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OXI1 protein kinase is required for plant immunity against Pseudomonas syringae in Arabidopsis
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Petersen, Lindsay N., Ingle, Robert A., Knight, Marc R. and Denby, Katherine J.. (2009) OXI1 protein kinase is required for plant immunity against Pseudomonas syringae in Arabidopsis. Journal of Experimental Botany, Vol.60 (No.13). pp. 3727-3735. ISSN 0022-0957
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Official URL: http://dx.doi.org/10.1093/jxb/erp219
Abstract
Expression of the Arabidopsis Oxidative Signal-Inducible1 (OXI1) serine/threonine protein kinase gene (At3g25250) is induced by oxidative stress. The kinase is required for root hair development and basal defence against the oomycete pathogen Hyaloperonospora parasitica, two separate H2O2-mediated processes. In this study, the role of OXI1 during pathogenesis was characterized further. Null oxi1 mutants are more susceptible to both virulent and avirulent strains of the biotrophic bacterial pathogen Pseudomonas syringae compared with the wild type, indicating that OXI1 positively regulates both basal resistance triggered by the recognition of pathogen-associated molecular patterns, as well as effector-triggered immunity. The level of OXI1 expression appears to be critical in mounting an appropriate defence response since OXI1 overexpressor lines also display increased susceptibility to biotrophic pathogens. The induction of OXI1 after P. syringae infection spatially and temporally correlates with the oxidative burst. Furthermore, induction is reduced in atrbohD mutants and after application of DPI (an inhibitor of NADPH oxidases) suggesting that reactive oxygen species produced through NADPH oxidases drives OXI1 expression during this plant–pathogen interaction.
| Item Type: | Journal Article |
|---|---|
| Alternative Title: | Role for OXI1 in plant immunity |
| Subjects: | S Agriculture > SB Plant culture |
| Divisions: | Faculty of Science > Life Sciences (2010- ) > Warwick HRI (2004-2010) |
| Library of Congress Subject Headings (LCSH): | Arabidopsis thaliana, Peronosporaceae, Pseudomonas syringae, Active oxygen -- Physiological effect, Transduction, Fungal diseases of plants, Plant diseases -- Genetic aspects, Plant immunology |
| Journal or Publication Title: | Journal of Experimental Botany |
| Publisher: | Oxford University Press |
| ISSN: | 0022-0957 |
| Date: | September 2009 |
| Volume: | Vol.60 |
| Number: | No.13 |
| Page Range: | pp. 3727-3735 |
| Identification Number: | 10.1093/jxb/erp219 |
| Status: | Peer Reviewed |
| Access rights to Published version: | Restricted or Subscription Access |
| Funder: | National Research Foundation (South Africa), University of Cape Town. Committee on Research (UoCT), Canon Collins Educational Trust for Southern Africa (CCETSA) |
| References: | Alvarez ME, Pennell RI, Meijer P-J, Ishikawa A, Dixon RA, Lamb C. Reactive oxygen intermediates mediate a systemic signal network in the establishment of plant immunity. Cell (1998) 92:773–784. Anthony RG, Khan S, Costa J, Pais MS, Bögre L. The Arabidopsis protein kinase PTI1-2 is activated by convergent phosphatidic acid and oxidative stress signaling pathways downstream of PDK1 and OXI1. Journal of Biological Chemistry (2006) 281:37536–37546. Asai T, Tena G, Plotnikova J, Willmann MR, Chiu W-L, Gomez-Gomez L, Boller T, Ausebel FM, Sheen J. MAP kinase signalling cascade in Arabidopsis innate immunity. Nature (2002) 415:977–983. Bradley DJ, Kjellbom P, Lamb CJ. Elicitor-induced and wound-induced oxidative cross-linking of a proline-rich plant-cell wall protein: a novel, rapid defense response. Cell (1992) 70:21–30. Cao H, Bowling SA, Gordon AS, Dong X. Characterization of an Arabidopsis mutant that is nonresponsive to inducers of systemic acquired resistance. The Plant Cell (1994) 6:1583–1592. Chamnongpol S, Willekens H, Moeder W, Langebartels C, Sandermann HJ, Montagu MV, Inzé D, Camp WV. Defense activation and enhanced pathogen tolerance induced by H2O2 in transgenic plants. Proceedings of the National Academy of Sciences, USA (1998) 95:5818–5823. Chen IC, Huang IC, Liu MJ, Wang ZG, Chung SS, Hsieh HL. Glutathione S-transferase interacting with far-red insensitive 219 is involved in phytochrome A-mediated signaling in Arabidopsis. Plant Physiology (2007) 143:1189–1202. Chinchilla D, Bauer Z, Regenass M, Boller T, Felix G. The Arabidopsis receptor kinase FLS2 binds flg22 and determines the specificity of flagellin perception. The Plant Cell (2006) 18:465–476. Choi HW, Kim YJ, Lee SC, Hong JK, Hwang BK. Hydrogen peroxide generation by the pepper extracellular peroxidase CaPO2 activates local and systemic cell death and defense response to bacterial pathogens. Plant Physiology (2007) 145:890–904. Chomczynski P, Sacchi N. Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Analytical Biochemistry (1987) 162:156–159. Clough SJ, Bent AF. Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. The Plant Journal (1998) 16:735–743. Constantinescu O, Fatehi J. Peronospora-like fungi (Chromista, Peronosporales) parasitic on Brassicaceae and related hosts. Nova Hedwigia (2002) 74:291–338.