Ryoji M, Katayama H, Fusamae H, Matsuda A, Sakai F, Utano H
Laboratory of Molecular Biology, Hiroshima Prefectural University, Shobara, Japan.
Nucleic Acids Res. 1996 Oct 15;24(20):4057-62. doi: 10.1093/nar/24.20.4057.
We examined DNA repair activities of a mitochondrial lysate derived from Xenopus laevis oocytes. Plasmid DNA, exposed to HCl, H2O2 or UV light, was used as the substrate for the in vitro repair reaction. DNA synthesis in the lysate was stimulated 2-8-fold by such lesions, indicating the presence of excision repair activities. This repair DNA synthesis was not affected by aphidicolin, but was sensitive to N-ethylmaleimide. Thus the mitochondrial DNA polymerase, i.e., pol gamma is indeed involved in the reaction. Actual repair of the depurinated DNA was demonstrated by using the polymerase chain reaction (PCR), where the amount of the amplified DNA fragment increased significantly if the depurinated template was incubated in the lysate prior to the PCR. UV-irradiated DNA, on the other hand, restored its ability as a PCR template only if the repair reaction was carried out under the light. Therefore, in this system, UV-induced damage is repaired mainly by photoreactivation. These results show that mitochondria of Xenopus oocytes possess excision repair as well as photolyase activities, and that the in vitro repair system described here should be useful for further molecular characterization of such DNA repair machinery.
我们检测了非洲爪蟾卵母细胞来源的线粒体裂解物的DNA修复活性。用暴露于盐酸、过氧化氢或紫外线下的质粒DNA作为体外修复反应的底物。这些损伤可使裂解物中的DNA合成增加2至8倍,表明存在切除修复活性。这种修复性DNA合成不受阿非迪霉素影响,但对N-乙基马来酰亚胺敏感。因此,线粒体DNA聚合酶,即聚合酶γ确实参与了该反应。通过聚合酶链反应(PCR)证明了脱嘌呤DNA的实际修复情况,如果在PCR之前将脱嘌呤模板在裂解物中孵育,扩增的DNA片段数量会显著增加。另一方面,紫外线照射的DNA只有在光照下进行修复反应时才能恢复其作为PCR模板的能力。因此,在该系统中,紫外线诱导的损伤主要通过光复活进行修复。这些结果表明,非洲爪蟾卵母细胞的线粒体具有切除修复以及光解酶活性,并且这里描述的体外修复系统应有助于对此类DNA修复机制进行进一步的分子表征。