Department of Pharmacology and Toxicology, University of Navarra, C/Irunlarrea 1, 31009 Pamplona, Spain.
Arch Toxicol. 2013 Jun;87(6):949-68. doi: 10.1007/s00204-013-1070-0. Epub 2013 May 18.
The comet assay (single cell gel electrophoresis) is the most common method for measuring DNA damage in eukaryotic cells or disaggregated tissues. The assay depends on the relaxation of supercoiled DNA in agarose-embedded nucleoids (the residual bodies remaining after lysis of cells with detergent and high salt), which allows the DNA to be drawn out towards the anode under electrophoresis, forming comet-like images as seen under fluorescence microscopy. The relative amount of DNA in the comet tail indicates DNA break frequency. The assay has been modified to detect various base alterations, by including digestion of nucleoids with a lesion-specific endonuclease. We describe here recent technical developments, theoretical aspects, limitations as well as advantages of the assay, and modifications to measure cellular antioxidant status and different types of DNA repair. We briefly describe the applications of this method in genotoxicity testing, human biomonitoring, and ecogenotoxicology.
彗星实验(单细胞凝胶电泳)是测量真核细胞或分散组织中 DNA 损伤的最常用方法。该实验依赖于琼脂糖包埋核小体中超螺旋 DNA 的松弛(用去污剂和高盐裂解细胞后残留的体),这使得 DNA 在电泳下被推向阳极,形成类似于荧光显微镜下看到的彗星样图像。彗星尾部的 DNA 相对含量表明 DNA 断裂频率。该实验通过用损伤特异性内切酶消化核小体来检测各种碱基改变而得到改良。我们在这里描述了该实验的最新技术进展、理论方面、局限性和优点,以及用于测量细胞抗氧化状态和不同类型 DNA 修复的改良方法。我们简要描述了该方法在遗传毒性测试、人体生物监测和生态遗传毒性学中的应用。