A molecular beacon strategy for the thermodynamic characterization of triplex DNA: Triplex formation at the promoter region of cyclin D1

被引:36
作者
Antony, T
Thomas, T
Sigal, LH
Shirahata, A
Thomas, TJ
机构
[1] UMDNJ, Robert Wood Johnson Med Sch, Dept Med, New Brunswick, NJ 08903 USA
[2] UMDNJ, Robert Wood Johnson Med Sch, Dept Environm & Community Med, New Brunswick, NJ 08903 USA
[3] UMDNJ, Robert Wood Johnson Med Sch, Dept Pediat, New Brunswick, NJ 08903 USA
[4] UMDNJ, Robert Wood Johnson Med Sch, Dept Mol Genet & Microbiol, New Brunswick, NJ 08903 USA
[5] UMDNJ, Robert Wood Johnson Med Sch, Canc Inst New Jersey, New Brunswick, NJ 08903 USA
[6] UMDNJ, Robert Wood Johnson Med Sch, Environm & Occupat Hlth Sci Inst, New Brunswick, NJ 08903 USA
[7] Josai Univ, Fac Pharmaceut Sci, Sakado, Saitama 35002, Japan
关键词
D O I
10.1021/bi010397z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We studied the formation of triplex DNA in the purine-pyrimidine-rich promoter site sequence of cyclin Dl, located at -116 to -99 from the transcription initiation site, with a molecular beacon comprised of a G-rich 18-mer triplex forming oligodeoxyribonucleotide. Formation of triplex DNA was monitored by enhanced fluorescence of the beacon, due to the weakening of fluorescence energy transfer, upon its binding to the target duplex. Electrophoretic mobility shift assay confirmed triplex DNA formation by these oligonucleotides. In low salt buffer (10 mM Na+), triplex DNA formation was not observed in the absence of a ligand such as spermine. At room temperature (22 degreesC), the equilibrium association constant (Ka) calculated in the presence of 1 muM spermine and 10 mM Na+ was 3.2 x 10(8) M-1. The K-a value was 1.0 x 10(9) M-1 in the presence of 150 mM Na+, and it increased by 10-fold by the addition of 1 mM spermine. DeltaH, DeltaS, and DeltaG of triplex DNA formation, calculated from the temperature dependence of K-a in the range of 20-45 degreesC, were -35.9 kcal/mol, -77 cal/(mol.K), and -13 kcal/mol, respectively, in the presence of 150 mM NaCl. The corresponding values were -52.9 kcal/mol, -132.5 cal/(mol.K), and -13.4 kcal/mol in the presence of 150 mM NaCl and 1 mM spermine. Structurally related polyamines exerted different degrees of triplex DNA stabilization, as determined by binding constant measurements. Comparison of spermine versus hexamine showed a 17-fold increase in the equilibrium association constant, whereas bis(ethyl) derivatization lead to a 4-fold decrease of this value. In the absence of added duplex and polyamines, the molecular beacon dissociated with a melting temperature of 67 degreesC. Thermodynamic parameters of beacon melting were calculated from the melting curve, and the DeltaH, DeltaS, and DeltaG values were 37.8 kcal/mol, 112 cal/(mol.K), and 4.4 kcal/mol, respectively. These results demonstrate that molecular beacons can be used for the direct determination of the equilibrium association constants and thermodynamic parameters of triplex DNA formation in the presence of ligands such as polyamines.
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页码:9387 / 9395
页数:9
相关论文
共 56 条
[1]   Antisense therapeutics [J].
Agrawal, S ;
Zhao, QY .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (04) :519-528
[2]   Thermodynamic and kinetic studies of the formation of triple helices between purine-rich deoxyribo-oligonucleotides and the promoter region of the human c-src proto-oncogene [J].
Aich, P ;
Ritchie, S ;
Bonham, K ;
Lee, JS .
NUCLEIC ACIDS RESEARCH, 1998, 26 (18) :4173-4177
[3]   The role of polyamines, Na+ and K+ in the formation of triple helices between purine oligonucleotides and the promoter region of the human c-src proto-oncogene [J].
Aich, P ;
Thomas, TJ ;
Lee, JS .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12) :2307-2310
[4]   Selectivity of spermine homologs on tripler DNA stabilization [J].
Antony, T ;
Thomas, T ;
Shirahata, A ;
Sigal, LH ;
Thomas, TJ .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1999, 9 (02) :221-231
[5]   Overexpression of cyclin D1 occurs in both squamous carcinomas and adenocarcinomas of the esophagus and in adenocarcinomas of the stomach [J].
Arber, N ;
Gammon, MD ;
Hibshoosh, H ;
Britton, JA ;
Zhang, Y ;
Schonberg, JB ;
Roterdam, H ;
Fabian, I ;
Holt, PR ;
Weinstein, IB .
HUMAN PATHOLOGY, 1999, 30 (09) :1087-1092
[6]  
Bloomfield V. A., 2000, NUCL ACIDS STRUCTURE
[7]   Thermodynamic basis of the enhanced specificity of structured DNA probes [J].
Bonnet, G ;
Tyagi, S ;
Libchaber, A ;
Kramer, FR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6171-6176
[8]   ENTHALPY ENTROPY COMPENSATIONS IN DRUG DNA-BINDING STUDIES [J].
BRESLAUER, KJ ;
REMETA, DP ;
CHOU, WY ;
FERRANTE, R ;
CURRY, J ;
ZAUNCZKOWSKI, D ;
SNYDER, JG ;
MARKY, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :8922-8926
[9]   DNA melting investigated by differential scanning calorimetry and Raman spectroscopy [J].
Duguid, JG ;
Bloomfield, VA ;
Benevides, JM ;
Thomas, GJ .
BIOPHYSICAL JOURNAL, 1996, 71 (06) :3350-3360
[10]   WIN SOME, LOSE SOME - ENTHALPY-ENTROPY COMPENSATION IN WEAK INTERMOLECULAR INTERACTIONS [J].
DUNITZ, JD .
CHEMISTRY & BIOLOGY, 1995, 2 (11) :709-712