Nonenzymatic synthesis of RNA and DNA oligomers on hexitol nucleic acid templates: The importance of the A structure

被引:53
|
作者
Kozlov, IA
Politis, PK
Van Aerschot, A
Busson, R
Herdewijn, P
Orgel, LE
机构
[1] Salk Inst Biol Studies, San Diego, CA 92186 USA
[2] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[3] Katholieke Univ Leuven, Rega Inst, Med Chem Lab, B-3000 Louvain, Belgium
关键词
D O I
10.1021/ja983958r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hexitol nucleic acid (HNA) is an analogue of DNA containing the standard nucleoside bases, but with a phosphorylated 1,5-anhydrohexitol backbone. HNA oligomers form duplexes having the nucleic acid A structure with complementary DNA or RNA oligomers. The HNA decacytidylate oligomer is an efficient template for the oligomerization of the 5'-phosphoroimidazolides of guanosine or deoxyguanosine. Comparison of the oligomerization efficiencies on HNA, RNA, and DNA decacytidylate templates under various conditions suggests strongly that only nucleic acid double helices with the A structure support efficient template-directed synthesis when 5'-phosphoroimidazolides of nucleosides are used as substrates.
引用
收藏
页码:2653 / 2656
页数:4
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