The Role of ABA in Plant Immunity is Mediated through the PYR1 Receptor

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dc.contributor.affiliationInstituto Universitario Mixto de Biología Molecular y Celular de Plantas
dc.contributor.authorGarcía-Andrade, Javieres_ES
dc.contributor.authorGonzález, Beatrizes_ES
dc.contributor.authorGonzalez-Guzman, Migueles_ES
dc.contributor.authorRodríguez Egea, Pedro Luís
dc.contributor.authorVera Vera, Pablo
dc.contributor.funderAgencia Estatal de Investigaciónes_ES
dc.date.accessioned2021-07-17T03:34:37Z
dc.date.available2021-07-17T03:34:37Z
dc.date.issued2020-08es_ES
dc.description.abstract[EN] ABA is involved in plant responses to a broad range of pathogens and exhibits complex antagonistic and synergistic relationships with salicylic acid (SA) and ethylene (ET) signaling pathways, respectively. However, the specific receptor of ABA that triggers the positive and negative responses of ABA during immune responses remains unknown. Through a reverse genetic analysis, we identified that PYR1, a member of the family of PYR/PYL/RCAR ABA receptors, is transcriptionally upregulated and specifically perceives ABA during biotic stress, initiating downstream signaling mediated by ABA-activated SnRK2 protein kinases. This exerts a damping effect on SA-mediated signaling, required for resistance to biotrophic pathogens, and simultaneously a positive control over the resistance to necrotrophic pathogens controlled by ET. We demonstrated that PYR1-mediated signaling exerted control on a priori established hormonal cross-talk between SA and ET, thereby redirecting defense outputs. Defects in ABA/PYR1 signaling activated SA biosynthesis and sensitized plants for immune priming by poising SA-responsive genes for enhanced expression. As a trade-off effect,pyr1-mediated activation of the SA pathway blunted ET perception, which is pivotal for the activation of resistance towards fungal necrotrophs. The specific perception of ABA by PYR1 represented a regulatory node, modulating different outcomes in disease resistance.en_EN
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationGarcía-Andrade, J.; González, B.; Gonzalez-Guzman, M.; Rodríguez Egea, PL.; Vera Vera, P. (2020). The Role of ABA in Plant Immunity is Mediated through the PYR1 Receptor. International Journal of Molecular Sciences. 21(16):1-21. https://doi.org/10.3390/ijms21165852es_ES
dc.description.issue16es_ES
dc.description.referencesMalamy, J., Carr, J. P., Klessig, D. F., & Raskin, I. (1990). Salicylic Acid: A Likely Endogenous Signal in the Resistance Response of Tobacco to Viral Infection. Science, 250(4983), 1002-1004. doi:10.1126/science.250.4983.1002es_ES
dc.description.referencesMétraux, J. P., Signer, H., Ryals, J., Ward, E., Wyss-Benz, M., Gaudin, J., … Inverardi, B. (1990). Increase in Salicylic Acid at the Onset of Systemic Acquired Resistance in Cucumber. Science, 250(4983), 1004-1006. doi:10.1126/science.250.4983.1004es_ES
dc.description.referencesGlazebrook, J. (2005). Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens. Annual Review of Phytopathology, 43(1), 205-227. doi:10.1146/annurev.phyto.43.040204.135923es_ES
dc.description.referencesVerhage, A., van Wees, S. C. M., & Pieterse, C. M. J. (2010). Plant Immunity: It’s the Hormones Talking, But What Do They Say?: Figure 1. Plant Physiology, 154(2), 536-540. doi:10.1104/pp.110.161570es_ES
