Abstract
Glutathione (GSH), the tripeptide (nonprotein) thiol (γ-glutamyl cysteinyl glycine) and ascorbic acid (AsA, vitamin C) are the most prominent and worth functional low molecular weight soluble antioxidants in plant cells. Environmental fluctuations can lead the plants/crops to abiotic stress conditions. Thus a prompt and effective response, involving many genes and biochemical–molecular mechanism to cope with these conditions is inevitable. In response to these stresses, the ratio of reduced glutathione (GSH) and oxidized form of glutathione (GSSG) tends to decrease due to the oxidation of GSH during the detoxification of reactive oxygen species and changes in its metabolism, which leads to the activation of various defence mechanisms through a redox signalling pathway, including several oxidants, antioxidants, and stress hormones. Glutathione along with AsA plays a pivotal role in protecting cell function. They detoxify H2O2 in the AsA–GSH cycle and are involved in cellular redox regulation and buffering. The ascorbate and glutathione (AsA/DHA and GSH/GSSG) redox pairs are often found to be coupled in plants favours net electron flow from reduced glutathione to dehydroascorbate (DHA). The antioxidation property of ascorbate and glutathione plays a key role in the redox signal transduction process. The plausible reasons could be: (a) signal transduction is influenced as ascorbate and glutathione regulate the cellular H2O2. (b) As these metabolites are responsible for regulating gene expression, so the compartment-specific variations in AsA/DHA and GSH/GSSG ratios may have substantial significance for redox signalling. The aim of present chapter is: firstly, to enlighten the pivotal role of AsA and GSH in plant metabolism and tolerance to abiotic stresses such as oxidative, drought, salinity, heat, and cold stress. Secondly, to emphasize the importance of identification and analysis of AsA–GSH genes responsible for multiple stress tolerance in plant species.
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References
Asada K (1999) The water-water cycle in chloroplasts: scavenging of active oxygen species and dissipation of excess photons. Annu Rev Plant Physiol Mol Biol 50:601–639
Anderson JV, Chevone BI, Hess JL (1992) Seasonal variation in the antioxidant system of eastern white pine needles: evidence for thermal dependence. Plant Physiol 98:501–508
Asada K (2000) The water-water cycle as alternative photon and electron sinks. Phil Trans R Soc Lond B 355:1419–1431
Asada K, Takahashi M (1978) Production and scavenging of activated oxygen in photosynthesis. In: Kyle DJ, Osmond CB, Arntzen CJ (eds) Photoinhibition. Elsevier Science Publishers, Amsterdam, The Netherlands, pp 227–287
Ball L, Accotto G-P, Bechtold U, Creissen G, Funck D, Jimenez A, Kular B, Leyland N, Mejia-Carranza J, Reynolds H, Karpinski S, Mullineaux PM (2004) Evidence for a direct link between glutathione biosynthesis and stress defense gene expression in Arabidopsis. Plant Cell 16:2448–2462
Beeor-Tzahar T, Ben-Hayyim G, Holland D, Faltin Z, Eshdat Y (1995) A stress-associated citrus protein is a distinct plant phospholipid hydroperoxide glutathione peroxidase. FEBS Lett 366:151–155
Bielawski W, Joy KW (1986) Reduced and oxidised glutathione and glutathione reductase activity in tissues of Pisum sativum. Planta 169:267–272
Blum A (1988) Plant Breeding for Stress Environment. CRC Press, Boca Raton, FL
Blumwald E (2000) Sodium transport and salt tolerance in plants. Curr Opin Cell Biol 12:431–434
Bohnert HJ, Sheveleva E (1998) Plant stress adaptations – making metabolism move. Curr Opin Plant Biol 1:267–274
Bohnert HJ, Qingqiu G, Pinghua L, Ma S (2006) Unraveling abiotic stress tolerance mechanisms – getting genomics going. Curr Opin Plant Biol 9:180–188
Bowler C, Van Montagu M, Inźe D (1992) Superoxide dismutase and stress tolerance. Annu Rev Plant Physiol Plant Mol Biol 43:83–116
