Abstract
Key message
Recent updates in JA biosynthesis, signaling pathways and the crosstalk between JA and others phytohormones in relation with plant responses to different stresses.
Abstract
In plants, the roles of phytohormone jasmonic acid (JA), amino acid conjugate (e.g., JA-Ile) and their derivative emerged in last decades as crucial signaling compounds implicated in stress defense and development in plants. JA has raised a great interest, and the number of researches on JA has increased rapidly highlighting the importance of this phytohormone in plant life. First, JA was considered as a stress hormone implicated in plant response to biotic stress (pathogens and herbivores) which confers resistance to biotrophic and hemibiotrophic pathogens contrarily to salicylic acid (SA) which is implicated in plant response to necrotrophic pathogens. JA is also implicated in plant responses to abiotic stress (such as soil salinity, wounding and UV). Moreover, some researchers have recently revealed that JA controls several physiological processes like root growth, growth of reproductive organs and, finally, plant senescence. JA is also involved in the biosynthesis of various metabolites (e.g., phytoalexins and terpenoids). In plants, JA signaling pathways are well studied in few plants essentially Arabidopsis thaliana, Nicotiana benthamiana, and Oryza sativa L. confirming the crucial role of this hormone in plants. In this review, we highlight the last foundlings about JA biosynthesis, JA signaling pathways and its implication in plant maturation and response to environmental constraints.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
Agurla S, Gahir S, Munemasa S, Murata M, Raghavendra AS (2018) Mechanism of stomatal closure in plants exposed to drought and cold stress. Adv Exp Med Biol 1081:215–232. https://doi.org/10.1007/978-981-13-1244-1_12
Ahmad P, Rasool S, Gul A, Sheikh SA, Akram NA, Ashraf M, Kazi AM, Gucel S (2016) Jasmonates: multifunctional roles in stress tolerance. Front Plant Sci 7:813. https://doi.org/10.3389/fpls.2016.00813
Ahmad P, Alyemeni MN, Wijaya L, Alam P et al (2017) Jasmonic acid alleviates negative impacts of cadmium stress by modifying osmolytes and antioxidants in faba bean (Vicia faba L.). Arch Agron Soil Sci 63(13):1889–1899
Aleman F, Yazaki J, Lee M, Takahashi Y, Kim AY, Li Z, Kinoshita T, Ecker JR, Schroeder JI (2016) An ABA-increased interaction of the PYL6 ABA receptor with MYC2 transcription factor: a putative link of ABA and JA signaling. Sci Rep 6:28941. https://doi.org/10.1038/srep28941
Ali E, Hussain N, Shamsi IH, Jabeen Z, Siddiqui MH, Lx J (2018) Role of jasmonic acid in improving tolerance of rapeseed (Brassica napus L.), to Cd toxicity. J Zhejiang Univ Sci B 19:130–146. https://doi.org/10.1631/jzus.B1700191
Alkhatib R, Maruthavanan J, Ghoshroy S, Steiner R, Sterling T, Creamer R (2012) Physiological and ultrastructural effects of lead on tobacco. Biol Plant 56:711–716. https://doi.org/10.1007/s10535-012-0241-9
Altaf-Ul-Amin M, Katsuragi T, Sato T, Kanaya S (2015) A glimpse to background and characteristics of major molecular biological networks. Biomed Res Int. https://doi.org/10.1155/2015/540297
Amoutzias GD, Robertson DL, Van de Peer Y, Oliver SG (2008) Choose your partners, dimerization in eukaryotic transcription factors. Trends Biochem Sci 33:220–229. https://doi.org/10.1016/j.tibs.2008.02.002
Argueso CT, Ferreira FJ, Kieber JJ (2009) Environmental perception avenues: The interaction of cytokinin and environmental response pathways. Plant Cell Environ 32:1147–1160. https://doi.org/10.1111/j.1365-3040.2009.01940.x
Avramova Z (2017) The jasmonic acid signaling and abscissic acid signaling pathways during one, but not repeated dehydratation stress: a nonspecific ‘paniky’ or a meaningful response? Plant Cell Env 40:1704–1710. https://doi.org/10.1111/pce.12967
Awan SA, Khan I, Rizwan M, Zhang X, Brestic M, Khan A, El-Sheikh MA, Alyemeni MN, Ali S, Huang L, Huang L (2020) Exogenous abscisic acid and jasmonic acid restrain polyethylene glycol-induced drought by improving the growth and antioxidative enzyme activities in pearl millet. Physiol Plant. https://doi.org/10.1111/ppl.13247
Ayala A, Muñoz MF, Argüelles S (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev. https://doi.org/10.1155/2014/360438
Azeem U (2018) Ameliorating Nickel stress by Jasmonic acid treatment in Zea mays L. Russ Agric Sci 44:209–215
Bali S, Kaur P, Sharma A, Ohri P, Bhardwaj R, Alyemeni MN et al (2017) Jasmonic acid-induced tolerance to root-knot nematodes in tomato plants through altered photosynthetic and antioxidative defense mechanisms. Protoplasma 255:471–484. https://doi.org/10.1007/s00709-017-1160-6
Bali S, Kaur P, Kohli SK, Ohri P, Thukral AK, Bhardwaj R, Wijaya L, Alyemeni MN, Ahmad P (2018) Jasmonic acid induced changes in physio-biochemical attributes and ascorbate-glutathione pathway in Lycopersicon esculentum under lead stress at different growth stages. Sci Total Environ 645:1344–1360. https://doi.org/10.1016/j.scitotenv.2018.07.164
Bali S, Jamwal VL, Kaur P, Kohli SK, Ohri P, Gandhi SG, Bardwaj R, Al-Huqail AA, Sidiqui MH, Ali HM, Ahmad P (2019a) Role of P-type ATPase metal transporters and plant immunity induced by jasmonic acid against Lead (Pb) toxicity in tomato. Ecotoxicol Environ Saf 174:283–294. https://doi.org/10.1016/j.ecoenv.2019.02.084
Bali S, Lakshmi V, Sukhmeen J, Kohli K, Kaur P, Tejpal R, Bhalla V, Gandhi SG, Bhardwi R, Al-Huqail AA, Sidiqui MH, Ali HM, Ahmad P (2019b) Jasmonic acid application triggers detoxification of lead (Pb) toxicity in tomato through the modifications of secondary metabolites and gene expression. Chemosphere. https://doi.org/10.1016/j.chemosphere.2019.06.188
Bargmann BOR, Laxalt AM, Ter Riet B, Testerink C, Merquiol E, Mosblech A, Leon-Reyes A, Pieterse CMJ, Haring MA, Heilmann I, Bartels D, Munnik T (2009) Reassessing the role of phospholipase D in the Arabidopsis wounding response. Plant Cell Environ 32:837–850. https://doi.org/10.1111/j.1365-3040.2009.01962.x
Bayram A, Tonga A (2018) cis-Jasmone treatments affect pests and beneficial insects of wheat (Triticum aestivum L.): the influence of doses and plant growth stages. Crop Prot 105:70–79. https://doi.org/10.1016/j.cropro.2017.11.011
