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The Dual Role of Reactive Oxygen Species as Signals that Influence Plant Stress Tolerance and Programmed Cell Death

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Reactive Oxygen Species

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Abstract

Reactive oxygen species (ROS) are molecules and radicals which are continuously made by the redox cascades of aerobic metabolism in plants. They may even act as a signal by altering the redox equilibrium of the cell, which can change how specific proteins work or how genes are expressed and respond to biotic and abiotic stress. The network of redox signals controls metabolism to regulate how energy is produced and utilized at every stage of plant growth by interfering with the main signaling molecules (hormones) to adapt to environmental changes. In normal conditions, plants have many ways to fight ROS, but when they are stressed, ROS starts building up and causes oxidative stress. This duality can only be achieved by strictly regulating ROS generation and consumption by the antioxidant defense system within cells. Indeed, ROS are involved in a wide variety of redox-governing actions within cells, which are necessary for maintaining cellular homeostasis. However, its excess synthesis has been linked to oxidative stress, a potentially harmful process that damages biomolecules and cellular structures and contributes to programmed cell death (PCD). The chapter provides a concise view of the dual role of ROS signaling in plant acclamatory defense processes and PCD.

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References

  • Akter S et al (2018) Chemical proteomics reveals new targets of cysteine sulfinic acid reductase. Nat Chem Biol 14:995–1004

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signaling transduction. Annu Rev Plant Biol 55:373

    Article  CAS  PubMed  Google Scholar 

  • Bendall DS, Howe CJ, Nisbet EG, Nisbet RE (2008) Photosynthetic and atmospheric evolution. Introduction. Philos Trans R Soc Lond Ser B Biol Sci 363(1504):2625–2628

    Article  Google Scholar 

  • Bhattacharjee S (2005) Reactive oxygen species and oxidative burst: roles in stress, senescence and signal. Curr Sci 89:1113–1121

    CAS  Google Scholar 

  • Bienert GP et al (2007) Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes. J Biol Chem 282:1183–1192

    Article  CAS  PubMed  Google Scholar 

  • Bose J, Rodrigo-Moreno A, Shabala S (2014) ROS homeostasis in halophytes in the context of salinity stress tolerance. J Exp Bot 65:1241–1257

    Article  CAS  PubMed  Google Scholar 

  • Breygina M, Klimenko E (2020) ROS and ions in cell Signaling during sexual plant reproduction. Int J Mol Sci 21:9476

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chae HB et al (2013) Thioredoxin reductase type C (NTRC) orchestrates enhanced thermotolerance to Arabidopsis by its redox-dependent holdase chaperone function. Mol Plant 6:323–336

    Article  CAS  PubMed  Google Scholar 

  • Chan KX et al (2016) Sensing and signaling of oxidative stress in chloroplasts by inactivation of the SAL1 phosphoadenosine phosphatase. Proc Natl Acad Sci U S A 113:E4567–E4576

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Das K, Roychoudhury A (2014) Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Front Environ Sci 2:53

    Article  Google Scholar 

  • Davletova S et al (2005) Cytosolic ascorbate peroxidase 1 is a central component of the reactive oxygen gene network of Arabidopsis. Plant Cell 17:268–281

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • De Smet B, Willems P, Fernandez-Fernandez AD, Alseekh S, Fernie AR, Messens J, Van Breusegem F (2019) In vivo detection of protein cysteine sulfenylation in plastids. Plant J 97(4):765–778

    Article  PubMed  Google Scholar 

  • Desikan R, Hancock JT, Ichimura K, Shinozaki K, Neill SJ (2001) Harpin induces activation of the Arabidopsis mitogen-activated protein kinases AtMPK4 and AtMPK6. Plant Physiol 126(4):1579–1587

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Desikan R, Reynolds A, Hancock TJ, Neill JS (1998) Harpin and hydrogen peroxide both initiate programmed cell death but have differential effects on defence gene expression in Arabidopsis suspension cultures. Biochem J 330(1):115–120

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dietz KJ, Turkan I, Krieger-Liszkay A (2016) Redox-and reactive oxygen species-dependent signaling into and out of the photosynthesizing chloroplast. Plant Physiol 171(3):1541–1550

