Mutational spectrum of the lacI gene in Escherichia coli K12 induced by low-energy ion beam

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 602, Issue 1-2, 2006, Pages 163-169

  Tang, Ming Li ^a   Wang, Shun Chang ^a   Wang, Tao ^a   Zhao, Shi Guang ^a   Wu, Yao Jing ^a   Wu, Li Jun ^a   Yu, Zeng Liang ^a  

^a INSTITUTE OF PLASMA PHYSICS   (China)

Author keywords

Escherichia coli; lacI gene; Low energy ion beam; Spectrum

Indexed keywords

NITROGEN; OXYGEN; TISSUE FACTOR PATHWAY INHIBITOR;

AMINO ACID SUBSTITUTION; ARTICLE; BACTERIAL GENE; BACTERIAL GENOME; BACTERIAL STRAIN; BASE PAIRING; CARCINOGEN DNA INTERACTION; CONTROLLED STUDY; DNA ADDUCT; ESCHERICHIA COLI; GAMMA RADIATION; GENE DELETION; GENE MUTATION; IN VIVO STUDY; LOW ENERGY RADIATION; MUTAGENESIS; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RADIATION DOSE; RADIATION MUTAGENESIS; SPECTRUM; WILD TYPE;

BACTERIAL PROTEINS; CELL SURVIVAL; DOSE-RESPONSE RELATIONSHIP, RADIATION; ESCHERICHIA COLI K12; FREE RADICALS; MUTATION; RADIATION, IONIZING; REPRESSOR PROTEINS;

ESCHERICHIA COLI;

EID: 33750632023     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2006.09.001     Document Type: Article

References (40)