Boyer JS (1982) Plant productivity and environment. Science 218:443–448
Bray EA, Bailey-Serres J, Weretilnyk E (2000) Responses to abiotic stresses. In: Gruissem W, Buchannan B, Jones R (eds) Biochemistry and molecular biology of plants. American Society of Plant Physiologists, Rockville, MD, pp 1158–1249
Buettner GR, Jurkiewicz BA (1996) Chemistry and biochemistry of ascorbic acid. In: Cadenas E, Packer L (eds) Handbook of antioxidants. Marcel Dekker, New York, pp 91–115
Burns JJ (1957) Missing step in man, monkey and guinea pig required for the biosynthesis of L-ascorbic acid. Nature 180:553
Chang CCC, Ball L, Fryer MJ, Baker NR, Karpinski S, Mullineaux PM (2004) Induction of ASCORBATE PEROXIDASE 2 expression in wounded Arabidopsis leaves does not involve known wound-signalling pathways but is associated with changes in photosynthesis. Plant J 38:499–511
Chapman D (1998) Phospholipase activity during plant growth anddevelopment and in response to environmental stress. Trends Plant Sci 3:419–426
Chen WJ, Zhu T (2004) Networks of transcription factors with roles in environmental stress response. Trends Plant Sci 9:591–596
Chinnusamy V, Jagendorf A, Zhu JK (2005) Understanding and improving salt tolerance in plants. Crop Sci 45:437–448
Choi HI, Hong JH, Ha J, Kang JY, Kim SY (2000) ABFs, a family of ABA-responsive element binding factors. J Biol Chem 275:1723–1730
Cobbett CS, May MJ, Howden R, Rolls B (1998) The glutathione deficient, cadmium-sensitive mutant, cad2-1 of Arabidopsis thaliana is deficient in g-glutamylcysteine synthetase. Plant J 16:73–78
Comba ME, Benavides MP, Tomaro ML (1998) Effect of salt stress on antioxidant defense system in soybean root nodules. Aus J Plant Physiol 25:665–671
Creissen GP, Firmin J, Fryer M, Kular B, Leyland N, Reynolds H, Pastori G, Wellburn F, Baker N, Wellburn A, Mullineaux PM (1999) Elevated glutathione biosynthetic capacity in the chloroplasts of transgenic tobacco plants paradoxically causes increased oxidative stress. Plant Cell 11:1277–1291
Davenport SB, Gallego SM, Benavides MP, Tomaro ML (2003) Behaviour of antioxidant defense system in the adaptive response to salt stress in Helianthus annuus L. cells. Plant Growth Regul 40:81–88
Demiral T, Turkan (2005) Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environ Exp Bot 53:247–257
Denby K, Gehring C (2005) Engineering drought and salinity tolerance in plants: lessons from genome-wide expression profiling in Arabidopsis. Trends Biotechnol 23:547–552
Desikan R, Mackerness SA-H, Hancock JT, Neill SJ (2001) Regulation of the Arabidopsis transcriptome by oxidative stress. Plant Physiol 127:159–172
Dionisio-Sese ML, Tobita S (1998) Antioxidant responses of rice seedlings to salinity stress. Plant Sci 135:1–9
Dron M, Clouse SD, Dixon RA, Lawton MA, Lamb CJ (1988) Glutathione and fungal elicitor regulation of a plant defense gene promoter in electroporated protoplasts. Proc Natl Acad Sci USA 85:6738–6742
Fadzilla NM, Finch RP, Burdon RH (1997) Salinity, oxidative stress and antioxidant responses in shoot cultures of rice. J Exp Bot 48:325–331
Fahmy AS, Mohamed TM, Mohamed SA, Saker MM (1998) Effect of salt stress on antioxidant activities in cell suspension cultures of cantaloupe (Cucumis melo). Egypt J Physiol Sci 22:315–326
Forti G, Elli G (1995) The function of ascorbic acid in photosynthetic phosphorylation. Plant Physiol 109:1207–1211
Foyer CH, Harbinson J (1994) Oxygen metabolism and the regulation of photosynthetic electron transport. In: Foyer CH, Mullineaux P (eds) Causes of photooxidative stresses and amelioration of defense systems in plants. CRC Press, Boca Raton, FL, pp 1–42
Foyer CH, Noctor G (2003) Redox sensing and signaling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol Plant 119:355–364
