Phytohormone-Mediated Regulation of Heat Stress Response in Plants

Prerostova, Sylva; Vankova, Radomira

doi:10.1007/978-981-19-4941-8_8

Sylva Prerostova³ &
Radomira Vankova³

685 Accesses
1 Citations
11 Altmetric

Abstract

Heat stress is one of the most devastating abiotic stresses that cause substantial yield loss around the world. Heat stress induces excessive production of reactive oxygen species, which negatively affect lipids, proteins and nucleic acids in plants. Protective mechanisms are tightly driven by phytohormones, the key molecules regulating plant growth, development and interactions with the environment. Hormonal cross-talk among abscisic acid, salicylic acid, jasmonic acid, ethylene, auxins, cytokinins, gibberellins, brassinosteroids, strigolactones and karrikins may promote stress tolerance, thermomorphogenesis as well as early senescence. Phytohormone synthesis and signalling are affected by temperature sensors and vice versa; they can influence production and function of the sensors. This chapter also summarizes plant sensing and signalling of high temperatures by calcium ions, hydrogen peroxide, reactive oxygen species, membrane lipids, phytochrome B, histone modifications, DNA remodelling, RNA stability and alternative splicing, methyl erythritol cyclodiphosphate (MEcPP), volatile compounds and changes in photosynthesis. The central regulatory role of phytochrome interacting factor 4 (PIF4), H₂O₂ and heat shock proteins (HSPs) is highlighted. Detail knowledge about molecular mechanisms is described in the relation to warm stress, heat shock, stress acclimation and stress memory. Organ-specific responses uncovered the key protective mechanisms in meristematic tissues and roots, which are driven by phytohormones. At the subcellular level, not only chloroplasts and mitochondria are involved in heat stress responses, but also endoplasmic reticulum and processes on plasma membrane are crucial for stress signalling. The unique scheme of heat-induced interactions among phytohormones is presented in this chapter. Possible ways of future research are suggested.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Log in via an institution

Chapter: USD 29.95; Price excludes VAT (USA)

eBook: USD 149.00; Price excludes VAT (USA)

Softcover Book: USD 199.99; Price excludes VAT (USA)

Hardcover Book: USD 199.99; Price excludes VAT (USA)

