Published June 30, 2020
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Relative contribution of LOX10, green leaf volatiles and JA to woundinduced local and systemic oxylipin and hormone signature in Zea mays (maize)
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- 1. Jiangxi Key Laboratory of Crop Physiology, Ecology and Genetic Breeding, Ministry of Education, Jiangxi Agricultural University, Nanchang, 330045, China & ∗ & Department of Plant Pathology and Microbiology, Texas A&M University, College Station, TX, 77843, USA
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He, Yongming, Borrego, Eli J., Gorman, Zachary, Huang, Pei-Cheng, Kolomiets, Michael V. (2020): Relative contribution of LOX10, green leaf volatiles and JA to woundinduced local and systemic oxylipin and hormone signature in Zea mays (maize). Phytochemistry (112334) 174: 1-15, DOI: 10.1016/j.phytochem.2020.112334, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112334
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- urn:lsid:plazi.org:pub:FFBBFFD07E1CFFAEFFB6F171B53AFFC9
References
- Allmann, S., Halitschke, R., Schuurink, R.C., Baldwin, I.T., 2010. Oxylipin channelling in Nicotiana attenuata: lipoxygenase 2 supplies substrates for green leaf volatile production. Plant Cell Environ. 33, 2028-2040. https://doi.org/10.1111/j.1365-3040. 2010.02203.x.
- Almeras, E., Stolz, S., Vollenweider, S., Reymond, P., Mene-Saffrane, L., Farmer, E.E., 2003. Reactive electrophile species activate defense gene expression in Arabidopsis. Plant J. 34, 205-216. https://doi.org/10.1046/j.1365-313X.2003.01718.x.
- Ameye, M., Allmann, S., Verwaeren, J., Smagghe, G., Haesaert, G., Schuurink, R.C., Audenaert, K., 2018. Green leaf volatile production by plants: a meta-analysis. New Phytol. 220, 666-683. https://doi.org/10.1111/nph.14671.
- Borrego, E.J., Kolomiets, M.V., 2016. Synthesis and functions of jasmonates in maize. Plants 5, 41. https://doi.org/10.3390/plants5040041.
- Bozorov, T.A., Dinh, S.T., Baldwin, I.T., 2017. JA but not JA-Ile is the cell-nonautonomous signal activating JA mediated systemic defenses to herbivory in Nicotiana attenuata. J. Integr. Plant Biol. 59, 552-571. https://doi.org/10.1111/jipb. 12545.
- 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.
- Brilli, F., Ruuskanen, T.M., Schnitzhofer, R., Muller, M., Breitenlechner, M., Bittner, V., Wohlfahrt, G., Loreto, F., Hansel, A., 2011. Detection of plant volatiles after leaf wounding and darkening by proton transfer reaction "time-of-flight" mass spectrometry (PTR-TOF). PloS One 6, e20419. https://doi.org/10.1371/journal.pone. 0020419.
- Chauvin, A., Caldelari, D., Wolfender, J., Farmer, E.E., 2013. Four 13-lipoxygenases contribute to rapid jasmonate synthesis in wounded Arabidopsis thaliana leaves: a role for lipoxygenase 6 in responses to long-distance wound signals. New Phytol. 197, 566-575. https://doi.org/10.1111/nph.12029.
- Chauvin, A., Lenglet, A., Wolfender, J.-L., Farmer, E.E., 2016. Paired hierarchical organization of 13-lipoxygenases in Arabidopsis. Plants 5, 16. https://doi.org/10.3390/ plants5020016.
- Chehab, E.W., Kaspi, R., Savchenko, T., Rowe, H., Negre-Zakharov, F., Kliebenstein, D., Dehesh, K., 2008. Distinct roles of jasmonates and aldehydes in plant-defense responses. PloS One 3, e1904. https://doi.org/10.1371/journal.pone.0001904.
- Chini, A., Monte, I., Zamarreno, A.M., Hamberg, M., Lassueur, S., Reymond, P., Weiss, S., Stintzi, A., Schaller, A., Porzel, A., Garcia-Mina, J.M., 2018. An OPR3-independent pathway uses 4, 5-didehydrojasmonate for jasmonate synthesis. Nat. Chem. Biol. 14, 171-178. https://doi.org/10.1038/nchembio.2540.
