Salicylic acid and jasmonic acid in plant immunity

Pingyu Zhang , Edan Jackson , Xin Li , Yuelin Zhang

Horticulture Research ›› 2025, Vol. 12 ›› Issue (7) : 82

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Horticulture Research ›› 2025, Vol. 12 ›› Issue (7) :82 DOI: 10.1093/hr/uhaf082
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Salicylic acid and jasmonic acid in plant immunity
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Abstract

Salicylic acid (SA) and jasmonic acid (JA) are the two most important phytohormones in plant immunity. While SA plays pivotal roles in local and systemic acquired resistance (SAR) against biotrophic pathogens, JA, on the other hand, contributes to defense against necrotrophic pathogens, herbivores, and induced systemic resistance (ISR). Over the past 30 years, extensive research has elucidated the biosynthesis, metabolism, physiological functions, and signaling of both SA and JA. Here, we present an overview of signaling pathways of SA and JA and how they interact with each other to fine-tune plant defense responses.

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Pingyu Zhang, Edan Jackson, Xin Li, Yuelin Zhang. Salicylic acid and jasmonic acid in plant immunity. Horticulture Research, 2025, 12(7): 82 DOI:10.1093/hr/uhaf082

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Conflict of interest statement

The authors declare that they have no conflict of interest.

References

[1]

Macho AP, Zipfel C. Plant PRRs and the activation of innate immune signaling. Mol Cell. 2014; 54:263-72

[2]

Ngou BPM, Ding P, Jones JDG. Thirty years of resistance: zig-zag through the plant immune system. Plant Cell. 2022; 34:1447-78

[3]

Jones JDG, Dangl JL. The plant immune system. Nature. 2006; 444:323-9

[4]

Fu ZQ, Dong X. Systemic acquired resistance: turning local infection into global defense. Annu Rev Plant Biol. 2013; 64: 839-63

[5]

Solano R, Gimenez-Ibanez S. Nuclear jasmonate and salicylate signaling and crosstalk in defense against pathogens. Front Plant Sci. 2013; 4:1-11

[6]

Pieterse CMJ, Van Der Does D, Zamioudis C. et al. Hormonal modulation of plant immunity. Annu Rev Cell Dev Biol. 2012; 28: 489-521

[7]

Li N, Han X, Feng D. et al. Signaling crosstalk between salicylic acid and ethylene/jasmonate in plant defense: do we under-stand what they are whispering? Int J Mol Sci. 2019; 20:671

[8]

Zhou Y, Xu S, Jiang N. et al. Engineering of rice varieties with enhanced resistances to both blast and bacterial blight dis-eases via CRISPR/Cas9. Plant Biotechnol J. 2022; 20:876-85

[9]

Zhu X, Zhao Y, Shi C-M. et al. Antagonistic control of rice immunity against distinct pathogens by the two transcription modules via salicylic acid and jasmonic acid pathways. Dev Cell. 2024; 59:1609-22.e4

[10]

Peng Y, Yang J, Li X. et al. Salicylic acid: biosynthesis and signaling. Annu Rev Plant Biol. 2021; 72:761-91

[11]

Zhang Y, Li X. Salicylic acid: biosynthesis, perception, and contributions to plant immunity. Curr Opin Plant Biol. 2019; 50: 29-36

[12]

Garcion C, Lohmann A, Lamodière E. et al. Characterization and biological function of the ISOCHORISMATE SYNTHASE2 gene of Arabidopsis. Plant Physiol. 2008; 147:1279-87

[13]

Wildermuth MC, Dewdney J, Wu G. et al. Isochorismate syn-thase is required to synthesize salicylic acid for plant defence. Nature. 2001; 414:562-5

[14]

Shine MB, Yang J-W, El-Habbak M. et al. Cooperative function-ing between phenylalanine ammonia lyase and isochorismate synthase activities contributes to salicylic acid biosynthesis in soybean. New Phytol. 2016; 212:627-36

[15]

Ogawa D, Nakajima N, Seo S. et al. The phenylalanine pathway is the main route of salicylic acid biosynthesis in tobacco mosaic virus-infected tobacco leaves. Plant Biotechnol. 2006; 23: 395-8

[16]

Serrano M, Wang B, Aryal B. et al. Export of salicylic acid from the chloroplast requires the multidrug and toxin extrusion-like transporter EDS5. Plant Physiol. 2013; 162:1815-21

[17]

Jagadeeswaran G, Raina S, Acharya BR. et al. Arabidopsis GH3-LIKE DEFENSE GENE 1 is required for accumulation of salicylic acid, activation of defense responses and resistance to Pseu-domonas syringae. Plant J. 2007; 51:234-46

[18]

Nobuta K, Okrent RA, Stoutemyer M. et al. The GH3 acyl adeny-lase family member PBS3 regulates salicylic acid-dependent defense responses in Arabidopsis. Plant Physiol. 2007; 144: 1144-56

[19]

Warren RF, Merritt PM, Holub E. et al. Identification of three putative signal transduction genes involved in R gene-specified disease resistance in Arabidopsis. Genetics. 1999; 152:401-12

[20]

Nawrath C, Heck S, Parinthawong N. et al. EDS5, an essential component of salicylic acid-dependent signaling for disease resistance in Arabidopsis, is a member of the MATE transporter family. Plant Cell. 2002; 14:275-86

[21]

Yamasaki K, Motomura Y, Yagi Y. et al. Chloroplast enve-lope localization of EDS5, an essential factor for salicylic acid biosynthesis in Arabidopsis thaliana. Plant Signal Behav. 2013; 8:e23603

[22]

Rekhter D, Lüdke D, Ding Y. et al. Isochorismate-derived biosynthesis of the plant stress hormone salicylic acid. Science. 2019; 365:498-502

[23]

Torrens-Spence MP, Bobokalonova A, Carballo V. et al. PBS3 and EPS1 complete salicylic acid biosynthesis from isochorismate in Arabidopsis. Mol Plant. 2019; 12:1577-86

[24]

Zhang YX, Xu SH, Ding PT. et al. Control of salicylic acid synthesis and systemic acquired resistance by two members of a plant-specific family of transcription factors. Proc Natl Acad Sci USA. 2010; 107:18220-5

[25]

Sun T, Zhang Y, Li Y. et al. ChIP-seq reveals broad roles of SARD1 and CBP60g in regulating plant immunity. Nat Commun. 2015; 6:10159

[26]

