Short-RNA selective binding of oligonucleotides modified using adenosine and guanosine derivatives that possess cyclohexyl phosphates as substituents

Org Biomol Chem. 2012 Feb 7;10(5):994-1006. doi: 10.1039/c1ob06580g. Epub 2011 Dec 5.

Abstract

We have developed new artificial oligonucleotides which distinguish short RNA targets from long ones. The modification of the 5' termini of oligonucleotides by using adenosine derivatives that possess a bulky cyclohexyl phosphate moiety at their base moiety and a phosphate group at the position of their 5'-hydroxyl group maximized their short RNA selectivity. The 2'-O-methyl-RNA (5'-XC(m)A(m)A(m)C(m)C(m)U(m)A(m)C(m)U(m)) having these modifications exhibits ca. 10 °C higher T(m) in the duplexes with the complementary short RNA (3'-GUUGGAUGA-5') than with the long RNA (3'-AUUAUAUGUUGGAUGAUGGUUA-5'). The oligodeoxynucleotides having the same modification exhibited similar selectivity. Such short-RNA selective binding of terminally modified oligonucleotides can be employed to distinguish between mature microRNAs and pre-microRNAs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / chemistry
  • Adenosine / metabolism*
  • Base Sequence
  • Binding Sites
  • Guanosine / chemistry
  • Guanosine / metabolism*
  • MicroRNAs / chemistry*
  • MicroRNAs / metabolism*
  • Oligonucleotides / chemistry
  • Oligonucleotides / metabolism*
  • Phosphates / chemistry
  • Phosphates / metabolism

Substances

  • MicroRNAs
  • Oligonucleotides
  • Phosphates
  • Guanosine
  • Adenosine