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Exposito-Rodriguez M, Laissue PP, Yvon-Durocher G, Smirnoff N, Mullineaux PM (2017) Photosynthesis-dependent H2O2 transfer from chloroplasts to nuclei provides a high-light signalling mechanism. Nat Commun 8:49

    Article  PubMed  PubMed Central  Google Scholar 

  • Flors C, Fryer MJ, Waring J, Reeder B, Bechtold U, Mullineaux PM, Nonell S, Wilson MT, Baker NR (2006) Imaging the production of singlet oxygen in vivo using a new fluorescent sensor, singlet oxygen sensor green®. J Exp Bot 57(8):1725–1734

    Article  CAS  PubMed  Google Scholar 

  • Foyer CH, Noctor G (2005) Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ 28(8):1056–1071

    Article  CAS  Google Scholar 

  • Gadjev I, Stone JM, Gechev TS (2008) Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide. Int Rev Cell Mol Biol 270:87–144. https://doi.org/10.1016/S1937-6448(08)01403-2

    Article  CAS  PubMed  Google Scholar 

  • Gauthier NC, Fardin MA, Roca-Cusachs P, Sheetz MP (2011) Temporary increase in plasma membrane tension coordinates the activation of exocytosis and contraction during cell spreading. Proc Natl Acad Sci 108(35):14467–14472

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • GawroÅ„ski P, WitoÅ„ D, Vashutina K, Bederska M, BetliÅ„ski B, Rusaczonek A, KarpiÅ„ski S (2014) Mitogen-activated protein kinase 4 is a salicylic acid-independent regulator of growth but not of photosynthesis in Arabidopsis. Mol Plant 7(7):1151–1166

    Article  PubMed  Google Scholar 

  • Gechev TS, Van Breusegem F, Stone JM, Denev I, Laloi C (2006) Reactive oxygen species as signals that modulate plant stress responses and programmed cell death. BioEssays 28(11):1091–1101

    Article  CAS  PubMed  Google Scholar 

  • Giesguth M, Sahm A, Simon S, Dietz KJ (2015) Redox-dependent translocation of the heat shock transcription factor AtHSFA8 from the cytosol to the nucleus in Arabidopsis thaliana. FEBS Lett 589:718–725

    Article  CAS  PubMed  Google Scholar 

  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48(12):909–930

    Article  CAS  PubMed  Google Scholar 

  • Girotti AW (2001) Photosensitized oxidation of membrane lipids: reaction pathways, cytotoxic effects and cytoprotective mechanisms. J Photochem Photobiol 63:103–113

    Article  CAS  Google Scholar 

  • Golani Y, Kaye Y, Gilhar O, Ercetin M, Gillaspy G, Levine A (2013) Inositol polyphosphate phosphatidylinositol 5-phosphatase9 (At5ptase9) controls plant salt tolerance by regulating endocytosis. Mol Plant 6(6):1781–1794

    Article  CAS  PubMed  Google Scholar 

  • Gull A, Lone AA, Wani NUI (2019) Biotic and abiotic stresses in plants. In (Ed.), Abiotic and Biotic stress in plants. IntechOpen. https://doi.org/10.5772/intechopen.85832

  • Gupta R, Luan S (2003) Redox control of protein tyrosine phosphatases and mitogen-activated protein kinases in plants. Plant Physiol 132:1149–1152

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Halliwell B (2006) Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol 141(2):312–322

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Halliwell B, Gutteridge JM (2015) Free radicals in biology and medicine. Oxford university press, USA

    Book  Google Scholar 

  • He H, Denecker J, Van Der Kelen K, Willems P, Pottie R, Phua SY, Hannah MA, Vertommen D, Van Breusegem F, Mhamdi A (2021) The Arabidopsis mediator complex subunit 8 regulates oxidative stress responses. Plant Cell 33(6):2032–2057

    Article  PubMed  PubMed Central  Google Scholar 

  • Hipsch M, Lampl N, Zelinger E, Barda O, Waiger D, Rosenwasser S (2021) Sensing stress responses in potato with whole-plant redox imaging. Plant Physiol 187(2):618–631

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Huang H, Ullah F, Zhou DX, Yi M, Zhao Y (2019) Mechanisms of ROS regulation of plant development and stress responses. Front Plant Sci 10:800

