bioRxiv (Cold Spring Harbor Laboratory) · 2020 · 68 citations · 51 references
Life SciencesInfectious DiseasesMolecular BiologyCell SignalingMolecular VirologySignal TransductionAntiviral ImmunityInnate Immune Signaling PathwaysInterferon ResponsesViral InfectionsViral PathogenesisViral PathologyAntiviral Innate SignalingAntiviral Signaling PathwaysHost Antiviral ResponseInterferon Response To Viral InfectionInterferon Signaling SuppressionSars-cov-2 InfectionViral Protein DegradationViral Protein Localization
of the viral genome contains a putative transmembrane domain, interacts with membrane proteins in multiple cellular compartments, and impairs antiviral processes in a lung epithelial cell line. Proteomic, interactome, and transcriptomic analyses, combined with bioinformatic analysis, revealed that expression of only this highly unstable small viral protein impaired interferon signaling, antigen presentation, and complement signaling, while inducing IL-6 signaling. Furthermore, we showed that interfering with ORF9c degradation by either proteasome inhibition or inhibition of the ATPase VCP blunted the effects of ORF9c. Our study indicated that ORF9c enables immune evasion and coordinates cellular changes essential for the SARS-CoV-2 life cycle. ONE-SENTENCE SUMMARY: SARS-CoV-2 ORF9c is the first human coronavirus protein localized to membrane, suppressing antiviral response, resembling full viral infection.
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STAR: ultrafast universal RNA-seq aligner
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Cutadapt removes adapter sequences from high-throughput sequencing reads
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