Skip to main content

Advertisement

Log in

Minimising toxicity of cadmium in plants—role of plant growth regulators

  • Review Article
  • Published:
Protoplasma Aims and scope Submit manuscript

Abstract

A range of man-made activities promote the enrichment of world-wide agricultural soils with a myriad of chemical pollutants including cadmium (Cd). Owing to its significant toxic consequences in plants, Cd has been one of extensively studied metals. However, sustainable strategies for minimising Cd impacts in plants have been little explored. Plant growth regulators (PGRs) are known for their role in the regulation of numerous developmental processes. Among major PGRs, plant hormones (such as auxins, gibberellins, cytokinins, abscisic acid, jasmonic acid, ethylene and salicylic acid), nitric oxide (a gaseous signalling molecule), brassinosteroids (steroidal phytohormones) and polyamines (group of phytohormone-like aliphatic amine natural compounds with aliphatic nitrogen structure) have gained attention by agronomist and physiologist as a sustainable media to induce tolerance in abiotic-stressed plants. Considering recent literature, this paper: (a) overviews Cd status in soil and its toxicity in plants, (b) introduces major PGRs and overviews their signalling in Cd-exposed plants, (c) appraises mechanisms potentially involved in PGR-mediated enhanced plant tolerance to Cd and (d) highlights key aspects so far unexplored in the subject area.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Achard P, Renou J, Berthome R, Harberd N, Genschik P (2008) Plant DELLAs restrain growth and promote survival of adversity by reducing the levels of reactive oxygen species. Curr Biol 18:656–660

    CAS  PubMed  Google Scholar 

  • Ahammed GJ, Choudhary SP, Chen S, Xia X et al (2013) Role of brassinosteroids in alleviation of phenanthrene-cadmium co-contamination-induced N photosynthetic inhibition and oxidative stress in tomato. J Exp Bot 64:199–213

    PubMed Central  CAS  PubMed  Google Scholar 

  • Ahmad A, Hayat S (2011) Brassinosteroids: a class of plant hormone. Springer, Dordrecht

    Google Scholar 

  • Alavi SMN, Arvin MJ, Kalantari KM (2014) Salicylic acid and nitric oxide alleviate osmotic stress in wheat (Triticum aestivum L.) seedlings. J Plant Intl 9:683–688

    Google Scholar 

  • Albersheim P, Darvill AG (1985) Oligosaccharins. Sci Am 253:58–64

    Google Scholar 

  • Alcázar R, Altabella T, Marco F, Bortolotti C et al (2010) Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta 231:1237–1249

    PubMed  Google Scholar 

  • Al-Hakimi AMA (2007) Modification of cadmium toxicity in pea seedlings by kinetin. Plant Soil Environ 53:129–135

    CAS  Google Scholar 

  • Alonso-Ramırez A, Rodrıguez D, Reyes D, Jimenez JA et al (2009) Evidence for a role of gibberellins in salicylic acid-modulated early plant responses to abiotic stress in Arabidopsis seeds. Plant Physiol 150:1335–1344

    PubMed Central  PubMed  Google Scholar 

  • An C, Mou Z (2011) Salicylic acid and its function in plant immunity. J Integr Plant Biol 53:412–428

    CAS  PubMed  Google Scholar 

  • Anjum NA, Ahamd I, Mohmood I, Pacheco M et al (2012) Modulation of glutathione and its related enzymes in plants’ responses to toxic metals and metalloids—a review. Environ Exp Bot 75:307–324

    CAS  Google Scholar 

  • Anjum NA, Umar S, Iqbal M (2014) Assessment of cadmium accumulation, toxicity, and tolerance in Brassicaceae and Fabaceae plants-implications for phytoremediation. Environ Sci Pollut Res 21:10286–10293

    CAS  Google Scholar 

  • Anuradha S, Rao SSR (2009) Effect of 24-epibrassinolide on the photosynthetic activity of radish plants under cadmium stress. Photosynthetica 47:317–320

    CAS  Google Scholar 

  • Aoyama T, Oka A (2003) Cytokinin signal transduction in plant cells. J Plant Res 116:221–231

    CAS  PubMed  Google Scholar 

  • Arasimowicz-Jelonek M, Floryszak-Wieczorek J, Gwozdz EA (2011) The message of nitric oxide in cadmium challenged plants. Plant Sci 181:612–620

    CAS  PubMed  Google Scholar 

  • Arata Y, Nagasawa-Iida A, Uneme H, Nakajima H et al (2010) The phenylquinazoline compound S-4893 is a non-competitive cytokinin antagonist that targets Arabidopsis cytokinin receptor CRE1 and promotes root growth in Arabidopsis and Rice. Plant Cell Physiol 51:2047–2059

    CAS  PubMed  Google Scholar 

  • Asensi-Fabado MA, Cela J, Müller M, Arrom L et al (2012) Enhanced oxidative stress in the ethylene-insensitive (ein3-1) mutant of Arabidopsis thaliana exposed to salt stress. J Plant Physiol 169:360–368

    CAS  PubMed  Google Scholar 

  • Asgher M, Khan MIR, Iqbal N, Masood A, Khan NA (2013) Cadmium tolerance in mustard cultivars: dependence on proline accumulation and nitrogen assimilation. J Fun Exp Bot 3:30–42