- Christensen, S.A., Huffaker, A., Kaplan, F., Sims, J., Ziemann, S., Doehlemann, G., Ji, L., Schmitz, R.J., Kolomiets, M.V., Alborn, H.T., Mori, N., Jander, G., Ni, X., Sartor, R.C., Byers, S., Abdo, Z., Schmelz, E.A., 2015. Maize death acids, 9-lipoxygenase-derived cyclopente(a)nones, display activity as cytotoxic phytoalexins and transcriptional mediators. Proc. Natl. Acad. Sci. U.S.A. 112, 11407-11412. https://doi.org/10.1073/ pnas.1511131112.
- Christensen, S.A., Kolomiets, M.V., 2011. The lipid language of plant-fungal interactions. Fungal Genet. Biol. 48, 4-14. https://doi.org/10.1016/j.fgb.2010.05.005.
- Christensen, S.A., Nemchenko, A., Borrego, E., Murray, I., Sobhy, I.S., Bosak, L., DeBlasio, S., Erb, M., Robert, C.A.M., Vaughn, K.A., Herrfurth, C., Tumlinson, J., Feussner, I., Jackson, D., Turlings, T.C.J., Engelberth, J., Nansen, C., Meeley, R., Kolomiets, M.V., 2013. The maize lipoxygenase, ZmLOX10, mediates green leaf volatile, jasmonate and herbivore-induced plant volatile production for defense against insect attack. Plant J. 74, 59-73. https://doi.org/10.1111/tpj.12101.
- Christensen, S.A., Nemchenko, A., Park, Y., Borrego, E., Huang, P.C., Schmelz, E.A., Kunze, S., Feussner, I., Yalpani, N., Meeley, R., Kolomiets, M.V., 2014. The novel monocot-specific 9-lipoxygenase ZmLOX12 is required to mount an effective jasmonate-mediated defense against fusarium verticillioides in maize. Mol. Plant Microbe Interact. 27, 1263-1276. https://doi.org/10.1094/MPMI-06-13-0184-R.
- Engelberth, J., Alborn, H.T., Schmelz, E.A., Tumlinson, J.H., 2004. Airborne signals prime plants against insect herbivore attack. Proc. Natl. Acad. Sci. U.S.A. 101, 1781-1785. https://doi.org/10.1073/pnas.0308037100.
- Engelberth, J., Contreras, C.F., Dalvi, C., Li, T., Engelberth, M., 2013. Early transcriptome analyses of Z-3-hexenol-treated Zea mays revealed distinct transcriptional networks and anti-herbivore defense potential of green leaf volatiles. PloS One 8, e77465. https://doi.org/10.1371/journal.pone.0077465.
- 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.
- Gao, X., Stumpe, M., Feussner, I., Kolomiets, M., 2008. A novel plastidial lipoxygenase of maize (Zea mays) ZmLOX6 encodes for a fatty acid hydroperoxide lyase and is uniquely regulated by phytohormones and pathogen infection. Planta 227, 491-503. https://doi.org/10.1007/s00425-007-0634-8.
- Ghanem, M.E., Ghars, M.A., Frettinger, P., Perez-Alfocea, F., Lutts, S., Wathelet, J., du Jardin, P., Fauconnier, M., 2012. Organ-dependent oxylipin signature in leaves and roots of salinized tomato plants (Solanum lycopersicum). J. Plant Physiol. 169, 1090-1101. https://doi.org/10.1016/j.jplph.2012.03.015.
- Glauser, G., Dubugnon, L., Mousavi, S.A.R., Rudaz, S., Wolfender, J., Farmer, E.E., 2009. Velocity estimates for signal propagation leading to systemic jasmonic acid accumulation in wounded Arabidopsis. J. Biol. Chem. 284, 34506-34513. https://doi. org/10.1074/jbc.M109.061432.
- Glazebrook, J., 2005. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol. 43, 205-227. https://doi.org/10.1146/ annurev.phyto.43.040204.135923.
