Expansion of triplex recognition codes by the use of novel bicyclic nucleoside derivatives (WNA)

Yosuke Taniguchi, Ayako Nakamura, Yusuke Senko, Keiichi Kodama, Fumi Nagatsugi, Shigeki Sasaki

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13 Citations (Scopus)


Recently, we have developed new base analogs (WNA) and demonstrated that WNA-&#6T538;T with thymine and WNA-C with cytosine stabilize non-natural antiparallel triplexes with a TA or a CG interrupting site, respectively. However, limitations in recognizable sequences with the WNA-containing TFO were also found. The objective of this study is to search better WNA analogs for expansion of triplex recognition codes to general duplex sequences. In this study, we designed new WNA analogs by systematic modification of the aromatic part and the recognition part. The new WNA analogs with the benzene ring substituted with bromide or cyanide have determined for selective stabilization of triplexes at a TA interrupting site, and general formation of triplexes having a TA interrupting site has been achieved.

Original languageEnglish
Pages (from-to)823-827
Number of pages5
JournalNucleosides, Nucleotides and Nucleic Acids
Issue number5-7
Publication statusPublished - Oct 20 2005
Externally publishedYes


All Science Journal Classification (ASJC) codes

  • Genetics
  • Biochemistry

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