Erixon K, Ahnström G
Mutat Res. 1979 Feb;59(2):257-71. doi: 10.1016/0027-5107(79)90164-7.
A simple and sensitive technique for detection of strand breaks in DNA has been further developed. The method has been used to follow UV-induced excision-repair in human fibroblasts. It has been possible to study the kinetics of enzymic reactions in intact cells, in which strand breaks in DNA are produced and sealed again. Hydroxyurea, 5-fluorodeoxyuridine and 1-beta-D-arabinofuranosylcytosine, potent inhibitors of DNA synthesis, drastically increased the number of breaks observed during the repair process. This was probably due to a decreased polymerase activity, which will cause the strand breaks formed by endonuclease to remain open longer. The initial rate of strand-break formation did not seem to be influenced by hydroxyurea or araC, and was about 4000 breaks per minute in a diploid genome, at a dose of 20 J/m2. After 5--30 min, depending on the dose of UV, the number of breaks reached a maximum and started to decrease again. Hydroxyurea decreased the rate of polymerization in the sites under repair. However, there was no concomitant reduction of repair-induced incorporation of [3H]thymidine and no reduction of the excision of pyrimidine dimers. It therefore seems that the action of the polymerase was not a rate-limiting event, but rather an earlier step. It is likely that the endonucleolytic activity determined the rate of repair. As a consequence, the endonuclease and polymerase cannot be bound in a permanent complex. Under certain assumptions, the time for repair of a site, i.e. the time from incision to final ligase sealing, can be estimated as between 3 and 10 min. Essentially no breaks were produced in Xeroderma pigmentosum cells belonging to complementation group A, and there was no enhancement by hydroxyurea. Cells from the variant type of Xeroderma pigmentosum behaved like normal cells in this respect.
一种用于检测DNA链断裂的简单而灵敏的技术得到了进一步发展。该方法已被用于追踪紫外线诱导的人成纤维细胞中的切除修复过程。已经能够研究完整细胞中酶促反应的动力学,在这些细胞中DNA链断裂产生后又重新封闭。羟基脲、5-氟脱氧尿苷和1-β-D-阿拉伯呋喃糖基胞嘧啶是DNA合成的有效抑制剂,它们极大地增加了修复过程中观察到的断裂数量。这可能是由于聚合酶活性降低,这将导致内切核酸酶形成的链断裂保持开放的时间更长。链断裂形成的初始速率似乎不受羟基脲或阿糖胞苷的影响,在二倍体基因组中,当紫外线剂量为20 J/m2时,约为每分钟4000个断裂。5-30分钟后,根据紫外线剂量的不同,断裂数量达到最大值,然后又开始下降。羟基脲降低了修复位点处的聚合速率。然而,修复诱导的[3H]胸腺嘧啶掺入并没有相应减少,嘧啶二聚体的切除也没有减少。因此,似乎聚合酶的作用不是限速事件,而是更早的步骤。很可能内切核酸酶活性决定了修复速率。因此,内切核酸酶和聚合酶不能以永久复合物的形式结合。在某些假设下,一个位点的修复时间,即从切口到最终连接酶封闭的时间,可以估计在3到10分钟之间。属于互补组A的着色性干皮病细胞基本上不产生断裂,羟基脲也没有增强作用。在这方面,着色性干皮病变异型的细胞表现得像正常细胞。