Roti Roti J L, Wright W D
Section of Cancer Biology, School of Medicine, Washington University, St. Louis, Missouri 63108.
Cytometry. 1987 Sep;8(5):461-7. doi: 10.1002/cyto.990080505.
An assay for visualization of DNA loops undergoing supercoiling changes has been developed. The assay utilizes the fluorescent dye, propidium iodide (PI), which intercalates into the DNA and under the proper conditions causes the supercoiling status of the DNA to change. Thus, the DNA can be seen as a fluorescent halo that changes diameter with PI concentration. At low PI concentrations (0-7.5 micrograms/ml) the supercoils are relaxed with increasing PI, while at higher PI concentrations (7.50-50 micrograms/ml) supercoils in the opposite winding sense are rewound with increasing PI. When HeLa cells were irradiated with 1-20 Gy of 137Cs gamma-rays, the ability to rewind the DNA supercoils was inhibited in a dose-dependent manner, presumably because of the presence of radiation-induced DNA strand breakage, which removed the topological constraints on the DNA loops. These lesions were repaired rapidly during post-irradiation incubation. The ability of the DNA loops to be rewound was restored within 8 min after 10 Gy of gamma-irradiation, such that no difference from control cells could be detected. The half-time for repair of the radiation-induced lesions that inhibit DNA rewinding was similar to that for repair of DNA single strand breaks. The assay has certain advantages over current methods for assaying DNA damage in that it involves measurement of single cells and it does not require the DNA to be labeled with radioactive precursors.
已开发出一种用于可视化发生超螺旋变化的DNA环的检测方法。该检测方法利用荧光染料碘化丙啶(PI),它可嵌入DNA中,并在适当条件下使DNA的超螺旋状态发生变化。因此,DNA可被视为一个荧光晕圈,其直径会随PI浓度而变化。在低PI浓度(0 - 7.5微克/毫升)下,随着PI浓度增加,超螺旋会松弛,而在较高PI浓度(7.50 - 50微克/毫升)下,相反缠绕方向的超螺旋会随着PI浓度增加而重新缠绕。当用1 - 20 Gy的¹³⁷Csγ射线照射HeLa细胞时,DNA超螺旋重新缠绕的能力受到剂量依赖性抑制,推测这是由于存在辐射诱导的DNA链断裂,从而消除了对DNA环的拓扑限制。这些损伤在照射后孵育期间迅速得到修复。在10 Gyγ射线照射后8分钟内,DNA环重新缠绕的能力得以恢复,以至于与对照细胞没有差异。抑制DNA重新缠绕的辐射诱导损伤的修复半衰期与DNA单链断裂的修复半衰期相似。该检测方法相对于目前用于检测DNA损伤的方法具有某些优势,因为它涉及单个细胞的测量,并且不需要用放射性前体标记DNA。