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有丝分裂染色体的 DNA 损伤焦点。

DNA Damage Foci on Metaphase Chromosomes.

机构信息

Department of Environmental & Radiological Health Sciences, Colorado State University, Fort Collins, CO, USA.

出版信息

Methods Mol Biol. 2023;2519:93-98. doi: 10.1007/978-1-0716-2433-3_10.

Abstract

After DNAs are damaged, DNA repair proteins accumulate and are activated at the DNA damaged site. These accumulated proteins are visualized as foci by fluorescent immunocytochemistry technique. This allows the DNA damage responses in interphase nuclei to be detected; it was earlier times difficult to analyze DNA damage in situ. In order to analyze DNA damage in interphase cells, either DNA is extracted to assay breaks biochemically, or premature chromosome condensation is conducted to observe as chromatin breaks. Although DNA damage-induced foci are typically analyzed in interphase cells, these foci can be also visualized on mitotic chromosomes. The foci where the repair proteins accumulate at the damage site is observed as mitotic chromosome break site. Since mitotic cells attach loosely or not attached to cell culture vessels, it is difficult to analyze foci on chromosomes in culture vessels under a microscope, so metaphase chromosome spread must be prepared for accurate analysis. The cytocentrifuge system is an ideal method to adhere mitotic cells to microscope slides for the fluorescent immunocytochemistry. This chapter introduces cytocentrifuge method to prepare metaphase spread for DNA damage foci analysis.

摘要

DNA 损伤后,DNA 修复蛋白在 DNA 损伤部位聚集并被激活。这些聚集的蛋白质通过荧光免疫细胞化学技术被可视化成焦点。这使得在间核中检测 DNA 损伤反应成为可能;在过去,分析原位 DNA 损伤是很困难的。为了分析间期中的细胞 DNA 损伤,要么提取 DNA 进行生化分析以检测断裂,要么进行过早的染色体浓缩以观察染色质断裂。尽管 DNA 损伤诱导的焦点通常在间期中的细胞中进行分析,但这些焦点也可以在有丝分裂染色体上观察到。在损伤部位聚集修复蛋白的焦点被观察为有丝分裂染色体断裂部位。由于有丝分裂细胞与细胞培养容器松散结合或不结合,因此在显微镜下分析培养容器中的染色体焦点很困难,因此必须准备中期染色体展开来进行准确分析。细胞离心系统是将有丝分裂细胞附着到显微镜载玻片上进行荧光免疫细胞化学的理想方法。本章介绍了用于制备中期展开以进行 DNA 损伤焦点分析的细胞离心方法。

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