Foyer CH, Noctor G (2005a) Oxidant and antioxidant signaling in plants a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ 28:1056–1071
Foyer CH, Noctor G (2005b) Redox homeostis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17:1866–1875
Frank W, Munnik T, Kerkmann K, Salamini F, Bartels D (2000) Water deficit triggers phospholipase D activity in the resurrection plant Craterostigma plantagineum. Plant Cell 12:111–124
Fryer MJ, Ball L, Oxborough K, Karpinski S, Mullineaux PM, Baker NR (2003) Control of ascorbate peroxidase 2 expression by hydrogen peroxide and leaf water status during excess light stress reveals a functional organisation of Arabidopsis leaves. Plant J 33:691–705
Gaber A, Yoshimura K, Tamoi M, Takeda T, Nakano Y, Shigeoka S (2004) Induction and functional analysis of two reduced nicotinamide adenine dinucleotide phosphate-dependent glutathione peroxidase-like proteins in Synechocystis PCC 6803 during the progression of oxidative stress. Plant Physiol 136:2855–2861
Gamble PE, Burke JJ (1984) Effect of water stress on the chloroplastic antioxidant system. I. Alterations in glutathione reductase activity. Plant Physiol 76:615–621
Grant JJ, Loake GJ (2000) Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiol 124:21–29
Gueta-Dahan Y, Yaniv Z, Zilinkas BA, Ben-Hayyim G (1997) Salt and oxidative stress: similar and specific responses and their relation to salt tolerance in citrus. Planta 203:460–469
Gullner G, Kómíves T (2001) The role of glutathione and glutathione-related enzymes in plant-pathogen interactions. In: Grill D, Tausz M, De Kok LJ (eds) Significance of glutathione to plant adaptation to the environment. Kluwer, Dordrecht, The Netherlands, pp 207–239
Hare PD, Cress WA, Van SJ (1998) Dissecting the roles of osmolyte accumulation during stress. Plant Cell Environ 21:535–553
Hausladen A, Alscher RG (1993) Glutathione. In: Alscher RG (ed) Antioxidants in higher plants. CRC Press, Boca Raton, FL, pp 1–30
Hernandez JA, Corpas FJ, Gomez M, Del Rio LA, Sevilla F (1993) Salt-induced oxidative stress mediated by activated oxygen species in pea leaf mitochondria. Physiol Plant 89:103–110
Hernandez JA, Olmos E, Corpas FJ, Sevilla F, del Rio LA (1995) Salt-induced oxidative stress in chloroplasts of pea plants. Plant Sci 105:151–167
Hernandez JA, Jimenez A, Mullineaux PM, Sevilla F (2000) Tolerance of pea (Pisum sativum L.) to long term salt stress is associated with induction of antioxidant defenses. Plant Cell Environ 23:853–862
Hernández JA, Ferrer MA, Jime’nez A, Barcelo’ AR, Sevilla F (2001) Antioxidant systems and O2-/H2O2 production in the apoplast of pea leaves. Its relation with salt-induced necrotic lesions in minor veins. Plant Physiol 127:817–831
Hess JL (1994) Free radical scavenging. In: Alscher RG, Wellburn AR (eds) Plant responses to the gaseous environment. Chapman & Hall, London, pp 165–180
Hoffmann AA, Parsons PA (1991) Evolutionary genetics and environmental stress. Oxford University Press, Oxford
Hoffmann AA, Parsons PA (1997) Extreme environmental change and evolution. Cambridge University Press, Cambridge, UK
Holmberg N, Bülow L (1998) Improving stress tolerance in plants by gene transfer. Trends Plant Sci 3:61–66
Huang C, He W, Guo J, Chang X, Su P, Zhang L (2005) Increased sensitivity to salt stress in an ascorbate-deficient Arabidopsis mutant. J Exp Bot 56:3041–3049
Ingram J, Bartels D (1996) The molecular basis of dehydration tolerance in plants. Annu Rev Plant Biol 47:377–403
Jimenez A, Hernandez JA, Pastori G, del Rio LA, Sevilla F (Dec 1998) Role of the ascorbate-glutathione cycle of mitochondria and peroxisomes in the senescence of pea leaves. Plant Physiol 118:1327–1335
Karpinski S, Escobar C, Karpinska B, Creissen G, Mullineaux PM (1997) Photosynthetic electron transport regulates the expression of cytosolic ascorbate peroxidase genes in Arabidopsis during excess light stress. Plant Cell 9:627–640
