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Transcriptional networks in plant immunity

Tsuda, Kenichi, Somssich, Imre E.·2015·New Phytologist

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Abstract

Summary: Next to numerous abiotic stresses, plants are constantly exposed to a variety of pathogens within their environment. Thus, their ability to survive and prosper during the course of evolution was strongly dependent on adapting efficient strategies to perceive and to respond to such potential threats. It is therefore not surprising that modern plants have a highly sophisticated immune repertoire consisting of diverse signal perception and intracellular signaling pathways. This signaling network is intricate and deeply interconnected, probably reflecting the diverse lifestyles and infection strategies used by the multitude of invading phytopathogens. Moreover it allows signal communication between developmental and defense programs thereby ensuring that plant growth and fitness are not significantly retarded. How plants integrate and prioritize the incoming signals and how this information is transduced to enable appropriate immune responses is currently a major research area. An important finding has been that pathogen‐triggered cellular responses involve massive transcriptional reprogramming within the host. Additional key observations emerging from such studies are that transcription factors (TF s) are often sites of signal convergence and that signal‐regulated TF s act in concert with other context‐specific TF s and transcriptional co‐regulators to establish sensory transcription regulatory networks required for plant immunity. Contents Summary 932 I. Introduction 932 II. Major transcription factor families involved in plant immunity 933 III. Regulation of transcriptional complexes 934 IV. Transcription factor networks in phytohormone signaling 938 V. Discussion and perspectives 941 Acknowledgements 943 References 943

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MYB transcription factors in Arabidopsis
Dubos, C., Stracke, R., Grotewold, E., Weisshaar, B., Martin, C., & Lepiniec, L. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.06.005 · Cited by 4,865
Network motifs: theory and experimental approaches
Alon, U. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2102 · Cited by 3,279
Hormonal Modulation of Plant Immunity
Pieterse, C. M. J., Van der Does, D., Zamioudis, C., Leon-Reyes, A., & Van Wees, S. C. M. (2012) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154055 · Cited by 2,998
MAP kinase signalling cascade in Arabidopsis innate immunity
Asai, T., Tena, G., Plotnikova, J., Willmann, M. R., Chiu, W.-L., Gomez-Gomez, L., Boller, T., Ausubel, F. M., & Sheen, J. (2002) · Nature · doi:10.1038/415977a · Cited by 2,726
WRKY transcription factors
Rushton, P. J., Somssich, I. E., Ringler, P., & Shen, Q. J. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.02.006 · Cited by 2,700
Self-citation
JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling
Thines, B., Katsir, L., Melotto, M., Niu, Y., Mandaokar, A., Liu, G., Nomura, K., He, S. Y., Howe, G. A., & Browse, J. (2007) · Nature · doi:10.1038/nature05960 · Cited by 2,520
The JAZ family of repressors is the missing link in jasmonate signalling
Chini, A., Fonseca, S., Fernández, G., Adie, B., Chico, J. M., Lorenzo, O., García-Casado, G., López-Vidriero, I., Lozano, F. M., Ponce, M. R., et al. (2007) · Nature · doi:10.1038/nature06006 · Cited by 2,432
Isochorismate synthase is required to synthesize salicylic acid for plant defence
Wildermuth, M. C., Dewdney, J., Wu, G., & Ausubel, F. M. (2001) · Nature · doi:10.1038/35107108 · Cited by 2,357
A Receptor Kinase-Like Protein Encoded by the Rice Disease Resistance Gene, Xa21
Song, W.-Y., Wang, G.-L., Chen, L.-L., Kim, H.-S., Pi, L.-Y., Holsten, T., Gardner, J., Wang, B., Zhai, W.-X., Zhu, L.-H., et al. (1995) · Science · doi:10.1126/science.270.5243.1804 · Cited by 2,292
The R2R3-MYB gene family in Arabidopsis thaliana
Stracke, R., Werber, M., & Weisshaar, B. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00199-0 · Cited by 2,197
Abiotic and biotic stress combinations
Suzuki, N., Rivero, R. M., Shulaev, V., Blumwald, E., & Mittler, R. (2014) · New Phytologist · doi:10.1111/nph.12797 · Cited by 2,153
Plant Stomata Function in Innate Immunity against Bacterial Invasion
Melotto, M., Underwood, W., Koczan, J., Nomura, K., & He, S. Y. (2006) · Cell · doi:10.1016/j.cell.2006.06.054 · Cited by 1,981
bZIP transcription factors in Arabidopsis
Jakoby, M., Weisshaar, B., Dröge-Laser, W., Vicente-Carbajosa, J., Tiedemann, J., Kroj, T., & Parcy, F. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(01)02223-3 · Cited by 1,849
Growth–Defense Tradeoffs in Plants: A Balancing Act to Optimize Fitness
Huot, B., Yao, J., Montgomery, B. L., & He, S. Y. (2014) · Molecular Plant · doi:10.1093/mp/ssu049 · Cited by 1,836
Isolation and Functional Analysis of Arabidopsis Stress-Inducible NAC Transcription Factors That Bind to a Drought-Responsive cis-Element in the early responsive to dehydration stress 1 Promoter[W]
Tran, L.-S. P., Nakashima, K., Sakuma, Y., Simpson, S. D., Fujita, Y., Maruyama, K., Fujita, M., Seki, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2004) · The Plant Cell · doi:10.1105/tpc.104.022699 · Cited by 1,511
ETHYLENE RESPONSE FACTOR1 Integrates Signals from Ethylene and Jasmonate Pathways in Plant Defense[W]
Lorenzo, O., Piqueras, R., Sánchez-Serrano, J. J., & Solano, R. (2003) · The Plant Cell · doi:10.1105/tpc.007468 · Cited by 1,405