Yalpani N, Leon J, Lawton MA. et al. Pathway of salicylic acid biosynthesis in healthy and virus-inoculated tobacco. Plant Physiol. 1993; 103:315-21

[27]

Vogt T. Phenylpropanoid biosynthesis. Mol Plant. 2010; 3:2-20

[28]

Huang J, Gu M, Lai Z. et al. Functional analysis of the Arabidop-sis PAL gene family in plant growth, development, and response to environmental stress. Plant Physiol. 2010; 153:1526-38

[29]

Duan L, Liu H, Li X. et al. Multiple phytohormones and phy-toalexins are involved in disease resistance to Magnaporthe oryzae invaded from roots in rice. Physiol Plant. 2014; 152:486-500

[30]

Xu L, Zhao H, Ruan W. et al. ABNORMAL INFLORESCENCE MERISTEM1 functions in salicylic acid biosynthesis to maintain proper reactive oxygen species levels for root meristem activity in rice. Plant Cell. 2017; 29:560-74

[31]

Bussell JD, Reichelt M, Wiszniewski AAG. et al. Peroxisomal ATP-binding cassette transporter COMATOSE and the multi-functional protein abnormal INFLORESCENCE MERISTEM are required for the production of benzoylated metabolites in Ara-bidopsis seeds. Plant Physiol. 2014; 164:48-54

[32]

Leon J, Yalpani N, Raskin I. et al. Induction of benzoic acid 2-hydroxylase in virus-inoculated tobacco. Plant Physiol. 1993; 103:323-8

[33]

Wu J, Zhu W, Zhao Q. Salicylic acid biosynthesis is not from phenylalanine in Arabidopsis. J Integr Plant Biol. 2023; 65:881-7

[34]

Ding P, Ding Y. Stories of salicylic acid: a plant defense hor-mone. Trends Plant Sci. 2020; 25:549-65

[35]

Lefevere H, Bauters L, Gheysen G. Salicylic acid biosynthesis in plants. Front Plant Sci. 2020; 11:338

[36]

Zhang Z, Li Q, Li Z. et al. Dual regulation role of GH3.5 in sali-cylic acid and auxin signaling during Arabidopsis-Pseudomonas syringae interaction. Plant Physiol. 2007; 145:450-64

[37]

Lim E-K, Doucet CJ, Li Y. et al. The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic acid, and other benzoates. JBiolChem. 2002; 277:586-92

[38]

Dean JV, Delaney SP. Metabolism of salicylic acid in wild-type, ugt74f1 and ugt74f2 glucosyltransferase mutants of Arabidopsis thaliana. Physiol Plant. 2008; 132:417-25

[39]

von Saint Paul V, Zhang W, Kanawati B. et al. The Arabidopsis glucosyltransferase UGT76B1 conjugates isoleucic acid and modulates plant defense and senescence. Plant Cell. 2011; 23: 4124-45

[40]

Noutoshi Y, Okazaki M, Kida T. et al. Novel plant immune-priming compounds identified via high-throughput chemical screening target salicylic acid glucosyltransferases in Ara-bidopsis. Plant Cell. 2012; 24:3795-804

[41]

Hu Y, Zhang M, Lu M. et al. Salicylic acid carboxyl glucosyl-transferase UGT87E7 regulates disease resistance in Camellia sinensis. Plant Physiol. 2021; 188:1507-20

[42]

Bauer S, Mekonnen DW, Hartmann M. et al. UGT76B1, a promis-cuous hub of small molecule-based immune signaling, gluco-sylates N-hydroxypipecolic acid, and balances plant immunity. Plant Cell. 2021; 33:714-34

[43]

Holmes EC, Chen Y-C, Mudgett MB. et al. Arabidopsis UGT76B1 glycosylates N-hydroxy-pipecolic acid and inactivates sys-temic acquired resistance in tomato. Plant Cell. 2021; 33:750-65

[44]

Hõrak H. How to achieve immune balance and harmony: glyco-syltransferase UGT76B1 inactivates N-hydroxy-pipecolic acid to suppress defense responses. Plant Cell. 2021; 33:453-4

[45]

Chen F, D’Auria JC, Tholl D. et al.An Arabidopsis thaliana gene for methylsalicylate biosynthesis, identified by a biochemical genomics approach, has a role in defense. Plant J. 2003; 36: 577-88

[46]

Shulaev V, Silverman P, Raskin I. Airborne signalling by methyl salicylate in plant pathogen resistance. Nature. 1997; 385: 718-21

[47]

Gong Q, Wang Y, He L. et al. Molecular basis of methyl-salicylate-mediated plant airborne defence. Nature. 2023; 622: 139-48

[48]

Zhang K, Halitschke R, Yin C. et al. Salicylic acid 3-hydroxylase regulates Arabidopsis leaf longevity by mediating salicylic acid catabolism. Proc Natl Acad Sci USA. 2013; 110: 14807-12

[49]

Zhang Y, Zhao L, Zhao J. et al. S5H/DMR6 encodes a salicylic acid 5-hydroxylase that fine-tunes salicylic acid homeostasis. Plant Physiol. 2017; 175:1082-93

[50]

Uknes S, Mauch-Mani B, Moyer M. et al. Acquired resistance in Arabidopsis. Plant Cell. 1992; 4:645-56

[51]

Ali S, Ganai BA, Kamili AN. et al. Pathogenesis-related proteins and peptides as promising tools for engineering plants with multiple stress tolerance. Microbiol Res. 2018;212-213:29-37

[52]

Van Loon LC, Antoniw JF. Comparison of the effects of salicylic acid and ethephon with virus-induced hypersensitivity and acquired resistance in tobacco. Neth J Plant Pathol. 1982; 88: 237-56

[53]

Cao H, Bowling SA, Gordon AS. et al. Characterization of an Ara-bidopsis mutant that is nonresponsive to inducers of systemic acquired resistance. Plant Cell. 1994; 6:1583-92

[54]

Shah J, Tsui F, Klessig DF. Characterization of a salicylic acid-insensitive mutant (sai1)of Arabidopsis thaliana, identified in a selective screen utilizing the SA-inducible expression of the tms2 gene. Mol Plant-Microbe Interact. 1997; 10:69-78

[55]

Delaney TP, Friedrich L, Ryals JA. Arabidopsis signal trans-duction mutant defective in chemically and biologically induced disease resistance. Proc Natl Acad Sci USA. 1995; 92: 6602-6

[56]

