Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1994 Nov 11;22(22):4634–4640. doi: 10.1093/nar/22.22.4634

Evidence for intramolecularly folded i-DNA structures in biologically relevant CCC-repeat sequences.

G Manzini 1, N Yathindra 1, L E Xodo 1
PMCID: PMC308511  PMID: 7984411

Abstract

The structural behaviour of repetitive cytosine DNA is examined in the oligodeoxynucleotide sequences of (CCCTAA)3CCCT (HTC4), GC(TCCC)3TCCT(TCCC)3 (KRC6) and the methylated (CCCT)3TCCT(CCCT)3C (KRM6) by circular dichroism (CD), gel electrophoresis (PAGE), and ultra violet (UV) absorbance studies. All the three sequences exhibit a pH-induced cooperative structural transition as monitored by CD. An intense positive CD band around 285 nm develops on lowering the pH from 8 to slightly acidic condition, indicative of the formation of base pairs between protonated cytosines. The oligomers are found to melt in a fully reversible and cooperative fashion, with a melting temperature (Tm) of around 50 degrees C at pH 5.5. The melting temperatures are independent from DNA concentration, indicative of an intramolecular process involved in the structural formation. PAGE experiments performed with 32P-labeled samples as well as with normal staining procedures show a predominantly single band migration for all the three oligomers suggestive of a unimolecular structure. From pH titrations the number of protons required for generating the structures formed by HTC4, KRC6 and KRM6 results to be around six. These findings strongly suggest that all the three sequences adopt an intramolecular i-motif structure. The demonstration of i-motif structure for KRC6, a critical functional stretch of the c-ki-ras promoter proto-oncogene, besides the human telomeric sequence HTC4, may be suggestive of larger significance in the functioning of DNA.

