The Cytomegalovirus M35 Protein Modulates Transcription of Ifnb1 and Other IRF3-Driven Genes by Direct Promoter Binding

Schwanke, H.; Goncalves Magalhaes, V.; Schmelz, S.; Wyler, E.; Hennig, T.; Guenther, T.; Grundhoff, A.; Doelken, L.; Landthaler, M.; van Ham, M.; Jaensch, L.; Buessow, K.; van den Heuvel, J.; Blankenfeldt, W.; Friedel, C. C.; Erhard, F.; Brinkmann, M. M.

doi:10.1101/2023.03.21.533612

bioRxiv · 10.1101/2023.03.21.533612

The Cytomegalovirus M35 Protein Modulates Transcription of Ifnb1 and Other IRF3-Driven Genes by Direct Promoter Binding

Schwanke, H.·Goncalves Magalhaes, V.·Schmelz, S.·Wyler, E.·Hennig, T.·Guenther, T.·Grundhoff, A.·Doelken, L.·Landthaler, M.·van Ham, M.·Jaensch, L.·Buessow, K.·van den Heuvel, J.·Blankenfeldt, W.·Friedel, C. C.·Erhard, F.·Brinkmann, M. M.

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Abstract

Induction of type I interferon (IFN) gene expression is among the first lines of cellular defence a virus encounters during primary infection. We previously identified the tegument protein M35 of murine cytomegalovirus (MCMV) as an essential antagonist of this antiviral system. M35 localizes to the nucleus and interferes with type I IFN induction downstream of pattern-recognition receptor (PRR) activation. Here, we report structural and mechanistic details of M35s function. Using electrophoretic mobility shift assays (EMSA), we demonstrate that purified M35 protein specifically binds to the regulatory DNA element that governs transcription of the first type I IFN gene induced in non-immune cells, Ifnb1. Determination of M35s crystal structure combined with reverse genetics revealed that homodimerisation is a key feature for M35s immunomodulatory activity. DNA-binding sites of M35 overlapped with the recognition elements of interferon regulatory factor 3 (IRF3), a key transcription factor activated by PRR signalling. Chromatin immunoprecipitation (ChIP) showed reduced binding of IRF3 to the host Ifnb1 promoter in the presence of M35. We furthermore defined the IRF3-dependent and the type I IFN signalling-responsive genes in murine fibroblasts by RNA sequencing of metabolically labelled transcripts (SLAM-seq), and assessed M35s global effect on gene expression. Stable expression of M35 broadly influenced the transcriptome in untreated cells and specifically down-regulated basal expression of IRF3-dependent genes, and during MCMV infection, M35 impaired expression of IRF3-responsive genes aside of Ifnb1. Our results suggest that M35-DNA binding directly antagonises gene induction by IRF3 and impairs the antiviral response more broadly than formerly recognised. ImportanceReplication of the ubiquitous human cytomegalovirus (CMV) in healthy individuals mostly goes unnoticed, but can impair foetal development or cause life-threatening symptoms in immunosuppressed or -deficient patients. Like other herpesviruses, CMV extensively manipulates its hosts and establishes lifelong latent infections. Murine CMV (MCMV) presents an important model system as it allows the study of CMV infection in the host organism. We previously showed that during entry, MCMV virions release the evolutionary conserved protein M35 protein to immediately dampen the antiviral type I interferon (IFN) response induced by pathogen detection. Here we show that M35 dimers bind to regulatory DNA elements and interfere with recruitment of interferon regulatory factor 3 (IRF3), a key factor for antiviral gene expression. Thereby, M35 interferes with expression of type I IFNs and other IRF3-dependent genes. Unrelated proteins from other herpesviruses employ the same mechanism, reflecting the importance for herpesviruses to avoid IRF3-mediated gene induction.

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Schwanke, H., Goncalves Magalhaes, V., Schmelz, S., Wyler, E., Hennig, T., Guenther, T., Grundhoff, A., Doelken, L., Landthaler, M., van Ham, M., Jaensch, L., Buessow, K., van den Heuvel, J., Blankenfeldt, W., Friedel, C. C., Erhard, F., Brinkmann, M. M.. 2023-03-21. The Cytomegalovirus M35 Protein Modulates Transcription of Ifnb1 and Other IRF3-Driven Genes by Direct Promoter Binding. https://doi.org/10.1101/2023.03.21.533612

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