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

Alonso-Ramírez, A., Rodríguez, D., Reyes, D., Jiménez, J. A., Nicolás, G., López-Climent, M., Gómez-Cadenas, A., & Nicolás, C. (2009). Evidence for a role of gibberellins in salicylic acid-modulated early plant responses to abiotic stress in Arabidopsis seeds. Plant Physiology, 150, 1335–1344. https://doi.org/10.1104/pp.109.139352
Article Google Scholar
Asthir, B. (2015). Mechanisms of heat tolerance in crop plants. Biologia Plantarum, 59, 620–628. https://doi.org/10.1007/s10535-015-0539-5
Article CAS Google Scholar
Bahuguna, R. N., & Jagadish, K. S. (2015). Temperature regulation of plant phenological development. Environmental and Experimental Botany, 111, 83–90. https://doi.org/10.1016/j.envexpbot.2014.10.007
Article CAS Google Scholar
Balti, I., Benny, J., Perrone, A., Caruso, T., Abdallah, D., Salhi-Hannachi, A., & Martinelli, F. (2020). Identification of conserved genes linked to responses to abiotic stresses in leaves among different plant species. Functional Plant Biology, 48, 54–71. https://doi.org/10.1071/FP20028
Article CAS Google Scholar
Bao, S., Hua, C., Shen, L., & Yu, H. (2020). New insights into gibberellin signaling in regulating flowering in Arabidopsis. Journal of Integrative Plant Biology, 62, 118–131. https://doi.org/10.1111/jipb.12892
Article CAS Google Scholar
Bellstaedt, J., Trenner, J., Lippmann, R., Poeschl, Y., Zhang, X., Friml, J., Quint, M., & Delker, C. (2019). A mobile auxin signal connects temperature sensing in cotyledons with growth responses in hypocotyls. Plant Physiology, 180, 757–766. https://doi.org/10.1104/pp.18.01377
Article CAS Google Scholar
Bielach, A., Hrtyan, M., & Tognetti, V. B. (2017). Plants under stress: Involvement of auxin and cytokinin. International Journal of Molecular Sciences, 18, 1427. https://doi.org/10.3390/ijms18071427
Article CAS Google Scholar
Biggs, M. S., Woodson, W. R., & Handa, A. K. (1988). Biochemical basis of high-temperature inhibition of ethylene biosynthesis in ripening tomato fruits. Physiologia Plantarum, 72, 572–578. https://doi.org/10.1111/j.1399-3054.1988.tb09167.x
Article CAS Google Scholar
Binder, B. M. (2020). Ethylene signaling in plants. The Journal of Biological Chemistry, 295, 7710–7725. https://doi.org/10.1074/jbc.REV120.010854
Article CAS Google Scholar
Bjornson, M., Balcke, G. U., Xiao, Y., de Souza, A., Wang, J. Z., Zhabinskaya, D., Tagkopoulos, I., Tissier, A., & Dehesh, K. (2017). Integrated omics analyses of retrograde signaling mutant delineate interrelated stress-response strata. The Plant Journal, 91, 70–84. https://doi.org/10.1111/tpj.13547
Article CAS Google Scholar
Casal, J. J., & Balasubramanian, S. (2019). Thermomorphogenesis. Annual Review of Plant Biology, 70, 321–346. https://doi.org/10.1146/annurev-arplant-050718-095919
Article CAS Google Scholar
Černý, M., Jedelský, P. L., Novák, J., Schlosser, A., & Brzobohatý, B. (2014). Cytokinin modulates proteomic, transcriptomic and growth responses to temperature shocks in Arabidopsis. Plant, Cell & Environment, 37, 1641–1655. https://doi.org/10.1111/pce.12270
Article CAS Google Scholar
Che, P., Bussell, J. D., Zhou, W., Estavillo, G. M., Pogson, B. J., & Smith, S. M. (2010). Signaling from the endoplasmic reticulum activates brassinosteroid signaling and promotes acclimation to stress in Arabidopsis. Science Signaling, 3, 69. https://doi.org/10.1126/scisignal.2001140
Article CAS Google Scholar
Chen, L., Huang, X. X., Zhao, S. M., Xiao, D. W., Xiao, L. T., Tong, J. H., Wang, W. S., Li, Y. J., Ding, Z., & Hou, B. K. (2020). IPyA glucosylation mediates light and temperature signaling to regulate auxin-dependent hypocotyl elongation in Arabidopsis. PNAS, 117, 6910–6917. https://doi.org/10.1073/pnas.2000172117
Article CAS Google Scholar
Chen, Z., Huang, Y., Yang, W., Chang, G., Li, P., Wei, J., Yuan, X., Huang, J., & Hu, X. (2019). The hydrogen sulfide signal enhances seed germination tolerance to high temperatures by retaining nuclear COP1 for HY5 degradation. Plant Science, 285, 34–43. https://doi.org/10.1016/j.plantsci.2019.04.024
Article CAS Google Scholar
Cheng, M. C., Liao, P. M., Kuo, W. W., & Lin, T. P. (2013). The Arabidopsis ETHYLENE RESPONSE FACTOR1 regulates abiotic stress-responsive gene expression by binding to different cis-acting elements in response to different stress signals. Plant Physiology, 162, 1566–1582. https://doi.org/10.1104/pp.113.221911
Article CAS Google Scholar
Chung, B. Y. W., Balcerowicz, M., Di Antonio, M., Jaeger, K. E., Geng, F., Franaszek, K., Marriott, P., Brierley, I., Firth, A. E., & Wigge, P. A. (2020). An RNA thermoswitch regulates daytime growth in Arabidopsis. Nature Plants, 6, 522–532. https://doi.org/10.1038/s41477-020-0633-3
Article CAS Google Scholar
Clarke, S. M., Cristescu, S. M., Miersch, O., Harren, F. J., Wasternack, C., & Mur, L. A. (2009). Jasmonates act with salicylic acid to confer basal thermotolerance in Arabidopsis thaliana. The New Phytologist, 182, 175–187. https://doi.org/10.1111/j.1469-8137.2008.02735.x
Article CAS Google Scholar
Clarke, S. M., Mur, L. A., Wood, J. E., & Scott, I. M. (2004). Salicylic acid dependent signaling promotes basal thermotolerance but is not essential for acquired thermotolerance in Arabidopsis thaliana. The Plant Journal, 38, 432–447. https://doi.org/10.1111/j.1365-313X.2004.02054.x
Article CAS Google Scholar
Cortijo, S., Charoensawan, V., Brestovitsky, A., Buning, R., Ravarani, C., Rhodes, D., van Noort, J., Jaeger, K. E., & Wigge, P. A. (2017). Transcriptional regulation of the ambient temperature response by H2A.Z nucleosomes and HSF1 transcription factors in Arabidopsis. Molecular Plant, 10, 1258–1273. https://doi.org/10.1016/j.molp.2017.08.014
Article CAS Google Scholar
De Cuyper, C., Struk, S., Braem, L., Gevaert, K., De Jaeger, G., & Goormachtig, S. (2017). Strigolactones, karrikins and beyond. Plant, Cell & Environment, 40, 1691–1703. https://doi.org/10.1111/pce.12996
Article CAS Google Scholar
Deng, Y., Humbert, S., Liu, J. X., Srivastava, R., Rothstein, S. J., & Howell, S. H. (2011). Heat induces the splicing by IRE1 of a mRNA encoding a transcription factor involved in the unfolded protein response in Arabidopsis. PNAS, 108, 7247–7252. https://doi.org/10.1073/pnas.1102117108
Article Google Scholar
Di, D. W., Wu, L., Zhang, L., An, C. W., Zhang, T. Z., Luo, P., Gao, H. H., Kriechbaumer, V., & Guo, G. Q. (2016). Functional roles of Arabidopsis CKRC2/YUCCA8 gene and the involvement of PIF4 in the regulation of auxin biosynthesis by cytokinin. Scientific Reports, 6, 36866. https://doi.org/10.1038/srep36866
Article CAS Google Scholar
di Donato, M., & Geisler, M. (2019). HSP 90 and co-chaperones: A multitaskers’ view on plant hormone biology. FEBS Letters, 593, 1415–1430. https://doi.org/10.1002/1873-3468.13499
Article CAS Google Scholar
Ding, Y., Huang, L., Jiang, Q., & Zhu, C. (2020). MicroRNAs as important regulators of heat stress responses in plants. Journal of Agricultural and Food Chemistry, 68, 11320–11326. https://doi.org/10.1021/acs.jafc.0c03597
Article CAS Google Scholar
Dobrá, J., Černý, M., Štorchová, H., Dobrev, P., Skalák, J., Jedelský, P. L., Lukšanová, H., Gaudinová, A., Pešek, B., Malbek, J., Vanek, T., Brzobohatý, B., & Vanková, R. (2015). The impact of heat stress targeting on the hormonal and transcriptomic response in Arabidopsis. Plant Science, 231, 52–61. https://doi.org/10.1016/j.plantsci.2014.11.005
Article CAS Google Scholar
Dong, F., Fu, X., Watanabe, N., Su, X., & Yang, Z. (2016). Recent advances in the emission and functions of plant vegetative volatiles. Molecules, 21, 124. https://doi.org/10.3390/molecules21020124
Article CAS Google Scholar
