2-Amino-7-deazaadenine forms stable base pairs with cytosine and thymine

Bioorg Med Chem Lett. 2002 Jan 7;12(1):97-9. doi: 10.1016/s0960-894x(01)00685-0.

Abstract

2-Amino-7-deazaadenine ((AD)A) was incorporated into oligodeoxynucleotides (ODN) and their base-pairing properties with natural nucleobases were investigated. In melting temperature (T(m)) experiments, the duplex containing an (AD)A/C base pair showed a high stability comparable to that containing (AD)A/T base pair. Destabilization of the duplex usually observed for existing degenerate bases was not observed. However, the incorporation efficiency of dCTP was only 1.8% for TTP in single-nucleotide insertion reactions using polymerase.

MeSH terms

  • Adenine / analogs & derivatives*
  • Adenine / chemistry*
  • Base Composition
  • Base Pairing*
  • Cytosine / chemistry*
  • Drug Stability
  • Oligodeoxyribonucleotides / chemistry
  • Temperature
  • Thymine / chemistry*

Substances

  • 2-amino-7-deazaadenine
  • Oligodeoxyribonucleotides
  • 7-deazaadenine
  • Cytosine
  • Adenine
  • Thymine