Le Henanff G, Heitz T, Mestre P. et al. Characterization of Vitis vinifera NPR1 homologs involved in the regulation of pathogenesis-related gene expression. BMC Plant Biol. 2009; 9:54

[57]

Zhang X, Francis MI, Dawson WO. et al. Over-expression of the Arabidopsis NPR1 gene in citrus increases resistance to citrus canker. Eur J Plant Pathol. 2010; 128:91-100

[58]

Wang Z, Zhang W-H, Ma L-Y. et al. Overexpression of Brassica napus NPR1 enhances resistance to Sclerotinia sclerotiorum in oilseed rape. Physiol Mol Plant Pathol. 2020; 110:101460

[59]

Ali S, Mir ZA, Tyagi A. et al. Overexpression of NPR1 in Brassica juncea confers broad spectrum resistance to fungal pathogens. Front Plant Sci. 2017; 8:1-16

[60]

Robertson CJ, Zhang X, Gowda S. et al. Overexpression of the Arabidopsis NPR1 protein in citrus confers tolerance to Huan-glongbing. J Citrus Pathol. 2018; 5:1-8

[61]

Lin W-C, Lu C-F, Wu J-W. et al. Transgenic tomato plants expressing the Arabidopsis NPR1 gene display enhanced resis-tance to a spectrum of fungal and bacterial diseases. Transgenic Res. 2004; 13:567-81

[62]

Cao H, Li X, Dong X. Generation of broad-spectrum disease resistance by overexpression of an essential regulatory gene in systemic acquired resistance. Proc Natl Acad Sci USA. 1998; 95: 6531-36

[63]

Rochon A, Boyle P, Wignes T. et al. The coactivator function of Arabidopsis NPR1 requires the core of its BTB/POZ domain and the oxidation of C-terminal cysteines. Plant Cell. 2006; 18: 3670-85

[64]

Kumar S, Zavaliev R, Wu Q. et al. Structural basis of NPR1 in activating plant immunity. Nature. 2022; 605:561-6

[65]

Cao H, Glazebrook J, Clarke JD. et al. The Arabidopsis NPR1 gene that controls systemic acquired resistance encodes a novel protein containing ankyrin repeats. Cell. 1997; 88:57-63

[66]

Zhang Y, Fan W, Kinkema M. et al. Interaction of NPR1 with basic leucine zipper protein transcription factors that bind sequences required for salicylic acid induction of the PR-1 gene. Proc Natl Acad Sci USA. 1999; 96:6523-8

[67]

Zhou J-M, Trifa Y, Silva H. et al. 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. Mol Plant-Microbe Interact. 2000; 13:191-202

[68]

Zhang Y, Tessaro MJ, Lassner M. et al. Knockout analysis of Arabidopsis transcription factors TGA2, TGA5,and TGA6 reveals their redundant and essential roles in systemic acquired resis-tance. Plant Cell. 2003; 15:2647-53

[69]

Johnson C, Boden E, Arias J. Salicylic acid and NPR1 induce the recruitment of trans-activating TGA factors to a defense gene promoter in Arabidopsis. Plant Cell. 2003; 15:1846-58

[70]

Fu ZQ, Yan S, Saleh A. et al. NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants. Nature. 2012; 486: 228-32

[71]

Ding Y, Sun T, Ao K. et al. Opposite roles of salicylic acid receptors NPR1 and NPR3/NPR4 in transcriptional regulation of plant immunity. Cell. 2018; 173:1454-67.e15

[72]

Zhang Y, Cheng YT, Qu N. et al. Negative regulation of defense responses in Arabidopsis by two NPR1 paralogs. Plant J. 2006; 48: 647-56

[73]

Liu Y, Sun T, Sun Y. et al. Diverse roles of the salicylic acid receptors NPR1 and NPR3/NPR4 in plant immunity. Plant Cell. 2020; 32:4002-16

[74]

Delaney TP, Uknes S, Vernooij B. et al. A central role of salicylic acid in plant disease resistance. Science. 1994; 266: 1247-50

[75]

Vernooij B, Reist LFM, KolditzJawhar R. et al. Salicylic acid is not the translocated signal responsible for inducing systemic acquired resistance but is required in signal transduction. Plant Cell. 1994; 6:959-65

[76]

Gaffney T, Friedrich L, Vernooij B. et al. Requirement of salicylic acid for the induction of systemic acquired resistance. Science. 1993; 261:754-6

[77]

Bartsch M, Bednarek P, Vivancos PD. et al. Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-beta-d-xyloside in Arabidopsis resistance to pathogens and ageing of leaves. JBiolChem. 2010; 285:25654-65

[78]

Silverman P, Seskar M, Kanter D. et al. Salicylic acid in rice (biosynthesis, conjugation, and possible role). Plant Physiol. 1995; 108:633-9

[79]

Yang Y, Qi M, Mei C. Endogenous salicylic acid protects rice plants from oxidative damage caused by aging as well as biotic and abiotic stress. Plant J. 2004; 40:909-19

[80]

Yuan Y, Zhong S, Li Q. et al. Functional analysis of rice NPR1-like genes reveals that OsNPR1/NH1 is the rice orthologue confer-ring disease resistance with enhanced herbivore susceptibility. Plant Biotechnol J. 2007; 5:313-24

[81]

Chern M-S, Fitzgerald HA, Yadav RC. et al. Evidence for a disease-resistance pathway in rice similar to the NPR1-mediated signaling pathway in Arabidopsis. Plant J. 2001; 27: 101-13

[82]

Qi P-F, Balcerzak M, Rocheleau H. et al. Jasmonic acid and abscisic acid play important roles in host-pathogen interaction between Fusarium graminearum and wheat during the early stages of fusarium head blight. Physiol Mol Plant Pathol. 2016; 93: 39-48

[83]

Qi P-F, Zhang Y-Z, Liu C-H. et al. Functional analysis of FgNahG clarifies the contribution of salicylic acid to wheat (Triticum aestivum) resistance against Fusarium head blight. Toxins. 2019; 11:59

[84]

Ngou BPM, Jones JDG, Ding P. Plant immune networks. Trends Plant Sci. 2022; 27:255-73

[85]

Tsuda K, Sato M, Glazebrook J. et al. Interplay between MAMP-triggered and SA-mediated defense responses. Plant J. 2008; 53: 763-75

[86]

Yi SY, Shirasu K, Moon JS. et al. The activated SA and JA signal-ing pathways have an influence on flg22-triggered oxidative burst and callose deposition. PLoS One. 2014; 9:e88951

