Seres D S, Fornace A J
Biochim Biophys Acta. 1982 Sep 27;698(3):237-42. doi: 10.1016/0167-4781(82)90153-1.
In this investigation, normal and Fanconi's anemia fibroblasts were exposed to high concentrations of oxygen and the effects of this treatment on DNA were analyzed by alkaline elution. No DNA single-strand breaks were detected in either cell type with up to 20 h incubation in high(50-95%) concentrations of O2. No evidence of DNA damage by O2 could be detected with an endonuclease preparation from Micrococcus luteus. Cells which have been treated with various DNA-damaging agents in the presence of the polymerase inhibitor cytosine arabinoside have been shown to accumulate DNA single-strand breaks during DNA excision repair. When cells were treated with the polymerase inhibitor in 50 or 95% O2, a low level of DNA single-strand breaks accumulated in both cells types. However, no significant differences in the frequency of DNA single-strand breaks were detected between normal and Fanconi's anemia cells after exposure to high O2.
在本研究中,将正常和成范科尼贫血的成纤维细胞暴露于高浓度氧气中,并通过碱性洗脱分析这种处理对DNA的影响。在高达20小时的50%-95%高浓度氧气孵育下,两种细胞类型均未检测到DNA单链断裂。用藤黄微球菌的核酸内切酶制剂未检测到氧气造成DNA损伤的证据。在聚合酶抑制剂阿糖胞苷存在的情况下,用各种DNA损伤剂处理的细胞已显示在DNA切除修复过程中积累DNA单链断裂。当细胞在50%或95%氧气中用聚合酶抑制剂处理时,两种细胞类型中均积累了低水平的DNA单链断裂。然而,暴露于高氧后,正常细胞和范科尼贫血细胞之间在DNA单链断裂频率上未检测到显著差异。