| [1] |
Li Y, Wang H, Zhang Y, Martin C. 2018. Can the world's favorite fruit, tomato, provide an effective biosynthetic chassis for high-value metabolites? Plant Cell Reports 37:1443−50 doi: 10.1007/s00299-018-2283-8 |
| [2] |
Raiola A, Rigano MM, Calafiore R, Frusciante L, Barone A. 2014. Enhancing the health-promoting effects of tomato fruit for biofortified food. Mediators of Inflammation 2014:139873 doi: 10.1155/2014/139873 |
| [3] |
Fonseca S, Chini A, Hamberg M, Adie B, Porzel A, et al. 2009. (+)-7-iso-Jasmonoyl-L-isoleucine is the endogenous bioactive jasmonate. Nature Chemical Biology 5:344−50 doi: 10.1038/nchembio.161 |
| [4] |
Wasternack C, Song S. 2017. Jasmonates: biosynthesis, metabolism, and signaling by proteins activating and repressing transcription. Journal of Experimental Botany 68:1303−21 doi: 10.1093/jxb/erw443 |
| [5] |
Wasternack C, Strnad M. 2018. Jasmonates: news on occurrence, biosynthesis, metabolism and action of an ancient group of signaling compounds. International Journal of Molecular Sciences 19:2539 doi: 10.3390/ijms19092539 |
| [6] |
Wasternack C, Feussner I. 2018. The oxylipin pathways: biochemistry and function. Annual Review of Plant Biology 69:363−86 doi: 10.1146/annurev-arplant-042817-040440 |
| [7] |
Vick BA, Zimmerman DC. 1983. The biosynthesis of jasmonic acid: a physiological role for plant lipoxygenase. Biochemical and Biophysical Research Communications 111:470−77 doi: 10.1016/0006-291X(83)90330-3 |
| [8] |
Guan L, Denkert N, Eisa A, Lehmann M, Sjuts I, et al. 2019. JASSY, a chloroplast outer membrane protein required for jasmonate biosynthesis. Proceedings of the National Academy of Sciences of the United States of America 116:10568−75 doi: 10.1073/pnas.1900482116 |
| [9] |
Theodoulou FL, Job K, Slocombe SP, Footitt S, Holdsworth M, et al. 2005. Jasmonic acid levels are reduced in COMATOSE ATP-binding cassette transporter mutants. Implications for transport of jasmonate precursors into peroxisomes. Plant Physiology 137:835−40 doi: 10.1104/pp.105.059352 |
| [10] |
Schaller F, Biesgen C, Müssig C, Altmann T, Weiler EW. 2000. 12-Oxophytodienoate reductase 3 (OPR3) is the isoenzyme involved in jasmonate biosynthesis. Planta 210:979−84 doi: 10.1007/s004250050706 |
| [11] |
Wasternack C, Hause B. 2013. Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Annals of Botany 111:1021−58 doi: 10.1093/aob/mct067 |
| [12] |
Stintzi A, Browse J. 2000. The Arabidopsis male-sterile mutant, opr3, lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis. Proceedings of the National Academy of Sciences of the United States of America 97:10625−30 doi: 10.1073/pnas.190264497 |
| [13] |
Griffiths G. 2020. Jasmonates: biosynthesis, perception and signal transduction. Essays in Biochemistry 64:501−12 doi: 10.1042/EBC20190085 |
| [14] |
Wasternack C, Hause B. 2018. A bypass in jasmonate biosynthesis – the OPR3-independent formation. Trends in Plant Science 23:276−79 doi: 10.1016/j.tplants.2018.02.011 |
| [15] |
Chini A, Monte I, Zamarreño AM, Hamberg M, Lassueur S, et al. 2018. An OPR3-independent pathway uses 4, 5-didehydrojasmonate for jasmonate synthesis. Nature Chemical Biology 14:171−78 doi: 10.1038/nchembio.2540 |
| [16] |