[87]

Tateda C, Zhang Z, Shrestha J. et al. Salicylic acid regulates Ara-bidopsis microbial pattern receptor kinase levels and signaling. Plant Cell. 2014; 26:4171-87

[88]

Lukan T, Pompe-Novak M, Baebler Š. et al. Precision transcrip-tomics of viral foci reveals the spatial regulation of immune-signaling genes and identifies RBOHD as an important player in the incompatible interaction between potato virus Y and potato. Plant J. 2020; 104:645-61

[89]

Wu D, Tian H, Xu F. et al. The prodomain of Arabidopsis metacaspase 2 positively regulates immune signaling medi-ated by pattern-recognition receptors. New Phytol. 2024; 241: 430-43

[90]

Betsuyaku S, Katou S, Takebayashi Y. et al. Salicylic acid and jasmonic acid pathways are activated in spatially different domains around the infection site during effector-triggered immunity in Arabidopsis thaliana. Plant Cell Physiol. 2018; 59: 8-16

[91]

Radojičić A, Li X, Zhang Y. Salicylic acid: a double-edged sword for programed cell death in plants. Front Plant Sci. 2018; 9:1133

[92]

Nawrath C, Métraux J-P. Salicylic acid induction-deficient mutants of Arabidopsis express PR-2 and PR-5 and accumulate high levels of camalexin after pathogen inoculation. Plant Cell. 1999; 11:1393-404

[93]

Dewdney J, Reuber TL, Wildermuth MC. et al. Three unique mutants of Arabidopsis identify eds loci required for limiting growth of a biotrophic fungal pathogen. Plant J. 2000; 24:205-18

[94]

Devadas SK, Raina R. Preexisting systemic acquired resistance suppresses hypersensitive response-associated cell death in Arabidopsis hrl1 mutant. Plant Physiol. 2002; 128:1234-44

[95]

Feys BJ. Direct interaction between the Arabidopsis disease resistance signaling proteins, EDS1 and PAD4. EMBO J. 2001; 20: 5400-11

[96]

Lapin D, Bhandari DD, Parker JE. Origins and immunity net-working functions of EDS1 family proteins. Annu Rev Phy-topathol. 2020; 58:253-76

[97]

Jirage D, Tootle TL, Reuber TL. et al. Arabidopsis thaliana PAD4 encodes a lipase-like gene that is important for salicylic acid signaling. Proc Natl Acad Sci USA. 1999; 96:13583-8

[98]

Parker JE, Holub EB, Frost LN. et al.Characterization of eds1,a mutation in Arabidopsis suppressing resistance to Peronospora parasitica specified by several different RPP genes. Plant Cell. 1996; 8:2033-46

[99]

Aarts N, Metz M, Holub E. et al. Different requirements for EDS1 and NDR1 by disease resistance genes define at least two R gene-mediated signaling pathways in Arabidopsis. Proc Natl Acad Sci USA. 1998; 95:10306-11

[100]

Yang J, Xiong C, Li S. et al. Evolution patterns of NBS genes in the genus Dendrobium and NBS-LRR gene expression in D. officinale by salicylic acid treatment. BMC Plant Biol. 2022; 22:529

[101]

Yamamoto S, Katagiri M, Maeno H. et al. Salicylate hydroxylase, a monooxygenase requiring flavin adenine dinucleotide. JBiol Chem. 1965; 240:3408-13

[102]

Hartmann M, Zeier T, Bernsdorff F. et al. Flavin monooxygenase-generated N-hydroxypipecolic acid is a critical element of plant systemic immunity. Cell. 2018; 173:456-69.e16

[103]

Yildiz I, Mantz M, Hartmann M. et al. The mobile SAR sig-nal N-hydroxypipecolic acid induces NPR1-dependent tran-scriptional reprogramming and immune priming. Plant Physiol. 2021; 186:1679-705

[104]

Chen Y-C, Holmes EC, Rajniak J. et al. N-hydroxy-pipecolic acid is a mobile metabolite that induces systemic disease resistance in Arabidopsis. Proc Natl Acad Sci USA. 2018;115:E4920-29

[105]

Hartmann M, Zeier J. N-hydroxypipecolic acid and salicylic acid: a metabolic duo for systemic acquired resistance. Curr Opin Plant Biol. 2019; 50:44-57

[106]

Sun T, Huang J, Xu Y. et al. Redundant CAMTA transcription factors negatively regulate the biosynthesis of salicylic acid and N-hydroxypipecolic acid by modulating the expression of SARD1 and CBP60g. Mol Plant. 2020; 13:144-56

[107]

Wasternack C, Hause B. Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Ann Bot. 2013; 111:1021-58

[108]

Li M, Yu G, Cao C. et al. Metabolism, signaling, and transport of jasmonates. Plant Communs. 2021; 2:100231

[109]

Wasternack C, Song SS. Jasmonates: biosynthesis, metabolism, and signaling by proteins activating and repressing transcrip-tion. JExp Bot. 2017; 68:1303-21

[110]

Ellinger D, Stingl N, Kubigsteltig II. et al. DONGLE and DEFEC-TIVE IN ANTHER DEHISCENCE1 lipases are not essential for wound-and pathogen-induced jasmonate biosynthesis: redun-dant lipases contribute to jasmonate formation. Plant Physiol. 2010; 153:114-27

[111]

Hyun Y, Choi S, Hwang H-J. et al. Cooperation and functional diversification of two closely related galactolipase genes for jasmonate biosynthesis. Dev Cell. 2008; 14:183-92

[112]

Ryu SB. Phospholipid-derived signaling mediated by phospho-lipase A in plants. Trends Plant Sci. 2004; 9:229-35

[113]

Ishiguro S, Kawai-Oda A, Ueda J. et al. The DEFECTIVE IN ANTHER DEHISCIENCE gene encodes a novel phospholipase A1 catalyzing the initial step of jasmonic acid biosynthesis, which synchronizes pollen maturation, anther dehiscence, and flower opening in Arabidopsis. Plant Cell. 2001; 13:2191-209

[114]

Bannenberg G, Martínez M, Hamberg M. et al. Diversity of the enzymatic activity in the lipoxygenase gene family of Arabidop-sis thaliana. Lipids. 2009; 44:85-95

[115]

Ziegler J, Hamberg M, Miersch O. et al. Purification and char-acterization of allene oxide cyclase from dry corn seeds. Plant Physiol. 1997; 114:565-73