- Gorman, Z., Christensen, S.A., Yan, Y., He, Y., Borrego, E., Kolomiets, M.V., 2020. Green leaf volatiles and jasmonic acid enhance susceptibility to anthracnose diseases caused by Colletotrichum graminicola in maize. Mol. Plant Pathol. https://doi.org/10.1111/ mpp.12924.
- Halitschke, R., Ziegler, J., Keinanen, M., Baldwin, I.T., 2004. Silencing of hydroperoxide lyase and allene oxide synthase reveals substrate and defense signaling crosstalk in Nicotiana attenuata. Plant J. 40, 35-46. https://doi.org/10.1111/j.1365-313X.2004. 02185.x.
- Heitz, T., Widemann, E., Lugan, R., Miesch, L., Ullmann, P., Desaubry, L., Holder, E., Grausem, B., Kandel, S., Miesch, M., Werck-Reichhart, D., Pinot, F., 2012. Cytochromes P450 CYP94C1 and CYP94B3 catalyze two successive oxidation steps of plant hormone jasmonoyl-isoleucine for catabolic turnover. J. Biol. Chem. 287, 6296-6306. https://doi.org/10.1074/jbc.M111.316364.
- Heyer, M., Reichelt, M., Mithofer, A., 2018. A holistic approach to analyze systemic jasmonate accumulation in individual leaves of Arabidopsis rosettes upon wounding. Front. Plant Sci. 9, 1569. https://doi.org/10.3389/fpls.2018.01569.
- Howe, G.A., Jander, G., 2008. Plant immunity to insect herbivores. Annu. Rev. Plant Biol. 59, 41-66. https://doi.org/10.1146/annurev.arplant.59.032607.092825.
- Kallenbach, M., Gilardoni, P.A., Allmann, S., Baldwin, I.T., Bonaventure, G., 2011. C12 derivatives of the hydroperoxide lyase pathway are produced by product recycling through lipoxygenase-2 in Nicotiana attenuata leaves. New Phytol. 191, 1054-1068. https://doi.org/10.1146/10.1111/j.1469-8137.2011.03767.x.
- Kim, E., Choi, E., Kim, Y., Cho, K., Lee, A., Shim, J., Rakwal, R., Agrawal, G.K., Han, O., 2003. Dual positional specificity and expression of non-traditional lipoxygenase induced by wounding and methyl jasmonate in maize seedlings. Plant Mol. Biol. 52, 1203-1213. https://doi.org/10.1023/B:PLAN.0000004331.94803.b0.
- Koo, A.J.K., Gao, X., Daniel Jones, A., Howe, G.A., 2009. A rapid wound signal activates the systemic synthesis of bioactive jasmonates in Arabidopsis. Plant J. 59, 974-986. https://doi.org/10.1016/10.1111/j.1365-313X.2009.03924.x.
- Koo, A.J., Thireault, C., Zemelis, S., Poudel, A.N., Zhang, T., Kitaoka, N., Brandizzi, F., Matsuura, H., Howe, G.A., 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.
- Lee, B., Lee, S., Ryu, C.M., 2012. Foliar aphid feeding recruits rhizosphere bacteria and primes plant immunity against pathogenic and non-pathogenic bacteria in pepper. Ann. Bot. 110, 281-290. https://doi.org/10.1093/aob/mcs055.
- Leon, J., Royo, J., Vancanneyt, G., Sanz, C., Silkowski, H., Griffiths, G., Sanchez-Serrano, J.J., 2002. Lipoxygenase H1 gene silencing reveals a specific role in supplying fatty acid hydroperoxides for aliphatic aldehyde production. J. Biol. Chem. 277, 416-423. https://doi.org/10.1074/jbc.M107763200.
- Li, L., Li, C., Lee, G.I., Howe, G.A., 2002. Distinct roles for jasmonate synthesis and action in the systemic wound response of tomato. Proc. Natl. Acad. Sci. U.S.A. 99, 6416-6421. https://doi.org/10.1073/pnas.072072599.
- Li, T., Cofer, T., Engelberth, M., Engelberth, J., 2016. Defense priming and jasmonates: a role for free fatty acids in insect elicitor-induced long distance signaling. Plants 5, 5. https://doi.org/10.3390/plants5010005.
