Monomolecular G-quadruplex structures with inversion of polarity sites: new topologies and potentiality

Nucleic Acids Res. 2017 Aug 21;45(14):8156-8166. doi: 10.1093/nar/gkx566.

Abstract

In this paper, we report investigations, based on circular dichroism, nuclear magnetic resonance spectroscopy and electrophoresis methods, on three oligonucleotide sequences, each containing one 3'-3' and two 5'-5' inversion of polarity sites, and four G-runs with a variable number of residues, namely two, three and four (mTG2T, mTG3T and mTG4T with sequence 3'-TGnT-5'-5'-TGnT-3'-3'-TGnT-5'-5'-TGnT-3' in which n = 2, 3 and 4, respectively), in comparison with their canonical counterparts (TGnT)4 (n = 2, 3 and 4). Oligonucleotides mTG3T and mTG4T have been proven to form very stable unprecedented monomolecular parallel G-quadruplex structures, characterized by three side loops containing the inversion of polarity sites. Both G-quadruplexes have shown an all-syn G-tetrad, while the other guanosines adopt anti glycosidic conformations. All oligonucleotides investigated have shown a noteworthy antiproliferative activity against lung cancer cell line Calu 6 and colorectal cancer cell line HCT-116 p53-/-. Interestingly, mTG3T and mTG4T have proven to be mostly resistant to nucleases in a fetal bovine serum assay. The whole of the data suggest the involvement of specific pathways and targets for the biological activity.

MeSH terms

  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Circular Dichroism
  • Electrophoresis, Polyacrylamide Gel
  • G-Quadruplexes*
  • HCT116 Cells
  • Humans
  • Magnetic Resonance Spectroscopy
  • Nucleic Acid Conformation*
  • Nucleic Acid Denaturation*
  • Oligonucleotides / chemistry*
  • Oligonucleotides / genetics
  • Oligonucleotides / pharmacology
  • Temperature

Substances

  • Oligonucleotides