    Article  PubMed  PubMed Central  Google Scholar 

  • Huang S, Van Aken O, Schwarzländer M, Belt K, Millar AH (2016) The roles of mitochondrial reactive oxygen species in cellular signaling and stress response in plants. Plant Physiol 171(3):1551–1559

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Inupakutika MA, Sengupta S, Devireddy AR, Azad RK, Mittler R (2016) The evolution of reactive oxygen species metabolism. J Exp Bot 67:5933–5943

    Article  CAS  PubMed  Google Scholar 

  • Iyer NJ, Jia X, Sunkar R, Tang G, Mahalingam R (2012) microRNAs responsive to ozone-induced oxidative stress in Arabidopsis thaliana. Plant Signal Behav 7:484–491

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jabs T, Dietrich RA, Dangl JL (1996) Initiation of runaway cell death in an Arabidopsis mutant by extracellular superoxide. Science 273:1853–1856

    Article  CAS  PubMed  Google Scholar 

  • Kärkönen A, Kuchitsu K (2015) Reactive oxygen species in cell wall metabolism and development in plants. Phytochemistry 112:22–32

    Article  PubMed  Google Scholar 

  • Kaya H, Nakajima R, Iwano M, Kanaoka MM, Kimura S, Takeda S, Kawarazaki T, Senzaki E, Hamamura Y, Higashiyama T, Takayama S (2014) Ca2+-activated reactive oxygen species production by Arabidopsis RbohH and RbohJ is essential for proper pollen tube tip growth. Plant Cell 26(3):1069–1080

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kerchev P, Waszczak C, Lewandowska A, Willems P, Shapiguzov A, Li Z, Alseekh S, Mühlenbock P, Hoeberichts FA, Huang J, Van Der Kelen K (2016) Lack of GLYCOLATE OXIDASE1, but not GLYCOLATE OXIDASE2, attenuates the photorespiratory phenotype of CATALASE2-deficient Arabidopsis. Plant Physiol 171(3):1704–1719

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Koukalova B, Kovarik A, Fajkus J, Siroky J (1997) Chromatin fragmentation associated with apoptotic changes in tobacco cells exposed to cold stress. FEBS Lett 414:289–292

    Article  CAS  PubMed  Google Scholar 

  • Krieger-Liszkay A (2005) Singlet oxygen production in photosynthesis. J Exp Bot 56:337–346

    Article  CAS  PubMed  Google Scholar 

  • Krieger-Liszkay A, Fufezan C, Trebst A (2008) Singlet oxygen production in photosystem II and related protection mechanism. Photosynth Res 98:551–564

    Article  CAS  PubMed  Google Scholar 

  • Lam E (2004) Controlled cell death, plant survival and development. Nat Rev Mol Cell Biol 5:305–315

    Article  CAS  PubMed  Google Scholar 

  • Levine A, Tenhaken R, Dixon R, Lamb C (1994) H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79:583–593

    Article  CAS  PubMed  Google Scholar 

  • Li Z, Wakao S, Fischer BB, Niyogi KK (2009) Sensing and responding to excess light. Annu Rev Plant Biol 60:239–260

    Article  CAS  PubMed  Google Scholar 

  • Liang X, Zhou JM (2018) Receptor-like cytoplasmic kinases: central players in plant receptor kinase–mediated signaling. Annu Rev Plant Biol 69:267–299

    Article  CAS  PubMed  Google Scholar 

  • Liu D et al (2021) Tobacco transcription factor bHLH123 improves salt tolerance by activating NADPH oxidase NtRbohE expression. Plant Physiol 186:1706–1720

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Locato V, Gadaleta C, De Gara L, De Pinto MC (2008) Production of reactive species and modulation of antioxidant network in response to heat shock: a critical balance for cell fate. Plant Cell Environ 31(11):1606–1619

    Article  CAS  PubMed  Google Scholar 

  • López-Huertas E, Corpas FJ, Sandalio LM, Del Río LA (1999) Characterization of membrane polypeptides from pea leaf peroxisomes involved in superoxide radical generation. Biochem J 337(3):531–536

    Article  PubMed  PubMed Central  Google Scholar 

  • MAPK Group (2002) Mitogen-activated protein kinase cascades in plants: a new nomenclature. Trends Plant Sci 7:301–308

    Article  Google Scholar 

  • Martins L et al (2020) Redox modification of the iron-sulfur glutaredoxin GRXS17 activates holdase activity and protects plants from heat stress. Plant Physiol 184:676–692

