| First Author | Yu Z | Year | 2022 |
| Journal | Commun Biol | Volume | 5 |
| Issue | 1 | Pages | 943 |
| PubMed ID | 36085336 | Mgi Jnum | J:329012 |
| Mgi Id | MGI:7339606 | Doi | 10.1038/s42003-022-03911-x |
| Citation | Yu Z, et al. (2022) TOB1 attenuates IRF3-directed antiviral responses by recruiting HDAC8 to specifically suppress IFN-beta expression. Commun Biol 5(1):943 |
| abstractText | Interferon regulatory factor 3 (IRF3) is a key transcription factor required for the secretion of type I interferons (IFN-alpha/beta) and initiation of antiviral immune response. However, the negative feedback regulator of IRF3-directed antiviral response remains unknown. In this study, we demonstrated that viral infection induced the interaction of the transducer of ERBB2.1 (TOB1) with IRF3, which bound to the promoter region of Ifnb1 in macrophages. TOB1 inhibited Ifnb1 transcription by disrupting IRF3 binding and recruiting histone deacetylase 8 (HDAC8) to the Ifnb1 promoter region. Consequently, TOB1 attenuated IRF3-directed IFN-beta expression in virus-infected macrophages. Tob1 deficiency enhanced antiviral response and suppressed viral replication in vivo. Thus, we identified TOB1 as a feedback inhibitor of host antiviral innate immune response and revealed a mechanism underlying viral immune escape. |