MAPK Cascades in Plant Disease Resistance Signaling
Meng, X., & Zhang, S. (2013) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-082712-102314 · Cited by 1,367
Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1
Solano, R., Stepanova, A., Chao, Q., & Ecker, J. R. (1998) · Genes & Development · doi:10.1101/gad.12.23.3703 · Cited by 1,287
The Role of WRKY Transcription Factors in Plant Immunity
Pandey, S. P., & Somssich, I. E. (2009) · Plant Physiology · doi:10.1104/pp.109.138990 · Cited by 1,277
Self-citation
The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense[W]
Li, J., Brader, G., & Palva, E. T. (2004) · The Plant Cell · doi:10.1105/tpc.016980 · Cited by 1,207
Plant pattern-recognition receptors
Zipfel, C. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.05.004 · Cited by 1,159
How do plants achieve immunity? Defence without specialized immune cells
Spoel, S. H., & Dong, X. (2012) · Nature Reviews Immunology · doi:10.1038/nri3141 · Cited by 1,112
MYC2: The Master in Action
Kazan, K., & Manners, J. M. (2013) · Molecular Plant · doi:10.1093/mp/sss128 · Cited by 1,081
NAC transcription factors in plant abiotic stress responses
Nakashima, K., Takasaki, H., Mizoi, J., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2012) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2011.10.005 · Cited by 1,055
Concomitant Activation of Jasmonate and Ethylene Response Pathways Is Required for Induction of a Plant Defensin Gene in Arabidopsis
Penninckx, I. A. M. A., Thomma, B. P. H. J., Buchala, A., Métraux, J.-P., & Broekaert, W. F. (1998) · The Plant Cell · doi:10.1105/tpc.10.12.2103 · Cited by 1,037
APETALA 2/Ethylene Responsive Factor (AP 2/ERF) transcription factors: mediators of stress responses and developmental programs
Licausi, F., Ohme‐Takagi, M., & Perata, P. (2013) · New Phytologist · doi:10.1111/nph.12291 · Cited by 1,020
NINJA connects the co-repressor TOPLESS to jasmonate signalling
Pauwels, L., Barbero, G. F., Geerinck, J., Tilleman, S., Grunewald, W., Pérez, A. C., Chico, J. M., Bossche, R. V., Sewell, J., Gil, E., et al. (2010) · Nature · doi:10.1038/nature08854 · Cited by 1,018
Jasmonate Passes Muster: A Receptor and Targets for the Defense Hormone
Browse, J. (2009) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092007 · Cited by 944
Plant Responses to Ethylene Gas Are Mediated by SCFEBF1/EBF2-Dependent Proteolysis of EIN3 Transcription Factor
Guo, H., & Ecker, J. R. (2003) · Cell · doi:10.1016/s0092-8674(03)00969-3 · Cited by 928
Differential innate immune signalling via Ca2+ sensor protein kinases
Boudsocq, M., Willmann, M. R., McCormack, M., Lee, H., Shan, L., He, P., Bush, J., Cheng, S.-H., & Sheen, J. (2010) · Nature · doi:10.1038/nature08794 · Cited by 887
Comparing signaling mechanisms engaged in pattern-triggered and effector-triggered immunity
Tsuda, K., & Katagiri, F. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.04.006 · Cited by 884
Self-citation
Phosphorylation of a WRKY Transcription Factor by Two Pathogen-Responsive MAPKs Drives Phytoalexin Biosynthesis in Arabidopsis
Mao, G., Meng, X., Liu, Y., Zheng, Z., Chen, Z., & Zhang, S. (2011) · The Plant Cell · doi:10.1105/tpc.111.084996 · Cited by 876
Phosphorylation of 1-Aminocyclopropane-1-Carboxylic Acid Synthase by MPK6, a Stress-Responsive Mitogen-Activated Protein Kinase, Induces Ethylene Biosynthesis in Arabidopsis[W]
Liu, Y., & Zhang, S. (2004) · The Plant Cell · doi:10.1105/tpc.104.026609 · Cited by 863
Roles of NAC transcription factors in the regulation of biotic and abiotic stress responses in plants
Nuruzzaman, M., Sharoni, A. M., & Kikuchi, S. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00248 · Cited by 857
COI1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine
Katsir, L., Schilmiller, A. L., Staswick, P. E., He, S. Y., & Howe, G. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802332105 · Cited by 821
DELLAs Modulate Jasmonate Signaling via Competitive Binding to JAZs
Hou, X., Lee, L. Y. C., Xia, K., Yan, Y., & Yu, H. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.10.024 · Cited by 813
Encoding and Decoding Cellular Information through Signaling Dynamics
Purvis, J. E., & Lahav, G. (2013) · Cell · doi:10.1016/j.cell.2013.02.005 · Cited by 798
The Arabidopsis CORONATINE INSENSITIVE1 Protein Is a Jasmonate Receptor
Yan, J., Zhang, C., Gu, M., Bai, Z., Zhang, W., Qi, T., Cheng, Z., Peng, W., Luo, H., Nan, F., et al. (2009) · The Plant Cell · doi:10.1105/tpc.109.065730 · Cited by 792
A Genomic Approach to Identify Regulatory Nodes in the Transcriptional Network of Systemic Acquired Resistance in Plants
Wang, D., Amornsiripanitch, N., & Dong, X. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020123 · Cited by 774
Calcium-dependent protein kinase/NADPH oxidase activation circuit is required for rapid defense signal propagation
Dubiella, U., Seybold, H., Durian, G., Komander, E., Lassig, R., Witte, C., Schulze, W. X., & Romeis, T. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221294110 · Cited by 760
Shaping the calcium signature
McAinsh, M. R., & Pittman, J. K. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2008.02682.x · Cited by 756
Nuclear Activity of MLA Immune Receptors Links Isolate-Specific and Basal Disease-Resistance Responses
Shen, Q.-H., Saijo, Y., Mauch, S., Biskup, C., Bieri, S., Keller, B., Seki, H., Ülker, B., Somssich, I. E., & Schulze-Lefert, P. (2007) · Science · doi:10.1126/science.1136372 · Cited by 751
