Trgovcević Z, Petranović D, Salaj-Smic E, Petranović M, Trinajstić N, Jericević Z
Mutat Res. 1983 Feb;112(1):17-22. doi: 10.1016/0167-8817(83)90020-2.
Post-UV DNA synthesis in Escherichia coli uvrA recA cells was studied. A low dose of UV radiation (0.07 J/m2), which caused no degradation of the dimer-containing DNA, was used. This enabled us to make a direct comparison between DNA synthesis on the normal template and DNA synthesis on the UV-damaged template. There was no change in the post-UV DNA synthesis kinetics during the first 60 min of post-irradiation incubation. A reduced rate of DNA synthesis was observed at later post-UV times when the dimers are expected to have passed through the normal replication complex. This reduced rate of DNA synthesis was associated with loss of the biological activity of the DNA. We suggest that the gaps opposite dimers rather than dimers per se interfere with normal replication, thus leading to cell death of uvrA recA bacteria.
对大肠杆菌uvrA recA细胞中的紫外线后DNA合成进行了研究。使用了低剂量的紫外线辐射(0.07 J/m²),该剂量不会导致含二聚体的DNA降解。这使我们能够直接比较正常模板上的DNA合成与紫外线损伤模板上的DNA合成。在照射后孵育的前60分钟内,紫外线后DNA合成动力学没有变化。在紫外线照射后的后期,当预计二聚体已通过正常复制复合体时,观察到DNA合成速率降低。这种DNA合成速率的降低与DNA生物活性的丧失有关。我们认为,二聚体对面的缺口而非二聚体本身会干扰正常复制,从而导致uvrA recA细菌的细胞死亡。