Bettencourt-Dias Mónica, Goshima Gohta
Cell Cycle Regulation Lab, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Methods Mol Biol. 2009;545:39-62. doi: 10.1007/978-1-60327-993-2_3.
Genetic studies on model organisms, particularly yeasts and Drosophila melanogaster, have proven powerful in identifying the cell cycle machinery and its regulatory mechanisms. In more recent years RNAi has been used in a variety of genome-wide screens and single molecule studies to elucidate the mechanisms of cell cycle progression. In Drosophila cultured cells, RNAi is extremely simple, and a strong effect can be observed by adding the dsRNA to the cultured cells, with few complications of off-target effects. Functions in cell cycle progression can be followed by a variety of assays. One of the advantages of these cells is that they allow high-resolution spatiotemporal observations to be made by microscopy, with no particular complexity in terms of media and temperature. Here we discuss protocols for RNAi in Drosophila S2 culture cells, followed by the study of mitotic progression, through immunocytochemistry, live imaging, and flow cytometry analysis.
对模式生物,特别是酵母和黑腹果蝇的遗传学研究,已证明在识别细胞周期机制及其调控机制方面很有成效。近年来,RNA干扰已被用于各种全基因组筛选和单分子研究,以阐明细胞周期进程的机制。在果蝇培养细胞中,RNA干扰极其简单,通过向培养细胞中添加双链RNA就能观察到强烈的效果,而且脱靶效应的并发症很少。细胞周期进程中的功能可以通过多种检测方法来追踪。这些细胞的优点之一是,它们允许通过显微镜进行高分辨率的时空观察,在培养基和温度方面没有特别复杂的情况。在这里,我们讨论果蝇S2培养细胞中RNA干扰的实验方案,随后通过免疫细胞化学、实时成像和流式细胞术分析来研究有丝分裂进程。