Staswick PE, Tiryaki I. 2004. The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. The Plant Cell 16:2117−27 doi: 10.1105/tpc.104.023549 |
| [17] |
Staswick PE. 2009. The tryptophan conjugates of jasmonic and indole-3-acetic acids are endogenous auxin inhibitors. Plant Physiology 150:1310−21 doi: 10.1104/pp.109.138529 |
| [18] |
Kramell R, Schmidt J, Herrmann G, Schliemann W. 2005. N-(jasmonoyl)tyrosine-derived compounds from flowers of broad beans (Vicia faba). Journal of Natural Products 68:1345−49 doi: 10.1021/np0501482 |
| [19] |
Li Q, Zheng J, Li S, Huang G, Skilling SJ, et al. 2017. Transporter-mediated nuclear entry of jasmonoyl-isoleucine is essential for jasmonate signaling. Molecular Plant 10:695−708 doi: 10.1016/j.molp.2017.01.010 |
| [20] |
Pauwels L, Barbero GF, Geerinck J, Tilleman S, Grunewald W, et al. 2010. NINJA connects the co-repressor TOPLESS to jasmonate signalling. Nature 464:788−91 doi: 10.1038/nature08854 |
| [21] |
Chini A, Fonseca S, Fernández G, Adie B, Chico JM, et al. 2007. The JAZ family of repressors is the missing link in jasmonate signalling. Nature 448:666−71 doi: 10.1038/nature06006 |
| [22] |
Thines B, Katsir L, Melotto M, Niu Y, Mandaokar A, et al. 2007. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nature 448:661−65 doi: 10.1038/nature05960 |
| [23] |
Yan Y, Stolz S, Chételat A, Reymond P, Pagni M, et al. 2007. A downstream mediator in the growth repression limb of the jasmonate pathway. The Plant Cell 19:2470−83 doi: 10.1105/tpc.107.050708 |
| [24] |
Xie DX, Feys BF, James S, Nieto-Rostro M, Turner JG. 1998. COI1: an Arabidopsis gene required for jasmonate-regulated defense and fertility. Science 280:1091−94 doi: 10.1126/science.280.5366.1091 |
| [25] |
Xu L, Liu F, Lechner E, Genschik P, Crosby WL, et al. 2002. The SCF(COI1) ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis. The Plant Cell 14:1919−35 doi: 10.1105/tpc.003368 |
| [26] |
Yan J, Zhang C, Gu M, Bai Z, Zhang W, et al. 2009. The Arabidopsis CORONATINE INSENSITIVE1 protein is a jasmonate receptor. The Plant Cell 21:2220−36 doi: 10.1105/tpc.109.065730 |
| [27] |
Sheard LB, Tan X, Mao H, Withers J, Ben-Nissan G, et al. 2010. Jasmonate perception by inositol-phosphate-potentiated COI1-JAZ co-receptor. Nature 468:400−5 doi: 10.1038/nature09430 |
| [28] |
Huang H, Chen Y, Wang S, Qi T, Song S. 2023. Jasmonate action and crosstalk in flower development and fertility. Journal of Experimental Botany 74:1186−97 doi: 10.1093/jxb/erac251 |
| [29] |
Huang H, Liu B, Liu L, Song S. 2017. Jasmonate action in plant growth and development. Journal of Experimental Botany 68:1349−59 doi: 10.1093/jxb/erw495 |
| [30] |
Yan C, Xie D. 2015. Jasmonate in plant defence: sentinel or double agent? Plant Biotechnology Journal 13:1233−40 doi: 10.1111/pbi.12417 |
| [31] |
Wang J, Wu D, Wang Y, Xie D. 2019. Jasmonate action in plant defense against insects. Journal of Experimental Botany 70:3391−400 doi: 10.1093/jxb/erz174 |
| [32] |
Yan L, Zhai Q, Wei J, Li S, Wang B, et al. 2013. Role of tomato lipoxygenase D in wound-induced jasmonate biosynthesis and plant immunity to insect herbivores. PLoS Genetics 9:e1003964 doi: 10.1371/journal.pgen.1003964 |
| [33] |
