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1999 | 46 | 3 |

Tytuł artykułu

Mutagenic specificity of imidazole ring-opened 7-methylpurines in M13mp 18 phage DNA

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The most abundant lesion formed in DNA upon modification with methylating agents 7-methylguanine, under alkaline conditions is converted into 2,6-diamino-4-hydroxy-5N-methyl-formamidopyrimidine (Fapy-7MeGua). We have previously shown that treatment of dimethylsulfate methylated DNA with NaOH creates mutagenic base derivatives leading to a 60-fold increase in the frequency of A-->G transitions and a 2-3-fold increase of G-->T and G-->C transversions. We have analyzed which lesions lead to these mutations. We compared mutagenic spectra in the lacZ gene of M13mp18 phage DNA modified with dimethylsulfate and NaOH after selective elimination of damaged bases from molecules used for transfection into SOS-induced E. coli. Partial elimination of Fapy-7MeGua from phage DNA performed by its digestion with formamidopyrimidine-DNA glycosylase resulted in a 2-3-fold decrease of G-->T and G-->C transversions. Selective depurination of methylated bases (9 h, 37°C, pH 7,0) resulting in almost complete loss of 7MeAde as demonstrated by HPLC analysis of (3H)MNU alkylated phage DNA used as a probe, caused a dramatic, 9-fold decrease of A-->G transitions. Alkali-catalysed rearrangement of 7MeAde was followed by HPLC analysis of (3H)MNU alkylated polyA and polydA. After incubation of these oligonucleotides in NaOH, 7MeAde disappeared from both chromatograms, but only in polyA, 2 new peaks migrating with retention time different from that of 1MeAde, 3MeAde or 7MeAde were detected, suggesting formation of two rotameric forms of Fapy-7MeAde as observed for Fapy-7MeGua. Thus the miscoding lesion, giving rise to A-->G transitions derived from 7MeAde was Fapy-7MeAde. Fapy-7MeGua was at least an order of magnitude less mutagenic, but in SOS-induced cells it gave rise to G-->T and G-->C transversions.

Wydawca

-

Rocznik

Tom

46

Numer

3

Opis fizyczny

p.785-799,fig.

Twórcy

autor
  • Polish Academy of Sciences, A.Pawinskiego 5a, 02-106 Warsaw, Poland
autor
autor

