Abstract
Many environmental metals are co-carcinogens, eliciting their effects via inhibition of DNA repair. Apurinic/apyrimidinic (AP) endonuclease 1 (Ape1) is the major mammalian abasic endonuclease and initiates repair of this cytotoxic/mutagenic lesion by incising the DNA backbone via a Mg(2+)-dependent reaction. In this study we examined the effects of arsenite [As(III)], cadmium [Cd(II)], cobalt [Co(II)], iron [Fe(II)], nickel [Ni(II)], and lead [Pb(II)] at concentrations ranging from 0.3 to 100 microM on the incision activity of Ape1 in the presence of 1 mM MgCl(subscript)2(/subscript). Pb(II) and Fe(II) inhibited Ape1 activity at each of the concentrations tested, with an IC(subscript)50(/subscript) (half-maximal inhibitory concentration) of 0.61 and 1.0 microM, respectively. Cd(II) also inhibited Ape1 activity but only at concentrations > 10 microM. No inhibition was seen with As(III), Co(II), or Ni(II). A similar inhibition pattern was observed with the homologous Escherichia coli protein, exonuclease III, but no inhibition was seen with the structurally distinct AP endonuclease E. coli endonuclease IV, indicating a targeted effect of Pb(II), Fe(II), and Cd(II) on the Ape1-like repair enzymes. Excess nonspecific DNA did not abrogate the metal inactivation, suggesting a protein-specific effect. Notably, Cd(II), Fe(II), and Pb(II) [but not As(III), Co(II), or Ni(II)] inhibited AP endonuclease activity in whole-cell extracts but had no significant effect on single nucleotide gap filling, 5'-flap endonuclease, and nick ligation activities, supporting the idea of selective inactivation of Ape1 in cells. Our results are the first to identify a potential DNA repair enzyme target for lead and suggest a means by which these prevalent environmental metals may elicit their deleterious effects.
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- Asmuss M., Mullenders L. H., Eker A., Hartwig A. Differential effects of toxic metal compounds on the activities of Fpg and XPA, two zinc finger proteins involved in DNA repair. Carcinogenesis. 2000 Nov;21(11):2097–2104. doi: 10.1093/carcin/21.11.2097. [DOI] [PubMed] [Google Scholar]
- Beernink P. T., Segelke B. W., Hadi M. Z., Erzberger J. P., Wilson D. M., 3rd, Rupp B. Two divalent metal ions in the active site of a new crystal form of human apurinic/apyrimidinic endonuclease, Ape1: implications for the catalytic mechanism. J Mol Biol. 2001 Apr 6;307(4):1023–1034. doi: 10.1006/jmbi.2001.4529. [DOI] [PubMed] [Google Scholar]
- Chou Kai-Ming, Cheng Yung-Chi. An exonucleolytic activity of human apurinic/apyrimidinic endonuclease on 3' mispaired DNA. Nature. 2002 Feb 7;415(6872):655–659. doi: 10.1038/415655a. [DOI] [PubMed] [Google Scholar]
- Demple B., Harrison L. Repair of oxidative damage to DNA: enzymology and biology. Annu Rev Biochem. 1994;63:915–948. doi: 10.1146/annurev.bi.63.070194.004411. [DOI] [PubMed] [Google Scholar]
