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The SOS induction of umu'-'lacZ fusion gene by oxidative damage is influenced by polyamines in Escherichia coli

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Abstract

We report that polyamines have an effect on the SOS response of the umu operon in polyamine-deficient mutant and wild-type Escherichia coli strains carrying the umu'-'lacZ fusion. H2O2 effectively induces umu'-'lacZ in the wild type, but not significantly in the mutant strain. Exogenous polyamines did not restore the umu induction in the mutant to the wild-type level. In logarithmically growing cells, the basal expression of umu gene in the mutant is about five times higher than that of the wild type. The addition of polyamines to the growth medium markedly reduces the basal expression to the wild-type level. This reduction is due not to growth rate but to the polyamine itself. Our results suggest that polyamines are essentially involved in the SOS induction of the umu operon in E. coli.

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References

  • Carlios A, Touati D. Isolation of superoxide dismutase mutants in Escherichia coli: is superoxide dismutase necessary for aerobic life? EMBO J. 1986;5:623–30.

    Google Scholar 

  • Giannakouros T, Nikolakaki H, Georgatsos JG. Concentration-dependent effects of natural polyamines on peptide chain initiation and elongation in a cell-free system of protein synthesis. Mol Cell Biochem. 1990;99:9–19.

    Google Scholar 

  • Ha HC, Yager JD, Woster PA, Casero Jr CA. Structural specificity of polyamines and polyamine analogues in the protection of DNA from strand breaks induced by reactive oxygen species. Biochem Biophys Res Commun. 1998;244:298–303.

    Google Scholar 

  • Hafner EW, Tabor CW, Tabor H. Mutants of Escherichia coli that do not contain 1,4-diaminobutane (putrescine) or spermidine. J Biol Chem. 1979;254:12419–26.

    Google Scholar 

  • Huang SC, Panagiotidis CA, Canellakis ES. Transcriptional effect of polyamines on ribosomal proteins and polyamine-synthesizing enzymes in Escherichia coli. Proc Natl Acad Sci USA. 1990;87:3464–8.

    Google Scholar 

  • Karahalios P, Mamos P, Vynios DH, Papaioannou P, Kalpaxis DL. The effect of acylated polyamine derivatives on polyamine uptake mechanism, cell growth, and polyamine pools in Escherichia coli, and the pursuit of structure/activity relationships. Eur J Biochem. 1998;252:998–1004.

    Google Scholar 

  • Khan AU, Mascio P, Medeiros MH, Wilson T. Spermine and spermidine protection of plasmid DNA against single-strand breaks induced by singlet oxygen. Proc Natl Acad Sci USA. 1992;89:11428–30.

    Google Scholar 

  • Little JW, Mount DW. The SOS regulatory system of Escherichia coli. Cell. 1982;29:11–22.

    Google Scholar 

  • Miller JH. Experiments in molecular genetics. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 1972:352–5.

    Google Scholar 

  • Minton KW, Tabor H, Tabor CW. Paraquat toxicity is increased in Escherichia coli defective in the synthesis of polyamines. Proc Natl Acad Sci USA. 1990;87:2851–5.

    Google Scholar 

  • Oh TJ, Kim IG. Polyamines protect against DNA strand breaks and aid cell survival against irradiation in Escherichia coli. Biotechnol Tech. 1998;12:755–8.

    Google Scholar 

  • Panagiotidis CA, Blackburn S, Low KB, Canellakis ES. Biosynthesis of polyamines in ornithine decarboxylase, arginine decarboxylase, and agmatine ureahydrolase deletion mutants of Escherichia coli K-12. Proc Natl Acad Sci USA. 1987;84: 4423–7.

    Google Scholar 

  • Rajalakshmi S, Rao PM, Sarma DS. Studies on carcinogen chromatin-DNA interaction: inhibition of N-methyl-N-nitrosourea-induced methylation of chromatin-DNA by spermine and distamycin A. Biochemistry. 1978;17:4515–8.

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T. Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 1992;1:21–83.

    Google Scholar 

  • Shinagawa H, Kato T, Ise T, Makino T, Nakata A. Cloning and characterization of the umu operon responsible for inducible mutagenesis in Escherichia coli. Gene. 1983;23:167–74.

    Google Scholar 

  • Smith BT, Walker GC. Mutagenesis and more: umuDC and the Escherichia coli SOS response. Genetics. 1998;148:1599–610.

    Google Scholar 

  • Snyder RD, Lachmann PJ. Hyperthermia, polyamine depletion and inhibition of X-ray-induced DNA strand break repair. Radiat Res. 1989;120:121–8.

    Google Scholar 

  • Spotheim-Maurizot M, Ruiz S, Sabattier R, Charlier M. Radioprotection of DNA by polyamines. Int J Radiat Biol. 1995;68:571–7.

    Google Scholar 

  • Tabor H, Tabor CW. Polyamines. Annu Rev Biochem. 1984;53:749–90.

    Google Scholar 

  • Tabor H, Hafner EW, Tabor CW. Construction of an Escherichia coli strain unable to synthesize putrescine, spermidine, or cadaverine: characterization of two genes controlling lysine decarboxylase. J Bacteriol. 1980;144:952–6.

    Google Scholar 

  • Walker GC. Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli. Microbiol Rev. 1984;48:60–93.

    Google Scholar 

  • Witkin EM. Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bacteriol Rev. 1976;40:869–907.

    Google Scholar 

Download references

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Oh, T., Kim, I. The SOS induction of umu'-'lacZ fusion gene by oxidative damage is influenced by polyamines in Escherichia coli. Cell Biol Toxicol 15, 291–297 (1999). https://doi.org/10.1023/A:1007663701589

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  • DOI: https://doi.org/10.1023/A:1007663701589

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