- Lunde, C., Kimberlin, A., Leiboff, S., Koo, A.J., Hake, S., 2019. Tasselseed5 overexpresses a wound-inducible enzyme, ZmCYP94B1, that affects jasmonate catabolism, sex determination, and plant architecture in maize. Commun. Biol. 2, 114. https://doi.org/ 10.1038/s42003-019-0354-1.
- Matsui, K., Sugimoto, K., Mano, J., Ozawa, R., Takabayashi, J., 2012. Differential metabolisms of green leaf volatiles in injured and intact parts of a wounded leaf meet distinct ecophysiological requirements. PloS One 7, e36433. https://doi.org/10. 1371/journal.pone.0036433.
- Mochizuki, S., Sugimoto, K., Koeduka, T., Matsui, K., 2016. Arabidopsis lipoxygenase 2 is essential for formation of green leaf volatiles and five-carbon volatiles. FEBS Lett. 590, 1017-1027. https://doi.org/10.1371/10.1002/1873-3468.12133.
- Mosblech, A., Feussner, I., Heilmann, I., 2009. Oxylipins: structurally diverse metabolites from fatty acid oxidation. Plant Physiol. Biochem. (Paris) 47, 511-517. https://doi. org/10.1016/j.plaphy.2008.12.011.
- Nakashima, A., von Reuss, S.H., Tasaka, H., Nomura, M., Mochizuki, S., Iijima, Y., Aoki, K., Shibata, D., Boland, W., Takabayashi, J., Matsui, K., 2013. Traumatin- and Dinortraumatin-containing Galactolipids in Arabidopsis: their formation in tissuedisrupted leaves as counterparts of green leaf volatiles. J. Biol. Chem. 288, 26078-26088. https://doi.org/10.1074/jbc.M113.487959.
- Nemchenko, A., Kunze, S., Feussner, I., Kolomiets, M., 2006. Duplicate maize 13-lipoxygenase genes are differentially regulated by circadian rhythm, cold stress, wounding, pathogen infection, and hormonal treatments. J. Exp. Bot. 57, 3767-3779. https://doi.org/10.1093/jxb/erl137.
- Ogunola, O.F., Hawkins, L.K., Mylroie, E., Kolomiets, M.V., Borrego, E., Tang, J.D., Williams, W.P., Warburton, M.L., 2017. Characterization of the maize lipoxygenase gene family in relation to aflatoxin accumulation resistance. PloS One 12, e181265. https://doi.org/10.1371/journal.pone.0181265.
- Ollerstam, O., Larsson, S., 2003. Salicylic acid mediates resistance in the willow Salix viminalis against the gall midge Dasineura marginemtorquens. J. Chem. Ecol. 29, 163-174. https://doi.org/10.1023/A:1021936832258.
- Pare, P.W., Tumlinson, J.H., 1999. Plant volatiles as a defense against insect herbivores. Plant Physiol. 121, 325-332. https://doi.org/10.1104/pp.121.2.325.
- Park, Y., Kunze, S., Ni, X., Feussner, I., Kolomiets, M.V., 2010. Comparative molecular and biochemical characterization of segmentally duplicated 9-lipoxygenase genes ZmLOX4 and ZmLOX5 of maize. Planta 231, 1425-1437. https://doi.org/10.1007/ s00425-010-1143-8.
- Qi, J., Sun, G., Wang, L., Zhao, C., Hettenhausen, C., Schuman, M.C., Baldwin, I.T., Li, J., Song, J., Liu, Z., Xu, G., Lu, X., Wu, J., 2016. Oral secretions from Mythimna separata insects specifically induce defence responses in maize as revealed by high-dimensional biological data. Plant Cell Environ. 39, 1749-1766. https://doi.org/10.1111/ pce.12735.
