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. 1997 Feb;179(4):1096–1101. doi: 10.1128/jb.179.4.1096-1101.1997

Saccharomyces cerevisiae exhibits a yAP-1-mediated adaptive response to malondialdehyde.

H E Turton 1, I W Dawes 1, C M Grant 1
PMCID: PMC178803  PMID: 9023189

Abstract

Malondialdehyde (MDA) is a highly reactive aldehyde generally formed as a consequence of lipid peroxidation. MDA has been inferred to have mutagenic and cytotoxic roles and possibly to be a participant in the onset of atherosclerosis. Wild-type Saccharomyces cerevisiae acquires resistance to a lethal dose (5 mM) of MDA following prior exposure to a nonlethal concentration (1 mM). This response was completely inhibited by cycloheximide (50 microg ml(-1)), indicating a requirement for protein synthesis for adaptation. Furthermore, we have examined the roles of glutathione (GSH), mitochondrial function, and yAP-1-mediated transcription in conferring resistance and adaptation to MDA. A yap1 disruption mutant exhibited the greatest sensitivity and was unable to adapt to MDA, implicating yAP-1 in both the adaptive response and constitutive survival. The effect of MDA on GSH mutants indicated a role for GSH in initial resistance, whereas resistance acquired through adaptation was independent of GSH. Likewise, respiratory mutants (petite mutants) were sensitive to MDA but were still able to mount an adaptive response similar to that of the wild type, excluding mitochondria from any role in adaptation. MDA was detected in yeast cells by the thiobarbituric acid test and subsequent high-pressure liquid chromatography separation. Elevated levels were detected following treatment with hydrogen peroxide. However, the MDA-adaptive response was independent of that to H2O2.