Boter M, Golz JF, Giménez-Ibañez S, Fernandez-Barbero G, Franco-Zorrilla JM, Solano R (2015) FILAMENTOUS FLOWER is a direct target of JAZ3 and modulates responses to jasmonate. Plant Cell 27:3160–3174. https://doi.org/10.1105/tpc.15.00220
Branch C, Hwang CF, Navarre DA, Williamson VM (2004) Salicylic acid is part of the Mi-1-mediated defense response to root-knot nematode in tomato. Mol Plant Microbe Interact 17:351–356. https://doi.org/10.1094/MPMI.2004.17.4.351
Brioudes F, Joly C, Szécsi J, Varaud E, Leroux J, Bellvert F, Bertrand C, Bendahmane M (2009) Jasmonate controls late development stages of petal growth in Arabidopsis thaliana. Plant J 60:1070–1080. https://doi.org/10.1111/j.1365-313X.2009.04023.x
Browse J (2009) Jasmonate passes muster, a receptor and targets for the defense hormone. Annu Rev Plant Biol 60:183–205. https://doi.org/10.1146/annurev.arplant.043008.092007
Bruckhoff V, Haroth S, Feussner K, Konig S, Brodhun F, Feussner I (2016) Functional characterization of CYP94-genes and identification of a novel jasmonate catabolite in flowers. PLoS ONE 11(7):e0159875. https://doi.org/10.1371/journal.pone.0159875
Cai XT, Xu P, Zhao PX, Liu R, Yu LH, Xiang CB (2014) Arabidopsis ERF109 mediates crosstalk between jasmonic acid and auxin biosynthesis during lateral root formation. Nat Commun 5:5833. https://doi.org/10.1038/ncomms6833
Carretero-Paulet L, Galstyan A, Roig-Villanova I, MartínezGarcía JF, Bilbao-Castro JR, Robertson DL (2010) Genome-wide classification and evolutionary analysis of the bHLH family of transcription factors in Arabidopsis, poplar, rice, moss, and algae. Plant Physiol 153:1398–1412. https://doi.org/10.1104/pp.110.153593
Carvalho RF, Campos ML, Azevedo RA (2013) The role of phytochromes in stress tolerance. Salt stress plants. Springer, Berlin, pp 283–299. https://doi.org/10.1111/j.1744-7909.2011.01081.x
Chandler JW, Werr W (2015) Cytokinin–auxin crosstalk in cell type specification. Trends Plant Sci 20:291–300. https://doi.org/10.1016/j.tplants.2015.02.003
Chen Q, Sun J, Zhai Q, Zhou W, Qi L, Xu L, Wang B, Chen R, Jiang H, Qi J et al (2011) The basic helix-loop-helix transcription factor MYC2 directly represses PLETHORA expression during jasmonate-mediated modulation of the root stem cell niche in Arabidopsis. Plant Cell 23:3335–3352. https://doi.org/10.1105/tpc.111.089870
Chen R, Jiang H, Li L, Zhai Q, Qi L, Zhou W, Liu X, Li H, Zheng W, Sun J et al (2012) The Arabidopsis Mediator subunit MED25 differentially regulates jasmonate and abscisic acid signaling through interacting with the MYC2 and ABI5 transcription factors. Plant Cell 24:2898–2916. https://doi.org/10.1105/tpc.112.098277
Chen J, Sonobe K, Ogawa N, Masuda S, Nagatani A, Kobayashi Y, Ohta H (2013) Inhibition of Arabidopsis hypocotyl elongation by jasmonates is enhanced under red light in phytochrome B dependent manner. J Plant Res 126:161–168. https://doi.org/10.1007/s10265-012-0509-3
Chico JM, Fernández-Barbero G, Chini A, Fernández-Calvo P, Díez-Díaz M, Solano R (2014) Repression of jasmonate-dependent defenses by shade involves differential regulation of protein stability of MYC transcription factors and their JAZ repressors in Arabidopsis. Plant Cell 26:1967–1980. https://doi.org/10.1105/tpc.114.125047
Chini A, Fonseca S, Fernández G, Adie B, Chico JM, Lorenzo O, García-Casado G, López-Vidriero I, Lozano FM, Ponce MR et al (2007) The JAZ family of repressors is the missing link in jasmonate signaling. Nature 448:666–671. https://doi.org/10.1038/nature06006
Chini A, Boter M, Solano R (2009a) Plant oxylipins, COI1/ JAZs/MYC2 as the core jasmonic acid-signaling module. FEBS J 276:4682–4692. https://doi.org/10.1111/j.1742-4658.2009.07194.x
Chini A, Fonseca S, Chico JM, Fernández-Calvo P, Solano R (2009b) The ZIM domain mediates homo- and heteromeric interactions between Arabidopsis JAZ proteins. Plant J 59:77–87. https://doi.org/10.1111/j.1365-313X.2009.03852.x
Chini A, Gimenez-Ibanez S, Goossens A, Solano R (2016) Redundancy and specificity in jasmonate signaling. Curr Opin Plant Biol 33:147–156. https://doi.org/10.1016/j.pbi.2016.07.005
Chini A, Monte I, Zamarreno AM, Hamberg M, Lassueur S, Reymond P et al (2018) An OPR3-independent pathway uses 4,5-didehydrojasmonate for jasmonate synthesis. Nat Chem Biol 14:171. https://doi.org/10.1038/nchembio.2540
Choudhary SP, Yu JQ, Yamaguchi-Shinozaki K, Shinozaki K, Tran LS (2012) Benefits of brassinosteroid crosstalk. Trends Plant Sci 17:594–605. https://doi.org/10.1016/j.tplants.2012.05.012
Dabrowska P, Boland W (2007) iso-OPDA: An Early Precursor of cis-Jasmone in Plants? ChemBioChem 8:2281–2285. https://doi.org/10.1002/cbic.200700464
Dar TA, Uddin M, Khan MMA, Hakeem KR, Jaleel H (2015) Jasmonates counter plant stress: a review. Environ Exp Bot 115:49–57. https://doi.org/10.1016/j.envexpbot.2015.02.010
Dave A, Hernandez ML, He ZS, Andriotis VME, Vaistij FE, Larson TR et al (2011) 12-oxo-phytodienoic acid accumulation during seed development represses seed germination in Arabidopsis. Plant Cell 23:583–599. https://doi.org/10.1105/tpc.110.081489
de Ollas C, Arbona V, GóMez-Cadenas A (2015) Jasmonoyl isoleucine accumulation is needed for abscisic acid build-up in roots of Arabidopsis under water stress conditions. Plant Cell Environ 38(10):2157–2170. https://doi.org/10.1111/pce.12536
Delker C, Stenzel I, Hause B, Miersch O, Feussner I, Wasternack C (2006) Jasmonate biosynthesis in Arabidopsis thaliana—enzymes, products, regulation. Plant Biol 8:297–306. https://doi.org/10.1055/s-2006-923935
Demianski AJ, Chung KM, Kunkel BN (2012) Analysis of Arabidopsis JAZ gene expression during Pseudomonas syringae pathogenesis. Mol Plant Pathol 13:46–57. https://doi.org/10.1111/j.1364-3703.2011.00727.x
Demidchik V, Shabala S (2017) Mechanisms of cytosolic calcium elevation in plants: the role of ion channels, calcium extrusion systems and NADPH oxidase-mediated ‘ROS-Ca2+ Hub.’ Funct Plant Biol 45(2):9–27. https://doi.org/10.1071/FP16420
Deng X, Wang J, Li Y, Wu S, Yang S, Chao J, Chen Y, Zhang X, Shi M, Tian W (2018) Comparative transcriptome analysis reveals phytohormone signaling, heat shock module and ROS scavenger mediate the cold-tolerance of rubber tree. Sci Rep 8:4931. https://doi.org/10.1038/s41598-018-23094-y