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Maurel C et al (2015) Aquaporins in plants. Physiol Rev 95:1321–1358

    Article  CAS  PubMed  Google Scholar 

  • Mhamdi A, Van Breusegem F (2018) Reactive oxygen species in plant development. Development 145(15):164376

    Article  Google Scholar 

  • Miller G, Schlauch K, Tam R, Cortes D, Torres MA, Shulaev V, Dangl JL, Mittler R (2009) The plant NADPH oxidase RBOHD mediates rapid systemic signaling in response to diverse stimuli. Sci Signal 2(84):45

    Article  Google Scholar 

  • Miller GA, Suzuki N, Ciftci-Yilmaz SU, Mittler RO (2004) Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant Cell Environ 33:453–467

    Article  Google Scholar 

  • Mittler R (2017) ROS are good. Trends Plant Sci 22:11–19

    Article  CAS  PubMed  Google Scholar 

  • Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9:490–498

    Article  CAS  PubMed  Google Scholar 

  • Mittler R, Zandalinas SI, Fichman Y, Van Breusegem F (2022) Reactive oxygen species signalling in plant stress responses. Nat Rev Mol Cell Biol 23:663–679

    Article  CAS  PubMed  Google Scholar 

  • Mittler R, Zilinskas BA (1992) Molecular cloning and characterization of a gene encoding pea cytosolic ascorbate peroxidase. J Biol Chem 267:21802–21807

    Article  CAS  PubMed  Google Scholar 

  • Müller P, Li XP, Niyogi KK (2001) Non-photochemical quenching. A response to excess light energy. Plant Physiol 125:1558–1566

    Article  PubMed  PubMed Central  Google Scholar 

  • Murphy MP (2009) How mitochondria produce reactive oxygen species. Biochem J 417:1–3

    Article  CAS  PubMed  Google Scholar 

  • Noctor G, De Paepe R, Foyer CH (2007) Mitochondrial redox biology and homeostasis in plants. Trends Plant Sci 12:125–134

    Article  CAS  PubMed  Google Scholar 

  • Nomura H, Komori T, Uemura S, Kanda Y, Shimotani K, Nakai K, Furuichi T, Takebayashi K, Sugimoto T, Sano S, Suwastika IN (2012) Chloroplast-mediated activation of plant immune signalling in Arabidopsis. Nat Commun 3:926

    Article  PubMed  Google Scholar 

  • Ohama N, Sato H, Shinozaki K, Yamaguchi-Shinozaki K (2017) Transcriptional regulatory network of plant heat stress response. Trends Plant Sci 22:53–65

    Article  CAS  PubMed  Google Scholar 

  • Overmyer K, Tuominen H, Kettunen R, Betz C, Langebartels C, Sandermann H Jr, Kangasjärvi J (2000) Ozone-sensitive Arabidopsis rcd1 mutant reveals opposite roles for ethylene and jasmonate signaling pathways in regulating superoxide-dependent cell death. Plant Cell 12:1849–1862

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pennell RI, Lamb C (1997) Programmed cell death in plants. Plant Cell 9:1157–1168

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • de Pinto MC, Paradiso A, Leonetti P, De Gara L (2006) Hydrogen peroxide, nitric oxide and cytosolic ascorbate peroxidase at the crossroad between defence and cell death. Plants J 48:784–795

    Article  Google Scholar 

  • Pitzschke A, Djamei A, Bitton F, Hirt H (2009) A major role of the MEKK1-MKK1/ 2-MPK4 pathway in ROS signalling. Mol Plant 2:120–137

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pitzschke A, Hirt H (2009) Disentangling the complexity of mitogen-activated protein kinases and reactive oxygen species signalling. Plant Physiol 149:606–615

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Podolyan A, Maksimov N, Breygina M (2019) Redox-regulation of ion homeostasis in growing lily pollen tubes. J Plant Physiol 243

    Google Scholar 

  • Rasmusson AG, Geisler DA, Møller IM (2008) The multiplicity of dehydrogenases in the electron transport chain of plant mitochondria. Mitochondrion 8:47–60

    Article  CAS  PubMed  Google Scholar 

  • Raza A, Razzaq A, Mehmood SS, Zou X, Zhang X, Lv Y, Xu J (2019) Impact of climate change on crops adaptation and strategies to tackle its outcome: a review. Plants (Basel) 8(2):34.s

