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One pathway is triggered by the inositol-requiring enzyme 1 (IRE1), which splices the X-box binding protein 1 (Xbp1) mRNA, thereby enabling expression of XBP1s. Another UPR pathway activates the activating transcription factor 6 (ATF6). Here we show that murine cytomegalovirus (MCMV), a prototypic \u03b2-herpesvirus, harnesses the UPR to regulate its own life cycle. MCMV activates the IRE1-XBP1 pathway early post infection to relieve repression by XBP1u, the product of the unspliced Xbp1 mRNA. XBP1u inhibits viral gene expression and replication by blocking the activation of the viral major immediate-early promoter by XBP1s and ATF6. These findings reveal a redundant function of XBP1s and ATF6 as activators of the viral life cycle, and an unexpected role of XBP1u as a potent repressor of both XBP1s and ATF6-mediated activation.<\/jats:p>","DOI":"10.7554\/elife.51804","type":"journal-article","created":{"date-parts":[[2020,2,17]],"date-time":"2020-02-17T08:00:22Z","timestamp":1581926422000},"source":"Crossref","is-referenced-by-count":33,"title":["Repression of viral gene expression and replication by the unfolded protein response effector XBP1u"],"prefix":"10.7554","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0820-7041","authenticated-orcid":true,"given":"Florian","family":"Hinte","sequence":"first","affiliation":[{"name":"Heinrich Pette Institute, Leibniz Institute for Experimental Virology, Hamburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9529-2701","authenticated-orcid":true,"given":"Eelco","family":"van 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