Self-citation
The AP2/ERF Domain Transcription Factor ORA59 Integrates Jasmonic Acid and Ethylene Signals in Plant Defense
Pré, M., Atallah, M., Champion, A., De Vos, M., Pieterse, C. M. J., & Memelink, J. (2008) · Plant Physiology · doi:10.1104/pp.108.117523 · Cited by 736
Derepression of ethylene-stabilized transcription factors (EIN3/EIL1) mediates jasmonate and ethylene signaling synergy in Arabidopsis
Zhu, Z., An, F., Feng, Y., Li, P., Xue, L., A, M., Jiang, Z., Kim, J.-M., To, T. K., Li, W., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103959108 · Cited by 734
EIN3-Dependent Regulation of Plant Ethylene Hormone Signaling by Two Arabidopsis F Box Proteins
Potuschak, T., Lechner, E., Parmentier, Y., Yanagisawa, S., Grava, S., Koncz, C., & Genschik, P. (2003) · Cell · doi:10.1016/s0092-8674(03)00968-1 · Cited by 733
Physical interaction between RRS1-R, a protein conferring resistance to bacterial wilt, and PopP2, a type III effector targeted to the plant nucleus
Deslandes, L., Olivier, J., Peeters, N., Feng, D. X., Khounlotham, M., Boucher, C., Somssich, I., Genin, S., & Marco, Y. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1230660100 · Cited by 729
Self-citation
Interaction of NPR1 with basic leucine zipper protein transcription factors that bind sequences required for salicylic acid induction of the PR-1 gene
Zhang, Y., Fan, W., Kinkema, M., Li, X., & Dong, X. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6523 · Cited by 714
Genome-Wide Classification and Evolutionary Analysis of the bHLH Family of Transcription Factors in Arabidopsis, Poplar, Rice, Moss, and Algae
Carretero-Paulet, L., Galstyan, A., Roig-Villanova, I., Martínez-García, J. F., Bilbao-Castro, J. R., & Robertson, D. L. (2010) · Plant Physiology · doi:10.1104/pp.110.153593 · Cited by 681
Coronatine Promotes Pseudomonas syringae Virulence in Plants by Activating a Signaling Cascade that Inhibits Salicylic Acid Accumulation
Zheng, X.-Y., Spivey, N. W., Zeng, W., Liu, P.-P., Fu, Z. Q., Klessig, D. F., He, S. Y., & Dong, X. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.04.014 · Cited by 653
Targets of AtWRKY6 regulation during plant senescence and pathogen defensePreprint
Robatzek, S., & Somssich, I. E. (2002) · Genes & Development · doi:10.1101/gad.222702 · Cited by 649
Self-citation
RNA silencing suppression by plant pathogens: defence, counter-defence and counter-counter-defence
Pumplin, N., & Voinnet, O. (2013) · Nature Reviews Microbiology · doi:10.1038/nrmicro3120 · Cited by 642
CTR1 phosphorylates the central regulator EIN2 to control ethylene hormone signaling from the ER membrane to the nucleus in Arabidopsis
Ju, C., Yoon, G. M., Shemansky, J. M., Lin, D. Y., Ying, Z. I., Chang, J., Garrett, W. M., Kessenbrock, M., Groth, G., Tucker, M. L., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214848109 · Cited by 637
Disease resistance or growth: the role of plant hormones in balancing immune responses and fitness costs
Denancé, N., Sánchez-Vallet, A., Goffner, D., & Molina, A. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00155 · Cited by 634
Plant immunity: the EDS1 regulatory node
Wiermer, M., Feys, B. J., & Parker, J. E. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.05.010 · Cited by 623
Ca2+/calmodulin regulates salicylic-acid-mediated plant immunity
Du, L., Ali, G. S., Simons, K. A., Hou, J., Yang, T., Reddy, A. S. N., & Poovaiah, B. W. (2009) · Nature · doi:10.1038/nature07612 · Cited by 592
The Arabidopsis NPR1 Disease Resistance Protein Is a Novel Cofactor That Confers Redox Regulation of DNA Binding Activity to the Basic Domain/Leucine Zipper Transcription Factor TGA1
Després, C., Chubak, C., Rochon, A., Clark, R., Bethune, T., Desveaux, D., & Fobert, P. R. (2003) · The Plant Cell · doi:10.1105/tpc.012849 · Cited by 591
Arabidopsis WRKY38 and WRKY62 Transcription Factors Interact with Histone Deacetylase 19 in Basal Defense
Kim, K.-C., Lai, Z., Fan, B., & Chen, Z. (2008) · The Plant Cell · doi:10.1105/tpc.107.055566 · Cited by 579
Antagonistic Interaction between Systemic Acquired Resistance and the Abscisic Acid–Mediated Abiotic Stress Response in Arabidopsis
Yasuda, M., Ishikawa, A., Jikumaru, Y., Seki, M., Umezawa, T., Asami, T., Maruyama-Nakashita, A., Kudo, T., Shinozaki, K., Yoshida, S., et al. (2008) · The Plant Cell · doi:10.1105/tpc.107.054296 · Cited by 568
Arabidopsis WRKY33 Is a Key Transcriptional Regulator of Hormonal and Metabolic Responses toward Botrytis cinerea Infection
Birkenbihl, R. P., Diezel, C., & Somssich, I. E. (2012) · Plant Physiology · doi:10.1104/pp.111.192641 · Cited by 568
Self-citation
Chromatin modification acts as a memory for systemic acquired resistance in the plant stress response
Jaskiewicz, M., Conrath, U., & Peterhänsel, C. (2011) · EMBO reports · doi:10.1038/embor.2010.186 · Cited by 556
Pseudomonas syringae pv. tomato hijacks the Arabidopsis abscisic acid signalling pathway to cause disease
de Torres‐Zabala, M., Truman, W., Bennett, M. H., Lafforgue, G., Mansfield, J. W., Rodriguez Egea, P., Bögre, L., & Grant, M. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601575 · Cited by 554
The MAP kinase substrate MKS1 is a regulator of plant defense responses
Andreasson, E., Jenkins, T., Brodersen, P., Thorgrimsen, S., Petersen, N. H., Zhu, S., Qiu, J., Micheelsen, P., Rocher, A., Petersen, M., et al. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600737 · Cited by 551
Self-citation
Plant Defense Genes Are Synergistically Induced by Ethylene and Methyl Jasmonate.