[116]

Howe GA, Lee GI, Itoh A. et al. Cytochrome P450-dependent metabolism of oxylipins in tomato. Cloning and expression of allene oxide synthase and fatty acid hydroperoxide lyase. Plant Physiol. 2000; 123:711-24

[117]

Ziegler J, Stenzel I, Hause B. et al. Molecular cloning of allene oxide cyclase: the enzyme establishing the stereochemistry of octadecanoids and jasmonates. JBiolChem. 2000; 275:19132-8

[118]

Stenzel I, Hause B, Miersch O. et al. Jasmonate biosynthesis and the allene oxide cyclase family of Arabidopsis thaliana. Plant Mol Biol. 2003; 51:895-911

[119]

Laudert D, Pfannschmidt U, Lottspeich F. et al. Cloning, molec-ular and functional characterization of Arabidopsis thaliana allene oxide synthase (CYP74), the first enzyme of the octadecanoid pathway to jasmonates. Plant Mol Biol. 1996; 31: 323-35

[120]

Park J-H, Halitschke R, Kim HB. et al. A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis. Plant J. 2002; 31:1-12

[121]

Stintzi A, Browse J. The Arabidopsis male-sterile mutant, opr3, lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis. Proc Natl Acad Sci USA. 2000; 97: 10625-30

[122]

Schaller F, Biesgen C, Müssig C. et al. 12-Oxophytodienoate reductase 3 (OPR3) is the isoenzyme involved in jasmonate biosynthesis. Planta. 2000; 210:979-84

[123]

Koo AJK, Chung HS, Kobayashi Y. et al. Identification of a per-oxisomal acyl-activating enzyme involved in the biosynthesis of jasmonic acid in Arabidopsis. JBiolChem. 2006; 281:33511-20

[124]

Chini A, Monte I, Zamarreño AM. et al. An OPR3-independent pathway uses 4,5-didehydrojasmonate for jasmonate synthe-sis. Nat Chem Biol. 2018; 14:171-8

[125]

Wasternack C, Hause B. A bypass in jasmonate biosynthe-sis—the OPR3-independent formation. Trends Plant Sci. 2018; 23: 276-9

[126]

Fu W, Jin G, Jiménez-Alemán GH. et al. The jasmonic acid-amino acid conjugates JA-Val and JA-Leu are involved in rice resistance to herbivores. Plant Cell Environ. 2022; 45:262-72

[127]

Yan J, Li S, Gu M. et al. Endogenous bioactive jasmonate is composed of a set of (+)-7-iso-JA-amino acid conjugates. Plant Physiol. 2016; 172:2154-64

[128]

Heitz T, Widemann E, Lugan R. et al. Cytochromes P450 CYP94C1 and CYP94B3 catalyze two successive oxidation steps of plant hormone jasmonoyl-isoleucine for catabolic turnover. JBiolChem. 2012; 287:6296-306

[129]

Koo AJ, Thireault C, Zemelis S. et al. Endoplasmic reticulum-associated inactivation of the hormone jasmonoyl-l-isoleucine by multiple members of the cytochrome P450 94 family in Arabidopsis. JBiolChem. 2014; 289:29728-38

[130]

Bruckhoff V, Haroth S, Feussner K. et al. Functional characteri-zation of CYP94-genes and identification of a novel jasmonate catabolite in flowers. PLoS One. 2016; 11:e0159875

[131]

Woldemariam MG, Onkokesung N, Baldwin IT. et al. Jasmonoyl-l-isoleucine hydrolase 1 (JIH1) regulates jasmonoyl-l-isoleucine levels and attenuates plant defenses against herbivores. Plant J. 2012; 72:758-67

[132]

Widemann E, Miesch L, Lugan R. et al. The amidohydrolases IAR3 and ILL6 contribute to jasmonoyl-isoleucine hormone turnover and generate 12-hydroxyjasmonic acid upon wound-ing in Arabidopsis leaves∗. JBiolChem. 2013; 288:31701-14

[133]

Smirnova E, Marquis V, Poirier L. et al. Jasmonic acid oxidase 2 hydroxylates jasmonic acid and represses basal defense and resistance responses against Botrytis cinerea infection. Mol Plant. 2017; 10:1159-73

[134]

Seo HS, Song JT, Cheong J-J. et al. Jasmonic acid carboxyl methyltransferase: a key enzyme for jasmonate-regulated plant responses. Proc Natl Acad Sci USA. 2001; 98:4788-93

[135]

Staswick PE, Tiryaki I, Rowe ML. Jasmonate response locus JAR1 and several related Arabidopsis genes encode enzymes of the firefly luciferase superfamily that show activity on jasmonic, salicylic, and indole-3-acetic acids in an assay for adenylation. Plant Cell. 2002; 14:1405-15

[136]

Staswick PE, Tiryaki I. The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell. 2004; 16:2117-27

[137]

Fonseca S, Chini A, Hamberg M. et al. (+)-7-iso-Jasmonoyl-l-isoleucine is the endogenous bioactive jasmonate. Nat Chem Biol. 2009; 5:344-50

[138]

Yan J, Zhang C, Gu M. et al. The Arabidopsis CORONATINE INSENSITIVE1 protein is a jasmonate receptor. Plant Cell. 2009; 21:2220-36

[139]

Pauwels L, Goossens A. The JAZ proteins: a crucial interface in the jasmonate signaling cascade. Plant Cell. 2011; 23:3089-100

[140]

Thines B, Katsir L, Melotto M. et al. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nature. 2007; 448:661-5

[141]

Chini A, Fonseca S, Fernández G. et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature. 2007; 448:666-71

[142]

Yan Y, Stolz S, Chételat A. et al. A downstream mediator in the growth repression limb of the jasmonate pathway. Plant Cell. 2007; 19:2470-83

[143]

Guo Q, Yoshida Y, Major IT. et al. JAZ repressors of metabolic defense promote growth and reproductive fitness in Arabidop-sis. Proc Natl Acad Sci USA. 2018;115:E10768-77

[144]

Campos ML, Yoshida Y, Major IT. et al. Rewiring of jasmonate and phytochrome B signalling uncouples plant growth-defense tradeoffs. Nat Commun. 2016; 7:12570

[145]

Pauwels L, Barbero GF, Geerinck J. et al. NINJA connects the co-repressor TOPLESS to jasmonate signalling. Nature. 2010; 464: 788-91

[146]

