Activation of the Jasmonate Biosynthesis Pathway in Roots in Drought Stress

Climate Change and Plant Abiotic Stress Tolerance

Volumn , Issue , 2013, Pages 325-342

  Poltronieri, Palmiro ^a   Taurino, Marco ^a   De Domenico, Stefania ^a   Bonsegna, Stefania ^a   Santino, Angelo ^a  

^a INSTITUTE OF SCIENCES OF FOOD PRODUCTION   (Italy)

Author keywords

Abiotic stress signaling; Drought; Jasmonate; microRNA; Soil environment; Symbiotic organism

Indexed keywords

AGRONOMY; BIOCHEMISTRY; BIODEGRADATION; BIOSYNTHESIS; CHEMICAL ACTIVATION; DROUGHT; PHYSIOLOGY; PLANT SHUTDOWNS; PLANTS (BOTANY); RNA; VOLATILE ORGANIC COMPOUNDS;

ABIOTIC STRESS; JASMONATES; MICRORNAS; SOIL ENVIRONMENT; SYMBIOTIC ORGANISM;

VOLATILE FATTY ACIDS;

EID: 84912064954     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527675265.ch13     Document Type: Chapter

References (70)

1. Xiong, L., Schumaker, K.S., and Zhu, J.K. (2002) Cell signalling during cold, drought, and salt stress. Plant Cell, 14, S165-S183.
2. Shinozaki, K. and Yamaguchi-Shinozaki, K. (2007) Gene networks involved in drought stress response and tolerance. J. Exp. Bot., 58, 221-227.
3. Jakab, G., Ton, J., Flors, V., Zimmerli, L., Métraux, J.P., and Mauch-Mani, B. (2005) Enhancing Arabidopsis salt and drought stress tolerance by chemical priming for its abscisic acid responses. Plant Physiol., 139, 267-274.
4. Borsani, O., Valpuesta, V., and Botella, M.A. (2001) Evidence for a role of salicylic acid in the oxidative damage generated by NaCl and osmotic stress in Arabidopsis seedlings. Plant Physiol., 126, 1024-1030.
5. Serrano, R., Mulet, J.M., Rios, G., Marquez, J.A., de Larriona, I.F., Leube, M.P., Mendizabal, I., Pascual-Ahuir, A., Proft, M., Ros, R. et al. (1999) A glimpse of the mechanisms of ion homeostasis during salt stress. J. Exp. Bot., 50, 1023-1036.
6. Hasegawa, P.M., Bressan, R.A., Zhu, J.K., and Bohnert, H.J. (2000) Plant cellular and molecular responses to high salinity. Annu. Rev. Plant Physiol. Plant Mol. Biol., 51, 463-499.
7. Rodriguez-Navarro, A. (2000) Potassium transport in fungi and plants. Biochim. Biophys. Acta, 1469, 1-30.
8. Spoel, S.H., Koornneef, A., Claessens, S.M.C., Korzelius, J.P., Van Pelt, J.A., Mueller, M.J., Buchala, A.J., Metraux, J.-P., Brown, R., Kazan, K., van Loon, L.C., Dong, X., and Pieterse, C.M. (2003) NPR1 modulates cross-talk between salicylate-and jasmonate-dependent defense pathways through a novel function in the cytosol. Plant Cell, 15, 760-770.
9. Memelink, J. (2009) Regulation of gene expression by jasmonate hormones. Phytochemistry, 70, 1560-1570.
10. Zarei, A., Körbes, A.P., Younessi, P., Montiel, G., Champion, A., and Memelink, J. (2011) Two GCC boxes and AP2/ERFdomain transcription factor ORA59 in jasmonate/ethylene-mediated activation of the PDF1.2 promoter in Arabidopsis. Plant Mol. Biol., 75, 321-331.
11. Gfeller, A., Dubugnon, L., Liechti, R., and Farmer, E.E. (2010) Jasmonate biochemical pathway. Sci. Signal., 3 (109), cm3.
12. Fujita, M., Fujita, Y., Noutoshi, Y., Takahashi, F., Narusaka, Y., Yamaguchi-Shinozaki, K., and Shinozaki, K. (2006) Crosstalk between biotic and abiotic stress responses: a current view from the points of convergence in the stress signaling networks. Curr. Opin. Plant Biol., 9, 436-442.
13. Goodger, J.Q.D. and Schachtman, D.P. (2010) Re-examining the role of ABA as the primary long-distance signal produced by water-stressed roots. Plant Signal. Behav., 5, 1298-1301.
14. Schaller, A. and Stintzi, A. (2009) Enzymes in jasmonate biosynthesis -structure, function, regulation. Phytochemistry, 70, 1532-1538.
15. Wasternack, C. (2007) Jasmonates: an up date on biosynthesis, signal transduction and action in plant stress response, growth and development. Ann. Bot., 100, 681-697.
