Abstract
The thermodynamic and kinetic parameters of triplex formation between four purine-rich oligonucleotides and a 22 bp pyrimidine. purine tract in the promoter region of the c-src gene were determined by fluorescence polarization studies. Three of these four oligonucleotides were 11 nt in length, corresponding to the left, central or right portion of the tract, while the fourth was a 22mer covering the whole tract. Binding constants ( Ka) were measured as a function of Mg2+ concentration (0-10 mM) and temperature (0-41 degrees C). In 10 mM Mg2+, K a for the left, central and right 11mers were 0.26, 0.75 and 1.4 x 10(8)/M, respectively, while for the 22mer the value was 1.8 x 10(8)/M at 22 degrees C. Under the same conditions, Ka was estimated by an electrophoretic band shift technique. The agreement between the two methods was acceptable for the 22mer but not for the 11mers. Kinetic measurements demonstrated that the rate of dissociation of the 22mer from the triplex was significantly slower than that of the 11mers, providing an explanation for the observed discrepancy. The entropy and enthalpy of triplex formation were calculated from van't Hoff plots. In all cases the entropy was favourable, especially for the 22mer and for the 11mer with the lowest guanine content. The enthalpy was unfavourable for the 22mer and most favourable for the 11mer with the highest guanine content. These results provide a thermodynamic explanation for length and sequence effects on the formation of purine.pyrimidine.purine triplexes.
Full Text
The Full Text of this article is available as a PDF (116.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alunni-Fabbroni M., Pirulli D., Manzini G., Xodo L. E. (A,G)-oligonucleotides form extraordinary stable triple helices with a critical R.Y sequence of the murine c-Ki-ras promoter and inhibit transcription in transfected NIH 3T3 cells. Biochemistry. 1996 Dec 17;35(50):16361–16369. doi: 10.1021/bi961750h. [DOI] [PubMed] [Google Scholar]
- Bonham K., Fujita D. J. Organization and analysis of the promoter region and 5' non-coding exons of the human c-src proto-oncogene. Oncogene. 1993 Jul;8(7):1973–1981. [PubMed] [Google Scholar]
- Brenowitz M., Senear D. F., Shea M. A., Ackers G. K. Quantitative DNase footprint titration: a method for studying protein-DNA interactions. Methods Enzymol. 1986;130:132–181. doi: 10.1016/0076-6879(86)30011-9. [DOI] [PubMed] [Google Scholar]
- Breslauer K. J., Frank R., Blöcker H., Marky L. A. Predicting DNA duplex stability from the base sequence. Proc Natl Acad Sci U S A. 1986 Jun;83(11):3746–3750. doi: 10.1073/pnas.83.11.3746. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Callahan D. E., Trapane T. L., Miller P. S., Ts'o P. O., Kan L. S. Comparative circular dichroism and fluorescence studies of oligodeoxyribonucleotide and oligodeoxyribonucleoside methylphosphonate pyrimidine strands in duplex and triplex formation. Biochemistry. 1991 Feb 12;30(6):1650–1655. doi: 10.1021/bi00220a030. [DOI] [PubMed] [Google Scholar]
- 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]
- 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]
- Devlin R., Studholme R. M., Dandliker W. B., Fahy E., Blumeyer K., Ghosh S. S. Homogeneous detection of nucleic acids by transient-state polarized fluorescence. Clin Chem. 1993 Sep;39(9):1939–1943. [PubMed] [Google Scholar]
- Durand M., Peloille S., Thuong N. T., Maurizot J. C. Triple-helix formation by an oligonucleotide containing one (dA)12 and two (dT)12 sequences bridged by two hexaethylene glycol chains. Biochemistry. 1992 Sep 29;31(38):9197–9204. doi: 10.1021/bi00153a012. [DOI] [PubMed] [Google Scholar]
- Eiseman E., Bolen J. B. src-related tyrosine protein kinases as signaling components in hematopoietic cells. Cancer Cells. 1990 Oct;2(10):303–310. [PubMed] [Google Scholar]
- Ellerton N. F., Isenberg I. Fluorescence polarization study of DNA--proflavine complexes. Biopolymers. 1969;8(6):767–786. doi: 10.1002/bip.1969.360080607. [DOI] [PubMed] [Google Scholar]
- 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]
