Involvement of Jasmonate Signaling Components in Salt Stress-Induced Stomatal Closure in Arabidopsis thaliana
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Flowers, T.J. and Colmer, T.D., Salinity tolerance in halophytes, New Phytol., 2008, vol. 179, no. 4, pp. 945–963. https://doi.org/10.1111/j.1469-8137.2008.02531.x
Munns, R., Comparative physiology of salt and water stress, Plant Cell Environ., 2002, vol. 25, pp. 239–250.https://doi.org/10.1046/j.0016-8025.2001.00808.x
Veselov, D.S., Markova, I.V., and Kudoyarova, G.R., A response of plants to salinization and formation of salt tolerance, Usp. Sovrem. Biol., 2007, vol. 127, no. 5, pp. 482–493.
Roelfsema, M.R.G. and Hedrich, R., In the light of stomatal opening: new insights into “The Watergate,” New Phytol., 2005, vol. 167, no. 3, pp. 665–691.https://doi.org/10.1111/j.1469-8137.2005.01460.x
Very, A.A., Robinson, M.F., Michael, F., Mansfield, T.A., and Sanders, D., Guard cell cation channels are involved in Na+-induced stomatal closure in a halophyte, Plant J., 1998, vol. 14, no. 5, pp. 509–521.https://doi.org/10.1046/j.1365-313X.1998.00147.x
Ma, Y., Zhang, We, Niu, J., Ren, Yu, and Zhang, F., Hydrogen sulfide may function downstream of hydrogen peroxide in salt stress-induced stomatal closure in Vicia faba, Funct. Plant Biol., 2018, vol. 46, no. 2, pp. 136–145. https://doi.org/10.1071/FP18096
Neill, S.J. and Burnett, E.C., Regulation of gene expression during water deficit stress, Plant Growth Regul., 1999, vol. 29, pp. 23–33. doi org/https://doi.org/10.1023/A:1006251631570
Suhita, D., Raghavendra, A.S., Kwak, J.M., and Vavasseur, A., Cytoplasmic alkalization precedes reactive oxygen species production during methyl jasmonate- and abscisic acid-induced stomatal closure, Plant Physiol., 2004, vol. 134, no. 4, pp. 1536–1545. https://doi.org/10.1104/pp.103.032250
Liu, J., Hou, Z.H., Liu, G.H., Hou, L.X., and Liu, X., Hydrogen sulfide may function downstream of nitric oxide in ethylene-induced stomatal closure in Vicia faba L., J. Integr. Agricult., 2012, vol. 11, pp. 1644–1653.https://doi.org/10.1016/S2095-3119(12)60167-1
Miura, K., Okamoto, H., Okuma, E., Shiba, H., Ka-mada, H., Hasegawa, P.M., and Murata, Y., SIZ1 deficiency causes reduced stomatal aperture and enhanced drought tolerance via controlling salicylic acid-induced accumulation of reactive oxygen species in Arabidopsis,Plant J., 2013, vol. 73, no. 1, pp. 91–104. https://doi.org/10.1111/tpj.12014
Melotto, M., Underwood, W., and He, S.Y., Role of stomata in plant innate immunity and foliar bacterial diseases, Annu. Rev. Phytopathol., 2008, vol. 46, pp. 101–122. https://doi.org/10.1146/annurev.phyto.121107.104959
Montillet, J.L., Leonhardt, N., Mondy, S., Tranchi-mand, S., Rumeau, D., Boudsocq, M., Garcia, A.V., Douki, T., Bigear, J., Lauriere, C., Chevalier, A., Castresana, C., and Hirt, H., An abscisic acid-independent oxylipin pathway controls stomatal closure and immune defense in Arabidopsis,PLoS Biol., 2013, vol. 11, no. 3. e1 001 513. https://doi.org/10.1371/journal.pbio.1001513
