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Proc Natl Acad Sci U S A. 1987 May; 84(10): 3189–3193.
PMCID: PMC304834
Endonuclease IV of Escherichia coli is induced by paraquat.
E Chan and B Weiss
Abstract
The addition of paraquat (methyl viologen) to a growing culture of Escherichia coli K-12 led within 1 hr to a 10- to 20-fold increase in the level of endonuclease IV, a DNase for apurinic/apyrimidinic sites. The induction was blocked by chloramphenicol. Increases of 3-fold or more were also seen with plumbagin, menadione, and phenazine methosulfate. H2O2 produced no more than a 2-fold increase in endonuclease IV activity. The following agents had no significant effect: streptonigrin, nitrofurantoin, tert-butyl hydroperoxide, gamma rays, 260-nm UV radiation, methyl methanesulfonate, mitomycin C, and ascorbate. Paraquat, plumbagin, menadione, and phenazine methosulfate are known to generate superoxide radical anions via redox cycling in vivo. A mutant lacking superoxide dismutase was unusually sensitive to induction by paraquat. In addition, endonuclease IV could be induced by merely growing the mutant in pure O2. The levels of endonuclease IV in uninduced or paraquat-treated cells were unaffected by mutations of oxyR, a H2O2-inducible gene that governs an oxidative-stress regulon. The results indicate that endonuclease IV is an inducible DNA-repair enzyme and that its induction can be mediated via the production of superoxide radicals.
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Selected References
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  • Ljungquist, S. A new endonuclease from Escherichia coli acting at apurinic sites in DNA. J Biol Chem. 1977 May 10;252(9):2808–2814. [PubMed]
  • Lindahl, T. DNA repair enzymes. Annu Rev Biochem. 1982;51:61–87. [PubMed]
  • Yajko, DM; Weiss, B. Mutations simultaneously affecting endonuclease II and exonuclease III in Escherichia coli. Proc Natl Acad Sci U S A. 1975 Feb;72(2):688–692. [PubMed]
  • Weiss, B. Endonuclease II of Escherichia coli is exonuclease III. J Biol Chem. 1976 Apr 10;251(7):1896–1901. [PubMed]
  • Cunningham, RP; Saporito, SM; Spitzer, SG; Weiss, B. Endonuclease IV (nfo) mutant of Escherichia coli. J Bacteriol. 1986 Dec;168(3):1120–1127. [PubMed]
  • Breimer, LH; Lindahl, T. DNA glycosylase activities for thymine residues damaged by ring saturation, fragmentation, or ring contraction are functions of endonuclease III in Escherichia coli. J Biol Chem. 1984 May 10;259(9):5543–5548. [PubMed]
  • Katcher, HL; Wallace, SS. Characterization of the Escherichia coli X-ray endonuclease, endonuclease III. Biochemistry. 1983 Aug 16;22(17):4071–4081. [PubMed]
  • Cunningham, RP; Weiss, B. Endonuclease III (nth) mutants of Escherichia coli. Proc Natl Acad Sci U S A. 1985 Jan;82(2):474–478. [PubMed]
  • Weiss, B; Cunningham, RP. Genetic mapping of nth, a gene affecting endonuclease III (thymine glycol-DNA glycosylase) in Escherichia coli K-12. J Bacteriol. 1985 May;162(2):607–610. [PubMed]
  • Milcarek, C; Weiss, B. Mutants of Escherichia coli with altered deoxyribonucleases. I. Isolation and characterization of mutants for exonuclease 3. J Mol Biol. 1972 Jul 21;68(2):303–318. [PubMed]
  • Carlioz, A; Touati, D. Isolation of superoxide dismutase mutants in Escherichia coli: is superoxide dismutase necessary for aerobic life? EMBO J. 1986 Mar;5(3):623–630. [PubMed]
  • Christman, MF; Morgan, RW; Jacobson, FS; Ames, BN. Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium. Cell. 1985 Jul;41(3):753–762. [PubMed]
