Ager D D, Dewey W C, Gardiner K, Harvey W, Johnson R T, Waldren C A
Radiation Oncology Research Laboratory, University of California, San Francisco 94143.
Radiat Res. 1990 May;122(2):181-7.
We have examined the use of pulsed-field gel electrophoresis (PFGE) to measure DNA double-strand breaks induced in CHO cells by ionizing radiation. The PFGE assay provides a simple method for the measurement of DNA double-strand breaks for doses as low as 3-4 Gy ionizing radiation, and appears applicable for the measurement of damage produced by any agent producing double-strand breaks. The conditions of transverse alternating field electrophoresis determined both the sensitivity of the assay and the ability to resolve DNA fragments with different sizes. For example, with 0.8% agarose and a 1-min pulse time at 250 V for 18 h of electrophoresis, 0.39% of the DNA per gray migrated into the gel, and only molecules less than 1500 kb could be resolved. With 0.56% agarose and a 60-min pulse time at 40 V for 6 days of electrophoresis, 0.55-0.90% of the DNA per gray migrated into the gel, and molecules between 1500 and 7000 kb could be resolved.
我们研究了使用脉冲场凝胶电泳(PFGE)来测量电离辐射在CHO细胞中诱导产生的DNA双链断裂。PFGE检测为测量低至3 - 4 Gy电离辐射剂量下的DNA双链断裂提供了一种简单方法,并且似乎适用于测量由任何产生双链断裂的试剂所造成的损伤。横向交变电场电泳的条件既决定了检测的灵敏度,也决定了分辨不同大小DNA片段的能力。例如,使用0.8%琼脂糖,在250 V下脉冲时间为1分钟,电泳18小时,每戈瑞有0.39%的DNA迁移到凝胶中,并且只能分辨小于1500 kb的分子。使用0.56%琼脂糖,在40 V下脉冲时间为60分钟,电泳6天,每戈瑞有0.55 - 0.90%的DNA迁移到凝胶中,并且可以分辨1500至7000 kb之间的分子。