Savchenko, T., Kolla, V.A., Wang, C.Q., Nasafi, Z., Hicks, D.R., Phadungchob, B., Chehab, W.E., Brandizzi, F., Froehlich, J., and Dehesh, K., Functional convergence of oxylipin and abscisic acid pathways controls stomatal closure in response to drought, Plant Physiol., 2014, vol. 164, no. 3, pp. 1151–1160. https://doi.org/10.1104/pp.113.234310
Gimenez-Ibanez, S., Boter, M., Ortigosa, A., García-Casado, G., Chini, A., Lewsey, M.G., Ecker, J.R., Ntoukakis, V., and Solano, R., JAZ2 controls stomata dynamics during bacterial invasion, New Phytol., 2017, vol. 213, no. 3, pp. 1378–1392. https://doi.org/10.1111/nph.14354
Pedranzani, H., Racagni, G., Alemano, S., Miersch, O., Ramirez, I., Pena-Cortes, H., Taleisnik, E., Machado-Domenech, E., and Abdala, G., Salt tolerant tomato plants show increased levels of jasmonic acid, Plant Growth Regul., 2003, vol. 41, no. 2, pp. 149–158.https://doi.org/10.1023/A:1027311319940
Dong H., Zhen Z., Peng J., Chang L., Gong Q., and Wang N.N., Loss of ACS7 confers abiotic stress tolerance by modulating ABA sensitivity and accumulation in Arabidopsis, J. Exp. Bot., 2011, vol. 62, no. 14, pp. 4875–4887. https://doi.org/10.1093/jxb/err143
Yastreb, T.O., Kolupaev, Yu.E., Shvidenko, N.V., and Dmitriev, A.P., Action of methyl jasmonate and salt stress on antioxidant system of Arabidopsis plants defective in jasmonate signaling genes, Ukr. Biochem. J., 2018, vol. 90, no. 5, pp. 50–59.https://doi.org/10.15407/ubj90.05.050
Lorenzo, O., Chico, J.M., Sanchez-Serrano, J.J., and Solano, R., JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis,Plant Cell, 2004, vol. 16, no. 7, pp. 1938–1950. https://doi.org/10.1105/tpc.022319
Anderson, J.P., Badruzsaufari, E., Schenk, P.M., Manners, J.M., Desmond, O.J., Ehlert, C., Maclean, D.J., Ebert, P.R., and Kazan K., Antagonistic inter-action between abscisic acid and jasmonate-ethylene signaling pathways modulates defense gene expression and disease resistance in Arabidopsis,Plant Cell, 2004, vol. 16, no. 12, pp. 3460–3479. https://doi.org/10.1105/tpc.104.025833
Honda, K., Yamada, N., Yoshida, R., Ihara, H., Sawa, T., Akaike, T., and Iwai, S., 8-Mercapto-cyclic GMP mediates hydrogen sulfide-induced stomatal closure in Arabidopsis,Plant Cell Physiol., 2015, vol. 56, no. 8, pp. 1481–1489. https://doi.org/10.1093/pcp/pcv069
Iakovenko, O.M., Kretynin, S.V., Kabachevskaya, E.M., Lyakhnovich, G.V., Volotovski, D.I., and Kravets, V.S., Role of phospholipase C in ABA regulation of stomata function, Ukr. Bot. J., 2008, vol. 65, no. 4, pp. 605–613.
Ismail, A., Riemann, M., and Nick, P., The jasmonate pathway mediates salt tolerance in grapevines, J. Exp. Bot., 2012, vol. 63, no. 5, pp. 2127–2139. https://doi.org/10.1093/jxb/err426
Dombrecht, B., Xue, G.P., Sprague, S.J., Kirkegaard, J.A., Ross, J.J., Reid, J.B., Fitt, G.P., Sewelam, N., Schenk, P.M., Manners, J.M., and Kazan, K., MYC2 differentially modulates diverse jasmonate-dependent functions in Arabidopsis, Plant Cell, 2007, vol. 19, no. 7, pp. 2225–2245.https://doi.org/10.1105/tpc.106.048017
