Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1998 Sep 1;26(17):3949–3954. doi: 10.1093/nar/26.17.3949

Poly(L-lysine)-graft-dextran copolymer: amazing effects on triplex stabilization under physiological pH and ionic conditions (in vitro).

A Ferdous 1, H Watanabe 1, T Akaike 1, A Maruyama 1
PMCID: PMC147801  PMID: 9705503

Abstract

Triplex DNA formation involving unmodified triplex-forming oligonucleotides (TFOs) is very unstable under physiological conditions. Here, we report a novel strategy to stabilize both purine and pyrimidine motif triplex DNA within the rat alpha1 (I) collagen gene promoter under physiologically relevant conditions by a poly(L-lysine)- graft -dextran copolymer. Using an in vitro electrophoretic mobility shift assay, we show that the copolymer almost completely abrogates the inhibitory effects of physiological concentrations of monovalent cations, particularly potassium ion (K+), on purine motif triplex formation involving very low concentrations of an unmodified guanine-rich TFO. Of importance, pH dependency in pyrimidine motif triplex formation involving an unmodified cytosine-rich TFO is also significantly overcome by the copolymer. Finally, the triplex-stabilizing efficiency of the copolymer is remarkably higher than that of other oligocations, like spermine and spermidine. We suggest that the ability of the graft copolymer to stabilize triplex DNA under physiologically relevant pH and salt concentrations will be a cue for further progress in the antigene strategy.

