May A, Nairn R S, Okumoto D S, Wassermann K, Stevnsner T, Jones J C, Bohr V A
Laboratory of Molecular Pharmacology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Biol Chem. 1993 Jan 25;268(3):1650-7.
We have analyzed gene-specific and strand-specific DNA damage and repair in the dihydrofolate reductase gene in hamster cells. Cells were UV-irradiated or treated with two types of chemotherapeutics, alkylating agents or cisplatin. UV-induced pyrimidine dimers were detected using a previously published technique in which the T4 endonuclease V enzyme is used to create nicks at the lesion sites. 6-4 photoproducts were detected in a similar assay using ABC excinuclease after prior reversal of the pyrimidine dimers with photolyase. Adducts formed by the alkylating agents nitrogen mustard and dimethyl sulfate were quantitated by generating strand breaks at basic sites after neutral depurination. Cisplatin-induced intrastrand adducts were detected with ABC excinuclease, and cisplatin interstrand cross-links were detected using a denaturation-reannealing reaction before electrophoresis. In accord with previous reports by other investigators, we find distinct strand specificity of the repair of pyrimidine dimers after UV; the transcribed strand was much more efficiently repaired than the nontranscribed strand. In contrast, there was little or no strand bias in the repair of the 6-4 photoproducts. For alkylating agents, a slight bias toward repair in the transcribed strand was found after treatment with nitrogen mustard, but there appeared to be no bias in the repair after treatment with dimethyl sulfate. Cisplatin interstrand cross-links are repaired with equal efficiency from the two strands, but the more common cisplatin-induced lesion, the intrastrand adduct, is preferentially repaired from the transcribed strand. In conclusion, there is strand bias in the repair of pyrimidine dimers and cisplatin intrastrand adducts, but the strand specificity of repair may not be a general feature for all DNA lesions, as we found little or no strand bias in the repair of other lesions studied.
我们分析了仓鼠细胞中二氢叶酸还原酶基因的基因特异性和链特异性DNA损伤及修复情况。细胞经紫外线照射或用两种化疗药物(烷基化剂或顺铂)处理。使用先前发表的技术检测紫外线诱导的嘧啶二聚体,该技术中使用T4内切核酸酶V在损伤位点产生切口。在用光裂合酶使嘧啶二聚体预先逆转后,在类似的测定中使用ABC核酸外切酶检测6-4光产物。通过在碱性位点中性脱嘌呤后产生链断裂来定量由烷基化剂氮芥和硫酸二甲酯形成的加合物。用ABC核酸外切酶检测顺铂诱导的链内加合物,在电泳前使用变性-复性反应检测顺铂链间交联。与其他研究人员先前的报告一致,我们发现紫外线照射后嘧啶二聚体修复存在明显的链特异性;转录链比非转录链修复效率高得多。相比之下,在6-4光产物的修复中几乎没有链偏向。对于烷基化剂,用氮芥处理后发现转录链的修复有轻微偏向,但用硫酸二甲酯处理后修复似乎没有偏向。顺铂链间交联从两条链修复的效率相同,但更常见的顺铂诱导损伤,即链内加合物,优先从转录链修复。总之,嘧啶二聚体和顺铂链内加合物的修复存在链偏向,但修复的链特异性可能不是所有DNA损伤的普遍特征,因为我们发现所研究的其他损伤的修复几乎没有链偏向。