Xu, Y., Chang, P., Liu, D., Narasimhan, M. L., Raghothama, K. G., Hasegawa, P. M., & Bressan, R. A. (1994) · The Plant Cell · doi:10.1105/tpc.6.8.1077 · Cited by 539
NPR1 Differentially Interacts with Members of the TGA/OBF Family of Transcription Factors That Bind an Element of the PR-1 Gene Required for Induction by Salicylic Acid
Zhou, J.-M., Trifa, Y., Silva, H., Pontier, D., Lam, E., Shah, J., & Klessig, D. F. (2000) · Molecular Plant-Microbe Interactions® · doi:10.1094/mpmi.2000.13.2.191 · Cited by 536
Knockout Analysis of Arabidopsis Transcription Factors TGA2, TGA5, and TGA6 Reveals Their Redundant and Essential Roles in Systemic Acquired Resistance
Zhang, Y., Tessaro, M. J., Lassner, M., & Li, X. (2003) · The Plant Cell · doi:10.1105/tpc.014894 · Cited by 517
Requirement of Functional Ethylene-Insensitive 2 Gene for Efficient Resistance of Arabidopsis to Infection by Botrytis cinerea
Thomma, B. P. H. J., Eggermont, K., Tierens, K. F. M.-J., & Broekaert, W. F. (1999) · Plant Physiology · doi:10.1104/pp.121.4.1093 · Cited by 512
Phytopathogen Effectors Subverting Host Immunity: Different Foes, Similar Battleground
Dou, D., & Zhou, J.-M. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.09.003 · Cited by 505
The Role of Ethylene in Host-Pathogen Interactions
Broekaert, W. F., Delauré, S. L., De Bolle, M. F. C., & Cammue, B. P. A. (2006) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.44.070505.143440 · Cited by 503
Arabidopsis MAP kinase 4 regulates gene expression through transcription factor release in the nucleus
Qiu, J., Fiil, B. K., Petersen, K., Nielsen, H. B., Botanga, C. J., Thorgrimsen, S., Palma, K., Suarez‐Rodriguez, M. C., Sandbech‐Clausen, S., Lichota, J., et al. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.147 · Cited by 503
Intervention of Phytohormone Pathways by Pathogen Effectors
Kazan, K., & Lyons, R. (2014) · The Plant Cell · doi:10.1105/tpc.114.125419 · Cited by 488
The Cytokinin-Activated Transcription Factor ARR2 Promotes Plant Immunity via TGA3/NPR1-Dependent Salicylic Acid Signaling in Arabidopsis
Choi, J., Huh, S. U., Kojima, M., Sakakibara, H., Paek, K.-H., & Hwang, I. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.011 · Cited by 473
Precision genome engineering and agriculture: opportunities and regulatory challenges
Voytas, D. F., & Gao, C. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001877 · Cited by 458
SA‐inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA‐responsive PDF1.2 transcription
Ndamukong, I., Abdallat, A. A., Thurow, C., Fode, B., Zander, M., Weigel, R., & Gatz, C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03039.x · Cited by 456
Control of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factors
Zhang, Y., Xu, S., Ding, P., Wang, D., Cheng, Y. T., He, J., Gao, M., Xu, F., Li, Y., Zhu, Z., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005225107 · Cited by 454
Dual-Level Regulation of ACC Synthase Activity by MPK3/MPK6 Cascade and Its Downstream WRKY Transcription Factor during Ethylene Induction in Arabidopsis
Li, G., Meng, X., Wang, R., Mao, G., Han, L., Liu, Y., & Zhang, S. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002767 · Cited by 453
Oxylipins: Structurally diverse metabolites from fatty acid oxidation
Mosblech, A., Feussner, I., & Heilmann, I. (2009) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2008.12.011 · Cited by 445
Phosphorylation of an ERF Transcription Factor by Arabidopsis MPK3/MPK6 Regulates Plant Defense Gene Induction and Fungal Resistance
Meng, X., Xu, J., He, Y., Yang, K.-Y., Mordorski, B., Liu, Y., & Zhang, S. (2013) · The Plant Cell · doi:10.1105/tpc.112.109074 · Cited by 429
Temporal transcriptional response to ethylene gas drives growth hormone cross-regulation in Arabidopsis
Chang, K. N., Zhong, S., Weirauch, M. T., Hon, G., Pelizzola, M., Li, H., Huang, S.-S. C., Schmitz, R. J., Urich, M. A., Kuo, D., et al. (2013) · eLife · doi:10.7554/elife.00675 · Cited by 427
RRS1 and RPS4 provide a dual Resistance‐gene system against fungal and bacterial pathogens
Narusaka, M., Shirasu, K., Noutoshi, Y., Kubo, Y., Shiraishi, T., Iwabuchi, M., & Narusaka, Y. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03949.x · Cited by 419
The Arabidopsis RPS4 bacterial-resistance gene is a member of the TIR-NBS-LRR family of disease-resistance genes
Gassmann, W., Hinsch, M., & Staskawicz, B. J. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00600.x · Cited by 416
Arabidopsis EIN3-binding F-box 1 and 2 form ubiquitin-protein ligases that repress ethylene action and promote growth by directing EIN3 degradation
Gagne, J. M., Smalle, J., Gingerich, D. J., Walker, J. M., Yoo, S.-D., Yanagisawa, S., & Vierstra, R. D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401698101 · Cited by 413
A critical role of two positively charged amino acids in the Jas motif of Arabidopsis JAZ proteins in mediating coronatine‐ and jasmonoyl isoleucine‐dependent interactions with the COI1 F‐box protein
Melotto, M., Mecey, C., Niu, Y., Chung, H. S., Katsir, L., Yao, J., Zeng, W., Thines, B., Staswick, P., Browse, J., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03566.x · Cited by 405
Interaction between MYC2 and ETHYLENE INSENSITIVE3 Modulates Antagonism between Jasmonate and Ethylene Signaling in Arabidopsis
Song, S., Huang, H., Gao, H., Wang, J., Wu, D., Liu, X., Yang, S., Zhai, Q., Li, C., Qi, T., et al. (2014) · The Plant Cell · doi:10.1105/tpc.113.120394 · Cited by 401
Structural Basis for Assembly and Function of a Heterodimeric Plant Immune Receptor