Li C, Liu G, Xu C, Lee GI, Bauer P, et al. 2003. The tomato suppressor of prosystemin-mediated responses2 gene encodes a fatty acid desaturase required for the biosynthesis of jasmonic acid and the production of a systemic wound signal for defense gene expression. The Plant Cell 15:1646−61 doi: 10.1105/tpc.012237 |
| [34] |
Li L, Zhao Y, McCaig BC, Wingerd BA, Wang J, et al. 2004. The tomato homolog of CORONATINE-INSENSITIVE1 is required for the maternal control of seed maturation, jasmonate-signaled defense responses, and glandular trichome development. The Plant Cell 16:126−43 doi: 10.1105/tpc.017954 |
| [35] |
Goetz S, Hellwege A, Stenzel I, Kutter C, Hauptmann V, et al. 2012. Role of cis-12-oxo-phytodienoic acid in tomato embryo development. Plant Physiology 158:1715−27 doi: 10.1104/pp.111.192658 |
| [36] |
Scalschi L, Sanmartín M, Camañes G, Troncho P, Sánchez-Serrano JJ, et al. 2015. Silencing of OPR3 in tomato reveals the role of OPDA in callose deposition during the activation of defense responses against Botrytis cinerea. The Plant Journal 81:304−15 doi: 10.1111/tpj.12728 |
| [37] |
Saito R, Hayashi K, Nomoto H, Nakayama M, Takaoka Y, et al. 2021. Extended JAZ degron sequence for plant hormone binding in jasmonate co-receptor of tomato SlCOI1-SlJAZ. Scientific Reports 11:13612 doi: 10.1038/s41598-021-93067-1 |
| [38] |
Du M, Zhao J, Tzeng DTW, Liu Y, Deng L, et al. 2017. MYC2 orchestrates a hierarchical transcriptional cascade that regulates jasmonate-mediated plant immunity in tomato. The Plant Cell 29:1883−906 doi: 10.1105/tpc.16.00953 |
| [39] |
Ding F, Wang C, Xu N, Zhang S, Wang M. 2022. SlMYC2 mediates jasmonate-induced tomato leaf senescence by promoting chlorophyll degradation and repressing carbon fixation. Plant Physiology and Biochemistry 180:27−34 doi: 10.1016/j.plaphy.2022.03.026 |
| [40] |
Wang Z, Gao M, Li Y, Zhang J, Su H, et al. 2022. The transcription factor SlWRKY37 positively regulates jasmonic acid- and dark-induced leaf senescence in tomato. Journal of Experimental Botany 73:6207−25 doi: 10.1093/jxb/erac258 |
| [41] |
Chen Y, Feng P, Tang B, Hu Z, Xie Q, et al. 2022. The AP2/ERF transcription factor SlERF. F5 functions in leaf senescence in tomato. Plant Cell Report 41:1181−95 doi: 10.1007/s00299-022-02846-1 |
| [42] |
Kang JH, Campos ML, Zemelis-Durfee S, Al-Haddad JM, Jones AD, et al. 2016. Molecular cloning of the tomato Hairless gene implicates actin dynamics in trichome-mediated defense and mechanical properties of stem tissue. Journal of Experimental Botany 67:5313−24 doi: 10.1093/jxb/erw292 |
| [43] |
Kang JH, Shi F, Jones AD, Marks MD, Howe GA. 2010. Distortion of trichome morphology by the hairless mutation of tomato affects leaf surface chemistry. Journal of Experimental Botany 61:1053−64 doi: 10.1093/jxb/erp370 |
| [44] |
Peiffer M, Tooker JF, Luthe DS, Felton GW. 2009. Plants on early alert: glandular trichomes as sensors for insect herbivores. New Phytologist 184:644−56 doi: 10.1111/j.1469-8137.2009.03002.x |
| [45] |
Luckwill LC. 1943. The genus Lycopersicon: a historical, biological and taxonomic survey of the wild and cultivated tomatoes. pp 44. Aberdeen, The University Press. |
| [46] |
McDowell ET, Kapteyn J, Schmidt A, Li C, Kang JH, et al. 2011. Comparative functional genomic analysis of Solanum glandular trichome types. Plant Physiology 155:524−39 doi: 10.1104/pp.110.167114 |
| [47] |
