Literature DB >> 3964658

Structural studies of the O6meG.C interaction in the d(C-G-C-G-A-A-T-T-C-O6meG-C-G) duplex.

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

Abstract

One- and two-dimensional nuclear magnetic resonance (NMR) experiments have been undertaken to investigate the conformation of the d(C1-G2-C3-G4-A5-A6-T7-T8-C9-O6meG10-C11-G12) self-complementary dodecanucleotide (henceforth called O6meG.C 12-mer), which contains C3.O6meG10 interactions in the interior of the helix. We observe intact base pairs at G2.C11 and G4.C9 on either side of the modification site at low temperature though these base pairs are kinetically destabilized in the O6meG.C 12-mer duplex compared to the G.C 12-mer duplex. One-dimensional nuclear Overhauser effects (NOEs) on the exchangeable imino protons demonstrate that the C3 and O6meG10 bases are stacked into the helix and act as spacers between the flanking G2.C11 and G4.C9 base pairs. The nonexchangeable base and H1', H2', H2'', H3', and H4' protons have been completely assigned in the O6meG.C 12-mer duplex at 25 degrees C by two-dimensional correlated (COSY) and nuclear Overhauser effect (NOESY) experiments. The observed NOEs and their directionality demonstrate that the O6meG.C 12-mer is a right-handed helix in which the O6meG10 and C3 bases maintain their anti conformation about the glycosidic bond at the modification site. The NOEs between the H8 of O6meG10 and the sugar protons of O6meG10 and adjacent C9 exhibit an altered pattern indicative of a small conformational change from a regular duplex in the C9-O6meG10 step of the O6meG.C 12-mer duplex. We propose a pairing scheme for the C3.O6meG10 interaction at the modification site. Three phosphorus resonances are shifted to low field of the normal spectral dispersion in the O6meG.C 12-mer phosphorus spectrum at low temperature, indicative of an altered phosphodiester backbone at the modification site. These NMR results are compared with the corresponding parameters in the G.C 12-mer, which contains Watson-Crick base pairs at the same position in the helix.

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Year:  1986        PMID: 3964658     DOI: 10.1021/bi00353a012

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  24 in total

1.  Replication past O(6)-methylguanine by yeast and human DNA polymerase eta.

Authors:  L Haracska; S Prakash; L Prakash
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

2.  High-resolution structure of a mutagenic lesion in DNA.

Authors:  G A Leonard; J Thomson; W P Watson; T Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

3.  Exploring the roles of nucleobase desolvation and shape complementarity during the misreplication of O(6)-methylguanine.

Authors:  Delia Chavarria; Andrea Ramos-Serrano; Ichiro Hirao; Anthony J Berdis
Journal:  J Mol Biol       Date:  2011-07-23       Impact factor: 5.469

4.  The structural basis for the mutagenicity of O(6)-methyl-guanine lesions.

Authors:  Joshua J Warren; Lawrence J Forsberg; Lorena S Beese
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-18       Impact factor: 11.205

5.  Evidence from in vitro replication that O6-methylguanine can adopt multiple conformations.

Authors:  M K Dosanjh; E L Loechler; B Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

6.  Accuracy of lesion bypass by yeast and human DNA polymerase eta.

Authors:  M T Washington; R E Johnson; L Prakash; S Prakash
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

7.  Structural basis for proficient incorporation of dTTP opposite O6-methylguanine by human DNA polymerase iota.

Authors:  Matthew G Pence; Jeong-Yun Choi; Martin Egli; F Peter Guengerich
Journal:  J Biol Chem       Date:  2010-10-20       Impact factor: 5.157

8.  Structure of the hydrogen bonding complex of O6-methylguanine with cytosine and thymine during DNA replication.

Authors:  T E Spratt; D E Levy
Journal:  Nucleic Acids Res       Date:  1997-08-15       Impact factor: 16.971

9.  Alkyl phosphotriester modified oligodeoxyribonucleotides. VI. NMR and UV spectroscopic studies of ethyl phosphotriester (Et) modified Rp-Rp and Sp-Sp duplexes, (d[GGAA(Et)TTCC])2.

Authors:  M F Summers; C Powell; W Egan; R A Byrd; W D Wilson; G Zon
Journal:  Nucleic Acids Res       Date:  1986-09-25       Impact factor: 16.971

10.  Protonated base pairs explain the ambiguous pairing properties of O6-methylguanine.

Authors:  L D Williams; B R Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

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