    Google Scholar 

  • Asgher M, Khan NA, Khan MIR, Fatma M, Masood A (2014) Ethylene production is associated with alleviation of cadmium-induced oxidative stress by sulfur in mustard types differing in ethylene sensitivity. Ecotoxicol Environ Saf 106:54–61

    CAS  PubMed  Google Scholar 

  • Astolfi S, Zuchi S, Passera C (2005) Effect of cadmium on H+-ATPase activity of plasma membrane vesicles isolated from roots of different S-supplied maize (Zea mays L.) plants. Plant Sci 169:361–368

    CAS  Google Scholar 

  • Auxtová O, Lisková D, Kákoniová D, Kubacková M et al (1995) Effect of galactoglucomannan-derived oligosaccharides on elongation growth of pea and spruce stem segments stimulated by auxin. Planta 196:420–424

    Google Scholar 

  • Bai X, Yang L, Tian M, Chen J et al (2011) Nitric oxide enhances desiccation tolerance of recalcitrant Antiaris toxicaria seeds via protein S-nitrosylation and carbonylation. PLoS ONE 6:e20714

    PubMed Central  CAS  PubMed  Google Scholar 

  • Bansal P, Sharma P, Goyal V (2002) Impact of lead and cadmium on enzyme of citric acid cycle in germinating pea seeds. Biol Plant 45:125–127

    CAS  Google Scholar 

  • Basra A (2000) Plant growth regulators in agriculture and horticulture: their role and commercial uses. CRC Press, Boca Raton

    Google Scholar 

  • Belkadhi A, De Haro A, Soengas P, Obregon S et al (2014) Salicylic acid increases tolerance to oxidative stress induced by hydrogen peroxide accumulation in leaves of cadmium-exposed flax (Linum usitatissimum L.). J Plant Interact 9:647–654

    Google Scholar 

  • Besson-Bard A, Pugin A, Wendehenne D (2008) New insights into nitric oxide signaling in plants. Annu Rev Plant Biol 59:21–39

    CAS  PubMed  Google Scholar 

  • Bhattacharya A, Kourmpetli S, Davey MR (2010) Practical applications of manipulating plant architecture by regulating gibberellin metabolism. J Plant Growth Regul 29:249–256

    CAS  Google Scholar 

  • Bishop GJ, Yokota T (2001) Plants steroid hormones, brassinosteroids: current highlights of molecular aspects on their synthesis/metabolism, transport, perception and response. Plant Cell Physiol 42:114–120

    CAS  PubMed  Google Scholar 

  • Bleecker AB, Kende H (2000) Ethylene: a gaseous signal molecule in plants. Annu Rev Cell Dev Biol 16:1–18

    CAS  PubMed  Google Scholar 

  • Bocova B, Huttova J, Mistrık I, Tamas L (2013) Auxin signalling is involved in cadmium-induced glutathione-S-transferase activity in barley root. Acta Physiol Plant 35:2685–2690

    CAS  Google Scholar 

  • Browse J (2009) Jasmonate passes muster: a receptor and targets for the defense hormone. Annu Rev Plant Biol 60:183–205

    CAS  PubMed  Google Scholar 

  • Bulak P, Walkiewicz A, Brzezińska M (2014) Plant growth regulators-assisted phytoextraction. Biol Plant 58:1–8

  • Calzadilla PI, Gazquez A, Maiale SJ, Ruiz OA, Bernardina MA (2014) Polyamines as indicators and modulators of the abiotic stress in plants. In: Anjum NA, Gill SS, Gill R (eds) Plant adaptation to environmental change: significance of amino acids and their derivatives. CABI, Wallingford, UK, pp 109–128

    Google Scholar 

  • Chao YY, Chen CY, Huang WD, Ching CH (2010) Salicylic acid-mediated hydrogen peroxide accumulation and protection against Cd toxicity in rice leaves. Plant Soil 329:327–337

    CAS  Google Scholar 

  • Chen Z, Zheng Z, Huang J, Lai Z, Fan B (2009) Biosynthesis of salicylic acid in plants. Plant Signal Behav 4:493–496

    PubMed Central  CAS  PubMed  Google Scholar 

  • Chen J, Yan Z, Li X (2014) Effect of methyl jasmonate on cadmium uptake and antioxidative capacity in Kandelia obovata seedlings under cadmium stress. Ecotoxicol Environ Saf 104:349–356

    CAS  PubMed  Google Scholar 

  • Chmielowska-Bąk J, Lefèvre I, Lutts S, Deckert J (2013) Short term signaling responses in roots of young soybean seedlings exposed to cadmium stress. J Plant Physiol 170:1585–1594

    PubMed  Google Scholar 

  • Choi J, Hwang I (2007) Cytokinin: perception, signal transduction, and role in plant growth and development. J Plant Biol 50:98–108

    CAS  Google Scholar 

  • Clemens S, Antosiewicz DM, Ward JM, Schachtman DP, Schroeder JI (1998) The plant cDNA LCT1 mediates the uptake of calcium and cadmium in yeast. Proc Natl Acad Sci U S A 95:12043–12048

