Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Methods Mol Biol. 2021;2267:145-157. doi: 10.1007/978-1-0716-1217-0_9.
Cell cycle progression, or its arrest upon checkpoint activation, is directed by a complex array of cellular processes dependent on the diffusion of chemical signals. These signals regulate the onset of each cell cycle phase and prevent undesired phase transitions. Functional complementation is a robust strategy to identify such signals, by which mutant phenotypes are rescued through complementation with candidate factors. Here we describe a method that reclaims a five-decade old mammalian cell-cell fusion strategy of functional complementation to study the molecular control of cell cycle progression. The generation of cell-cell fusions (heterokaryons) allows for the analysis, via immunofluorescence, of cell cycle regulator dynamics and evaluating the effective rescue of cell cycle progression in specific genetic settings.
细胞周期的推进,或者在检查点激活时的停滞,是由一系列复杂的细胞过程决定的,这些过程依赖于化学信号的扩散。这些信号调节每个细胞周期阶段的开始,并防止不期望的阶段转变。功能互补是一种强大的策略,可以通过该策略用候选因子来互补突变表型,从而鉴定这些信号。在这里,我们描述了一种方法,该方法重新利用了一个已有五十年历史的哺乳动物细胞融合功能互补策略,以研究细胞周期进程的分子控制。细胞融合(异核体)的产生允许通过免疫荧光分析细胞周期调节剂的动力学,并评估在特定遗传背景下细胞周期进程的有效挽救。