生物
病毒复制
病毒学
染色质
细胞生物学
基因
遗传学
病毒
作者
Emily A. Rex,Dahee Seo,Sruthi Chappidi,Chelsea Pinkham,Sabrynna Brito Oliveira,Aaron Embry,David B. Heisler,Yang Liu,Karolin Luger,Neal M. Alto,Flávio Guimarães da Fonseca,Robert C. Orchard,Dustin C. Hancks,Don B. Gammon
标识
DOI:10.1101/2023.02.08.527673
摘要
The FACT complex is an ancient chromatin remodeling factor comprised of Spt16 and SSRP1 subunits that regulates specific eukaryotic gene expression programs. However, whether FACT regulates host immune responses to infection was unclear. Here, we identify an antiviral pathway mediated by FACT, distinct from the interferon response, that restricts poxvirus replication. We show that early viral gene expression triggers nuclear accumulation of specialized, SUMOylated Spt16 subunits of FACT required for expression of ETS-1, a downstream transcription factor that activates a virus restriction program. However, poxvirus-encoded A51R proteins block ETS-1 expression by outcompeting SSRP1 for binding to SUMOylated Spt16 in the cytosol and by tethering SUMOylated Spt16 to microtubules. Moreover, we show that A51R antagonism of FACT enhances both poxvirus replication in human cells and viral virulence in mice. Finally, we demonstrate that FACT also restricts unrelated RNA viruses, suggesting a broad role for FACT in antiviral immunity. Our study reveals the F ACT- E TS-1 A ntiviral R esponse (FEAR) pathway to be critical for eukaryotic antiviral immunity and describes a unique mechanism of viral immune evasion.
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