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. 1997 May;114(1):79–88. doi: 10.1104/pp.114.1.79

Jasmonate-Inducible Genes Are Activated in Rice by Pathogen Attack without a Concomitant Increase in Endogenous Jasmonic Acid Levels.

P Schweizer 1, A Buchala 1, P Silverman 1, M Seskar 1, I Raskin 1, J P Metraux 1
PMCID: PMC158281  PMID: 12223690

Abstract

The possible role of the octadecanoid signaling pathway with jasmonic acid (JA) as the central component in defense-gene regulation of pathogen-attacked rice was studied. Rice (Oryza sativa L.) seedlings were treated with JA or inoculated with the rice blast fungus Magnaporthe grisea (Hebert) Barr., and gene-expression patterns were compared between the two treatments. JA application induced the accumulation of a number of pathogenesis-related (PR) gene products at the mRNA and protein levels, but pathogen attack did not enhance the levels of (-)-JA during the time required for PR gene expression. Pathogen-induced accumulation of PR1-like proteins was reduced in plants treated with tetcyclacis, a novel inhibitor of jasmonate biosynthesis. There was an additive and negative interaction between JA and an elicitor from M. grisea with respect to induction of PR1-like proteins and of an abundant JA-and wound-induced protein of 26 kD, respectively. Finally, activation of the octadecanoid signaling pathway and induction of a number of PR genes by exogenous application of JA did not confer local acquired resistance to rice. The data suggest that accumulation of nonconjugated (-)-JA is not necessary for induction of PR genes and that JA does not orchestrate localized defense responses in pathogen-attacked rice. Instead, JA appears to be embedded in a signaling network with another pathogen-induced pathway(s) and may be required at a certain minimal level for induction of some PR genes.

