https://doi.org/10.4081/jbr.2023.11706
Exploring the interplay of phytohormones and polyamines in drought-stressed Cress (Lepidium sativum L.) leaves
Submitted: September 2, 2023
Accepted: December 1, 2023
Published: December 14, 2023
Accepted: December 1, 2023
Abstract Views: 470
PDF: 175
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
The study investigated prolonged drought stress effects on phytohormone and polyamine levels in cress (Lepidium sativum L.) leaves, elucidating plant responses to harsh environments. Phytohormones, 12-oxophytodienoic acid (OPDA), Jasmonic acid (JA), Jasmonyl-Isoleucine (JA-Ile), Abscisic acid (ABA), and salicylic acid (SA) increased, especially ABA that rose consistently. Indole-3-acetic acid (IAA) responded akin to ABA and SA. Cytokinins such as zeatin (ZT) and isopentenyl adenine (iP) diversified drought tolerance, ZT fell sharply, and iP remained stable. Gibberellic acid (GA3) declined, while brassinolide (BL) surged with prolonged drought. Polyamines reduced, indicating sensitivity to severe drought. Findings uncovered intricate regulatory mechanisms for plant acclimation to water scarcity. Interaction of OPDA, JA, JA-Ile, ABA, SA, IAA, ZT, iP, GA3, BL, and polyamines contributes to drought coping and physiological balance. Insights into cress leaf response and drought tolerance mechanisms contribute significantly to plant drought acclimation understanding.
Alkhsabah IA, Alsharafa KY, Kalaji HM. Effects of abiotic factors on internal homeostasis of Mentha spicata leaves. Appl Ecol Env Res 2018;16:2537-64.
DOI: https://doi.org/10.15666/aeer/1603_25372564
Al-Sammarraie ON, Alsharafa KY, Al-Limoun MO, et al. Effect of various abiotic stressors on some biochemical indices of Lepidium sativum plants. Sci Rep 2020;10:21131.
DOI: https://doi.org/10.1038/s41598-020-78330-1
Dietz KJ, Zörb C, Geilfus CM. Drought and crop yield. Plant Biol (Stuttg) 2021;23:881-93.
DOI: https://doi.org/10.1111/plb.13304
Taleb MH, Majidi MM, Pirnajmedin F, Maibody SAMM. Plant functional trait responses to cope with drought in seven cool-season grasses. Sci Rep 2023;13:5285
DOI: https://doi.org/10.1038/s41598-023-31923-y
Wahab A, Abdi G, Saleem MH, et al. Plants’ physio-biochemical and phyto-hormonal responses to alleviate the adverse effects of drought stress: A comprehensive review. Plants 2022;11:1620.
DOI: https://doi.org/10.3390/plants11131620
Seleiman MF, Al-Suhaibani N, Ali N, et al. Drought stress impacts on plants and different approaches to alleviate its adverse effects. Plants 2021;10:259.
DOI: https://doi.org/10.3390/plants10020259
Nandy S, Mandal S, Gupta SK, et al. Role of polyamines in molecular regulation and cross-talks against drought tolerance in plants. J Plant Growth Regul 2022;1-17.
Napieraj N, Janicka M, Reda M. Interactions of polyamines and phytohormones in plant response to abiotic stress. Plants 2023;12:1159.
DOI: https://doi.org/10.3390/plants12051159
Sharma A, Shahzad B, Kumar V, et al. Phytohormones regulate accumulation of osmolytes under abiotic stress. Biomolecules 2019;9:285.
DOI: https://doi.org/10.3390/biom9070285
Muhammad Aslam M, Waseem M, Jakada BH, et al. Mechanisms of abscisic acid-mediated drought stress responses in plants. Int J Mol Sci 2022;23:1084.
DOI: https://doi.org/10.3390/ijms23031084
Hai NN, Chuong NN, Tu NHC, et al. Role and regulation of cytokinins in plant response to drought stress. Plants 2020;9:422.
DOI: https://doi.org/10.3390/plants9040422
Gujjar RS, Roytrakul S, Chuekong W, Supaibulwatana K. A synthetic cytokinin influences the accumulation of leaf soluble sugars and sugar transporters, and enhances the drought adaptability in rice. 3 Biotech 2021;11:1-14.