    PubMed Central  CAS  PubMed  Google Scholar 

  • Cui W, Li L, Gao Z, Wu H et al (2012) Haem oxygenase-1 is involved in salicylic acid-induced alleviation of oxidative stress due to cadmium stress in Medicago sativa. J Exp Bot 63:5521–5534

    PubMed Central  CAS  PubMed  Google Scholar 

  • Curie C, Cassin G, Couch D, Divol F, Higuchi K et al (2009) Metal movement within the plant: contribution of nicotianamine and yellow stripe 1-like transporters. Ann Bot 103:1–11

    PubMed Central  CAS  PubMed  Google Scholar 

  • Cutler SR, Rodriguez PL, Finkelstein RR, Abrams SR (2010) Abscisic acid: emergence of a core signaling network. Annu Rev Plant Biol 61:651–679

    CAS  PubMed  Google Scholar 

  • DalCorso G, Farinati S, Furini A (2010) Regulatory networks of cadmium stress in plants. Plant Signal Behav 5:663–667

    PubMed Central  CAS  PubMed  Google Scholar 

  • Davies PJ (2010) Plant hormones: biosynthesis, signal transduction, action!, revised 3rd edn. Springer, Dordrecht

  • De Michele R, Vurro E, Rigo C, Costa A et al (2009) Nitric oxide is involved in cadmium-induced programmed cell death in Arabidopsis suspension cultures. Plant Physiol 150:217–228

    PubMed Central  PubMed  Google Scholar 

  • Dias MC, Monteiro C, Moutinho-Pereira J, Correia C et al (2013) Cadmium toxicity affects photosynthesis and plant growth at different levels. Acta Physiol Plant 35:1281–1289

    CAS  Google Scholar 

  • Du H, Liu H, Xiong L (2013) Endogenous auxin and jasmonic acid levels are differentially modulated by abiotic stresses in rice. Front Plant Sci 4:397

    PubMed Central  PubMed  Google Scholar 

  • El-Mashad AA, Mohamed HI (2012) Brassinolide alleviates salt stress and increases antioxidant activity of cowpea plants (Vigna sinensis). Protoplasma 249:625–635

    CAS  PubMed  Google Scholar 

  • Elobeid M, Gobel C, Feussner I, Polle A (2012) Cadmium interferes with auxin physiology and lignification in poplar. J Exp Bot 63:1413–1421

    PubMed Central  CAS  PubMed  Google Scholar 

  • Fayez KA, Bazaid SA (2014) Improving drought and salinity tolerance in barley by application of salicylic acid and potassium nitrate. J Saudi Soc Agric Sci 13:45–55

    Google Scholar 

  • Fediuc E, Lips SH, Erdei L (2005) O-acetylserine (thiol) lyase activity in Phragmites and Typha plants under cadmium and NaCl stress conditions and the involvement of ABA in the stress response. J Plant Physiol 162:865–872

    CAS  PubMed  Google Scholar 

  • Gallego SM, Pena LB, Barcia RA, Azpilicueta CE et al (2012) Unravelling cadmium toxicity and tolerance in plants: insight into regulatory mechanisms. Environ Exp Bot 83:33–46

    CAS  Google Scholar 

  • Gemrotová M, Kulkarni MG, Stirk WA, Strnad M et al (2013) Seedlings of medicinal plants treated with either a cytokinin antagonist (PI-55) or an inhibitor of cytokinin degradation (INCYDE) are protected against the negative effects of cadmium. Plant Growth Regul 71:137–145

    Google Scholar 

  • George E, Hall M, Klerk GJ (2008a) Plant growth regulators III: gibberellins, ethylene, abscisic acid, their analogues and inhibitors; miscellaneous compounds. In: George E, Hall M, Klerk GJ (eds) Plant propagation by tissue culture. Springer, Dordrecht, The Netherlands, pp 227–281

    Google Scholar 

  • George E, Hall M, Klerk GJ (2008b) Plant growth regulators II: cytokinins, their analogues and antagonists. In: George E, Hall M, Klerk GJ (eds) Plant propagation by tissue culture. Springer, Dordrecht, The Netherlands, pp 205–226

    Google Scholar 

  • Ghanashyam C, Jain M (2009) Role of auxin-responsive genes in biotic stress responses. Plant Signal Behav 4:846–848

    PubMed Central  CAS  PubMed  Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Gill SS, Tuteja N (2010b) Polyamines and abiotic stress tolerance in plants. Plant Signal Behav 5:26–33

    PubMed Central  CAS  PubMed  Google Scholar 

  • Gill SS, Khan NA, Tuteja N (2012) Cadmium at high dose perturbs growth, photosynthesis and nitrogen metabolism while at low dose it up regulates sulfur assimilation and antioxidant machinery in garden cress (Lepidium sativum L.). Plant Sci 182:112–120

    CAS  PubMed  Google Scholar 

  • Gill SS, Hasanuzzaman M, Nahar K, Macovei A, Tuteja N (2013) Importance of nitric oxide in cadmium stress tolerance in crop plants. Plant Physiol Biochem 63:254–261

    CAS  PubMed  Google Scholar 

  • Gomez CA, Arbona V, Jacas J, PrimoMillo E, Talon M (2002) Abscisic acid reduces leaf abscission and increases salt tolerance in citrus plants. J Plant Growth Regul 21:234–240

