Frameshifts, base substitutions and minute deletions constitute X-ray-induced mutations in the endogenous tonB gene of Escherichia coli K12

Mutation Research - DNA Repair

Volumn 385, Issue 3, 1997, Pages 259-267

  Kanbashi, Kenji ^a   Wang, Xue ^a   Komura, Jun Ichiro ^b   Ono, Tetsuya ^b   Yamamoto, Kazuo ^a  

^a TOHOKU UNIVERSITY   (Japan)

^b TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Irradiation in vivo; Mutation spectrum; tonB gene; X ray

Indexed keywords

ARTICLE; DELETION MUTANT; DNA REPLICATION; ESCHERICHIA COLI; FRAMESHIFT MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PLASMID; PRIORITY JOURNAL; RADIATION MUTAGENESIS;

BACTERIAL PROTEINS; CHROMOSOME MAPPING; COLIPHAGES; DNA DAMAGE; DNA, BACTERIAL; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; FRAMESHIFT MUTATION; GAMMA RAYS; MEMBRANE PROTEINS; MUTATION; PLASMIDS; POINT MUTATION; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; TRANSFECTION;

ESCHERICHIA COLI; NEGIBACTERIA;

EID: 0031423412     PISSN: 09218777     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0921-8777(97)00056-6     Document Type: Article

References (31)

1. Hutchinson F. Chemical changes induced in DNA by ionizing radiation. Prog. Nucleic Acid Res. Mol. Biol. 32:1985;115-154.
2. 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.
3. Ayaki H., Higo K., Yamamoto O. Specificity of ionizing radiation-induced mutagenesis in the lac region of single-stranded bacteriophage M13 mp10 DNA. Nucleic Acids Res. 14:1986;5013-5018.
4. 60Co γ-rays induce predominantly C/G to G/C transversions in double-stranded M13 DNA. Nucleic Acids Res. 16:1988;8147-8156.
5. Takimoto K., Uchino K., Ishizaki K., Ikenaga M. Specificity of mutational DNA sequence changes induced by X-rays in the cloned Escherichia coli crp gene. Mutation Res. 254:1991;199-206.
6. Waters L.C., Sikpi M.O., Preston R.J., Mitra S., Jaberaboansari A. Mutations induced by ionizing radiation in a plasmid replicated in human cells. I. Similar, nonrandom distribution of mutations in unirradiated and X-irradiated DNA. Radiat. Res. 127:1991;190-201.
7. Hutchinson F. Published data on mutagenesis by ionizing radiation of plasmids in solution probably reflect in part the specificity of adventitious transition metal ions complexed to the DNA. Mutation Res. 281:1992;261-266.
8. Glickman B.W., Rietveld K., Aaron C.S. γ-Ray induced mutational spectrum in the lacI gene of Escherichia coli: comparison of induced and spontaneous spectra at the molecular level. Mutation Res. 69:1980;1-12.
9. Ise T., Kato T., Glickman B.W. Spectra of base substitution mutations induced in Escherichia coli by tritiated water and the decay of incorporated tritiated thymidine. Radiat. Res. 97:1984;200-210.
10. Tindall K.R., Stein J., Hutchinson F. Changes in DNA base sequence induced by gamma-ray mutagenesis of lambda bacteriophage and prophage. Genetics. 118:1988;551-560.
11. d mutations in Escherichia coli K-12. Mutation Res. 309:1994;147-163.
12. Kitamura K., Torii Y., Matsuoka C., Yamamoto K. DNA sequence changes in mutations in the tonB gene on the chromosome of Escherichia coli K12: insertion elements dominate the spontaneous spectra. Jpn. J. Genet. 70:1995;35-46.
13. Kitamura K., Yamamoto K. Mutagenic specificity of ultraviolet light in the tonB gene on the chromosome of Escherichia coli uvrA cells. Biochem. Biophys. Res. Commun. 220:1996;496-501.
14. - cells. Biochem. Biophys. Res. Commun. 227:1996;334-339.
15. Ishii Y., Kondo S. Spontaneous and radiation-induced deletion mutations in Escherichia coli strains with different DNA repair capacities. Mutation Res. 16:1972;13-25.
16. Akasaka S., Yamamoto K. Construction of Escherichia coli K12 phr deletion and insertion mutants by gene replacement. Mutation Res. 254:1991;27-35.
17. Kimura H., Higuchi H., Iyehara-Ogawa H., Kato T. Sequence analysis of X-ray-induced mutations occurring in a cDNA of the human hprt gene integrated into mammalian chromosomal DNA. Radiat. Res. 134:1993;202-208.
18. Sargentini N.J., Smith K.C. Ionizing and ultraviolet radiation-induced reversion of sequenced frameshift mutations in Escherichia coli: a new role for umuDC suggested by delayed photoreactivation. Mutation Res. 179:1987;55-63.
19. Streisinger G., Okada Y., Emrich J., Newton J., Tsugita A., Terzaghi E., Inoue M. Frameshift mutations and the genetic code. Cold Spring Harbor Symp. Quant. Biol. 31:1966;77-84.
20. Ripley L.S. Model for the participation of quasi-palindromic DNA sequences in frameshift mutation. Proc. Natl. Acad. Sci. USA. 79:1982;4128-4132.
21. Bebenek K., Kunkel T.A. Frameshift errors initiated by nucleotide misincorporation. Proc. Natl. Acad. Sci. USA. 87:1990;4946-4950.
22. Albertini A.M., Hofer M., Calos M.P., Miller J.H. On the formation of spontaneous deletions: the importance of short sequence homologies in the generation of large deletions. Cell. 29:1982;319-328.
23. Sargentini N.J., Smith K.C. Involvement of RecB-mediated (but not RecF-mediated) repair of DNA double-strand breaks in the gamma-radiation production of long deletions in Escherichia coli. Mutation Res. 265:1992;83-101.
24. Ootsuyama A., Makino H., Nagao M., Ochiai A., Yamauchi Y., Tanooka H. Frequent p53 mutation in mouse tumors induced by repeated beta-irradiation. Mol. Carcinog. 11:1994;236-242.
25. Raha M., Hutchinson F. Deletions induced by gamma rays in the genome of Escherichia coli. J. Mol. Biol. 220:1991;193-198.
26. Anton M., Heller K.J. Functional analysis of a C-terminally altered TonB protein of Escherichia coli. Gene. 105:1990;23-29.
27. Lejeune P., Danchin A. Mutations in the bglY gene increase the frequency of spontaneous deletions in Escherichia coli K-12. Proc. Natl. Acad. Sci. USA. 87:1990;360-363.
28. Schofield M.A., Agbunag R., Michaels M.L., Miller J.H. Cloning and sequencing of Escherichia coli mutR shows its identity to topB, encoding topoisomerase III. J. Bacteriol. 174:1992;5168-5170.
29. DiGate R.J., Marians K.J. Molecular cloning and DNA sequence analysis of Escherichia coli topB, the gene encoding topoisomerase III. J. Biol. Chem. 264:1989;17924-17930.
30. Hulton C.S., Seirafi A., Hinton J.C., Sidebotham J.M., Waddell L., Pavitt G.D., Owen-Hughes T., Spassky A., Buc H., Higgins C.F. Histone-like protein H1 (H-NS), DNA supercoiling, and gene expression in bacteria. Cell. 63:1990;631-642.
31. Uematsu N., Eda S., Yamamoto K. An Escherichia coli topB mutant increases deletion and frameshift mutations in the supF target gene. Mutation Res. 383:1997;223-230.