Full text

PDF
4634

Images in this article

Selected References

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

  1. Ahmed S., Henderson E. Formation of novel hairpin structures by telomeric C-strand oligonucleotides. Nucleic Acids Res. 1992 Feb 11;20(3):507–511. doi: 10.1093/nar/20.3.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ahmed S., Kintanar A., Henderson E. Human telomeric C-strand tetraplexes. Nat Struct Biol. 1994 Feb;1(2):83–88. doi: 10.1038/nsb0294-83. [DOI] [PubMed] [Google Scholar]
  3. Brown F., Newman J., Stott J., Porter A., Frisby D., Newton C., Carey N., Fellner P. Poly(C) in animal viral RNAs. Nature. 1974 Sep 27;251(5473):342–344. doi: 10.1038/251342a0. [DOI] [PubMed] [Google Scholar]
  4. Cooney M., Czernuszewicz G., Postel E. H., Flint S. J., Hogan M. E. Site-specific oligonucleotide binding represses transcription of the human c-myc gene in vitro. Science. 1988 Jul 22;241(4864):456–459. doi: 10.1126/science.3293213. [DOI] [PubMed] [Google Scholar]
  5. Dayn A., Samadashwily G. M., Mirkin S. M. Intramolecular DNA triplexes: unusual sequence requirements and influence on DNA polymerization. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11406–11410. doi: 10.1073/pnas.89.23.11406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Edwards E. L., Patrick M. H., Ratliff R. L., Gray D. M. A.T and C.C+ base pairs can form simultaneously in a novel multistranded DNA complex. Biochemistry. 1990 Jan 23;29(3):828–836. doi: 10.1021/bi00455a033. [DOI] [PubMed] [Google Scholar]
  7. Gehring K., Leroy J. L., Guéron M. A tetrameric DNA structure with protonated cytosine.cytosine base pairs. Nature. 1993 Jun 10;363(6429):561–565. doi: 10.1038/363561a0. [DOI] [PubMed] [Google Scholar]
  8. Gray D. M. A circular dichroism study of poly dG, poly dC, and poly dG:dC. Biopolymers. 1974;13(10):2087–2102. doi: 10.1002/bip.1974.360131011. [DOI] [PubMed] [Google Scholar]
  9. Gray D. M., Cui T., Ratliff R. L. Circular dichroism measurements show that C.C+ base pairs can coexist with A.T base pairs between antiparallel strands of an oligodeoxynucleotide double-helix. Nucleic Acids Res. 1984 Oct 11;12(19):7565–7580. doi: 10.1093/nar/12.19.7565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gray D. M., Morgan A. R., Ratliff R. L. A comparison of the circular dichroism spectra of synthetic DNA sequences of the homopurine . homopyrimidine and mixed purine- pyrimidine types. Nucleic Acids Res. 1978 Oct;5(10):3679–3695. doi: 10.1093/nar/5.10.3679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gray D. M., Vaughan M. Circular dichroism spectra show that repeating dinucleotide DNAs may form helices in which every other base is looped out. Nucleic Acids Res. 1980 Aug 25;8(16):3695–3707. doi: 10.1093/nar/8.16.3695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hoffman E. K., Trusko S. P., Freeman N., George D. L. Structural and functional characterization of the promoter region of the mouse c-Ki-ras gene. Mol Cell Biol. 1987 Jul;7(7):2592–2596. doi: 10.1128/mcb.7.7.2592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hoffman E. K., Trusko S. P., Murphy M., George D. L. An S1 nuclease-sensitive homopurine/homopyrimidine domain in the c-Ki-ras promoter interacts with a nuclear factor. Proc Natl Acad Sci U S A. 1990 Apr;87(7):2705–2709. doi: 10.1073/pnas.87.7.2705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Leroy J. L., Gehring K., Kettani A., Guéron M. Acid multimers of oligodeoxycytidine strands: stoichiometry, base-pair characterization, and proton exchange properties. Biochemistry. 1993 Jun 15;32(23):6019–6031. doi: 10.1021/bi00074a013. [DOI] [PubMed] [Google Scholar]
  15. Leroy J. L., Guéron M., Mergny J. L., Hélène C. Intramolecular folding of a fragment of the cytosine-rich strand of telomeric DNA into an i-motif. Nucleic Acids Res. 1994 May 11;22(9):1600–1606. doi: 10.1093/nar/22.9.1600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lyamichev V. I., Mirkin S. M., Danilevskaya O. N., Voloshin O. N., Balatskaya S. V., Dobrynin V. N., Filippov S. A., Frank-Kamenetskii M. D. An unusual DNA structure detected in a telomeric sequence under superhelical stress and at low pH. Nature. 1989 Jun 22;339(6226):634–637. doi: 10.1038/339634a0. [DOI] [PubMed] [Google Scholar]
  17. Marck C., Thiele D., Schneider C., Guschlbauer W. Protonated polynucleotides structures - 22.CD study of the acid-base titration of poly(dG).poly(dC). Nucleic Acids Res. 1978 Jun;5(6):1979–1996. doi: 10.1093/nar/5.6.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. McKeon C., Schmidt A., de Crombrugghe B. A sequence conserved in both the chicken and mouse alpha 2(I) collagen promoter contains sites sensitive to S1 nuclease. J Biol Chem. 1984 May 25;259(10):6636–6640. [PubMed] [Google Scholar]
  19. Michel D., Gillet G., Volovitch M., Pessac B., Calothy G., Brun G. Expression of a novel gene encoding a 51.5 kD precursor protein is induced by different retroviral oncogenes in quail neuroretinal cells. Oncogene Res. 1989;4(2):127–136. [PubMed] [Google Scholar]
  20. Orbons L. P., van der Marel G. A., van Boom J. H., Altona C. Hairpin and duplex formation of the DNA octamer d(m5C-G-m5C-G-T-G-m5C-G) in solution. An NMR study. Nucleic Acids Res. 1986 May 27;14(10):4187–4196. doi: 10.1093/nar/14.10.4187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pestov D. G., Dayn A., Siyanova EYu, George D. L., Mirkin S. M. H-DNA and Z-DNA in the mouse c-Ki-ras promoter. Nucleic Acids Res. 1991 Dec 11;19(23):6527–6532. doi: 10.1093/nar/19.23.6527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Sen D., Gilbert W. Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosis. Nature. 1988 Jul 28;334(6180):364–366. doi: 10.1038/334364a0. [DOI] [PubMed] [Google Scholar]
  23. Shen C. K. Superhelicity induces hypersensitivity of a human polypyrimidine . polypurine DNA sequence in the human alpha 2-alpha 1 globin intergenic region to S1 nuclease digestion--high resolution mapping of the clustered cleavage sites. Nucleic Acids Res. 1983 Nov 25;11(22):7899–7910. doi: 10.1093/nar/11.22.7899. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Sundquist W. I., Klug A. Telomeric DNA dimerizes by formation of guanine tetrads between hairpin loops. Nature. 1989 Dec 14;342(6251):825–829. doi: 10.1038/342825a0. [DOI] [PubMed] [Google Scholar]
  25. Tautz D., Renz M. Simple DNA sequences of Drosophila virilis isolated by screening with RNA. J Mol Biol. 1984 Jan 15;172(2):229–235. doi: 10.1016/s0022-2836(84)80041-8. [DOI] [PubMed] [Google Scholar]
  26. Voloshin O. N., Veselkov A. G., Belotserkovskii B. P., Danilevskaya O. N., Pavlova M. N., Dobrynin V. N., Frank-Kamenetskii M. D. An eclectic DNA structure adopted by human telomeric sequence under superhelical stress and low pH. J Biomol Struct Dyn. 1992 Feb;9(4):643–652. doi: 10.1080/07391102.1992.10507945. [DOI] [PubMed] [Google Scholar]
  27. Weiner A. M. Eukaryotic nuclear telomeres: molecular fossils of the RNP world? Cell. 1988 Jan 29;52(2):155–158. doi: 10.1016/0092-8674(88)90501-6. [DOI] [PubMed] [Google Scholar]
  28. Williamson J. R., Raghuraman M. K., Cech T. R. Monovalent cation-induced structure of telomeric DNA: the G-quartet model. Cell. 1989 Dec 1;59(5):871–880. doi: 10.1016/0092-8674(89)90610-7. [DOI] [PubMed] [Google Scholar]
  29. Xodo L. E., Manzini G., Quadrifoglio F., van der Marel G. A., van Boom J. H. Oligodeoxynucleotide folding in solution: loop size and stability of B-hairpins. Biochemistry. 1988 Aug 23;27(17):6321–6326. doi: 10.1021/bi00417a018. [DOI] [PubMed] [Google Scholar]

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

RESOURCES