DOI: https://doi.org/10.1007/s13205-021-02908-3
Pérez-Llorca M, Pollmann S, Müller M. Ethylene and jasmonates signaling network mediating secondary metabolites under abiotic stress. Int J Mol Sci 2023;24:5990.
DOI: https://doi.org/10.3390/ijms24065990
Chen K, Li GJ, Bressan RA, et al. Abscisic acid dynamics, signaling, and functions in plants. J Integr Plant Biol 2020;62:25-54.
DOI: https://doi.org/10.1111/jipb.12899
Shao J, Huang K, Batool M, et al. Versatile roles of polyamines in improving abiotic stress tolerance of plants. Front Plant Sci 2022;13:1003155.
DOI: https://doi.org/10.3389/fpls.2022.1003155
Cao ZY, Sun LH, Mou RX, et al. Profiling of phytohormones and their major metabolites in rice using binary solid-phase extraction and liquid chromatography-triple quadrupole mass spectrometry. J Chromatogr A 2016;1451:67-74.
DOI: https://doi.org/10.1016/j.chroma.2016.05.011
Savchenko T, Kolla VA, Wang CQ, et al. Functional convergence of oxylipin and abscisic acid pathways controls stomatal closure in response to drought. Plant Physiol 2014;164:1151-60.
DOI: https://doi.org/10.1104/pp.113.234310
Kienow L, Schneider K, Bartsch M, et al. Jasmonates meet fatty acids: functional analysis of a new acyl-coenzyme A synthetase family from Arabidopsis thaliana. J Exp Bot 2008;59:403-19.
DOI: https://doi.org/10.1093/jxb/erm325
Ribot C, Zimmerli C, Farmer EE, et al. Induction of the Arabidopsis PHO1; H10 gene by 12-oxo-phytodienoic acid but not jasmonic acid via a CORONATINE INSENSITIVE1-dependent pathway. Plant Physiol 2008;147:696-706.
DOI: https://doi.org/10.1104/pp.108.119321
Ali MS, Baek KH. Jasmonic acid signaling pathway in response to abiotic stresses in plants. Int J Mol Sci 2020;21:621.
DOI: https://doi.org/10.3390/ijms21020621
Iqbal S, Wang X, Mubeen I, et al. Phytohormones trigger drought tolerance in crop plants: outlook and future perspectives. Front Plant Sci 2022;12:3378.
DOI: https://doi.org/10.3389/fpls.2021.799318
Per TS, Khan MIR, Anjum NA, et al. Jasmonates in plants under abiotic stresses: Crosstalk with other phytohormones matters. Environ Exp Bot 2018;145:104-20.
DOI: https://doi.org/10.1016/j.envexpbot.2017.11.004
Salvi P, Manna M, Kaur H, et al. Phytohormone signaling and crosstalk in regulating drought stress response in plants. Plant Cell Rep 2021;40:1305-29.
DOI: https://doi.org/10.1007/s00299-021-02683-8
Wang X, Li Q, Xie J, et al. Abscisic acid and jasmonic acid are involved in drought priming-induced tolerance to drought in wheat. Crop J 2021;9:120-32.
DOI: https://doi.org/10.1016/j.cj.2020.06.002
Alsharafa K, Vogel MO, Oelze ML, et al. Kinetics of retrograde signalling initiation in the high light response of Arabidopsis thaliana. Philos Trans R Soc Lond B Biol Sci 2014;369:20130424.
DOI: https://doi.org/10.1098/rstb.2013.0424
Yi R, Du R, Wang J, et al. Dioxygenase JID1 mediates the modification of OPDA to regulate jasmonate homeostasis. Cell Discov 2023;9:39.
DOI: https://doi.org/10.1038/s41421-023-00530-6
Arnold MD, Gruber C, Floková K, et al. The recently identified isoleucine conjugate of cis-12-oxo-phytodienoic acid is partially active in cis-12-oxo-phytodienoic acid-specific gene expression of Arabidopsis thaliana. PloS One 2016;11:e0162829.
