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The Hypernodulating nts Mutation Induces Jasmonate Synthetic Pathway in Soybean Leaves  

Seo, Hak Soo (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Li, Jinjie (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Lee, Sun-Young (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Yu, Jae-Woong (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Kim, Kil-Hyun (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Lee, Suk-Ha (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Lee, In-Jung (Department of Applied Biosciences, Kyungpook National University)
Paek, Nam-Chon (Department of Plant Science and Research Institute of Agriculture and Life Sciences, Seoul National University)
Abstract
Symbiotic nitrogen fixation with nitrogen-fixing bacteria in the root nodules is a distinctly beneficial metabolic process in legume plants. Legumes control the nodule number and nodulation zone through a systemic negative regulatory system between shoot and root. Mutation in the soybean NTS gene encoding GmNARK, a CLAVATA1-like serine/threonine receptor-like kinase, causes excessive nodule development called hypernodulation. To examine the effect of nts mutation on the gene expression profile in the leaves, suppression subtractive hybridization was performed with the trifoliate leaves of nts mutant 'SS2-2' and the wild-type (WT) parent 'Sinpaldalkong2', and 75 EST clones that were highly expressed in the leaves of the SS2-2 mutant were identified. Interestingly, the expression of jasmonate (JA)-responsive genes such as vspA, vspB, and Lox2 were upregulated, whereas that of a salicylate-responsive gene PR1a was suppressed in the SS2-2 mutant. In addition, the level of JA was about two-fold higher in the leaves of the SS2-2 mutant than in those of the WT under natural growth conditions. Moreover, the JA-responsive gene expression persists in the leaves of SS2-2 mutant without rhizobia infection in the roots. Taken together, our results suggest that the nts mutation increases JA synthesis in mature leaves and consequently leads to constitutive expression of JA-responsive genes which is irrelevant to hypernodulation in the root.
Keywords
Hypernodulation; Jasmonate; NTS; Salicylate; Soybean; SSH; vspA; vspB;
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1 Nakagawa, T. and Kawaguchi, M. (2006) Shoot-applied MeJA suppresses root nodulation in Lotus japonicus. Plant Cell Physiol. 47, 176−180
2 Nutman, P. S. (1952) Host-factors influencing infection and nodule development in leguminous plants. Proc. R Soc. Lond. B Biol. Sci. 139, 176−185
3 Oka-Kira, E. and Kawaguchi, M. (2006) Long-distance signaling to control root nodule number. Curr. Opin. Plant Biol. 9, 496−502
4 Benedetti, C. E., Xie, D., and Turner, J. G. (1995) coi1-dependent expression of an Arabidopsis vegetative storage protein in flowers and siliques and in response to coronatine or methyl jasmonate. Plant Physiol. 109, 567−572
5 Diatchenko, L., Lukyanov, S., Lau, Y. F., and Siebert, P. D. (1999) Suppression subtractive hybridization: a versatile method for identifying differentially expressed genes. Methods Enzymol. 303, 349−380   DOI
6 Ellis, C., Karafyllidis, I., Wasternack, C., and Turner, J. G. (2002) The Arabidopsis mutant cev1 links cell wall signaling to jasmonate and ethylene responses. Plant Cell 14, 1557− 1566
7 Ha, B. K. and Lee, S. H. (2001) Growth, nitrogen metabolism and nodulation of hypernodulating soybean mutant as effected by soil fertility. Korean J. Crop Sci. 46, 145−149
8 Lorenzo, O., Piqueras, R., Sanchez-Serrano, J. J., and Solano, R. (2003) ETHYLENE RESPONSE FACTOR1 integrates signals from ethylene and jasmonate pathways in plant defense. Plant Cell 15, 165−178
9 Krusell, L., Madsen, L. H., Sato, S., Aubert, G., Genua, A., et al. (2002) Shoot control of root development and nodulation is mediated by a receptor-like kinase. Nature 420, 422−426
10 Norman-Setterblad, C., Vidal, S., and Palva, E. T. (2000) Interacting signal pathways control defense gene expression in Arabidopsis in response to cell wall-degrading enzymes from Erwinia carotovora. Mol. Plant Microbe Interact. 13, 430− 438
