Department of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
Science. 2015 Oct 30;350(6260):568-71. doi: 10.1126/science.aab3291. Epub 2015 Sep 24.
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.
环鸟苷酸-腺苷酸合酶 (cGAS) 检测细胞内 DNA 并通过衔接蛋白 STING 发出信号,从而启动针对 DNA 病毒的抗病毒反应。然而,DNA 病毒是否可以阻止 cGAS-STING 途径的激活在很大程度上仍是未知的。在这里,我们鉴定了 DNA 肿瘤病毒的致癌基因,包括人乳头瘤病毒 (HPV) 的 E7 和腺病毒的 E1A,它们是 cGAS-STING 途径的有效且特异性抑制剂。我们表明,这些致癌蛋白的 LXCXE 基序对于阻断视网膜母细胞瘤肿瘤抑制因子是必不可少的,对于拮抗 DNA 感应也很重要。E1A 和 E7 与 STING 结合,沉默这些致癌基因可恢复 cGAS-STING 途径。我们的研究结果揭示了一种宿主-病毒冲突,这可能塑造了病毒致癌基因的进化。