    Article  Google Scholar 

  • Rentel MC, Lecourieux D, Ouaked F, Usher SL, Petersen L, Okamoto H, Knight H, Peck SC, Grierson CS, Hirt H, Knight MR (2004) OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis. Nature 427(6977):858–861

    Article  CAS  PubMed  Google Scholar 

  • Rodrigues O et al (2017) Aquaporins facilitate hydrogen peroxide entry into guard cells to mediate ABA and pathogen-triggered stomatal closure. Proc Natl Acad Sci U S A 114:9200–9205

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sandalio LM, Romero-Puertas MC (2015) Peroxisomes sense and respond to environmental cues by regulating ROS and RNS signalling networks. Ann Bot 116:475–485

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Saxena I, Srikanth S, Chen Z (2016) Cross talk between H2O2 and interacting signal molecules under plant stress response. Front Plant Sci 28:570

    Google Scholar 

  • Shapiguzov A et al (2019) Arabidopsis RCD1 coordinates chloroplast and mitochondrial functions through interaction with ANAC transcription factors. Elife 8:e43284

    Article  PubMed  PubMed Central  Google Scholar 

  • Shumbe L, Chevalier A, Legeret B, Taconnat L, Monnet F, Havaux M (2016) Singlet oxygen-induced cell death in Arabidopsis under high-light stress is controlled by OXI1 kinase. Plant Physiol 170:1757–1771

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sies H, Jones DP (2020) Reactive oxygen species (ROS) as pleiotropic physiological signalling agents. Nat Rev Mol Cell Biol 21:363–383

    Article  CAS  PubMed  Google Scholar 

  • Silver DM et al (2013) Insight into the redox regulation of the phosphoglucan phosphatase SEX4 involved in starch degradation. FEBS J 280:538–548

    Article  CAS  PubMed  Google Scholar 

  • Simon HU, Haj-Yehia A, Levi Schaffer F (2000) Role of reactive oxygen species in apoptosis induction. Apoptosis 5:415–418

    Article  CAS  PubMed  Google Scholar 

  • Singh A, Kumar A, Yadav S, Singh IK (2019) Reactive oxygen species-mediated signaling during abiotic stress. Plant Gene 18:100173

    Article  CAS  Google Scholar 

  • Smirnoff N, Arnaud D (2019) Hydrogen peroxide metabolism and functions in plants. New Phytol 221:1197–1214

    Article  CAS  PubMed  Google Scholar 

  • Swidzinski JA, Sweetlove LJ, Leaver CJ (2002) A custom microarray analysis of gene expression during programmed cell death in Arabidopsis thaliana. Plant J 30(4):431–446

    Article  CAS  PubMed  Google Scholar 

  • Thomas SG, Franklin-Tong VE (2004) Self-incompatibility triggers programmed cell death in Papaver pollen. Nature 429(6989):305–309

    Article  CAS  PubMed  Google Scholar 

  • Tochigi M, Inoue T, Suzuki-Karasaki M, Ochiai T, Ra C, Suzuki-Karasaki Y (2013) Hydrogen peroxide induces cell death in human TRAIL-resistant melanoma through intracellular superoxide generation. Int J Oncol 42(3):863–872

    Article  CAS  PubMed  Google Scholar 

  • Torres MA, Dangl JL, Jones JDGG (2002) Arabidopsis gp91 phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response. Proc Natl Acad Sci U S A 99:517–522

    Article  CAS  PubMed  Google Scholar 

  • Tran D et al (2013) Post-transcriptional regulation of GORK channels by superoxide anion contributes to increases in outward-rectifying K+ currents. New Phytol 198:1039–1048

    Article  CAS  PubMed  Google Scholar 

  • Turrens JF (2003) Mitochondrial formation of reactive oxygen species. J Physiol 552:335–344. https://doi.org/10.1113/jphysiol.2003.049478

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Vacca RA, Valenti D, Bobba A, de Pinto MC, Merafina RS, De Gara L, Passarella S, Marra E (2007) Proteasome function is required for activation of programmed cell death in heat shocked tobacco bright-yellow 2 cells. FEBS Lett 581:917–922