11 Seo, H. S., Song, J. T., Cheong, J. J., Lee, Y. H., Lee, Y.W., et al. (2001) Jasmonic acid carboxyl methyltransferase: a key enzyme for jasmonate-regulated plant responses. Proc. Natl. Acad. Sci. USA 98, 4788−4793
12 Caetano-Anolles G. and Gresshoff P. M. (1990) Early induction of feedback regulatory responses governing nodulation in soybean. Plant Sci. 71, 69−81
13 Staswick, P. E. (1990) Novel regulation of vegetative storage protein genes. Plant Cell 2, 1−6
14 Tang, Z., Sadka, A., Morishige, D. T., and Mullet, J. E. (2001) Homeodomain leucine zipper proteins bind to the phosphate response domain of the soybean VspB tripartite promoter. Plant Physiol. 125, 797−809
15 Lee, H. S., Chae, Y. A., Park, E. H., Kim, Y. W., Yun, K. I., et al. (1997) Introduction, development, and characterization of supernodulating soybean mutant. Korean J. Crop Sci. 42, 247− 253
16 Sivasankar, S., Sheldrick, B., and Rothstein, S. J. (2000) Expression of allene oxide synthase determines defense gene activation in tomato. Plant Physiol. 122, 1335−1342
17 Creelman, R. A., Tierney, M. L., and Mullet, J. E. (1992) Jasmonic acid/methyl jasmonate accumulate in wounded soybean hypocotyls and modulate wound gene expression. Proc. Natl. Acad. Sci. USA 89, 4938−4941
18 Sun, J., Cardoza, V., Mitchell, D. M., Bright, L., Oldroyd, G., et al. (2006) Crosstalk between jasmonic acid, ethylene and Nod factor signaling allows integration of diverse inputs for regulation of nodulation. Plant J. 46, 961−970
19 Halim, V. A., Vess, A., Scheel, D., and Rosahl, S. (2006) The role of salicylic acid and jasmonic acid in pathogen defence. Plant Biol. 8, 307−313
20 Mason, H. S. and Mullet, J. E. (1990) Expression of two soybean vegetative storage protein genes during development and in response to water deficit, wounding, and jasmonic acid. Plant Cell 2, 569−579
21 Peters, N. K., Frost, J. W., and Long, S. R. (1986) A plant flavone, luteolin, induces expression of Rhizobium meliloti nodulation genes. Science 233, 977−980   DOI
22 Stacey, G., McAlvin, C. B., Kim, S. Y., Olivares, J., and Soto, M. J. (2006b) Effects of endogenous salicylic acid on nodulation in the model legumes Lotus japonicus and Medicago truncatula. Plant Physiol. 141, 1473−1481
23 Penninckx, I. A., Thomma, B. P., Buchala, A., Métraux J. P., and Broekaert, W. F. (1998) Concomitant activation of jasmonate and ethylene response pathways is required for induction of a plant defensin gene in Arabidopsis. Plant Cell 10, 2103− 2113
24 Searle, I. R., Men, A. E., Laniya, T. S., Buzas, D. M., Iturbe- Ormaetxe, I., et al. (2003) Long-distance signaling in nodulation directed by a CLAVATA1-like receptor kinase. Science 299, 109−121
25 Reymond, P. and Farmer, E. E. (1998) Jasmonate and salicylate as global signals for defense gene expression. Curr. Opin. Plant Biol. 1, 404−411
26 Rojo, E., Leon, J., and Sanchez-Serrano, J. J. (1999) Cross-talk between wound signaling pathways determines local versus systemic gene expression in Arabidopsis thaliana. Plant J. 20, 135−142
27 Stacey, G., Libault, M., Brechenmacher, L., Wan, J., and May, G. D. (2006a) Genetics and functional genomics of legume nodulation. Curr. Opin. Plant Biol. 9, 110−121
28 Delves, A. C., Mathews, A., Day, D. A., Carter, A. S., Carroll, B. J., et al. (1986) Regulation of the soybean-rhizobium nodule symbiosis by shoot and root factors. Plant Physiol. 82, 588− 590
29 Lee, B. K., Park, M. R., Srinivas, B., Chun, J. C., Kwon, I. S., et al. (2003) Induction pf phenylalanine ammonia-lyase gene expression by paraquat and stress-related hormones in Rehmannia glutinosa. Mol. Cells 16, 34−39
30 Creelman, R. A. and Mullet, J. E. (1995) Jasmonic acid distribution and action in plants: regulation during development and response to biotic and abiotic stress. Proc. Natl. Acad. Sci. USA 92, 4114−4119
31 Staswick, P. E. (1997) The occurrence and gene expression of vegetative storage proteins and a Rubisco complex protein in several perennial soybean species. J. Exp. Bot. 48, 2031− 2036