Mahas Ahmed, Ali Zahir, Tashkandi Manal, Mahfouz Magdy M
Laboratory for Genome Engineering, Division of Environmental and Biological Sciences and Engineering, 4700 King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.
Methods Mol Biol. 2019;1917:311-326. doi: 10.1007/978-1-4939-8991-1_23.
Targeted modification of plant genomes is a powerful strategy for investigating and engineering cellular systems, paving the way for the discovery and development of important, novel agricultural traits. Cas9, an RNA-guided DNA endonuclease from the type II adaptive immune CRISPR system of the prokaryote Streptococcus pyogenes, has gained widespread popularity as a genome-editing tool for use in a wide array of cells and organisms, including model and crop plants. Effective genome engineering requires the delivery of the Cas9 protein and guide RNAs into target cells. However, in planta genome modification faces many hurdles, including the difficulty in efficiently delivering genome engineering reagents to the desired tissues. We recently developed a Tobacco rattle virus (TRV)-mediated genome engineering system for Nicotiana benthamiana. Using this platform, genome engineering reagents can be delivered into all plant parts in a simple, efficient manner, facilitating the recovery of progeny plants with the desired genomic modifications, thus bypassing the need for transformation and tissue culture. This platform expands the utility of the CRISPR/Cas9 system for in planta, targeted genome modification. Here, we provide a detailed protocol explaining the methodologies used to develop and implement TRV-mediated genome engineering in N. benthamiana. The protocol described here can be extended to any other plant species susceptible to systemic infection by TRV. However, this approach is not limited to vectors derived from TRV, as other RNA viruses could be used to develop similar delivery platforms.
对植物基因组进行靶向修饰是研究和改造细胞系统的有力策略,为发现和培育重要的新型农业性状铺平了道路。Cas9是一种来自化脓性链球菌原核生物II型适应性免疫CRISPR系统的RNA引导的DNA内切酶,作为一种基因组编辑工具,已在包括模式植物和作物在内的多种细胞和生物体中广泛应用。有效的基因组工程需要将Cas9蛋白和引导RNA导入靶细胞。然而,植物体内的基因组修饰面临许多障碍,包括难以将基因组工程试剂有效地递送至所需组织。我们最近开发了一种用于本氏烟草的烟草脆裂病毒(TRV)介导的基因组工程系统。利用该平台,基因组工程试剂可以以简单、高效的方式递送至所有植物部位,有助于获得具有所需基因组修饰的后代植株,从而无需进行转化和组织培养。该平台扩展了CRISPR/Cas9系统在植物体内进行靶向基因组修饰的应用。在此,我们提供了一份详细的方案,解释了用于在本氏烟草中开发和实施TRV介导的基因组工程的方法。这里描述的方案可以扩展到任何其他易受TRV系统感染的植物物种。然而,这种方法不限于源自TRV的载体,因为其他RNA病毒也可用于开发类似的递送平台。