Schilmiller AL, Moghe GD, Fan P, Ghosh B, Ning J, et al. 2015. Functionally divergent alleles and duplicated loci encoding an acyltransferase contribute to acylsugar metabolite diversity in Solanum trichomes. The Plant Cell 27:1002−17 doi: 10.1105/tpc.15.00087 |
| [48] |
Balcke GU, Bennewitz S, Bergau N, Athmer B, Henning A, et al. 2017. Multi-omics of tomato glandular trichomes reveals distinct features of central carbon metabolism supporting high productivity of specialized metabolites. The Plant Cell 29:960−83 doi: 10.1105/tpc.17.00060 |
| [49] |
Hua B, Chang J, Xu Z, Han X, Xu M, et al. 2021. HOMEODOMAIN PROTEIN8 mediates jasmonate-triggered trichome elongation in tomato. New Phytologist 230:1063−77 doi: 10.1111/nph.17216 |
| [50] |
Boughton AJ, Hoover K, Felton GW. 2005. Methyl jasmonate application induces increased densities of glandular trichomes on tomato, Lycopersicon esculentum. Journal of Chemical Ecology 31:2211−16 doi: 10.1007/s10886-005-6228-7 |
| [51] |
Yang C, Li H, Zhang J, Luo Z, Gong P, et al. 2011. A regulatory gene induces trichome formation and embryo lethality in tomato. Proceedings of the National Academy of Sciences of the United States of America 108:11836−41 doi: 10.1073/pnas.1100532108 |
| [52] |
Kanwar MK, Yu J, Zhou J. 2018. Phytomelatonin: recent advances and future prospects. Journal of Pineal Research 65:e12526 doi: 10.1111/jpi.12526 |
| [53] |
Hua B, Chang J, Han X, Xu Z, Hu S, et al. 2022. H and HL synergistically regulate jasmonate-triggered trichome formation in tomato. Horticulture Research 9:uhab080 doi: 10.1093/hr/uhab080 |
| [54] |
Hua B, Chang J, Wu M, Xu Z, Zhang F, et al. 2021. Mediation of JA signalling in glandular trichomes by the woolly/SlMYC1 regulatory module improves pest resistance in tomato. Plant Biotechnology Journal 19:375−93 doi: 10.1111/pbi.13473 |
| [55] |
Shu P, Li Z, Min D, Zhang X, Ai W, et al. 2020. CRISPR/Cas9-Mediated SlMYC2 mutagenesis adverse to Tomato plant growth and meja-induced fruit resistance to Botrytis cinerea. Journal of Agricultural and Food Chemistry 68:5529−38 doi: 10.1021/acs.jafc.9b08069 |
| [56] |
Dobritzsch S, Weyhe M, Schubert R, Dindas J, Hause G, et al. 2015. Dissection of jasmonate functions in tomato stamen development by transcriptome and metabolome analyses. BMC Biology 13:28 doi: 10.1186/s12915-015-0135-3 |
| [57] |
Niwa T, Suzuki T, Takebayashi Y, Ishiguro R, Higashiyama T, et al. 2018. Jasmonic acid facilitates flower opening and floral organ development through the upregulated expression of SlMYB21 transcription factor in tomato. Bioscience, Biotechnology, and Biochemistry 82:292−303 doi: 10.1080/09168451.2017.1422107 |
| [58] |
Schubert R, Dobritzsch S, Gruber C, Hause G, Athmer B, et al. 2019. Tomato MYB21 acts in ovules to mediate jasmonate-regulated fertility. The Plant Cell 31:1043−62 doi: 10.1105/tpc.18.00978 |
| [59] |
Zhang Y, Xing H, Wang H, Yu L, Yang Z, et al. 2022. SlMYC2 interacted with the SlTOR promoter and mediated JA signaling to regulate growth and fruit quality in tomato. Frontiers in Plant Science 13:1013445 doi: 10.3389/fpls.2022.1013445 |
| [60] |
Liu L, Wei J, Zhang M, Zhang L, Li C, et al. 2012. Ethylene independent induction of lycopene biosynthesis in tomato fruits by jasmonates. Journal of Experimental Botany 63:5751−61 doi: 10.1093/jxb/ers224 |
