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dc.contributor.authorHarwardt, Thomas
dc.contributor.authorLukas, Simone
dc.contributor.authorZenger, Marion
dc.contributor.authorReitberger, Tobias
dc.contributor.authorDanzer, Daniela
dc.contributor.authorÜbner, Theresa
dc.contributor.authorMunday, Diane C.
dc.contributor.authorNevels, Michael
dc.contributor.authorPaulus, Christina
dc.date.accessioned2016-07-13T09:30:10Z
dc.date.available2016-07-13T09:30:10Z
dc.date.issued2016-07-07
dc.identifier.citationHarwardt , T , Lukas , S , Zenger , M , Reitberger , T , Danzer , D , Übner , T , Munday , D C , Nevels , M & Paulus , C 2016 , ' Human cytomegalovirus immediate-early 1 protein rewires upstream STAT3 to downstream STAT1 signaling switching an IL6-type to an IFNγ-like response ' , PLoS Pathogens , vol. 12 , no. 7 , e1005748 . https://doi.org/10.1371/journal.ppat.1005748en
dc.identifier.issn1553-7366
dc.identifier.otherPURE: 244283704
dc.identifier.otherPURE UUID: 238d8cc0-e43e-4d66-a831-b3fc94616f91
dc.identifier.otherRIS: urn:E0DA536A1E28E624048E73BD75E9332B
dc.identifier.otherScopus: 84982975819
dc.identifier.otherORCID: /0000-0002-7115-407X/work/28624005
dc.identifier.otherORCID: /0000-0002-4123-5629/work/47136629
dc.identifier.otherWOS: 000383366400032
dc.identifier.urihttp://hdl.handle.net/10023/9124
dc.descriptionMN and CP were supported by the Wellcome Trust (www.wellcome.ac.uk) Institutional Strategic Support Fund and CP was supported by the Deutsche Forschungsgemeinschaft (PA 815/2-1; www.dfg.de).en
dc.description.abstractThe human cytomegalovirus (hCMV) major immediate-early 1 protein (IE1) is best known for activating transcription to facilitate viral replication. Here we present transcriptome data indicating that IE1 is as significant a repressor as it is an activator of host gene expression. Human cells induced to express IE1 exhibit global repression of IL6- and oncostatin M-responsive STAT3 target genes. This repression is followed by STAT1 phosphorylation and activation of STAT1 target genes normally induced by IFNγ. The observed repression and subsequent activation are both mediated through the same region (amino acids 410 to 445) in the C-terminal domain of IE1, and this region serves as a binding site for STAT3. Depletion of STAT3 phenocopies the STAT1-dependent IFNγ-like response to IE1. In contrast, depletion of the IL6 receptor (IL6ST) or the STAT kinase JAK1 prevents this response. Accordingly, treatment with IL6 leads to prolonged STAT1 instead of STAT3 activation in wild-type IE1 expressing cells, but not in cells expressing a mutant protein (IE1dl410-420) deficient for STAT3 binding. A very similar STAT1-directed response to IL6 is also present in cells infected with a wild-type or revertant hCMV, but not an IE1dl410-420 mutant virus, and this response results in restricted viral replication. We conclude that IE1 is sufficient and necessary to rewire upstream IL6-type to downstream IFNγ-like signaling, two pathways linked to opposing actions, resulting in repressed STAT3- and activated STAT1-responsive genes. These findings relate transcriptional repressor and activator functions of IE1 and suggest unexpected outcomes relevant to viral pathogenesis in response to cytokines or growth factors that signal through the IL6ST-JAK1-STAT3 axis in hCMV-infected cells. Our results also reveal that IE1, a protein considered to be a key activator of the hCMV productive cycle, has an unanticipated role in tempering viral replication.
dc.format.extent39
dc.language.isoeng
dc.relation.ispartofPLoS Pathogensen
dc.rights© 2016 Harwardt et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectQR Microbiologyen
dc.subjectBDCen
dc.subject.lccQRen
dc.titleHuman cytomegalovirus immediate-early 1 protein rewires upstream STAT3 to downstream STAT1 signaling switching an IL6-type to an IFNγ-like responseen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Biologyen
dc.contributor.institutionUniversity of St Andrews.Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1371/journal.ppat.1005748
dc.description.statusPeer revieweden


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