Jung Ha-il, Yan Jiapei, Zhai Zhiyang, Vatamaniuk Olena K
Department of Crop and Soil Sciences, Cornell University, Ithaca, NY, 14853, USA.
Methods Mol Biol. 2015;1284:433-52. doi: 10.1007/978-1-4939-2444-8_22.
The protoplast transient assay system has been widely used for rapid functional analyses of genes using cellular and biochemical approaches. This system has been increasingly employed for functional genetic studies using double-stranded (ds) RNA interference (RNAi). Here, we describe a modified procedure for the isolation of protoplasts from leaf mesophyll cells of 14-day-old Arabidopsis thaliana. This modification significantly simplifies and speeds up functional studies without compromising the yield and the viability of protoplasts. We also present the procedure for the isolation and transfection of protoplasts from mesophyll cells of an emerging model grass species, Brachypodium distachyon. Further, we detail procedures for RNAi-based functional studies of genes using transient expression of in vitro synthesized dsRNA in protoplasts.
原生质体瞬时分析系统已被广泛用于通过细胞和生化方法对基因进行快速功能分析。该系统越来越多地用于利用双链(ds)RNA干扰(RNAi)进行功能基因研究。在此,我们描述了一种从14日龄拟南芥叶片叶肉细胞中分离原生质体的改良方法。这种改良显著简化并加速了功能研究,同时不影响原生质体的产量和活力。我们还介绍了从新兴模式禾本科植物短柄草叶肉细胞中分离和转染原生质体的方法。此外,我们详细说明了利用体外合成的dsRNA在原生质体中瞬时表达进行基于RNAi的基因功能研究的程序。