MOE Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua-Peking Joint Center for Life Sciences, Center for Plant Biology, Tsinghua University, Beijing, China.
MOE Key Laboratory of Bioinformatics and the Center of Biomedical Analysis, School of Life Sciences, Tsinghua University, Beijing, China.
J Virol. 2019 Mar 5;93(6). doi: 10.1128/JVI.01675-18. Print 2019 Mar 15.
In plants, RNA-directed DNA methylation (RdDM)-mediated transcriptional gene silencing (TGS) is a natural antiviral defense against geminiviruses. Several geminiviral proteins have been shown to target the enzymes related to the methyl cycle or histone modification; however, it remains largely unknown whether and by which mechanism geminiviruses directly inhibit RdDM-mediated TGS. In this study, we showed that (CLCuMuV) V2 directly interacts with AGO4 (NbAGO4) and that the L76S mutation in V2 (V2) abolishes such interaction. We further showed that V2, but not V2, can suppresses RdDM and TGS. Silencing of inhibits TGS, reduces the viral methylation level, and enhances CLCuMuV DNA accumulation. In contrast, the V2 substitution mutant attenuates CLCuMuV infection and enhances the viral methylation level. These findings reveal that CLCuMuV V2 contributes to viral infection by interaction with NbAGO4 to suppress RdDM-mediated TGS in plants. In plants, the RNA-directed DNA methylation (RdDM) pathway is a natural antiviral defense mechanism against geminiviruses. However, how geminiviruses counter RdDM-mediated defense is largely unknown. Our findings reveal that V2 contributes to viral infection by interaction with NbAGO4 to suppress RNA-directed DNA methylation-mediated transcriptional gene silencing in plants. Our work provides the first evidence that a geminiviral protein is able to directly target core RdDM components to counter RdDM-mediated TGS antiviral defense in plants, which extends our current understanding of viral counters to host antiviral defense.
在植物中,RNA 指导的 DNA 甲基化 (RdDM) 介导的转录基因沉默 (TGS) 是一种天然的抗病毒防御机制,可抵御双生病毒。已经发现几种双生病毒蛋白靶向与甲基化循环或组蛋白修饰相关的酶;然而,双生病毒是否以及通过何种机制直接抑制 RdDM 介导的 TGS 仍然很大程度上未知。在这项研究中,我们表明 (CLCuMuV) V2 直接与 AGO4 (NbAGO4) 相互作用,并且 V2 中的 L76S 突变 (V2) 会破坏这种相互作用。我们进一步表明,V2 而不是 V2 可以抑制 RdDM 和 TGS。沉默 抑制 TGS,降低病毒甲基化水平,并增强 CLCuMuV DNA 积累。相比之下,V2 取代突变体削弱了 CLCuMuV 感染并增强了病毒甲基化水平。这些发现表明,CLCuMuV V2 通过与 NbAGO4 相互作用来抑制植物中 RdDM 介导的 TGS,从而有助于病毒感染。在植物中,RNA 指导的 DNA 甲基化 (RdDM) 途径是一种天然的抗病毒防御机制,可抵御双生病毒。然而,双生病毒如何对抗 RdDM 介导的防御在很大程度上是未知的。我们的研究结果表明,V2 通过与 NbAGO4 相互作用来抑制植物中的 RNA 指导的 DNA 甲基化介导的转录基因沉默,从而有助于病毒感染。我们的工作首次提供了证据表明,一种双生病毒蛋白能够直接靶向核心 RdDM 成分来对抗植物中 RdDM 介导的 TGS 抗病毒防御,这扩展了我们对病毒对抗宿主抗病毒防御的现有理解。