dc.description.referencesBroekaert, W. F., Delauré, S. L., De Bolle, M. F. C., & Cammue, B. P. A. (2006). The Role of Ethylene in Host-Pathogen Interactions. Annual Review of Phytopathology, 44(1), 393-416. doi:10.1146/annurev.phyto.44.070505.143440es_ES
dc.description.referencesGrant, M. R., & Jones, J. D. G. (2009). Hormone (Dis)harmony Moulds Plant Health and Disease. Science, 324(5928), 750-752. doi:10.1126/science.1173771es_ES
dc.description.referencesPieterse, C. M. J., Van der Does, D., Zamioudis, C., Leon-Reyes, A., & Van Wees, S. C. M. (2012). Hormonal Modulation of Plant Immunity. Annual Review of Cell and Developmental Biology, 28(1), 489-521. doi:10.1146/annurev-cellbio-092910-154055es_ES
dc.description.referencesThaler, J. S., & Bostock, R. M. (2004). INTERACTIONS BETWEEN ABSCISIC-ACID-MEDIATED RESPONSES AND PLANT RESISTANCE TO PATHOGENS AND INSECTS. Ecology, 85(1), 48-58. doi:10.1890/02-0710es_ES
dc.description.referencesSpoel, S. H., Koornneef, A., Claessens, S. M. C., Korzelius, J. P., Van Pelt, J. A., Mueller, M. J., … Pieterse, C. M. J. (2003). NPR1 Modulates Cross-Talk between Salicylate- and Jasmonate-Dependent Defense Pathways through a Novel Function in the Cytosol. The Plant Cell, 15(3), 760-770. doi:10.1105/tpc.009159es_ES
dc.description.referencesThomma, B. P. H. J., Eggermont, K., Tierens, K. F. M.-J., & Broekaert, W. F. (1999). Requirement of Functional Ethylene-Insensitive 2Gene for Efficient Resistance of Arabidopsis to Infection by Botrytis cinerea  . Plant Physiology, 121(4), 1093-1101. doi:10.1104/pp.121.4.1093es_ES
dc.description.referencesGu, Y.-Q., Yang, C., Thara, V. K., Zhou, J., & Martin, G. B. (2000). Pti4 Is Induced by Ethylene and Salicylic Acid, and Its Product Is Phosphorylated by the Pto Kinase. The Plant Cell, 12(5), 771-785. doi:10.1105/tpc.12.5.771es_ES
dc.description.referencesBerrocal-Lobo, M., Molina, A., & Solano, R. (2002). Constitutive expression ofETHYLENE-RESPONSE-FACTOR1inArabidopsisconfers resistance to several necrotrophic fungi. The Plant Journal, 29(1), 23-32. doi:10.1046/j.1365-313x.2002.01191.xes_ES
dc.description.referencesDı́az, J., ten Have, A., & van Kan, J. A. L. (2002). The Role of Ethylene and Wound Signaling in Resistance of Tomato to Botrytis cinerea  . Plant Physiology, 129(3), 1341-1351. doi:10.1104/pp.001453es_ES
dc.description.referencesLeslie, C. A., & Romani, R. J. (1988). Inhibition of Ethylene Biosynthesis by Salicylic Acid. Plant Physiology, 88(3), 833-837. doi:10.1104/pp.88.3.833es_ES
dc.description.referencesChen, H., Xue, L., Chintamanani, S., Germain, H., Lin, H., Cui, H., … Zhou, J.-M. (2009). ETHYLENE INSENSITIVE3 and ETHYLENE INSENSITIVE3-LIKE1 Repress SALICYLIC ACID INDUCTION DEFICIENT2 Expression to Negatively Regulate Plant Innate Immunity in Arabidopsis    . The Plant Cell, 21(8), 2527-2540. doi:10.1105/tpc.108.065193es_ES
dc.description.referencesHuang, P., Dong, Z., Guo, P., Zhang, X., Qiu, Y., Li, B., … Guo, H. (2019). Salicylic Acid Suppresses Apical Hook Formation via NPR1-Mediated Repression of EIN3 and EIL1 in Arabidopsis. The Plant Cell, 32(3), 612-629. doi:10.1105/tpc.19.00658es_ES
dc.description.referencesSpoel, S. H., Johnson, J. S., & Dong, X. (2007). Regulation of tradeoffs between plant defenses against pathogens with different lifestyles. Proceedings of the National Academy of Sciences, 104(47), 18842-18847. doi:10.1073/pnas.0708139104es_ES
