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The Expression Patterns of AtBSMT1 and AtSAGT1 Encoding a Salicylic Acid (SA) Methyltransferase and a SA Glucosyltransferase, Respectively, in Arabidopsis Plants with Altered Defense Responses

  • Song, Jong Tae (School of Applied Biosciences, Kyungpook National University) ;
  • Koo, Yeon Jong (School of Agricultural Biotechnology, Seoul National University) ;
  • Park, Jong-Beum (School of Applied Biosciences, Kyungpook National University) ;
  • Seo, Yean Joo (School of Applied Biosciences, Kyungpook National University) ;
  • Cho, Yeon-Jeong (School of Applied Biosciences, Kyungpook National University) ;
  • Seo, Hak Soo (Department of Plant Bioscience, Seoul National University) ;
  • Choi, Yang Do (School of Agricultural Biotechnology, Seoul National University)
  • Received : 2009.05.11
  • Accepted : 2009.06.24
  • Published : 2009.08.31

Abstract

We reported previously that overexpression of a salicylic acid (SA) methyltransferase1 gene from rice (OsBSMT1) or a SA glucosyltransferase1 gene from Arabidopsis thaliana (AtSAGT1) leads to increased susceptibility to Pseudomonas syringae due to reduced SA levels. To further examine their roles in the defense responses, we assayed the transcript levels of AtBSMT1 or AtSAGT1 in plants with altered levels of SA and/or other defense components. These data showed that AtSAGT1 expression is regulated partially by SA, or nonexpressor of pathogenesis related protein1, whereas AtBSMT1 expression was induced in SA-deficient mutant plants. In addition, we produced the transgenic Arabidopsis plants with RNAi-mediated inhibition of AtSAGT1 and isolated a null mutant of AtBSMT1, and then analyzed their phenotypes. A T-DNA insertion mutation in the AtBSMT1 resulted in reduced methyl salicylate (MeSA) levels upon P. syringae infection. However, accumulation of SA and glucosyl SA was similar in both the atbsmt1 and wild-type plants, indicating the presence of another SA methyltransferase or an alternative pathway for MeSA production. The AtSAGT1-RNAi line exhibited no altered phenotypes upon pathogen infection, compared to wild-type plants, suggesting that (an)other SA glucosyltransferase(s) in Arabidopsis plants may be important for the pathogenesis of P. syringae.