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Selected References

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  1. Burger R. M., Berkowitz A. R., Peisach J., Horwitz S. B. Origin of malondialdehyde from DNA degraded by Fe(II) x bleomycin. J Biol Chem. 1980 Dec 25;255(24):11832–11838. [PubMed] [Google Scholar]
  2. Collinson L. P., Dawes I. W. Inducibility of the response of yeast cells to peroxide stress. J Gen Microbiol. 1992 Feb;138(2):329–335. doi: 10.1099/00221287-138-2-329. [DOI] [PubMed] [Google Scholar]
  3. Debouzy J. C., Fauvelle F., Vezin H., Brasme B., Chancerelle Y. Interaction of the malonyldialdehyde molecule with membranes. A differential scanning calorimetry, 1H-, 31P-NMR and ESR study. Biochem Pharmacol. 1992 Nov 3;44(9):1787–1793. doi: 10.1016/0006-2952(92)90073-r. [DOI] [PubMed] [Google Scholar]
  4. Draper H. H., Squires E. J., Mahmoodi H., Wu J., Agarwal S., Hadley M. A comparative evaluation of thiobarbituric acid methods for the determination of malondialdehyde in biological materials. Free Radic Biol Med. 1993 Oct;15(4):353–363. doi: 10.1016/0891-5849(93)90035-s. [DOI] [PubMed] [Google Scholar]
  5. Esterbauer H. Cytotoxicity and genotoxicity of lipid-oxidation products. Am J Clin Nutr. 1993 May;57(5 Suppl):779S–786S. doi: 10.1093/ajcn/57.5.779S. [DOI] [PubMed] [Google Scholar]
  6. Esterbauer H., Schaur R. J., Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes. Free Radic Biol Med. 1991;11(1):81–128. doi: 10.1016/0891-5849(91)90192-6. [DOI] [PubMed] [Google Scholar]
  7. Flattery-O'Brien J., Collinson L. P., Dawes I. W. Saccharomyces cerevisiae has an inducible response to menadione which differs from that to hydrogen peroxide. J Gen Microbiol. 1993 Mar;139(3):501–507. doi: 10.1099/00221287-139-3-501. [DOI] [PubMed] [Google Scholar]
  8. Grant C. M., Collinson L. P., Roe J. H., Dawes I. W. Yeast glutathione reductase is required for protection against oxidative stress and is a target gene for yAP-1 transcriptional regulation. Mol Microbiol. 1996 Jul;21(1):171–179. doi: 10.1046/j.1365-2958.1996.6351340.x. [DOI] [PubMed] [Google Scholar]
  9. Grant C. M., MacIver F. H., Dawes I. W. Glutathione is an essential metabolite required for resistance to oxidative stress in the yeast Saccharomyces cerevisiae. Curr Genet. 1996 May;29(6):511–515. doi: 10.1007/BF02426954. [DOI] [PubMed] [Google Scholar]
  10. Grant C. M., Maciver F. H., Dawes I. W. Stationary-phase induction of GLR1 expression is mediated by the yAP-1 transcriptional regulatory protein in the yeast Saccharomyces cerevisiae. Mol Microbiol. 1996 Nov;22(4):739–746. doi: 10.1046/j.1365-2958.1996.d01-1727.x. [DOI] [PubMed] [Google Scholar]
  11. Gutteridge J. M. Aspects to consider when detecting and measuring lipid peroxidation. Free Radic Res Commun. 1986;1(3):173–184. doi: 10.3109/10715768609083149. [DOI] [PubMed] [Google Scholar]
  12. Gutteridge J. M. Thiobarbituric acid-reactivity following iron-dependent free-radical damage to amino acids and carbohydrates. FEBS Lett. 1981 Jun 15;128(2):343–346. doi: 10.1016/0014-5793(81)80113-5. [DOI] [PubMed] [Google Scholar]
  13. Hoff H. F., O'Neil J. Structural and functional changes in LDL after modification with both 4-hydroxynonenal and malondialdehyde. J Lipid Res. 1993 Jul;34(7):1209–1217. [PubMed] [Google Scholar]
  14. Imai T., Ohno T. Measurement of yeast intracellular pH by image processing and the change it undergoes during growth phase. J Biotechnol. 1995 Jan 15;38(2):165–172. doi: 10.1016/0168-1656(94)00130-5. [DOI] [PubMed] [Google Scholar]
  15. Jain A., Mårtensson J., Stole E., Auld P. A., Meister A. Glutathione deficiency leads to mitochondrial damage in brain. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1913–1917. doi: 10.1073/pnas.88.5.1913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Jentzsch A. M., Bachmann H., Fürst P., Biesalski H. K. Improved analysis of malondialdehyde in human body fluids. Free Radic Biol Med. 1996;20(2):251–256. doi: 10.1016/0891-5849(95)02043-8. [DOI] [PubMed] [Google Scholar]
  17. Kappus H. A survey of chemicals inducing lipid peroxidation in biological systems. Chem Phys Lipids. 1987 Nov-Dec;45(2-4):105–115. doi: 10.1016/0009-3084(87)90062-4. [DOI] [PubMed] [Google Scholar]
