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Efficient virus-induced gene silencing in plants using a modified geminivirus DNA1 component

机译:使用改性的Geminivirus DNA1组分在植物中有效的病毒诱导基因沉默

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Virus-induced gene silencing (VIGS) is currently recognized as a powerful reverse genetics tool for application in functional genomics. DNA1, a satellite-like and single-stranded DNA molecule associated with begomoviruses (Family Geminiviridae), has been shown to replicate autonomously but requires the helper virus for its dissemination. We developed a VIGS vector based on the DNA1 component of tobacco curly shoot virus (TbCSV), a monopartite begomovirus, by inserting a multiple cloning site between the replication-associated protein open reading frame and the A-rich region for subsequent insertion of DNA fragments of genes targeted for silencing. When a host gene (sulphur, Su) or transgene (green fluorescent protein, GFP) was inserted into the modified DNA1 vector and co-agroinoculated with TbCSV, efficient silencing of the cognate gene was observed in Nicotiana benthamiana plants. More interestingly, we demonstrated that this modified DNA1 could effectively suppress GFP in transgenic N. benthamiana or endogenous Su in tobacco plants when co-agroinoculated with tomato yellow leaf curl China virus (TYLCCNV), another monopartite begomovirus that does not induce any viral symptoms. A gene-silencing system in Nicotiana spp., Solanum lycopersicum and Petunia hybrida plants was then established using TYLCCNV and the modified DNA1 vector. The system can be used to silence genes involved in meristem and flower development. The modified DNA1 vector was used to silence the AtTOM homologous genes (NbTOM1 and NbTOM3) in N. benthamiana. Silencing of NbTOM1 or NbTOM3 can reduce tobamovirus multiplication to a lower level, and silencing of both genes simultaneously can completely inhibit tobamovirus multiplication. Previous studies have reported that DNA1 is associated with both monopartite and bipartite begomoviruses, as well as curtoviruses. This vector system can therefore be applied for the study, analysis and discovery of gene function in a variety of important crop plants.
机译:病毒诱导的基因沉默(Vigs)目前被认为是在功能基因组学中施用的强大反向遗传工具。 DNA1,与前饲料缺血病毒(家庭精灵)相关的卫星和单链DNA分子(Geminiviridae),已被证明是自主重建的,但需要辅助病毒进行散发。我们通过在复制相关蛋白质开放阅读框架和富含A的富含区域之间插入多个克隆部位的烟草卷发病毒(TBCSV)的DNA1组分,基于烟草卷曲病毒(TBCSV)的DNA1组分开发了Vigs载体,以便在富含DNA片段中插入DNA碎片靶向沉默的基因。当将宿主基因(硫,Su)或转基因(绿色荧光蛋白,GFP)插入修饰的DNA1载体中并与TBCSV共同吞噬时,在尼古拉·南·南部植物中观察到同源基因的有效沉默。更有趣的是,当与番茄黄叶卷曲中国病毒(Tylccnv)共同农业植物,这种改性DNA1可以有效地抑制转基因N. Benthamiana或内源Su在烟草植物中的GFP。然后使用TylCCNV和改性DNA1载体建立了尼古拉斯纳SPP中的基因沉默系统。该系统可用于沉默于符合公司和花发育的沉默基因。修饰的DNA1载体用于沉默于N必需的抗体同源基因(NBTOM1和NBTOM3)。沉默NBTOM1或NBTOM3可以将烟草病毒倍增降低到较低水平,同时两种基因的沉默可以完全抑制麻黄血管倍增。以前的研究报告说,DNA1与单颗粒和二分血管病毒以及瘢痕病有关。因此,可以应用该载体系统在各种重要作物植物中的基因功能的研究,分析和发现。

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