DOI: https://doi.org/10.1371/journal.pone.0162829
Schulze A, Zimmer M, Mielke S, et al. Wound-induced shoot-to-root relocation of JA-Ile precursors coordinates Arabidopsis growth. Mol Plant 20191;2:1383-94.
DOI: https://doi.org/10.1016/j.molp.2019.05.013
Wasternack C, Song S. Jasmonates: biosynthesis, metabolism, and signaling by proteins activating and repressing transcription. J Exp Bot 2017;68:1303-21.
DOI: https://doi.org/10.1093/jxb/erw443
Yang J, Duan G, Li C, et al. The crosstalks between jasmonic acid and other plant hormone signaling highlight the involvement of jasmonic acid as a core component in plant response to biotic and abiotic stresses. Front Plant Sci 2019;10:1349.
DOI: https://doi.org/10.3389/fpls.2019.01349
Mahmud S, Ullah C, Kortz A, et al. Constitutive expression of JASMONATE RESISTANT 1 induces molecular changes that prime the plants to better withstand drought. Plant Cell Environ 2022;10:2906-22.
DOI: https://doi.org/10.1111/pce.14402
Pandey S, Chakraborty D. Salicylic acid and drought stress response: biochemical to molecular crosstalk. In: Tripathi B, Müller M (eds) Stress Responses in Plants. Springer, Cham; 2015.
DOI: https://doi.org/10.1007/978-3-319-13368-3_10
Sidhu GPS, Bali AS. Plant responses to drought stress: role of brassinosteroids. In: Brassinosteroids in plant developmental biology and stress tolerance. Cambridge: Academic Press; 2022. pp. 201-16.
DOI: https://doi.org/10.1016/B978-0-12-813227-2.00012-6
Singh PK, Srivastava D, Tiwari P, et al. Drought tolerance in plants: molecular mechanism and regulation of signaling molecules. In: Plant signaling molecules. Woodhead Publishing; 2019. pp. 105-23.
DOI: https://doi.org/10.1016/B978-0-12-816451-8.00006-X
Zhang Y, Li Y, Hassan MJ, et al. Indole-3-acetic acid improves drought tolerance of white clover via activating auxin, abscisic acid and jasmonic acid related genes and inhibiting senescence genes. BMC Plant Biol 2020;20:150.
DOI: https://doi.org/10.1186/s12870-020-02354-y
Verma V, Ravindran P, Kumar PP. Plant hormone-mediated regulation of stress responses. BMC Plant Biol 2016;16:86.
DOI: https://doi.org/10.1186/s12870-016-0771-y
Hallmark HT, Rashotte AM. Cytokinin isopentenyladenine and its glucoside isopentenyladenine‐9G delay leaf senescence through activation of cytokinin‐associated genes. Plant Direct 2020;4:e00292.
DOI: https://doi.org/10.1002/pld3.292
Shohat H, Cheriker H, Kilambi HV, et al. Inhibition of gibberellin accumulation by water deficiency promotes fast and long‐term ‘drought avoidance’ responses in tomato. New Phytol 2021;232:1985-98.
DOI: https://doi.org/10.1111/nph.17709
Zhang C, Huang Z. Effects of endogenous abscisic acid, jasmonic acid, polyamines, and polyamine oxidase activity in tomato seedlings under drought stress. Sci Hortic 2013;159:172-7.
DOI: https://doi.org/10.1016/j.scienta.2013.05.013
Skowron E, Trojak M. Effect of exogenously-applied abscisic acid, putrescine and hydrogen peroxide on drought tolerance of barley. Biologia 2021;76:453-68.
DOI: https://doi.org/10.2478/s11756-020-00644-2
How to Cite
Alsharafa, K. Y. (2023). Exploring the interplay of phytohormones and polyamines in drought-stressed Cress (<i>Lepidium sativum</i> L.) leaves. Journal of Biological Research - Bollettino Della Società Italiana Di Biologia Sperimentale, 96(2). https://doi.org/10.4081/jbr.2023.11706
Copyright (c) 2023 the Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.