Dong, H., Zhen, Z., Peng, J., Chang, L., Gong, Q., & Wang, N. N. (2011). Loss of ACS7 confers abiotic stress tolerance by modulating ABA sensitivity and accumulation in Arabidopsis. Journal of Experimental Botany, 62, 4875–4887. https://doi.org/10.1093/jxb/err143
Article CAS Google Scholar
Fang, X., Zhao, G., Zhang, S., Li, Y., Gu, H., Li, Y., Zhao, Q., & Qi, Y. (2019). Chloroplast-to-nucleus signaling regulates microRNA biogenesis in Arabidopsis. Developmental Cell, 48, 371–382. https://doi.org/10.1016/j.devcel.2018.11.046
Article CAS Google Scholar
Fatma, M., Iqbal, N., Sehar, Z., Alyemeni, M. N., Kaushik, P., Khan, N. A., & Ahmad, P. (2021). Methyl jasmonate protects the PS II system by maintaining the stability of chloroplast D1 protein and accelerating enzymatic antioxidants in heat-stressed wheat plants. Antioxidants, 10, 1216. https://doi.org/10.3390/antiox10081216
Article CAS Google Scholar
Feraru, E., Feraru, M. I., Barbez, E., Waidmann, S., Sun, L., Gaidora, A., & Kleine-Vehn, J. (2019). PILS6 is a temperature-sensitive regulator of nuclear auxin input and organ growth in Arabidopsis thaliana. PNAS, 116, 3893–3898. https://doi.org/10.1073/pnas.1814015116
Article CAS Google Scholar
Field, C. B., Barros, V. R., Mach, K., & Mastrandrea, M. (2014). Climate change 2014: Impacts, adaptation, and vulnerability (Vol. 1). Cambridge University Press Cambridge.
Book Google Scholar
Finka, A., Cuendet, A. F., Maathuis, F. J., Saidi, Y., & Goloubinoff, P. (2012). Plasma membrane cyclic nucleotide gated calcium channels control land plant thermal sensing and acquired thermotolerance. Plant Cell, 24, 3333–3348. https://doi.org/10.1105/tpc.112.095844
Article CAS Google Scholar
Fujii, Y., Tanaka, H., Konno, N., Ogasawara, Y., Hamashima, N., Tamura, S., Hasegawa, S., Hayasaki, Y., Okajima, K., & Kodama, Y. (2017). Phototropin perceives temperature based on the lifetime of its photoactivated state. PNAS, 114, 9206–9211. https://doi.org/10.1073/pnas.1704462114
Article CAS Google Scholar
Gajdošová, S., Spíchal, L., Kamínek, M., Hoyerová, K., Novák, O., Dobrev, P. I., Galuszka, P., Klíma, P., Gaudinová, A., Žižková, E., Hanuš, J., Dančák, M., Trávníček, B., Pešek, B., Krupička, M., Vaňková, R., Strnad, M., & Motyka, V. (2011). Distribution, biological activities, metabolism, and the conceivable function of cis-zeatin-type cytokinins in plants. Journal of Experimental Botany, 62, 2827–2840. https://doi.org/10.1093/jxb/erq457
Article CAS Google Scholar
Gao, F., Han, X., Wu, J., Zheng, S., Shang, Z., Sun, D., Zhou, R., & Li, B. (2012). A heat-activated calcium-permeable channel–Arabidopsis cyclic nucleotide-gated ion channel 6–is involved in heat shock responses. The Plant Journal, 70, 1056–1069. https://doi.org/10.1111/j.1365-313X.2012.04969.x
Article CAS Google Scholar
Grossiord, C., Buckley, T. N., Cernusak, L. A., Novick, K. A., Poulter, B., Siegwolf, R. T., Sperry, J. S., & McDowell, N. G. (2020). Plant responses to rising vapor pressure deficit. The New Phytologist, 226, 1550–1566. https://doi.org/10.1111/nph.16485
Article Google Scholar
Hahm, J., Kim, K., Qiu, Y., & Chen, M. (2020). Increasing ambient temperature progressively disassembles Arabidopsis phytochrome B from individual photobodies with distinct thermostabilities. Nature Communications, 11, 1660. https://doi.org/10.1038/s41467-020-15526-z
Article CAS Google Scholar
Havko, N. E., Das, M. R., McClain, A. M., Kapali, G., Sharkey, T. D., & Howe, G. A. (2020). Insect herbivory antagonizes leaf cooling responses to elevated temperature in tomato. PNAS, 117, 2211–2217. https://doi.org/10.1073/pnas.1913885117
Article CAS Google Scholar
Hayes, S., Schachtschabel, J., Mishkind, M., Munnik, T., & Arisz, S. A. (2021). Hot topic: Thermosensing in plants. Plant, Cell & Environment, 44, 1987–1991. https://doi.org/10.1111/pce.13979
Article CAS Google Scholar
Hedden, P., & Thomas, S. G. (2012). Gibberellin biosynthesis and its regulation. Biochemical Journal, 444, 11–25. https://doi.org/10.1042/BJ20120245
Article CAS Google Scholar
Hilker, M., & Schmülling, T. (2019). Stress priming, memory, and signalling in plants. Plant, Cell & Environment, 42, 753–761. https://doi.org/10.1111/pce.13526
Article CAS Google Scholar
Hluska, T., Hlusková, L., & Emery, R. J. (2021). The Hulks and the Deadpools of the cytokinin universe: A dual strategy for cytokinin production, translocation, and signal transduction. Biomolecules, 11, 209. https://doi.org/10.3390/biom11020209
Article CAS Google Scholar
Hossain, M. A., Li, Z. G., Hoque, T. S., Burritt, D. J., Fujita, M., & Munné-Bosch, S. (2018). Heat or cold priming-induced cross-tolerance to abiotic stresses in plants: Key regulators and possible mechanisms. Protoplasma, 255, 399–412. https://doi.org/10.1007/s00709-017-1150-8
Article CAS Google Scholar
Hsieh, E. J., Cheng, M. C., & Lin, T. P. (2013). Functional characterization of an abiotic stress-inducible transcription factor AtERF53 in Arabidopsis thaliana. Plant Molecular Biology, 82, 223–237. https://doi.org/10.1007/s11103-013-0054-z
Article CAS Google Scholar
Hu, Q., Zhang, S., & Huang, B. (2018). Strigolactones and interaction with auxin regulating root elongation in tall fescue under different temperature regimes. Plant Science, 271, 34–39. https://doi.org/10.1016/j.plantsci.2018.03.008
Article CAS Google Scholar
Hu, Q., Zhang, S., & Huang, B. (2019). Strigolactones promote leaf elongation in tall fescue through upregulation of cell cycle genes and downregulation of auxin transport genes in tall fescue under different temperature regimes. International Journal of Molecular Sciences, 20, 1836. https://doi.org/10.3390/ijms20081836
Article CAS Google Scholar
Hu, T., Liu, S. Q., Amombo, E., & Fu, J. M. (2015). Stress memory induced rearrangements of HSP transcription, photosystem II photochemistry and metabolism of tall fescue (Festuca arundinacea Schreb.) in response to high-temperature stress. Frontiers in Plant Science, 6, 403. https://doi.org/10.3389/fpls.2015.00403
Article Google Scholar
Hua, B. G., Mercier, R. W., Zielinski, R. E., & Berkowitz, G. A. (2003). Functional interaction of calmodulin with a plant cyclic nucleotide gated cation channel. Plant Physiology and Biochemistry, 41, 945–954. https://doi.org/10.1016/j.plaphy.2003.07.006
Article CAS Google Scholar
Huot, B., Castroverde, C. D. M., Velásquez, A. C., Hubbard, E., Pulman, J. A., Yao, J., Childs, K. L., Tsuda, K., Montgomery, B. L., & He, S. Y. (2017). Dual impact of elevated temperature on plant defence and bacterial virulence in Arabidopsis. Nature Communications, 8, 1808. https://doi.org/10.1038/s41467-017-01674-2
Article CAS Google Scholar
Hurný, A., Cuesta, C., Cavallari, N., Ötvös, K., Duclercq, J., Dokládal, L., Montesinos, J. C., Gallemí, M., Semerádová, H., Rauter, T., & Stenzel, I. (2020). Synergistic on auxin and cytokinin 1 positively regulates growth and attenuates soil pathogen resistance. Nature Communications, 11, 2170. https://doi.org/10.1038/s41467-020-15895-5
Article CAS Google Scholar
Hwang, I., Sheen, J., & Müller, B. (2012). Cytokinin signaling networks. Annual Review of Plant Biology, 63, 353–380. https://doi.org/10.1146/annurev-arplant-042811-105503
Article CAS Google Scholar
Ibañez, C., Delker, C., Martinez, C., Bürstenbinder, K., Janitza, P., Lippmann, R., Ludwig, W., Sun, H., James, G. V., Klecker, M., & Grossjohann, A. (2018). Brassinosteroids dominate hormonal regulation of plant thermomorphogenesis via BZR1. Current Biology, 28, 303–310. https://doi.org/10.1016/j.cub.2017.11.077
Article CAS Google Scholar
Islam, M. R., Feng, B., Chen, T., Tao, L., & Fu, G. (2018). Role of abscisic acid in thermal acclimation of plants. Journal of Plant Biology, 61, 255–264. https://doi.org/10.1007/s12374-017-0429-9
Article CAS Google Scholar
