Temperature‐Gradient gel electrophoresis of nucleic acids: Analysis of conformational transitions, sequence variations, and protein‐nucleic acid interactions

Temperature‐gradient gel electrophoresis (TGGE) is applied to analyze conformational transitions and sequence variations of nucleic acids and protein‐nucleic acid interactions. A linear and highly reproducible temperature‐gradient is established perpendicular or parallel to the direction of the electrophoresis. The instrument consists of an electrically insulated metal plate, which is heated at one edge and cooled at the other edge by two thermostating baths and is used as an ancillary device for commercial horizontal gel electrophoresis instruments. Biopolymers are separated in TGGE according to size, shape and thermal stability of their conformational transitions. If the temperature‐gradient is established perpendicular to the electrophoresis, monomolecular conformational transitions of nucleic acids show up as continuous transition curves; strand‐separation leads to discontinuous transitions. In the studies on viroid RNA it was shown that natural circular viroid RNA undergoes one highly cooperative transition detected by TGGE as a drastic retardation in mobility. Oligomeric replication intermediates of viroids exhibit coexisting structures which could not be detected by any other technique. Double‐stranded satellite RNA from cucumber mosaic virus is a mixture of sequence variants, all of which have the identical length of 335 nucleotides. In TGGE six different strains were resolved. Sequence variants of viroids were analyzed by hybridizing viroid RNA to (–)strand viroid RNA transcripts from viroid cDNA clones. Sequence variations lead to mismatches in the double strands and thereby to a shift of the transition curve to lower temperature. Mutations in plasmids, particularly in cloned inserts, were detected by mixing plasmids of two different clones, linearizing, denaturing, renaturing, and searching for shifts in the transition curves, which are generated by mismatch‐formation during the renaturation of (+)‐ and (−)strands from different clones. Examples are given for different viroid clones and HIV‐clones from one and the same patient. In another example, clones with point mutations from site‐directed mutagenesis are analyzed and selected by TGGE. TGGE is also applied to study the effect of amino acid exchanges in the Tet repressor from E. coli on the thermal stability of the represser and on the mode of binding of the repressor to the operator DNA. The results are discussed under the aspect that TGGE may be applied as routine analytical laboratory procedure.

[1]  E. Helm,et al.  Isolation frequency and growth properties of HIV‐variants: Multiple simultaneous variants in a patient demonstrated by molecular cloning , 1987, Journal of medical virology.

[2]  D. Riesner,et al.  Temperature-gradient gel electrophoresis. Thermodynamic analysis of nucleic acids and proteins in purified form and in cellular extracts. , 1987, Biophysical chemistry.

[3]  D. Riesner Physical-Chemical Properties , 1987 .

[4]  D. Crothers,et al.  Free energy of imperfect nucleic acid helices. II. Small hairpin loops. , 1973, Journal of molecular biology.

[5]  Lynn C. Klotz,et al.  A New Spectroscopic Approach to the Determination of Helical Secondary Structure in Ribonucleic Acids , 1963 .

[6]  L. Adams,et al.  Ultrasensitive silver‐based color staining of polypeptides in polyacrylamide gels , 1981 .

[7]  D Riesner,et al.  Mismatches in DNA double strands: thermodynamic parameters and their correlation to repair efficiencies. , 1986, Nucleic acids research.

[8]  H. Domdey,et al.  Nucleotide sequence and secondary structure of potato spindle tuber viroid , 1978, Nature.

[9]  J. Visvader,et al.  Eleven new sequence variants of citrus exocortis viroid and the correlation of sequence with pathogenicity. , 1985, Nucleic acids research.

[10]  R. Myers,et al.  Recent advances in the development of methods for detecting single-base substitutions associated with human genetic diseases. , 1986, Cold Spring Harbor symposia on quantitative biology.

[11]  N. Davidson,et al.  Rates of formation and thermal stabilities of RNA:DNA and DNA:DNA duplexes at high concentrations of formamide. , 1977, Nucleic acids research.

[12]  E. Grinfeld,et al.  Searching for gene defects by denaturing gradient gel electrophoresis. , 1986, Cold Spring Harbor symposia on quantitative biology.

[13]  W. Hillen,et al.  Engineered Tet repressor mutants with single tryptophan residues as fluorescent probes. Solvent accessibilities of DNA and inducer binding sites and interaction with tetracycline. , 1987, The Journal of biological chemistry.

[14]  R. Korneluk,et al.  Rapid and reliable dideoxy sequencing of double-stranded DNA. , 1985, Gene.

[15]  D. Riesner,et al.  Conversion of circular viroid molecules to linear strands , 1979 .

[16]  Michael Zuker,et al.  Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information , 1981, Nucleic Acids Res..

[17]  J. Parvin,et al.  Detection of single base substitutions in influenza virus RNA molecules by denaturing gradient gel electrophoresis of RNA-RNA or DNA-RNA heteroduplexes. , 1986, Virology.