Full Text

The Full Text of this article is available as a PDF (199.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Beal P. A., Dervan P. B. Second structural motif for recognition of DNA by oligonucleotide-directed triple-helix formation. Science. 1991 Mar 15;251(4999):1360–1363. doi: 10.1126/science.2003222. [DOI] [PubMed] [Google Scholar]
  2. Cheng A. J., Van Dyke M. W. Monovalent cation effects on intermolecular purine-purine-pyrimidine triple-helix formation. Nucleic Acids Res. 1993 Dec 11;21(24):5630–5635. doi: 10.1093/nar/21.24.5630. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cheng A. J., Van Dyke M. W. Oligodeoxyribonucleotide length and sequence effects on intramolecular and intermolecular G-quartet formation. Gene. 1997 Sep 15;197(1-2):253–260. doi: 10.1016/s0378-1119(97)00269-2. [DOI] [PubMed] [Google Scholar]
  4. Chojkier M., Brenner D. A. Therapeutic strategies for hepatic fibrosis. Hepatology. 1988 Jan-Feb;8(1):176–182. doi: 10.1002/hep.1840080132. [DOI] [PubMed] [Google Scholar]
  5. Dagle J. M., Weeks D. L. Positively charged oligonucleotides overcome potassium-mediated inhibition of triplex DNA formation. Nucleic Acids Res. 1996 Jun 1;24(11):2143–2149. doi: 10.1093/nar/24.11.2143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Faruqi A. F., Krawczyk S. H., Matteucci M. D., Glazer P. M. Potassium-resistant triple helix formation and improved intracellular gene targeting by oligodeoxyribonucleotides containing 7-deazaxanthine. Nucleic Acids Res. 1997 Feb 1;25(3):633–640. doi: 10.1093/nar/25.3.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Frank-Kamenetskii M. D., Mirkin S. M. Triplex DNA structures. Annu Rev Biochem. 1995;64:65–95. doi: 10.1146/annurev.bi.64.070195.000433. [DOI] [PubMed] [Google Scholar]
  8. Gee J. E., Revankar G. R., Rao T. S., Hogan M. E. Triplex formation at the rat neu gene utilizing imidazole and 2'-deoxy-6-thioguanosine base substitutions. Biochemistry. 1995 Feb 14;34(6):2042–2048. doi: 10.1021/bi00006a026. [DOI] [PubMed] [Google Scholar]
  9. Grigoriev M., Praseuth D., Guieysse A. L., Robin P., Thuong N. T., Hélène C., Harel-Bellan A. Inhibition of gene expression by triple helix-directed DNA cross-linking at specific sites. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3501–3505. doi: 10.1073/pnas.90.8.3501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hampel K. J., Crosson P., Lee J. S. Polyamines favor DNA triplex formation at neutral pH. Biochemistry. 1991 May 7;30(18):4455–4459. doi: 10.1021/bi00232a012. [DOI] [PubMed] [Google Scholar]
  11. Hélène C. The anti-gene strategy: control of gene expression by triplex-forming-oligonucleotides. Anticancer Drug Des. 1991 Dec;6(6):569–584. [PubMed] [Google Scholar]
  12. Jin R. Z., Breslauer K. J., Jones R. A., Gaffney B. L. Tetraplex formation of a guanine-containing nonameric DNA fragment. Science. 1990 Oct 26;250(4980):543–546. doi: 10.1126/science.2237404. [DOI] [PubMed] [Google Scholar]
  13. Joseph J., Kandala J. C., Veerapanane D., Weber K. T., Guntaka R. V. Antiparallel polypurine phosphorothioate oligonucleotides form stable triplexes with the rat alpha1(I) collagen gene promoter and inhibit transcription in cultured rat fibroblasts. Nucleic Acids Res. 1997 Jun 1;25(11):2182–2188. doi: 10.1093/nar/25.11.2182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lichtler A., Stover M. L., Angilly J., Kream B., Rowe D. W. Isolation and characterization of the rat alpha 1(I) collagen promoter. Regulation by 1,25-dihydroxyvitamin D. J Biol Chem. 1989 Feb 25;264(6):3072–3077. [PubMed] [Google Scholar]
  15. Marchand C., Bailly C., Nguyen C. H., Bisagni E., Garestier T., Hélène C., Waring M. J. Stabilization of triple helical DNA by a benzopyridoquinoxaline intercalator. Biochemistry. 1996 Apr 16;35(15):5022–5032. doi: 10.1021/bi952908l. [DOI] [PubMed] [Google Scholar]
  16. Maruyama A., Katoh M., Ishihara T., Akaike T. Comb-type polycations effectively stabilize DNA triplex. Bioconjug Chem. 1997 Jan-Feb;8(1):3–6. doi: 10.1021/bc960071g. [DOI] [PubMed] [Google Scholar]
  17. Maruyama A., Watanabe H., Ferdous A., Katoh M., Ishihara T., Akaike T. Characterization of interpolyelectrolyte complexes between double-stranded DNA and polylysine comb-type copolymers having hydrophilic side chains. Bioconjug Chem. 1998 Mar-Apr;9(2):292–299. doi: 10.1021/bc9701510. [DOI] [PubMed] [Google Scholar]
