines. TRIM56 overexpression enhanced IFN-β promoter activation after double-stranded DNA stimulation whereas TRIM56 knockdown abrogated it. TRIM56 interacted with STING and targeted it for lysine 63-linked ubiquitination. This modification induced STING dimerization, which was a prerequisite for recruitment of the antiviral kinase TBK1 and subsequent induction of IFN-β. Taken together, these results indicate that TRIM56 is an interferon-inducible E3 ubiquitin ligase that modulates STING to confer double-stranded DNA-mediated innate immune responses. The ubiquitin ligase TRIM56 regulates innate immune responses to intracellular double-stranded DNA.
Organism species: Homo sapiens (Human)
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Organism species: Mus musculus (Mouse)
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