    Google Scholar 

  • Goncalves JF, Nicoloso FT, Becker AG, Pereira LB et al (2009) Photosynthetic pigments content, δ-aminolevulinic acid dehydratase and acid phosphatase activities and mineral nutrients concentration in cadmium-exposed Cucumis sativus L. Biologia 64:310–318

    CAS  Google Scholar 

  • Groppa MD, Tomaro ML, Benavides MP (2001) Polyamines as protectors against cadmium or copper-induced oxidative damage in sunflower leaf discs. Plant Sci 161:481–488

    CAS  Google Scholar 

  • Gupta R, Chakrabarty SK (2013) Gibberellic acid in plant—still a mystery unresolved. Plant Signal Behav 8:e25504

    PubMed Central  PubMed  Google Scholar 

  • Gupta UC, Gupta SC (1998) Trace element toxicity relationships to crop production and livestock and human health: implications for management. J Commun Soil Sci Plant 29:1491–1522

    CAS  Google Scholar 

  • Ha S, Vankova R, Yamaguchi-Shinozaki K, Shinozaki K, Tran LSP (2012) Cytokinins: metabolism and function in plant adaptation to environmental stresses. Trends Plant Sci 17:172–179

    CAS  PubMed  Google Scholar 

  • Hadi F, Ali N, Ahmad A (2014) Enhanced phytoremediation of cadmium-contaminated soil by Parthenium hysterophorus plant: effect of gibberellic acid (GA3) and synthetic chelator, alone and in combinations. Biorem J 18:46–55

    CAS  Google Scholar 

  • Han RM, Lefèvre I, Albacete A, Pérez-Alfocea F et al (2013) Antioxidant enzyme activities and hormonal status in response to Cd stress in the wetland halophyte Kosteletzkya virginica under saline conditions. Physiol Plant 147:352–368

    CAS  PubMed  Google Scholar 

  • Hasanuzzaman M, Nahar K, Alam M, Fujita M (2012) Exogenous nitric oxide alleviates high temperature induced oxidative stress in wheat (Triticum aestivum L.) seedlings by modulating the antioxidant defense and glyoxalase system. Aust J Crop Sci 6:1314

    CAS  Google Scholar 

  • Hashem HA (2014) Cadmium toxicity induces lipid peroxidation and alters cytokinin content and antioxidant enzyme activities in soybean. Botany 92:1–7

    CAS  Google Scholar 

  • Hooykaas PJ, Hall MA, Libbenga KR (1999) Biochemistry and molecular biology of plant hormones. Elsevier, Amsterdam

    Google Scholar 

  • Horvath E, Szalai G, Janda T (2007) Induction of abiotic stress tolerance by salicylic acid signalling. J Plant Growth Regul 26:290–300

    CAS  Google Scholar 

  • Hsu YT, Kao CH (2003) Role of abscisic acid in cadmium tolerance of rice (Oryza sativa L.) seedlings. Plant Cell Environ 26:867–874

    CAS  PubMed  Google Scholar 

  • Hsu YT, Kao CH (2004) Cadmium toxicity is reduced by nitric oxide in rice leaves. Plant Growth Regul 42:227–238

    CAS  Google Scholar 

  • Hsu YT, Kao CH (2007) Cadmium-induced oxidative damage in rice leaves is reduced by polyamines. Plant Soil 291:27–37

    CAS  Google Scholar 

  • Hu YF, Zhou G, Na XF, Yang L et al (2013) Cadmium interferes with maintenance of auxin homeostasis in Arabidopsis seedlings. J Plant Physiol 170:965–975

    CAS  PubMed  Google Scholar 

  • Huang B, Chu CH, Chen SL, Juan HF, Chen TM (2006) A proteomics study of the mung bean epicotyl regulated by brassinosteroids under conditions of chilling stress. Cell Mol Biol Lett 11:264–278

    CAS  PubMed  Google Scholar 

  • IARC (1994) Beryllium, cadmium, mercury, and exposures in the glass manufacturing industry[M]. In: Monographs on the evaluation of carcinogenic risks to humans. Lyon: WHO Press 58:444

  • Igarashi K, Kashiwagi K (2000) Polyamines: mysterious modulators of cellular functions. Biochem Biophys Res Commun 271:559–564

    CAS  PubMed  Google Scholar 

  • Iqbal M, Ashraf M (2013) Gibberellic acid mediated induction of salt tolerance in wheat plants: growth, ionic partitioning, photosynthesis, yield and hormonal homeostasis. Environ Exp Bot 86:76–85

    CAS  Google Scholar 

  • Iqbal N, Nazar R, Khan MIR, Masood A, Khan NA (2011) Role of gibberellins in regulation of source-sink relations under optimal and limiting environmental conditions. Curr Sci 100:7

    Google Scholar 

  • Iqbal N, Trivellini A, Masood A, Ferrante A, Khan NA (2013) Current understanding on ethylene signaling in plants: the influence of nutrient availability. Plant Physiol Biochem 73:128–138

    CAS  PubMed  Google Scholar 

  • Jain M, Khurana JP (2009) Transcript profiling reveals diverse roles of auxin-responsive genes during reproductive development and abiotic stress in rice. FEBS J 276:3148–3162