- Demple B., Herman T., Chen D. S. Cloning and expression of APE, the cDNA encoding the major human apurinic endonuclease: definition of a family of DNA repair enzymes. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11450–11454. doi: 10.1073/pnas.88.24.11450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Erzberger J. P., Barsky D., Schärer O. D., Colvin M. E., Wilson D. M., 3rd Elements in abasic site recognition by the major human and Escherichia coli apurinic/apyrimidinic endonucleases. Nucleic Acids Res. 1998 Jun 1;26(11):2771–2778. doi: 10.1093/nar/26.11.2771. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fatur Tanja, Lah Tamara T., Filipic Metka. Cadmium inhibits repair of UV-, methyl methanesulfonate- and N-methyl-N-nitrosourea-induced DNA damage in Chinese hamster ovary cells. Mutat Res. 2003 Aug 28;529(1-2):109–116. doi: 10.1016/s0027-5107(03)00112-x. [DOI] [PubMed] [Google Scholar]
- Gorman M. A., Morera S., Rothwell D. G., de La Fortelle E., Mol C. D., Tainer J. A., Hickson I. D., Freemont P. S. The crystal structure of the human DNA repair endonuclease HAP1 suggests the recognition of extra-helical deoxyribose at DNA abasic sites. EMBO J. 1997 Nov 3;16(21):6548–6558. doi: 10.1093/emboj/16.21.6548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hadi Masood Z., Ginalski Krzysztof, Nguyen Lam H., Wilson David M., 3rd Determinants in nuclease specificity of Ape1 and Ape2, human homologues of Escherichia coli exonuclease III. J Mol Biol. 2002 Feb 22;316(3):853–866. doi: 10.1006/jmbi.2001.5382. [DOI] [PubMed] [Google Scholar]
- Hartwig A., Asmuss M., Ehleben I., Herzer U., Kostelac D., Pelzer A., Schwerdtle T., Bürkle A. Interference by toxic metal ions with DNA repair processes and cell cycle control: molecular mechanisms. Environ Health Perspect. 2002 Oct;110 (Suppl 5):797–799. doi: 10.1289/ehp.02110s5797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartwig A. Role of DNA repair inhibition in lead- and cadmium-induced genotoxicity: a review. Environ Health Perspect. 1994 Sep;102 (Suppl 3):45–50. doi: 10.1289/ehp.94102s345. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartwig Andrea, Pelzer Anke, Asmuss Monika, Bürkle Alexander. Very low concentrations of arsenite suppress poly(ADP-ribosyl)ation in mammalian cells. Int J Cancer. 2003 Mar 10;104(1):1–6. doi: 10.1002/ijc.10911. [DOI] [PubMed] [Google Scholar]
- Hartwig Andrea, Schwerdtle Tanja. Interactions by carcinogenic metal compounds with DNA repair processes: toxicological implications. Toxicol Lett. 2002 Feb 28;127(1-3):47–54. doi: 10.1016/s0378-4274(01)00482-9. [DOI] [PubMed] [Google Scholar]
- Hayes R. B. The carcinogenicity of metals in humans. Cancer Causes Control. 1997 May;8(3):371–385. doi: 10.1023/a:1018457305212. [DOI] [PubMed] [Google Scholar]
- Heinen Christopher D., Schmutte Christoph, Fishel Richard. DNA repair and tumorigenesis: lessons from hereditary cancer syndromes. Cancer Biol Ther. 2002 Sep-Oct;1(5):477–485. doi: 10.4161/cbt.1.5.160. [DOI] [PubMed] [Google Scholar]
- Hitzfeld B., Taylor D. M. Characteristics of lead adaptation in a rat kidney cell line. I. Uptake and subcellular and subnuclear distribution of lead. Mol Toxicol. 1989 Jul-Sep;2(3):151–162. [PubMed] [Google Scholar]
- Hoeijmakers J. H. Genome maintenance mechanisms for preventing cancer. Nature. 2001 May 17;411(6835):366–374. doi: 10.1038/35077232. [DOI] [PubMed] [Google Scholar]
- Huang Xi. Iron overload and its association with cancer risk in humans: evidence for iron as a carcinogenic metal. Mutat Res. 2003 Dec 10;533(1-2):153–171. doi: 10.1016/j.mrfmmm.2003.08.023. [DOI] [PubMed] [Google Scholar]