[CrossRef][Web of Science] Denby KJ, Jason LJM, Murray SL, Last RL. ups1, an Arabidopsis thaliana camalexin accumulation mutant defective in multiple defence signalling pathways. The Plant Journal (2005) 41:673–684. Fry SC, Willis SC, Patterson AEJ. Intraprotoplasmic and wall-localized fromation of arabinoxylan-cound diferulates and larger ferulate coupling products in maize cell-suspension cultures. Planta (2000) 211:679–692. Gomez-Gomez L, Bauer Z, Boller T. Both the extracellular leucine-rich-repeat domain and the kinase activity of FLS2 are required for flagellin binding and signalling in Arabidopsis. The Plant Cell (2001) 13:1155–1163. Grant JJ, Byung-Wook Loake GJ. Oxidative burst and cognate redox signalling reported by luciferase imaging: identification of a signal network that functions independently of ethylene, SA and Me-JA but is dependent on MAPKK activity. The Plant Journal (2000) 24:569–582. Grant JJ, Loake GJ. Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiology (2000) 124:21–29. Ingle RA, Carstens M, Denby KJ. PAMP recognition and the plant–pathogen arms race. BioEssays (2006) 28:880–889. Jones JD, Dangl JL. The plant immune system. Nature (2006) 444:323–329. Keppler LD, Baker CJ, Atkinson MM. Activated oxygen production during a bacteria induced hypersensitive reaction in tobacco suspension cells. Phytopathology (1989) 79:974–978. King EO, Ward MK, Raney DE. Two simple media for the demonstration of phycocynin and fluorescein. Journal of Laboratory and Clinical Medicine (1954) 44:301–307. Lamb C, Dixon RA. The oxidative burst in plant disease resistance. Annual Review of Plant Physiology and Plant Molecular Biology (1997) 48:251–275. Levine A, Tenhaken R, Dixon R, Lamb C. H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell (1994) 79:583–593. Mackey D, Holt BF, Wiig A, Dangl JL. RIN4 interacts with Pseudomonas syringae Type III effector molecules and is required for RPM1-mediated resistance in Arabidopsis. Cell (2002) 108:743–754. Menke FLH, Pelt JA, Pieterse CMJ, Klessig DF. Silencing of the mitogen-activated protein kinase MPK6 compromises disease resistance in Arabidopsis. The Plant Cell (2004) 16:897–907. Murray SL, Thomson C, Chini A, Read N, Loake G. Characterization of a novel, defense-related Arabidopsis mutant, cir1, isolated by luciferase imaging. Molecular Plant–Microbe Interactions (2002) 15:557–566. Murray SL, Ingle RA, Petersen LN, Denby KJ. Basal resistance against Pseudomonas syringae in Arabidopsis involves WRKY53 and a protein with homology to a nematode resistance protein. Molecular Plant–Microbe Interactions (2007) 20:1431–1438. Nawrath C, Métraux J-P. Salicylic acid induction-deficient mutants of Arabidopsis express PR-2 and PR-5 and accumulate high levels of camalexin after pathogen inoculation. The Plant Cell (1999) 11:1393–1404. Parker JE, Holub EB, Frost LN, Falk A, Gunn ND, Daniels MJ. Characterization of eds1, a mutation in Arabidopsis suppressing resistance to Peronospora parasitica specified by several different RPP genes. The Plant Cell (1996) 8:2033–2046. Pavet V, Olmos E, Kiddle G, Mowla S, Kumar S, Antoniw J, Alvarez ME, Foyer CH. Ascorbic acid deficiency activates cell death and disease resistance responses in Arabidopsis. Plant Physiology (2005) 139:1291–1303. Pineiro M, Gomez-Mena C, Schaffer R, Martinez-Zapater JM, Coupland G. EARLY BOLTING IN SHORT DAYS is related to chromatin remodeling factors and regulates flowering in Arabidopsis by repressing FT. The Plant Cell (2003) 15:1552–1562. Rentel M. Signal transduction in response to active oxygen species in Arabidopsis thaliana (2002) PhD thesis, University of Oxford. Rentel MC, Lecourieux D, Ouaked F, et al. OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis. Nature (2004) 427:858–861. Tao Y, Xie Z, Chen W, Glazebrook J, Chang H-S, Han B, Zhu T, Zou G, Katagiri F. Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae. The Plant Cell (2003) 15:317–330. Thomma BP, Penninckx IA, Broekaert WF, Cammue BP. The complexity of disease signaling in Arabidopsis. Current Opinion in Immunology (2001) 13:63–68. Torres MA, Dangl JL, Jones JDG. Arabidopsis gp91phox homologues AtrbohD and AtrbohF are required for the accumulation of reactive oxygen intermediates in the plant defence response. Proceedings of the National Academy of Sciences, USA (2002) 99:517–522. Torres MA, Jones JDC, Dangl JL. Reactive oxygen species signaling in response to pathogens. Plant Physiology (2006) 141:373–378. Wu G, Shortt BJ, Lawrence EB, Leon J, Fitzsimmons KC, Levine EB, Raskin I, Shah DM. Activation of host defence mechanisms by elevated production of H2O2 in transgenic plants. Plant Physiology (1997) 115:427–435. Zhou J, Lho Y-T, Bressan RA, Martin GB. The tomato gene Pti1 encodes a serine/threoning kinase that is phosphorylated by Pto and Is involved in the hypersensitive response. Cell (1995) 83:925–935. Zhou N, Tootle TL, Tsui F, Klessig DF, Glazebrook J. PAD4 functions upstream from salicylic acid to control defense responses in Arabidopsis. The Plant Cell (1998) 10:1021–1030. |
| URI: | http://wrap.warwick.ac.uk/id/eprint/1105 |
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