Rex Emily A, Seo Dahee, Chappidi Sruthi, Pinkham Chelsea, Oliveira Sabrynna Brito, Embry Aaron, Heisler David, Liu Yang, Luger Karolin, Alto Neal M, da Fonseca Flávio Guimarães, Orchard Robert, Hancks Dustin, Gammon Don B
bioRxiv. 2023 Feb 8:2023.02.08.527673. doi: 10.1101/2023.02.08.527673.
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.
FACT复合物是一种古老的染色质重塑因子,由Spt16和SSRP1亚基组成,可调节特定的真核基因表达程序。然而,FACT是否调节宿主对感染的免疫反应尚不清楚。在此,我们确定了一条由FACT介导的抗病毒途径,该途径不同于干扰素反应,可限制痘病毒复制。我们发现早期病毒基因表达会触发FACT的特殊SUMO化Spt16亚基的核积累,而ETS-1的表达需要这些亚基,ETS-1是一种激活病毒限制程序的下游转录因子。然而,痘病毒编码的A51R蛋白通过在细胞质中与SSRP1竞争结合SUMO化Spt16并将SUMO化Spt16拴系到微管上,从而阻断ETS-1的表达。此外,我们表明A51R对FACT的拮抗作用增强了痘病毒在人细胞中的复制以及在小鼠中的病毒毒力。最后,我们证明FACT也能限制无关的RNA病毒,这表明FACT在抗病毒免疫中具有广泛作用。我们的研究揭示了FACT-ETS-1抗病毒反应(FEAR)途径对真核抗病毒免疫至关重要,并描述了一种独特的病毒免疫逃逸机制。