Williams, S. J., Sohn, K. H., Wan, L., Bernoux, M., Sarris, P. F., Segonzac, C., Ve, T., Ma, Y., Saucet, S. B., Ericsson, D. J., et al. (2014) · Science · doi:10.1126/science.1247357 · Cited by 370
Flg22 regulates the release of an ethylene response factor substrate from MAP kinase 6 in Arabidopsis thaliana via ethylene signaling
Bethke, G., Unthan, T., Uhrig, J. F., Pöschl, Y., Gust, A. A., Scheel, D., & Lee, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810206106 · Cited by 361
A Mitogen-activated Protein Kinase Kinase Kinase Mediates Reactive Oxygen Species Homeostasis in Arabidopsis
Nakagami, H., Soukupová, H., Schikora, A., Zárský, V., & Hirt, H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605293200 · Cited by 357
A fungal-responsive MAPK cascade regulates phytoalexin biosynthesis in Arabidopsis
Ren, D., Liu, Y., Yang, K.-Y., Han, L., Mao, G., Glazebrook, J., & Zhang, S. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711301105 · Cited by 354
Roles of CAMTA transcription factors and salicylic acid in configuring the low‐temperature transcriptome and freezing tolerance of Arabidopsis
Kim, Y., Park, S., Gilmour, S. J., & Thomashow, M. F. (2013) · The Plant Journal · doi:10.1111/tpj.12205 · Cited by 348
MEKK1 Is Required for flg22-Induced MPK4 Activation in Arabidopsis Plants
Suarez-Rodriguez, M. C., Adams-Phillips, L., Liu, Y., Wang, H., Su, S.-H., Jester, P. J., Zhang, S., Bent, A. F., & Krysan, P. J. (2007) · Plant Physiology · doi:10.1104/pp.106.091389 · Cited by 347
ETHYLENE INSENSITIVE3 and ETHYLENE INSENSITIVE3-LIKE1 Repress SALICYLIC ACID INDUCTION DEFICIENT2 Expression to Negatively Regulate Plant Innate Immunity in Arabidopsis
Chen, H., Xue, L., Chintamanani, S., Germain, H., Lin, H., Cui, H., Cai, R., Zuo, J., Tang, X., Li, X., et al. (2009) · The Plant Cell · doi:10.1105/tpc.108.065193 · Cited by 335
Bifurcation of Arabidopsis NLR Immune Signaling via Ca2+-Dependent Protein Kinases
Gao, X., Chen, X., Lin, W., Chen, S., Lu, D., Niu, Y., Li, L., Cheng, C., McCormack, M., Sheen, J., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003127 · Cited by 331
A bHLH-Type Transcription Factor, ABA-INDUCIBLE BHLH-TYPE TRANSCRIPTION FACTOR/JA-ASSOCIATED MYC2-LIKE1, Acts as a Repressor to Negatively Regulate Jasmonate Signaling in Arabidopsis
Nakata, M., Mitsuda, N., Herde, M., Koo, A. J. K., Moreno, J. E., Suzuki, K., Howe, G. A., & Ohme-Takagi, M. (2013) · The Plant Cell · doi:10.1105/tpc.113.111112 · Cited by 331
A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors
Burch-Smith, T. M., Schiff, M., Caplan, J. L., Tsao, J., Czymmek, K., & Dinesh-Kumar, S. P. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050068 · Cited by 329
Antagonism between salicylic and abscisic acid reflects early host–pathogen conflict and moulds plant defence responses
De Torres Zabala, M., Bennett, M. H., Truman, W. H., & Grant, M. R. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03875.x · Cited by 327
The Mediator Complex Subunit PFT1 Is a Key Regulator of Jasmonate-Dependent Defense in Arabidopsis
Kidd, B. N., Edgar, C. I., Kumar, K. K., Aitken, E. A., Schenk, P. M., Manners, J. M., & Kazan, K. (2009) · The Plant Cell · doi:10.1105/tpc.109.066910 · Cited by 324
CBP60g and SARD1 play partially redundant critical roles in salicylic acid signaling
Wang, L., Tsuda, K., Truman, W., Sato, M., Nguyen, L. V., Katagiri, F., & Glazebrook, J. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04655.x · Cited by 319
Self-citation
Arabidopsis Mitogen-Activated Protein Kinase Kinases MKK1 and MKK2 Have Overlapping Functions in Defense Signaling Mediated by MEKK1, MPK4, and MKS1
Qiu, J.-L., Zhou, L., Yun, B.-W., Nielsen, H. B., Fiil, B. K., Petersen, K., MacKinlay, J., Loake, G. J., Mundy, J., & Morris, P. C. (2008) · Plant Physiology · doi:10.1104/pp.108.120006 · Cited by 316
Arabidopsis CaM Binding Protein CBP60g Contributes to MAMP-Induced SA Accumulation and Is Involved in Disease Resistance against Pseudomonas syringae
Wang, L., Tsuda, K., Sato, M., Cohen, J. D., Katagiri, F., & Glazebrook, J. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000301 · Cited by 309
Self-citation
A Prominent Role of the Flagellin Receptor FLAGELLIN-SENSING2 in Mediating Stomatal Response to Pseudomonas syringae pv tomato DC3000 in Arabidopsis
Zeng, W., & He, S. Y. (2010) · Plant Physiology · doi:10.1104/pp.110.157016 · Cited by 297
Durable panicle blast-resistance gene Pb1 encodes an atypical CC-NBS-LRR protein and was generated by acquiring a promoter through local genome duplication
Hayashi, N., Inoue, H., Kato, T., Funao, T., Shirota, M., Shimizu, T., Kanamori, H., Yamane, H., Hayano-Saito, Y., Matsumoto, T., et al. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04348.x · Cited by 294
MEKK1 Is Required for MPK4 Activation and Regulates Tissue-specific and Temperature-dependent Cell Death in Arabidopsis
Ichimura, K., Casais, C., Peck, S. C., Shinozaki, K., & Shirasu, K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605319200 · Cited by 293
Overproduction of salicylic acid in plants by bacterial transgenes enhances pathogen resistance
Verberne, M. C., Verpoorte, R., Bol, J. F., Mercado-Blanco, J., & Linthorst, H. J. M. (2000) · Nature Biotechnology · doi:10.1038/77347 · Cited by 290
Filamentous pathogen effector functions: of pathogens, hosts and microbiomes
Rovenich, H., Boshoven, J. C., & Thomma, B. P. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.05.001 · Cited by 288
Ethylene signaling: simple ligand, complex regulation
Merchante, C., Alonso, J. M., & Stepanova, A. N. (2013) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2013.08.001 · Cited by 284
Connecting Growth and Defense: The Emerging Roles of Brassinosteroids and Gibberellins in Plant Innate Immunity