dc.description.referencesCutler, S. R., Rodriguez, P. L., Finkelstein, R. R., & Abrams, S. R. (2010). Abscisic Acid: Emergence of a Core Signaling Network. Annual Review of Plant Biology, 61(1), 651-679. doi:10.1146/annurev-arplant-042809-112122es_ES
dc.description.referencesMauch-Mani, B., & Mauch, F. (2005). The role of abscisic acid in plant–pathogen interactions. Current Opinion in Plant Biology, 8(4), 409-414. doi:10.1016/j.pbi.2005.05.015es_ES
dc.description.referencesAsselbergh, B., De Vleesschauwer, D., & Höfte, M. (2008). Global Switches and Fine-Tuning—ABA Modulates Plant Pathogen Defense. Molecular Plant-Microbe Interactions®, 21(6), 709-719. doi:10.1094/mpmi-21-6-0709es_ES
dc.description.referencesFan, J., Hill, L., Crooks, C., Doerner, P., & Lamb, C. (2009). Abscisic Acid Has a Key Role in Modulating Diverse Plant-Pathogen Interactions      . Plant Physiology, 150(4), 1750-1761. doi:10.1104/pp.109.137943es_ES
dc.description.referencesSánchez-Vallet, A., López, G., Ramos, B., Delgado-Cerezo, M., Riviere, M.-P., Llorente, F., … Molina, A. (2012). Disruption of Abscisic Acid Signaling Constitutively Activates Arabidopsis Resistance to the Necrotrophic Fungus Plectosphaerella cucumerina    . Plant Physiology, 160(4), 2109-2124. doi:10.1104/pp.112.200154es_ES
dc.description.referencesAdie, B. A. T., Pérez-Pérez, J., Pérez-Pérez, M. M., Godoy, M., Sánchez-Serrano, J.-J., Schmelz, E. A., & Solano, R. (2007). ABA Is an Essential Signal for Plant Resistance to Pathogens Affecting JA Biosynthesis and the Activation of Defenses in Arabidopsis. The Plant Cell, 19(5), 1665-1681. doi:10.1105/tpc.106.048041es_ES
dc.description.referencesGarcía-Andrade, J., Ramírez, V., Flors, V., & Vera, P. (2011). Arabidopsis ocp3 mutant reveals a mechanism linking ABA and JA to pathogen-induced callose deposition. The Plant Journal, 67(5), 783-794. doi:10.1111/j.1365-313x.2011.04633.xes_ES
dc.description.referencesJensen, M. K., Hagedorn, P. H., de Torres-Zabala, M., Grant, M. R., Rung, J. H., Collinge, D. B., & Lyngkjaer, M. F. (2008). Transcriptional regulation by an NAC (NAM-ATAF1,2-CUC2) transcription factor attenuates ABA signalling for efficient basal defence towardsBlumeria graminisf. sp.hordeiin Arabidopsis. The Plant Journal, 56(6), 867-880. doi:10.1111/j.1365-313x.2008.03646.xes_ES
dc.description.referencesDe Torres-Zabala, M., Truman, W., Bennett, M. H., Lafforgue, G., Mansfield, J. W., Rodriguez Egea, P., … Grant, M. (2007). Pseudomonas syringae pv. tomato hijacks the Arabidopsis abscisic acid signalling pathway to cause disease. The EMBO Journal, 26(5), 1434-1443. doi:10.1038/sj.emboj.7601575es_ES
dc.description.referencesMine, A., Berens, M. L., Nobori, T., Anver, S., Fukumoto, K., Winkelmüller, T. M., … Tsuda, K. (2017). Pathogen exploitation of an abscisic acid- and jasmonate-inducible MAPK phosphatase and its interception by Arabidopsis immunity. Proceedings of the National Academy of Sciences, 114(28), 7456-7461. doi:10.1073/pnas.1702613114es_ES
dc.description.referencesPeng, Z., Hu, Y., Zhang, J., Huguet-Tapia, J. C., Block, A. K., Park, S., … White, F. F. (2019). Xanthomonas translucens commandeers the host rate-limiting step in ABA biosynthesis for disease susceptibility. Proceedings of the National Academy of Sciences, 116(42), 20938-20946. doi:10.1073/pnas.1911660116es_ES
dc.description.referencesChen, W., Provart, N. J., Glazebrook, J., Katagiri, F., Chang, H.-S., Eulgem, T., … Zhu, T. (2002). Expression Profile Matrix of Arabidopsis Transcription Factor Genes Suggests Their Putative Functions in Response to Environmental Stresses[W]. The Plant Cell, 14(3), 559-574. doi:10.1105/tpc.010410es_ES
dc.description.referencesAnderson, J. P., Badruzsaufari, E., Schenk, P. M., Manners, J. M., Desmond, O. J., Ehlert, C., … Kazan, K. (2004). Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis. The Plant Cell, 16(12), 3460-3479. doi:10.1105/tpc.104.025833es_ES
dc.description.referencesYang, Z., Tian, L., Latoszek-Green, M., Brown, D., & Wu, K. (2005). Arabidopsis ERF4 is a transcriptional repressor capable of modulating ethylene and abscisic acid responses. Plant Molecular Biology, 58(4), 585-596. doi:10.1007/s11103-005-7294-5es_ES
dc.description.referencesDittrich, M., Mueller, H. M., Bauer, H., Peirats-Llobet, M., Rodriguez, P. L., Geilfus, C.-M., … Hedrich, R. (2019). The role of Arabidopsis ABA receptors from the PYR/PYL/RCAR family in stomatal acclimation and closure signal integration. Nature Plants, 5(9), 1002-1011. doi:10.1038/s41477-019-0490-0es_ES
dc.description.referencesHubbard, K. E., Nishimura, N., Hitomi, K., Getzoff, E. D., & Schroeder, J. I. (2010). Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions. Genes & Development, 24(16), 1695-1708. doi:10.1101/gad.1953910es_ES
dc.description.referencesKlingler, J. P., Batelli, G., & Zhu, J.-K. (2010). ABA receptors: the START of a new paradigm in phytohormone signalling. Journal of Experimental Botany, 61(12), 3199-3210. doi:10.1093/jxb/erq151es_ES
dc.description.referencesRaghavendra, A. S., Gonugunta, V. K., Christmann, A., & Grill, E. (2010). ABA perception and signalling. Trends in Plant Science, 15(7), 395-401. doi:10.1016/j.tplants.2010.04.006es_ES
dc.description.referencesUmezawa, T., Sugiyama, N., Mizoguchi, M., Hayashi, S., Myouga, F., Yamaguchi-Shinozaki, K., … Shinozaki, K. (2009). Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis. Proceedings of the National Academy of Sciences, 106(41), 17588-17593. doi:10.1073/pnas.0907095106es_ES
dc.description.referencesVlad, F., Rubio, S., Rodrigues, A., Sirichandra, C., Belin, C., Robert, N., … Merlot, S. (2009). Protein Phosphatases 2C Regulate the Activation of the Snf1-Related Kinase OST1 by Abscisic Acid inArabidopsis . The Plant Cell, 21(10), 3170-3184. doi:10.1105/tpc.109.069179es_ES
dc.description.referencesFujii, H., Chinnusamy, V., Rodrigues, A., Rubio, S., Antoni, R., Park, S.-Y., … Zhu, J.-K. (2009). In vitro reconstitution of an abscisic acid signalling pathway. Nature, 462(7273), 660-664. doi:10.1038/nature08599es_ES
dc.description.referencesMa, Y., Szostkiewicz, I., Korte, A., Moes, D., Yang, Y., Christmann, A., & Grill, E. (2009). Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors. Science, 324(5930), 1064-1068. doi:10.1126/science.1172408es_ES
dc.description.referencesPark, S.-Y., Fung, P., Nishimura, N., Jensen, D. R., Fujii, H., Zhao, Y., … Cutler, S. R. (2009). Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins. Science, 324(5930), 1068-1071. doi:10.1126/science.1173041es_ES
dc.description.referencesUmezawa, T., Sugiyama, N., Takahashi, F., Anderson, J. C., Ishihama, Y., Peck, S. C., & Shinozaki, K. (2013). Genetics and Phosphoproteomics Reveal a Protein Phosphorylation Network in the Abscisic Acid Signaling Pathway in Arabidopsis thaliana. Science Signaling, 6(270). doi:10.1126/scisignal.2003509es_ES
dc.description.referencesGonzalez-Guzman, M., Pizzio, G. A., Antoni, R., Vera-Sirera, F., Merilo, E., Bassel, G. W., … Rodriguez, P. L. (2012). Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid. The Plant Cell, 24(6), 2483-2496. doi:10.1105/tpc.112.098574es_ES
dc.description.referencesGonzález-Guzmán, M., Rodríguez, L., Lorenzo-Orts, L., Pons, C., Sarrión-Perdigones, A., Fernández, M. A., … Rodríguez, P. L. (2014). Tomato PYR/PYL/RCAR abscisic acid receptors show high expression in root, differential sensitivity to the abscisic acid agonist quinabactin, and the capability to enhance plant drought resistance. Journal of Experimental Botany, 65(15), 4451-4464. doi:10.1093/jxb/eru219es_ES
dc.description.referencesHelander, J. D. M., Vaidya, A. S., & Cutler, S. R. (2016). Chemical manipulation of plant water use. Bioorganic & Medicinal Chemistry, 24(3), 493-500. doi:10.1016/j.bmc.2015.11.010es_ES
dc.description.referencesAntoni, R., Gonzalez-Guzman, M., Rodriguez, L., Rodrigues, A., Pizzio, G. A., & Rodriguez, P. L. (2011). Selective Inhibition of Clade A Phosphatases Type 2C by PYR/PYL/RCAR Abscisic Acid Receptors    . Plant Physiology, 158(2), 970-980. doi:10.1104/pp.111.188623es_ES
dc.description.referencesTischer, S. V., Wunschel, C., Papacek, M., Kleigrewe, K., Hofmann, T., Christmann, A., & Grill, E. (2017). Combinatorial interaction network of abscisic acid receptors and coreceptors fromArabidopsis thaliana. Proceedings of the National Academy of Sciences, 114(38), 10280-10285. doi:10.1073/pnas.1706593114es_ES
dc.description.referencesAntoni, R., Gonzalez-Guzman, M., Rodriguez, L., Peirats-Llobet, M., Pizzio, G. A., Fernandez, M. A., … Rodriguez, P. L. (2012). PYRABACTIN RESISTANCE1-LIKE8 Plays an Important Role for the Regulation of Abscisic Acid Signaling in Root      . Plant Physiology, 161(2), 931-941. doi:10.1104/pp.112.208678es_ES
dc.description.referencesFujii, H., Verslues, P. E., & Zhu, J.-K. (2007). Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis. The Plant Cell, 19(2), 485-494. doi:10.1105/tpc.106.048538es_ES
dc.description.referencesGarcía-Andrade, J., Ramírez, V., López, A., & Vera, P. (2013). Mediated Plastid RNA Editing in Plant Immunity. PLoS Pathogens, 9(10), e1003713. doi:10.1371/journal.ppat.1003713es_ES
dc.description.referencesRubio, S., Rodrigues, A., Saez, A., Dizon, M. B., Galle, A., Kim, T.-H., … Rodriguez, P. L. (2009). Triple Loss of Function of Protein Phosphatases Type 2C Leads to Partial Constitutive Response to Endogenous Abscisic Acid      . Plant Physiology, 150(3), 1345-1355. doi:10.1104/pp.109.137174es_ES
dc.description.referencesSchweighofer, A., Hirt, H., & Meskiene, I. (2004). Plant PP2C phosphatases: emerging functions in stress signaling. Trends in Plant Science, 9(5), 236-243. doi:10.1016/j.tplants.2004.03.007es_ES
dc.description.referencesCarrasco, J. L. (2003). A novel transcription factor involved in plant defense endowed with protein phosphatase activity. The EMBO Journal, 22(13), 3376-3384. doi:10.1093/emboj/cdg323es_ES
dc.description.referencesCarrasco, J. L., Castelló, M. J., Naumann, K., Lassowskat, I., Navarrete-Gómez, M., Scheel, D., & Vera, P. (2014). Arabidopsis Protein Phosphatase DBP1 Nucleates a Protein Network with a Role in Regulating Plant Defense. PLoS ONE, 9(3), e90734. doi:10.1371/journal.pone.0090734es_ES
dc.description.referencesClarke, J. D., Volko, S. M., Ledford, H., Ausubel, F. M., & Dong, X. (2000). Roles of Salicylic Acid, Jasmonic Acid, and Ethylene in cpr-Induced Resistance in Arabidopsis. The Plant Cell, 12(11), 2175-2190. doi:10.1105/tpc.12.11.2175es_ES
dc.description.referencesWildermuth, M. C., Dewdney, J., Wu, G., & Ausubel, F. M. (2001). Isochorismate synthase is required to synthesize salicylic acid for plant defence. Nature, 414(6863), 562-565. doi:10.1038/35107108es_ES
dc.description.referencesGarcion, C., Lohmann, A., Lamodière, E., Catinot, J., Buchala, A., Doermann, P., & Métraux, J.-P. (2008). Characterization and Biological Function of the ISOCHORISMATE SYNTHASE2 Gene of Arabidopsis. Plant Physiology, 147(3), 1279-1287. doi:10.1104/pp.108.119420es_ES
dc.description.referencesMauch-Mani, B., Baccelli, I., Luna, E., & Flors, V. (2017). Defense Priming: An Adaptive Part of Induced Resistance. Annual Review of Plant Biology, 68(1), 485-512. doi:10.1146/annurev-arplant-042916-041132es_ES
dc.description.referencesGaffney, T., Friedrich, L., Vernooij, B., Negrotto, D., Nye, G., Uknes, S., … Ryals, J. (1993). Requirement of Salicylic Acid for the Induction of Systemic Acquired Resistance. Science, 261(5122), 754-756. doi:10.1126/science.261.5122.754es_ES
dc.description.referencesCheng, W.-H., Endo, A., Zhou, L., Penney, J., Chen, H.-C., Arroyo, A., … Sheen, J. (2002). A Unique Short-Chain Dehydrogenase/Reductase in Arabidopsis Glucose Signaling and Abscisic Acid Biosynthesis and Functions. The Plant Cell, 14(11), 2723-2743. doi:10.1105/tpc.006494es_ES
dc.description.referencesKoiwai, H., Nakaminami, K., Seo, M., Mitsuhashi, W., Toyomasu, T., & Koshiba, T. (2004). Tissue-Specific Localization of an Abscisic Acid Biosynthetic Enzyme, AAO3, in Arabidopsis. Plant Physiology, 134(4), 1697-1707. doi:10.1104/pp.103.036970es_ES
dc.description.referencesEndo, A., Koshiba, T., Kamiya, Y., & Nambara, E. (2008). Vascular system is a node of systemic stress responses. Plant Signaling & Behavior, 3(12), 1138-1140. doi:10.4161/psb.3.12.7145es_ES
dc.description.referencesEndo, A., Sawada, Y., Takahashi, H., Okamoto, M., Ikegami, K., Koiwai, H., … Nambara, E. (2008). Drought Induction of Arabidopsis 9-cis-Epoxycarotenoid Dioxygenase Occurs in Vascular Parenchyma Cells    . Plant Physiology, 147(4), 1984-1993. doi:10.1104/pp.108.116632es_ES
dc.description.referencesAlvarez, M. E., Pennell, R. I., Meijer, P.-J., Ishikawa, A., Dixon, R. A., & Lamb, C. (1998). Reactive Oxygen Intermediates Mediate a Systemic Signal Network in the Establishment of Plant Immunity. Cell, 92(6), 773-784. doi:10.1016/s0092-8674(00)81405-1es_ES
dc.description.referencesYu, A., Lepere, G., Jay, F., Wang, J., Bapaume, L., Wang, Y., … Navarro, L. (2013). Dynamics and biological relevance of DNA demethylation in Arabidopsis antibacterial defense. Proceedings of the National Academy of Sciences, 110(6), 2389-2394. doi:10.1073/pnas.1211757110es_ES
dc.description.referencesFlors, V., Ton, J., Van Doorn, R., Jakab, G., García-Agustín, P., & Mauch-Mani, B. (2007). Interplay between JA, SA and ABA signalling during basal and induced resistance against Pseudomonas syringae and Alternaria brassicicola. The Plant Journal, 54(1), 81-92. doi:10.1111/j.1365-313x.2007.03397.xes_ES
dc.description.referencesPétriacq, P., Stassen, J. H. M., & Ton, J. (2016). Spore Density Determines Infection Strategy by the Plant Pathogenic Fungus Plectosphaerella cucumerina. Plant Physiology, 170(4), 2325-2339. doi:10.1104/pp.15.00551es_ES
dc.description.referencesKoornneef, A., & Pieterse, C. M. J. (2008). Cross Talk in Defense Signaling. Plant Physiology, 146(3), 839-844. doi:10.1104/pp.107.112029es_ES
dc.description.referencesTon, J., Flors, V., & Mauch-Mani, B. (2009). The multifaceted role of ABA in disease resistance. Trends in Plant Science, 14(6), 310-317. doi:10.1016/j.tplants.2009.03.006es_ES
dc.description.referencesDe Vleesschauwer, D., Yang, Y., Vera Cruz, C., & Höfte, M. (2010). Abscisic Acid-Induced Resistance against the Brown Spot Pathogen Cochliobolus miyabeanus in Rice Involves MAP Kinase-Mediated Repression of Ethylene Signaling      . Plant Physiology, 152(4), 2036-2052. doi:10.1104/pp.109.152702es_ES
dc.description.referencesDe Torres Zabala, M., Bennett, M. H., Truman, W. H., & Grant, M. R. (2009). Antagonism between salicylic and abscisic acid reflects early host-pathogen conflict and moulds plant defence responses. The Plant Journal, 59(3), 375-386. doi:10.1111/j.1365-313x.2009.03875.xes_ES
dc.description.referencesBelin, C., de Franco, P.-O., Bourbousse, C., Chaignepain, S., Schmitter, J.-M., Vavasseur, A., … Thomine, S. (2006). Identification of Features Regulating OST1 Kinase Activity and OST1 Function in Guard Cells  . Plant Physiology, 141(4), 1316-1327. doi:10.1104/pp.106.079327es_ES
dc.description.referencesPlanes, M. D., Niñoles, R., Rubio, L., Bissoli, G., Bueso, E., García-Sánchez, M. J., … Serrano, R. (2014). A mechanism of growth inhibition by abscisic acid in germinating seeds of Arabidopsis thaliana based on inhibition of plasma membrane H+-ATPase and decreased cytosolic pH, K+, and anions. Journal of Experimental Botany, 66(3), 813-825. doi:10.1093/jxb/eru442es_ES
dc.description.sponsorshipThis research was founded by the Spanish AEI agency by grant BIO2017-82503-R to P.L.R. and by grant RTI2018-098501-B-I00 to P.V.es_ES
dc.description.upvformatpfin21es_ES
dc.description.upvformatpinicio1es_ES
dc.description.volume21es_ES
dc.identifier.doi10.3390/ijms21165852es_ES
dc.identifier.eissn1422-0067es_ES
dc.identifier.pmcidPMC7461614es_ES
dc.identifier.pmid32824010es_ES
dc.identifier.urihttps://riunet.upv.es/handle/10251/169415
dc.languageIngléses_ES
dc.publisherMDPI AGes_ES
dc.relation.ispartofInternational Journal of Molecular Scienceses_ES
dc.relation.pasarelaS\433477es_ES
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dc.relation.references10.1126/science.250.4983.1002es_ES
dc.relation.references10.1126/science.250.4983.1004es_ES
dc.relation.references10.1146/annurev.phyto.43.040204.135923es_ES
dc.relation.references10.1104/pp.110.161570es_ES
dc.relation.references10.1146/annurev.phyto.44.070505.143440es_ES
dc.relation.references10.1126/science.1173771es_ES
dc.relation.references10.1146/annurev-cellbio-092910-154055es_ES
dc.relation.references10.1890/02-0710es_ES
dc.relation.references10.1105/tpc.009159es_ES
dc.relation.references10.1104/pp.121.4.1093es_ES
dc.relation.references10.1105/tpc.12.5.771es_ES
dc.relation.references10.1046/j.1365-313x.2002.01191.xes_ES
dc.relation.references10.1104/pp.001453es_ES
dc.relation.references10.1104/pp.88.3.833es_ES
dc.relation.references10.1105/tpc.108.065193es_ES
dc.relation.references10.1105/tpc.19.00658es_ES
dc.relation.references10.1073/pnas.0708139104es_ES
dc.relation.references10.1146/annurev-arplant-042809-112122es_ES
dc.relation.references10.1016/j.pbi.2005.05.015es_ES
