Andreassen Paul R, Skoufias Dimitrios A, Margolis Robert L
Institut de Biologie Structurale, J-P Ebel (CEA-CNRS-UJF), Grenoble, France.
Methods Mol Biol. 2004;281:213-25. doi: 10.1385/1-59259-811-0:213.
The spindle-assembly checkpoint involves signaling at kinetochores, which leads to the arrest of mitotic progression in the absence of microtubule attachment or spindle tension. Here, we detail procedures for the analysis of the spindle-assembly checkpoint in adherent mammalian cells. These techniques focus on pharmacological approaches and immunofluorescence microscopy to verify the state of spindle assembly, kinetochore attachment of microtubules and spindle tension, chromosome positioning, and kinetochore signaling by the Mad2 or Bub1 checkpoint proteins. We also describe a bi-parameter flow cytometric assay, using either MPM-2 or anti-phospho-(Ser10)-histone H3 antibodies, for quantitating mitotic cells.
纺锤体组装检验点涉及动粒处的信号传导,在没有微管附着或纺锤体张力的情况下,这会导致有丝分裂进程停滞。在此,我们详细介绍了用于分析贴壁哺乳动物细胞中纺锤体组装检验点的方法。这些技术着重于药理学方法和免疫荧光显微镜检查,以验证纺锤体组装状态、微管的动粒附着和纺锤体张力、染色体定位以及Mad2或Bub1检验点蛋白的动粒信号传导。我们还描述了一种双参数流式细胞术检测方法,使用MPM-2或抗磷酸化(Ser10)-组蛋白H3抗体来定量有丝分裂细胞。