Structural mechanism of CRL4‐instructed STAT2 degradation via a novel cytomegaloviral DCAF receptor. (10th February 2023)

• Record Type: Journal Article
• Authors: Le‐Trilling, Vu Thuy Khanh; Banchenko, Sofia; Paydar, Darius; Leipe, Pia Madeleine; Binting, Lukas; Lauer, Simon; Graziadei, Andrea; Klingen, Robin; Gotthold, Christine; Bürger, Jörg; Bracht, Thilo; Sitek, Barbara; Jan Lebbink, Robert; Malyshkina, Anna; Mielke, Thorsten; Rappsilber, Juri; Spahn, Christian MT; Voigt, Sebastian; Trilling, Mirko; Schwefel, David
• Is Part Of: EMBO journal. Volume 42:Number 5(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2023-02-10
• Subjects: cullin‐RING ubiquitin ligases -- cytomegalovirus -- interferon -- ubiquitin–proteasome system -- viral DCAF; Molecular biology -- Periodicals; 572.805
• DOI: 10.15252/embj.2022112351
• Languages: English
• ISSNs: 0261-4189

Abstract

Abstract: Human cytomegalovirus (CMV) is a ubiquitously distributed pathogen whose rodent counterparts such as mouse and rat CMV serve as common infection models. Here, we conducted global proteome profiling of rat CMV‐infected cells and uncovered a pronounced loss of the transcription factor STAT2, which is crucial for antiviral interferon signalling. Via deletion mutagenesis, we found that the viral protein E27 is required for CMV‐induced STAT2 depletion. Cellular and in vitro analyses showed that E27 exploits host‐cell Cullin4‐RING ubiquitin ligase (CRL4) complexes to induce poly‐ubiquitylation and proteasomal degradation of STAT2. Cryo‐electron microscopy revealed how E27 mimics molecular surface properties of cellular CRL4 substrate receptors called DCAFs (DDB1‐ and Cullin4‐associated factors), thereby displacing them from the catalytic core of CRL4. Moreover, structural analyses showed that E27 recruits STAT2 through a bipartite binding interface, which partially overlaps with the IRF9 binding site. Structure‐based mutations in M27, the murine CMV homologue of E27, impair the interferon‐suppressing capacity and virus replication in mouse models, supporting the conserved importance of DCAF mimicry for CMV immune evasion. Synopsis: Viruses can hijack the cellular ubiquitin–proteasome system to induce the degradation of antiviral host factors. Here, a combination of proteomic, biochemical, structural and virological analyses explains how cytomegaloviruses hijack Cullin4‐RING ubiquitin ligases for the removal of STAT2, a key signalling hub of the antiviral interferon response. The rat cytomegalovirus‐encoded protein E27 induces proteasomal STAT2 degradation E27 binds and exploits DDB1‐containing Cullin4‐RING ubiquitin ligases (CRL4) by mimicking endogenous CRL4 substrate receptors, DCAFs Cryo‐EM shows that E27 recruits STAT2 via a bipartite interface, positioning STAT2 for CRL4‐catalysed ubiquitylation The homologous mouse cytomegalovirus factor M27 establishes interferon resistance in mouse models via CRL4‐mediated STAT2 degradation Abstract : Cytomegaloviruses exploit host ubiquitin ligases to induce ubiquitylation and proteasomal degradation of STAT2, a key signalling hub of the antiviral interferon response.