Nonenzymatic Synthesis of RNA and DNA Oligomers on Hexitol Nucleic Acid Templates:  The Importance of the A Structure

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 t...

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Veröffentlicht in:Journal of the American Chemical Society 1999-03, Vol.121 (12), p.2653-2656
Hauptverfasser: Kozlov, Igor A, Politis, Panagiotis K, Van Aerschot, Arthur, Busson, Roger, Herdewijn, Piet, Orgel, Leslie E
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Sprache:eng
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Zusammenfassung: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.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja983958r