Shen Wan-Xia, Au Phil Chi Khang, Shi Bu-Jun, Smith Neil A, Dennis Elizabeth S, Guo Hui-Shan, Zhou Chang-Yong, Wang Ming-Bo
National Citrus Engineering Research Center, Citrus Research Institute, Southwest University Chongqing, China ; Commonwealth Scientific and Industrial Research Organisation Plant Industry Canberra, ACT, Australia.
Commonwealth Scientific and Industrial Research Organisation Plant Industry Canberra, ACT, Australia.
Front Plant Sci. 2015 Apr 24;6:281. doi: 10.3389/fpls.2015.00281. eCollection 2015.
Viral satellite RNAs (satRNAs) are small subviral RNAs and depend on the helper virus for replication and spread. satRNAs can attenuate helper virus-induced symptoms, the mechanism of which remains unclear. Here, we show that two virus-encoded suppressors of RNA silencing (VSRs), Cucumber mosaic virus (CMV) 2b and Tombusvirus P19, suppress hairpin RNA (hpRNA)-induced silencing of a β-glucuronidase (GUS) gene in Nicotiana benthamiana. This suppression can be overcome by CMV Y-satellite RNA (Y-Sat) via the Y-Sat-derived small interfering RNAs (siRNAs), which bind to the VSRs and displace the bound hpGUS-derived siRNAs. We also show that microRNA target gene expression in N. tabacum was elevated by CMV infection, presumably due to function of the 2b VSR, but this upregulation of microRNA target genes was reversed in the presence of Y-Sat. These results suggest that satRNA infection minimizes the effect of VSRs on host siRNA and microRNA-directed silencing. Our results suggest that the high abundance of satRNA-derived siRNAs contributes to symptom attenuation by binding helper virus-encoded VSRs, minimizing the capacity of the VSRs to bind host siRNA and miRNA and interfere with their function.
病毒卫星RNA(satRNAs)是小型亚病毒RNA,依赖辅助病毒进行复制和传播。satRNAs能够减轻辅助病毒诱导的症状,但其机制尚不清楚。在此,我们表明两种病毒编码的RNA沉默抑制因子(VSRs),即黄瓜花叶病毒(CMV)2b和番茄丛矮病毒P19,可抑制本氏烟草中发夹RNA(hpRNA)诱导的β-葡萄糖醛酸酶(GUS)基因沉默。CMV Y卫星RNA(Y-Sat)通过Y-Sat衍生的小干扰RNA(siRNAs)可克服这种抑制作用,这些siRNAs与VSRs结合并取代结合的hpGUS衍生的siRNAs。我们还表明,CMV感染可提高烟草中微小RNA靶基因的表达,这可能是由于2b VSR的作用,但在存在Y-Sat的情况下,微小RNA靶基因的这种上调被逆转。这些结果表明,satRNA感染可将VSRs对宿主siRNA和微小RNA介导的沉默的影响降至最低。我们的结果表明,高丰度的satRNA衍生的siRNAs通过结合辅助病毒编码的VSRs有助于减轻症状,使VSRs结合宿主siRNA和miRNA并干扰其功能的能力降至最低。