  • Bachmann, BJ. Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972 Dec;36(4):525–557. [PubMed]
  • White, BJ; Hochhauser, SJ; Cintron, NM; Weiss, B. Genetic mapping of xthA, the structural gene for exonuclease III in Escherichia coli K-12. J Bacteriol. 1976 Jun;126(3):1082–1088. [PubMed]
  • Demple, B; Halbrook, J. Inducible repair of oxidative DNA damage in Escherichia coli. Nature. 304(5925):466–468. [PubMed]
  • BEERS, RF, Jr; SIZER, IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem. 1952 Mar;195(1):133–140. [PubMed]
  • Smith, PK; Krohn, RI; Hermanson, GT; Mallia, AK; Gartner, FH; Provenzano, MD; Fujimoto, EK; Goeke, NM; Olson, BJ; Klenk, DC. Measurement of protein using bicinchoninic acid. Anal Biochem. 1985 Oct;150(1):76–85. [PubMed]
  • Walker, GC. Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli. Microbiol Rev. 1984 Mar;48(1):60–93. [PubMed]
  • Hassan, HM; Fridovich, I. Intracellular production of superoxide radical and of hydrogen peroxide by redox active compounds. Arch Biochem Biophys. 1979 Sep;196(2):385–395. [PubMed]
  • Youngman, RJ; Osswald, WF; Elstner, EF. Mechanisms of oxygen activation by nitrofurantoin and relevance to its toxicity. Biochem Pharmacol. 1982 Dec 1;31(23):3723–3729. [PubMed]
  • Richter, HE; Loewen, PC. Induction of catalase in Escherichia coli by ascorbic acid involves hydrogen peroxide. Biochem Biophys Res Commun. 1981 Jun 16;100(3):1039–1046. [PubMed]
  • Hassan, HM; Fridovich, I. Enzymatic defenses against the toxicity of oxygen and of streptonigrin in Escherichia coli. J Bacteriol. 1977 Mar;129(3):1574–1583. [PubMed]
  • Morgan, RW; Christman, MF; Jacobson, FS; Storz, G; Ames, BN. Hydrogen peroxide-inducible proteins in Salmonella typhimurium overlap with heat shock and other stress proteins. Proc Natl Acad Sci U S A. 1986 Nov;83(21):8059–8063. [PubMed]
  • Fridovich, I. The biology of oxygen radicals. Science. 1978 Sep 8;201(4359):875–880. [PubMed]
  • Farr, SB; D'Ari, R; Touati, D. Oxygen-dependent mutagenesis in Escherichia coli lacking superoxide dismutase. Proc Natl Acad Sci U S A. 1986 Nov;83(21):8268–8272. [PubMed]
  • Halliwell, B; Gutteridge, JM. Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J. 1984 Apr 1;219(1):1–14. [PubMed]
  • Hutchinson, F. Chemical changes induced in DNA by ionizing radiation. Prog Nucleic Acid Res Mol Biol. 1985;32:115–154. [PubMed]
  • Brawn, K; Fridovich, I. DNA strand scission by enzymically generated oxygen radicals. Arch Biochem Biophys. 1981 Feb;206(2):414–419. [PubMed]
  • Winterbourn, CC. Production of hydroxyl radicals from paraquat radicals and H2O2. FEBS Lett. 1981 Jun 15;128(2):339–342. [PubMed]
  • Youngman, RJ; Elstner, EF. Oxygen species in paraquat toxicity: the crypto-OH radical. FEBS Lett. 1981 Jul 6;129(2):265–268. [PubMed]
  • Van Hemmen, JJ; Meuling, WJ. Inactivation of biologically active DNA by gamma-ray-induced superoxide radicals and their dismutation products singlet molecular oxygen and hydrogen peroxide. Biochim Biophys Acta. 1975 Aug 21;402(2):133–141. [PubMed]
  • Demple, B; Johnson, A; Fung, D. Exonuclease III and endonuclease IV remove 3' blocks from DNA synthesis primers in H2O2-damaged Escherichia coli. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7731–7735. [PubMed]
  • Brawn, MK; Fridovich, I. Increased superoxide radical production evokes inducible DNA repair in Escherichia coli. J Biol Chem. 1985 Jan 25;260(2):922–925. [PubMed]
  • Farr, SB; Natvig, DO; Kogoma, T. Toxicity and mutagenicity of plumbagin and the induction of a possible new DNA repair pathway in Escherichia coli. J Bacteriol. 1985 Dec;164(3):1309–1316. [PubMed]