16. Hughes, R.K., De Domenico, S., and Santino, A. (2009) Plant Cytochromes CYP74: biochemical features, endocellular localisation, activation mechanism in plant defence and improvements for industrial applications. ChemBioChem, 10, 1122-1133.
17. Mueller, M.J. and Berger, S. (2009) Reactive electrophilic oxylipins: pattern recognition and signalling. Phytochemistry, 70, 1511-1521.
18. Delker, C., Stenzel, I., Hause, B., Miersch, O., Feussner, I., and Wasternack, C. (2006) Jasmonate biosynthesis in Arabidopsis thaliana: enzymes, products, regulation. Plant Biol., 8, 297-306.
19. Stenzel, I., Otto, M., Delker, C., Kirmse, N., Schmidt, D., Miersch, O., Hause, B., and Wasternack, C. (2012) ALLENE OXIDE CYCLASE (AOC) gene family members of Arabidopsis thaliana: tissue-and organspecific promoter activities and in vivo heteromerization. J. Exp. Bot., 63, 6125-6138.
20. Wang, Y.-Q., Feechan, A., Yun, B.-W., Shafiei, R., Hofmann, A., Taylor, P., Xue, P., Yang, F.-Q., Xie, Z.-S., Pallas, J.A., Chu, C. C., and Loake, G.J. (2009) S-nitrosylation of AtSABP3 antagonizes the expression of plant immunity. J. Biol. Chem., 284, 2131-2137.
21. Romero-Puertas, M.C., Laxa, M., Mattè, A., Zaninotto, F., Finkemeier, I., Jones, A.M.E., Perazolli, M., Vandelle, E., Dietz, K.-J., and Delledonne, M. (2007) S-nitrosylation of peroxiredoxin II E promotes peroxynitrite mediated tyrosine nitration. Plant Cell, 19, 4120-4130.
22. Reumann, S. (2011) Toward a definition of the complete proteome of plant peroxisomes: where experimental proteomics must be complemented by bioinformatics. Proteomics, 9, 11.
23. Kataya, A.R.A. and Reumann, S. (2010) Arabidopsis glutathione reductase 1 is dually targeted to peroxisomes and the cytosol. Plant Signal. Behav., 2, 5.
24. Wasternack, C. and House, B. (2013) Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Ann. Bot. 111, 1021-1058.
25. Koo, A.J., Gao, X., Jones, A.D., and Howe, G.A. (2009) A rapid wound signal activates the systemic synthesis of bioactive jasmonates in Arabidopsis. Plant J., 59, 974-986.
26. Pauwels, L. and Goossens, A. (2011) The JAZ proteins: a crucial interface in the jasmonate signaling cascade. Plant Cell, 23, 3089-3100.
27. Geng, X., Cheng, J., Gangadharan, A., and Mackey, D. (2012) The coronatine toxin of Pseudomonas syringae is a multifunctional suppressor of Arabidopsis defense. Plant Cell, 24, 4763-4774.
28. Melotto, M., Underwood, W., Koczan, J., Nomura, K., and He, S.Y. (2006) Plant stomata function in innate immunity against bacterial invasion. Cell, 126, 969-980.
29. Tiryaki, I. and Staswick, P.E. (2002) An Arabidopsis mutant defective in jasmonate response is allelic to the auxin-signaling mutant axr1. Plant Physiol., 130, 887-894.
30. Lorenzo, O. and Solano, R. (2005) Molecular players regulating the jasmonate signalling network. Curr. Opin. Plant Biol., 8, 532-540.
31. Matsuzaki, Y., Ogawa-Ohnishi, M., Mori, A., and Matsubayashi, Y. (2010) Secreted peptide signals required for maintenance of root stem cell niche in Arabidopsis. Science, 329, 1065-1067.
32. Matsubayashi, Y. and Sakagami, Y. (2006) Peptide hormones in plants. Annu. Rev. Plant Biol., 57, 649-674.
33. Amano, Y., Tsubouchi, H., Shinohara, H., Ogawa, M., and Matsubayashi, Y. (2007). Tyrosine-sulfated glycopeptide involved in cellular proliferation and expansion in Arabidopsis. Proc. Natl. Acad. Sci. USA, 104, 18333-18338.
34. Kwezi, L., Ruzvidzo, O., Wheeler, J.I., Govender, K., Iacuone, S., Thompson, P.E., Gehring, C., and Irving, H.R. (2011) The phytosulfokine (PSK) receptor is capable of guanylate cyclase activity and enabling cyclic GMP-dependent signaling in plants. J. Biol. Chem., 286, 22580-22588.
35. Md Rahim, A., Busatto, N., and Trainotti, L. (2013) Peach ripening transcriptomics unveils new and unexpected targets for the improvement of drupe quality, in From Plant Genomics to Plant Biotechnology (eds P. Poltronieri, N. Burbulis, and C. Fogher), Woodhead, Cambridge, in press.