| [61] |
Miersch O, Neumerkel J, Dippe M, Stenzel I, Wasternack C. 2008. Hydroxylated jasmonates are commonly occurring metabolites of jasmonic acid and contribute to a partial switch-off in jasmonate signaling. New Phytologist 177:114−27 doi: 10.1111/j.1469-8137.2007.02252.x |
| [62] |
Fowler JH, Narváez-Vásquez J, Aromdee DN, Pautot V, Holzer FM, et al. 2009. Leucine aminopeptidase regulates defense and wound signaling in tomato downstream of jasmonic acid. The Plant Cell 21:1239−51 doi: 10.1105/tpc.108.065029 |
| [63] |
Li Z, Peng R, Yao Q. 2021. SlMYB14 promotes flavonoids accumulation and confers higher tolerance to 2, 4, 6-trichlorophenol in tomato. Plant Science 303:110796 doi: 10.1016/j.plantsci.2020.110796 |
| [64] |
Chen Y, Kim P, Kong L, Wang X, Tan W, et al. 2022. A dual-function transcription factor, SlJAF13, promotes anthocyanin biosynthesis in tomato. Journal of Experimental Botany 73:5559−80 doi: 10.1093/jxb/erac209 |
| [65] |
Chen H, Jones AD, Howe GA. 2006. Constitutive activation of the jasmonate signaling pathway enhances the production of secondary metabolites in tomato. FEBS Letters 580:2540−46 doi: 10.1016/j.febslet.2006.03.070 |
| [66] |
Abdelkareem A, Thagun C, Nakayasu M, Mizutani M, Hashimoto T, et al. 2017. Jasmonate-induced biosynthesis of steroidal glycoalkaloids depends on COI1 proteins in tomato. Biochemical and Biophysical Research Communications 489:206−10 doi: 10.1016/j.bbrc.2017.05.132 |
| [67] |
Cárdenas PD, Sonawane PD, Pollier J, Vanden Bossche R, Dewangan V, et al. 2016. GAME9 regulates the biosynthesis of steroidal alkaloids and upstream isoprenoids in the plant mevalonate pathway. Nature Communications 7:10654 doi: 10.1038/ncomms10654 |
| [68] |
Wang Y, Mostafa S, Zeng W, Jin B. 2021. Function and mechanism of jasmonic acid in plant responses to abiotic and biotic stresses. International Journal of Molecular Sciences 22:8568 doi: 10.3390/ijms22168568 |
| [69] |
Xu B, Wang J, Peng Y, Huang H, Sun L, et al. 2022. SlMYC2 mediates stomatal movement in response to drought stress by repressing SlCHS1 expression. Frontiers in Plant Science 13:952758 doi: 10.3389/fpls.2022.952758 |
| [70] |
Zhao W, Huang H, Wang J, Wang X, Xu B, et al. 2023. Jasmonic acid enhances osmotic stress responses by MYC2-mediated inhibition of protein phosphatase 2C1 and response regulators 26 transcription factor in tomato. The Plant Journal 113:546−61 doi: 10.1111/tpj.16067 |
| [71] |
Pan C, Yang D, Zhao X, Jiao C, Yan Y, et al. 2019. Tomato stigma exsertion induced by high temperature is associated with the jasmonate signalling pathway. Plant, Cell & Environment 42:1205−21 doi: 10.1111/pce.13444 |
| [72] |
Min D, Li F, Zhang X, Cui X, Shu P, et al. 2018. SlMYC2 involved in methyl jasmonate-induced tomato fruit chilling tolerance. Journal of Agricultural and Food Chemistry 66:3110−17 doi: 10.1021/acs.jafc.8b00299 |
| [73] |
Min D, Zhou J, Li J, Ai W, Li Z, et al. 2021. SlMYC2 targeted regulation of polyamines biosynthesis contributes to methyl jasmonate-induced chilling tolerance in tomato fruit. Postharvest Biology and Technology 174:111443 doi: 10.1016/j.postharvbio.2020.111443 |
| [74] |