De Bruyne, L., Höfte, M., & De Vleesschauwer, D. (2014) · Molecular Plant · doi:10.1093/mp/ssu050 · Cited by 282
Trojan Horse Strategy in Agrobacterium Transformation: Abusing MAPK Defense Signaling
Djamei, A., Pitzschke, A., Nakagami, H., Rajh, I., & Hirt, H. (2007) · Science · doi:10.1126/science.1148110 · Cited by 275
Transcription Dynamics in Plant Immunity
Moore, J. W., Loake, G. J., & Spoel, S. H. (2011) · The Plant Cell · doi:10.1105/tpc.111.087346 · Cited by 272
The Arabidopsis miR472-RDR6 Silencing Pathway Modulates PAMP- and Effector-Triggered Immunity through the Post-transcriptional Control of Disease Resistance Genes
Boccara, M., Sarazin, A., Thiébeauld, O., Jay, F., Voinnet, O., Navarro, L., & Colot, V. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1003883 · Cited by 268
Phosphorylation of the Nicotiana benthamiana WRKY8 Transcription Factor by MAPK Functions in the Defense Response
Ishihama, N., Yamada, R., Yoshioka, M., Katou, S., & Yoshioka, H. (2011) · The Plant Cell · doi:10.1105/tpc.110.081794 · Cited by 265
Dual Regulation of Gene Expression Mediated by Extended MAPK Activation and Salicylic Acid Contributes to Robust Innate Immunity in Arabidopsis thaliana
Tsuda, K., Mine, A., Bethke, G., Igarashi, D., Botanga, C. J., Tsuda, Y., Glazebrook, J., Sato, M., & Katagiri, F. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1004015 · Cited by 265
Self-citation
Arabidopsis thaliana class-II TGA transcription factors are essential activators of jasmonic acid/ethylene-induced defense responses: Class-II TGA factors activate JA/ET-induced responses
Zander, M., La Camera, S., Lamotte, O., Métraux, J.-P., & Gatz, C. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04044.x · Cited by 265
Mitogen-activated protein kinase 3 and 6 regulate Botrytis cinerea-induced ethylene production in Arabidopsis: MAPKs regulate pathogen-induced ethylene production
Han, L., Li, G.-J., Yang, K.-Y., Mao, G., Wang, R., Liu, Y., & Zhang, S. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04318.x · Cited by 263
Transcriptional control of plant defence responses
Buscaill, P., & Rivas, S. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.04.004 · Cited by 262
Transcription Factor Families Have Much Higher Expansion Rates in Plants than in Animals
Shiu, S.-H., Shih, M.-C., & Li, W.-H. (2005) · Plant Physiology · doi:10.1104/pp.105.065110 · Cited by 250
CAMTAs: Calmodulin‐binding transcription activators from plants to human
Finkler, A., Ashery-Padan, R., & Fromm, H. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.07.051 · Cited by 247
The transcriptional regulator BZR1 mediates trade-off between plant innate immunity and growth
Lozano-Durán, R., Macho, A. P., Boutrot, F., Segonzac, C., Somssich, I. E., & Zipfel, C. (2013) · eLife · doi:10.7554/elife.00983 · Cited by 245
Self-citation
Phosphorylation-Coupled Proteolysis of the Transcription Factor MYC2 Is Important for Jasmonate-Signaled Plant Immunity
Zhai, Q., Yan, L., Tan, D., Chen, R., Sun, J., Gao, L., Dong, M.-Q., Wang, Y., & Li, C. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003422 · Cited by 241
WRKY Transcription Factors Involved in Activation of SA Biosynthesis Genes
van Verk, M. C., Bol, J. F., & Linthorst, H. J. (2011) · BMC Plant Biology · doi:10.1186/1471-2229-11-89 · Cited by 238
The bHLH Transcription Factor HBI1 Mediates the Trade-Off between Growth and Pathogen-Associated Molecular Pattern–Triggered Immunity in Arabidopsis
Fan, M., Bai, M.-Y., Kim, J.-G., Wang, T., Oh, E., Chen, L., Park, C. H., Son, S.-H., Kim, S.-K., Mudgett, M. B., et al. (2014) · The Plant Cell · doi:10.1105/tpc.113.121111 · Cited by 237
Export of Salicylic Acid from the Chloroplast Requires the Multidrug and Toxin Extrusion-Like Transporter EDS5
Serrano, M., Wang, B., Aryal, B., Garcion, C., Abou-Mansour, E., Heck, S., Geisler, M., Mauch, F., Nawrath, C., & Métraux, J.-P. (2013) · Plant Physiology · doi:10.1104/pp.113.218156 · Cited by 233
Perception of the plant immune signal salicylic acid
Yan, S., & Dong, X. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.04.006 · Cited by 231
Calcium and Reactive Oxygen Species Rule the Waves of Signaling
Steinhorst, L., & Kudla, J. (2013) · Plant Physiology · doi:10.1104/pp.113.222950 · Cited by 231
MAPK phosphorylation‐induced stabilization of ACS6 protein is mediated by the non‐catalytic C‐terminal domain, which also contains the cis‐determinant for rapid degradation by the 26S proteasome pathway
Joo, S., Liu, Y., Lueth, A., & Zhang, S. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03404.x · Cited by 230
Plant–bacterial pathogen interactions mediated by type III effectors
Feng, F., & Zhou, J.-M. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2012.03.004 · Cited by 230
Blast resistance of CC-NB-LRR protein Pb1 is mediated by WRKY45 through protein–protein interaction
Inoue, H., Hayashi, N., Matsushita, A., Xinqiong, L., Nakayama, A., Sugano, S., Jiang, C.-J., & Takatsuji, H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222155110 · Cited by 226
From Pioneers to Team Players: TGA Transcription Factors Provide a Molecular Link Between Different Stress Pathways
Gatz, C. (2013) · Molecular Plant-Microbe Interactions® · doi:10.1094/mpmi-04-12-0078-ia · Cited by 225
Jasmonate-Activated MYC2 Represses ETHYLENE INSENSITIVE3 Activity to Antagonize Ethylene-Promoted Apical Hook Formation in Arabidopsis
Zhang, X., Zhu, Z., An, F., Hao, D., Li, P., Song, J., Yi, C., & Guo, H. (2014) · The Plant Cell · doi:10.1105/tpc.113.122002 · Cited by 220
Basic Helix-Loop-Helix Transcription Factors JASMONATE-ASSOCIATED MYC2-LIKE1 (JAM1), JAM2, and JAM3 Are Negative Regulators of Jasmonate Responses in Arabidopsis
