生物
病毒性表皮
先天免疫系统
DNA
细胞生物学
免疫系统
病毒学
遗传学
作者
Guangjun Xu,Chong Liu,Sheng Zhou,Quanjin Li,Yun Feng,Panpan Sun,Feng Han,Yina Gao,Jingpeng Zhu,Xiaohua Luo,Qi Zhan,Songqin Liu,Shu Zhu,Hongyu Deng,Dong Liu,Pu Gao
出处
期刊:Molecular Cell
[Elsevier]
日期:2021-07-01
卷期号:81 (13): 2823-2837.e9
被引量:59
标识
DOI:10.1016/j.molcel.2021.05.002
摘要
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.
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