    CAS  PubMed  Google Scholar 

  • Jain M, Ghanashyam C, Bhattacharjee A (2010) Comprehensive expression analysis suggests overlapping and specific roles of rice glutathione-S-transferase genes during development and stress responses. BMC Genomics 11:73

    PubMed Central  PubMed  Google Scholar 

  • Janeczko A, Kościelniak J, Pilipowicz M, Lu-kaszewska S (2005) Protection of winter rape photosystem 2 by 24-epibrassinolide under cadmium stress. Photosynthetica 43:293–298

    CAS  Google Scholar 

  • Janicka-Russak M, Kabała K, Burzyński M (2012) Different effect of cadmium and copper on H+-ATPase activity in plasma membrane vesicles from Cucumis sativus roots. J Exp Bot 63:4133–4142

    PubMed Central  CAS  PubMed  Google Scholar 

  • Jemâa E, Saida A, Sadok B (2011) Impact of indole-3-butyric acid and indole-3-acetic acid on the lateral roots growth of Arabidopsis under salt stress conditions. Aust J Agri Eng 2:18

    Google Scholar 

  • Kaminek M, Motyka V, Vankova R (1997) Regulation of cytokinin content in plant cells. Physiol Plant 101:689–700

    CAS  Google Scholar 

  • Kang DJ, Seo YJ, Lee JD, Ishii R, Kim K, Shin DH et al (2005) Jasmonic acid differentially affects growth, ion uptake and abscisic acid concentration in salt-tolerant and salt-sensitive rice cultivars. J Agron Crop Sci 191:273–282

    CAS  Google Scholar 

  • Kazan K, Manners JM (2012) JAZ repressors and the orchestration of phytohormone crosstalk. Trends Plant Sci 17:22–31

    CAS  PubMed  Google Scholar 

  • Keramat B, Kalantari KM, Arvin MJ (2009) Effects of methyl jasmonate in regulating cadmium induced oxidative stress in soybean plant (Glycine max L.). Afr J Micro Res 3:240–244

    CAS  Google Scholar 

  • Khan MIR, Khan NA (2014) Ethylene reverses photosynthetic inhibition by nickel and zinc in mustard through changes in PS II activity, photosynthetic nitrogen use efficiency, and antioxidant metabolism. Protoplasma 251:1007–1019

    CAS  PubMed  Google Scholar 

  • Khan MIR, Iqbal N, Masood A, Khan NA (2012a) Variation in salt tolerance of wheat cultivars: role of glycinebetaine and ethylene. Pedosphere 22:746–754

    CAS  Google Scholar 

  • Khan NA, Nazar R, Iqbal N, Anjum NA (2012b) Phytohormones and abiotic stress tolerance in plants. Springer Verlag, Berlin

    Google Scholar 

  • Khan MIR, Iqbal N, Masood A, Per TS, Khan NA (2013) Salicylic acid alleviates adverse effects of heat stress on photosynthesis through changes in proline production and ethylene formation. Plant Signal Behav 8:e26374

    PubMed Central  PubMed  Google Scholar 

  • Khan MIR, Asgher M, Khan NA (2014) Alleviation of salt-induced photosynthesis and growth inhibition by salicylic acid involves glycinebetaine and ethylene in mungbean (Vigna radiata L.). Plant Physiol Biochem 80:67–74

    CAS  PubMed  Google Scholar 

  • Kollárová K, Lišková D, Lux A (2007) Influence of galactoglucomannan oligosaccharides on root culture of Karwinskia humboldtiana. Plant Cell Tissue Org Cult 91:9–19

    Google Scholar 

  • Kollárová K, Vatehová Z, Slováková L, Lišková D (2010) Interaction of galactoglucomannan oligosaccharides with auxin in mung bean primary root. Plant Physiol Biochem 48:401–406

    PubMed  Google Scholar 

  • Kováčik J, Babula P, Klejdus B, Hedbavny J, Jarosova M (2014) Unexpected behavior of some nitric oxide modulators under cadmium excess in plant tissue. PLoS ONE 9:e91685

    PubMed Central  PubMed  Google Scholar 

  • Krantev A, Yordanova R, Janda T, Szalai G, Popova L (2008) Treatment with salicylic acid decreases the effect of cadmium on photosynthesis in maize plants. J Plant Physiol 165:920–931

    CAS  PubMed  Google Scholar 

  • Krishna P (2003) Brassinosteroid-mediated stress responses. J Plant Growth Regul 22:289–297

    CAS  PubMed  Google Scholar 

  • Kučerová D, Kollárová K, Zelko I, Vatehová Z, Lišková D (2014) Galactoglucomannan oligosaccharides alleviate cadmium stress in Arabidopsis. J Plant Physiol 171:518–524

    PubMed  Google Scholar 

  • Kudo T, Kiba T, Sakakibara H (2010) Metabolism and long-distance translocation of cytokinins. J Integr Plant Biol 52:53–60

    CAS  PubMed  Google Scholar 

  • Kumar M, Bijo AJ, Baghel RS, Reddy CRK, Jha B (2012) Selenium and spermine alleviate cadmium induced toxicity in the red seaweed Gracilaria dura by regulating antioxidants and DNA methylation. Plant Physiol Biochem 51:129–138

