4.2 Article

SYNTHESIS AND PROPERTIES OF OLIGONUCLEOTIDES CONTAINING 3′-O,4′-C-ETHYLENEOXY-BRIDGED 5-METHYLURIDINES

Journal

HETEROCYCLES
Volume 97, Issue 1, Pages 306-313

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-18-S(T)20

Keywords

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Funding

  1. JSPS KAKENHI [JP17K18295]
  2. Takeda Science Foundation
  3. Grants-in-Aid for Scientific Research [17K18295] Funding Source: KAKEN

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A phosphoramidite of 3'-O,4'-C-ethyleneoxy-bridged 5-methyluridine (3',4'-EoNA-T) was successfully incorporated into oligonucleotides, and their abilities to form duplexes with RNA and DNA as well as triplexes with double-stranded DNA were evaluated. The stabilities of the duplexes formed between RNA and 3',4'-EoNA-modified oligonucleotides were only slightly lower than those of the natural DNA RNA duplex, while the duplexes formed between 3',4'-EoNA-modified oligonucleotides and DNA were drastically less stable than the natural DNA-DNA duplex. Moreover, under the same conditions as the UV-melting experiments of the duplexes, 3',4'-EoNA-modified oligonucleotides were unable to form triplexes with dsDNA. These results showed that oligonucleotides containing 3',4'-EoNA-T had excellent RNA selectivity.

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