CAS Key Laboratory of Infection and Immunity, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Mol Cell. 2021 Jul 1;81(13):2823-2837.e9. doi: 10.1016/j.molcel.2021.05.002. Epub 2021 May 19.
DNA-induced liquid-liquid phase separation of cyclic GMP-AMP synthase (cGAS) triggers a potent response to detect pathogen infection and promote innate immune signaling. Whether and how pathogens manipulate cGAS-DNA condensation to mediate immune evasion is unknown. We report the identification of a structurally related viral tegument protein family, represented by ORF52 and VP22 from gamma- and alpha-herpesvirinae, respectively, that employs a conserved mechanism to restrict cGAS-DNA phase separation. ORF52/VP22 proteins accumulate into, and effectively disrupt, the pre-formed cGAS-DNA condensation both in vitro and in cells. The inhibition process is dependent on DNA-induced liquid-liquid phase separation of the viral protein rather than a direct interaction with cGAS. Moreover, highly abundant ORF52 proteins carried within viral particles are able to target cGAS-DNA phase separation in early infection stage. Our results define ORF52/VP22-type tegument proteins as a family of inhibitors targeting cGAS-DNA phase separation and demonstrate a mechanism for how viruses overcome innate immunity.
DNA 诱导的环鸟苷酸-腺苷酸合酶 (cGAS) 液-液相分离触发了一种强大的反应,以检测病原体感染并促进先天免疫信号转导。目前还不清楚病原体是否以及如何操纵 cGAS-DNA 凝聚来介导免疫逃避。我们报告了一种结构相关的病毒被膜蛋白家族的鉴定,该家族由γ和α疱疹病毒亚科的 ORF52 和 VP22 代表,分别采用保守机制来限制 cGAS-DNA 相分离。ORF52/VP22 蛋白在体外和细胞内积累并有效地破坏预先形成的 cGAS-DNA 凝聚。该抑制过程依赖于病毒蛋白的 DNA 诱导液-液相分离,而不是与 cGAS 的直接相互作用。此外,病毒颗粒内大量存在的 ORF52 蛋白能够在早期感染阶段靶向 cGAS-DNA 相分离。我们的结果将 ORF52/VP22 型被膜蛋白定义为一类靶向 cGAS-DNA 相分离的抑制剂,并展示了病毒克服先天免疫的一种机制。