Walker P R, Kokileva L, LeBlanc J, Sikorska M
Institute for Biological Sciences, National Research Council of Canada, Ottawa.
Biotechniques. 1993 Dec;15(6):1032-40.
DNA fragmentation during apoptosis proceeds through an ordered series of stages commencing with the production of DNA fragments of 300 kbp, which are then degraded to fragments of 50 kbp. The 50-kbp fragments are further degraded, in some but not all cells, to smaller fragments (10-40 kbp) and release the small oligonucleosome fragments that are recognized as the characteristic DNA ladder on conventional agarose gels. Methodology is presented for the detection of the initial stages of DNA fragmentation using pulsed-field gel electrophoresis or a combination of pulsed-field gel electrophoresis and conventional agarose gel electrophoresis that allows detection of the DNA ladder in the same sample. A new method for the detection of high molecular weight DNA fragments on conventional agarose gels is presented, together with a rationale for the analysis of DNA fragmentation during apoptosis.
细胞凋亡过程中的DNA片段化通过一系列有序阶段进行,始于产生300 kbp的DNA片段,随后这些片段被降解为50 kbp的片段。在一些但并非所有细胞中,50 kbp的片段会进一步降解为更小的片段(10 - 40 kbp),并释放出小的寡核小体片段,这些片段在传统琼脂糖凝胶上被识别为特征性的DNA梯带。本文介绍了使用脉冲场凝胶电泳或脉冲场凝胶电泳与传统琼脂糖凝胶电泳相结合的方法来检测DNA片段化的初始阶段,该方法能够在同一样本中检测到DNA梯带。本文还介绍了一种在传统琼脂糖凝胶上检测高分子量DNA片段的新方法,以及分析细胞凋亡过程中DNA片段化的基本原理。