Isono, K., Tsukimoto, R., Iuchi, S., Shinozawa, A., Yotsui, I., Sakata, Y., & Taji, T. (2021). An ER–golgi tethering factor SLOH4/MIP3 is involved in long-term heat tolerance of Arabidopsis. Plant & Cell Physiology, 62, 272–279. https://doi.org/10.1093/pcp/pcaa157
Article CAS Google Scholar
Janda, T., Prerostová, S., Vanková, R., & Darkó, É. (2021). Crosstalk between light-and temperature-mediated processes under cold and heat stress conditions in plants. International Journal of Molecular Sciences, 22, 8602. https://doi.org/10.3390/ijms22168602
Article CAS Google Scholar
Jha, U. C., Nayyar, H., & Siddique, K. H. (2021). Role of phytohormones in regulating heat stress acclimation in agricultural crops. Journal of Plant Growth Regulation. https://doi.org/10.1007/s00344-021-10362-x
Jiang, J., & Dehesh, K. (2021). Plastidial retrograde modulation of light and hormonal signaling: An odyssey. The New Phytologist, 230, 931–937. https://doi.org/10.1111/nph.17192
Article CAS Google Scholar
Jiang, J., Xiao, Y., Chen, H., Hu, W., Zeng, L., Ke, H., Ditengou, F. A., Devisetty, U., Palme, K., Maloof, J., & Dehesh, K. (2020). Retrograde induction of phyB orchestrates ethylene-auxin hierarchy to regulate growth. Plant Physiology, 183, 1268–1280. https://doi.org/10.1104/pp.20.00090
Article CAS Google Scholar
Jin, H., Pang, L., Fang, S., Chu, J., Li, R., & Zhu, Z. (2018). High ambient temperature antagonizes ethylene-induced exaggerated apical hook formation in etiolated Arabidopsis seedlings. Plant, Cell & Environment, 41, 2858–2868. https://doi.org/10.1111/pce.13417
Article CAS Google Scholar
Jochum, G. M., Mudge, K. W., & Thomas, R. B. (2007). Elevated temperatures increase leaf senescence and root secondary metabolite concentrations in the understory herb Panax quinquefolius (Araliaceae). American Journal of Botany, 94, 819–826. https://doi.org/10.3732/ajb.94.5.819
Article CAS Google Scholar
Jones, M. A. (2019). Retrograde signalling as an informant of circadian timing. The New Phytologist, 221, 1749–1753. https://doi.org/10.1111/nph.15525
Article Google Scholar
Kamínek, M. (2015). Tracking the story of cytokinin research. Journal of Plant Growth Regulation, 34, 723–739. https://doi.org/10.1007/s00344-015-9543-4
Article CAS Google Scholar
Keller, M. A., Piedrafita, G., & Ralser, M. (2015). The widespread role of non-enzymatic reactions in cellular metabolism. Current Opinion in Biotechnology, 34, 153–161. https://doi.org/10.1016/j.copbio.2014.12.020
Article CAS Google Scholar
Khan, M. I. R., Fatma, M., Per, T. S., Anjum, N. A., & Khan, N. A. (2015). Salicylic acid-induced abiotic stress tolerance and underlying mechanisms in plants. Frontiers in Plant Science, 6, 462. https://doi.org/10.3389/fpls.2015.00462
Article Google Scholar
Khan, M. I. R., Iqbal, N., Masood, A., Per, T. S., & Khan, N. A. (2013). Salicylic acid alleviates adverse effects of heat stress on photosynthesis through changes in proline production and ethylene formation. Plant Signaling & Behavior, 8, e26374. https://doi.org/10.4161/psb.26374
Article CAS Google Scholar
Kim, C., Kim, S. J., Jeong, J., Park, E., Oh, E., Park, Y. I., Lim, P. O., & Choi, G. (2020). High ambient temperature accelerates leaf senescence via PHYTOCHROME-INTERACTING FACTOR 4 and 5 in Arabidopsis. Molecules and Cells, 43, 645. https://doi.org/10.14348/molcells.2020.0117
Article CAS Google Scholar
Kim, S., Hwang, G., Kim, S., Thi, T. N., Kim, H., Jeong, J., Kim, J., Kim, J., Choi, G., & Oh, E. (2020). The epidermis coordinates thermoresponsive growth through the phyB-PIF4-auxin pathway. Nature Communications, 11, 1053. https://doi.org/10.1038/s41467-020-14905-w
Article CAS Google Scholar
Kramna, B., Prerostova, S., & Vankova, R. (2019). Strigolactones in an experimental context. Plant Growth Regulation, 88, 113–128. https://doi.org/10.1007/s10725-019-00502-5
Article CAS Google Scholar
Kumar, S. V., & Wigge, P. A. (2010). H2A.Z-containing nucleosomes mediate the thermosensory response in Arabidopsis. Cell, 140, 136–147. https://doi.org/10.1016/j.cell.2009.11.006
Article CAS Google Scholar
Lancaster, L. T., & Humphreys, A. M. (2020). Global variation in the thermal tolerances of plants. PNAS, 117, 13580–13587. https://doi.org/10.1073/pnas.1918162117
Article CAS Google Scholar
Lantz, A. T., Allman, J., Weraduwage, S. M., & Sharkey, T. D. (2019). Isoprene: New insights into the control of emission and mediation of stress tolerance by gene expression. Plant, Cell & Environment, 42, 2808–2826. https://doi.org/10.1111/pce.13629
Article CAS Google Scholar
Larkindale, J., Hall, J. D., Knight, M. R., & Vierling, E. (2005). Heat stress phenotypes of Arabidopsis mutants implicate multiple signaling pathways in the acquisition of thermotolerance. Plant Physiology, 138, 882–897. https://doi.org/10.1104/pp.105.062257
Article CAS Google Scholar
Lau, O. S., Song, Z., Zhou, Z., Davies, K. A., Chang, J., Yang, X., Wang, S., Lucyshyn, D., Tay, I. H., Wigge, P. A., & Bergmann, D. C. (2018). Direct control of SPEECHLESS by PIF4 in the high-temperature response of stomatal development. Current Biology, 28, 1273–1280. https://doi.org/10.1016/j.cub.2018.02.054
Article CAS Google Scholar
Legris, M., Klose, C., Burgie, E. S., Rojas, C. C. R., Neme, M., Hiltbrunner, A., Wigge, P. A., Schafer, E., Vierstra, R. D., & Casal, J. J. (2016). Phytochrome B integrates light and temperature signals in Arabidopsis. Science, 354, 897–900. https://doi.org/10.1126/science.aaf5656
Article CAS Google Scholar
Lesk, C., Rowhani, P., & Ramankutty, N. (2016). Influence of extreme weather disasters on global crop production. Nature, 529, 84–87. https://doi.org/10.1038/nature16467
Article CAS Google Scholar
Li, N., Bo, C., Zhang, Y., & Wang, L. (2021). PIF4 and PIF5 proteins promote heat stress induced leaf senescence in Arabidopsis. Journal of Experimental Botany, 72, 4577–4589. https://doi.org/10.1093/jxb/erab158
Article CAS Google Scholar
Li, N., Euring, D., Cha, J. Y., Lin, Z., Lu, M., Huang, L. J., & Kim, W. Y. (2021). Plant hormone-mediated regulation of heat tolerance in response to global climate change. Frontiers in Plant Science, 11, 2318. https://doi.org/10.3389/fpls.2020.627969
Article Google Scholar
Li, S., Zhou, X., Chen, L., Huang, W., & Yu, D. (2010). Functional characterization of Arabidopsis thaliana WRKY39 in heat stress. Molecules and Cells, 29, 475–483. https://doi.org/10.1007/s10059-010-0059-2
Article CAS Google Scholar
Liao, H., Tang, R., Zhang, X., Luan, S., & Yu, F. (2017). FERONIA receptor kinase at the crossroads of hormone signaling and stress responses. Plant & Cell Physiology, 58, 1143–1150. https://doi.org/10.1093/pcp/pcx048
Article CAS Google Scholar
Lin, J. S., Kuo, C. C., Yang, I. C., Tsai, W. A., Shen, Y. H., Lin, C. C., Liang, Y. C., Li, Y. C., Kuo, Y. W., King, Y. C., Lai, H. M., & Jeng, S. T. (2018). MicroRNA160 modulates plant development and heat shock protein gene expression to mediate heat tolerance in Arabidopsis. Frontiers in Plant Science, 9, 68. https://doi.org/10.3389/fpls.2018.00068
Article Google Scholar
Ling, Y., Serrano, N., Gao, G., Atia, M., Mokhtar, M., Woo, Y. H., Bazin, J., Veluchamy, A., Benhamed, M., Crespi, M., Gehring, C., Reddy, A. S. N., & Mahfouz, M. M. (2018). Thermopriming triggers splicing memory in Arabidopsis. Journal of Experimental Botany, 69, 2659–2675. https://doi.org/10.1093/jxb/ery062
Article CAS Google Scholar
Liu, J., Feng, L., Li, J., & He, Z. (2015). Genetic and epigenetic control of plant heat responses. Frontiers in Plant Science, 6, 267. https://doi.org/10.3389/fpls.2015.00267
Article Google Scholar
Lubovská, Z., Dobrá, J., Štorchová, H., Wilhelmová, N., & Vanková, R. (2014). Cytokinin oxidase/dehydrogenase overexpression modifies antioxidant defense against heat, drought and their combination in Nicotiana tabacum plants. Journal of Plant Physiology, 171, 1625–1633. https://doi.org/10.1016/j.jplph.2014.06.021