Ding F, Ren L, Xie F, Wang M, Zhang S. 2021. Jasmonate and melatonin act synergistically to potentiate cold tolerance in tomato plants. Frontiers in Plant Science 12:763284 doi: 10.3389/fpls.2021.763284 |
| [75] |
Wang F, Guo Z, Li H, Wang M, Onac E, et al. 2016. Phytochrome A and B function antagonistically to regulate cold tolerance via abscisic acid-dependent jasmonate signaling. Plant Physiology 170:459−71 doi: 10.1104/pp.15.01171 |
| [76] |
Ding F, Wang X, Li Z, Wang M. 2023. Jasmonate positively regulates cold tolerance by promoting ABA biosynthesis in tomato. Plants 12:60 doi: 10.3390/plants12010060 |
| [77] |
Bali S, Jamwal VL, Kohli SK, Kaur P, Tejpal R, et al. 2019. Jasmonic acid application triggers detoxification of lead (Pb) toxicity in tomato through the modifications of secondary metabolites and gene expression. Chemosphere 235:734−48 doi: 10.1016/j.chemosphere.2019.06.188 |
| [78] |
Thaler JS, Stout MJ, Karban R, Duffey SS. 2001. Jasmonate-mediated induced plant resistance affects a community of herbivores. Ecological Entomology 26:312−24 doi: 10.1046/j.1365-2311.2001.00324.x |
| [79] |
Li C, Schilmiller AL, Liu G, Lee GI, Jayanty S, et al. 2005. Role of β-oxidation in jasmonate biosynthesis and systemic wound signaling in tomato. The Plant Cell 17:971−86 doi: 10.1105/tpc.104.029108 |
| [80] |
Tian D, Peiffer M, De Moraes CM, Felton GW. 2014. Roles of ethylene and jasmonic acid in systemic induced defense in tomato (Solanum lycopersicum) against Helicoverpa zea. Planta 239:577−89 doi: 10.1007/s00425-013-1997-7 |
| [81] |
Zhang P, Wei J, Zhao C, Zhang Y, Li C, et al. 2019. Airborne host-plant manipulation by whiteflies via an inducible blend of plant volatiles. Proceedings of the National Academy of Sciences of the United States of America 116:7387−96 doi: 10.1073/pnas.1818599116 |
| [82] |
Escobar-Bravo R, Chen G, Kim HK, Grosser K, van Dam NM, et al. 2019. Ultraviolet radiation exposure time and intensity modulate tomato resistance to herbivory through activation of jasmonic acid signaling. Journal of Experimental Botany 70:315−27 doi: 10.1093/jxb/ery347 |
| [83] |
Hu C, Wei C, Ma Q, Dong H, Shi K, et al. 2021. Ethylene response factors 15 and 16 trigger jasmonate biosynthesis in tomato during herbivore resistance. Plant Physiology 185:1182−97 doi: 10.1093/plphys/kiaa089 |
| [84] |
Hu C, Wu S, Li J, Dong H, Zhu C, et al. 2022. Herbivore-induced Ca2+ signals trigger a jasmonate burst by activating ERF16-mediated expression in tomato. New Phytologist 236:1796−808 doi: 10.1111/nph.18455 |
| [85] |
Cooper WR, Jia L, Goggin L. 2005. Effects of jasmonate-induced defenses on root-knot nematode infection of resistant and susceptible tomato cultivars. Journal of Chemical Ecology 31:1953−67 doi: 10.1007/s10886-005-6070-y |
| [86] |
Fan J, Hu C, Zhang L, Li Z, Zhao F, Wang S. 2015. Jasmonic acid mediates tomato’s response to root knot nematodes. Journal of Plant Growth Regulation 34:196−205 doi: 10.1007/s00344-014-9457-6 |
| [87] |
Sun Y, Cao H, Yin J, Kang L, Ge F. 2010. Elevated CO2 changes the interactions between nematode and tomato genotypes differing in the JA pathway. Plant, Cell & Environment 33:729−39 doi: 10.1111/j.1365-3040.2009.02098.x |
| [88] |
