Yu Ru, Chen Caixia, Cao Weilin, Liu Hongmei, Zhou Shumei, Song Yunzhi, Zhu Changxiang
State Key Laboratory of Crop Biology, Shandong Key Laboratory of Crop Biology, Shandong Agricultural University, Tai'an, 271018, Shandong, People's Republic of China.
Arch Virol. 2018 Nov;163(11):3073-3081. doi: 10.1007/s00705-018-3969-5. Epub 2018 Aug 10.
In plants, viral replication can be inhibited through gene silencing, which is mediated by short interfering RNA (siRNA) or microRNA (miRNA). However, under natural conditions, viruses are extremely susceptible to mutations that may decrease the efficiency of cleavage of these small RNAs (sRNAs). Therefore, a single sRNA may not provide a sufficient degree of viral resistance to transgenic plants. Potato virus Y necrotic strain (PVY) and Potato virus Y common strain (PVY) are the two major PVY strains that cause systemic necrosis and mottling, respectively, in tobacco. In this study, we designed specific siRNAs and miRNAs to target two regions of the PVY replicase gene (NIb). Eight plant expression vectors containing one or two sRNAs were constructed. Luciferase activity assays showed that the designed sRNAs successfully cleaved the NIb gene of PVY and PVY, and the vector carrying a combined siRNA- and miRNA-based short hairpin RNA (shRNA) demonstrated the strongest inhibitory effect. These effects were confirmed through the acquisition of PVY and PVY resistance in transgenic sRNA-expressing Nicotiana tabacum plants. This phenomenon could be related to a plant defense mechanism in which siRNA and miRNA pathways are complementary and interact to achieve gene silencing. Furthermore, there is a tendency for the homologous small RNA sequences (PVY) to be more effective in conferring resistance than those with imperfect homology (PVY). Overall, these findings confirm that the use of a combined siRNA- and miRNA-based shRNAs is a promising approach for introducing viral resistance to plants through genetic engineering.
在植物中,病毒复制可通过基因沉默被抑制,基因沉默由小分子干扰RNA(siRNA)或微小RNA(miRNA)介导。然而,在自然条件下,病毒极易发生突变,这可能会降低这些小RNA(sRNA)的切割效率。因此,单一的sRNA可能无法为转基因植物提供足够程度的病毒抗性。马铃薯Y病毒坏死株(PVY)和马铃薯Y病毒普通株(PVY)是分别导致烟草系统性坏死和斑驳的两种主要PVY株系。在本研究中,我们设计了特异性siRNA和miRNA来靶向PVY复制酶基因(NIb)的两个区域。构建了八个含有一个或两个sRNA的植物表达载体。荧光素酶活性测定表明,设计的sRNA成功切割了PVY和PVY的NIb基因,携带基于siRNA和miRNA的组合短发夹RNA(shRNA)的载体表现出最强的抑制作用。通过在表达sRNA的转基因烟草植株中获得对PVY和PVY 的抗性,证实了这些效果。这种现象可能与一种植物防御机制有关,在该机制中,siRNA和miRNA途径相互补充并相互作用以实现基因沉默。此外,同源小RNA序列(PVY)比具有不完全同源性的序列(PVY)在赋予抗性方面更有效。总体而言,这些发现证实,使用基于siRNA和miRNA的组合shRNA是一种通过基因工程赋予植物病毒抗性的有前景的方法。