Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants

Plant Journal

Volumn 34, Issue 3, 2003, Pages 363-375

  Thoma, Ingeborg ^a   Loeffler, Christiane ^a   Sinha, Alok K ^a   Gupta, Meetu ^a   Krischke, Markus ^a   Steffan, Bert ^b   Roitsch, Thomas ^a   Mueller, Martin J ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

12 oxo phytodienoic; Isoprostane; Jasmonic acid; Phytoprostane; Prostaglandin

Indexed keywords

CATALYSIS; CELL CULTURE; ENZYMES; FREE RADICALS; GENES; OXIDATION; OXYGEN;

OXIDATIVE STRESS;

PLANTS (BOTANY);

ARABIDOPSIS; BETA-FRUCTOFURANOSIDASE; BOTRYTIS; CELLS, CULTURED; CYCLOPENTANES; ENZYME ACTIVATION; ENZYME INDUCTION; GENE EXPRESSION REGULATION, PLANT; GLUTATHIONE TRANSFERASE; GLYCOSIDE HYDROLASES; IMMUNITY, NATURAL; ISOPROSTANES; LYCOPERSICON ESCULENTUM; MITOGEN-ACTIVATED PROTEIN KINASES; MOLECULAR STRUCTURE; PEROXIDES; PHENYLALANINE AMMONIA-LYASE; PLANT EXTRACTS; PLANTS; REACTIVE OXYGEN SPECIES; SCOPOLETIN; TERPENES; TOBACCO;

BOTRYOTINIA FUCKELIANA; BOTRYTIS; FUNGI; LYCOPERSICON ESCULENTUM; NICOTIANA TABACUM;

EID: 0038367940     PISSN: 09607412     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-313X.2003.01730.x     Document Type: Article

References (40)