Dhakarey R, Raorane ML, Treumann A, Peethambaran PK, Schendel RR, Sahi VP, Hause B, Bunzel M, Henry A, Kohli A, Riemann M (2017) Physiological and Proteomic Analysis of the Rice Mutant cpm2 Suggests a Negative Regulatory Role of Jasmonic Acid in Drought Tolerance. Front Plant Sci 8:1903
Ding Y, Liu N, Virlouvet L, Riethoven JJ, Fromm M, Avramova Z (2013) Four distinct types of dehydration stress memory genes in Arabidopsis thaliana. BMC Plant Boil 13:229. https://doi.org/10.3390/ijms21041446
Disi JO, Zebelo S, Ngumbi E, Fadamiro HY (2017) cis-Jasmone primes defense pathways in tomato via emission of volatile organic compounds and regulation of genes with consequences for Spodoptera exigua oviposition. Arthropod Plant Interact 11:591–602. https://doi.org/10.1007/s11829-017-9503-y
Dombrecht B, Xue GP, Sprague SJ, Kirkegaard JA, Ross JJ, Reid JB, Fitt GP, Sewelam N, Schenk PM, Manners JM et al (2007) MYC2 differentially modulates diverse jasmonate-dependent functions in Arabidopsis. Plant Cell 19:2225–2245. https://doi.org/10.1105/tpc.106.048017
Dubois M, Van den Broeck L, Inzé D (2018) The pivotal role of ethylene in plant growth. Trends Plant Sci 23(4):311–323. https://doi.org/10.1016/j.tplants.2018.01.003
Farhangi-Abriz S, Ghassemi-Golezani K (2018) How can salicylic acid and jasmonic acid mitigate salt toxicity in soybean plants? Ecotox Environ Saf 147:1010–1016. https://doi.org/10.1016/j.ecoenv.2017.09.070
Fernández-Calvo P, Chini A, Fernández-Barbero G, Chico JM, Gimenez-Ibanez S, Geerinck J, Eeckhout D, Schweizer F, Godoy M, Franco-Zorrilla JM et al (2011) 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 23:701–715. https://doi.org/10.1105/tpc.110.080788
Feussner I, Wasternack C (2002) The lipoxygenase pathway. Annu Rev Plant Biol 53:275–297. https://doi.org/10.1146/annurev.arplant.53.100301.135248
Feys B, Benedetti CE, Penfold CN, Turner JG (1994) Arabidopsis mutants selected for resistance to the phytotoxin coronatine are male sterile, insensitive to methyl jasmonate, and resistant to a bacterial pathogen. Plant Cell 6:751–759. https://doi.org/10.1105/tpc.6.5.751
Figueiredo DD, Köhler C (2018) Auxin: a molecular trigger of seed development. Genes Dev 32:479–490. https://doi.org/10.1101/gad.312546.118
Figueroa P, Browse J (2012) The Arabidopsis JAZ2 promoter contains a G-box and thymidine-rich module that is necessary and sufficient for jasmonate-dependent activation by MYC transcription factors and repression by JAZ proteins. Plant Cell Physiol 53:330–343. https://doi.org/10.1093/pcp/pcr178
Fu ZQ, Yan S, Saleh A, Wang W, Ruble J, Oka N, Mohan R, Spoel SH, Tada Y, Zheng N, Dong X (2012) NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants. Nature 486:228–232. https://doi.org/10.1038/nature11162
Fujimoto T, Tomitaka Y, Abe H, Tsuda S, Futai K, Mizukubo T (2011) Expression profile of jasmonic acid-induced genes and the induced resistance against the root-knot nematode (Meloidogyne incognita) in tomato plants (Solanum lycopersicum) after foliar treatment with methyl jasmonate. J Plant Physiol 168:1084–1097. https://doi.org/10.1016/j.jplph.2010.12.002
Gasperini D, Chételat A, Acosta IF, Goossens J, Pauwels L, Goossens A, Dreos R, Alfonso E, Farmer EE (2015) Multilayered organization of jasmonate signaling in the regulation of root growth. PLoS Genet 11:e1005300. https://doi.org/10.1371/journal.pgen.1005300
Gatz C (2013) From pioneers to team players: TGA transcription factors provide a molecular link between different stress pathways. MPMI 26:151–159. https://doi.org/10.1094/MPMI-04-12-0078-IA
Genva M, Akong FO, Andersson MX, Deleu M, Lins L, Fauconnier ML (2019) New insights into the biosynthesis of esterified oxylipins and their involvement in plant defense and developmental mechanisms. Phytochem Rev 18:343–358. https://doi.org/10.1007/s11101-018-9595-8
Gimenez-Ibanez S, Boter M, Fernández-Barbero G, Chini A, Rathjen JP, Solano R (2014) The bacterial effector HopX1 targets JAZ transcriptional repressors to activate jasmonate signaling and promote infection in Arabidopsis. PLoS Biol 12:e1001792. https://doi.org/10.1371/journal.pbio.1001792
Göbel C, Feussner I (2009) Methods for the analysis of oxylipins in plants. Phytochem 70:1485–1503. https://doi.org/10.1016/j.phytochem.2009.07.040
Górnik K, Badowiec A, Weidner S (2014) The effect of seed conditioning, short-term heat shock and salicylic, jasmonic acid or brasinolide on sunflower (Helianthus annuus L.) chilling resistance and polysome formation. Acta Physiol Plant 36:2547–2554. https://doi.org/10.1007/s11738-014-1626-5
Griffiths G (2020) Jasmonates: biosynthesis, perception and signal transduction. Essays Biochem. https://doi.org/10.1042/EBC20190085
Grunewald W, Vanholme B, Pauwels L, Plovie E, Inzé D, Gheysen G, Goossens A (2009) Expression of the Arabidopsis jasmonate signalling repressor JAZ1/TIFY10A is stimulated by auxin. EMBO Rep 10:923–938. https://doi.org/10.1038/embor.2009.103
Guan L, Denkertb N, Eisaa A, Lehmanna M, Sjutsa I, Weiberga A, Solla J, Meineckeb M, Schwenkert S (2019) JASSY, a chloroplast outer membrane protein required for jasmonate biosynthesis. Proc Natl Acad Sci USA 116:10568–10575. https://doi.org/10.1073/pnas.1900482116
Guo J, Pang Q, Wang L, Yu P, Li N, Yan X (2012) Proteomic identification of MYC2-dependent jasmonate-regulated proteins in Arabidopsis thaliana. Proteome Sci 10:57
Gutierrez L, Mongelard G, Flokova K et al (2012) Auxin controls Arabidopsis adventitious root initiation by regulating jasmonic acid homeostasis. Plant Cell 24:2515–2527. https://doi.org/10.1105/tpc.112.099119
Haroth S, Feussner K, Kelly AA, Zienkiewicz K, Shaikhqasem A, Herrfurth C et al (2019) The glycosyl transferase UGT76E1 significantly contributes to 12-O-glucopyranosyl-jasmonic acid formation in wounded Arabidopsis thaliana leaves. J Biol Chem 294:9858–9872. https://doi.org/10.1074/jbc.RA119.007600
Havko NE, Major IT, Jewell JB, Attaran E, Browse J, Howe GA (2016) Control of carbon assimilation and partitioning by jasmonate: an accounting of growth-defense tradeoffs. Plants 5:7. https://doi.org/10.3390/plants5010007
Hiruma K, Nishiuchi T, Kato T, Bednarek P, Okuno T, SchulzeLefert P, Takano Y (2011) Arabidopsis ENHANCED DISEASE RESISTANCE 1 is required for pathogen-induced expression of plant defensins in nonhost resistance, and acts through interference of MYC2-mediated repressor function. Plant J 67:980–992. https://doi.org/10.1111/j.1365-313X.2011.04651.x