36. Whitford, R., Fernandez, A., Tejos, R., Cuéllar Pérez, A., Kleine-Vehn F. J., Vanneste, S., Drozdzecki, A., Leitner, J., Abas, L., Aerts, M., Hoogewijs, K., Baster, P., De Groodt, R., Lin, Y.-C., Storme, V., Van de Peer, Y., Beeckman, T., Madder, A., Devreese, B., Luschnig, C., Friml, J., and Hilson, P. (2012). GOLVEN secretory peptides regulate auxin carrier turnover during plant gravitropic responses. Dev. Cell, 22, 678-685.
37. Busatto, N. (2012). Functional characterization of a ripening induced RGFlike peptide hormone in peach, PhD Thesis, University of Padua.
38. Kistner, C. and Parniske, M. (2002) Evolution of signal transduction in intracellular symbiosis. Trends Plant Sci., 7, 511-518.
39. Pawlowski, K. and Sirrenberg, A. (2003) Symbiosis between Frankia and actinorhizal plants: root nodules of non-legumes. Indian J. Exp. Biol., 41, 1165-1183.
40. Varma, A., Verma, S., Sudha, Sahay, N., Bütehorn, B., and Franken, P. (1999) Piriformospora indica, a cultivable plant-growth-promoting root endophyte. Appl. Environ. Microbiol., 65, 2741-2744.
41. Schäfer, P., Pfiffi, S., Voll, L.M., Zajic, D., Chandler, P.M., Waller, F., Scholz, U., Pons-Kühnemann, J., Sonnewald, S., Sonnewald, U., and Kogel, K.H. (2009) Manipulation of plant innate immunity and gibberellin as factor of compatibility in the mutualistic association of barley roots with Piriformospora indica. Plant J., 59, 461-474.
42. Singh, L.P., Singh Gill, S., and Tuteja, N. (2011) Unraveling the role of fungal symbionts in plant abiotic stress tolerance. Plant Signal. Behav., 6, 175-191.
43. Franken, P. (2012) The plant strengthening root endophyte Piriformospora indica: potential application and the biology behind. Appl. Microbiol. Biotechnol., 96, 1455-1464.
44. Verbruggen, E., van der Heijden, M.G.A., Rillig, M.A., and Kiers, E.T. (2013) Mycorrhizal fungal establishment in agricultural soils: factors determining inoculation success. New Phytol., 197, 1104-1109.
45. Jung, S.C., Martienz-Medina, A., Lopez-Raez, J.A., and Pozo, M.J. (2012) Mycorrhiza-induced resistance and priming of plant defenses. J. Chem. Ecol., 38, 651-664.
46. Taghavi, S., Can der Leilie, D., Hoffman, A., Zhang, Y.-B., Walla, M.D., Vangronsveld, J., Newman, L., and Monchy, S. (2010) Genome sequence of the plant growth promoting endophytic bacterium Enterobacter sp. 638. PLoS Genet., 6, e10000943.
47. Horchani, F., Prevot, M., Boscari, A., Evangelisti, E., Meilhoc, E., Bruand, C., Raymond, P., Boncompagni, E., Aschi-Smiti, S., Puppo, A., and Brouquisse, R. (2011) Both plant and bacterial nitrate reductases contribute to nitric oxide production in Medicago truncatula nitrogen-fixing nodules. Plant Physiol., 155, 1023-1036.
48. Barea, J.M., Pozo, M.J., Azcon, R., and Azcon-Aguilar, C. (2005) Microbial cooperation in the rhizosphere. J. Exp. Bot., 56, 1761-1768.
49. Correa-Aragunde, N., Graziano, M., and Lamattina, L. (2004) Nitric oxide plays a central role in determining lateral root development in tomato. Planta, 218, 900-905.
50. Pagnussat, G.C., Simontacchi, M., Puntarulo, S., and Lamattina, L. (2002) Nitric oxide is required for root organogenesis. Plant Physiol., 129, 954-956.
51. Poltronieri, P., Bonsegna, S., De Domenico, S., and Santino, A. (2011) Molecular mechanisms in plant abiotic stress response. Field Veg. Crop Res., 48, 15-24.
52. Schäfer, P., Pfiffi, S., Voll, L.M., Zajic, D., Chandler, P.M., Waller, F., Scholz, U., Pons-Kühnemann, J., Sonnewald, S., Sonnewald, U., and Kogel, K.-H. (2009). Manipulation of plant innate immunity and gibberellin as factor of compatibility in the mutualistic association of barley roots with Piriformospora indica. Plant J., 59, 461-474.
53. Baltrushat, H., Fodor, J., Harrach, B.D., Niemczyk, E., Barna, B., Gullnet, G., Janeczko, A., Kogel, K.-H., Schäfer, P., Schwarczinger, I., Zuccaro, A., and Skoczowski, A. (2008) Salt stress tolerance of barley induced by the root endophyte Piriformospora indica is associated with a strong increase in antioxidants. New Phytol., 180, 501-510.
