Literature DB >> 3016288

Covalent carcinogenic O6-methylguanosine lesions in DNA. Structural studies of the O6 meG X A and O6meG X G interactions in dodecanucleotide duplexes.

D J Patel, L Shapiro, S A Kozlowski, B L Gaffney, R A Jones.   

Abstract

High-resolution proton and phosphorus nuclear magnetic resonance studies are reported on the self-complementary d(C1-G2-N3-G4-A5-A6-T7-T8-C9-O6meG10-C11-G12) duplexes (henceforth called O6meG X A 12-mer when N3 = A3 and O6meG X G 12-mer when N3 = G3), which contain symmetry-related A3 X O6meG10 and G3 X O6meG10 interactions in the interior of the helices. We observe inter-base-pair nuclear Overhauser effects (NOE) between the base protons at the N3 X O6meG10 modification site and protons of flanking G2 X C11 and G4 X C9 base-pairs, indicative of the stacking of N3 and O6meG10 bases in both O6meG X A 12-mer and O6meG X G 12-mer duplexes. We have assigned all the base and a majority of the sugar protons from two-dimensional proton-correlated and nuclear Overhauser effect experiments on the O6meG X A 12-mer duplex and O6meG X G 12-mer duplex in solution. The observed NOEs establish that the A3 and O6meG10 at the modification site and all other residues adopt the anti configuration about the glycosidic bond, and that the O6meG X A 12-mer forms a right-handed duplex. The interaction between the bulky purine A3 and O6meG10 residues in the anti orientation results in large proton chemical shift perturbations at the (G2-A3-G4) X (C9-O6meG10-C11) segments of the helix. By contrast, we demonstrate that the O6meG10 residue adopts a syn configuration, while all other bases adopt an anti configuration about the glycosidic bond in the right-handed O6meG X G 12-mer duplex. This results in altered NOE patterns between the base protons of O6meG10 and the base and sugar protons of flanking C9 and C11 residues in the O6meG X G 12-mer duplex. The phosphorus backbone is perturbed at the modification site in both duplexes, since the phosphorus resonances are dispersed over 2 parts per million in the O6meG X A 12-mer and over 1 part per million in the O6meG X G 12-mer compared to a 0.5 part per million dispersion for an unperturbed DNA helix. We propose tentative pairing schemes for the A3 X O6meG10 and G3 X O6meG10 interactions in the above dodecanucleotide duplexes.

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Year:  1986        PMID: 3016288     DOI: 10.1016/s0022-2836(86)80014-6

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  8 in total

1.  Two-dimensional NMR investigation of a bent DNA fragment: assignment of the proton resonances and preliminary structure analysis.

Authors:  A Kintanar; R E Klevit; B R Reid
Journal:  Nucleic Acids Res       Date:  1987-07-24       Impact factor: 16.971

2.  One- and two-dimensional NMR studies on the conformation of DNA containing the oligo(dA)oligo(dT) tract.

Authors:  M Katahira; H Sugeta; Y Kyogoku; S Fujii; R Fujisawa; K Tomita
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

3.  Free Energy Landscape and Conformational Kinetics of Hoogsteen Base Pairing in DNA vs. RNA.

Authors:  Dhiman Ray; Ioan Andricioaei
Journal:  Biophys J       Date:  2020-09-02       Impact factor: 4.033

4.  DNA alkylation repair limits spontaneous base substitution mutations in Escherichia coli.

Authors:  W J Mackay; S Han; L D Samson
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

5.  A historical account of Hoogsteen base-pairs in duplex DNA.

Authors:  Evgenia N Nikolova; Huiqing Zhou; Federico L Gottardo; Heidi S Alvey; Isaac J Kimsey; Hashim M Al-Hashimi
Journal:  Biopolymers       Date:  2013-12       Impact factor: 2.505

6.  Structural characterization of a 2:1 distamycin A.d(CGCAAATTGGC) complex by two-dimensional NMR.

Authors:  J G Pelton; D E Wemmer
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

7.  Alternative pathways for the in vivo repair of O6-alkylguanine and O4-alkylthymine in Escherichia coli: the adaptive response and nucleotide excision repair.

Authors:  L Samson; J Thomale; M F Rajewsky
Journal:  EMBO J       Date:  1988-07       Impact factor: 11.598

8.  Metal-dependent conformational activation explains highly promutagenic replication across O6-methylguanine by human DNA polymerase β.

Authors:  Myong-Chul Koag; Seongmin Lee
Journal:  J Am Chem Soc       Date:  2014-04-02       Impact factor: 15.419

  8 in total

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