  18. Kistler M., Summer K. H., Eckardt F. Isolation of glutathione-deficient mutants of the yeast Saccharomyces cerevisiae. Mutat Res. 1986 Feb;173(2):117–120. doi: 10.1016/0165-7992(86)90087-4. [DOI] [PubMed] [Google Scholar]
  19. Kuge S., Jones N. YAP1 dependent activation of TRX2 is essential for the response of Saccharomyces cerevisiae to oxidative stress by hydroperoxides. EMBO J. 1994 Feb 1;13(3):655–664. doi: 10.1002/j.1460-2075.1994.tb06304.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Lee H. S., Csallany A. S. Measurement of free and bound malondialdehyde in vitamin E-deficient and -supplemented rat liver tissues. Lipids. 1987 Feb;22(2):104–107. doi: 10.1007/BF02534861. [DOI] [PubMed] [Google Scholar]
  21. Li Z. S., Szczypka M., Lu Y. P., Thiele D. J., Rea P. A. The yeast cadmium factor protein (YCF1) is a vacuolar glutathione S-conjugate pump. J Biol Chem. 1996 Mar 15;271(11):6509–6517. doi: 10.1074/jbc.271.11.6509. [DOI] [PubMed] [Google Scholar]
  22. Moradas-Ferreira P., Costa V., Piper P., Mager W. The molecular defences against reactive oxygen species in yeast. Mol Microbiol. 1996 Feb;19(4):651–658. doi: 10.1046/j.1365-2958.1996.403940.x. [DOI] [PubMed] [Google Scholar]
  23. Ohkawa H., Ohishi N., Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979 Jun;95(2):351–358. doi: 10.1016/0003-2697(79)90738-3. [DOI] [PubMed] [Google Scholar]
  24. Ohtake Y., Yabuuchi S. Molecular cloning of the gamma-glutamylcysteine synthetase gene of Saccharomyces cerevisiae. Yeast. 1991 Dec;7(9):953–961. doi: 10.1002/yea.320070907. [DOI] [PubMed] [Google Scholar]
  25. Ohyashiki T., Sakata N., Matsui K. A decrease of lipid fluidity of the porcine intestinal brush-border membranes by treatment with malondialdehyde. J Biochem. 1992 Mar;111(3):419–423. doi: 10.1093/oxfordjournals.jbchem.a123772. [DOI] [PubMed] [Google Scholar]
  26. Poli G., Dianzani M. U., Cheeseman K. H., Slater T. F., Lang J., Esterbauer H. Separation and characterization of the aldehydic products of lipid peroxidation stimulated by carbon tetrachloride or ADP-iron in isolated rat hepatocytes and rat liver microsomal suspensions. Biochem J. 1985 Apr 15;227(2):629–638. doi: 10.1042/bj2270629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Pryor W. A., Stanley J. P., Blair E. Autoxidation of polyunsaturated fatty acids: II. A suggested mechanism for the formation of TBA-reactive materials from prostaglandin-like endoperoxides. Lipids. 1976 May;11(5):370–379. doi: 10.1007/BF02532843. [DOI] [PubMed] [Google Scholar]
  28. Salmon S., Mazière C., Auclair M., Theron L., Santus R., Mazière J. C. Malondialdehyde modification and copper-induced autooxidation of high-density lipoprotein decrease cholesterol efflux from human cultured fibroblasts. Biochim Biophys Acta. 1992 Apr 23;1125(2):230–235. doi: 10.1016/0005-2760(92)90050-6. [DOI] [PubMed] [Google Scholar]
  29. Schnell N., Krems B., Entian K. D. The PAR1 (YAP1/SNQ3) gene of Saccharomyces cerevisiae, a c-jun homologue, is involved in oxygen metabolism. Curr Genet. 1992 Apr;21(4-5):269–273. doi: 10.1007/BF00351681. [DOI] [PubMed] [Google Scholar]
  30. Sies H., de Groot H. Role of reactive oxygen species in cell toxicity. Toxicol Lett. 1992 Dec;64-65 Spec No:547–551. doi: 10.1016/0378-4274(92)90230-h. [DOI] [PubMed] [Google Scholar]
  31. Steels E. L., Learmonth R. P., Watson K. Stress tolerance and membrane lipid unsaturation in Saccharomyces cerevisiae grown aerobically or anaerobically. Microbiology. 1994 Mar;140(Pt 3):569–576. doi: 10.1099/00221287-140-3-569. [DOI] [PubMed] [Google Scholar]
  32. Vaca C. E., Vodicka P., Hemminki K. Determination of malonaldehyde-modified 2'-deoxyguanosine-3'-monophosphate and DNA by 32P-postlabelling. Carcinogenesis. 1992 Apr;13(4):593–599. doi: 10.1093/carcin/13.4.593. [DOI] [PubMed] [Google Scholar]
  33. Wu A. L., Moye-Rowley W. S. GSH1, which encodes gamma-glutamylcysteine synthetase, is a target gene for yAP-1 transcriptional regulation. Mol Cell Biol. 1994 Sep;14(9):5832–5839. doi: 10.1128/mcb.14.9.5832. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Yang M. H., Schaich K. M. Factors affecting DNA damage caused by lipid hydroperoxides and aldehydes. Free Radic Biol Med. 1996;20(2):225–236. doi: 10.1016/0891-5849(95)02039-x. [DOI] [PubMed] [Google Scholar]

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