Karpinski S, Reynolds H, Karpinska B, Wingsle G, Creissen G, Mullineaux P (1999) Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis. Science 284:654–657
Kasuga M, Liu Q, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1999) Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor. Nat Biotechnol 17:287–291
Kiddle G, Pastori GM, Bernard S, Pignocchi C, Antoniw J, Verrier PJ, Foyer CH (2003) Effects of leaf ascorbate content on defense and photosynthesis gene expression in Arabidopsis thaliana. Antioxid Redox Signal 5:23–32
Kukreja S, Nandwal AS, Kumar N, Sharma SK, Unvi V, Sharma PK (2005) Plant water status, H2O2 scavenging enzymes, ethylene evolution and membrane integrity of Cicer arietinum roots as affected by salinity. Biol Plant 49:305–308
Lin CC, Kao CH (2000) Effect of NaCl stress on H2O2 metabolism in rice leaves. Plant Growth Regul 30:151–155
Link G, Tiller K, Baginsky S (1997) Glutathione, a regulator of chloroplast transcription. In: Hatzios KK (ed) Regulation of enzymatic systems detoxifying xenobiotics in plants. Kluwer, Dordrecht, The Netherlands, pp 125–137
lnzé D, Van Montagu M (1995) Oxidative stress in plants. Curr Opin Biotech 6:153–158
Mahalingam R, Gomez-Buitrago A, Eckardt N, Shah N, Guevara-Garcia A (2003) Characterizing the stress/defense transcriptome of Arabidopsis. Genome Biol 4:R20
Maurel C (1997) Aquaporins and water permeability of plant membranes. Annu Rev Plant Biol 48:399–429
Meyer A (2009) The integration of glutathione homeostasis and redox signaling. J Plant Physiol 165:1390–1403
Meyer AJ, Fricker MD (2002) Control of demand-driven biosynthesis of glutathione in green Arabidopsis suspension culture cells. Plant Physiol 130:1927–1937
Millar AH, Mittova V, Kiddle G (2003) Control of ascorbate synthesis by respiration and its implications for stress responses. Plant Physiol 133:443–447
Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
Mittova V, Theodoulou FL, Kiddle G, Gomez L, Volokita M, Tal M, Foyer CH, Guy M (2003a) Coordinate induction of glutathione biosynthesis and glutathione-metabolizing enzymes is correlated with salt tolerance in tomato. FEBS Lett 554:417–421
Mittova V, Tal M, Volokita M, Guy M (2003b) Up-regulation of the leaf mitochondrial and peroxisomal antioxidative systems in response to salt-induced oxidative stress in the wild salt-tolerant tomato species Lycopersicon pennellii. Plant Cell Environ 26:845–856
Molina A, Bueno P, Marín MC, Rosales MPR, Belver A, Venema K, Donaire JP (2002) Involvement of endogenous salicylic acid content, lipoxygenase and antioxidant enzyme activities in the response of tomato cell suspension cultures to NaCl. New Phytol 156:409–415
Moran JF, Becana M, Iturbe-Ormaetxe I, Frechilla S, Klucas RV, Aparicio-Tejo P (1994) Drought induces oxidative stress in pea plants. Planta 194:346–352
Munnik T, Ligterink W, Meskiene I, Calderini O, Beyerly J, Musgrave A, Hirt H (1999) Distinct osmo-sensing protein kinase pathways are involved in signaling moderate and severe hyper-osmotic stress. Plant J 20:381–388
Navari-Izzo F, Meneguzzo S, Loggini B, Vazzana C, Sgherri CLM (1997) The role of the glutathione system during dehydration of Boea hygroscopica. Physiol Plant 99:23–30
Neill SJ, Desikan R, Hancock JT (2002) Hydrogen peroxide signalling. Curr Opin Plant Biol 5:388–395
Nijs D, Kelley PM (1991) Vitamins C and E donate single hydrogen atoms in vivo. FEBS Lett 284:147–151
Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
Noctor G, Gomez L, Vanacker H, Foyer CH (2002) Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling. J Exp Bot 53:1283–1304
Op den Camp RGL, Przbyla D, Ochsenbein C, Laloi C, Kim C, Danon A, Wagner D, Hideg E, Gobel C, Feussner I, Nater M, Apel K (2003) Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. Plant Cell 15:2320–2332
Ort DR, Baker NR (2002) A photoprotective role for O2 as an alternative electron sink in photosynthesis. Curr Opin Plant Biol 5:193–198
