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High-resolution Structure of a Mutagenic Lesion in DNA

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Specialty Science
Date 1990 Dec 1
PMID 2263612
Citations 29
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Abstract

The self-complementary dodecanucleotide d[CGC(m6G)AATTTGCG]2 (where m6G is O6-methylguanine), which contains two m6G.T base pairs, has been analyzed by x-ray diffraction methods and the structure has been refined to a residual error of R = 0.185 at 2.0-A resolution. The m6G.T mispair closely resembles a Watson-Crick base pair and there are very few structural differences between the m6G.T duplex and the native analogue. The similarity between the m6G.T base pair and a normal G.C base pair explains the failure of mismatch repair enzymes to recognize and remove this mutagenic lesion. A series of ultraviolet melting studies over a wide pH range on a related dodecamer indicate that the m6G.C mispair can exist in two conformations; one is a wobble pair and the other is a protonated Watson-Crick pair. The former, which predominates at physiological pH, will be removed by normal proofreading and repair enzymes, whereas the latter is likely to escape detection. Hence, the occasional occurrence of the protonated m6G.C base pair may explain why the presence of m6G in genomic DNA does not always give rise to a mutation.

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References
1.
Olsson M, Lindahl T . Repair of alkylated DNA in Escherichia coli. Methyl group transfer from O6-methylguanine to a protein cysteine residue. J Biol Chem. 1980; 255(22):10569-71. View

2.
Mitra G, Pauly G, Kumar R, Pei G, Hughes S, Moschel R . Molecular analysis of O6-substituted guanine-induced mutagenesis of ras oncogenes. Proc Natl Acad Sci U S A. 1989; 86(22):8650-4. PMC: 298345. DOI: 10.1073/pnas.86.22.8650. View

3.
Miller E, Miller J . Searches for ultimate chemical carcinogens and their reactions with cellular macromolecules. Cancer. 1981; 47(10):2327-45. DOI: 10.1002/1097-0142(19810515)47:10<2327::aid-cncr2820471003>3.0.co;2-z. View

4.
Karran P, Marinus M . Mismatch correction at O6-methylguanine residues in E. coli DNA. Nature. 1982; 296(5860):868-9. DOI: 10.1038/296868a0. View

5.
Reddy E, Reynolds R, Santos E, Barbacid M . A point mutation is responsible for the acquisition of transforming properties by the T24 human bladder carcinoma oncogene. Nature. 1982; 300(5888):149-52. DOI: 10.1038/300149a0. View