Hou X, Lee LYC, Xia K, Yan Y, Yu H (2010) DELLAs modulate jasmonate signaling via competitive binding to JAZs. Dev Cell 19:884–894. https://doi.org/10.1016/j.devcel.2010.10.024
Howe GA (2010) Ubiquitin ligase-coupled receptors extend their reach to jasmonate. Plant Physiol 154:471–474. https://doi.org/10.1104/pp.110.161190
Ilyas N, Gull R, Mazhar R, Saeed M, Kanwal S, Shabir S, Bibi F (2017) Influence of salicylic acid and jasmonic acid on wheat under drought stress. Commun Soil Sci Plant Anal 48:2715–2723. https://doi.org/10.1080/00103624.2017.1418370
Ishiguro S, Kawai-Oda A, Ueda J, Nishida I, Okada K (2001) 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 13:2191–2209. https://doi.org/10.1105/tpc.010192
Ishimaru Y, Oikawa T, Suzuki T, Takeishi S, Matsuura H, Takahashi K et al (2017) GTR1 is a jasmonic acid and jasmonoyl-L-isoleucine transporter in Arabidopsis thaliana. Biosci Biotechnol Biochem 81:249–255. https://doi.org/10.1080/09168451
Jang G, Chang SH, Um TY, Lee S, Kim JK, Do Choi Y (2017) Antagonistic interaction between jasmonic acid and cytokinin in xylem development. Sci Rep 7:10212. https://doi.org/10.1038/s41598-017-10634-1
Jang G, Yoon Y, Choi YD (2019) Jasmonic acid modulates xylem development by controlling expression of PIN-FORMED 7. Plant Signal Behav 14(9):1637664. https://doi.org/10.1080/15592324.2019.1637664
Jang G, Yoon Y, Choi YD (2020) Crosstalk with jasmonic acid integrates multiple responses in plant development. Int J Mol Sci 21:305. https://doi.org/10.3390/ijms21010305
Jewell JB, Browse J (2016) Epidermal jasmonate perception is sufficient for all aspects of jasmonate-mediated male fertility in Arabidopsis. Plant J 85:634–647. https://doi.org/10.1111/tpj.13131
Jiang Y, Liang G, Yang S, Yu D (2014) Arabidopsis WRKY57 functions as a node of convergence for jasmonic acid- and auxin-mediated signaling in jasmonic acid-induced leaf senescence. Plant Cell 26:230–245. https://doi.org/10.1105/tpc.113.117838
Kammerhofer N, Radakovic Z, Regis JM, Dobrev P, Vankova R, Grundler FM et al (2015) Role of stress-related hormones in plant defence during early infection of the cyst nematode Heterodera schachtii in Arabidopsis. New Phytol 207:778–789. https://doi.org/10.1111/nph.13395
Kazan K (2015) Diverse roles of jasmonates and ethylene in abiotic stress tolerance. Trends Plant Sci 20:219–229. https://doi.org/10.1016/j.tplants.2015.02.001
Kazan K, Manners JM (2013) MYC2: The Master in Action. Mol Plant 6:686–703. https://doi.org/10.1093/mp/sss128
Khan MIR, Syeed S, Nazar R, Anjum NA (2012) An insight into the role of salicylic acid and Jasmonic acid in salt stress tolerance. Phytohormones and abiotic stress tolerance in plants. Springer, Berlin, pp 277–300. https://doi.org/10.1007/978-3-642-25829-9
Kieber JJ, Schaller GE (2018) Cytokinin signaling in plant development. Development 145:149344. https://doi.org/10.1242/dev.149344
Kim J, Chang C, Tucker ML (2015) To grow old: regulatory role of ethylene and jasmonic acid in senescence. Front Plant Sci 6:20. https://doi.org/10.3389/fpls.2015.00020
Kitaoka N, Kawaide H, Amano N, Matsubara T, Nabeta K, Takahashi K et al (2014) CYP94B3 activity against jasmonic acid amino acid conjugates and the elucidation of 12-O-beta-glucopyranosyl-jasmonoyl-L-isoleucine as an additional metabolite. Phytochem 99:6–13. https://doi.org/10.1016/j.phytochem.2013.12.019
Koo AJ, Thireault C, Zemelis S, Poudel AN, Zhang T, Kitaoka N et al (2014) Endoplasmic reticulum-associated inactivation of the hormone jasmonoyl-L-isoleucine by multiple members of the cytochrome P450 94 family in Arabidopsis. J Biol Chem 289:29728–29738. https://doi.org/10.1074/jbc.M114.603084
Kyndt T, Vieira P, Gheysen G, De Almeida-Engler J (2013) Nematode feeding sites: unique organs in plant roots. Planta 238:807–818. https://doi.org/10.1007/s00425-013-1923-z
Kyndt T, Nahar K, Haeck A, Verbeek R, Demeestere K, Gheysen G (2017) Interplay between carotenoids, abscisic acid and jasmonate guides the compatible rice-Meloidogyne graminicola interaction. Front Plant Sci 8:951. https://doi.org/10.3389/fpls.2017.00951
Li L, Zhao Y, McCaig BC, Wingerd BA, Wang J, Whalon ME, Pichersky E, Howe GA (2004) The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development. Plant Cell 16:126–143. https://doi.org/10.1105/tpc.017954
Li N, Han X, Feng D, Yuan D, Huang LJ (2019) Signaling crosstalk between salicylic acid and ethylene/jasmonate in plant defense: Do we understand what they are whispering? Int J Mol Sci 20:671
Liu X, Hou X (2018) Antagonistic regulation of ABA and GA in metabolism and signaling pathways. Front Plant Sci 9:251. https://doi.org/10.3389/fpls.2018.00251
Liu L, Li H, Zeng H, Cai Q, Zhou X, Yin C (2016a) Exogenous jasmonic acid and cytokinin antagonistically regulate rice flag leaf senescence by mediating chlorophyll degradation, membrane deterioration, and senescence-associated genes expression. J Plant Growth Regul 35:366–376. https://doi.org/10.3390/ijms21010305
Liu L, Sonbol FM, Huot B, Gu Y, Withers J, Mwimba M, Yao J, He SY, Dong X (2016b) Salicylic acid receptors activate jasmonic acid signalling through a non-canonical pathway to promote effector-triggered immunity. Nat Commun 7:13099. https://doi.org/10.1038/ncomms13099
Liu J, Moore S, Chen C, Lindsey K (2017) Crosstalk complexities between auxin, cytokinin, and ethylene in Arabidopsis root development: from experiments to systems modeling, and back again. Mol Plant 10:1480–1496. https://doi.org/10.1016/j.molp.2017.11.002
Luo J, Xia W, Cao P, Xiao Z, Zhang Y, Liu M, Zhan C, Wang N (2019) Integrated transcriptome analysis reveals plant hormones jasmonic acid and salicylic acid coordinate growth and defense responses upon fungal infection in poplar. Biomolecules 9:12. https://doi.org/10.3390/biom9010012
Luo H, He WW, Li DJ, Bao YH, Riaz A, Xiao YD et al (2020) Effect of methyl jasmonate on carotenoids biosynthesis in germinated maize kernels. Food Chem 307:125525. https://doi.org/10.1016/j.foodchem.2019.125525
Mahonem AP, Ten Tusscher K, Siligato R, Smetana O, Diaz-Trivino S, Salojarvi J, Wachsman G, Prasad K, Heidstra R, Scheres B (2014) PLETHORA gradient formation mechanism separates auxin responses. Nature 515:125–129. https://doi.org/10.1038/nature13663