- Faucon B., Mergny J. L., Héléne C. Effect of third strand composition on the triple helix formation: purine versus pyrimidine oligodeoxynucleotides. Nucleic Acids Res. 1996 Aug 15;24(16):3181–3188. doi: 10.1093/nar/24.16.3181. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Freier S. M., Kierzek R., Jaeger J. A., Sugimoto N., Caruthers M. H., Neilson T., Turner D. H. Improved free-energy parameters for predictions of RNA duplex stability. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9373–9377. doi: 10.1073/pnas.83.24.9373. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ito T., Smith C. L., Cantor C. R. Sequence-specific DNA purification by triplex affinity capture. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):495–498. doi: 10.1073/pnas.89.2.495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kibler-Herzog L., Kell B., Zon G., Shinozuka K., Mizan S., Wilson W. D. Sequence dependent effects in methylphosphonate deoxyribonucleotide double and triple helical complexes. Nucleic Acids Res. 1990 Jun 25;18(12):3545–3555. doi: 10.1093/nar/18.12.3545. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krakauer H., Sturtevant J. M. Heats of the helix-coil transitions of the poly A-poly U complexes. Biopolymers. 1968 Apr;6(4):491–512. doi: 10.1002/bip.1968.360060406. [DOI] [PubMed] [Google Scholar]
- Mergny J. L., Collier D., Rougée M., Montenay-Garestier T., Hélène C. Intercalation of ethidium bromide into a triple-stranded oligonucleotide. Nucleic Acids Res. 1991 Apr 11;19(7):1521–1526. doi: 10.1093/nar/19.7.1521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Park Y. W., Breslauer K. J. Drug binding to higher ordered DNA structures: netropsin complexation with a nucleic acid triple helix. Proc Natl Acad Sci U S A. 1992 Jul 15;89(14):6653–6657. doi: 10.1073/pnas.89.14.6653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pilch D. S., Brousseau R., Shafer R. H. Thermodynamics of triple helix formation: spectrophotometric studies on the d(A)10.2d(T)10 and d(C+3T4C+3).d(G3A4G3).d(C3T4C3) triple helices. Nucleic Acids Res. 1990 Oct 11;18(19):5743–5750. doi: 10.1093/nar/18.19.5743. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Plum G. E., Park Y. W., Singleton S. F., Dervan P. B., Breslauer K. J. Thermodynamic characterization of the stability and the melting behavior of a DNA triplex: a spectroscopic and calorimetric study. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9436–9440. doi: 10.1073/pnas.87.23.9436. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Plum G. E., Pilch D. S., Singleton S. F., Breslauer K. J. Nucleic acid hybridization: triplex stability and energetics. Annu Rev Biophys Biomol Struct. 1995;24:319–350. doi: 10.1146/annurev.bb.24.060195.001535. [DOI] [PubMed] [Google Scholar]
- Roberts R. W., Crothers D. M. Specificity and stringency in DNA triplex formation. Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9397–9401. doi: 10.1073/pnas.88.21.9397. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ross P. D., Scruggs R. L. Heat of the reaction forming the three-stranded poly (A + 2U) complex. Biopolymers. 1965;3(4):491–496. doi: 10.1002/bip.1965.360030410. [DOI] [PubMed] [Google Scholar]
- Rougée M., Faucon B., Mergny J. L., Barcelo F., Giovannangeli C., Garestier T., Hélène C. Kinetics and thermodynamics of triple-helix formation: effects of ionic strength and mismatches. Biochemistry. 1992 Sep 29;31(38):9269–9278. doi: 10.1021/bi00153a021. [DOI] [PubMed] [Google Scholar]
- Scaria P. V., Shafer R. H. Binding of ethidium bromide to a DNA triple helix. Evidence for intercalation. J Biol Chem. 1991 Mar 25;266(9):5417–5423. [PubMed] [Google Scholar]
- Shea R. G., Ng P., Bischofberger N. Thermal denaturation profiles and gel mobility shift analysis of oligodeoxynucleotide triplexes. Nucleic Acids Res. 1990 Aug 25;18(16):4859–4866. doi: 10.1093/nar/18.16.4859. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shindo H., Torigoe H., Sarai A. Thermodynamic and kinetic studies of DNA triplex formation of an oligohomopyrimidine and a matched duplex by filter binding assay. Biochemistry. 1993 Aug 31;32(34):8963–8969. doi: 10.1021/bi00085a030. [DOI] [PubMed] [Google Scholar]
- Singleton S. F., Dervan P. B. Equilibrium association constants for oligonucleotide-directed triple helix formation at single DNA sites: linkage to cation valence and concentration. Biochemistry. 1993 Dec 7;32(48):13171–13179. doi: 10.1021/bi00211a028. [DOI] [PubMed] [Google Scholar]
- Tanha J., Lee J. S. Thermodynamic analysis of monoclonal antibody binding to duplex DNA. Nucleic Acids Res. 1997 Apr 1;25(7):1442–1449. doi: 10.1093/nar/25.7.1442. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xodo L. E., Manzini G., Quadrifoglio F. Spectroscopic and calorimetric investigation on the DNA triplex formed by d(CTCTTCTTTCTTTTCTTTCTTCTC) and d(GAGAAGAAAGA) at acidic pH. Nucleic Acids Res. 1990 Jun 25;18(12):3557–3564. doi: 10.1093/nar/18.12.3557. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang M., Ghosh S. S., Millar D. P. Direct measurement of thermodynamic and kinetic parameters of DNA triple helix formation by fluorescence spectroscopy. Biochemistry. 1994 Dec 27;33(51):15329–15337. doi: 10.1021/bi00255a014. [DOI] [PubMed] [Google Scholar]