刺
生物
DNA
病毒学
先天免疫系统
干扰素基因刺激剂
免疫系统
DNA病毒
病毒
基因
细胞生物学
基因组
遗传学
生物化学
工程类
航空航天工程
作者
Laura Lau,Elizabeth Gray,Rebecca Brunette,Daniel B. Stetson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2015-09-25
卷期号:350 (6260): 568-571
被引量:399
标识
DOI:10.1126/science.aab3291
摘要
Cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS) detects intracellular DNA and signals through the adapter protein STING to initiate the antiviral response to DNA viruses. Whether DNA viruses can prevent activation of the cGAS-STING pathway remains largely unknown. Here, we identify the oncogenes of the DNA tumor viruses, including E7 from human papillomavirus (HPV) and E1A from adenovirus, as potent and specific inhibitors of the cGAS-STING pathway. We show that the LXCXE motif of these oncoproteins, which is essential for blockade of the retinoblastoma tumor suppressor, is also important for antagonizing DNA sensing. E1A and E7 bind to STING, and silencing of these oncogenes in human tumor cells restores the cGAS-STING pathway. Our findings reveal a host-virus conflict that may have shaped the evolution of viral oncogenes.
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