    CAS  PubMed  Google Scholar 

  • Kumari A, Sheokand S, Swaraj K (2010) Nitric oxide induced alleviation of toxic effects of short term and long term Cd stress on growth, oxidative metabolism and Cd accumulation in Chickpea. Braz J Plant Physiol 22:271–284

    Google Scholar 

  • Kupper H, Parameswaran A, Leitenmaier B, Trtílek M, Šetlík I (2007) Cadmium‐induced inhibition of photosynthesis and long‐term acclimation to cadmium stress in the hyperaccumulator Thlaspi caerulescens. New Phytol 175:655–674

    PubMed  Google Scholar 

  • Kusano T, Yamaguchi K, Berberich T, Takahashi Y (2007) The polyamine spermine rescues Arabidopsis from salinity and drought stresses. Plant Signal Behav 2:251–252

    PubMed Central  PubMed  Google Scholar 

  • Kyozuka J (2007) Control of shoot and root meristem function by cytokinin. Curr Opin Plant Biol 10:442–446

    CAS  PubMed  Google Scholar 

  • Lakimova ET, Woltering EJ, Kapchina-Toteva VM et al (2008) Cadmium toxicity in cultured tomato cells-role of ethylene, proteases and oxidative stress in cell death signaling. Cell Biol Int 32:1521–1529

    Google Scholar 

  • Laspina NV, Groppa MD, Tomaro ML, Benavides MP (2005) Nitric oxide protects sunflower leaves against Cd-induced oxidative stress. Plant Sci 169:323–330

    CAS  Google Scholar 

  • Lee HE, Shin D, Park SR, Han SE, Jeong MJ, Kwon TR et al (2007) Ethylene responsive element binding protein 1(StEREBP1) from Solanum tuberosum increases tolerance to abiotic stress in transgenic potato plants. Biochem Biophys Res Commun 353:863–868

    CAS  PubMed  Google Scholar 

  • Leitner M, Vandelle E, Gaupels F, Bellin D et al (2009) NO signals in the haze: nitric oxide signalling in plant defence. Curr Opin Plant Biol 12:451–458

    CAS  PubMed  Google Scholar 

  • Lequeux H, Hermans C, Lutts S, Verbruggen N (2010) Response to copper excess in Arabidopsis thaliana: impact on the root system architecture, hormone distribution, lignin accumulation and mineral profile. Plant Physiol Biochem 48:673–682

    CAS  PubMed  Google Scholar 

  • Li X, Cai J, Liu F, Dai T, Cao W, Jiang D (2014) Exogenous abscisic acid application during grain filling in winter wheat improves cold tolerance of offspring’s seedlings. J Agric Crop Sci. doi:10.1111/jac.12064

    Google Scholar 

  • Liao WB, Huang GB, Yu JH, Zhang ML (2012) Nitric oxide and hydrogen peroxide alleviate drought stress in marigold explants and promote its adventitious root development. Plant Physiol Biochem 58:6–15

    CAS  PubMed  Google Scholar 

  • Lindblad MS, Dahlman O, Sjöberg J, Albertsson AC (2009) Modified galactoglucomannans from forestry waste-water for films and hydrogels. In: Edgar KJ, Heinze T, Buchanan CM (eds) Polysaccharide materials: performance by design. ACS Symposium Series, vol. 1017, American Chemical Society, pp 185–198

  • Lišková D, Auxtová O, Kákoniová D, Kubačková M et al (1995) Biological activity of galactoglucomannan-derived oligosaccharides. Planta 196:425–429

    Google Scholar 

  • Litwack G (2005) Plant hormones. Vol. 72, vitamins and hormones advances in research and applications, vol 72. Elsevier Academic Press, San Diego

    Google Scholar 

  • Liu JH, Kitashiba H, Wang J, Ban Y, Moriguchi T (2007) Polyamines and their ability to provide environmental stress tolerance to plants. Plant Biotechnol 24:117–126

    CAS  Google Scholar 

  • Liu K, Shen L, Sheng J (2008) Improvement in cadmium tolerance of tomato seedlings with an antisense DNA for 1-aminocyclopropane-1-carboxylate synthase. J Plant Nutr 31:809–827

    CAS  Google Scholar 

  • Liu Y, Jiang H, Zhao Z, An L (2010) Nitric oxide synthase like activity-dependent nitric oxide production protects against chilling-induced oxidative damage in Chorispora bungeana suspension cultured cells. Plant Physiol Biochem 48:936–944

    CAS  PubMed  Google Scholar 

  • Ljung K (2013) Auxin metabolism and homeostasis during plant development. Development 140:943–950

    CAS  PubMed  Google Scholar 

  • Lundqvist J, Teleman A, Junel L, Zacchi G et al (2002) Isolation and characterization of galactoglucomannan from spruce (Picea abies). Carbohydr Polym 48:29e39

    Google Scholar 

  • Lux A, Martinka M, Vaculík M, White PJ (2011) Root responses to cadmium in the rhizosphere: a review. J Exp Bot 62:21–37

    CAS  PubMed  Google Scholar 

  • Maksymiec W (2011) Effects of jasmonate and some other signalling factors on bean and onion growth during the initial phase of cadmium action. Biol Plant 55:112–118

