Molecular Virology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
School of Biological Sciences, University of East Anglia, Norwich, UK.
Planta. 2020 Jul 1;252(1):11. doi: 10.1007/s00425-020-03417-y.
RNA-dependent RNA polymerase 1 of Nicotiana tabacum modulates ToLCGV pathogenesis by influencing a number of defence-related genes in N. benthamiana plants. Key means of plants protecting themselves from the invading viruses is through RNA silencing. RNA-dependent RNA polymerase-1 (RDR1) is one of the crucial proteins of the RNA silencing pathway, which is induced after infection by viruses. RDR1 functions in the generation of small interfering RNAs (siRNAs) against the viral genome, thus it is antiviral in nature. Here, we used the transgenic Nicotiana benthamiana plant expressing N. tabacum NtRDR1 and observed reduced susceptibility towards Tomato leaf curl Gujarat virus (ToLCGV) infection compared to the wild-type N. benthamiana plants. To understand the reason for such reduced susceptibility, we prepared high-definition small RNA (sRNA) cDNA libraries from ToLCGV-infected wild-type N. benthamiana and NtRDR1 expressing N. benthamiana lines and carried out next-generation sequencing (NGS). We found that upon ToLCGV infection the majority of siRNAs generated from the host genome were of the 24 nucleotide (nt) class, while viral siRNAs (vsiRNAs) were of the 21-22-nt class, indicating that transcriptional gene silencing (TGS) is the major pathway for silencing of host genes while viral genes are silenced, predominantly, by post transcriptional gene silencing (PTGS) pathways. We estimated the changes in the expression of various defence-related genes, such as Constitutively Photomorphogenic-9 (COP9) signalosome (CSN) complex subunit-7, Pentatricopeptide repeat containing protein (PPRP), Laccase-3, Glutathione peroxidase-1 (GPX-1), Universal stress protein (USP) A-like protein, Heat shock transcription factor B4 (HSTF-B4), Auxin response factor-18 (ARF18), WRKY-6 and Short chain dehydrogenase reductase-3a. The differential expression of these genes might be linked with the enhanced tolerance of NtRDR1 N. benthamiana transgenic plants to ToLCGV. Our study suggests that reduced expression of subunit-7 of CSN complex and WRKY6, and increased expression of USPA-like protein might be linked with the reduced susceptibility of NtRDR1-transgenic N. benthamiana plants to ToLCGV.
烟草依赖 RNA 聚合酶 1 通过影响烟草原生质体中许多与防御相关的基因来调节 ToLCGV 发病。植物保护自身免受入侵病毒侵害的主要手段是通过 RNA 沉默。RNA 依赖的 RNA 聚合酶-1(RDR1)是 RNA 沉默途径的关键蛋白之一,该蛋白在病毒感染后被诱导。RDR1 的功能是针对病毒基因组产生小干扰 RNA(siRNA),因此它在本质上是抗病毒的。在这里,我们使用表达烟草 NtRDR1 的转基因烟草原生质体,并观察到与野生型烟草原生质体相比,对番茄卷叶古尔冈病毒(ToLCGV)感染的敏感性降低。为了了解这种敏感性降低的原因,我们从 ToLCGV 感染的野生型烟草原生质体和表达 NtRDR1 的烟草原生质体系中制备了高清小 RNA(sRNA)cDNA 文库,并进行了下一代测序(NGS)。我们发现,在 ToLCGV 感染后,宿主基因组产生的大多数 siRNAs 为 24 个核苷酸(nt)类,而病毒 siRNAs(vsiRNAs)为 21-22-nt 类,表明转录基因沉默(TGS)是沉默宿主基因的主要途径,而病毒基因主要通过转录后基因沉默(PTGS)途径沉默。我们估计了各种防御相关基因表达的变化,如组成型光形态发生 9(COP9)信号体(CSN)复合物亚基-7、五肽重复蛋白(PPRP)、漆酶-3、谷胱甘肽过氧化物酶-1(GPX-1)、通用应激蛋白(USP)A 样蛋白、热休克转录因子 B4(HSTF-B4)、生长素响应因子-18(ARF18)、WRKY-6 和短链脱氢酶还原酶-3a。这些基因的差异表达可能与 NtRDR1 烟草原生质体转基因植物对 ToLCGV 的增强耐受性有关。我们的研究表明,CSN 复合物亚基-7 和 WRKY6 的表达降低,以及 USPA 样蛋白的表达增加可能与 NtRDR1 转基因烟草原生质体对 ToLCGV 的敏感性降低有关。