| Literature DB >> 30988430 |
Tingting Guo1,2, Yibo Zuo1,2, Liping Qian1,2, Jin Liu1,2, Yukang Yuan1,2, Kailin Xu1, Ying Miao1,2, Qian Feng1,2, Xiangjie Chen1,2, Lincong Jin1,2, Liting Zhang1,2, Chunsheng Dong3, Sidong Xiong4,5, Hui Zheng6,7.
Abstract
Outbreaks of viral infections are a global health burden. Although type I interferon (IFN-I) exerts broad-spectrum antiviral effects, its antiviral efficacy in host cells is largely restricted by viruses. How the antiviral efficacy of IFN-I can be improved remains to be explored. Here, we identified the ADP-ribosyltransferase poly(ADP-ribose) polymerase family member 11 (PARP11) as a potent regulator of IFN-I antiviral efficacy. PARP11 does not restrict IFN-I production induced by vesicular stomatitis virus or Sendai virus but inhibits the strength of IFN-I-activated signalling. Mechanistically, PARP11 mono-ADP-ribosylates the ubiquitin E3 ligase β-transducin repeat-containing protein (β-TrCP). Mono-ADP-ribosylation of β-TrCP promotes IFNα/β receptor subunit 1 (IFNAR1) ubiquitination and degradation. Moreover, PARP11 expression is upregulated by virus infections, including vesicular stomatitis virus, herpes simplex virus-1 and influenza A virus, thus promoting ADP-ribosylation-mediated viral evasion. We further highlight the potential for repurposing clinical ADP-ribosylation inhibitors. We found that rucaparib can target PARP11 to stabilize IFNAR1 and therefore exhibits efficient enhancement of IFN-I signalling and the host antiviral response. Consequently, rucaparib renders mice more resistant to viral infection. Our study updates the understanding of how β-TrCP regulates its substrates and may provide a druggable target for improving IFN antiviral efficacy.Entities:
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Year: 2019 PMID: 30988430 DOI: 10.1038/s41564-019-0428-3
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745