- Jin Yong Hwan, Clark Alan B., Slebos Robbert J. C., Al-Refai Hanan, Taylor Jack A., Kunkel Thomas A., Resnick Michael A., Gordenin Dmitry A. Cadmium is a mutagen that acts by inhibiting mismatch repair. Nat Genet. 2003 Jul;34(3):326–329. doi: 10.1038/ng1172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kasprzak Kazimierz S. Oxidative DNA and protein damage in metal-induced toxicity and carcinogenesis. Free Radic Biol Med. 2002 May 15;32(10):958–967. doi: 10.1016/s0891-5849(02)00809-2. [DOI] [PubMed] [Google Scholar]
- Ke Ya, Ming Qian Zhong. Iron misregulation in the brain: a primary cause of neurodegenerative disorders. Lancet Neurol. 2003 Apr;2(4):246–253. doi: 10.1016/s1474-4422(03)00353-3. [DOI] [PubMed] [Google Scholar]
- Kelley Mark R., Kow Yoke W., Wilson David M., 3rd Disparity between DNA base excision repair in yeast and mammals: translational implications. Cancer Res. 2003 Feb 1;63(3):549–554. [PubMed] [Google Scholar]
- Klaassen C. D., Liu J., Choudhuri S. Metallothionein: an intracellular protein to protect against cadmium toxicity. Annu Rev Pharmacol Toxicol. 1999;39:267–294. doi: 10.1146/annurev.pharmtox.39.1.267. [DOI] [PubMed] [Google Scholar]
- Lowry David F., Hoyt David W., Khazi Fayaz A., Bagu John, Lindsey Andrea G., Wilson David M., 3rd Investigation of the role of the histidine-aspartate pair in the human exonuclease III-like abasic endonuclease, Ape1. J Mol Biol. 2003 May 30;329(2):311–322. doi: 10.1016/s0022-2836(03)00382-6. [DOI] [PubMed] [Google Scholar]
- Ludwig D. L., MacInnes M. A., Takiguchi Y., Purtymun P. E., Henrie M., Flannery M., Meneses J., Pedersen R. A., Chen D. J. A murine AP-endonuclease gene-targeted deficiency with post-implantation embryonic progression and ionizing radiation sensitivity. Mutat Res. 1998 Oct 21;409(1):17–29. doi: 10.1016/s0921-8777(98)00039-1. [DOI] [PubMed] [Google Scholar]
- Meira L. B., Devaraj S., Kisby G. E., Burns D. K., Daniel R. L., Hammer R. E., Grundy S., Jialal I., Friedberg E. C. Heterozygosity for the mouse Apex gene results in phenotypes associated with oxidative stress. Cancer Res. 2001 Jul 15;61(14):5552–5557. [PubMed] [Google Scholar]
- Mol C. D., Hosfield D. J., Tainer J. A. Abasic site recognition by two apurinic/apyrimidinic endonuclease families in DNA base excision repair: the 3' ends justify the means. Mutat Res. 2000 Aug 30;460(3-4):211–229. doi: 10.1016/s0921-8777(00)00028-8. [DOI] [PubMed] [Google Scholar]
- Mol C. D., Izumi T., Mitra S., Tainer J. A. DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination [corrected]. Nature. 2000 Jan 27;403(6768):451–456. doi: 10.1038/35000249. [DOI] [PubMed] [Google Scholar]
- Méplan C., Mann K., Hainaut P. Cadmium induces conformational modifications of wild-type p53 and suppresses p53 response to DNA damage in cultured cells. J Biol Chem. 1999 Oct 29;274(44):31663–31670. doi: 10.1074/jbc.274.44.31663. [DOI] [PubMed] [Google Scholar]
- Palecek E., Brázdová M., Cernocká H., Vlk D., Brázda V., Vojtesek B. Effect of transition metals on binding of p53 protein to supercoiled DNA and to consensus sequence in DNA fragments. Oncogene. 1999 Jun 17;18(24):3617–3625. doi: 10.1038/sj.onc.1202710. [DOI] [PubMed] [Google Scholar]
- Petrat Frank, de Groot Herbert, Sustmann Reiner, Rauen Ursula. The chelatable iron pool in living cells: a methodically defined quantity. Biol Chem. 2002 Mar-Apr;383(3-4):489–502. doi: 10.1515/BC.2002.051. [DOI] [PubMed] [Google Scholar]