Zhang F, Yao J, Ke J. et al. Structural basis of JAZ repression of MYC transcription factors in jasmonate signalling. Nature. 2015; 525:269-73

[147]

Feys B, Benedetti CE, Penfold CN. et al.Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male sterile, insensitive to methyl jasmonate, and resistant to a bacterial pathogen. Plant Cell. 1994; 6:751-9

[148]

Xu L, Liu F, Lechner E. et al. The SCFCOI1 ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis. Plant Cell. 2002; 14:1919-35

[149]

Zheng X-y, Spivey NW, Zeng W. et al. Coronatine promotes Pseudomonas syringae virulence in plants by activating a signal-ing cascade that inhibits salicylic acid accumulation. Cell Host Microbe. 2012; 11:587-96

[150]

Devoto A, Nieto-Rostro M, Xie D. et al. COI1 links jasmonate signalling and fertility to the SCF ubiquitin-ligase complex in Arabidopsis. Plant J. 2002; 32:457-66

[151]

Lorenzo O, Chico JM, Sánchez-Serrano JJ. et al. JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis. Plant Cell. 2004; 16:1938-50

[152]

Dombrecht B, Xue GP, Sprague SJ. et al. MYC2 differentially modulates diverse jasmonate-dependent functions in Ara-bidopsis. Plant Cell. 2007; 19:2225-45

[153]

Fernández-Calvo P, Chini A, Fernández-Barbero G. et al. The Arabidopsis bHLH transcription factors MYC3 and MYC4 are targets of JAZ repressors and act additively with MYC2 in the activation of jasmonate responses. Plant Cell. 2011; 23: 701-15

[154]

Cheng Z, Sun L, Qi T. et al. The bHLH transcription factor MYC3 interacts with the jasmonate ZIM-domain proteins to mediate jasmonate response in Arabidopsis. Mol Plant. 2011; 4:279-88

[155]

Niu Y, Figueroa P, Browse J. Characterization of JAZ-interacting bHLH transcription factors that regulate jasmonate responses in Arabidopsis. JExp Bot. 2011; 62:2143-54

[156]

Çevik V, Kidd BN, Zhang P. et al. MEDIATOR25 acts as an inte-grative hub for the regulation of jasmonate-responsive gene expression in Arabidopsis. Plant Physiol. 2012; 160:541-55

[157]

Chen R, Jiang H, Li L. et al. The Arabidopsis mediator subunit MED25 differentially regulates jasmonate and abscisic acid signaling through interacting with the MYC2 and ABI5 tran-scription factors. Plant Cell. 2012; 24:2898-916

[158]

Thomma BPHJ, Eggermont K, Broekaert WF. et al. Disease development of several fungi on Arabidopsis can be reduced by treatment with methyl jasmonate. Plant Physiol Biochem. 2000; 38:421-7

[159]

Fujimoto T, Tomitaka Y, Abe H. et al. Expression profile of jas-monic acid-induced genes and the induced resistance against the root-knot nematode (Meloidogyne incognita) in tomato plants (Solanum lycopersicum) after foliar treatment with methyl jas-monate. J Plant Physiol. 2011; 168:1084-97

[160]

Zhu Z, Tian S. Resistant responses of tomato fruit treated with exogenous methyl jasmonate to Botrytis cinerea infection. Sci Hortic. 2012; 142:38-43

[161]

Sun Y, Xiao J, Jia X. et al. The role of wheat jasmonic acid and ethylene pathways in response to Fusarium graminearum infection. Plant Growth Regul. 2016; 80:69-77

[162]

Ameye M, Audenaert K, De Zutter N. et al. Priming of wheat with the green leaf volatile Z-3-hexenyl acetate enhances defense against Fusarium graminearum but boosts deoxynivalenol pro-duction. Plant Physiol. 2015; 167:1671-84

[163]

Duan Z, Lv G, Shen C. et al. The role of jasmonic acid signalling in wheat (Triticum aestivum L.) powdery mildew resistance reac-tion. Eur J Plant Pathol. 2014; 140:169-83

[164]

Doostkam M, Sohrabi F, Modarresi M. et al. Genetic variation of cucumber (Cucumis sativus L.) cultivars to exogenously applied jasmonic acid to induce resistance to Liriomyza sativae. Arthro-pod Plant Interact. 2023; 17:289-99

[165]

Nahar K, Kyndt T, De Vleesschauwer D. et al. The jasmonate pathway is a key player in systemically induced defense against root knot nematodes in rice. Plant Physiol. 2011; 157:305-16

[166]

Cooper WR, Jia L, Goggin L. Effects of jasmonate-induced defenses on root-knot nematode infection of resistant and susceptible tomato cultivars. JChemEcol. 2005; 31:1953-67

[167]

Hu YF, You J, Li CJH. et al. Exogenous application of methyl jasmonate induces defence against in soybean. Nematology. 2017; 19:293-304

[168]

Soriano IR, Asenstorfer RE, Schmidt O. et al. Inducible flavone in oats (Avena sativa) is a novel defense against plant-parasitic nematodes. Phytopathology. 2004; 94:1207-14

[169]

Wang J, Wu D, Wang Y. et al. Jasmonate action in plant defense against insects. JExp Bot. 2019; 70:3391-400

[170]

Kessler A, Halitschke R, Baldwin IT. Silencing the jasmonate cascade: induced plant defenses and insect populations. Sci-ence. 2004; 305:668-68

[171]

Aubert Y, Widemann E, Miesch L. et al. CYP94-mediated jasmonoyl-isoleucine hormone oxidation shapes jasmonate profiles and attenuates defence responses to Botrytis cinerea infection. JExp Bot. 2015; 66:3879-92

[172]

Halitschke R, Baldwin IT. Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuata. Plant J. 2003; 36:794-807

[173]

Paschold A, Halitschke R, Baldwin IT. Co(i)-ordinating defenses: NaCOI1 mediates herbivore-induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoid-ing defenses. Plant J. 2007; 51:79-91

[174]

Chehab EW, Kim S, Savchenko T. et al. Intronic T-DNA insertion renders Arabidopsis opr3 a conditional jasmonic acid-producing mutant. Plant Physiol. 2011; 156:770-8

[175]

Schilmiller AL, Koo AJK, Howe GA. Functional diversification of acyl-coenzyme A oxidases in jasmonic acid biosynthesis and action. Plant Physiol. 2007; 143:812-24

[176]

Staswick PE, Su W, Howell SH. Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant. Proc Natl Acad Sci USA. 1992; 89: 6837-40