Bibliografia

  • Basu, A.K., Wood, M.L., Niedernhofer, L.J., Ramos, L.A. & Essigmann, J.M. (1993) Muta­genic and genotoxic effects of three vinyl chlo­ride-induced DNA lesions: l,A^-Etheno- adenine, S^-ethenocytosine and 4-amino-5- (imidazol-2-yl)imidazole. Biochemistry 32, 12793-12801.
  • Beranek, D.T., Weiss, C.C., Evans, F.E., Chetsanga, C.J. & Kadlubar, F.F. (1983) Identi­fication of iV5-methyl-JV5-formyl-2,5,6-tria- mino-4-hydroxypyrimidine as a major adduct in rat liver DNA after treatment with the car- cinogens, JV,jV-dimethylnitrosamine or 1,2-dimethylhydrazine. Biochem. Biophys. Res. Commun. 110, 625-631.
  • Bjelland, S. & Seeberg, E. (1996) Different effi­ciencies of the Tag and AlkA DNA glycosylases from Escherichia coli in the removal of 3-methyladenine from single-stranded DNA. FEBS Lett 397, 127-129.
  • Bodell, WJ. & Singer, B. (1979) Influence of hy­drogen bonding in DNA and polynucleotides on reaction of nitrogens and oxygens toward ethylnitrosourea. Biochemistry 18, 2860- 2863.
  • Boiteux, S., Belleney, J.f Roques, B.P. & Laval, J. (1984) Two rotameric forms of open ring 7-methylguanine are present in alkylated poly­nucleotides. Nucleic Acids Res. 12, 5429- 5439.
  • Boiteux, S., O'Connor, T.R. & Laval, J. (1987) Formamidopyrimidine-DNA glycosylase of Escherichia coli: Cloning and sequencing of the fog structural gene arid overproducing of the protein. EMBO J. 6. 3177-3183.
  • Boiteux, S., Bichara, M., Fuchs, R.PP. & Laval, J. (1989) Excision of the imidazole ring-opened form of N-2-aminofluorene-C(8)-guanine adduct in poly(dG-dC) by Escherichia coli formamidopyrimidine-DNA glycosylase. Carcinogenesis 10, 1905-1909.
  • Boiteux, S., O'Connor, T.R., Lederer, F., Gouyette, A. & Laval, J. (1990) Homogeneous Esche­richia coli FPG protein. A DNA glycosylase which excises imidazole ring-opened purines and nicks DNA at apurinic/apyrimidinic sites. J. Biol Chem. 265, 3916-3922.
  • Castaing, B., Geiger, A., Seliger, H., Nehls, P., Laval, J., Zelwer, C. & Boiteux, S. (1993) Cleav­age and binding of a DNA fragment containing a single 8-oxoguanine by wild type and mutant FPG proteins. Nucleic Acids Res. 21, 2899- 2905.
  • Cussac, C. & Laval, F. (1996) Reduction of the tox­icity and mutagenicity of aziridine in mamma­lian cells harboring the Escherichia coli fpg gene. Nucleic Acids Res. 24, 1742-1746.
  • Dizdaroglu, M. (1992) Oxidative damage to DNA in mammalian chromatin. Mutai. Res. 275, 331-342.
  • Dizdaroglu, M. (1994) Chemical determination of oxidative DNA damage by gas chromatogra- phy-mass spectrometry. Methods Enzymol. 234, 3-16.
  • Djuric, Z., Heilbrun, L.K., Reading, B.A., Broomer, A., Veleriote, F.A. & Martino, S. (1991) Effects of a low-fat diet on levels of oxi­dative damage to DNA in human peripheral nucleated blood cells. J. Natl Cancer Inst. 83, 766-769.
  • Fujita, S. & Steenken, S., (1981) Pattern of OH radical addition to uracil and methyl- and car­bon substituted uracils: Electron transfer of OH adducts with N,N,N',N' tetramethyl- phenylenediamine and tetranitromethane. J. Am. Chem. Soc. 103, 2540-2545.
  • Gill, R.D., Cussac, C., Souhami, R.L. & Laval, F. (1996) Increased resistance to N,N',N"-tn- ethylenethiophosphoramide (thiotepa) in cells expressing the Escherichia coli formamido- pyrimidine-DNA glycosylase. Cancer Res. 15, 3721-3724.
  • Grąziewicz, M.-A., Zastawny, T.H., Oliriski, R. & Tudek, B. (1999) SOS-dependent A-*G transi­tions induced by hydroxyl radical generating system hyooxanthine/xanthine oxidase/Fe+3 /EDTA are accompanied by the increase of Fapyadenine content in M13mpl8 phage DNA. MutaL Res. 434, 41-52.
  • Haines, JA, Reese, C.B. & Todd, J.L. (1962) The methylation of guanosine and related com­pounds with diazomethane. J. Chem. Soc. 5281-5288.
  • Hazra, T.K., Izumi, T., Maidt, L., Floyd, R.A. & Mitra, S. (1998) The presence of two distinct 8-oxoguanine repair enzymes in human cells: Their potential complementary roles in pre­venting mutation. Nucleic Acids Res. 26, 5116-5122.
  • Hemminki, K. (1984) Reaction of ethyleneimine with guanosine and deoxyguanosine. Chem. Biol Interact. 48, 249-260.
  • Hemminki, K. & Kallama, S. (1986) Reactions of nitrogen mustards with DNA. IARC Scu Publ. 78, 55-70.
  • Horsfall, M.J., Gordon, A.J.E., Burns, P.A., Zielenska, M., van der Vliet, G.M.E. & Glickman, B.W. (1990) Mutational specificity of alkylating agents and the influence of DNA repair. Environ. Mol Mutagen. 15, 107-122.
  • Hsieh, D.P. & Atkinson, D.N. (1991) Bisfuranoid mycotoxins: Their genotoxicity and carcinoge­nicity. Adv. Exp. Med. Biol 283, 525-532.
  • Kadlubar, F.F., Beranek, D.T., Weiss, C.C., Evans, F.E., Cox, R. & Irving, C.C. (1984) Character­ization of the purine ring-opened 7-methyl- guanine and its persistence in rat bladder epi­thelial DNA after treatment with the carcino­gen JV-methylnitrosourea. Carcinogenesis 5, 587-592.
  • Karahalil, B., Girard, P.M., Boiteux, S. & Dizdaroglu, M. (1998) Substrate specificity of the Oggl protein of Saccharomyces cerevisiae: Excision of guanine lesions produced in DNA by ionizing radiation — or hydrogen perox­ide/metal ion-generated free radicals. Nucleic Acids Res. 26, 1228-1233.
  • Kunkel, T.A. (1984) Mutational specificity of depurination. Proc. Natl Acad. Sci. U.S.A. 81, 1494-1498.
  • Lawley, P.D. & Brookes, P. (1964) Methylation of adenine in deoxyadenylic acid or deoxyribonu­cleic acid at N-7. Biochem. J. 92, 19c-20c.
  • Matijasevic, Z., Stering, A., Niu, T.Q., Aus­tin-Ritchie, D.B. & Ludlum, D. (1996) Release of sulfur mustard modified DNA bases by E. coli -methyladenine DNA glycosylase. Carcinogenesis 17, 2249-2252.
  • Messing, J. (1983) New M13 vectors for cloning. Methods Enzymol. 101, 20-78.
  • O'Connor, T.R., Boiteux, S. & Laval, J. (1988) Ring-opened 7-methylguanine residues in DNA are a block to in vitro DNA synthesis. Nur cleic Acids Res. 16, 5879-5894.
  • Sambrook, J., Fritsch, E.F. & Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual. 2nd edn., Cold Spring Laboratory Press, Cold Spring Harbour, New York.
  • Senturker, S., Auffret van der Kemp, P., You, H.J., Doetsch, P.W., Dizdaroglu, M. & Boiteux, S. (1998) Substrate specificities of the ntgl and ntg2 proteins of Saccharomyces cerevisiae for oxidized DNA bases are not identical. Nucleic Acids Res. 26, 5270-5276.
  • Singer, B. & Grunberger, D. (19S3) Molecular Biol­ogy of Mutagens and Carcinogens. Plenum Press, New York.
  • Singer, B., Sun, L. & Fraenkel-Conrat, H. (1974) Reaction of adenosine with ethylating agents. Biochemistry 23, 1913-1920.
  • Tudek, B., Boiteux, S. & Laval, J. (1992) Biological properties of imidazole ring-opened N7-me- thylguanine in Ml3mpl8 phage DNA. Nucleic Acids Res. 20, 3070-3084.
  • Tudek, B., VanZeeland, A.A., Kusmierek, J.T. & Laval, J. (1998) Activity of Escherichia coli DNA-glycosylases on DNA damaged by methyl- ating and ethylating agents and influence of 3-substituted adenine derivatives. Mutat. Res. 407, 169-186.

Typ dokumentu

Bibliografia

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