Literature DB >> 3211742

Sequence-specific recognition of the major groove of DNA by oligodeoxynucleotides via triple helix formation. Footprinting studies.

J C François1, T Saison-Behmoaras, C Hélène.   

Abstract

Homopyrimidine oligodeoxynucleotides recognize the major groove of the DNA double helix at homopurine.homopyrimidine sequences by forming local triple helices. The oligonucleotide is bound parallel to the homopurine strand of the duplex. This binding can be revealed by a footprinting technique using copper-phenanthroline as a cleaving reagent. Oligonucleotide binding in the major groove prevents cleavage by copper-phenanthroline. The cleavage patterns on opposite strands of the duplex at the boundaries of the triple helix are asymmetric. They are shifted to the 3'-side, indicating that the copper-phenanthroline chelate binds in the minor groove of the duplex structure. Binding of the chelate at the junction between the triple and the double helix is not perturbed on the 5'-side of the bound homopyrimidine oligonucleotide. In contrast, a strong enhancement of cleavage is observed on the purine-containing strand at the triplex-duplex junction on the 3'-side of the homopyrimidine oligonucleotide.

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Year:  1988        PMID: 3211742      PMCID: PMC339056          DOI: 10.1093/nar/16.24.11431

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  25 in total

1.  DNAse footprinting: a simple method for the detection of protein-DNA binding specificity.

Authors:  D J Galas; A Schmitz
Journal:  Nucleic Acids Res       Date:  1978-09       Impact factor: 16.971

2.  [Interaction of ethidium hydrobromate (EH) with polyribonucleotides. Applications to the study of hybridization reactions].

Authors:  J B Le Pecq; C Paoletti
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1965-06-28

3.  RNA polymerase nascent product analysis.

Authors:  M Takanami
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

4.  Visualization of drug--nucleic acid interactions at atomic resolution. VI. Structure of two drug--dinucleoside monophosphate crystalline complexes, ellipticine--5-iodocytidylyy (3'-5') guanosine and 3,5,6,8-tetramethyl-N-methyl phenanthrolinium--5-iodocytidylyl (3'-5') guanosine.

Authors:  S C Jain; K K Bhandary; H M Sobell
Journal:  J Mol Biol       Date:  1979-12-25       Impact factor: 5.469

Review 5.  Interactions between functional groups in protein-nucleic acid associations.

Authors:  C Hélène; G Lancelot
Journal:  Prog Biophys Mol Biol       Date:  1982       Impact factor: 3.667

6.  Nuclease activity of 1,10-phenanthroline-copper ion. Conformational analysis and footprinting of the lac operon.

Authors:  A Spassky; D S Sigman
Journal:  Biochemistry       Date:  1985-12-31       Impact factor: 3.162

7.  Structures for the polynucleotide complexes poly(dA) with poly (dT) and poly(dT) with poly(dA) with poly (dT).

Authors:  S Arnott; E Selsing
Journal:  J Mol Biol       Date:  1974-09-15       Impact factor: 5.469

8.  Secondary structure specificity of the nuclease activity of the 1,10-phenanthroline-copper complex.

Authors:  L E Pope; D S Sigman
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

9.  Map of distamycin, netropsin, and actinomycin binding sites on heterogeneous DNA: DNA cleavage-inhibition patterns with methidiumpropyl-EDTA.Fe(II).

Authors:  M W Van Dyke; R P Hertzberg; P B Dervan
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

10.  Equilibrium studies of ethidium--polynucleotide interactions.

Authors:  J L Bresloff; D M Crothers
Journal:  Biochemistry       Date:  1981-06-09       Impact factor: 3.162

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  35 in total

1.  Sequence-specific photo-induced cross-linking of the two strands of double-helical DNA by a psoralen covalently linked to a triple helix-forming oligonucleotide.

Authors:  M Takasugi; A Guendouz; M Chassignol; J L Decout; J Lhomme; N T Thuong; C Hélène
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

2.  Photofootprinting of DNA triplexes.

Authors:  V I Lyamichev; O N Voloshin; M D Frank-Kamenetskii; V N Soyfer
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

3.  Uranyl photofootprinting of triple helical DNA.

Authors:  P E Nielsen
Journal:  Nucleic Acids Res       Date:  1992-06-11       Impact factor: 16.971

4.  DNA protein interactions at the interferon-responsive promoter elements: potential for an H-DNA conformation.

Authors:  C Roy; B Lebleu
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

5.  Triple helix formation by purine-rich oligonucleotides targeted to the human dihydrofolate reductase promoter.

Authors:  S W Blume; J E Gee; K Shrestha; D M Miller
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

6.  Inhibition of gene transcription by purine rich triplex forming oligodeoxyribonucleotides.

Authors:  C Roy
Journal:  Nucleic Acids Res       Date:  1993-06-25       Impact factor: 16.971

7.  Potassium-resistant triple helix formation and improved intracellular gene targeting by oligodeoxyribonucleotides containing 7-deazaxanthine.

Authors:  A F Faruqi; S H Krawczyk; M D Matteucci; P M Glazer
Journal:  Nucleic Acids Res       Date:  1997-02-01       Impact factor: 16.971

8.  Divalent transition metal cations counteract potassium-induced quadruplex assembly of oligo(dG) sequences.

Authors:  S W Blume; V Guarcello; W Zacharias; D M Miller
Journal:  Nucleic Acids Res       Date:  1997-02-01       Impact factor: 16.971

9.  Improved bioactivity of G-rich triplex-forming oligonucleotides containing modified guanine bases.

Authors:  Faye A Rogers; Janice A Lloyd; Meetu Kaushik Tiwari
Journal:  Artif DNA PNA XNA       Date:  2014

10.  Triple-helix formation by oligonucleotides containing the three bases thymine, cytosine, and guanine.

Authors:  C Giovannangéli; M Rougée; T Garestier; N T Thuong; C Hélène
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

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