Padh H (1990) Cellular functions of ascorbic acid. Biochem Cell Biol 68:1166–1173
Pastori GM, Foyer CH (2002) Common components, networks, and pathways of cross-tolerance to stress. The central role of “redox” and abscisic acid-mediated controls. Plant Physiol 129:460–468
Pastori GM, Kiddle G, Antoniw J, Bernard S, Veljovic-Jovanovic S, Verrier PJ, Noctor G, Foyer CH (2003) Leaf vitamin C contents modulate plant defense transcripts and regulate genes controlling development through hormone signaling. Plant Cell 15:939–951
Pellegrineschi A, Reynolds M, Pacheco M, Brito RM, Almeraya R (2004) Stress-induced expression in wheat of the Arabidopsis thaliana DREB1A gene delays water stress symptoms under greenhouse conditions. Genome 47:493–500
Potters G, De Gara L, Asard H, Horemans N (2002) Ascorbate and glutathione: guardians of the cell cycle, partners in crime? Plant Physiol Biochem 40:537–548
Price AM, Atherton NM, Hendry GAF (1989) Plants under drought-stress generate activated oxygen. Free Radic Res Commun 8:61–66
Rawlins MR, Leaver CJ, May MJ (1995) Characterisation of a cDNA encoding Arabidopsis glutathione synthetase. FEBS Lett 376:81–86
Reddy AR, Chaitanya KV, Vivekanandan M (2004) Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161:1189–1202
Roxas VP, Smith RK, Allen ER, Allen RD (1997) Over expression of glutathione S-transferase/glutathione peroxidase enhances the growth of transgenic tobacco seedlings during stress. Nat Biotech 15:988–991
Roxas VP, Lodhi SA, Garrett DK, Mahan JR, Allen RD (2000) Stress tolerance in transgenic tobacco seedlings that overexpress glutathione S-transferase/glutathione peroxidase. Plant Cell Rep 41:1229–1234
Ruiz JM, Blumwald E (2002) Salinity-induced glutathione synthesis in Brassica napus. Planta 214:965–969
Sairam PK, Saxena DC (2000) Oxidative stress and antioxidants in wheat genotypes: possible mechanism of water stress tolerance. J Agron Crop Sci 184:55–61
Sairam RK, Srivastava GC, Agarwal S, Meena RC (2005) Differences in antioxidant activity in response to salinity stress in tolerant and susceptible wheat genotypes. Biol Plant 49:85–91
Schöffl F, Prandl R, Reindl A (1998) Regulation of the heat-shock response. Plant Physiol 117:1135–1141
Serrano R, Mulet JM, Rios G, Marquez JA, de Larrinoa IF, Leube MP, Mendizabal I, Pascual-Ahuir A, Proft M, Ros R, Montesinos C (1999) A glimpse of the mechanisms of ion homeostasis during salt stress. J Exp Bot 50:1023–1036
Shalata A, Mittova V, Volokita M, Guy M, Tal M (2001) Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: the root antioxidative system. Physiol Plant 112:487–494
Shao HB, Liang ZS, Shao MA (2005a) Adaptation of higher plants to stresses and stress signal transduction. Acta Ecol Sin 25:1871–1882
Shao HB, Liang ZS, Shao MA (2005b) Dynamic changes of anti-oxidative enzymes of 10 wheat genotypes at soil water deficits. Biointerfaces 42:187–195
Shao HB, Liang ZS, Shao MA, Sun Q, Hu ZM (2005c) Investigation on dynamic changes of photosynthetic characteristics of 10 wheat (Triticum aestivum L.) genotypes during two vegetative-growth stages at water deficits. Biointerfaces 43:221–227
Shao HB, Chu LY, Zhao CX, Guo QJ, Liu XA, Ribaut JM (2006) Plant gene regulatory net work system under abiotic stress. Acta Biol Sezeged 50:1–9
Shao HB, Jiang SY, Li FM, Chu LY, Zhao CX, Shao MA, Zhao XN, Li F (2007) Some advances in plant stress physiology and their implications in the systems biology era. Biointerfaces 54:33–36
Shinozaki K, Yamaguchi-Shinozaki K (1997) Gene expression and signal transduction in water-stress response. Plant Physiol 115:327–334
Shinozaki K, Yamaguchi-Shinozaki K (2000) Molecular responses to dehydration and low temperature: differences and cross-talk between two stress signalling pathways. Curr Opin Plant Biol 3:217–223