1. Chen Y., Jiang B., Chen Y., Ding X., Liu X., Chen C., Guo X., and Yin G. Formation of plasmid DNA strand breaks induced by low-energy ion beam: indicating of nuclear stopping effects. Radiat. Environ. Biophys. 37 (1998) 101-106
2. Zhao Y., Tan Z., Qiu G.Y., and Du Y.H. Electrophoresis examination strand breaks in plasmid DNA by low-energy nitrogen ion irradiation. Nucl. Instrum. Methods Phys. Res. B211 (2003) 211-218
3. Shi H.B., Shao C.L., and Yu Z.L. Dose effect of keV ions irradiation on adenine and cytosine. Acta Biophys. Sin. 17 (2001) 731-735
4. Du Y.H., Huang S.H., Tan Z., Lin Y.Z., and Liu G.Y. Dertermination of DNA single-strand breaks by low-energy heavy ion and analysis of dose-effect curves. Chin. Sci. Bull. 44 (1999) 711-714
5. Yu Z.L. An Introduction of Ion Beam Biotechnology (2006), Springer Press, NY
6. Wu L.J., and Yu Z.L. Radiobiological effects of low-energy ion beam on wheat. Radiat. Environ. Biophys. 40 (2001) 53-57
7. Yu Z.L., and Deng J.G. Mutation breeding by ion implantation. Nucl. Instrum. Methods Phys. Res. B59 (1991) 705-708
8. 2 by low-energy heavy ions. Radiat. Res. 35 (1968) 472-478
9. Phanchaisri B., Yu L.D., Anuntalabhochai S., Chandej R., Apavatjrut P., Vilaithong T., and Brown I.G. Characteristics of heavy ion beam-bombarded bacteria induced direct DNA transfer. Surf. Coat. Technol. 158-159 (2002) 624-629
10. Yang J.B., Wu L.J., Li L., Yu Z.L., and Xu ZH. Sequence analysis of lacZ-mutations induced by ion beam irradiation in double-stranded M13mp18DNA. Sci. China (Series C) 40 (1997) 107-112
11. Wang Q., Zhang G., Du Y.H., Zhao Y., and Qiu G.Y. Low-energy 30 keV carbon ion induced mutation spectrum in the LacZ gene of M13mp18 double-stranded DNA. Mutat. Res. 528 (2003) 55-60
12. 60Co-gamma ray irradiation in Escherichia coli. Gen. Mol. Boil. 27 (2004) 284-290
13. Murata-Kamiya N., Kamiya H., Iwamoto N., and Kasai H. Formation of a mutagen, glyoxal from DNA treated with oxygen free radicals. Carcinogenesis 162 (1995) 251-2253
14. Sedwick W.D., Brown O.E., and Glickman B.W. Deoxyuridine misincorporation causes site-specific mutational lesions in the lacI gene of Escherichia coli. Mutat. Res. 162 (1986) 7-12
15. Halliday J.A., and Glickman B.W. Mechanisms of spontaneous mutation in DNA repair-proficient Escherichia coli. Mutat. Res. 250 (1991) 55-71
16. Kato T.Y., Oda Y., and Glickman B.W. Randomness of base substitution mutations in the lacI gene of Escherichia coli by ionizing radiation. Radiat. Res. 101 (1985) 402-406
17. Fujikawa K., Kamiya H., and Kasai H. The mutations induced by oxidatively damaged nucleotides, 5-formyl-dUTP and 5-hydroxy-dCTP, in Escherichia coli. Nucleic Acids Res. 26 (1998) 4582-4587
18. Stuart G.R., Oda Y., de Boer J.G., and Glickman B.W. No change in spontaneous mutation frequency or specificity in dietary restricted mice. Carcinogenesis 21 (2000) 317-319
19. Kohler S.W., Proyost G.S., Fieck A., Kretz P.L., Bullock W.O., Sorge J.A., Putman D.L., and Short J.M. Spectra of spontaneous and mutagen-induced mutations in the lacI gene in transgenic mice. Proc. Natl. Sci. U.S.A. 88 (1991) 7958-7962
20. Wijker C.A., Lafleur M.V.M., Steeg H.V., Mohn G.R., and Retel J. γ-Radiation-induced mutation spectrum in the episomal lacI gene of Escherichia coli under oxic conditions. Mutat. Res. 349 (1996) 229-239
21. Wijker C.A., Slotman B.J., and Lafleur M.V.M. Mutagenic effect by phenylalanine during γ-irradiation in aqueous solution under oxic conditions. Mutat. Res. 454 (2000) 71-76
22. JianLi J., Malgorzata P., Glickman B.W., and Maria Z. Molecular analysis of mutations induced by ethylating N-nitroso compounds in the lacI gene of Escherichia coli. Mutat. Res. 352 (1996) 39-45
23. d mutations in Escherichia coli umuC122::Tn5:differential requirement for umuC at G:C vs. A:T sites and for the production of transversions vs. transitions. Mutat. Res. 311 (1994) 175-189
24. Miller J.H. Experiments in Molecular Genetics (1972), Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
25. Miller J.H. A Short Course in Bacteria Genetics (1992), Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
26. Ono T., Negishi K., and Hayatsu H. Spectra of superoxide-induced mutations in the lacI gene of a wild type and a mutM strain of Escherichia coli K-12. Mutat. Res. 326 (1995) 175-183
27. Kuipers G.K., Slotman B.J., and Lafleur M.V.M. The importance of using absolute mutant frequencies to compare mutation spectra. Mutat. Res. 479 (2001) 95-99
28. Murata-Kamiya N., Kamiya H., Kaji H., and Kasai H. Mutational specificity of glyoxal, a product of DNA oxidation, in the lacI gene of wild type Escherichia coli W3110. Mutat. Res. 377 (1997) 255-262
29. Asada S., Takano M., and Shibasaki I. Mutation induced by drying of Escherichia coli on a hydrophobic filter membrane. Appl. Environ. Microbiol. 40 (1980) 274-281
30. Tanaka Y., Yoh M., Takeda Y., and Miwatani T. Induction of mutation in Escherichia coli by freeze-drying. Appl. Environ. Microbiol. 37 (1979) 369-372
31. Miller J.H., and Low K.B. Specificity of mutagenesis resulting from the induction of the SOS system in the absence of mutagenic treatment. Cell 37 (1984) 675-682
32. Yatagai F., Michael J., Low H., and Glickman B.W. Specificity of SOS mutagenesis in native M131acI phage. J. Bacteriol. (1991) 7996-7999
33. Eichenbaum Z., and Livneh Z. UV light induces IS10 transposition in Escherichia coli. Genetics 149 (1998) 1173-1181
34. Repine J.E., Pfenninge D.W., Talmage D.W., Berger E.M., and Pettijohn D.E. Dimethyl sulfoxide prevents DNA niking mediated by ionizing radiation or iron/hydrogen peroxide-generated hydroxyl radical. Proc. Natl. Acad. Sci. U.S.A. 78 (1981) 1001-1003
35. Pezeshk A. The effect of ionizing radiation on DNA: the role of thiols as radioprotectors. Life Sci. 74 (2004) 2423-2429
36. Wijker C.A., Wientjes N.M., and Lafleur M.V.M. Mutation spectrum in the lacI gene, induced by γ-radiation in aqueous solution under oxic conditions. Mutat. Res. 403 (1998) 137-147
37. Wijker C.A., and Lafleur M.V.M. Influence of the UV-activated SOS response on the γ-radiation -induced mutation spectrum in the lacI gene. Mutat. Res. 408 (1998) 195-201
38. Glickman B.W., Rietveld K., and Aaron C.S. γ-Ray induced mutational spectrum in the lacI gene of Escherichia coli, comparison of induced and spontaneous spectra at molecular level. Mutat. Res. 69 (1980) 1-12
39. Murata-Kamiya N., Kaji H., and Kasai H. Deficient nucleotide excision repair increases base-pair substitutions but decreases TGGC frameshifts induced by Methylglyoxal in Escherichia coli. Mutat. Res. 442 (1999) 19-28
40. Dianov G.L., Sleeth K.M., Dianova I.I., and Allinson S.L. Repair of abasic sites in DNA. Mutat. Res. 531 (2003) 157-163