College of Horticulture and Plant Protection, Inner Mongolia Agricultural University, Hohhot, China.
College of Plant Protection, Northwest A&F University, Yangling, China.
Plant Signal Behav. 2024 Dec 31;19(1):2358270. doi: 10.1080/15592324.2024.2358270. Epub 2024 May 26.
Trans-acting small interfering RNAs (tasiRNAs) are 21-nt phased (phased siRNAs) resulting from successive DCL-catalyzed processing from the end of a double-stranded RNA substrate originating from the RDR of an AGO-catalyzed cleaved RNA at a micro RNA target site. Plant tasiRNAs have been synthesized to produce synthetic tasiRNAs (syn-tasiRNAs) targeting viral RNAs that confer viral resistance. In this study, we engineered syn-tasiRNAs to target potato virus Y (PVY) infection by replacing five native siRNAs of TAS1c with 210-bp fragments from the coat protein (CP) region of the PVY genome. The results showed that the transient expression of syn-tasiR-CPpvy2 in Nicotiana benthamiana (N. benthamiana) plants conferred antiviral resistance, supported by the absence of PVY infection symptoms and viral accumulation. This indicated that syn-tasiR-CPpvy2 successfully targeted and silenced the PVY CP gene, effectively inhibiting viral infection. syn-tasiR-CPpvy1 displayed attenuated symptoms and decreased viral accumulation in these plants However, severe symptoms of PVY infection and a similar amount of viral accumulation as the control were observed in plants expressing syn-tasiR-CPpvy3. syn-tasiR-CPpvy/pvx, which targets both PVY and potato virus X (PVX), was engineered using a single precursor. After the transient expression of syn-tasiR-CPpvy/pvx3 and syn-tasiR-CPpvy/pvx5 in N. benthamiana, the plants were resistant to both PVY and PVX. These results suggested that engineered syn-tasiRNAs could not only specifically induce antiviral resistance against one target virus but could also be designed for multi-targeted silencing of different viruses, thereby preventing complex virus infection in plants.
反式作用小干扰 RNA(tasiRNA)是 21nt 相(相 siRNA),由双链 RNA 底物的末端经 DCL 催化加工而成,该双链 RNA 底物源自 AGO 催化切割的 RNA 的 RDR,切割位点位于 micro RNA 靶位。植物 tasiRNA 已被合成以产生针对病毒 RNA 的合成 tasiRNA(syn-tasiRNA),从而赋予病毒抗性。在这项研究中,我们通过用来自 PVY 基因组外壳蛋白(CP)区的 210bp 片段替换 TAS1c 的五个天然 siRNA,来设计靶向 PVY 感染的 syn-tasiRNA。结果表明,在 Nicotiana benthamiana(N. benthamiana)植物中瞬时表达 syn-tasiR-CPpvy2 可赋予抗病毒抗性,这一结果得到了 PVY 感染症状和病毒积累缺失的支持。这表明 syn-tasiR-CPpvy2 成功靶向并沉默了 PVY CP 基因,有效抑制了病毒感染。然而,在表达 syn-tasiR-CPpvy1 的植物中观察到症状减弱和病毒积累减少,但与对照相比,PVY 感染的严重症状和类似量的病毒积累。针对 PVY 和马铃薯病毒 X(PVX)的 syn-tasiR-CPpvy/pvx 是使用单个前体工程设计的。在 N. benthamiana 中瞬时表达 syn-tasiR-CPpvy/pvx3 和 syn-tasiR-CPpvy/pvx5 后,植物对 PVY 和 PVX 均具有抗性。这些结果表明,工程化的 syn-tasiRNA 不仅可以特异性诱导针对一种靶标病毒的抗病毒抗性,还可以设计用于不同病毒的多靶向沉默,从而防止植物中复杂病毒的感染。