Macovei Anca, Donà Mattia, Carbonera Daniela, Balestrazzi Alma
Department of Biology and Biotechnology 'Lazzaro Spallanzani', University of Pavia, Pavia, Italy.
Gregor Mendel Institute (GMI), Vienna Biocenter (VBC), Austrian Academy of Science, Vienna, Austria.
Methods Mol Biol. 2018;1743:107-115. doi: 10.1007/978-1-4939-7668-3_10.
DNA diffusion assay is a simple, sensitive and reliable technique which allows the assessment of programmed cell death (PCD) or necrosis events based on nuclear morphology. It consists in isolating nuclei from plant material, which are then embedded in agarose and subjected to lysis in alkaline buffers. Under these conditions, and due to the presence of abundant alkali-labile sites in the DNA, small pieces of DNA diffuse in the agarose gel giving a specific halo appearance when stained with fluorescent dyes like DAPI (4',6-diamidino-2-phenylindole). Here, we describe an optimized protocol for DNA diffusion assay applied to different types of plant cells/tissues, indicating all the critical steps required for a successful experimental procedure.
DNA扩散测定是一种简单、灵敏且可靠的技术,它能够基于细胞核形态评估程序性细胞死亡(PCD)或坏死事件。该技术包括从植物材料中分离细胞核,然后将其包埋在琼脂糖中,并在碱性缓冲液中进行裂解。在这些条件下,由于DNA中存在大量对碱不稳定的位点,DNA小片段会在琼脂糖凝胶中扩散,用DAPI(4',6-二脒基-2-苯基吲哚)等荧光染料染色时会呈现出特定的晕圈外观。在此,我们描述了一种适用于不同类型植物细胞/组织的DNA扩散测定优化方案,指明了成功进行实验所需的所有关键步骤。