Grubb Jennifer, Brown M Scott, Bishop Douglas K
Department of Radiation and Cellular Oncology, University of Chicago.
Department of Radiation and Cellular Oncology, University of Chicago; Department of Molecular Genetics and Cell Biology, University of Chicago.
J Vis Exp. 2015 Aug 9(102):e53081. doi: 10.3791/53081.
The small size of nuclei of the budding yeast Saccharomyces cerevisiae limits the utility of light microscopy for analysis of the subnuclear distribution of chromatin-bound proteins. Surface spreading of yeast nuclei results in expansion of chromatin without loss of bound proteins. A method for surface spreading balances fixation of DNA bound proteins with detergent treatment. The method demonstrated is slightly modified from that described by Josef Loidl and Franz Klein. The method has been used to characterize the localization of many chromatin-bound proteins at various stages of the mitotic cell cycle, but is especially useful for the study of meiotic chromosome structures such as meiotic recombinosomes and the synaptonemal complex. We also describe a modification that does not require use of Lipsol, a proprietary detergent, which was called for in the original procedure, but no longer commercially available. An immunostaining protocol that is compatible with the chromosome spreading method is also described.
出芽酵母酿酒酵母的细胞核体积小,限制了光学显微镜在分析与染色质结合蛋白的亚核分布方面的应用。酵母细胞核的表面铺展可使染色质扩张而不损失结合蛋白。一种表面铺展方法是通过洗涤剂处理平衡与DNA结合蛋白的固定。所展示的方法是对Josef Loidl和Franz Klein所描述的方法进行了轻微修改。该方法已被用于表征许多与染色质结合蛋白在有丝分裂细胞周期各个阶段的定位,但对于研究减数分裂染色体结构(如减数分裂重组体和联会复合体)特别有用。我们还描述了一种改进方法,该方法不需要使用Lipsol(一种专有洗涤剂),原始方法中需要使用该洗涤剂,但现在已不再商业化供应。还描述了一种与染色体铺展方法兼容的免疫染色方案。