Interaction of human nuclear topoisomerase I with guanosine quartet-forming and guanosine-rich single-stranded DNA and RNA oligonucleotides

J Biol Chem. 2002 Mar 15;277(11):8906-11. doi: 10.1074/jbc.M106372200. Epub 2001 Dec 26.

Abstract

Human nuclear DNA topoisomerase I (top1) plays a crucial role in DNA replication, transcription, and chromosome condensation. In this study, we show that intra- and intermolecular guanosine quartets (G-quartets) can inhibit top1-mediated DNA cleavage at a high affinity site. Top1-mediated DNA cleavage was also inhibited by a 16-mer single-stranded oligodeoxynucleotide (ODN) containing a G-rich sequence (G(2)T(2)G(5)TG(2)TG(3)) and by its RNA equivalent, neither of which form G-quartet structures. A comparison of various single-stranded ODN for their ability to inhibit top1-mediated DNA cleavage indicated that G-rich sequences containing repeats of 2 or 3 consecutive guanines interspaced with thymines specifically inhibited top1. We also found that both single-stranded and G-quartet-forming ODNs bind to top1 without being cleaved by the enzyme. These results demonstrate that either DNA or RNA G-rich single-stranded and G-quartet-forming oligonucleotides can bind to top1 and prevent cleavage of duplex DNA.

MeSH terms

  • Base Sequence
  • Camptothecin / pharmacology
  • Cell Nucleus / enzymology*
  • DNA Topoisomerases, Type I / metabolism*
  • DNA, Single-Stranded / chemistry
  • DNA, Single-Stranded / metabolism*
  • Guanosine / chemistry*
  • Humans
  • Oligodeoxyribonucleotides / chemistry
  • Oligodeoxyribonucleotides / metabolism*
  • Oligoribonucleotides / metabolism*

Substances

  • DNA, Single-Stranded
  • Oligodeoxyribonucleotides
  • Oligoribonucleotides
  • Guanosine
  • DNA Topoisomerases, Type I
  • Camptothecin