Lu Rui, Folimonov Alexey, Shintaku Michael, Li Wan-Xiang, Falk Bryce W, Dawson William O, Ding Shou-Wei
Center for Plant Cell Biology, Institute for Integrative Genome Biology, and Department of Plant Pathology, University of California, Riverside, CA 92521, USA.
Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15742-7. doi: 10.1073/pnas.0404940101. Epub 2004 Oct 25.
Viral infection in both plant and invertebrate hosts requires a virus-encoded function to block the RNA silencing antiviral defense. Here, we report the identification and characterization of three distinct suppressors of RNA silencing encoded by the approximately 20-kb plus-strand RNA genome of citrus tristeza virus (CTV). When introduced by genetic crosses into plants carrying a silencing transgene, both p20 and p23, but not coat protein (CP), restored expression of the transgene. Although none of the CTV proteins prevented DNA methylation of the transgene, export of the silencing signal (capable of mediating intercellular silencing spread) was detected only from the F(1) plants expressing p23 and not from the CP- or p20-expressing F(1) plants, demonstrating suppression of intercellular silencing by CP and p20 but not by p23. Thus, intracellular and intercellular silencing are each targeted by a CTV protein, whereas the third, p20, inhibits silencing at both levels. Notably, CP suppresses intercellular silencing without interfering with intracellular silencing. The novel property of CP suggests a mechanism distinct to p20 and all of the other viral suppressors known to interfere with intercellular silencing and that this class of viral suppressors may not be consistently identified by Agrobacterium coinfiltration because it also induces RNA silencing against the infiltrated suppressor transgene. Our analyses reveal a sophisticated viral counter-defense strategy that targets the silencing antiviral pathway at multiple steps and may be essential for protecting CTV with such a large RNA genome from antiviral silencing in the perennial tree host.
病毒感染植物和无脊椎动物宿主都需要病毒编码的功能来阻断RNA沉默抗病毒防御。在此,我们报告了对柑橘衰退病毒(CTV)约20 kb正链RNA基因组编码的三种不同RNA沉默抑制子的鉴定和表征。当通过遗传杂交引入携带沉默转基因的植物中时,p20和p23能恢复转基因的表达,但外壳蛋白(CP)不能。尽管CTV的任何一种蛋白都不能阻止转基因的DNA甲基化,但仅在表达p23的F1植物中检测到沉默信号(能够介导细胞间沉默传播)的输出,而在表达CP或p20的F1植物中未检测到,这表明CP和p20抑制细胞间沉默,而p23不抑制。因此,细胞内和细胞间沉默分别由一种CTV蛋白靶向,而第三种蛋白p20在两个水平上均抑制沉默。值得注意的是,CP抑制细胞间沉默而不干扰细胞内沉默。CP的这种新特性表明其机制不同于p20以及所有已知干扰细胞间沉默的其他病毒抑制子,并且这类病毒抑制子可能无法通过农杆菌共浸润一致地鉴定出来,因为它也会诱导针对浸润的抑制子转基因的RNA沉默。我们的分析揭示了一种复杂的病毒反防御策略,该策略在多个步骤靶向沉默抗病毒途径,对于保护具有如此大RNA基因组的CTV在多年生树木宿主中免受抗病毒沉默可能至关重要。