Kino K, Sugiyama H
Division of Biofunctional Molecules, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Surugadai, Kanda, Chiyoda-ku, Tokyo 101-0062, Japan.
Nucleic Acids Symp Ser. 2000(44):139-40. doi: 10.1093/nass/44.1.139.
Oxidation of d(A6GGA6)/d(T6CCT6) with sensitizer under different UV irradiation periods was examined. Enzymatic digestion of photolysate revealed that the amount of 8-oxoG initially increased with decrease of G and then decreased with the formation of Iz. In order to investigate whether Iz was formed by one electron oxidation of 8-oxoG through long-range hole migration, photoirradiation of anthraquinone-linked oligomer was examined. The results clearly demonstrated that 8-oxoG was efficiently converted to Iz under irradiation conditions. These results suggest that Iz generated from 8-oxoG induces GC->CG transversion under oxidative condition.
研究了在不同紫外线照射时间下敏化剂对d(A6GGA6)/d(T6CCT6)的氧化作用。对光解产物的酶促消化显示,8-氧代鸟嘌呤(8-oxoG)的量最初随着鸟嘌呤(G)的减少而增加,然后随着Iz的形成而减少。为了研究Iz是否通过8-oxoG的单电子氧化经长程空穴迁移形成,对蒽醌连接的寡聚物进行了光照射研究。结果清楚地表明,在照射条件下8-oxoG能有效地转化为Iz。这些结果表明,在氧化条件下,由8-oxoG产生的Iz会诱导GC→CG颠换。