Keywords

Acknowledgement

Supported by : Korea Research Foundation

References

  1. Attaran, E., Zeier, T.E., Griebel, T., and Zeier J. (2009). Methyl salicylate production and jasmonate signaling are not essential for systemic acquired resistance in Arabidopsis. Plant Cell 21, 954-971 https://doi.org/10.1105/tpc.108.063164
  2. Baldwin, I.T., Halitschke, R., Paschold, A., von Dahl, C.C., and Preston, C.A. (2006). Volatile signaling in plant-plant interactions: 'talking trees' in the genomics era. Science 311, 812-815 https://doi.org/10.1126/science.1118446
  3. Cao, H., Bowling, S.A., Gordon, S., and Dong, X. (1994). Characterization of an Arabidopsis mutant that is nonresponsive to inducers of systemic acquired resistance. Plant Cell 6, 1583-1592 https://doi.org/10.1105/tpc.6.11.1583
  4. Chen, F., D'Auria, J.C., Tholl, D., Ross, J.R., Gershenzon, J., Noel, J.P., and Pichersky, E. (2003). An Arabidopsis thaliana gene for methylsalicylate biosynthesis, identified by a biochemical genomics approach, has a role in defense. Plant J. 36, 577-588 https://doi.org/10.1046/j.1365-313X.2003.01902.x
  5. Dean, J., and Delaney, S. (2008). Metabolism of salicylic acid in wild-type, ugt74f1 and ugt74f2 glucosyltransferase mutants of Arabidopsis thaliana. Physiol. Plant. 132, 417-425 https://doi.org/10.1111/j.1399-3054.2007.01041.x
  6. Dean, J., Mohammed, L.A., and Fitzpatrick, T. (2005). The formation, vacuolar localization, and tonoplast transport of salicylic acid glucose conjugates in tobacco cell suspension cultures. Planta 221, 287-296 https://doi.org/10.1007/s00425-004-1430-3
  7. Delaney, T.P., Uknes, S., Vernooij, B., Friedrich, L., Weymann, K., Negrotto, D., Gaffney, T., Gut-Rella, M., Kessmann, H., Ward, E., et al. (1994). A central role of salicylic acid in plant disease resistance. Science 266, 1247-1250 https://doi.org/10.1126/science.266.5188.1247
  8. Edwards, R. (1994). Conjugation and metabolism of salicylic acid in tobacco. J. Plant Physiol. 143, 609-614 https://doi.org/10.1016/S0176-1617(11)81146-6
  9. Engelberth, J., Schmelz, E.A., Alborn, H.T., Cardoza, Y.J., Huang, J., and Tumlinson, J.H. (2003). Simulaneous quantification of jasmonic acid and salicylic acid in plants by vapor-phase extraction extraction and gas chromatography-chemical ionization-mass spectrometry. Anal. Biochem. 312, 242-250 https://doi.org/10.1016/S0003-2697(02)00466-9
  10. Gaffney, T., Friedrich, L., Vernooij, B., Negrotto, D., Nye, G., Uknes, S., Ward, E., Kessmann, H., and Ryals, J. (1993). Requirement of salicylic acid for the induction systemic acquired resistance. Science 261, 754-756 https://doi.org/10.1126/science.261.5122.754
  11. Kim, M.G., Kim, S.Y., Kim, W.Y., Mackey, D., and Lee, S.Y. (2008). Responses of Arabidopsis thaliana to challenge by Pseudomo-nas syringae. Mol. Cells 25, 323-331
  12. Koo, Y.J., Kim, M.A., Kim, E.H., Song, J.T., Jung, C., Moon, J.-K., Kim, J.-H., Seo, H.S., Song, S.I., Kim, J.-K., et al. (2007). Overexpression of salicylic acid carboxyl methyltransferase reduces salicylic acid-mediated pathogen resistance in Arabidopsis thaliana. Plant Mol. Biol. 64, 1-15 https://doi.org/10.1007/s11103-006-9123-x
  13. Kroczek, R.A., and Siebert, E. (1990). Optimization of Northern analysis by vaccum-blotting, RNA transfer, visualization and ultraviolet fixation. Anal. Biochem. 184, 90-95 https://doi.org/10.1016/0003-2697(90)90017-4
  14. Lee, H.-I., and Raskin, I. (1998). Glucosylation of salicylic acid in Nicotiana tabacum cv. Xanthi-nc. Phytopathology 88, 692-697 https://doi.org/10.1094/PHYTO.1998.88.7.692
  15. Lee, H.-I., Leon, J., and Raskin, I. (1995). Biosynthesis and metabolism of salicylic acid. Proc. Natl. Acad. Sci. USA 92, 4076-4079 https://doi.org/10.1073/pnas.92.10.4076
  16. Loake, G., and Grant, M. (2007). Salicyllic acid in plant defense-the players and protagonists. Curr. Opin. Plant Biol. 10, 466-472 https://doi.org/10.1016/j.pbi.2007.08.008
  17. Lim, E.-K., Doucet, C.J., Li, Y., Elias, L., Worrall, D., Spencer, S.P., Ross, J., and Bowles, D.J. (2002). The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic acid, and other benzoates. J. Biol. Chem. 277, 586-592 https://doi.org/10.1074/jbc.M109287200
  18. Park, S.W., Kaimoyo, E., Kumar, D., Mosher, S., and Klessig, D.F. (2007). Methyl salicylate is a critical mobile signal for plant systemic acquired resistance. Science 318, 113-116 https://doi.org/10.1126/science.1147113
  19. Rate, D.N., 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 https://doi.org/10.1046/j.0960-7412.2001.1075umedoc.x
  20. Rate, D.N., Cuenca, J.V., Bowman, G.R., and Greenberg, J.T. (1999). The gain-of-function Arabidopsis acd6 mutant reveals novel regulation and function of the salicylic acid signaling pathway in controlling cell death, defense, and cell growth. Plant Cell 11, 1695-1708 https://doi.org/10.1105/tpc.11.9.1695
  21. Seskar, M., Shulaev, V., and Raskin, I. (1998). Endogenous methyl salicylate in pathogen-inoculated tobacco plants. Plant Physiol. 116, 387-392 https://doi.org/10.1104/pp.116.1.387
  22. Shulaev, V., Silverman, P., and Raskin, I. (1997). Airborne signaling by methyl salicylate in plant pathogen resistance. Nature 385, 718-721 https://doi.org/10.1038/385718a0
  23. Song, J.T. (2006). Induction of a salicylic acid glucosyltransferase, AtSGT1, is an early disease response in Arabidopsis thaliana. Mol. Cells 22, 233-238
  24. Song, J.T., Koo, Y.J., Seo, H.S., Kim, M.C., Choi, Y.D., and Kim, J.H. (2008). Overexpression of AtSGT1, an Arabidopsis salicylic acid glucosyltransferase, leads to increased susceptibility to Pseudomonas syringae. Phytochemistry 69, 1128-1134 https://doi.org/10.1016/j.phytochem.2007.12.010
  25. Vlot, A.C., Liu, P.P., Cameron, R.K., Park, S.W., Yang, Y., Kumar, D., Zhou, F., Padukkavidana, T., Gustafsson, C., Pichersky, E., et al. (2008). Identification of likely orthologs of tobacco salicylic acid-binding protein 2 and their role in systemic acquired resistance in Arabidopsis thaliana. Plant J. 56, 445-456 https://doi.org/10.1111/j.1365-313X.2008.03618.x
  26. Wildermuth, M.C., Dewdney, J., Wu, G., and Ausubel F.M. (2001). Isochorismate synthase is required to synthesize salicylic acid for plant defense. Nature 414, 562-565 https://doi.org/10.1038/35107108
  27. Zhou, N., Tootle, T.L., Tsui, F., Klessig, D.F., and Glazebrook, J. (1998). PAD4 functions upstream from salicylic acid to control defense responses in Arabidopsis. Plant Cell 10, 1021-1030 https://doi.org/10.1105/tpc.10.6.1021

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