Francis A A, Blevins R D, Carrier W L, Smith D P, Regan J D
Biochim Biophys Acta. 1979 Jul 26;563(2):385-92. doi: 10.1016/0005-2787(79)90057-1.
The effect on DNA repair in ultraviolet-irradiated human skin fibroblasts by hydroxyurea has been examined in this study using three independent methods for measuring DNA repair:the 5-bromodeoxyuridine photolysis assay which measures DNA repair replication, chromatographic measurement of thymine-containing dimers, and measurement of specific ultraviolet-endonuclease-sensitive sites in irradiated DNA. Little effect of hydroxyurea was observed at the concentration of 2 mM, which is often used to inhibit semiconservative DNA synthesis; however, 10 mM hydroxyurea resulted in marked inhibition (65--70%) of excision repair. This inhibition was accompanied by a possible doubling in the size of the repaired region. The accumulation of large numbers of single-strand breaks following ultraviolet irradiation and hydroxyurea incubation seen by other investigators was not observed with the normal skin fibroblasts used in this study. A comparison of hydroxyurea effects on the different DNA repair assays indicates inhibition of one step in DNA repair also results in varying degrees of inhibition of other steps as well.
本研究采用三种独立的测量DNA修复的方法,检测了羟基脲对紫外线照射的人皮肤成纤维细胞中DNA修复的影响:5-溴脱氧尿苷光解测定法,用于测量DNA修复复制;含胸腺嘧啶二聚体的色谱测量法;以及测量受照射DNA中特定的紫外线内切酶敏感位点。在通常用于抑制半保留DNA合成的2 mM浓度下,未观察到羟基脲有明显影响;然而,10 mM羟基脲导致切除修复受到显著抑制(65%-70%)。这种抑制伴随着修复区域大小可能加倍。本研究中使用的正常皮肤成纤维细胞未观察到其他研究者所发现的紫外线照射和羟基脲孵育后大量单链断裂的积累。对羟基脲对不同DNA修复检测的影响进行比较表明,对DNA修复某一步骤的抑制也会导致其他步骤不同程度的抑制。