- Saeed, A.I., Sharov, V., White, J., Li, J., Liang, W., Bhagabati, N., Braisted, J., Klapa, M., Currier, T., Thiagarajan, M., Sturn, A., Snuffin, M., Rezantsev, A., Popov, D., Ryltsov, A., Kostukovich, E., Borisovsky, I., Liu, Z., Vinsavich, A., Trush, V., Quackenbush, J., 2003. TM4: a free, open-source system for microarray data management and analysis. Biotechniques 34, 374-378. https://doi.org/10.2144/03342mt01.
- Salch, Y.P., Grove, M.J., Takamura, H., Gardner, H.W., 1995. Characterization of a C-5,13-cleaving enzyme of 13(S)-hydroperoxide of linolenic acid by soybean seed. Plant Physiol. 108, 1211-1218. https://doi.org/10.1104/pp.108.3.1211.
- Scala, A., Allmann, S., Mirabella, R., Haring, M., Schuurink, R., 2013. Green leaf volatiles: a plant's multifunctional weapon against herbivores and pathogens. Int. J. Mol. Sci. 14, 17781-17811. https://doi.org/10.3390/ijms140917781.
- Schulze, A., Zimmer, M., Mielke, S., Stellmach, H., Melnyk, C.W., Hause, B., Gasperini, D., 2019. Wound-induced shoot-to-root relocation of JA-Ile precursors coordinates Arabidopsis growth. Mol. Plant 12, 1383-1394. https://doi.org/10.1016/j.molp. 2019.05.013.
- Schuman, M.C., Baldwin, I.T., 2016. The layers of plant responses to insect herbivores. Annu. Rev. Entomol. 61, 373-394. https://doi.org/10.1146/annurev-ento-010715- 023851.
- Shen, J., Tieman, D., Jones, J.B., Taylor, M.G., Schmelz, E., Huffaker, A., Bies, D., Chen, K., Klee, H.J., 2014. A 13-lipoxygenase, TomloxC, is essential for synthesis of C5 flavour volatiles in tomato. J. Exp. Bot. 65, 419-428. https://doi.org/10.1093/jxb/ ert382.
- Steppuhn, A., Gaquerel, E., Baldwin, I.T., 2010. The two α-dox genes of Nicotiana attenuata: overlapping but distinct functions in development and stress responses. BMC Plant Biol. 10, 171. https://doi.org/10.1186/1471-2229-10-171.
- Szczegielniak, J., Borkiewicz, L., Szurmak, B., Lewandowska-Gnatowska, E., Statkiewicz, M., Klimecka, M., Ciesla, J., Muszynska, G., 2012. Maize calcium-dependent protein kinase (ZmCPK11): local and systemic response to wounding, regulation by touch and components of jasmonate signaling. Physiol. Plantarum 146, 1-14. https://doi.org/ 10.1111/j.1399-3054.2012.01587.x.
- 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.
- Thaler, J.S., Bostock, R.M., 2004. Interactions between abscisic-acid-mediated responses and plant resistance to pathogens and insects. Ecology 85, 48-58. https://doi.org/10. 1890/02-0710.
- Tolley, J.P., Nagashima, Y., Gorman, Z., Kolomiets, M.V., Koiwa, H., 2018. Isoform-specific subcellular localization of Zea mays lipoxygenases and oxo-phytodienoate reductase 2. Plant Gene 13, 36-41. https://doi.org/10.1016/j.plgene.2017.12.002.
- Tong, X., Qi, J., Zhu, X., Mao, B., Zeng, L., Wang, B., Li, Q., Zhou, G., Xu, X., Lou, Y., He, Z., 2012. The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway. Plant J. 71, 763-775. https://doi.org/10.1111/j. 1365-313X.2012.05027.x.
- Tzin, V., Hojo, Y., Strickler, S.R., Bartsch, L.J., Archer, C.M., Ahern, K.R., Zhou, S., Christensen, S.A., Galis, I., Mueller, L.A., Jander, G., 2017. Rapid defense responses in maize leaves induced by Spodoptera exigua caterpillar feeding. J. Exp. Bot. 68, 4709-4723. https://doi.org/10.1093/jxb/erx274.
- van Den Dool, H., Kratz, P.H., 1963. A generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. J. Chromatogr. 11, 463-471. https://doi.org/10.1016/S0021-9673(01)80947-X.
