Goshima Gohta
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8602, Japan.
Methods Cell Biol. 2010;97:259-75. doi: 10.1016/S0091-679X(10)97015-5.
The Drosophila S2 cell line is popularly used to study mitosis. In this cell line, multiple genes can be easily and efficiently knocked down by RNA interference (RNAi), and the associated mitotic phenotypes can be assessed with high-resolution microscopy after immunofluorescence or in a living cell. However, compared to untransformed cells in wild-type organisms such as yeasts or worms, mitosis in the S2 cell line is more variable and often looks abnormal even in RNAi-untreated cells. Therefore, in order to judge whether a phenotype is derived from RNAi of the target gene or is simply a variation of control cells, it is critical to prepare proper control samples and perform objective imaging and image analysis. Here, we discuss how bona fide mitotic phenotypes associated with RNAi can be identified, avoiding selecting false positives, in S2 cells.
果蝇S2细胞系广泛用于研究有丝分裂。在该细胞系中,多个基因可通过RNA干扰(RNAi)轻松、高效地敲低,并且在免疫荧光后或在活细胞中可用高分辨率显微镜评估相关的有丝分裂表型。然而,与酵母或蠕虫等野生型生物体中的未转化细胞相比,S2细胞系中的有丝分裂更具变异性,即使在未经RNAi处理的细胞中也常常看起来异常。因此,为了判断一种表型是源自靶基因的RNAi还是仅仅是对照细胞的变异,准备合适的对照样本并进行客观成像和图像分析至关重要。在这里,我们讨论如何在S2细胞中识别与RNAi相关的真正有丝分裂表型,避免选择假阳性。