  18. Milligan J. F., Krawczyk S. H., Wadwani S., Matteucci M. D. An anti-parallel triple helix motif with oligodeoxynucleotides containing 2'-deoxyguanosine and 7-deaza-2'-deoxyxanthosine. Nucleic Acids Res. 1993 Jan 25;21(2):327–333. doi: 10.1093/nar/21.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Moser H. E., Dervan P. B. Sequence-specific cleavage of double helical DNA by triple helix formation. Science. 1987 Oct 30;238(4827):645–650. doi: 10.1126/science.3118463. [DOI] [PubMed] [Google Scholar]
  20. Musso M., Van Dyke M. W. Polyamine effects on purine-purine-pyrimidine triple helix formation by phosphodiester and phosphorothioate oligodeoxyribonucleotides. Nucleic Acids Res. 1995 Jun 25;23(12):2320–2327. doi: 10.1093/nar/23.12.2320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Olivas W. M., Maher L. J., 3rd Competitive triplex/quadruplex equilibria involving guanine-rich oligonucleotides. Biochemistry. 1995 Jan 10;34(1):278–284. doi: 10.1021/bi00001a034. [DOI] [PubMed] [Google Scholar]
  22. Olivas W. M., Maher L. J., 3rd Overcoming potassium-mediated triplex inhibition. Nucleic Acids Res. 1995 Jun 11;23(11):1936–1941. doi: 10.1093/nar/23.11.1936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Orson F. M., Thomas D. W., McShan W. M., Kessler D. J., Hogan M. E. Oligonucleotide inhibition of IL2R alpha mRNA transcription by promoter region collinear triplex formation in lymphocytes. Nucleic Acids Res. 1991 Jun 25;19(12):3435–3441. doi: 10.1093/nar/19.12.3435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Pilch D. S., Levenson C., Shafer R. H. Structure, stability, and thermodynamics of a short intermolecular purine-purine-pyrimidine triple helix. Biochemistry. 1991 Jun 25;30(25):6081–6088. doi: 10.1021/bi00239a001. [DOI] [PubMed] [Google Scholar]
  25. Postel E. H., Flint S. J., Kessler D. J., Hogan M. E. Evidence that a triplex-forming oligodeoxyribonucleotide binds to the c-myc promoter in HeLa cells, thereby reducing c-myc mRNA levels. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):8227–8231. doi: 10.1073/pnas.88.18.8227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rajagopal P., Feigon J. Triple-strand formation in the homopurine:homopyrimidine DNA oligonucleotides d(G-A)4 and d(T-C)4. Nature. 1989 Jun 22;339(6226):637–640. doi: 10.1038/339637a0. [DOI] [PubMed] [Google Scholar]
  27. Sen D., Gilbert W. A sodium-potassium switch in the formation of four-stranded G4-DNA. Nature. 1990 Mar 29;344(6265):410–414. doi: 10.1038/344410a0. [DOI] [PubMed] [Google Scholar]
  28. Silver G. C., Nguyen C. H., Boutorine A. S., Bisagni E., Garestier T., Hélène C. Conjugates of oligonucleotides with triplex-specific intercalating agents. Stabilization of triple-helical DNA in the promoter region of the gene for the alpha-subunit of interleukin 2 (IL-2R alpha). Bioconjug Chem. 1997 Jan-Feb;8(1):15–22. doi: 10.1021/bc9600675. [DOI] [PubMed] [Google Scholar]
  29. Singleton S. F., Dervan P. B. Influence of pH on the equilibrium association constants for oligodeoxyribonucleotide-directed triple helix formation at single DNA sites. Biochemistry. 1992 Nov 17;31(45):10995–11003. doi: 10.1021/bi00160a008. [DOI] [PubMed] [Google Scholar]
  30. Tabor C. W., Tabor H. Polyamines. Annu Rev Biochem. 1984;53:749–790. doi: 10.1146/annurev.bi.53.070184.003533. [DOI] [PubMed] [Google Scholar]
  31. Thomas T., Thomas T. J. Selectivity of polyamines in triplex DNA stabilization. Biochemistry. 1993 Dec 21;32(50):14068–14074. doi: 10.1021/bi00213a041. [DOI] [PubMed] [Google Scholar]
  32. Vasquez K. M., Wensel T. G., Hogan M. E., Wilson J. H. High-affinity triple helix formation by synthetic oligonucleotides at a site within a selectable mammalian gene. Biochemistry. 1995 May 30;34(21):7243–7251. doi: 10.1021/bi00021a040. [DOI] [PubMed] [Google Scholar]
  33. Wagner E., Cotten M., Foisner R., Birnstiel M. L. Transferrin-polycation-DNA complexes: the effect of polycations on the structure of the complex and DNA delivery to cells. Proc Natl Acad Sci U S A. 1991 May 15;88(10):4255–4259. doi: 10.1073/pnas.88.10.4255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wang G., Seidman M. M., Glazer P. M. Mutagenesis in mammalian cells induced by triple helix formation and transcription-coupled repair. Science. 1996 Feb 9;271(5250):802–805. doi: 10.1126/science.271.5250.802. [DOI] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES