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

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

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dc.contributor.author García-Andrade, Javier es_ES
dc.contributor.author González, Beatriz es_ES
dc.contributor.author Gonzalez-Guzman, Miguel es_ES
dc.contributor.author Rodríguez Egea, Pedro Luís es_ES
dc.contributor.author Vera Vera, Pablo es_ES
dc.date.accessioned 2021-07-17T03:34:37Z
dc.date.available 2021-07-17T03:34:37Z
dc.date.issued 2020-08 es_ES
dc.identifier.uri http://hdl.handle.net/10251/169415
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. es_ES
dc.description.sponsorship This 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.language Inglés es_ES
dc.publisher MDPI AG es_ES
dc.relation.ispartof International Journal of Molecular Sciences es_ES
dc.rights Reconocimiento (by) es_ES
dc.subject ABA es_ES
dc.subject Ethylene es_ES
dc.subject Pathogens es_ES
dc.subject Plant immunity es_ES
dc.subject PYR1 es_ES
dc.subject Salicylic acid es_ES
dc.subject.classification BIOQUIMICA Y BIOLOGIA MOLECULAR es_ES
dc.title The Role of ABA in Plant Immunity is Mediated through the PYR1 Receptor es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.3390/ijms21165852 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-098501-B-I00/ES/NUEVOS MEDIADORES DE LA ACTIVACION DE MECANISMOS DE RESISTENCIA Y DE FACTORES SUSCEPTIBILIDAD DE LA PLANTA A MICROORGANISMOS PATOGENOS/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/BIO2017-82503-R/ES/REGULACION DE LA SEÑALIZACION DEL ABA Y TOLERANCIA A SEQUIA MEDIANTE E3 UBIQUITIN LIGASAS QUE REGULAN EL RECAMBIO DE RECEPTORES Y FOSFATASAS 2C/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes es_ES
dc.description.bibliographicCitation García-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/ijms21165852 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.3390/ijms21165852 es_ES
dc.description.upvformatpinicio 1 es_ES
dc.description.upvformatpfin 21 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 21 es_ES
dc.description.issue 16 es_ES
dc.identifier.eissn 1422-0067 es_ES
dc.identifier.pmid 32824010 es_ES
dc.identifier.pmcid PMC7461614 es_ES
dc.relation.pasarela S\433477 es_ES
dc.contributor.funder Agencia Estatal de Investigación es_ES
dc.description.references Malamy, 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.250.4983.1002 es_ES
dc.description.references Métraux, 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.250.4983.1004 es_ES
dc.description.references Glazebrook, J. (2005). Contrasting Mechanisms of Defense Against Biotrophic and Necrotrophic Pathogens. Annual Review of Phytopathology, 43(1), 205-227. doi:10.1146/annurev.phyto.43.040204.135923 es_ES
dc.description.references Verhage, 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.110.161570 es_ES
dc.description.references Broekaert, 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.44.070505.143440 es_ES
dc.description.references Grant, M. R., & Jones, J. D. G. (2009). Hormone (Dis)harmony Moulds Plant Health and Disease. Science, 324(5928), 750-752. doi:10.1126/science.1173771 es_ES
dc.description.references Pieterse, 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-092910-154055 es_ES
dc.description.references Thaler, 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:10.1890/02-0710 es_ES
dc.description.references Spoel, 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.009159 es_ES
dc.description.references Thomma, 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.121.4.1093 es_ES
dc.description.references Gu, 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.12.5.771 es_ES
dc.description.references Berrocal-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.x es_ES
dc.description.references Dı́az, 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.001453 es_ES
dc.description.references Leslie, C. A., & Romani, R. J. (1988). Inhibition of Ethylene Biosynthesis by Salicylic Acid. Plant Physiology, 88(3), 833-837. doi:10.1104/pp.88.3.833 es_ES
dc.description.references Chen, 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.108.065193 es_ES
dc.description.references Huang, 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.19.00658 es_ES
dc.description.references Spoel, 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.0708139104 es_ES
dc.description.references Cutler, 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-042809-112122 es_ES
dc.description.references Mauch-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.2005.05.015 es_ES
dc.description.references Asselbergh, 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-21-6-0709 es_ES
dc.description.references Fan, 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.109.137943 es_ES
dc.description.references Sánchez-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.112.200154 es_ES
dc.description.references Adie, 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.106.048041 es_ES
dc.description.references García-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.x es_ES
dc.description.references Jensen, 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.x es_ES
dc.description.references De 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.7601575 es_ES
dc.description.references Mine, 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.1702613114 es_ES
dc.description.references Peng, 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.1911660116 es_ES
dc.description.references Chen, 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.010410 es_ES
dc.description.references Anderson, 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.104.025833 es_ES
dc.description.references Yang, 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/s11103-005-7294-5 es_ES
dc.description.references Dittrich, 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/s41477-019-0490-0 es_ES
dc.description.references Hubbard, 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.1953910 es_ES
dc.description.references Klingler, 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/erq151 es_ES
dc.description.references Raghavendra, 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.2010.04.006 es_ES
dc.description.references Umezawa, 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.0907095106 es_ES
dc.description.references Vlad, 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.109.069179 es_ES
dc.description.references Fujii, 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/nature08599 es_ES
dc.description.references Ma, 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.1172408 es_ES
dc.description.references Park, 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.1173041 es_ES
dc.description.references Umezawa, 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.2003509 es_ES
dc.description.references Gonzalez-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.112.098574 es_ES
dc.description.references González-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/eru219 es_ES
dc.description.references Helander, 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.2015.11.010 es_ES
dc.description.references Antoni, 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.111.188623 es_ES
dc.description.references Tischer, 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.1706593114 es_ES
dc.description.references Antoni, 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.112.208678 es_ES
dc.description.references Fujii, 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.106.048538 es_ES
dc.description.references García-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.1003713 es_ES
dc.description.references Rubio, 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.109.137174 es_ES
dc.description.references Schweighofer, 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.2004.03.007 es_ES
dc.description.references Carrasco, 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/cdg323 es_ES
dc.description.references Carrasco, 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.0090734 es_ES
dc.description.references Clarke, 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.12.11.2175 es_ES
dc.description.references Wildermuth, 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:10.1038/35107108 es_ES
dc.description.references Garcion, 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.108.119420 es_ES
dc.description.references Mauch-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-042916-041132 es_ES
dc.description.references Gaffney, 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.261.5122.754 es_ES
dc.description.references Cheng, 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.006494 es_ES
dc.description.references Koiwai, 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.103.036970 es_ES
dc.description.references Endo, 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.3.12.7145 es_ES
dc.description.references Endo, 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.108.116632 es_ES
dc.description.references Alvarez, 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)81405-1 es_ES
dc.description.references Yu, 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.1211757110 es_ES
dc.description.references Flors, 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.x es_ES
dc.description.references Pétriacq, 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.15.00551 es_ES
dc.description.references Koornneef, A., & Pieterse, C. M. J. (2008). Cross Talk in Defense Signaling. Plant Physiology, 146(3), 839-844. doi:10.1104/pp.107.112029 es_ES
dc.description.references Ton, 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.2009.03.006 es_ES
dc.description.references De 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.109.152702 es_ES
dc.description.references De 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.x es_ES
dc.description.references Belin, 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.106.079327 es_ES
dc.description.references Planes, 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/eru442 es_ES


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