The effect of single base-pair mismatches on the duplex stability of d(T-A-T-T-A-A-T-A-T-C-A-A-G-T-T-G) . d(C-A-A-C-T-T-G-A-T-A-T-T-A-A-T-A).

The stabilitye and dynamics of the duplex d(T-A-T-T-A-A--T-A-T-C-A-A-G-T-T-G) . d(C-A-A-C-T-T-G-A-T-A-T-T-A-A-T-A) has been studied by means of ultraviolet-melting, temperature-jump relaxation kinetics, stopped-flow and NMR spectroscopy. In addition, the influence of the mismatches A . A, G . T, A .C and T . C,-incorporated in this double helix through the introduction of non-complementary bases in the second strand, on these parameters has been investigated. The thermodynamic parameters characterizing the melting of the duplexes have been determined. Interestingly, a substantial decrease was observed for the values of the melting enthalpy when proceeding from 0.015 M to 0.1 M NaCl solutions. All duplexes that contain mismatches have melting temperatures below that of the totally complementary double helix. On the basis of NMR experiments and differences in the free enthalpy values between the totally complementary double helix and the duplexes with mismatches, it could be concluded that some degree of stacking of the two mispaired bases between the neighbouring base pairs is maintained. At 1 M NaCl the enthalpy and entropy of the helix-to-coil transition of the totally complementary double helix are in good agreement with values calculated on the basis of the thermodynamic data of Borer et al. [Borer, Ph. N., Dengler, B. & Tinoco, I. (1974) J. Mol. Biol. 86, 843--853] which were derived for RNA. The kinetics of the complementary duplex and duplexes with G . T and A . C mismatches were studied by means of stopped-flow and temperature-jump techniques. The rate constants of formation are the same for the three double helices. The decrease in stability of the duplexes with mismatches is therefore entirely due to an increase of the dissociation constant. In temperature-jump experiments very often a fast relaxation process is observed in addition to the relaxation characterizing the disruption of the double helix. This fast relaxation process is customarily attributed to base destacking in the single helix. By combining temperature-jump relaxation kinetics with NMR melting experiments, it is shown that at the low temperature side of the melting transition this fast relaxation process is caused by rapid changes in the double-helical structure.

[1]  C. W. Hilbers,et al.  Effective water resonance suppression in 1D- and 2D-FT-1H-NMR spectroscopy of biopolymers in aqueous solution. , 1983, Biopolymers.

[2]  K. Breslauer,et al.  Salt‐dependent conformational transitions in the self‐complementary deoxydodecanucleotide d(CGCAATTCGCG): Evidence for hairpin formation , 1983, Biopolymers.

[3]  K. Breslauer,et al.  Calorimetric determination of base‐stacking enthalpies in double‐helical DNA molecules , 1982, Biopolymers.

[4]  D. Patel,et al.  DNA conformation, dynamics, and interactions in solution. , 1982, Science.

[5]  D. Patel,et al.  Extra adenosine stacks into the self-complementary d(CGCAGAATTCGCG) duplex in solution. , 1982, Biochemistry.

[6]  D. Patel,et al.  Premelting and melting transitions in the d(CGCGAATTCGCG) self-complementary duplex in solution. , 1982, Biochemistry.

[7]  D. Patel,et al.  Structure and energetics of a hexanucleotide duplex with stacked trinucleotide ends formed by the sequence d(GAATTCGCG). , 1982, Biochemistry.

[8]  D. Patel,et al.  Structure, dynamics, and energetics of deoxyguanosine . thymidine wobble base pair formation in the self-complementary d(CGTGAATTCGCG) duplex in solution. , 1982, Biochemistry.

[9]  G. A. van der Marel,et al.  Construction of viable and lethal mutations in the origin of bacteriophage 'phi' X174 using synthetic oligodeoxyribonucleotides. , 1981, Journal of molecular biology.

[10]  H. Heus,et al.  Destabilization of secondary structure in 16S ribosomal RNA by dimethylation of two adjacent adenosines. , 1981, Nucleic acids research.

[11]  I. Tinoco,et al.  Comparative study of ribonucleotides, deoxyribonucleotides, and hybrid oligonucleotide helixes by nuclear magnetic resonance , 1981 .

[12]  James Feeney,et al.  Data shift accumulation and alternate delay accumulation techniques for overcoming the dynamic range problem , 1980 .

[13]  J. Shaffer,et al.  Hybridization of synthetic oligodeoxyribonucleotides to ΦX 174 DNA: the effect of single base pair mismatch , 1979 .

[14]  J. H. Boom,et al.  2,2,2-Tribromoethyl 2-Chloro-4-t-butylphenyl Phosphorochloridate: A Convenient Phosphorylating Agent for the Synthesis of DNA-Fragments by the Phosphotriester Approach , 1979 .

[15]  P. Weisbeek,et al.  Nucleotide sequence of the origin of replication in bacteriophage ΦX174 RF DNA , 1978, Nature.

[16]  J. Hurwitz,et al.  Role of DNA gyrase in phiX replicative-form replication in vitro. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[17]  I. Tinoco,et al.  Calorimetric and spectroscopic investigation of the helix-to-coil transition of a ribo-oligonucleotide: rA7U7. , 1975, Journal of molecular biology.

[18]  A. Redfield,et al.  Dynamic range in Fourier transform proton magnetic resonance , 1975 .

[19]  D. Patel,et al.  Proton nuclear magnetic resonance investigations of fraying in double-stranded d-ApTpGpCpApT in aqueous solution , 1975 .

[20]  D. Crothers,et al.  The molecular mechanism of thermal unfolding of Escherichia coli formylmethionine transfer RNA. , 1974, Journal of molecular biology.

[21]  I. Tinoco,et al.  Stability of ribonucleic acid double-stranded helices. , 1974, Journal of molecular biology.

[22]  D. Crothers,et al.  Improved estimation of secondary structure in ribonucleic acids. , 1973, Nature: New biology.

[23]  D. Crothers,et al.  Free energy of imperfect nucleic acid helices. 3. Small internal loops resulting from mismatches. , 1973, Journal of molecular biology.

[24]  O. Uhlenbeck,et al.  Thermodynamics and kinetics of the helix‐coil transition of oligomers containing GC base pairs , 1973 .

[25]  D M Crothers,et al.  Relaxation kinetics of dimer formation by self complementary oligonucleotides. , 1971, Journal of molecular biology.

[26]  R. L. Baldwin,et al.  Helix formation by d(TA) oligomers. 3. Electrostatic effects. , 1970, Journal of molecular biology.

[27]  S. Lifson,et al.  Dependence of the melting temperature of DNA on salt concentration , 1965, Biopolymers.

[28]  R. Shulman Biological applications of magnetic resonance , 1979 .

[29]  C. W. Hilbers HYDROGEN-BONDED PROTON EXCHANGE AND ITS EFFECT ON NMR SPECTRA OF NUCLEIC ACIDS , 1979 .

[30]  D. Crothers,et al.  Thermodynamic and kinetic properties of short RNA helices: the oligomer sequence AnGCUn. , 1974, Nucleic acids research.