    Article  CAS  PubMed  Google Scholar 

  • Van Hautegem T, Waters AJ, Goodrich J, Nowack MK (2015) Only in dying, life: programmed cell death during plant development. Trends Plant Sci 20(2):102–113

    Article  PubMed  Google Scholar 

  • Vogel MO, Moore M, König K, Pecher P, Alsharafa K, Lee J, Dietz KJ (2014) Fast retrograde signaling in response to high light involves metabolite export, MITOGEN-ACTIVATED PROTEIN KINASE6, and AP2/ERF transcription factors in Arabidopsis. Plant Cell 26:1151–1165

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wang L et al (2020) The Arabidopsis SAFEGUARD1 suppresses singlet oxygen-induced stress responses by protecting grana margins. Proc Natl Acad Sci U S A 117:6918–6927

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Waszczak C, Akter S, Eeckhout D, Persiau G, Wahni K, Bodra N, Van Molle I, De Smet B, Vertommen D, Gevaert K, De Jaeger G (2014) Sulfenome mining in Arabidopsis thaliana. Proc Natl Acad Sci U S A 111:11545–11550

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • **e HT, Wan ZY, Li S, Zhang Y (2014) Spatiotemporal production of reactive oxygen species by NADPH oxidase is critical for tapetal programmed cell death and pollen development in Arabidopsis. Plant Cell 26(5):2007–2023

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yamasaki H, Ogura MP, Kingjoe KA, Cohen MF (2019) D-cysteine-induced rapid root abscission in the water fern azolla pinnata: implications for the linkage between d-amino acid and reactive sulfur species (RSS) in plant environmental responses. Antioxidants 8:411

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Yin Y et al (2018) BZR1 transcription factor regulates heat stress tolerance through FERONIA receptor-like kinase-mediated reactive oxygen species signaling in tomato. Plant Cell Physiol 59:2239–2254

    CAS  PubMed  Google Scholar 

  • Zaffagnini M, De Mia M, Morisse S, Di Giacinto N, Marchand CH, Maes A, Lemaire SD, Trost P (2016) Protein S-nitrosylation in photosynthetic organisms: a comprehensive overview with future perspectives. Biochim Biophys Acta (BBA)-Proteins and Proteomics 1864(8):952–966

    Article  CAS  PubMed  Google Scholar 

  • Zhang Z, Wu Y, Gao M, Zhang J, Kong Q, Liu Y, Ba H, Zhou J, Zhang Y (2012) Disruption of PAMP-induced MAP kinase cascade by a Pseudomonas syringae effector activates plant immunity mediated by the NB-LRR protein SUMM2. Cell Host Microbe 11:253–263

    Article  CAS  PubMed  Google Scholar 

  • Zhu JK (2016) Abiotic stress signaling and responses in plants. Cell 167:313–324

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zou JJ et al (2015) Arabidopsis CALCIUM-DEPENDENT PROTEIN KINASE8 and CATALASE3 function in abscisic acid-mediated signaling and H2O2 homeostasis in stomatal guard cells under drought stress. Plant Cell 27:1445–1460

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Authors and Affiliations

  1. Department of Botany, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, India

    Mohd Soban Ali, Asif Hussain Hajam & Gausiya Bashri

  2. Ranjan Plant Physiology and Biochemistry Laboratory, Department of Botany, University of Allahabad, Prayagraj, India

    Mohammad Suhel & Sheo Mohan Prasad

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  1. Mohd Soban Ali
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  3. Mohammad Suhel
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  1. Botany Section, School of Sciences, Maulana Azad National Urdu University, Hyderabad, India

    Mohammad Faizan

  2. Faculty of Life Sciences, Department of Botany, Aligarh Muslim University, Aligrah, India

    Shamsul Hayat

  3. Botany Section, School of Sciences, Maulana Azad National Urdu University, Hyderabad, India

    S. Maqbool Ahmed

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Ali, M.S., Hajam, A.H., Suhel, M., Prasad, S.M., Bashri, G. (2023). The Dual Role of Reactive Oxygen Species as Signals that Influence Plant Stress Tolerance and Programmed Cell Death. In: Faizan, M., Hayat, S., Ahmed, S.M. (eds) Reactive Oxygen Species. Springer, Singapore. https://doi.org/10.1007/978-981-19-9794-5_10

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