- Varsani, S., Grover, S., Zhou, S., Koch, K.G., Huang, P.C., Kolomiets, M.V., Williams, W.P., Heng-Moss, T., Sarath, G., Luthe, D.S., Jander, G., Louis, J., 2019. 12-oxo-phytodienoic acid acts as a regulator of maize defense against corn leaf aphid. Plant Physiol. 179, 1402-1415. https://doi.org/10.1104/pp.18.01472.
- Vicente, J., Cascon, T., Vicedo, B., Garcia-Agustin, P., Hamberg, M., Castresana, C., 2012. Role of 9-lipoxygenase and α-dioxygenase oxylipin pathways as modulators of local and systemic defense. Mol. Plant 5, 914-928. https://doi.org/10.1093/mp/ssr105.
- Vos, I.A., Verhage, A., Schuurink, R.C., Watt, L.G., Pieterse, C.M.J., Van Wees, S.C.M., 2013. Onset of herbivore-induced resistance in systemic tissue primed for jasmonatedependent defenses is activated by abscisic acid. Front. Plant Sci. 4, 539. https://doi. org/10.3389/fpls.2013.00539.
- Walters, D.R., Cowley, T., Weber, H., 2006. Rapid accumulation of trihydroxy oxylipins and resistance to the bean rust pathogen uromyces fabae following wounding in vicia faba. Ann. Bot. 97, 779-784. https://doi.org/10.1093/aob/mcl034.
- Wang, K.D., Borrego, E.J., Kenerley, C.M., Kolomiets, M.V., 2020. Oxylipins other than jasmonic acid are xylem-resident signals regulating systemic resistance induced by Trichoderma virens in maize. Plant Cell 32, 166-185. https://doi.org/10.1105/tpc.19. 00487.
- Wang, R., Shen, W., Liu, L., Jiang, L., Liu, Y., Su, N., Wan, J., 2008. A novel lipoxygenase gene from developing rice seeds confers dual position specificity and responds to wounding and insect attack. Plant Mol. Biol. 66, 401-414. https://doi.org/10.1007/ s11103-007-9278-0.
- Wang, S., Saito, T., Ohkawa, K., Ohara, H., Shishido, M., Ikeura, H., Takagi, K., Ogawa, S., Yokoyama, M., Kondo, S., 2016. Alpha-Ketol linolenic acid (KODA) application affects endogenous abscisic acid, jasmonic acid and aromatic volatiles in grapes infected by a pathogen (Glomerella cingulata). J. Plant Physiol. 192, 90-97. https://doi. org/10.1016/j.jplph.2016.01.009.
- 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. Annals of Botany. Ann. Bot. 111, 1021-1058. https://doi.org/10.1093/ aob/mct067.
- Weber, H., Vick, B.A., Farmer, E.E., 1997. Dinor-oxo-phytodienoic acid: a new hexadecanoid signal in the jasmonate family. Proc. Natl. Acad. Sci. U.S.A. 94, 10473-10478. https://doi.org/10.1073/pnas.94.19.10473.
- Wittek, F., Hoffmann, T., Kanawati, B., Bichlmeier, M., Knappe, C., Wenig, M., Schmitt- Kopplin, P., Parker, J.E., Schwab, W., Vlot, A.C., 2014. Arabidopsis ENHANCED DISEASE SUSCEPTIBILITY1 promotes systemic acquired resistance via azelaic acid and its precursor 9-oxo nonanoic acid. J. Exp. Bot. 65, 5919-5931. https://doi.org/ 10.1093/jxb/eru331.
- Yan, Y., Christensen, S., Isakeit, T., Engelberth, J., Meeley, R., Hayward, A., Emery, R.J.N., Kolomiets, M.V., 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.
- Yokoyama, M., Yamaguchi, S., Inomata, S., Komatsu, K., Yoshida, S., Iida, T., Yokokawa, Y., Yamaguchi, M., Kaihara, S., Takimoto, A., 2000. Stress-induced factor involved in flower formation of Lemna is an α-ketol derivative of linolenic acid. Plant Cell Physiol. 41, 110-113. https://doi.org/10.1093/pcp/41.1.110.