Specificity of mutations induced by riboflavin mediated photosensitization in the supF gene of Escherichia coli

Mutation Research - Genetic Toxicology and Environmental Mutagenesis

Volumn 420, Issue 1-3, 1998, Pages 7-13

  Tano, Keizo ^a   Akasaka, Susumu ^b   Hashimoto, Mitsumasa ^a   Asano, Midori ^c   Yamamoto, Kazuo ^d   Utsumi, Hiroshi ^a   Takimoto, Koichi ^e  

^a KYOTO UNIVERSITY   (Japan)

^b OSAKA PREFECTURAL INSTITUTE OF PUBLIC HEALTH   (Japan)

^c TAIHO PHARMACEUTICAL CO LTD   (Japan)

^d TOHOKU UNIVERSITY   (Japan)

^e YAMAGUCHI UNIVERSITY   (Japan)

Author keywords

Escherichia coli; mutM; mutY; Oxidative DNA damage; Photosensitization; pUB3; Riboflavin; supF; Transversion

Indexed keywords

RIBOFLAVIN;

ARTICLE; CONTROLLED STUDY; DNA DAMAGE; ESCHERICHIA COLI; MUTATION; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; OXIDATION; PHOTOSENSITIZATION; PRIORITY JOURNAL;

BASE SEQUENCE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DNA GLYCOSYLASES; DNA, BACTERIAL; DNA-FORMAMIDOPYRIMIDINE GLYCOSYLASE; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; GENES, SUPPRESSOR; GUANINE; LIGHT; MOLECULAR SEQUENCE DATA; MUTATION; N-GLYCOSYL HYDROLASES; PHOTOSENSITIZING AGENTS; PLASMIDS; RIBOFLAVIN; RNA, TRANSFER; SEQUENCE ANALYSIS, DNA;

ESCHERICHIA COLI;

EID: 0032420607     PISSN: 13835718     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1383-5718(98)00137-5     Document Type: Article

References (33)