[177]

Zhang M, Li W, Zhang T. et al. Botrytis cinerea-induced F-box protein 1 enhances disease resistance by inhibiting JAO/JOX-mediated jasmonic acid catabolism in Arabidopsis. Mol Plant. 2024; 17:297-311

[178]

Penninckx IA, Eggermont K, Terras FR. et al. Pathogen-induced systemic activation of a plant defensin gene in Arabidopsis follows a salicylic acid-independent pathway. Plant Cell. 1996; 8: 2309-23

[179]

Lin C, Lan C, Li X. et al. A pair of nuclear factor Y transcription factors act as positive regulators in jasmonate signaling and disease resistance in Arabidopsis. J Integr Plant Biol. 2024; 66: 2042-57

[180]

Li C, Liu G, Xu C. et al. The tomato suppressor of prosystemin-mediated responses 2 gene encodes a fatty acid desaturase required for the biosynthesis of jasmonic acid and the produc-tion of a systemic wound signal for defense gene expression. Plant Cell. 2003; 15:1646-61

[181]

El Oirdi M, El Rahman TA, Rigano L. et al. Botrytis cinerea manip-ulates the antagonistic effects between immune pathways to promote disease development in tomato. Plant Cell. 2011; 23: 2405-21

[182]

Fan J, Hu C, Zhang L. et al. Jasmonic acid mediates tomato’s response to root knot nematodes. J Plant Growth Regul. 2015; 34: 196-205

[183]

Thaler JS, Owen B, Higgins VJ. The role of the jasmonate response in plant susceptibility to diverse pathogens with a range of lifestyles. Plant Physiol. 2004; 135:530-8

[184]

AbuQamar S, Chai MF, Luo HL. et al. Tomato protein kinase 1b mediates signaling of plant responses to necrotrophic fungi and insect herbivory. Plant Cell. 2008; 20:1964-83

[185]

Campos ML, Kang J-H, Howe GA. Jasmonate-triggered plant immunity. JChemEcol. 2014; 40:657-75

[186]

Riemann M, Haga K, Shimizu T. et al. Identification of rice allene oxide cyclase mutants and the function of jasmonate for defence against. Plant J. 2013; 74:226-38

[187]

Yan Y, Christensen S, Isakeit T. et al. Disruption of OPR7 and OPR8 reveals the versatile functions of jasmonic acid in maize development and defense. Plant Cell. 2012; 24:1420-36

[188]

Huang SJ, Wang CH, Wang L. et al. Loss-of-function of activates the jasmonate pathway and promotes maize resistance to corn leaf aphids. Plant Biotechnol J. 2024; 22:3326-41

[189]

Pré M, Atallah M, Champion A. et al. The AP2/ERF domain transcription factor ORA59 integrates jasmonic acid and ethylene signals in plant defense. Plant Physiol. 2008; 147: 1347-57

[190]

Lorenzo O, Piqueras R, Sánchez-Serrano JJ. et al. ETHYLENE RESPONSE FACTOR1 integrates signals from ethylene and jasmonate pathways in plant defense. Plant Cell. 2003; 15 165-78

[191]

Chen C-Y, Liu Y-Q, Song W-M. et al. An effector from cotton bollworm oral secretion impairs host plant defense signaling. Proc Natl Acad Sci USA. 2019; 116:14331-8

[192]

Chen X, Liu Y-Q, Wu M-N. et al. A highly accumulated secre-tory protein from cotton bollworm interacts with basic helix-loop-helix transcription factors to dampen plant defense. New Phytol. 2023; 237:265-78

[193]

Patkar RN, Benke PI, Qu Z. et al. A fungal monooxygenase-derived jasmonate attenuates host innate immunity. Nat Chem Biol. 2015; 11:733-40

[194]

Pieterse CMJ, Zamioudis C, Berendsen RL. et al. Induced sys-temic resistance by beneficial microbes. Annu Rev Phytopathol. 2014; 52:347-75

[195]

Pieterse CM, van Wees SC, van Pelt JA. et al. A novel signaling pathway controlling induced systemic resistance in Arabidop-sis. Plant Cell. 1998; 10:1571-80

[196]

Pozo MJ, Van Der Ent S, Van Loon LC. et al. Transcription factor MYC2 is involved in priming for enhanced defense during rhizobacteria-induced systemic resistance in Arabidop-sis thaliana. New Phytol. 2008; 180:511-23

[197]

Li L, Li C, Lee GI. et al. Distinct roles for jasmonate synthesis and action in the systemic wound response of tomato. Proc Natl Acad Sci USA. 2002; 99:6416-21

[198]

Li M, Wang F, Li S. et al. Importers drive leaf-to-leaf jasmonic acid transmission in wound-induced systemic immunity. Mol Plant. 2020; 13:1485-98

[199]

Jung SC, Martinez-Medina A, Lopez-Raez JA. et al. Mycorrhiza-induced resistance and priming of plant defenses. JChemEcol. 2012; 38:651-64

[200]

Cameron DD, Neal AL, van Wees SCM. et al. Mycorrhiza-induced resistance: more than the sum of its parts? Trends Plant Sci. 2013; 18:539-45

[201]

Yan C, Xie D. Jasmonate in plant defence: sentinel or double agent? Plant Biotechnol J. 2015; 13:1233-40

[202]

Penacortes H, Albrecht T, Prat S. et al. Aspirin prevents wound-induced gene expression in tomato leaves by blocking jasmonic acid biosynthesis. Planta. 1993; 191:123-8

[203]

Monte I. Jasmonates and salicylic acid: evolution of defense hormones in land plants. Curr Opin Plant Biol. 2023; 76:102470

[204]

Doherty HM, Selvendran RR, Bowles DJ. The wound response of tomato plants can be inhibited by aspirin and related hydroxy-benzoic acids. Physiol Mol Plant Pathol. 1988; 33:377-84

[205]

Spoel SH, Koornneef A, Claessens SMC. et al. NPR1 modu-lates cross-talk between salicylate-and jasmonate-dependent defense pathways through a novel function in the cytosol. Plant Cell. 2003; 15:760-70

[206]

Costarelli A, Bianchet C, Ederli L. et al. Salicylic acid induced by herbivore feeding antagonizes jasmonic acid mediated plant defenses against insect attack. Plant Signal Behav. 2020; 15:1704517

[207]

