Edenberg H J
Biophys J. 1976 Aug;16(8):849-60. doi: 10.1016/S0006-3495(76)85735-9.
DNA replication in ultraviolet-irradiated HeLa cells was studied by two different techniques: measurements of the kinetics of semiconservative DNA synthesis, and DNA fiber autoradiography. In examining the kinetics of semiconservative DNA synthesis, density label was used to avoid measuring the incorporation due to repair replication. The extent of inhibition varied with time. After doses of less than 10J/m2 the rate was initially depressed but later showed some recovery. After higher doses, a constant, low rate of synthesis was seen for at least the initial 6 h. An analysis of these data indicated that the inhibition of DNA synthesis could be explained by replication forks halting at pyrimidine dimers. DNA fiber autoradiography was used to further characterize replication after ultraviolet irradiation. The average length of labeled segments in irradiated cells increased in the time immediately after irradiation, and then leveled off. This is the predicted pattern if DNA synthesis in each replicon continued at its previous rate until a lesion is reached, and then halted. The frequency of lesions that block synthesis is approximately the same as the frequency of pyrimidine dimers.
通过两种不同技术研究了紫外线照射的HeLa细胞中的DNA复制:半保留DNA合成动力学测量和DNA纤维放射自显影。在检查半保留DNA合成动力学时,使用密度标记来避免测量由于修复复制导致的掺入。抑制程度随时间变化。剂量小于10J/m2时,速率最初降低,但后来有所恢复。更高剂量后,至少在最初6小时内观察到合成速率恒定且较低。对这些数据的分析表明,DNA合成的抑制可以通过复制叉在嘧啶二聚体处停止来解释。DNA纤维放射自显影用于进一步表征紫外线照射后的复制。照射后立即,受照射细胞中标记片段的平均长度增加,然后趋于稳定。如果每个复制子中的DNA合成以其先前的速率继续进行,直到到达损伤处然后停止,这就是预测的模式。阻断合成的损伤频率与嘧啶二聚体的频率大致相同。