Mao YB, Liu YQ, Chen DY, Chen FY, Fang X, Hong GJ, Wang LJ, Wang JW, Chen XY (2017) Jasmonate response decay and defense metabolite accumulation contributes to age-regulated dynamics of plant insect resistance. Nat Commun 8:13925. https://doi.org/10.1038/ncomms13925
Martìnez-Medina A, Fernandez I, Lok GB, Pozo MJ, Pieterse CM, Van Wees SC (2017) Shifting from priming of salicylic acid- to jasmonic acid-regulated defences by Trichoderma protects tomato against the root knot nematode Meloidogyne incognita. New Phytol 213:1363–1377. https://doi.org/10.1111/nph.14251
Matsu R, Amanu R, Takahashi K, Tagushi Y, Saburi W, Mori H, Kondo N, Matsuda K, Matsuura H (2017) Elucidation of the biosynthetic pathway of cis-jasmonate in Lasiodiplodia theobromae. Sci Rep 7:6688. https://doi.org/10.1038/s41598-017-05851-7
Matthes MC, Bruce TJA, Ton J, Verrier PJ, Pickett JA, Napier JA (2010) The transcriptome of cis-jasmone-induced resistance in Arabidopsis thaliana and its role in indirect defence. Planta 232:1163–1180. https://doi.org/10.1007/s00425-010-1244-4
Meldau S, Ullman-Zeunert L, Govind G, Bartram S, Baldwin IT (2012) MAPK-dependent JA and SA signaling in Nicotiana attenuate affects plant growth and fitness during competition with conspecifics. BMC Plant Biol 12:213. https://doi.org/10.1186/1471-2229-12-213
Melillo MT, Leonetti P, Bongiovanni M, Castagnone-Sereno P, Bleve-Zacheo T (2006) Modulation of reactive oxygen species activities and H2O2 accumulation during compatible and incompatible tomato-root-knot nematode interactions. New Phytol 170:501–512. https://doi.org/10.1111/j.1469-8137.2006.01724.x
Melotto M, Underwood W, Koczan J, Nomura K, He SY (2006) Plant stomata function in innate immunity against bacterial invasion. Cell 126:969–980. https://doi.org/10.1016/j.cell.2006.06.054
Molinari S, Fanelli E, Leonetti P (2014) Expression of tomato salicylic acid (SA)-responsive pathogenesis-related genes in Mi-1-mediated and SA-induced resistance to root-knot nematodes. Mol Plant Pathol 15:255–264. https://doi.org/10.1111/mpp.12085
Monte I, Hamberg M, Chini A, Gimenez-Ibanez S, García-Casado G, Porzel A, Pazos F, Boter M, Solano R (2014) Rational design of a ligand-based antagonist of jasmonate perception. Nat Chem Biol 10:671–676. https://doi.org/10.1038/nchembio.1575
Mosblech A, Thurow C, Gatz C, Feussner I, Heilmann I (2011) Jasmonic acid perception by COI1 involves inositol polyphosphates in Arabidopsis thaliana. Plant J 65:949–957. https://doi.org/10.1111/j.1365-313X.2011.04480.x
Mutar SS, Fattah FA (2013) Red light-induced systemic resistance to root knot nematodes in tomato. J Biol Agric Healthc 3:110–114. https://doi.org/10.3389/fpls.2018.00899
Nahar K, Kyndt T, De Vleesschauwer D, Höfte M, Gheysen G (2011) The jasmonate pathway is a key player in systemically induced defense against root knot nematodes in rice. Plant Physiol 157:305–316. https://doi.org/10.1104/pp.111.177576
Nakata M, Mitsuda N, Herde M, Koo AJ, Moreno JE, Suzuki K, Howe GA, Ohme-Takagi M (2013) 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. Plant Cell 25:1641–1656. https://doi.org/10.1105/tpc.113.111112
Narvaez-Vasquez J, Florin-Christensen J, Ryan CA (1999) Positional specificity of a phospholipase A activity induced by wounding, systemin, and oligosaccharide elicitors in tomato leaves. Plant Cell 11:2249–2260. https://doi.org/10.1105/tpc.11.11.2249
Nilsson AK, Fahlberg P, Johansson ON, Hamberg M, Andersson MX, Ellerstrom M (2016) The activity of hydroperoxide lyase 1 regulates accumulation of galactolipids containing 12-oxo-phytodienoic acid in Arabidopsis. J Exp Bot 67:5133–5144. https://doi.org/10.1093/jxb/erw278
Nitschke S, Cortleven A, Iven T, Feussner I, Havaux M, Riefler M, Schmülling T (2016) Circadian stress regimes affect the circadian clock and cause jasmonic acid-dependent cell death in cytokinin-deficient Arabidopsis plants. Plant Cell 28:1616–1639. https://doi.org/10.1105/tpc.16.00016
Noriega G, Cruz DS, Batlle A, Tomaro M, Balestrasse K (2012) Heme oxygenase is involved in the protection exerted by Jasmonic acid against Cadmium stress in Soybean roots. J Plant Growth Regul 31:79–89. https://doi.org/10.1007/s00344-011-9221-0
Pauwels L, Goossens A (2011) The JAZ proteins, a crucial interface in the jasmonate signaling cascade. Plant Cell 23:3089–3100. https://doi.org/10.1105/tpc.111.089300
Pauwels L, Barbero GF, Geerinck J, Tilleman S, Grunewald W, Pérez AC, Chico JM, Bossche RV, Sewell J, Gil E et al (2010) NINJA connects the co-repressor TOPLESS to jasmonate signaling. Nature 464:788–791. https://doi.org/10.1038/nature08854
Per TS, Iqbal M, Khan R, Anjum NA, Masood A, Hussain SJ (2018) Jasmonates in plants under abiotic stresses: Crosstalk with other phytohormones matters. Environ Exp Bot 145:104–120. https://doi.org/10.1016/j.envexpbot.2017.11.004
Pieterse CMJ (2012) Rewiring of the jasmonate signaling pathway in Arabidopsis during insect herbivory. Front Plant Sci 2:1–12. https://doi.org/10.3389/fpls.2011.00047
Pires N, Dolan L (2010) Origin and diversification of basic-helix-loop-helix proteins in plants. Mol Biol Evol 27:862–874. https://doi.org/10.1093/molbev/msp288
Pottosin I, Velarde-Buendía AM, Bose J, Zepeda-Jazo I, Shabala S, Dobrovinskaya O (2014) Crosstalk between reactive oxygen species and polyamines in regulation of ion transport across the plasma membrane: implications for plant adaptive responses. J Exp Bot 65:1271–1283. https://doi.org/10.1093/jxb/ert423
Qi J, Zhou G, Yang L, Erb M, Lu Y, Sun X, Cheng J, Lou Y (2011) The chloroplast-localized phospholipases D α4 and α5 regulate herbivore-induced direct and indirect defenses in rice. Plant Physiol 157:1987–1999. https://doi.org/10.1104/pp.111.183749
Qi T, Huang H, Wu D, Yan J, Qi Y, Song S, Xie D (2014) Arabidopsis DELLA and JAZ proteins bind the WD-repeat/bHLH/MYB complex to modulate gibberellin and jasmonate signaling synergy. Plant Cell 26:1118–1133. https://doi.org/10.1105/tpc.113.121731
Qi T, Huang H, Song S, Xie D (2015) Regulation of jasmonate-mediated stamen development and seed production by a bHLH-MYB complex in Arabidopsis. Plant Cell 27:1620–1633. https://doi.org/10.1105/tpc.15.00116