- Porter D. W., Yakushiji H., Nakabeppu Y., Sekiguchi M., Fivash M. J., Jr, Kasprzak K. S. Sensitivity of Escherichia coli (MutT) and human (MTH1) 8-oxo-dGTPases to in vitro inhibition by the carcinogenic metals, nickel(II), copper(II), cobalt(II) and cadmium(II). Carcinogenesis. 1997 Sep;18(9):1785–1791. doi: 10.1093/carcin/18.9.1785. [DOI] [PubMed] [Google Scholar]
- Roy N. K., Rossman T. G. Mutagenesis and comutagenesis by lead compounds. Mutat Res. 1992 Dec;298(2):97–103. doi: 10.1016/0165-1218(92)90034-w. [DOI] [PubMed] [Google Scholar]
- Silbergeld Ellen K. Facilitative mechanisms of lead as a carcinogen. Mutat Res. 2003 Dec 10;533(1-2):121–133. doi: 10.1016/j.mrfmmm.2003.07.010. [DOI] [PubMed] [Google Scholar]
- Suh D., Wilson D. M., 3rd, Povirk L. F. 3'-phosphodiesterase activity of human apurinic/apyrimidinic endonuclease at DNA double-strand break ends. Nucleic Acids Res. 1997 Jun 15;25(12):2495–2500. doi: 10.1093/nar/25.12.2495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waalkes Michael P. Cadmium carcinogenesis. Mutat Res. 2003 Dec 10;533(1-2):107–120. doi: 10.1016/j.mrfmmm.2003.07.011. [DOI] [PubMed] [Google Scholar]
- Waisberg Michael, Joseph Pius, Hale Beverley, Beyersmann Detmar. Molecular and cellular mechanisms of cadmium carcinogenesis. Toxicology. 2003 Nov 5;192(2-3):95–117. doi: 10.1016/s0300-483x(03)00305-6. [DOI] [PubMed] [Google Scholar]
- Wilson D. M., 3rd, Barsky D. The major human abasic endonuclease: formation, consequences and repair of abasic lesions in DNA. Mutat Res. 2001 May 10;485(4):283–307. doi: 10.1016/s0921-8777(01)00063-5. [DOI] [PubMed] [Google Scholar]
- Wilson D. M., 3rd, Takeshita M., Grollman A. P., Demple B. Incision activity of human apurinic endonuclease (Ape) at abasic site analogs in DNA. J Biol Chem. 1995 Jul 7;270(27):16002–16007. doi: 10.1074/jbc.270.27.16002. [DOI] [PubMed] [Google Scholar]
- Wilson David M., 3rd Properties of and substrate determinants for the exonuclease activity of human apurinic endonuclease Ape1. J Mol Biol. 2003 Jul 25;330(5):1027–1037. doi: 10.1016/s0022-2836(03)00712-5. [DOI] [PubMed] [Google Scholar]
- Winters T. A., Henner W. D., Russell P. S., McCullough A., Jorgensen T. J. Removal of 3'-phosphoglycolate from DNA strand-break damage in an oligonucleotide substrate by recombinant human apurinic/apyrimidinic endonuclease 1. Nucleic Acids Res. 1994 May 25;22(10):1866–1873. doi: 10.1093/nar/22.10.1866. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xanthoudakis S., Smeyne R. J., Wallace J. D., Curran T. The redox/DNA repair protein, Ref-1, is essential for early embryonic development in mice. Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):8919–8923. doi: 10.1073/pnas.93.17.8919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zharkov Dmitry O., Rosenquist Thomas A. Inactivation of mammalian 8-oxoguanine-DNA glycosylase by cadmium(II): implications for cadmium genotoxicity. DNA Repair (Amst) 2002 Aug 6;1(8):661–670. doi: 10.1016/s1568-7864(02)00074-5. [DOI] [PubMed] [Google Scholar]
- Zheng W. Toxicology of choroid plexus: special reference to metal-induced neurotoxicities. Microsc Res Tech. 2001 Jan 1;52(1):89–103. doi: 10.1002/1097-0029(20010101)52:1<89::AID-JEMT11>3.0.CO;2-2. [DOI] [PMC free article] [PubMed] [Google Scholar]