Lawrence T S, Davis M A, Normolle D P
Department of Radiation Oncology, School of Medicine, University of Michigan, Ann Arbor 48109, USA.
Radiat Res. 1995 Dec;144(3):282-7.
We have used biphasic linear ramping pulsed-field gel electrophoresis (PFGE) to understand the effect of incorporation of bromodeoxyuridine (BrdUrd) on radiation-induced DNA damage and repair. This technique permits a determination of the fragment size distribution produced immediately after irradiation as well as during the repair period. We found that incorporation of BrdUrd increased the induction and decreased the repair of radiation damage. The fragment size distribution was consistent with a random breakage model. When we found that significantly more damage was detected after irradiation of deproteinized DNA compared to intact cells, we studied the effects of BrdUrd incorporation on the radiation response of cells or DNA at various phases of preparation for electrophoresis: cells adherent to the culture dish (A), trypsinized cells (B), agarose-embedded cells (C) and deproteinized DNA (D). Although there was a general tendency to detect more damage when irradiation was performed later in the preparation process, steps B and C were the only successive steps which were significantly different. These findings demonstrate that incorporation of BrdUrd randomly increases the induction of radiation damage and decreases its repair at the level of 200 kbp to 5 Mbp fragments. Furthermore, they confirm that the amount of damage detected depends upon the conditions of the cells or DNA at the time of irradiation.
我们使用双相线性递增脉冲场凝胶电泳(PFGE)来了解掺入溴脱氧尿苷(BrdUrd)对辐射诱导的DNA损伤和修复的影响。该技术能够确定照射后即刻以及修复期间产生的片段大小分布。我们发现,掺入BrdUrd会增加辐射损伤的诱导并减少其修复。片段大小分布与随机断裂模型一致。当我们发现与完整细胞相比,脱蛋白DNA照射后检测到的损伤明显更多时,我们研究了在电泳制备的各个阶段掺入BrdUrd对细胞或DNA辐射反应的影响:贴壁于培养皿的细胞(A)、胰蛋白酶消化的细胞(B)、琼脂糖包埋的细胞(C)和脱蛋白DNA(D)。尽管在制备过程中较晚进行照射时通常有检测到更多损伤的趋势,但步骤B和C是仅有的两个有显著差异的连续步骤。这些发现表明,掺入BrdUrd会随机增加辐射损伤的诱导,并在200 kbp至5 Mbp片段水平上减少其修复。此外,它们证实检测到的损伤量取决于照射时细胞或DNA的状态。