1. Bolwell, G.P. (1999) Role of active oxygen species and NO in plant defense responses. Curr. Opin. Plant Biol. 2, 287-294.
2. Bradford, M.M. (1976) A rapid and sensitive method for quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254.
3. Chen, Y., Morrow, J.D. and Roberts, L.J.I.I. (1999) Formation of reactive cyclopentenone compounds in vivo as products of the isoprostane pathway. J. Biol. Chem. 274, 10863-10868.
4. Chong, J., Baltz, R., Schmitt, C., Beffa, R., Fritig, B. and Saindrenan, P. (2002) Downregulation of a pathogen-responsive tobacco UDP-Glc: phenylpropanoid glucosyltransferase reduces scopoletin glucoside accumulation, enhances oxidative stress, and weakens virus resistance. Plant Cell, 14, 1093-1107.
5. Chromczynski, P. and Sacchi, N. (1987) Single step method of RNA isolation by acid guanidium thyocynate-phenol-chloroform extraction. Anal. Biochem. 162, 166-169.
6. Cracowski, J.L., Devillier, P., Durand, T., Stanke-Labesque, F. and Bessard, G. (2001) Vascular biology of the isoprostanes. J. Vasc. Res. 38, 93-103.
7. Godt, D.E. and Roitsch, T. (1997) Differential regulation of a tomato invertase gene family suggests an important function of extracellular isoenzymes in establishing and maintaining sink metabolism. Plant Physiol. 115, 273-282.
8. Govrin, E.M. and Levine, A. (2000) The hypersensitive response facilitates plant infection by necrotrophic pathogen Botrytis cinerea. Curr. Biol. 10, 761-767.
9. Goy, P.A., Signer, H., Reist, R., Aichholz, R., Blum, W., Schmidt, E. and Kessmann, H. (1993) Accumulation of scopoletin is associated with high disease resistance of the hybrid Nicotiana glutinosa x Nicotiana debneyi. Planta, 191, 200-206.
10. Gundlach, H., Müller, M.J., Kutchan, T.M. and Zenk, M.H. (1992) Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures. Proc. Natl. Acad. Sci. USA, 89, 2389-2393.
11. Gundlach, H. and Zenk, M.H. (1998) Biological activity and biosynthesis of pentacyclic oxylipins: the linoleic acid pathway. Phytochemistry, 47, 527-537.
12. 1) from α-linolenic acid in plants. Free Radic. Biol. Med. 28, 720-726.
13. 1) in plants. Plant Physiol. 124, 1293-1303.
14. - from the oxidative burst are essential components in triggering defense gene activation and phytoalexin synthesis in parsley. Proc. Natl. Acad. Sci. USA, 94, 4800-4805.
15. 2-Isoprostanes as an index of oxidative stress in vivo. Free Radic. Biol. Med. 28, 505-513.
16. Janssen, L.J. (2001) Isoprostanes: an overview and putative roles in pulmonary pathophysiology. Am. J. Physiol. Lung Cell Mol. Physiol. 280, L1067-L1082.
17. Keinänen, M., Oldham, N.J. and Baldwin, I.T. (2001) Rapid HPLC screening of jasmonate-induced increases in tobacco alkaloids, phenolics, and diterpene glycosides in Nicotiana attenuata. J. Agric. Food Chem. 49, 3553-3558.
18. Kovtun, Y., Chiu, W.-L., Tena, G. and Sheen, J. (2000) Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants. Proc. Natl. Acad. Sci. USA, 97, 2940-2945.
19. Lawson, J.A., Rokach, J. and FitzGerald, G.A. (1999) Isoprostanes: formation, analysis and use as indices of lipid peroxidation in vivo. J. Biol. Chem. 274, 24441-24444.
20. Link, V.L., Hofmann, M.G., Sinha, A.K., Ehness, R., Strnad, M. and Roitsch, T. (2002) Biochemical evidence for the activation of distinct subsets of mitogen-activated protein kinases by voltage and defense-related stimuli. Plant. Physiol. 128, 271-281.
21. 2-isoprostanes) are formed in situ in phospholipids. Proc. Natl. Acad. Sci. USA, 89, 10721-10725.
22. Morrow, J.D., Harris, T.M. and Roberts, L.J. (1990) Noncyclooxygenase oxidative formation of a series of novel prostaglandins: analytical ramifications for measurement of eicosanoids. Anal. Biochem. 184, 1-10.
23. Muckenschnabel, I., Williamson, B., Goodman, B.A., Lyon, G.D., Stewart, D. and Deighton, N. (2001) Markers for oxidative stress associated with soft rots in French beans (Phaseolus vulgaris) infected by Botrytis cinerea. Planta, 212, 376-381.
24. Mueller, M.J. (1998) Radically novel prostaglandins in animals and plants: the isoprostanes. Chem. Biol. 5, 323-333.
25. Mueller, M.J. and Brodschelm, W. (1994) Quantification of jasmonic acid by capillary gas chromatography-negative chemical ionization-mass spectrometry. Anal. Biochem. 218, 425-435.
26. Parchmann, S., Gundlach, H. and Mueller, M.J. (1997) Induction of 12-oxo-phytodienoic acid in wounded plants and elicited plant cell cultures. Plant Physiol. 115, 1057-1064.
27. 1 from α-linolenic acid in plants. J. Biol. Chem. 273, 32650-32655.
28. Pratico, D., Lawson, J.A., Rokach, J. and FitzGerald, G.A. (2001) The isoprostanes in biology and medicine. Trends Endocrinol. Metab. 12, 243-247.
29. Rate, D. and Greenberg, J.T. (2001) The Arabidopsis aberrant growth and death2 mutant shows resistance to Pseudomonas syringae and reveals a role for NPR1 in suppressing hypersensitive cell death. Plant J. 27, 203-211.
30. Roberts, L.J. and Morrow, J.D. (1997) The generation and actions of isoprostanes. Biochim. Biophys. Acta, 1345, 121-135.
31. Roberts, L.J. and Morrow, J.D. (2002) Products of the isoprostane pathway: unique bioactive compounds and markers of lipid peroxidation. Cell. Mol. Life Sci. 59, 808-820.
32. Roitsch, T. (1999) Source-sink regulation by sugar and stress. Curr. Opin. Plant Biol. 2, 198-206.
33. Rokach, J., Khanapure, S.P., Hwang, S.-W., Adiyaman, M., Lawson, J.A. and FitzGerald, G.A. (1997) Nomenclature of isoprostanes: a proposal. Prostaglandins, 54, 853-873.
34. Sharan, M., Taguchi, G., Gonda, K., Jouke, T., Shimosaka, M., Hayashida, N. and Okazaki, M. (1998) Effects of methyl jasmonate and elicitor on the activation of phenylalanine ammonia-lyase and the accumulation of scopoletin and scopolin in tobacco cell cultures. Plant Sci. 132, 13-19.
35. Stintzi, A., Weber, H., Reymond, P., Browse, J. and Farmer, E.E. (2001) Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proc. Natl. Acad. Sci. USA, 98, 12837-12842.
36. Tierens, K.F.M.-J., Thomma, B.P.H.J., Bari, R.P., Garmier, M., Eggermont, K., Brouwer, M., Penninckx, I.A.M.A., Broekaert, W.F. and Cammue, B.P.A. (2002) ESA1, an Arabidopsis mutant with enhanced susceptibility to a range of necrotrophic fungal pathogens, shows a distorted induction of defense responses by reactive oxygen generating compounds. Plant J. 29, 131-140.
37. Vollenweider, S., Weber, H., Stolz, S., Chetelat, A. and Farmer, E.E. (2000) Fatty acid ketodienes and fatty acid ketotrienes: michael addition acceptors that accumulate in wounded and diseased Arabidopsis leaves. Plant J. 24, 467-476.
38. Vranova, E., Inze, D. and Van Breusegem, F. (2002) Signal transduction during oxidative stress. J. Exp. Bot. 53, 1227-1236.
39. Wojtaszek, P. (1997) Oxidative burst: an early plant response to pathogen infection. Biochem. J. 322, 681-692.
40. Zhang, S. and Klessig, D.F. (1997) Salicylic acid activates a 48-kD MAP kinase in tobacco. Plant Cell, 9, 809-824.