Yuan H-M, Liu W-C, Lu Y-T. CATALASE 2 coordinates SA-mediated repression of both auxin accumulation and ja biosynthesis in plant defenses. Cell Host Microbe. 2017; 21: 143-55

[208]

Gordy JW, Leonard BR, Blouin D. et al. Comparative effective-ness of potential elicitors of plant resistance against Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae) in four crop plants. PLoS One. 2015; 10:e0136689

[209]

Spoel SH, Johnson JS, Dong X. Regulation of tradeoffs between plant defenses against pathogens with different lifestyles. Proc Natl Acad Sci USA. 2007; 104:18842-7

[210]

Luna E, Bruce TJA, Roberts MR. et al. Next-generation systemic acquired resistance. Plant Physiol. 2012; 158:844-53

[211]

Nomoto M, Skelly MJ, Itaya T. et al. Suppression of MYC tran-scription activators by the immune cofactor NPR1 fine-tunes plant immune responses. Cell Rep. 2021; 37:110125

[212]

Li R, Wang L, Li Y. et al. Knockout of SlNPR1 enhances tomato plants resistance against Botrytis cinerea by modulating ROS homeostasis and JA/ET signaling pathways. Physiol Plant. 2020; 170:569-79

[213]

Leon-Reyes A, Spoel SH, De Lange ES. et al. Ethylene modu-lates the role of NONEXPRESSOR OF PATHOGENESIS-RELATED GENES1 in cross talk between salicylate and jasmonate signal-ing. Plant Physiol. 2009; 149:1797-809

[214]

Zander M, La Camera S, Lamotte O. et al. 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. Plant J. 2009; 61: 200-10

[215]

Ndamukong I, Abdallat AA, Thurow C. et al. SA-inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA-responsive PDF1.2 transcription. Plant J. 2007; 50: 128-39

[216]

Zander M, Chen S, Imkampe J. et al. Repression of the Arabidop-sis thaliana jasmonic acid/ethylene-induced defense pathway by TGA-interacting glutaredoxins depends on their C-terminal ALWL motif. Mol Plant. 2012; 5:831-40

[217]

Zander M, Thurow C, Gatz C. Characterization of a salicylic acid-insensitive mutant (sai1)of Arabidopsis thaliana, identified in a selective screen utilizing the SA-inducible expression of the tms2 gene. Plant Physiol. 2014; 165:1671-83

[218]

Li J, Brader G, Palva ET. The WRKY70 transcription factor: a node of convergence for jasmonate-mediated and salicylate-mediated signals in plant defense. Plant Cell. 2004; 16:319-31

[219]

Li J, Brader G, Kariola T. et al. WRKY70 modulates the selection of signaling pathways in plant defense. Plant J. 2006; 46:477-91

[220]

Zhou M, Lu Y, Bethke G. et al. WRKY70 prevents axenic acti-vation of plant immunity by direct repression of SARD1. New Phytol. 2018; 217:700-12

[221]

Wang D, Amornsiripanitch N, Dong X. A genomic approach to identify regulatory nodes in the transcriptional network of systemic acquired resistance in plants. PLoS Path. 2006; 2:e123

[222]

Laurie-Berry N, Joardar V, Street IH. et al. The Arabidopsis thaliana JASMONATE INSENSITIVE 1 gene is required for sup-pression of salicylic acid-dependent defenses during infec-tion by Pseudomonas syringae. Mol Plant-Microbe Interact. 2006; 19: 789-800

[223]

Kloek AP, Verbsky ML, Sharma SB. et al. Resistance to Pseudomonas syringae conferred by an Arabidopsis thaliana coronatine-insensitive (coi1) mutation occurs through two dis-tinct mechanisms. Plant J. 2001; 26:509-22

[224]

Gimenez-Ibanez S, Zamarreño AM, García-Mina JM. et al. An evolutionarily ancient immune system governs the interac-tions between Pseudomonas syringae and an early-diverging land plant lineage. Curr Biol. 2019; 29:2270-81.e4

[225]

Melotto M, Mecey C, Niu Y. et al. 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. Plant J. 2008; 55:979-88

[226]

Bu Q, Jiang H, Li C-B. et al. Role of the Arabidopsis thaliana NAC transcription factors ANAC019 and ANAC055 in regulating jasmonic acid-signaled defense responses. Cell Res. 2008; 18: 756-67

[227]

Du M, Zhai Q, Deng L. et al. Closely related NAC transcrip-tion factors of tomato differentially regulate stomatal closure and reopening during pathogen attack. Plant Cell. 2014; 26: 3167-84

[228]

Chung SH, Rosa C, Scully ED. et al. Herbivore exploits orally secreted bacteria to suppress plant defenses. Proc Natl Acad Sci USA. 2013; 110:15728-33

[229]

Zhao J, Liu Y, Xu S. et al. Mealybug salivary microbes inhibit induced plant defenses. Pest Manag Sci. 2023; 79:4034-47

[230]

Diezel C, von Dahl CC, Gaquerel E. et al. Different lepidopteran elicitors account for cross-talk in herbivory-induced phytohor-mone signaling. Plant Physiol. 2009; 150:1576-86

[231]

MurLAJ, KentonP, AtzornR. et al. The outcomes of concentration-specific interactions between salicylate and jas-monate signaling include synergy, antagonism, and oxidative stress leading to cell death. Plant Physiol. 2006; 140:249-62

[232]

Zhang N, Zhou S, Yang D. et al. Revealing shared and distinct genes responding to JA and SA signaling in Arabidopsis by meta-analysis. Front Plant Sci. 2020; 11:908

[233]

Tsuda K, Sato M, Stoddard T. et al. Network properties of robust immunity in plants. PLoS Genet. 2009; 5:e1000772

[234]

Ullah C, Tsai C-J, Unsicker SB. et al. Salicylic acid activates poplar defense against the biotrophic rust fungus Melampsora larici-populina via increased biosynthesis of catechin and proan-thocyanidins. New Phytol. 2019; 221:960-75

[235]

Ullah C, Schmidt A, Reichelt M. et al. Lack of antagonism between salicylic acid and jasmonate signalling pathways in poplar. New Phytol. 2022; 235:701-17

[236]

Tamaoki D, Seo S, Yamada S. et al. Jasmonic acid and salicylic acid activate a common defense system in rice. Plant Signal Behav. 2013; 8:e24260

[237]

Garg R, Tyagi AK, Jain M. Microarray analysis reveals overlap-ping and specific transcriptional responses to different plant hormones in rice. Plant Signal Behav. 2012; 7:951-56

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