[18]  H. Klump,et al.  Calorimetric measurements of the transition enthalpy of DNA in aqueous urea solutions. , 1977, Biochimica et biophysica acta.

[19]  D. Turner,et al.  Improved free-energy parameters for predictions of RNA duplex stability. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[20]  J. J. Salvo,et al.  A simple and efficient procedure for saturation mutagenesis using mixed oligodeoxynucleotides. , 1986, Gene.

[21]  T. Creighton Electrophoretic analysis of the unfolding of proteins by urea. , 1979, Journal of molecular biology.

[22]  G. Steger,et al.  Helix-coil transitions in double-stranded viral RNA. Fine resolution melting and ionic strength dependence. , 1980, Biochimica et biophysica acta.

[23]  Gerhard Steger,et al.  Double-stranded cucumovirus associated RNA 5: experimental analysis of necrogenic and non-necrogenic variants by temperature-gradient gel electrophore sis , 1987, Nucleic Acids Res..

[24]  D. Smith,et al.  Nucleotide sequence of a full-length infectious clone of the Indonesian strain of tomato apical stunt viroid (TASV). , 1987, Nucleic acids research.

[25]  Thomas A. Kunkel,et al.  Rapid and efficient site-specific mutagenesis without phenotypic selection. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[26]  C. Gatz,et al.  Control of expression of the Tn10-encoded tetracycline resistance operon. II. Interaction of RNA polymerase and TET repressor with the tet operon regulatory region. , 1984, Journal of molecular biology.

[27]  A. van Kammen,et al.  Molecular cloning and characterization of a complete DNA copy of potato spindle tuber viroid RNA. , 1982, Nucleic acids research.

[28]  R. Owens,et al.  Mutational analysis of potato spindle tuber viroid reveals complex relationships between structure and infectivity. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Gerhard Steger,et al.  Double-stranded cucumovirus associated RNA 5: which sequence variations may be detected by optical melting and temperature-gradient gel electrophoresis? , 1987, Nucleic Acids Res..

[30]  W. Hillen,et al.  Tryptophan in alpha-helix 3 of Tet repressor forms a sequence-specific contact with tet operator in solution. , 1987, The Journal of biological chemistry.

[31]  Homer Jacobson,et al.  Intramolecular Reaction in Polycondensations. I. The Theory of Linear Systems , 1950 .

[32]  D. Poland,et al.  Recursion relation generation of probability profiles for specific‐sequence macromolecules with long‐range correlations , 1974, Biopolymers.

[33]  R. Owens,et al.  Structural similarities between viroids and transposable genetic elements. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[34]  D. Thatcher,et al.  Denaturation of proteins and nucleic acids by thermal-gradient electrophoresis. , 1981, The Biochemical journal.

[35]  L. Lerman,et al.  Sequence-determined DNA separations. , 1984, Annual review of biophysics and bioengineering.

[36]  H. Hofmann,et al.  Correlation between structure and pathogenicity of potato spindle tuber viroid (PSTV) , 1985, The EMBO journal.

[37]  A. Suyama,et al.  Local stability of DNA and RNA secondary structure and its relation to biological functions. , 1986, Progress in biophysics and molecular biology.

[38]  D. Riesner,et al.  Fine structure melting of viroids as studied by kinetic methods. , 1979, Nucleic acids research.

[39]  S. Coutts Thermodynamics and kinetics of G-C base pairing in the isolated extra arm of serine-specific transfer RNA from yeast. , 1971, Biochimica et biophysica acta.

[40]  R. Jaenicke,et al.  [12]Refolding and association of oligomeric proteins , 1986 .

[41]  R. Nussinov,et al.  Fast algorithm for predicting the secondary structure of single-stranded RNA. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[42]  G. Steger,et al.  Conformational transitions in viroids and virusoids: comparison of results from energy minimization algorithm and from experimental data. , 1984, Journal of biomolecular structure & dynamics.

[43]  J. Kaper,et al.  Cucumber mosaic virus-associated RNA 5. V. Extensive nucleotide sequence homology among CARNA 5 preparations of different CMV strains. , 1978, Virology.

[44]  G. Shaw,et al.  Molecular cloning and characterization of the HTLV-III virus associated with AIDS , 1984, Nature.

[45]  D. Riesner,et al.  Diagnostic Procedure for Detection of Viroids and Viruses with Circular RNAs by “Return”–Gel Electrophoresis , 1986 .

[46]  G. Steger,et al.  Analysis of RNA structures by temperature-gradient gel electrophoresis: viroid replication and processing. , 1988, Gene.

[47]  W. Hillen,et al.  Thermal denaturation of engineered tet repressor proteins and their complexes with tet operator and tetracycline studied by temperature gradient gel electrophoresis. , 1988, Analytical biochemistry.