Reeves PH, Ellis CM, Ploense SE et al (2012) A regulatory network for coordinated flower maturation. PLoS Genet 8:e1002506. https://doi.org/10.1371/journal.pgen.1002506
Ren C, Han C, Peng W, Huang Y, Peng Z, Xiong X, Zhu Q, Gao B, Xie D (2009) A leaky mutation in DWARF4 reveals an antagonistic role of brassinosteroid in the inhibition of root growth by jasmonate in Arabidopsis. Plant Physiol 151:1412–1420. https://doi.org/10.1104/pp.109.140202
Robson F, Okamoto H, Patrick E, Harris SR, Wasternack C, Brearley C, Turner JG (2010) Jasmonate and phytochrome A signaling in Arabidopsis wound and shade responses are integrated through JAZ1 stability. Plant Cell 22:1143–1160. https://doi.org/10.1105/tpc.109.067728
Ruan J, Zhou Y, Zhou M, Yan J, Khurshid M, Weng W et al (2019) Jasmonic acid signaling pathway in plants. Inter J Mol Sci 20(10):2479. https://doi.org/10.3390/ijms20102479
Sadeghnezhad E, Sharifi M, Zare-Maivan H, Chashmi NA (2020) Time-dependent behavior of phenylpropanoid pathway in response to methyl jasmonate in Scrophularia striata cell cultures. Plant Cell Rep 39:227–243. https://doi.org/10.1007/s00299-019-02486-y
Sanchez-Aguayo I, Rodrıguez-Galan JM, Garcıa R, Torreblanca J, Pardo JM (2004) Salt stress enhances xylem development and expression of S-adenosyl-L-methionine synthase in lignifying tissues of tomato plants. Planta 220:278–285. https://doi.org/10.1007/s00425-004-1350-2
Saniewski M, Ueda J, Miyamoto K (2002) Relationships between jasmonates and auxin in regulation of some physiological processes in higher plants. Acta Physiol Plant 24:211. https://doi.org/10.1007/s11738-002-0013-9
Savchenko T, Kolla VA, Wang CQ et al (2014) Functional convergence of oxylipin and abscisic acid pathways controls stomatal closure in response to drought. Plant Physiol 164:1151–1160. https://doi.org/10.1104/pp.113.234310
Sayyari M, Babalar M, Kalantari S, Martínez-Romeroa D, Guilléna F, Serranob M, Valeroa D (2010) Vapour treatments with methyl salicylate or methyl jasmonate alleviated chilling injury and enhanced antioxidant potential during postharvest storage of pomegranates. Food Chem 124:964–970. https://doi.org/10.1016/j.foodchem.2010.07.036
Schaller F (2001) Enzymes of the biosynthesis of octadecanoid-derived signaling molecules. J Exp Bot 52:11–23
Scheer JM, Ryan CA Jr (2002) The systemin receptor SR160 from Lycopersicon peruvianum is a member of the LRR receptor kinase family. Proc Natl Acad Sci USA 99:9585–9590. https://doi.org/10.1073/pnas.132266499
Sethi V, Raghuram B, Sinha AK, Chattopadhyay S (2014) A mitogen activated protein kinase cascade module, MKK3-MPK6 and MYC2, is involved in blue light-mediated seedling development in Arabidopsis. Plant Cell 26:3343–3357. https://doi.org/10.1105/tpc.114.128702
Sewelam N, Kazan K, Schenk PM (2016) Global Plant Stress Signaling: Reactive Oxygen Species at the Crossroad. Front Plant Sci 7:187. https://doi.org/10.3389/fpls.2016.00187
Sharma P, Dubey RS (2005) Lead toxicity in plants. Braz J Plant Physiol 17:35–52. https://doi.org/10.1590/s1677-04202005000100004
Shi J, Ma CY, Qi DD, Lv HP, Yang T, Peng QH et al (2015) Transcriptional responses and flavor volatiles biosynthesis in methyl jasmonate-treated tea leaves. BMC Plant Biol 15:233. https://doi.org/10.1186/s12870-015-0609-z
Shim JS, Jung C, Lee S, Min K, Lee YW, Choi Y, Lee JS, Song JT, Kim JK, Choi YD (2013) AtMYB44 regulates WRKY70 expression and modulates antagonistic interaction between salicylic acid and jasmonic acid signaling. Plant J 73:483–495. https://doi.org/10.1111/tpj.12051
Siddiqi KS, Husen A (2019) Plant response to jasmonates: current developments and their role in changing environment. Bull Nat Res Centre 43(1):1–11. https://doi.org/10.1186/s42269-019-0195-6
Siddique S, Matera C, Radakovic ZS, Shamim Hasan M, Gutbrod P, Rozanska E (2014) Parasitic worms stimulate host NADPH oxidases to produce reactive oxygen species that limit plant cell death and promote infection. Sci Signal 7:ra33. https://doi.org/10.1126/scisignal.2004777
Simm S, Papasotiriou DG, Ibrahim M, Leisegang MS, Müller B, Schorge T, Karas M, Mirus O, Sommer MS, Schleiff E (2013) Defining the core proteome of the chloroplast envelope membranes. Front Plant Sci 4:11. https://doi.org/10.3389/fpls.2013.00011
Singh S, Singh A, Kumar S, Mittal P, Singh IK (2020) Protease inhibitors: recent advancement in its usage as a potential biocontrol agent for insect pest management. Insect Sci 27:186–201. https://doi.org/10.1111/1744-7917.12641
Sirhindi G, Mir MA, Sharma P, Gill SS, Kaur H, Mushtaq R (2015) Modulatory role of jasmonic acid on photosynthetic pigments, antioxidants and stress markers of Glycine max L. under nickel stress. Physiol Mol Biol Plants 21:559–565. https://doi.org/10.1007/s12298-015-0320-4
Song S, Qi T, Huang H, Ren Q, Wu D, Chang C, Peng W, Liu Y, Peng J, Xie D (2011) The Jasmonate-ZIM domain proteins interact with the R2R3-MYB transcription factors MYB21 and MYB24 to affect Jasmonate-regulated stamen development in Arabidopsis. Plant Cell 23:1000–1013. https://doi.org/10.1105/tpc.111.083089
Song S, Qi T, Huang H, Xie D (2013) Regulation of stamen development by coordinated actions of jasmonate, auxin, and gibberellin in Arabidopsis. Mol Plant 6:1065–1073. https://doi.org/10.1093/mp/sst054
Song S, Huang H, Gao H et al (2014) Interaction between MYC2 and ETHYLENE INSENSITIVE3 modulates antagonism between jasmonate and ethylene signaling in Arabidopsis. Plant Cell 26:263–279. https://doi.org/10.1105/tpc.113.120394
Song LX, Xu XC, Wang FN, Wang Y, Xia XJ, Shi K et al (2017) Brassinosteroids act as a positive regulator for resistance against root-knot nematode involving RESPIRATORY BURST OXIDASE HOMOLOG-dependent activation of MAPKs in tomato. Plant Cell Environ 41:1113–1125. https://doi.org/10.1111/pce.12952
Sopel HS, Gary JL (2011) Redox-based protein modifications: the missing link in plant immune signaling. Curr Opin Plant Biol 14:358–364. https://doi.org/10.1016/j.pbi.2011.03.007
Staswick PE, Tiryaki I (2004) The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell 16:2117–2127. https://doi.org/10.1105/tpc.104.023549
Suarez Rodriguez MC, Petersen M, Mundy J (2010) Mitogen-Activated Protein Kinase Signaling in Plants. Annu Rev Plant Biol 61:621–649. https://doi.org/10.1146/annurev-arplant-042809-112252
