Oda Y, Uesugi S, Ikehara M, Nishimura S, Kawase Y, Ishikawa H, Inoue H, Ohtsuka E
Faculty of Pharmaceutical Sciences, Osaka University, Japan.
Nucleic Acids Res. 1991 Apr 11;19(7):1407-12. doi: 10.1093/nar/19.7.1407.
The effects of hydroxylation at the C8 of a deoxyguanosine residue in DNA were studied by NMR analysis of a self-complementary dodecanucleotide, d(C1-G2-C3-oh8G4-A5-A6-T7-T8-C9-G10-C11-G12), which has an 8-hydroxy-2'-deoxyguanosine (oh8dG) residue at the 4th position. NMR data indicate that the 8-hydroxyguanine (oh8G) base takes a 6,8-diketo tautomeric form and is base-paired to C with Watson-Crick type hydrogen bonds in a B-form structure. The thermal stability of the duplex is reduced, but the overall structure is much the same as that of the unmodified d(CGCGAATTCGCG) duplex. The structural changes caused by 8-hydroxylation of the deoxyguanosine, if any, are localized near the modification site.
通过对一个自互补十二聚体d(C1-G2-C3-oh8G4-A5-A6-T7-T8-C9-G10-C11-G12)进行核磁共振分析,研究了DNA中脱氧鸟苷残基C8位羟基化的影响,该十二聚体在第4位有一个8-羟基-2'-脱氧鸟苷(oh8dG)残基。核磁共振数据表明,8-羟基鸟嘌呤(oh8G)碱基呈6,8-二酮互变异构形式,并在B型结构中通过沃森-克里克型氢键与C碱基配对。双链体的热稳定性降低,但整体结构与未修饰的d(CGCGAATTCGCG)双链体大致相同。脱氧鸟苷8-羟基化引起的结构变化(如果有的话)局限于修饰位点附近。