dc.relation.references10.1094/MPMI-21-6-0709es_ES
dc.relation.references10.1104/pp.109.137943es_ES
dc.relation.references10.1104/pp.112.200154es_ES
dc.relation.references10.1111/j.1365-313X.2004.02028.xes_ES
dc.relation.references10.1105/tpc.106.048041es_ES
dc.relation.references10.1111/j.1365-313X.2011.04633.xes_ES
dc.relation.references10.1007/s10142-006-0041-4es_ES
dc.relation.references10.1111/j.1365-313X.2008.03646.xes_ES
dc.relation.references10.1038/sj.emboj.7601575es_ES
dc.relation.references10.1073/pnas.1702613114es_ES
dc.relation.references10.1073/pnas.1911660116es_ES
dc.relation.references10.1105/tpc.010410es_ES
dc.relation.references10.1105/tpc.104.025833es_ES
dc.relation.references10.1007/s11103-005-7294-5es_ES
dc.relation.references10.1038/s41477-019-0490-0es_ES
dc.relation.references10.1101/gad.1953910es_ES
dc.relation.references10.1093/jxb/erq151es_ES
dc.relation.references10.1016/j.tplants.2010.04.006es_ES
dc.relation.references10.1073/pnas.0907095106es_ES
dc.relation.references10.1105/tpc.109.069179es_ES
dc.relation.references10.1038/nature08599es_ES
dc.relation.references10.1126/science.1172408es_ES
dc.relation.references10.1126/science.1173041es_ES
dc.relation.references10.1126/scisignal.2003509es_ES
dc.relation.references10.1105/tpc.112.098574es_ES
dc.relation.references10.1093/jxb/eru219es_ES
dc.relation.references10.1016/j.bmc.2015.11.010es_ES
dc.relation.references10.1104/pp.111.188623es_ES
dc.relation.references10.1073/pnas.1706593114es_ES
dc.relation.references10.1104/pp.112.208678es_ES
dc.relation.references10.1073/pnas.0903144106es_ES
dc.relation.references10.1105/tpc.106.048538es_ES
dc.relation.references10.1371/journal.ppat.1003713es_ES
dc.relation.references10.1371/journal.pgen.1002434es_ES
dc.relation.references10.1104/pp.109.137174es_ES
dc.relation.references10.1016/j.tplants.2004.03.007es_ES
dc.relation.references10.1093/emboj/cdg323es_ES
dc.relation.references10.1371/journal.pone.0090734es_ES
dc.relation.references10.1105/tpc.12.11.2175es_ES
dc.relation.references10.1038/35107108es_ES
dc.relation.references10.1104/pp.108.119420es_ES
dc.relation.references10.1371/journal.ppat.1003445es_ES
dc.relation.references10.1146/annurev-arplant-042916-041132es_ES
dc.relation.references10.1126/science.261.5122.754es_ES
dc.relation.references10.1105/tpc.006494es_ES
dc.relation.references10.1104/pp.103.036970es_ES
dc.relation.references10.4161/psb.3.12.7145es_ES
dc.relation.references10.1104/pp.108.116632es_ES
dc.relation.references10.1016/S0092-8674(00)81405-1es_ES
dc.relation.references10.1073/pnas.1211757110es_ES
dc.relation.references10.1111/j.1365-313X.2007.03397.xes_ES
dc.relation.references10.1104/pp.15.00551es_ES
dc.relation.references10.1104/pp.107.112029es_ES
dc.relation.references10.1016/j.tplants.2009.03.006es_ES
dc.relation.references10.1104/pp.109.152702es_ES
dc.relation.references10.1111/j.1365-313X.2009.03875.xes_ES
dc.relation.references10.1104/pp.106.079327es_ES
dc.relation.references10.1093/jxb/eru442es_ES
dc.rightsReconocimiento (by)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectABAes_ES
dc.subjectEthylenees_ES
dc.subjectPathogenses_ES
dc.subjectPlant immunityes_ES
dc.subjectPYR1es_ES
dc.subjectSalicylic acides_ES
dc.subject.classificationBIOQUIMICA Y BIOLOGIA MOLECULARes_ES
dc.titleThe Role of ABA in Plant Immunity is Mediated through the PYR1 Receptores_ES
dc.typeArtículoes_ES
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