Sasaki-Sekimoto, Y., Jikumaru, Y., Obayashi, T., Saito, H., Masuda, S., Kamiya, Y., Ohta, H., & Shirasu, K. (2013) · Plant Physiology · doi:10.1104/pp.113.220129 · Cited by 220
Transcriptional regulation by an NAC (NAM–ATAF1,2–CUC2) transcription factor attenuates ABA signalling for efficient basal defence towards Blumeria graminis f. sp.hordei in Arabidopsis
Jensen, M. K., Hagedorn, P. H., De Torres‐Zabala, M., Grant, M. R., Rung, J. H., Collinge, D. B., & Lyngkjaer, M. F. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03646.x · Cited by 218
Tell me more: roles of NPRs in plant immunity
Pajerowska-Mukhtar, K. M., Emerine, D. K., & Mukhtar, M. S. (2013) · Trends in Plant Science · doi:10.1016/j.tplants.2013.04.004 · Cited by 216
At MYB 44 regulates WRKY 70 expression and modulates antagonistic interaction between salicylic acid and jasmonic acid signaling
Shim, J. S., Jung, C., Lee, S., Min, K., Lee, Y., Choi, Y., Lee, J. S., Song, J. T., Kim, J., & Choi, Y. D. (2013) · The Plant Journal · doi:10.1111/tpj.12051 · Cited by 211
Ubiquitination during Plant Immune Signaling
Marino, D., Peeters, N., & Rivas, S. (2012) · Plant Physiology · doi:10.1104/pp.112.199281 · Cited by 208
The ABC transporter BcatrB from Botrytis cinerea exports camalexin and is a virulence factor on Arabidopsis thaliana
Stefanato, F. L., Abou‐Mansour, E., Buchala, A., Kretschmer, M., Mosbach, A., Hahn, M., Bochet, C. G., Métraux, J., & Schoonbeek, H. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03794.x · Cited by 203
Recent Advances in Calcium/Calmodulin-Mediated Signaling with an Emphasis on Plant-Microbe Interactions
Poovaiah, B. W., Du, L., Wang, H., & Yang, T. (2013) · Plant Physiology · doi:10.1104/pp.113.220780 · Cited by 202
The Arabidopsis MAP kinase kinase MKK1 participates in defence responses to the bacterial elicitor flagellin
Mészáros, T., Helfer, A., Hatzimasoura, E., Magyar, Z., Serazetdinova, L., Rios, G., Bardóczy, V., Teige, M., Koncz, C., Peck, S., et al. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02888.x · Cited by 198
bZIPs and WRKYs: two large transcription factor families executing two different functional strategies
Llorca, C. M., Potschin, M., & Zentgraf, U. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00169 · Cited by 197
Novel Positive Regulatory Role for the SPL6 Transcription Factor in the N TIR-NB-LRR Receptor-Mediated Plant Innate Immunity
Padmanabhan, M. S., Ma, S., Burch-Smith, T. M., Czymmek, K., Huijser, P., & Dinesh-Kumar, S. P. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003235 · Cited by 195
TAL effectors – pathogen strategies and plant resistance engineering
Boch, J., Bonas, U., & Lahaye, T. (2014) · New Phytologist · doi:10.1111/nph.13015 · Cited by 191
A single amino acid insertion in the WRKY domain of the Arabidopsis TIR–NBS–LRR–WRKY‐type disease resistance protein SLH1 (sensitive to low humidity 1) causes activation of defense responses and hypersensitive cell death
Noutoshi, Y., Ito, T., Seki, M., Nakashita, H., Yoshida, S., Marco, Y., Shirasu, K., & Shinozaki, K. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02500.x · Cited by 190
JAV1 Controls Jasmonate-Regulated Plant Defense
Hu, P., Zhou, W., Cheng, Z., Fan, M., Wang, L., & Xie, D. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.04.027 · Cited by 187
Repression of the Arabidopsis thaliana Jasmonic Acid/Ethylene-Induced Defense Pathway by TGA-Interacting Glutaredoxins Depends on Their C-Terminal ALWL Motif
Zander, M., Chen, S., Imkampe, J., Thurow, C., & Gatz, C. (2012) · Molecular Plant · doi:10.1093/mp/ssr113 · Cited by 186
Epigenetic control of plant immunity
ALVAREZ, M. E., NOTA, F., & CAMBIAGNO, D. A. (2010) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2010.00621.x · Cited by 181
Metabolism of salicylic acid in wild‐type, ugt74f1 and ugt74f2 glucosyltransferase mutants of Arabidopsis thaliana
Dean, J. V., & Delaney, S. P. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2007.01041.x · Cited by 180
The Arabidopsis thaliana mitogen‐activated protein kinases MPK 3 and MPK 6 target a subclass of ‘VQ‐motif’‐containing proteins to regulate immune responses
Pecher, P., Eschen‐Lippold, L., Herklotz, S., Kuhle, K., Naumann, K., Bethke, G., Uhrig, J., Weyhe, M., Scheel, D., & Lee, J. (2014) · New Phytologist · doi:10.1111/nph.12817 · Cited by 175
Epigenetic Control of a Transcription Factor at the Cross Section of Two Antagonistic Pathways
Alvarez-Venegas, R., Abdallat, A. A., Guo, M., Alfano, J. R., & Avramova, Z. (2007) · Epigenetics · doi:10.4161/epi.2.2.4404 · Cited by 170
An alternative polyadenylation mechanism coopted to the Arabidopsis RPP7 gene through intronic retrotransposon domestication
Tsuchiya, T., & Eulgem, T. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312545110 · Cited by 167
Comparison of phytohormone signaling mechanisms
Shan, X., Yan, J., & Xie, D. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.09.006 · Cited by 164
MED18 interaction with distinct transcription factors regulates multiple plant functions
Lai, Z., Schluttenhofer, C. M., Bhide, K., Shreve, J., Thimmapuram, J., Lee, S. Y., Yun, D.-J., & Mengiste, T. (2014) · Nature Communications · doi:10.1038/ncomms4064 · Cited by 164
Barley MLA Immune Receptors Directly Interfere with Antagonistically Acting Transcription Factors to Initiate Disease Resistance Signaling
Chang, C., Yu, D., Jiao, J., Jing, S., Schulze-Lefert, P., & Shen, Q.-H. (2013) · The Plant Cell · doi:10.1105/tpc.113.109942 · Cited by 163
A new eye on NLR proteins: focused on clarity or diffused by complexity?
