Fox M E, Feldman B J, Chu G
Department of Medicine, Stanford University School of Medicine, California 94305.
Mol Cell Biol. 1994 Dec;14(12):8071-7. doi: 10.1128/mcb.14.12.8071-8077.1994.
DNA photolyase binds to and repairs cyclobutane pyrimidine dimers induced by UV radiation. Here we demonstrate that in the yeast Saccharomyces cerevisiae, photolyase also binds to DNA damaged by the anticancer drugs cis-diamminedichloroplatinum (cis-DDP) and nitrogen mustard (HN2) and by the alkylating agent N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Surprisingly, mutations in photolyase were associated with resistance of yeast cells to cis-DDP, MNNG, 4-nitroquinoline oxide (4NQO), and HN2. Transformation of yeast photolyase mutants with the photolyase gene increased sensitivity to these agents. Thus, while the binding of photolyase to DNA damaged by UV radiation aids survival of the cell, binding to DNA damaged by other agents may interfere with cell survival, perhaps by making the lesions inaccessible to the nucleotide excision repair system.
DNA光解酶可结合并修复由紫外线辐射诱导形成的环丁烷嘧啶二聚体。在此我们证明,在酿酒酵母中,光解酶还可结合因抗癌药物顺二氯二氨铂(顺铂)、氮芥(HN2)以及烷化剂N-甲基-N'-硝基-N-亚硝基胍(MNNG)而受损的DNA。令人惊讶的是,光解酶中的突变与酵母细胞对顺铂、MNNG、4-硝基喹啉氧化物(4NQO)和HN2的抗性相关。用光解酶基因转化酵母光解酶突变体可增加其对这些药物的敏感性。因此,虽然光解酶与紫外线辐射损伤的DNA结合有助于细胞存活,但与其他药物损伤的DNA结合可能会干扰细胞存活,也许是通过使损伤无法被核苷酸切除修复系统识别。