Sun YC, Cao HF, Yin J, Kang L, Ge F (2010) Elevated CO2 changes the interactions between nematode and tomato genotypes differing in the JA pathway. Plant Cell Environ 33:729–739. https://doi.org/10.1371/journal.pone.0019751
Sun JQ, Hong-Ling J, Li CY (2011) Systemin/jasmonate-mediated systemic defense signaling in tomato. Mol Plant 4:607–615. https://doi.org/10.1093/mp/ssr008
Taki N, Sasaki-Sekimoto Y, Obayashi T, Kikuta A, Kobayashi K, Ainai T, Yagi K, Sakurai N, Suzuki H, Masuda T, Takamiya K, Shibata D, Kobayashi Y, Ohta H (2005) 12-oxo-phytodienoic acid triggers expression of a distinct set of genes and plays a role in wound-induced gene expression in Arabidopsis. Plant Physiol 139:1268–1283. https://doi.org/10.1104/pp.105.067058
Tang G, Ma J, Hause B, Nick P, Riemann M (2020) Jasmonate is required for the response to osmotic stress in rice. Environ Exp Bot 175:104047. https://doi.org/10.1016/j.envexpbot.2020.104047
Thatcher LF, Cevik V, Grant M, Zhai B, Jones JD, Manners JM, Kazan K (2016) Characterization of a JAZ7 activation-tagged Arabidopsis mutant with increased susceptibility to the fungal pathogen Fusarium oxysporum. J Exp Bot 67:2367–2386. https://doi.org/10.1093/jxb/erw040
Theodoulou FL, Job K, Slocombe SP, Footitt S, Holdsworth M, Baker A, Larson TR, Graham IA (2005) Jasmonic acid levels are reduced in COMATOSE ATP-binding cassette transporter mutants. Implications for transport of jasmonate precursors into peroxisome. Plant Physiol 137:835–840. https://doi.org/10.1104/pp.105.059352
Thines B, Katsir L, Melotto M, Niu Y, Mandaokar A, Liu G, Nomura K, He SY, Howe GA, Browse J (2007) JAZ repressor proteins are targets of the SCF COI1 complex during jasmonate signaling. Nature 448:661–665. https://doi.org/10.1038/nature05960
Thireault C, Shyu C, Yoshida Y, St Aubin B, Campos ML, Howe GA (2015) Repression of jasmonate signaling by a non-TIFY JAZ protein in Arabidopsis. Plant J 82:669–679. https://doi.org/10.1111/tpj.12841
Toledo-Ortiz G, Huq E, Quail PH (2003) The Arabidopsis basic/helix-loop-helix transcription factor family. Plant Cell 15:1749–1770. https://doi.org/10.1105/tpc.013839
Turner JG, Ellis C, Devoto A (2002) The jasmonate signal pathway. Plant Cell 14:S153–S164. https://doi.org/10.1105/tpc.000679
Tuteja N, Gill SS (2013) Salicylic acid: a novel plant growth regulator-role in physiological processes and abiotic stresses under changing environments. Climate change and plant abiotic stress tolerance. Wiley-VCH, Weinheim, pp 939–990. https://doi.org/10.1002/9783527675265.ch36
Ueda J, Kato J (1982) Inhibition of cytokinin-induced plant growth by jasmonic acid and its methyl ester. Physiol Plant 54(3):249–252. https://doi.org/10.1111/j.1399-3054.1982.tb00255.x
Um TY, Lee HY, Lee S, Chang SH, Chung PJ, Oh KB, Kim JK, Jang G, Choi YD (2018) JASMONATE ZIM-DOMAIN PROTEIN 9 interacts with SLENDER RICE 1 to mediate the antagonistic interaction between jasmonic and gibberellic acid signals in rice. Front Plant Sci 9:1866. https://doi.org/10.3389/fpls.2018.01866
van Wees SC, De Swart EA, Van Pelt JA, Van Loon LC, Pieterse CM (2000) Enhancement of induced disease resistance by simultaneous activation of salicylate- and jasmonate-dependent defense pathways in Arabidopsis thaliana. Proc Natl Acad Sci USA 97:8711–8716. https://doi.org/10.1073/pnas.130425197
Wager A, Browse J (2012) Social network, JAZ protein interactions expand our knowledge of jasmonate signaling. Front Plant Physiol 3:41. https://doi.org/10.3389/fpls.2012.00041
Wang Y, Yuan G, Yuan S, Duan W, Wang P, Bai J, Zhang F, Gao S, Zhang L, Zhao C (2016) TaOPR2 encodes a 12-oxo-phytodienoic acid reductase involved in the biosynthesis of jasmonic acid in wheat (Triticum aestivum L.). Biochem Biophys Res Commun 470:233–238. https://doi.org/10.1016/j.bbrc.2016.01.043
Wang K, Guo Q, Froehlich JE, Hersh HL, Zienkiewicz A, Howe GA et al (2019) Two abscisic acid-responsive plastid lipase genes involved in jasmonic acid biosynthesis in Arabidopsis thaliana. Plant Cell 30:1006–1022. https://doi.org/10.1105/tpc.18.00250
Wang Y, Hou Y, Qi J, Wang H, Wang S, Tang S, Tong X, Zhang J (2020) Abscissic acid promotes jasmonic acid biosynthesis via a “SAPK10-bZIP72-AOC” pathway to synergistically inhibit seed germination in rice (Oryza sativa). New Phytol 228:1336–1353. https://doi.org/10.1111/NPH.16774
Wang X, Li Q, Xie J, Huang M, Cai J, Zhou Q, Dai T, Jiang D (2021) Abscisic acid and jasmonic acid are involved in drought priming-induced tolerance to drought in wheat. Crop J 9:120–132. https://doi.org/10.1016/j.cj.2020.06.002
Wasternack C, Feussner I (2018) The oxylipin pathways: biochemistry and function. Ann Rev Plant Biol 69:363–386. https://doi.org/10.1146/annurev-arplant-042817-040440
Wasternack C, Hause B (2007) 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 111:1021–1058. https://doi.org/10.1093/aob/mct067
Wasternack C, Hause B (2019) The missing link in jasmonic acid biosynthesis. Nat Plants 5:776–777
Xiao HM, Cai WJ, Ye TT, Ding J, Feng YQ (2018) Spatio-temporal profiling of abscisic acid, indoleacetic acid and jasmonic acid in single rice seed during seed germination. Anal Chim Acta 1031:119–127. https://doi.org/10.1016/j.aca.2018.05.055
Xie DX, Feys BF, James S, Nieto-Rostro M, Turner JG (1998) COI1: an Arabidopsis gene required for jasmonate-regulated defense and fertility. Sci 280:1091–1094. https://doi.org/10.1126/science.280.5366.1091
Xu L, Liu F, Lechner E, Genschik P, Crosby WL, Ma H, Peng W, Huang D, Xie D (2002) The SCFCOI1 ubiquitin ligase complexes are required for jasmonate response in Arabidopsis. Plant Cell 14:1919–1935. https://doi.org/10.1105/tpc.003368
Xu Q, Truong TT, Barrero JM, Jacobsen JV, Hocart CH, Gubler F (2016) A role for jasmonates in the release of dormancy by cold stratification in wheat. J Exp Bot 67:3497–3508. https://doi.org/10.1093/jxb/erw172
Yadav V, Mallappa C, Gangappa SN, Bhatia S, Chattopadhyay S (2005) A basic helix-loop-helix transcription factor in Arabidopsis, MYC2, acts as a repressor of blue light-mediated photomorphogenic growth. Plant Cell 17:1953–1966. https://doi.org/10.1105/tpc.105.032060
Yan J, Zhang C, Gu M et al (2009) The Arabidopsis CORONATINE INSENSITIVE1 protein is a jasmonate receptor. Plant Cell 21:2220–2236. https://doi.org/10.1105/tpc.109.065730