Bonardi, V., Cherkis, K., Nishimura, M. T., & Dangl, J. L. (2012) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.12.006 · Cited by 161
A High-Throughput Screening System for Arabidopsis Transcription Factors and Its Application to Med25-Dependent Transcriptional Regulation
Ou, B., Yin, K., Liu, S.-N., Yan, Y., Gu, T., Hui, J. M. W., Zhang, L., Miao, J., Kondou, Y., Matsui, M., et al. (2011) · Molecular Plant · doi:10.1093/mp/ssr002 · Cited by 157
Plant Calcium-Permeable Channels
Swarbreck, S. M., Colaço, R., & Davies, J. M. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.220855 · Cited by 156
A Comprehensive Structure–Function Analysis ofArabidopsisSNI1 Defines Essential Regions and Transcriptional Repressor Activity
Mosher, R. A., Durrant, W. E., Wang, D., Song, J., & Dong, X. (2006) · The Plant Cell · doi:10.1105/tpc.105.039677 · Cited by 154
Activation of the Arabidopsis thaliana Mitogen-Activated Protein Kinase MPK11 by the Flagellin-Derived Elicitor Peptide, flg22
Bethke, G., Pecher, P., Eschen‐Lippold, L., Tsuda, K., Katagiri, F., Glazebrook, J., Scheel, D., & Lee, J. (2011) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-11-11-0281 · Cited by 153
Self-citation
Manipulation of salicylate content in Arabidopsis thaliana by the expression of an engineered bacterial salicylate synthase
Mauch, F., Mauch‐Mani, B., Gaille, C., Kull, B., Haas, D., & Reimmann, C. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.00940.x · Cited by 151
VIP1 response elements mediate mitogen-activated protein kinase 3-induced stress gene expression
Pitzschke, A., Djamei, A., Teige, M., & Hirt, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905599106 · Cited by 146
A Catalogue of Eukaryotic Transcription Factor Types, Their Evolutionary Origin, and Species Distribution
Weirauch, M. T., & Hughes, T. R. (2011) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-90-481-9069-0_3 · Cited by 138
Alternative Splicing in Plant Immunity
Yang, S., Tang, F., & Zhu, H. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150610424 · Cited by 137
Regulation of plant immunity through ubiquitin‐mediated modulation of Ca2+–calmodulin– A t SR 1/ CAMTA 3 signaling
Zhang, L., Du, L., Shen, C., Yang, Y., & Poovaiah, B. W. (2014) · The Plant Journal · doi:10.1111/tpj.12473 · Cited by 127
The CALMODULIN-BINDING PROTEIN60 Family Includes Both Negative and Positive Regulators of Plant Immunity
Truman, W., Sreekanta, S., Lu, Y., Bethke, G., Tsuda, K., Katagiri, F., & Glazebrook, J. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.227108 · Cited by 122
Self-citation
The Pseudomonas syringae type III effector tyrosine phosphatase HopAO1 suppresses innate immunity in Arabidopsis thaliana
Underwood, W. R., Zhang, S., & He, S. Y. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03262.x · Cited by 105
Tight Interconnection and Multi-Level Control of Arabidopsis MYB44 in MAPK Cascade Signalling
Persak, H., & Pitzschke, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057547 · Cited by 102
There's More to the Picture Than Meets the Eye: Nitric Oxide Cross Talk with Ca2+ Signaling
Jeandroz, S., Lamotte, O., Astier, J., Rasul, S., Trapet, P. L., Besson‐Bard, A., Bourque, S., Nicolas-Francès, V., Ma, W., Berkowitz, G. A., et al. (2013) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.220624 · Cited by 99
Cytokinins for immunity beyond growth, galls and green islands
Naseem, M., Wölfling, M., & Dandekar, T. (2014) · Trends in Plant Science · doi:10.1016/j.tplants.2014.04.001 · Cited by 88
Spatial and temporal organization of signaling pathways
Housden, B. E., & Perrimon, N. (2014) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2014.07.008 · Cited by 86
NLR-Associating Transcription Factor bHLH84 and Its Paralogs Function Redundantly in Plant Immunity
Xu, F., Kapos, P., Cheng, Y., Li, M., Zhang, Y., & Li, X. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004312 · Cited by 83
Chromatin modification and remodelling: a regulatory landscape for the control of Arabidopsis defence responses upon pathogen attack
Berr, A., Ménard, R., Heitz, T., et al. (2012) · Cellular Microbiology · doi:10.1111/j.1462-5822.2012.01785.x · Cited by 77
The function of the Mediator complex in plant immunity
An, C., & Mou, Z. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.23182 · Cited by 68
Molecular and spatial constraints on NB-LRR receptor signaling
Heidrich, K., Blanvillain‐Baufumé, S., & Parker, J. E. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2012.03.015 · Cited by 59
Modeling genomic regulatory networks with big data
Bolouri, H. (2014) · Trends in Genetics · doi:10.1016/j.tig.2014.02.005 · Cited by 59
Arabidopsis TNL-WRKY domain receptor RRS1 contributes to temperature-conditioned RPS4 auto-immunity
Heidrich, K., Tsuda, K., Blanvillain‐Baufumé, S., Wirthmueller, L., Bautor, J., & Parker, J. E. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00403 · Cited by 58
Self-citation
New clues in the nucleus: transcriptional reprogramming in effector-triggered immunity
Bhattacharjee, S., Garner, C. M., & Gassmann, W. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00364 · Cited by 43
Updates on the model and the evolution of cytokinin signaling
Gruhn, N., & Heyl, A. (2013) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2013.09.001 · Cited by 33
A High-Throughput Screening System for Arabidopsis Transcription Factors and Its Application to Med25-Dependent Transcriptional Regulation
Oua, Kang-Quan, Yin, Y., Sai-Nan, Liu, Yan, Yang, Tren, Gu, Jennifer, et al. (2011) · 分子植物：英文版 · Cited by 26

Disease Resistance Mechanisms in Plants
Andersen, E. J., Ali, S., Byamukama, E., Yen, Y., & Nepal, M. P. (2018) · Genes · doi:10.3390/genes9070339 · Cited by 434
Transcriptional Regulation of Pattern-Triggered Immunity in Plants
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See all 552

Authors: Tsuda, K., & Somssich, I. E.
Venue: New Phytologist
Publisher: Wiley
Published: 2015-01-26
Volume: 206
Issue: 3
Pages: 932-947
ISSN: 0028-646X (ISSN-L)
1469-8137
DOI: 10.1111/nph.13286
OpenAlex: W2139333496
Cited by: 552
References: 174
FWCI: 41.86
Type: journal article
Language: en
Open access: closed

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Transcriptional networks in plant immunity

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