Zhao W, Li Z, Fan J, Hu C, Yang R, et al. 2015. Identification of jasmonic acid-associated microRNAs and characterization of the regulatory roles of the miR319/TCP4 module under root-knot nematode stress in tomato. Journal of Experimental Botany 66:4653−67 doi: 10.1093/jxb/erv238 |
| [89] |
Shang Y, Wang K, Sun S, Zhou J, Yu J. 2019. COP9 Signalosome CSN4 and CSN5 subunits are involved in jasmonate-dependent defense against root-knot nematode in Tomato. Frontiers in Plant Science 10:1223 doi: 10.3389/fpls.2019.01223 |
| [90] |
ZZou J, Zhao Q, Yang T, Shang Y, Ahammed GJ, et al. 2022. The E3 ubiquitin ligase RING1 interacts with COP9 Signalosome Subunit 4 to positively regulate resistance to root-knot nematodes in Solanum lycopersicum L. Plant Science 322:111344 doi: 10.1016/j.plantsci.2022.111344 |
| [91] |
Wang G, Hu C, Zhou J, Liu Y, Cai J, et al. 2019. Systemic root-shoot signaling drives jasmonate-based root defense against nematodes. Current Biology 29:3430−3438.E4 doi: 10.1016/j.cub.2019.08.049 |
| [92] |
Xu X, Fang P, Zhang H, Chi C, Song L, et al. 2019. Strigolactones positively regulate defense against root-knot nematodes in tomato. Journal of Experimental Botany 70:1325−37 doi: 10.1093/jxb/ery439 |
| [93] |
AbuQamar S, Chai MF, Luo H, Song F, Mengiste T. 2008. Tomato protein kinase 1b mediates signaling of plant responses to necrotrophic fungi and insect herbivory. The Plant Cell 20:1964−83 doi: 10.1105/tpc.108.059477 |
| [94] |
Campos ML, Kang JH, Howe GA. 2014. Jasmonate-triggered plant immunity. Journal of Chemical Ecology 40:657−75 doi: 10.1007/s10886-014-0468-3 |
| [95] |
Thaler JS, Owen B, Higgins VJ. 2004. The role of the jasmonate response in plant susceptibility to diverse pathogens with a range of lifestyles. Plant Physiology 135:530−38 doi: 10.1104/pp.104.041566 |
| [96] |
Min D, Li F, Cui X, Zhou J, Li J, et al. 2020. SlMYC2 are required for methyl jasmonate-induced tomato fruit resistance to Botrytis cinerea. Food Chemistry 310:125901 doi: 10.1016/j.foodchem.2019.125901 |
| [97] |
Liu Y, Du M, Deng L, Shen J, Fang M, et al. 2019. MYC2 regulates the termination of jasmonate signaling via an autoregulatory negative feedback loop. The Plant Cell 31:106−27 doi: 10.1105/tpc.18.00405 |
| [98] |
Zhang L, Song Y, Liu K, Gong F. 2021. The tomato Mediator subunit MED8 positively regulates plant response to Botrytis cinerea. Journal of Plant Physiology 266:153533 doi: 10.1016/j.jplph.2021.153533 |
| [99] |
Jaiswal N, Liao CJ, Mengesha B, Han H, Lee S, et al. 2022. Regulation of plant immunity and growth by tomato receptor-like cytoplasmic kinase TRK1. New Phytologist 233:458−78 doi: 10.1111/nph.17801 |
| [100] |
Huang H, Zhao W, Li C, Qiao H, Song S, et al. 2022. SlVQ15 interacts with jasmonate-ZIM domain proteins and SlWRKY31 to regulate defense response in tomato. Plant Physiology 190:828−42 doi: 10.1093/plphys/kiac275 |
| [101] |
Ortigosa A, Gimenez-Ibanez S, Leonhardt N, Solano R. 2019. Design of a bacterial speck resistant tomato by CRISPR/Cas9-mediated editing of SlJAZ2. Plant Biotechnology Journal 17:665−73 doi: 10.1111/pbi.13006 |
| [102] |
Zhao Y, Thilmony R, Bender CL, Schaller A, He SY, et al. 2003. Virulence systems of Pseudomonas syringae pvtomato promote bacterial speck disease in tomato by targeting the jasmonate signaling pathway. The Plant Journal 36:485−99 doi: 10.1046/j.1365-313X.2003.01895.x |