    CAS  Google Scholar 

  • Maksymiec W, Krupa Z (2006) The effects of short-term exposure to Cd, excess Cu ions and jasmonate on oxidative stress appearing in Arabidopsis thaliana. Environ Exp Bot 57:187–194

    CAS  Google Scholar 

  • Maksymiec W, Wojcik M, Krupa Z (2007) Variation in oxidative stress and photochemical activity in Arabidopsis thaliana leaves subjected to cadmium and excess copper in the presence or absence of jasmonate and ascorbate. Chemosphere 66:421–427

    CAS  PubMed  Google Scholar 

  • Mano Y, Nemoto K (2012) The pathway of auxin biosynthesis in plants. J Exp Bot 63:2853–2872

    CAS  PubMed  Google Scholar 

  • Martin GC (1983) Commercial uses of gibberellins. In: Crozier A (ed) The biochemistry and physiology of gibberellins. Praeger, New York, pp 395–444

    Google Scholar 

  • Martinka M, Vaculik M, Lux A (2014) Plant cell responses to cadmium and zinc. In: Nick P, Opatrný Z (eds) Applied plant cell biology. Springer, Plant Cell Monogr 22:209–246

  • Masood A, Khan NA (2013) Ethylene and gibberellic acid interplay in regulation of photosynthetic capacity inhibition by cadmium. Plant Biochem Physiol. doi:10.4172/jpbp.1000111

    Google Scholar 

  • Masood A, Iqbal N, Khan NA (2012) Role of ethylene in alleviation of cadmium-induced photosynthetic capacity inhibition by sulphur in mustard. Plant Cell Environ 35:524–533

    CAS  PubMed  Google Scholar 

  • Matsuoka M (2003) Gibberellins signaling: how do plant cells respond to GA signals? J Plant Growth Regul 22:123–125

    CAS  Google Scholar 

  • Meng H, Hua S, Shamsi IH, Jilani G, Li Y, Jiang L (2009) Cadmium-induced stress on the seed germination and seedling growth of Brassica napus L, and its alleviation through exogenous plant growth regulators. Plant Growth Regul 58:47–59

    CAS  Google Scholar 

  • Metwally A, Safronova VI, Belimov AA, Dietz KJ (2005) Genotypic variation of the response to cadmium toxicity in Pisum sativum L. J Exp Bot 56:167–178

    CAS  PubMed  Google Scholar 

  • Miller CO (1961) A kinetin-like compound in maize. Proc Natl Acad Sci U S A 47:170–174

    PubMed Central  CAS  PubMed  Google Scholar 

  • Minocha R, Majumdar R, Minocha SC (2014) Polyamines and abiotic stress in plants: a complex relationship. Front Plant Sci 5:175

    PubMed Central  PubMed  Google Scholar 

  • Mobin M, Khan NA (2007) Photosynthetic activity, pigment composition and antioxidative response of two mustard (Brassica juncea) cultivars differing in photosynthetic capacity subjected to cadmium stress. J Plant Physiol 164:601–610

    CAS  PubMed  Google Scholar 

  • Mockaitis K, Estelle M (2008) Auxin receptors and plant development: a new signaling paradigm. Annu Rev Cell Dev Biol 24:55–80

    CAS  PubMed  Google Scholar 

  • Mohamed MM, Abdel-Razik KE (2005) Interactive effect of heavy metals and gibberellic acid on mitotic activity and some metabolic changes of Vicia faba L. plants. Cytologia 70:275–282

    Google Scholar 

  • Montero-Palmero MB, Martín-Barranco A, Escobar C, Hernández LE (2013) Early transcriptional responses to mercury: a role for ethylene in mercury-induced stress. New Phytol 201:116–130

    PubMed  Google Scholar 

  • Mora-Herrera ME, López-Delgado HA (2007) Freezing tolerance and antioxidant activity in potato microplants induced by abscisic acid treatment. Am J Potato Res 84:467–475

    CAS  Google Scholar 

  • Munshaw GC, Ervin EH, Beasley JS, Shang C, Zhang X, Parrish DJ (2011) Effects of late‐season ethephon applications on cold tolerance parameters of four bermudagrass cultivars. Crop Sci 50:1022–1029

    Google Scholar 

  • Murkowski A (2001) Heat stress and spermidine: effect on chlorophyll fluorescence in tomato plants. Biol Plant 44:53–57

    CAS  Google Scholar 

  • Mysliwa-Kurdziel B, Strzalka K (2002) Influence of metals on the biosynthesis of photosynthetic pigments. In: Prasad MNV, Strzalka K (eds) Physiology and biochemistry of metal toxicity and tolerance in plants. Springer, Dordrecht, The Netherlands, pp 201–228

    Google Scholar 

  • Nagajyoti PC, Lee KD, Sreekanth TVM (2010) Heavy metals, occurrence and toxicity for plants: a review. Environ Chem Lett 8:199–216

    CAS  Google Scholar 

  • Nayyar H, Chander S (2004) Protective effects of polyamines against oxidative stress induced by water and cold stress in chickpea. J Agron Crop Sci 190:355–365

    CAS  Google Scholar 

  • Nayyar H, Bains TS, Kumar S (2005) Chilling stressed chickpea seedlings: effect of cold acclimation, calcium and abscisic acid on cryoprotective solutes and oxidative damage. Environ Exp Bot 54:275–285