Article CAS Google Scholar
Lynas, M. (2020). Our final warning: Six degrees of climate emergency. HarperCollins.
Google Scholar
Macková, H., Hronková, M., Dobrá, J., Turečková, V., Novák, O., Lubovská, Z., Motyka, V., Haisel, D., Hájek, T., Prášil, I. T., Gaudinová, A., Štorchová, H., Ge, E., Werner, T., Schmülling, T., & Vanková, R. (2013). Enhanced drought and heat stress tolerance of tobacco plants with ectopically enhanced cytokinin oxidase/dehydrogenase gene expression. Journal of Experimental Botany, 64, 2805–2815. https://doi.org/10.1093/jxb/ert131
Article CAS Google Scholar
Marczak, M., Cieśla, A., Janicki, M., Kasprowicz-Maluśki, A., Kubiak, P., & Ludwików, A. (2020). Protein phosphatases type 2C group A interact with and regulate the stability of ACC synthase 7 in Arabidopsis. Cell, 9, 978. https://doi.org/10.3390/cells9040978
Article CAS Google Scholar
Martins, S., Montiel-Jorda, A., Cayrel, A., Huguet, S., Paysant-Le Roux, C., Ljung, K., & Vert, G. (2017). Brassinosteroid signaling-dependent root responses to prolonged elevated ambient temperature. Nature Communications, 8, 309. https://doi.org/10.1038/s41467-017-00355-4
Article CAS Google Scholar
Matthes, M. S., Best, N. B., Robil, J. M., Malcomber, S., Gallavotti, A., & McSteen, P. (2019). Auxin EvoDevo: Conservation and diversification of genes regulating auxin biosynthesis, transport, and signaling. Molecular Plant, 12, 298–320. https://doi.org/10.1016/j.molp.2018.12.012
Article CAS Google Scholar
Merret, R., Carpentier, M. C., Favory, J. J., Picart, C., Descombin, J., Bousquet-Antonelli, C., Tillard, P., Lejay, L., Deragon, J. M., & Charng, Y. Y. (2017). Heat shock protein HSP101 affects the release of ribosomal protein mRNAs for recovery after heat shock. Plant Physiology, 174, 1216–1225. https://doi.org/10.1104/pp.17.00269
Article CAS Google Scholar
Mizoi, J., Kanazawa, N., Kidokoro, S., Takahashi, F., Qin, F., Morimoto, K., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2019). Heat-induced inhibition of phosphorylation of the stress-protective transcription factor DREB2A promotes thermotolerance of Arabidopsis thaliana. The Journal of Biological Chemistry, 294, 902–917. https://doi.org/10.1074/jbc.RA118.002662
Article CAS Google Scholar
Mongélard, G., Seemann, M., Boisson, A. M., Rohmer, M., Bligny, R., & Rivasseau, C. (2011). Measurement of carbon flux through the MEP pathway for isoprenoid synthesis by 31P-NMR spectroscopy after specific inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate reductase. Effect of light and temperature. Plant, Cell & Environment, 34, 1241–1247. https://doi.org/10.1111/j.1365-3040.2011.02322.x
Article CAS Google Scholar
Muench, M., Hsin, C. H., Ferber, E., Berger, S., & Müller, M. J. (2016). Reactive electrophilic oxylipins trigger a heat stress-like response through HSFA1 transcription factors. Journal of Experimental Botany, 67, 6139–6148. https://doi.org/10.1093/jxb/erw376
Article CAS Google Scholar
Müller, M., & Munné-Bosch, S. (2015). Ethylene response factors: A key regulatory hub in hormone and stress signaling. Plant Physiology, 169, 32–41. https://doi.org/10.1104/pp.15.00677
Article CAS Google Scholar
Nawkar, G. M., Kang, C. H., Maibam, P., Park, J. H., Jung, Y. J., Chae, H. B., Chi, I. H., Jung, I. J., Kim, W. Y., Yun, D. J., & Lee, S. Y. (2017). HY5, a positive regulator of light signaling, negatively controls the unfolded protein response in Arabidopsis. PNAS, 114, 2084–2089. https://doi.org/10.1073/pnas.1609844114
Article CAS Google Scholar
Nguyen, T. H., Itoh, S. G., Okumura, H., & Tominaga, M. (2021). Structural basis for promiscuous action of monoterpenes on TRP channels. Communications Biology, 4, 293. https://doi.org/10.1038/s42003-021-01776-0
Article CAS Google Scholar
Niu, Y., & Xiang, Y. (2018). An overview of biomembrane functions in plant responses to high-temperature stress. Frontiers in Plant Science, 9, 915. https://doi.org/10.3389/fpls.2018.00915
Article Google Scholar
Nolan, T. M., Vukašinović, N., Liu, D., Russinova, E., & Yin, Y. (2020). Brassinosteroids: multidimensional regulators of plant growth, development, and stress responses. Plant Cell, 32, 295–318. https://doi.org/10.1105/tpc.19.00335
Article CAS Google Scholar
Nomoto, Y., Kubozono, S., Yamashino, T., Nakamichi, N., & Mizuno, T. (2012). Circadian clock-and PIF4-controlled plant growth: A coincidence mechanism directly integrates a hormone signaling network into the photoperiodic control of plant architectures in Arabidopsis thaliana. Plant & Cell Physiology, 53, 1950–1964. https://doi.org/10.1093/pcp/pcs137
Article CAS Google Scholar
Ogweno, J. O., Song, X. S., Shi, K., Hu, W. H., Mao, W. H., Zhou, Y. H., Yu, J. Q., & Nogués, S. (2008). Brassinosteroids alleviate heat-induced inhibition of photosynthesis by increasing carboxylation efficiency and enhancing antioxidant systems in Lycopersicon esculentum. Journal of Plant Growth Regulation, 27, 49–57. https://doi.org/10.1007/s00344-007-9030-7
Article CAS Google Scholar
Olas, J. J., Apelt, F., Annunziata, M. G., John, S., Richard, S. I., Gupta, S., Kragler, F., Balazadeh, S., & Mueller-Roeber, B. (2021). Primary carbohydrate metabolism genes participate in heat stress memory at the shoot apical meristem of Arabidopsis thaliana. Molecular Plant, 14, 1508–1524. https://doi.org/10.1016/j.molp.2021.05.024
Article CAS Google Scholar
Omoarelojie, L. O., Kulkarni, M. G., Finnie, J. F., Pospíšil, T., Strnad, M., & van Staden, J. (2020). Synthetic strigolactone (rac-GR24) alleviates the adverse effects of heat stress on seed germination and photosystem II function in lupine seedlings. Plant Physiology and Biochemistry, 155, 965–979. https://doi.org/10.1016/j.plaphy.2020.07.043
Article CAS Google Scholar
Oyoshi, K., Katano, K., Yunose, M., & Suzuki, N. (2020). Memory of 5-min heat stress in Arabidopsis thaliana. Plant Signaling & Behavior, 15, 1778919. https://doi.org/10.1080/15592324.2020.1778919
Article CAS Google Scholar
Pan, T., Sun, X., Liu, Y., Li, H., Deng, G., Lin, H., & Wang, S. (2018). Heat stress alters genome-wide profiles of circular RNAs in Arabidopsis. Plant Molecular Biology, 96, 217–229. https://doi.org/10.1007/s11103-017-0684-7
Article CAS Google Scholar
Pazouki, L., Kanagendran, A., Li, S., Kännaste, A., Memari, H. R., Bichele, R., & Niinemets, Ü. (2016). Mono-and sesquiterpene release from tomato (Solanum lycopersicum) leaves upon mild and severe heat stress and through recovery: From gene expression to emission responses. Environmental and Experimental Botany, 132, 1–15. https://doi.org/10.1016/j.envexpbot.2016.08.003
Article CAS Google Scholar
Pistelli, L., Tonelli, M., Pellegrini, E., Cotrozzi, L., Pucciariello, C., Trivellini, A., Lorenzini, G., & Nali, C. (2019). Accumulation of rosmarinic acid and behaviour of ROS processing systems in Melissa officinalis L. under heat stress. Industrial Crops and Products, 138, 111469. https://doi.org/10.1016/j.indcrop.2019.111469
Article CAS Google Scholar
Poór, P., Nawaz, K., Gupta, R., Ashfaque, F., & Khan, M. I. R. (2021). Ethylene involvement in the regulation of heat stress tolerance in plants. Plant Cell Reports. https://doi.org/10.1007/s00299-021-02675-8
Prerostova, S., Dobrev, P. I., Gaudinova, A., Hosek, P., Soudek, P., Knirsch, V., & Vankova, R. (2017). Hormonal dynamics during salt stress responses of salt-sensitive Arabidopsis thaliana and salt-tolerant Thellungiella salsuginea. Plant Science, 264, 188–198. https://doi.org/10.1016/j.plantsci.2017.07.020
Article CAS Google Scholar
Prerostova, S., Dobrev, P. I., Kramna, B., Gaudinova, A., Knirsch, V., Spichal, L., Zatloukal, M., & Vankova, R. (2020). Heat acclimation and inhibition of cytokinin degradation positively affect heat stress tolerance of Arabidopsis. Frontiers in Plant Science, 11, 87. https://doi.org/10.3389/fpls.2020.00087
