Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2001 Aug 15;29(16):3289-96.
doi: 10.1093/nar/29.16.3289.

Thermodynamic stability of base pairs between 2-hydroxyadenine and incoming nucleotides as a determinant of nucleotide incorporation specificity during replication

Affiliations

Thermodynamic stability of base pairs between 2-hydroxyadenine and incoming nucleotides as a determinant of nucleotide incorporation specificity during replication

J Kawakami et al. Nucleic Acids Res. .

Abstract

We investigated the thermodynamic stability of double-stranded DNAs with an oxidative DNA lesion, 2-hydroxyadenine (2-OH-Ade), in two different sequence contexts (5'-GA*C-3' and 5'-TA*A-3', A* represents 2-OH-Ade). When an A*-N pair (N, any nucleotide base) was located in the center of a duplex, the thermodynamic stabilities of the duplexes were similar for all the natural bases except A (N = T, C and G). On the other hand, for the duplexes with the A*-N pair at the end, which mimic the nucleotide incorporation step, the stabilities of the duplexes were dependent on their sequence. The order of stability is T > G > C >> A in the 5'-GA*C-3' sequences and T > A > C > G in the 5'-TA*A-3' sequences. Because T/G/C and T/A are nucleotides incorporated opposite to 2-OH-Ade in the 5'-GA*C-3' and 5'-TA*A-3' sequences, respectively, these results agree with the tendency of mutagenic misincorporation of the nucleotides opposite to 2-OH-Ade in vitro. Thus, the thermodynamic stability of the A*-N base pair may be an important factor for the mutation spectra of 2-OH-Ade.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Oligodeoxyribonucleotides with a 5′-TA*A-3′ or 5′-GA*C-3′ sequence (underlined) used in this study. X denotes A or 2-OH-Ade; N represents A, G, C or T. A particular duplex is indicated as sequence series name followed by X–N base pair as subscript, e.g. [1]A*T indicates 5′-GGAATATTAGCTGGT-3′/5′-ACCAGCTA*ATATTCC-3′.
Figure 2
Figure 2
Normalized UV melting curves. (AD) Results for duplexes [1], [2], [3] and [4] in Figure 1, respectively. Melting behavior of control duplexes having A–T base pair as X–N are shown as curves drawn by crosses. Melting curves of duplexes with A*–A, A*–G, A*–C and A*–T are drawn by open squares, filled squares, open circles and filled circles, respectively. Each oligomer concentration was 5 µM, and measurements were done in 1 M NaCl-phosphate buffer pH 7.0.
Figure 3
Figure 3
Summary of stability as ΔG°37 for all 20 model duplexes. (AD) Results for duplexes [1], [2], [3] and [4], respectively. The data are aligned by the order of –ΔG°37 value. Inset shows ΔΔG°37 values against the ΔG°37 of control duplex with A–T base pair for evaluation of the effect of trinucleotides with 2-OH-Ade.
Figure 4
Figure 4
Molecular modeling of a base pair of 2-OH-Ade and adenine in a tetranucleotide model of AT closing 5′-TA*A-3′ sequence, 5′-CTA*A-3′/5′TA-3′. (A) Top view of the base pair. (B) Side view of the base pair with adjacent bases.

Similar articles

Cited by

References

    1. Wallace S.S. (1994) DNA damages processed by base excision repair: biological consequences. Int. J. Radiat. Biol., 66, 579–589. - PubMed
    1. Kasai H. and Nishimura,S. (1991) Formation of 8-hydroxydeoxyguanosine in DNA by oxygen radicals and its biological significance. In Sies,H. (ed.), Oxidative Stress: Oxidants and Antioxidants. Academic Press, San Diego, CA, pp. 99–116.
    1. Kamiya H., Miura,K., Ishikawa,H., Inoue,H., Nishimura,S. and Ohtsuka,E. (1992) c-Ha-ras containing 8-hydroxyguanine at codon 12 induces point mutations at the modified and adjacent positions. Cancer Res., 52, 3483–3485. - PubMed
    1. Kamiya H., Murata-Kamiya,N., Koizume,S., Inoue,H., Nishimura,S. and Ohtsuka,E. (1995) 8-Hydroxyguanine (7,8-dihydro-8-oxoguanine) in hot spots of the c-Ha-ras gene: effects of sequence contexts on mutation spectra. Carcinogenesis, 16, 883–889. - PubMed
    1. Wagner J., Kamiya,H. and Fuchs,R.P. (1997) Leading versus lagging strand mutagenesis induced by 7,8-dihydro-8-oxo-2′-deoxyguanosine in Escherichia coli. J. Mol. Biol., 265, 302–309. - PubMed

Publication types

MeSH terms