Wang Zhengming, Wang Xiao Yu, Martinho Claudia, Baulcombe David C
Department of Plant Sciences, University of Cambridge, Cambridge, UK.
Key Laboratory of Horticulture Biology, Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, Hubei, China.
Methods Mol Biol. 2022;2484:201-212. doi: 10.1007/978-1-0716-2253-7_15.
Loss-of-function analyses are essential to dissect the complex nature of biological processes, including gametogenesis. Virus-induced gene silencing (VIGS) has been widely used in crop species as an amenable and rapid way to generate gene knockdowns. As a transient assay, VIGS circumvents the generation of stable transgenic lines through laborious and time-consuming tissue culture techniques. VIGS involves inoculating plants during early development with genetically manipulated viral constructs carrying an endogenous gene target sequence. The viral infection triggers the host plant gene silencing machinery to process the viral genomic RNA into small RNAs (sRNAs) including the gene complementary region. The sRNAs with complementary sequences to the endogenous gene mediate posttranscriptional gene silencing of the targeted gene. Here, we provide a simple and reproducible VIGS protocol employing the tobacco rattle virus (TRV) in tomato (Solanum lycopersicum cv. M82). As it is stable at later developmental stages this approach is suitable for many traits in tomato including gametogenesis and it can be adapted to other crop species.
功能丧失分析对于剖析包括配子发生在内的生物过程的复杂本质至关重要。病毒诱导的基因沉默(VIGS)作为一种便捷且快速的产生基因敲低的方法,已在作物物种中广泛应用。作为一种瞬时检测方法,VIGS避免了通过繁琐且耗时的组织培养技术来生成稳定转基因系。VIGS包括在植物早期发育阶段用携带内源基因靶序列的基因工程病毒构建体接种植物。病毒感染触发宿主植物基因沉默机制,将病毒基因组RNA加工成包括基因互补区域在内的小RNA(sRNA)。与内源基因具有互补序列的sRNA介导靶基因的转录后基因沉默。在此,我们提供了一种简单且可重复的VIGS方案,该方案在番茄(Solanum lycopersicum cv. M82)中采用烟草脆裂病毒(TRV)。由于该方法在发育后期稳定,因此适用于番茄中的许多性状,包括配子发生,并且可以适用于其他作物物种。