Article Google Scholar
Prerostova, S., Jarosova, J., Dobrev, P. I., Hluskova, L., Motyka, V., Filepova, R., Knirsch, V., Gaudinova, A., Kieber, J., & Vankova, R. (2021). Heat stress targeting individual organs reveals the central role of roots and crowns in rice stress responses. Frontiers in Plant Science, 12, 799249. https://doi.org/10.3389/fpls.2021.799249
Article Google Scholar
Prerostova, S., Zupkova, B., Petrik, I., Simura, J., Nasinec, I., Kopecky, D., Knirsch, V., Gaudinova, A., Novak, O., & Vankova, R. (2021). Hormonal responses associated with acclimation to freezing stress in Lolium perenne. Environmental and Experimental Botany, 182, 104295. https://doi.org/10.1016/j.envexpbot.2020.104295
Article CAS Google Scholar
Quint, M., Delker, C., Franklin, K. A., Wigge, P. A., Halliday, K. J., & van Zanten, M. (2016). Molecular and genetic control of plant thermomorphogenesis. Nature Plants, 2, 15190. https://doi.org/10.1038/NPLANTS.2015.190
Article CAS Google Scholar
Ren, H., Park, M. Y., Spartz, A. K., Wong, J. H., & Gray, W. M. (2018). A subset of plasma membrane-localized PP2C.D phosphatases negatively regulate SAUR-mediated cell expansion in Arabidopsis. PLoS Genetics, 14, 1007455. https://doi.org/10.1371/journal.pgen.1007455
Article CAS Google Scholar
Romero-Montepaone, S., Sellaro, R., Hernando, C. E., Costigliolo-Rojas, C., Bianchimano, L., Ploschuk, E. L., Yanovsky, M. J., & Casal, J. J. (2021). Functional convergence of growth responses to shade and warmth in Arabidopsis. The New Phytologist, 231, 1890–1905. https://doi.org/10.1111/nph.17430
Article CAS Google Scholar
Sadeghnezhad, E., Sharifi, M., Zare-maivan, H., Khorsand, B., & Zahiri, J. (2019). Cross talk between energy cost and expression of methyl jasmonate-regulated genes: From DNA to protein. Journal of Plant Biochemistry and Biotechnology, 28, 230–243. https://doi.org/10.1007/s13562-018-0480-8
Article CAS Google Scholar
Saksena, H. B., Sharma, M., Singh, D., & Laxmi, A. (2020). The versatile role of glucose signalling in regulating growth, development and stress responses in plants. Journal of Plant Biochemistry and Biotechnology, 29, 687–699. https://doi.org/10.1007/s13562-020-00614-4
Article CAS Google Scholar
Samakovli, D., Tichá, T., Vavrdová, T., Ovečka, M., Luptovčiak, I., Zapletalová, V., Kuchařová, A., Křenek, P., Krasylenko, Y., Margaritopoulou, T., Roka, L., Milioni, D., Komis, G., Hatzopoulos, P., & Šamaj, J. (2020). YODA-HSP90 module regulates phosphorylation-dependent inactivation of SPEECHLESS to control stomatal development under acute heat stress in Arabidopsis. Molecular Plant, 13, 612–633. https://doi.org/10.1016/j.molp.2020.01.001
Article CAS Google Scholar
Sharma, L., Dalal, M., Verma, R. K., Kumar, S. V., Yadav, S. K., Pushkar, S., Kushwaha, S. R., Bhowmik, A., & Chinnusamy, V. (2018). Auxin protects spikelet fertility and grain yield under drought and heat stresses in rice. Environmental and Experimental Botany, 150, 9–24. https://doi.org/10.1016/j.envexpbot.2018.02.013
Article CAS Google Scholar
Sharma, L., Priya, M., Kaushal, N., Bhandhari, K., Chaudhary, S., Dhankher, O. P., Prasad, V. P. V., Siddique, K. H. M., & Nayyar, H. (2020). Plant growth-regulating molecules as thermoprotectants: functional relevance and prospects for improving heat tolerance in food crops. Journal of Experimental Botany, 71, 569–594. https://doi.org/10.1093/jxb/erz333
Article CAS Google Scholar
Sharma, M., Banday, Z. Z., Shukla, B. N., & Laxmi, A. (2019). Glucose-regulated HLP1 acts as a key molecule in governing thermomemory. Plant Physiology, 180, 1081–1100. https://doi.org/10.1104/pp.18.01371
Article CAS Google Scholar
Shekhawat, K., Saad, M. M., Sheikh, A., Mariappan, K., Al-Mahmoudi, H., Abdulhakim, F., Eida, A. A., Jalal, R., Masmoudi, K., & Hirt, H. (2021). Root endophyte induced plant thermotolerance by constitutive chromatin modification at heat stress memory gene loci. EMBO Reports, 22, e51049. https://doi.org/10.15252/embr.202051049
Article CAS Google Scholar
Sheldrake, A. R. (2021). The production of auxin by dying cells. Journal of Experimental Botany, 72, 2288–22300. https://doi.org/10.1093/jxb/erab009
Article CAS Google Scholar
Shigeta, T., Zaizen, Y., Sugimoto, Y., Nakamura, Y., Matsuo, T., & Okamoto, S. (2015). Heat shock protein 90 acts in brassinosteroid signaling through interaction with BES1/BZR1 transcription factor. Journal of Plant Physiology, 178, 69–73. https://doi.org/10.1016/j.jplph.2015.02.003
Article CAS Google Scholar
Silva-Correia, J., Freitas, S., Tavares, R. M., Lino-Neto, T., & Azevedo, H. (2014). Phenotypic analysis of the Arabidopsis heat stress response during germination and early seedling development. Plant Methods, 10, 7. https://doi.org/10.1186/1746-4811-10-7
Article Google Scholar
Silva-Navas, J., Conesa, C. M., Saez, A., Navarro-Neila, S., Garcia-Mina, J. M., Zamarreño, A. M., Baigorri, R., Swarup, R., & Del Pozo, J. C. (2019). Role of cis-zeatin in root responses to phosphate starvation. The New Phytologist, 224, 242–257. https://doi.org/10.1111/nph.16020
Article CAS Google Scholar
Singh, R. K., Prasad, A., Maurya, J., & Prasad, M. (2021). Regulation of small RNA-mediated high temperature stress responses in crop plants. Plant Cell Reports. https://doi.org/10.1007/s00299-021-02745-x
Skalák, J., Černý, M., Jedelský, P., Dobrá, J., Ge, E., Novák, J., Hronková, M., Dobrev, P., Vanková, R., & Brzobohatý, B. (2016). Stimulation of ipt overexpression as a tool to elucidate the role of cytokinins in high temperature responses of Arabidopsis thaliana. Journal of Experimental Botany, 67, 2861–2873. https://doi.org/10.1093/jxb/erw129
Article CAS Google Scholar
Sobol, S., Chayut, N., Nave, N., Kafle, D., Hegele, M., Kaminetsky, R., Wünsche, J. N., & Samach, A. (2014). Genetic variation in yield under hot ambient temperatures spotlights a role for cytokinin in protection of developing floral primordia. Plant, Cell & Environment, 37, 643–657. https://doi.org/10.1111/pce.12184
Article CAS Google Scholar
Stief, A., Altmann, S., Hoffmann, K., Pant, B. D., Scheible, W. R., & Bäurle, I. (2014). Arabidopsis miR156 regulates tolerance to recurring environmental stress through SPL transcription factors. Plant Cell, 26, 1792–1807. https://doi.org/10.1105/tpc.114.123851
Article CAS Google Scholar
Su, Y., Huang, Y., Dong, X., Wang, R., Tang, M., Cai, J., Chen, J., Zhang, X., & Nie, G. (2021). Exogenous methyl jasmonate improves heat tolerance of perennial ryegrass through alteration of osmotic adjustment, antioxidant defense, and expression of jasmonic acid-responsive genes. Frontiers in Plant Science, 12, 664519. https://doi.org/10.3389/fpls.2021.664519
Article Google Scholar
Sun, G., Mei, Y., Deng, D., Xiong, L., Sun, L., Zhang, X., Wen, Z., Liu, S., You, X., Nasrullah, W. D., & Wang, N. N. (2017). N-terminus-mediated degradation of ACS7 is negatively regulated by senescence signaling to allow optimal ethylene production during leaf development in Arabidopsis. Frontiers in Plant Science, 8, 2066. https://doi.org/10.3389/fpls.2017.02066
Article Google Scholar
Sun, M., Jiang, F., Cen, B., Huo, H., & Wu, Z. (2019). Antioxidant enzymes act as indicators predicting intension of acquired and maintenance of acquired thermotolerance and the relationships between basal, acquired and maintenance of acquired thermotolerance of tomato. Scientia Horticulturae, 247, 130–137. https://doi.org/10.1016/j.scienta.2018.12.015
Article CAS Google Scholar