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Selected References

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  1. Andresen I., Becker W., Schlüter K., Burges J., Parthier B., Apel K. The identification of leaf thionin as one of the main jasmonate-induced proteins of barley (Hordeum vulgare). Plant Mol Biol. 1992 May;19(2):193–204. doi: 10.1007/BF00027341. [DOI] [PubMed] [Google Scholar]
  2. Bunker T. W., Koetje D. S., Stephenson L. C., Creelman R. A., Mullet J. E., Grimes H. D. Sink limitation induces the expression of multiple soybean vegetative lipoxygenase mRNAs while the endogenous jasmonic acid level remains low. Plant Cell. 1995 Aug;7(8):1319–1331. doi: 10.1105/tpc.7.8.1319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chandra S., Heinstein P. F., Low P. S. Activation of Phospholipase A by Plant Defense Elicitors. Plant Physiol. 1996 Mar;110(3):979–986. doi: 10.1104/pp.110.3.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chaudhry B., Müller-Uri F., Cameron-Mills V., Gough S., Simpson D., Skriver K., Mundy J. The barley 60 kDa jasmonate-induced protein (JIP60) is a novel ribosome-inactivating protein. Plant J. 1994 Dec;6(6):815–824. doi: 10.1046/j.1365-313x.1994.6060815.x. [DOI] [PubMed] [Google Scholar]
  5. Choi D., Bostock R. M., Avdiushko S., Hildebrand D. F. Lipid-derived signals that discriminate wound- and pathogen-responsive isoprenoid pathways in plants: methyl jasmonate and the fungal elicitor arachidonic acid induce different 3-hydroxy-3-methylglutaryl-coenzyme A reductase genes and antimicrobial isoprenoids in Solanum tuberosum L. Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2329–2333. doi: 10.1073/pnas.91.6.2329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Creelman R. A., Tierney M. L., Mullet J. E. Jasmonic acid/methyl jasmonate accumulate in wounded soybean hypocotyls and modulate wound gene expression. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4938–4941. doi: 10.1073/pnas.89.11.4938. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Doares S. H., Syrovets T., Weiler E. W., Ryan C. A. Oligogalacturonides and chitosan activate plant defensive genes through the octadecanoid pathway. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4095–4098. doi: 10.1073/pnas.92.10.4095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Farmer E. E. Fatty acid signalling in plants and their associated microorganisms. Plant Mol Biol. 1994 Dec;26(5):1423–1437. doi: 10.1007/BF00016483. [DOI] [PubMed] [Google Scholar]
  9. Farmer E. E., Ryan C. A. Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proc Natl Acad Sci U S A. 1990 Oct;87(19):7713–7716. doi: 10.1073/pnas.87.19.7713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Farmer E. E., Ryan C. A. Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. Plant Cell. 1992 Feb;4(2):129–134. doi: 10.1105/tpc.4.2.129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gundlach H., Müller M. J., Kutchan T. M., Zenk M. H. Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2389–2393. doi: 10.1073/pnas.89.6.2389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hildmann T., Ebneth M., Peña-Cortés H., Sánchez-Serrano J. J., Willmitzer L., Prat S. General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding. Plant Cell. 1992 Sep;4(9):1157–1170. doi: 10.1105/tpc.4.9.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hopke J., Donath J., Blechert S., Boland W. Herbivore-induced volatiles: the emission of acyclic homoterpenes from leaves of Phaseolus lunatus and Zea mays can be triggered by a beta-glucosidase and jasmonic acid. FEBS Lett. 1994 Sep 26;352(2):146–150. doi: 10.1016/0014-5793(94)00948-1. [DOI] [PubMed] [Google Scholar]
  14. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  15. Nojiri H., Sugimori M., Yamane H., Nishimura Y., Yamada A., Shibuya N., Kodama O., Murofushi N., Omori T. Involvement of Jasmonic Acid in Elicitor-Induced Phytoalexin Production in Suspension-Cultured Rice Cells. Plant Physiol. 1996 Feb;110(2):387–392. doi: 10.1104/pp.110.2.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ohta H., Shida K., Peng Y. L., Furusawa I., Shishiyama J., Aibara S., Morita Y. A Lipoxygenase Pathway Is Activated in Rice after Infection with the Rice Blast Fungus Magnaporthe grisea. Plant Physiol. 1991 Sep;97(1):94–98. doi: 10.1104/pp.97.1.94. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Peng Y. L., Shirano Y., Ohta H., Hibino T., Tanaka K., Shibata D. A novel lipoxygenase from rice. Primary structure and specific expression upon incompatible infection with rice blast fungus. J Biol Chem. 1994 Feb 4;269(5):3755–3761. [PubMed] [Google Scholar]
  18. Reimmann C., Dudler R. cDNA cloning and sequence analysis of a pathogen-induced thaumatin-like protein from rice (Oryza sativa). Plant Physiol. 1993 Mar;101(3):1113–1114. doi: 10.1104/pp.101.3.1113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Reimmann C., Ringli C., Dudler R. Complementary DNA cloning and sequence analysis of a pathogen-induced putative peroxidase from rice. Plant Physiol. 1992 Nov;100(3):1611–1612. doi: 10.1104/pp.100.3.1611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Schweizer P., Gees R., Mosinger E. Effect of Jasmonic Acid on the Interaction of Barley (Hordeum vulgare L.) with the Powdery Mildew Erysiphe graminis f.sp. hordei. Plant Physiol. 1993 Jun;102(2):503–511. doi: 10.1104/pp.102.2.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Seo S., Okamoto M., Seto H., Ishizuka K., Sano H., Ohashi Y. Tobacco MAP kinase: a possible mediator in wound signal transduction pathways. Science. 1995 Dec 22;270(5244):1988–1992. doi: 10.1126/science.270.5244.1988. [DOI] [PubMed] [Google Scholar]
  22. Silverman P., Seskar M., Kanter D., Schweizer P., Metraux J. P., Raskin I. Salicylic Acid in Rice (Biosynthesis, Conjugation, and Possible Role). Plant Physiol. 1995 Jun;108(2):633–639. doi: 10.1104/pp.108.2.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Simmons C. R., Litts J. C., Huang N., Rodriguez R. L. Structure of a rice beta-glucanase gene regulated by ethylene, cytokinin, wounding, salicylic acid and fungal elicitors. Plant Mol Biol. 1992 Jan;18(1):33–45. doi: 10.1007/BF00018454. [DOI] [PubMed] [Google Scholar]
  24. Swegle M., Kramer K. J., Muthukrishnan S. Properties of Barley Seed Chitinases and Release of Embryo-Associated Isoforms during Early Stages of Imbibition. Plant Physiol. 1992 Jul;99(3):1009–1014. doi: 10.1104/pp.99.3.1009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Xu Y., Chang PFL., Liu D., Narasimhan M. L., Raghothama K. G., Hasegawa P. M., Bressan R. A. Plant Defense Genes Are Synergistically Induced by Ethylene and Methyl Jasmonate. Plant Cell. 1994 Aug;6(8):1077–1085. doi: 10.1105/tpc.6.8.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Zhu Q., Dabi T., Beeche A., Yamamoto R., Lawton M. A., Lamb C. Cloning and properties of a rice gene encoding phenylalanine ammonia-lyase. Plant Mol Biol. 1995 Nov;29(3):535–550. doi: 10.1007/BF00020983. [DOI] [PubMed] [Google Scholar]

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