BASE-PAIRING OF 8-OXOGUANOSINE AND 8-OXO-2'-DEOXYGUANOSINE WITH 2'-DEOXYADENOSINE, 2'-DEOXYCYTOSINE, 2'-DEOXYGUANOSINE, AND THYMIDINE

Base pair formation between O-silyl derivatives of 8-oxoguanosine (8-O xoG) and 8-oxo-2'-deoxyguanosine (8-OxodG) with 2'-deoxyadenosine (dA) , 2'-deoxycytosine (dC), 2'-deoxyguanosine (dG), and thymidine (dThd) have been examined by NMR methods in chloroform. 8-OxoG and 8-OxodG fo rm base pairs with all four nucleosides, suggesting that they can mimi c the base pairing properties of any DNA base. In 8-OxodG.dA or 8-OxoG .dA base pairs both bases assume Hoogsteen geometry with respect to bo th bases. Hoogsteen and Watson-Crick base pairs are formed between 8-O xodG or 8-OxoG and either dThd or dG. Only Watson-Crick geometry is se en for 8-OxodG.dC and 8-OxoG.dC base pairs. In all base pairs the glyc osidic bond of 8-OxodG or 8-OxoG is syn and anti for the base pair par tner. Additional base pairing studies with the modified nucleosides 1- methyl-8-oxoguanosine (1-Me-8-oxoG), 7-methyl-8-oxoguanosine (7-Me-8-o xoG), and 8-methoxyguanosine (8-OMeG), modified nucleosides structural ly related to 8-OxoG and 8-OxodG, support the proposed base pair struc tures and aided in the determination of base pair geometry. Associatio n constants were determined for 8-OxoG.dN and 8-OxodG.dN (N = A, C, G, Thd) base pairs as well as the normal dThd.dA and dG-dC base pairs. T he magnitude of the association constants allows the relative stabilit ies of the base pairs to be determined: 8-OxodG(WC).dC (8-OxoG(WC).dC) almost-equal-to dG(WC).dC > 8-OxodG(H).dG (8-OxoG(H).dG) > 8-OxodG(H) .dA (8-OxoG(H).dA) > 8-OxodG(H).dThd (8-oxoG(H).dThd) almost-equal-to dThd.dA. The formation of these base pairs is consistent with the know n mutagenic nature of 8-oxo-2'-deoxyguanosine and with NMR studies of oligonucleotides containing the 8-oxoG modification.