Sýkorová, B., Kurešová, G., Daskalova, S., Trčková, M., Hoyerová, K., Raimanová, I., Motyka, V., Trávníčková, A., Elliott, M. C., & Kamínek, M. (2008). Senescence-induced ectopic expression of the A. tumefaciens ipt gene in wheat delays leaf senescence, increases cytokinin content, nitrate influx, and nitrate reductase activity, but does not affect grain yield. Journal of Experimental Botany, 59, 377–387. https://doi.org/10.1093/jxb/erm319
Article CAS Google Scholar
Thakur, M., Bhattacharya, S., Khosla, P. K., & Puri, S. (2019). Improving production of plant secondary metabolites through biotic and abiotic elicitation. Journal of Applied Research on Medicinal and Aromatic Plants, 12, 1–12. https://doi.org/10.1016/j.jarmap.2018.11.004
Article Google Scholar
Upadhyay, R. K., Handa, A. K., & Mattoo, A. K. (2019). Transcript abundance patterns of 9-and 13-lipoxygenase subfamily gene members in response to abiotic stresses (heat, cold, drought or salt) in tomato (Solanum lycopersicum L.) highlights member-specific dynamics relevant to each stress. Genes, 10, 683. https://doi.org/10.3390/genes10090683
Article CAS Google Scholar
van der Woude, L. C., Perrella, G., Snoek, B. L., van Hoogdalem, M., Novák, O., van Verk, M. C., van Kooten, H. N., Zorn, L. E., Tonckens, R., Dongus, J. A., Praat, M., Stouten, E. A., Proveniers, M. C. G., Vellutini, E., Patitaki, E., Shapulatov, U., Kohlen, W., Balasubramanian, S., Ljung, K., van der Krol, A. R., Smeekens, S., Kaiserli, E., & van Zanten, M. (2019). HISTONE DEACETYLASE 9 stimulates auxin-dependent thermomorphogenesis in Arabidopsis thaliana by mediating H2A.Z depletion. PNAS, 116, 25343–25354. https://doi.org/10.1073/pnas.1911694116
Article CAS Google Scholar
Vishwakarma, K., Upadhyay, N., Kumar, N., Yadav, G., Singh, J., Mishra, R. K., Kumar, V., Verma, V., Upadhyay, R. G., Pandey, M., & Sharma, S. (2017). Abscisic acid signaling and abiotic stress tolerance in plants: A review on current knowledge and future prospects. Frontiers in Plant Science, 8, 161. https://doi.org/10.3389/fpls.2017.00161
Article Google Scholar
Wang, L. J., Fan, L., Loescher, W., Duan, W., Liu, G. J., Cheng, J. S., Luo, H. B., & Li, S. H. (2010). Salicylic acid alleviates decreases in photosynthesis under heat stress and accelerates recovery in grapevine leaves. BMC Plant Biology, 10, 34. https://doi.org/10.1186/1471-2229-10-34
Article CAS Google Scholar
Wang, R., Zhang, Y., Kieffer, M., Yu, H., Kepinski, S., & Estelle, M. (2016). HSP90 regulates temperature-dependent seedling growth in Arabidopsis by stabilizing the auxin co-receptor F-box protein TIR1. Nature Communications, 7, 10269. https://doi.org/10.1038/ncomms
Article CAS Google Scholar
Wang, R. K., Wang, C. E., Fei, Y. Y., Gai, J. Y., & Zhao, T. J. (2013). Genome-wide identification and transcription analysis of soybean carotenoid oxygenase genes during abiotic stress treatments. Molecular Biology Reports, 40, 4737–4745. https://doi.org/10.1007/s11033-013-2570-y
Article CAS Google Scholar
Wang, X., Zhuang, L., Shi, Y., & Huang, B. (2017). Up-regulation of HSFA2c and HSPs by ABA contributing to improved heat tolerance in tall fescue and Arabidopsis. International Journal of Molecular Sciences, 18, 1981. https://doi.org/10.3390/ijms18091981
Article CAS Google Scholar
Wang, Y., Reiter, R. J., & Chan, Z. (2018). Phytomelatonin: A universal abiotic stress regulator. Journal of Experimental Botany, 69, 963–974. https://doi.org/10.1093/jxb/erx473
Article CAS Google Scholar
Wasternack, C., & Song, S. (2017). Jasmonates: Biosynthesis, metabolism, and signaling by proteins activating and repressing transcription. Journal of Experimental Botany, 68, 1303–1321. https://doi.org/10.1093/jxb/erw443
Article CAS Google Scholar
Wei, H., Jing, Y., Zhang, L., & Kong, D. (2021). Phytohormones and their crosstalk in regulating stomatal development and patterning. Journal of Experimental Botany, 72, 2356–2370. https://doi.org/10.1093/jxb/erab034
Article CAS Google Scholar
Wu, C., Tang, S., Li, G., Wang, S., Fahad, S., & Ding, Y. (2019). Roles of phytohormone changes in the grain yield of rice plants exposed to heat: A review. PeerJ, 7, e7792. https://doi.org/10.7717/peerj.7792
Article Google Scholar
Xu, Y., Tian, J., Gianfagna, T., & Huang, B. (2009). Effects of SAG12-ipt expression on cytokinin production, growth and senescence of creeping bentgrass (Agrostis stolonifera L.) under heat stress. Plant Growth Regulation, 57, 281–291. https://doi.org/10.1007/s10725-008-9346-8
Article CAS Google Scholar
Yang, D., Li, Y., Shi, Y., Cui, Z., Luo, Y., Zheng, M., Chen, J., Li, Y., Yin, Y., & Wang, Z. (2016). Exogenous cytokinins increase grain yield of winter wheat cultivars by improving stay-green characteristics under heat stress. PLoS ONE, 11, e0155437. https://doi.org/10.1371/journal.pone.0155437
Article CAS Google Scholar
Yao, Y., He, R. J., Xie, Q. L., Zhao, X. H., Deng, X. M., He, J. B., Song, L., He, J., Marchant, A., Chen, X. Y., & Wu, A. M. (2018). ETHYLENE RESPONSE FACTOR 74 (ERF74) plays an essential role in controlling a respiratory burst oxidase homolog D (RBOHD)-dependent mechanism in response to different stresses in Arabidopsis. The New Phytologist, 213, 1667–1681. https://doi.org/10.1111/nph.14278
Article CAS Google Scholar
Yin, Y., Qin, K., Song, X., Zhang, Q., Zhou, Y., Xia, X., & Yu, J. (2018). BZR1 transcription factor regulates heat stress tolerance through FERONIA receptor-like kinase-mediated reactive oxygen species signaling in tomato. Plant & Cell Physiology, 59, 2239–2254. https://doi.org/10.1093/pcp/pcy146
Article CAS Google Scholar
Yu, X., Zhang, W., Zhang, Y., Zhang, X., Lang, D., & Zhang, X. (2019). The roles of methyl jasmonate to stress in plants. Functional Plant Biology, 46, 197–212. https://doi.org/10.1071/FP18106
Article CAS Google Scholar
Yu, Y., Qi, Y., Xu, J., Dai, X., Chen, J., Dong, C. H., & Xiang, F. (2021). Arabidopsis WRKY71 regulates ethylene-mediated leaf senescence by directly activating EIN2, ORE1 and ACS2 genes. The Plant Journal, 107, 1819–1836. https://doi.org/10.1111/tpj.15433
Article CAS Google Scholar
Zhang, P., Yang, X., Chen, Y., Wei, Z., & Liu, F. (2021). Dissecting the combined effects of air temperature and relative humidity on water-use efficiency of barley under drought stress. Journal of Agronomy and Crop Science, 207, 606–617. https://doi.org/10.1111/jac.12475
Article CAS Google Scholar
Zhang, X. C., Millet, Y. A., Cheng, Z., Bush, J., & Ausubel, F. M. (2015). Jasmonate signalling in Arabidopsis involves SGT1b–HSP70–HSP90 chaperone complexes. Nature Plants, 1, 15049. https://doi.org/10.1038/nplants.2015.49
Article CAS Google Scholar
Zhao, H. J., Zhao, X. J., Ma, P. F., Wang, Y. X., Hu, W. W., Li, L. H., & Zhao, Y. D. (2011). Effects of salicylic acid on protein kinase activity and chloroplast D1 protein degradation in wheat leaves subjected to heat and high light stress. Acta Ecologica Sinica, 31, 259–263. https://doi.org/10.1016/j.chnaes.2011.06.006
Article Google Scholar
Zheng, Y., Yang, Z., Xu, C., Wang, L., Huang, H., & Yang, S. (2020). The interactive effects of daytime high temperature and humidity on growth and endogenous hormone concentration of tomato seedlings. Horticultural Science, 55, 1575–1583. https://doi.org/10.21273/HORTSCI15145-20
Article CAS Google Scholar
Zhou, J., Xia, X. J., Zhou, Y. H., Shi, K., Chen, Z., & Yu, J. Q. (2014). RBOH1-dependent H₂O₂ production and subsequent activation of MPK1/2 play an important role in acclimation-induced cross-tolerance in tomato. Journal of Experimental Botany, 65, 595–607. https://doi.org/10.1093/jxb/ert404
Article CAS Google Scholar
Zuo, Z., Weraduwage, S. M., Lantz, A. T., Sanchez, L. M., Weise, S. E., Wang, J., Childs, K. L., & Sharkey, T. D. (2019). Isoprene acts as a signaling molecule in gene networks important for stress responses and plant growth. Plant Physiology, 180, 124–152. https://doi.org/10.1104/pp.18.01391
Article CAS Google Scholar