Singh KB, Foley RC, Onate-Sanchez L (2002) Transcription factors in plant defense and stress responses. Curr Opin Plant Biol 5:430–436
Smirnoff N (1993) The role of active oxygen in the response of plants to water deficit and desiccation. New Phytol 125:27–58
Sreenivasulu N, Grimma B, Wobusa U, Weschkea W (2000) Differential response of antioxidant compounds to salinity stress in salt-tolerant and salt-sensitive seedlings of foxtail millet (Setaria italica). Physiol Plant 109:435–442
Srivalli B, Sharma G, Khanna-Chopra R (2003) Antioxidative defense system in an upland rice cultivar subjected to increasing intensity of water stress followed by recovery. Physiol Plant 119:503–512
Stockinger EJ, Gilmour SJ, Thomashow MF (1997) Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA 94:1035–1040
Sumithra K, Jutur PP, Dalton CB, Reddy AR (2006) Salinity-induced changes in two cultivars of Vigna radiata: responses of antioxidative and proline metabolism. Plant Growth Regul 50:11–22
Tsai YC, Hong CY, Liu LF, Kao CH (2005) Expression of ascorbate peroxidaes and glutathione reductase in roots of rice seedlings in respons to NaCl and H2O2. J Plant Physiol 162:291–299
Tyerman SD, Bohnert HJ, Maurel C, Steudle E, Smith JAC (1999) Plant aquaporins: their molecular biology, biophysics and significance for plant water relations. J Exp Bot 50:1055–1071
Vaidyanathan H, Sivakumar P, Chakrabarty R, Thomas G (2003) Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.) – differential responses in salt tolerant and sensitive varieties. Plant Sci 165:1411–1418
Veljovic-Jovanovic SD, Pignocchi C, Noctor G, Foyer CH (2001) Low ascorbic acid in the vtc1 mutant of Arabidopsis is associated with decreased growth and intracellular redistribution of the antioxidant system. Plant Physiol 127:426–435
Vernoux T, Wilson RC, Seeley KA, Reicheld JP, Muroy S, Brown S, Maughan SC, Cobbett CS, Van Montagu M, Inzé D, May MJ, Sung ZR (2000) The ROOT MERISTEMLESS/ CADMIUM SENSITIVE 2 gene defines a glutathione dependent pathway involved in initiation and maintenance of cell division during postembryonic root development. Plant Cell 12:97–110
Vierling E (1991) The roles of heat-shock proteins in plants. Annu Rev Plant Biol 42:579–620
Vinocur B, Altman A (2005) Recent advances in engineering plant tolerance to abiotic stress: achievements and limitations. Curr Opin Biotechnol 16:123–132
Wang W, Vinocur B, Altman A (2003) Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta 218:1–14
Wingate VPM, Lawton MA, Lamb CJ (1988) Glutathione causes a massive and selective induction of plant defense genes. Plant Physiol 87:206–210
Xiang C, Oliver DJ (1998) Glutathione metabolic genes co-ordinately respond to heavy metals and jasmonic acid in Arabidopsis. Plant Cell 10:1539–1550
Xiang C, Werner BL, Christensen EM, Oliver DJ (2001) The biological functions of glutathione revisited in Arabidopsis transgenic plants with altered glutathione levels. Plant Physiol 126:564–574
Zhu JK (2001) Cell signaling under salt, water and cold stresses. Curr Opin Plant Biol 4:401–406
Zimmermann S, Sentenac H (1999) Plant ion channels: from molecular structures to physiological functions. Curr Opin Plant Biol 2:477–482
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The work of our lab was supported by the Agricultural Ministry of China (the program code: 2009ZX08009-076B), Natural Science Foundation of China (the program code: 30671339 and 30971700), National High-Tech R&D Program (the program code: 2006AA10A113).
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Shamsi, I.H., Jiang, S., Hussain, N., Lin, X., Jiang, L. (2010). Coordinate Role of Ascorbate–Glutathione in Response to Abiotic Stresses. In: Anjum, N., Chan, MT., Umar, S. (eds) Ascorbate-Glutathione Pathway and Stress Tolerance in Plants. Springer, Dordrecht. https://doi.org/10.1007/978-90-481-9404-9_12
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