Balczon Ron, Wilson Misti, Bhatnagar Y M
Department of Cell Biology and Neuroscience, The University of South Alabama, Mobile, AL 36688, USA.
Chromosoma. 2003 Aug;112(2):96-102. doi: 10.1007/s00412-003-0248-2. Epub 2003 Jul 23.
A method has recently been established for inducing the physical detachment of kinetochores from chromosomes in human HeLa cells, and was used in the studies reported here to investigate the organization and function of dissociated HeLa kinetochores. Immunofluorescence labeling demonstrated that the detached HeLa kinetochores were relatively intact, with the number of detached kinetochores being only moderately more than the diploid number of chromosomes in HeLa cells. In addition, the detached kinetochores could be labeled with antibodies specific for the inner kinetochore plate, outer kinetochore, and subjacent centromeric heterochromatin. A functional assay demonstrated that detached kinetochores retained the capacity to activate the spindle checkpoint, leading to metaphase arrest. Analysis of kinetochore DNA indicated that it consisted primarily of DNA fragments of 130-160 kb in size, while the remainder of the chromosomes were sheared into much smaller fragments during the kinetochore detachment event. Further analysis of kinetochore DNA indicated that it was first cleaved into high molecular weight DNA (>200 kb) fragments during the initial stages of the kinetochore detachment process, and then underwent further maturation following nuclear envelope breakdown to give rise to the 130-160 kb fragment in detached kinetochores. Collectively, these data indicate that detached human kinetochores will be a useful system for investigating the organization, assembly, and function of human kinetochores.
最近建立了一种方法,可诱导人HeLa细胞中着丝粒从染色体上物理分离,并在此处报告的研究中用于研究解离后的HeLa着丝粒的组织和功能。免疫荧光标记显示,分离出的HeLa着丝粒相对完整,分离出的着丝粒数量仅略多于HeLa细胞中染色体的二倍体数量。此外,分离出的着丝粒可用针对着丝粒内板、着丝粒外板和邻近着丝粒异染色质的特异性抗体进行标记。功能分析表明,分离出的着丝粒保留了激活纺锤体检查点的能力,导致中期停滞。对着丝粒DNA的分析表明,它主要由大小为130 - 160 kb的DNA片段组成,而在着丝粒分离事件中,染色体的其余部分被剪切成小得多的片段。对着丝粒DNA的进一步分析表明,在着丝粒分离过程的初始阶段,它首先被切割成高分子量DNA(>200 kb)片段,然后在核膜破裂后经历进一步成熟,从而在分离出的着丝粒中产生130 - 160 kb的片段。总体而言,这些数据表明,分离出的人类着丝粒将是研究人类着丝粒的组织、组装和功能的有用系统。