Download references

Acknowledgements

Research in the authors’ laboratory is supported by funding from the Ministry of Education, Youth and Sports of CR: Inter-Excellence project No. LTAUSA17081 and from European Regional Development Fund-Project “Centre for Experimental Plant Biology,” grant number CZ.02.1.01/0.0/0.0/16_019/0000738 and by the Czech Science Foundation, grant number 20-22875S.

Author information

Authors and Affiliations

Laboratory of Hormonal Regulations in Plants, Institute of Experimental Botany, Czech Academy of Sciences, Prague, Czech Republic
Sylva Prerostova & Radomira Vankova

Authors

Sylva Prerostova
View author publications
You can also search for this author in PubMed Google Scholar
Radomira Vankova
View author publications
You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Sylva Prerostova .

Editor information

Editors and Affiliations

Department of Horticulture, College of Horticulture and Plant Protection, Henan University of Science and Technology, Luoyang, Henan, China
Golam Jalal Ahammed
Department of Horticulture, Zhejiang University, Hangzhou, China
Jingquan Yu

Rights and permissions

Reprints and permissions

Copyright information

About this chapter

Cite this chapter

Prerostova, S., Vankova, R. (2023). Phytohormone-Mediated Regulation of Heat Stress Response in Plants. In: Ahammed, G.J., Yu, J. (eds) Plant Hormones and Climate Change. Springer, Singapore. https://doi.org/10.1007/978-981-19-4941-8_8

Download citation

DOI: https://doi.org/10.1007/978-981-19-4941-8_8
Published: 01 January 2023
Publisher Name: Springer, Singapore
Print ISBN: 978-981-19-4940-1
Online ISBN: 978-981-19-4941-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)

Publish with us

Policies and ethics