Yan Y, Christensen S, Isakeit T, Engelberth J, Meeley R, Hayward A, Emery RJ, Kolomiets MV (2012) Disruption of OPR7 and OPR8 reveals the versatile functions of jasmonic acid in maize development and defense. Plant Cell 24:1420–1436. https://doi.org/10.1105/tpc.111.094151
Yan S, McLamore ES, Dong S, Gao H, Taguchi M, Wang N, Zhang T, Su X, Shen Y (2015) The role of plasma membrane H+-ATPase in jasmonate-induced ion fluxes and stomatal closure in Arabidopsis thaliana. Plant J 83:638–649. https://doi.org/10.1111/tpj.12915
Yang DL, Yao J, Mei CS, Tong XH, Zeng LJ, Li Q, Xiao LT, Sun TP, Li J, Deng XW (2012) Plant hormone jasmonate prioritizes defense over growth by interfering with gibberellin signaling cascade. Proc Natl Acad Sci USA 109:E1192–E1200. https://doi.org/10.1073/pnas.1201616109
Yang YX, Wang MM, Yin YL, Onac E, Zhou GF, Peng S et al (2015) RNA-seq analysis reveals the role of red light in resistance against Pseudomonas syringae pv. Tomato DC3000 in tomato plants. BMC Genom 16:120. https://doi.org/10.1186/s12864-015-1228-7
Yang YX, Wu C, Ahammed GJ, Wu C, Yang Z, Wan C, Chen J (2018) Red light-induced systemic resistance against root-knot nematode is mediated by a coordinated regulation of salicylic acid, jasmonic acid and redox signaling in watermelon. Front Plant Sci 9:899. https://doi.org/10.3389/fpls.2018.00899
Yang J, Duan G, Li C, Liu L, Han G, Zhang Y, Wang C (2019) The crosstalks between jasmonic acid and other plant hormone signaling highlight the involvement of jasmonic acid as a core component in plant response to biotic and abiotic stresses. Front Plant Sci 10:1349. https://doi.org/10.3389/fpls.2019.01349
Yin Y, Adachi Y, Nakamura Y, Munemasa S, Mori IC, Murata Y (2016) Involvement of OST1 protein kinase and PYR/PYL/RCAR receptors in methyl jasmonate-induced stomatal closure in Arabidopsis guard cells. Plant Cell Physiol 57:1779–1790. https://doi.org/10.1093/pcp/pcw102
Yoshida Y, Sano R, Wada T, Takabayashi J, Okada K (2009) Jasmonic acid control of GLABRA3 links inducible defense and trichome patterning in Arabidopsis. Develop 136:1039–1048. https://doi.org/10.1242/dev.030585
Yu J, Zhang Y, Di C, Zhang Q, Zhang K, Wang C, You Q, Yan H, Dai SY, Yuan JS (2015) JAZ7 negatively regulates dark-induced leaf senescence in Arabidopsis. J Exp Bot 67:751–762. https://doi.org/10.1093/jxb/erv487
Zander M, La Camera S, Lamotte O, Métraux JP, Gatz C (2010) Arabidopsis thaliana class-II TGA transcription factors are essential activators of jasmonic acid/ethylene-induced defense responses. Plant J 61:200–210. https://doi.org/10.1111/j.1365-313X.2009.04044.x
Zhai Q, Yan L, Tan D, Chen R, Sun J, Gao L, Dong MQ, Wang Y, Li Ch (2013) Phosphorylation-coupled proteolysis of the transcription factor MYC2 is important for jasmonate-signaled plant immunity. PLoS Genet 9(4):e1003422. https://doi.org/10.1371/journal.pgen.1003422
Zhai Q, Zhang X, Wu F, Feng H, Deng L, Xu L, Zhang M, Wang Q, Li C (2015) Transcriptional mechanism of jasmonate receptor COI1-mediated delay of flowering time in Arabidopsis. Plant Cell 27:2814–2828. https://doi.org/10.1105/tpc.15.00619
Zhang ZP, Baldwin IT (1997) Transport of [2-14C] jasmonic acid from leaves to roots mimics wound-induced changes in endogenous jasmonic acid pools in Nicotiana sylvestris. Planta 203:436–441
Zhang X, Zhu Z, An F, Hao D, Li P, Song J, Yi C, Guo H (2014) Jasmonate-activated MYC2 represses ETHYLENE INSENSITIVE3 activity to antagonize ethylene-promoted apical hook formation in Arabidopsis. Plant Cell 26:1105–1117. https://doi.org/10.1105/tpc.113.122002
Zhang F, Yao J, Ke J, Zhang L, Lam VQ, Xin XF, Zhou XE, Chen J, Brunzelle J, Griffin PR, Zhou M, Xu HE, Melcher K, He SY (2015) Structural basis of JAZ repression of MYC transcription factors in jasmonate signaling. Nature 525(7568):269–273. https://doi.org/10.1038/nature14661
Zhang X, Li M, Yang HH, Li XX, Cui ZJ (2018) Physiological responses of Suaeda glauca and Arabidopsis thaliana in phytoremediation of heavy metals. J Environ Manag 223:132–139. https://doi.org/10.1016/j.jenvman.2018.06.025
Zhang Y, He P, Ma X, Yang Z, Pang C, Yu J, Wang G, Friml J, Xiao G (2019) Auxin-mediated statolith production for root gravitropism. New Phytol 224:761–774. https://doi.org/10.1111/nph.15932
Zhao SY, Ma QF, Xu X, Li GZ, Hao L (2016) Tomato Jasmonic acid-deficient mutant spr2 seedling response to Cadmium stress. J Plant Growth Regul 35:603–610. https://doi.org/10.1007/s00344-015-9563-0
Zheng XY, Weaver NS, Weiqing Z, Liu PP, Fu ZQ, Klessig DF, He SY, Dong X (2012) Coronatine promotes Pseudomonas syringae virulence in plants by activating a signaling cascade that inhibits salicylic acid accumulation. Cell Host Microbe 11:587–596. https://doi.org/10.1016/j.chom.2012.04.014
Zhu Z, Lee B (2015) Friends or foes: new insights in jasmonate and ethylene co-actions. Plant Cell Physiol 56(3):414–420. https://doi.org/10.1093/pcp/pcu171
Zhu Z, An F, Feng Y, Li P, Xue L, Mu A, Jiang Z, Kim JM, To TK, Li W et al (2011) Derepression of ethylene-stabilized transcription factors (EIN3/EIL1) mediates jasmonate and ethylene signaling synergy in Arabidopsis. Proc Natl Acad Sci USA 108:12539–12544. https://doi.org/10.1073/pnas.1103959108
Zhu X, Chen J, Xie Z, Gao J, Ren G, Gao S, Zhou X, Kuai B (2015) Jasmonic acid promotes degreening via MYC2/3/4- and ANAC019/055/072-mediated regulation of major chlorophyll catabolic genes. Plant J 84:597–610. https://doi.org/10.1111/tpj.13030
Funding
This review received no external funding.
Author information
Authors and Affiliations
Contributions
MG and FB wrote the manuscript. AS and ML read and revised the manuscript. All the authors approved the final version of the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare no conflicts of interest.
Ethical approval
This review does not contain any studies with human participants or animals performed by any of the authors.
Additional information
Communicated by Aryadeep Roychoudhury.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Ghorbel, M., Brini, F., Sharma, A. et al. Role of jasmonic acid in plants: the molecular point of view. Plant Cell Rep 40, 1471–1494 (2021). https://doi.org/10.1007/s00299-021-02687-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00299-021-02687-4