1. Ames B.N. Dietry carcinogens and anticarcinogens, oxygen radicals and degenerative disease. Science. 221:1983;1256-1264.
2. Wood M.L., Dizdaroglu M., Gajewski E., Essigmann J.M. Mechanistic studies of ionizing radiation and oxidative mutagenesis: genetic effects of a single 8-hydroxyguanine (7-hydro-8-oxoguanine) residue inserted at a unique site in a viral genome. Biochemistry. 29:1990;7024-7032.
3. Shibutani S., Takeshita M., Grollman A.P. Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature. 349:1991;431-434.
4. Moriya M., Ou C., Bodepudi V., Johnson F., Takeshita M., Grollman A.P. Site specific mutagenesis using a gapped duplex vector: a study of translesion synthesis past 8-oxodeoxyguanosine in E. coli. Mutation Res. 254:1991;281-288.
5. Cheng K.C., Cahill D.S., Kasai H., Nishimura S., Loeb L.A. 8-hydroxyguanine, an abundant form of oxidative DNA damage, causes G→T and A→C substitutions. J. Biol. Chem. 267:1992;166-172.
6. Yamamoto K., Uraki F., Yonei S., Yukawa O. Enzymatic repair mechanisms for base modifications induced by oxygen radicals. J. Radiat. Res. 38:1997;1-4.
7. Floyd A.R., West M.S., Eneff K.L., Schneider J.E. Methylene blue plus light mediates 8-hydroxyguanine formation in DNA. Arch. Biochem. Biophys. 273:1989;106-111.
8. Kasai H., Yamaizumi Z., Berger M., Cadet J. Photosensitized formation of 7,8-dihydro-8-oxo-2′-deoxyguanosine (8-hydroxy-2′-deoxyguanosine) in DNA by riboflavin: a non singlet oxygen mediated reaction. J. Am. Chem. Soc. 114:1992;9692-9694.
9. Bessho T., Tano K., Nishimura S., Kasai H. Induction of mutations in mouse FM3A cells by treatment with riboflavin plus visible light and its possible relation with formation of 8-hydroxyguanine (7, 8-dihydro-8- oxoguanine) in DNA. Carcinogenesis. 14:1993;1069-1071.
10. Akasaka S., Takimoto K., Yamamoto K. G:C→T:A and G:C→C:G transversions are the predominant spontaneous mutations in the Escherichia coli supF gene: an improved lacZ (am) E. coli host designed for assaying pZ189 supF mutational specificity. Mol. Gen. Genet. 235:1992;173-178.
11. Akasaka S., Yamamoto K. Mutational specificity of the ferrous ion in a supF gene of Escherichia coli. Biochem. Biophys. Res. Commun. 213:1995;74-80.
12. J.H. Miller, A Short Course in Bacterial Genetics. A Laboratory Manual and Handbook for Escherichia coli and Related Bacteria (Handbook), Cold Spring Harbor Laboratory Press, USA, 1992, pp. 6-7.
13. Rodriguez H., Snow E.T., Bhat U., Loechler E.L. An Escherichia coli plasmid-based, mutational system in which supF mutants are selectable: insertion elements dominate the spontaneous spectra. Mutation Res. 270:1992;219-231.
14. Uematsu N., Edo S., Yamamoto K. An Escherichia coli topB mutant increases deletion and frameshift mutations in the supF target gene. Mutation Res. 383:1997;223-230.
15. Bessho T., Tano K., Kasai H., Nishimura S. Deficiency of 8-hydroxyguanine DNA endonuclease activity and accumulation of the 8-hydroxyguanine in mutator mutant (mutM) of Escherichia coli. Biochem. Biophys. Res. Commun. 188:1992;372-378.
16. Chung M.H., Kasai H., Jones D.S., Inoue H., Ishikawa H., Ohtsuka E., Nishimura S. An endonuclease activity of Escherichia coli that specifically removes 8-hydroxyguanine residues from DNA. Mutation Res. 254:1991;1-12.
17. Kasai H., Crain P.F., Kuchino Y., Nishimura S., Ootsuyama A., Tanooka H. Formation of 8-hydroxyguanine moiety in cellular DNA by agents producing oxygen radicals and evidence for its repair. Carcinogenesis. 7:1986;1849-1851.
18. Takimoto K., Yamamoto K., Sagara T., Ishizaki K. Spectrum of proton-induced mutagenesis of the Escherichia coli crp gene. Mutation Res. 314:1994;1-9.
19. Giroux C.N., Mis J.R.A., Pierce M.K., Kohalmi S.E., Kunz B.A. DNA sequence analysis of spontaneous mutations in the SUP4-o gene of Saccharomyces cerevisiae. Mol. Cell. Biol. 8:1988;978-981.
20. Mori T., Tano K., Takimoto K., Utsumi H. Formation of 8-hydroxyguanine and 2,6-diamino-4-hydroxy-5-formamidopyrimidine in DNA by riboflavin mediated photosensitization. Biochem. Biophys. Res. Commun. 242:1998;98-101.
21. Boiteux A., Laval J. Imidazole open ring 7-methylguanine: an inhibitor of DNA synthesis. Biochem. Biophys. Res. Commun. 110:1983;552-558.
22. Cabrera M., Nghiem Y., Miller J.H. MutM, a second mutator locus in Escherichia coli that generates G:C→T:A transversions. J. Bacteriol. 170:1988;5405-5407.
23. Michaels M.L., Pham L., Cruz C., Miller J.H. MutM, a protein that prevents GC→TA transversions, is formamidopyrimidine-DNA glycosylase. Nucl. Acids Res. 19:1991;3629-3632.
24. Nghiem Y., Cabrera M., Cupples C.G., Miller J.H. The mutY gene: a mutator locus in Escherichia coli that generates G:C→T:A transversions. Proc. Natl. Acad. Sci. USA. 85:1988;2709-2713.
25. Tajiri T., Maki H., Sekiguchi M. Functional cooperation of MutT, MutM and MutY proteins in preventing mutations caused by spontaneous oxidation of guanine nucleotide in Escherichia coli. Mutation Res. 336:1995;257-267.
26. Michaels M.L., Cruz C., Grollman A.P., Miller J.H. Evidence that MutY and MutM combine to prevent mutations by an oxidatively damaged form of guanine in DNA. Proc. Natl. Acad. Sci. USA. 89:1992;7022-7025.
27. Michaels M.L., Tchou J., Grollman A.P., Miller J.H. A repair system for 8-oxo-7,8-dihydrodeoxyguanine. Biochemistry. 31:1992;10964-10968.
28. Takimoto K., Tachibana A., Ayaki H., Yamamoto K. Spectrum of spontaneous mutations in the cyclic AMP receptor protein gene on chromosomal DNA of Escherichia coli. J. Radiat. Res. 38:1997;27-36.
29. Akasaka S., Yamamoto K. Hydrogen peroxide induces G:C to T:A and G:C to C:G transversions in the supF gene of Escherichia coli. Mol. Gen. Genet. 243:1994;500-505.
30. Epe B., Hegler J., Wild D. Singlet oxygen as an ultimately reactive species in Salmonella typhrimurium DNA damage induced by methylene blue plus visible light. Carcinogenesis. 10:1989;2019-2024.
31. McBride T.J., Schneider J.E., Floyd R.A., Loeb L.A. Mutations induced by methylene blue plus light in single-stranded M13mp2. Proc. Natl. Acad. Sci. USA. 89:1992;6866-6870.
32. Yatagai F., Holliday J.A., Glickman B.W. Specificity of recA441-mediated (tif-1) mutational events. Mol. Gen. Genet. 230:1991;75-80.
33. Tudek B., Laval J., Boiteux S. SOS-independent mutagenesis in lacZ induced by methylene blue plus visible light. Mol. Gen. Genet. 236:1993;433-439.