54. Schachman, D.P. and Goodger, J.Q.D. (2008) Chemical root to shoot signalling under drought. Trends Plant Sci., 13, 281-287.
55. Oldroyd, G.E. (2009) Plant science. Nodules and hormones. Science, 315, 52-53.
56. Hause, B. and Schaarschmidt, S. (2009) The role of jasmonates in mutualistic symbioses between plants and soil-born microorganisms. Phytochemistry, 70, 1589-1599.
57. Zhang, J., Subramanian, S., Zhang, Y., and Yu, O. (2007) Flavone synthases from Medicago truncatula are flavanone-2-hydroxylases and are important for nodulation. Plant Physiol., 144, 741-751.
58. Vellosillo, T., Martínez, M., López, M.A., Vicente, J., Cascón, T., Dolan, L., Hamberg, M., and Castresana, C. (2007) Oxylipins produced by the 9-lipoxygenase pathway in Arabidopsis regulate lateral root development and defense responses through a specific signaling cascade. Plant Cell, 19, 831-846.
59. Seki, M., Umezawa, T., Urano, K., and Shinozaki, K. (2007) Regulatory metabolic networks in drought stress response. Curr. Opin. Plant Biol., 10, 296-302.
60. Goodger, J.Q. and Schachtman, D.P. (2010) Re-examining the role of ABA as the primary long-distance signal produced by water-stressed roots. Plant Signal. Behav., 5, 1298-1301.
61. Molina, C., Rotter, B., Horres, R., Udupa, S.M., Besser, B., Bellarmino, L., Baum, M., Matsumura, H., Terauchi, R., Kahl, G., and Winter, P. (2008) SuperSAGE: the drought stress-responsive transcriptome of chickpea roots. BMC Genomics, 9, 553.
62. Molina, C., Zaman-Allah, M., Khan, F., Fatnassi, N., Horres, R., Rotter, B., Steinhauer, D., Amenc, L., Drevon, J.J., Winter, P., and Kahl, G. (2011) The saltresponsive transcriptome of chickpea roots and nodules via deepSuperSAGE. BMC Plant Biol., 11, 31.
63. Delker, C., Stenzel, I., Hause, B., Miersch, O., Feussner, I., and Wasternack, C. (2006) Jasmonate biosynthesis in Arabidopsis thaliana -enzymes, products, regulation. Plant Biol., 8, 297-306.
64. Gruber, V., Blanchet, S., Diet, A., Zahaf, O., Boualem, A., Kakar, K., Alunni, B., Udvardi, M., Frugier, F., and Crespi, M. (2009) Identification of transcription factors involved in root apex responses to salt stress in Medicago truncatula. Mol. Genet. Genomics, 281, 55-66.
65. De Domenico, S., Bonsegna, S., Horres, R., Pastor, V., Taurino, M., Poltronieri, P., Imtiaz, M., Kahl, G., Flors, V., Winter, P., and Santino, A. (2012) Transcriptomic analysis of oxylipin biosynthesis genes and chemical profiling reveal an early induction of jasmonates in chickpea roots under drought stress. Plant Physiol. Biochem., 61, 115-122.
66. Abdala, G., Miersch, O., Kramell, R., Vigliocco, A., Agostini, E., Forchetti, G., and Alemano, S. (2003) Jasmonate and octadecanoid occurrence in tomato hairy roots. Endogenous level changes in response to NaCl. J. Plant Growth Regul., 40, 21-27.
67. Buitink, J., Leger, J.J., Guisle, I., Vu, B.L., Wuilleme, S., Lamirault, G., Le, B.A., Le, M. N., Becker, A., Kuster, H., and Leprince, O. (2006) Transcriptome profiling uncovers metabolic and regulatory processes occurring during the transition from desiccation-sensitive to desiccation tolerant stages in Medicago truncatula seeds. Plant J., 47, 735-750.
68. Semeraro, C. (2010) Valutazione dell'espressione di geni della via di biosintesi delle ossilipine durante lo stress idrico in Cicer arietinum L., Master Thesis, University of Salento.
69. Galis, I., Gaquerel, E., Pandey, S.P., and Baldwin, J.T. (2009) Molecular mechanisms underlying plant memory in JA-mediated defence responses. Plant, Cell Environ., 32, 617-627.
70. Schommer, C., Palatnik, J.F., Aggarwal, P., Chételat, A., Cubas, P., Farmer, E.E., Nath, U., and Weigel, D. (2008) Control of jasmonate biosynthesis and senescence by miR319 targets. PLoS Biol., 6, e230.