Steinbrink Sandra, Boutros Michael
German Cancer Research Center, Heidelberg, Germany.
Methods Mol Biol. 2008;420:139-53. doi: 10.1007/978-1-59745-583-1_8.
RNA interference (RNAi) has become a widely used tool to analyze biological functions in vivo and in vitro. With the availability of an increasing number of Drosophila cell lines, a variety of different processes can be studied ranging from cell cycle control defects to signaling pathway activities and changes in cell morphology. Owing to the ease of RNAi in Drosophila cells, this experimental system has become a preferred method to screen for novel cellular factors, before their in depth analysis. We here describe the experimental procedures for RNAi experiments in cultured Drosophila cells, starting from the design of long double-stranded RNAs, their synthesis by in vitro transcription and application for cell-based RNAi experiments from low to high-throughput formats. Finally, we show how phenotype analysis can be performed using cell-based assays for luminescence or flow cytometric analysis as examples.
RNA干扰(RNAi)已成为一种广泛用于体内和体外分析生物学功能的工具。随着越来越多果蝇细胞系的出现,可以研究从细胞周期控制缺陷到信号通路活性以及细胞形态变化等各种不同的过程。由于在果蝇细胞中进行RNA干扰操作简便,在深入分析之前,这个实验系统已成为筛选新型细胞因子的首选方法。我们在此描述在培养的果蝇细胞中进行RNAi实验的实验步骤,从长双链RNA的设计开始,通过体外转录合成它们,并将其应用于从低通量到高通量形式的基于细胞的RNAi实验。最后,我们以基于细胞的发光测定或流式细胞术分析为例,展示如何进行表型分析。