    CAS  Google Scholar 

  • Nazar R, Iqbal N, Masood A, Khan MIR et al (2012) Cadmium toxicity in plants and role of mineral nutrients in its alleviation. Am J Plant Sci 3:1476–1489

    Google Scholar 

  • Nedjimi B, Daoud Y (2009) Cadmium accumulation in Atriplex halimus subsp. schweinfurthii and its influence on growth, proline, root hydraulic conductivity and nutrient uptake. Flora-Mor Dist Func Ecol Plants 204:316–324

    Google Scholar 

  • Nishiyama R, Watanabe Y, Fujita Y, Le DT et al (2011) Analysis of cytokinin mutants and regulation of cytokinin metabolic genes reveals important regulatory roles of cytokinins in drought, salt and abscisic acid responses, and abscisic acid biosynthesis. Plant Cell 23:2169–2183

    PubMed Central  CAS  PubMed  Google Scholar 

  • Noriega GO, Balestrasse KB, Batlle A, Tomaro ML (2007) Cadmium induced oxidative stress in soybean plants also by the accumulation of δ-aminolevulinic acid. Biometals 20:841–851

    CAS  PubMed  Google Scholar 

  • Noriega G, Caggiano E, Lecube MP, Santa Cruz D et al (2012a) The role of salicylic acid in the prevention of oxidative stress elicited by cadmium in soybean plants. Biometals 25:1155–1165

    CAS  PubMed  Google Scholar 

  • Noriega G, Cruz DS, Batlle A, Tomaro M, Balestrasse K (2012b) Heme oxygenase is involved in the protection exerted by jasmonic acid against cadmium stress in soybean roots. J Plant Growth Regul 31:79–89

    CAS  Google Scholar 

  • Parmar P, Kumari N, Sharma V (2013) Structural and functional alterations in photosynthetic apparatus of plants under cadmium stress. Bot Stud 54:45

    Google Scholar 

  • Piotrowska-Niczyporuk A, Bajguz A, Zambrzycka E, Godlewska-Zylkiewicz B (2012) Phytohormones as regulators of heavy metal biosorption and toxicity in green alga Chlorella vulgaris (Chlorophyceae). Plant Physiol Biochem 52:52–65

    CAS  PubMed  Google Scholar 

  • Polle A, Schützendübel A (2003) Heavy metal signalling in plants: linking cellular and organismic responses. In: Hirt H, Shinozaki K (eds) Plant responses to abiotic stress. Springer, Berlin, pp 187–215

    Google Scholar 

  • Poonam S, Kaur H, Geetika S (2013) Effect of jasmonic acid on photosynthetic pigments and stress markers in Cajanus cajan (L.) Mill sp. seedlings under copper stress. Am J Plant Sci 4:817–823

    Google Scholar 

  • Popova LP, Maslenkova LT, Yordanova RY, Ivanova AP et al (2009) Exogenous treatment with salicylic acid attenuates cadmium toxicity in pea seedlings. Plant Physiol Biochem 47:224–231

    CAS  PubMed  Google Scholar 

  • Qiu Z, Guo J, Zhu A, Zhang L, Zhang M (2014) Exogenous jasmonic acid can enhance tolerance of wheat seedlings to salt stress. Ecotoxicol Environ Saf 104:202–208

    CAS  PubMed  Google Scholar 

  • Richterová-Kučerová D, Kollárová K, Zelko I, Vatehová Z, Lišková D (2012) How do galactoglucomannan oligosaccharides regulate cell growth in epidermal and cortical tissues of mung bean seedlings? Plant Physiol Biochem 57:154–158

    PubMed  Google Scholar 

  • Rivas-San Vicente M, Plasencia J (2011) Salicylic acid beyond defence: its role in plant growth and development. J Exp Bot 62:3321–3338

    CAS  PubMed  Google Scholar 

  • Roberts J, Hooley R (1988) Plant growth regulators. Springer, New York, USA

    Google Scholar 

  • Rodriguez-Flores M, Rodriguez-Castellon E (1982) Lead and cadmium levels in soil and plants near highways and their correlation with traffic density. Environ Pollut Ser B 4:281–290

    CAS  Google Scholar 

  • Rodríguez-Serrano M, Romero-Puertas MC, Pazmiño DM et al (2009) Cellular response of pea plants to cadmium toxicity: cross talk between reactive oxygen species, nitric oxide, and calcium. Plant Physiol 150:229–243

    PubMed Central  PubMed  Google Scholar 

  • Saeedipour S (2011) Is salinity tolerance of rice lines related to endogenous ABA level or to the cellular ability for ABA synthesis under stress? Afr J Plant Sci 5:628–633

    CAS  Google Scholar 

  • Salt DE, Prince RC, Pickering IJ, Raskin I (1995) Mechanisms of cadmium mobility and accumulation in Indian mustard. Plant Physiol 109:1427–1433

    PubMed Central  CAS  PubMed  Google Scholar 

  • Sanita di Toppi L, Gabbrielli R (1999) Response to cadmium in higher plants. Environ Exp Bot 41:105–130

    Google Scholar 

  • Schellingen K, Der Straeten DV, Vandenbussche F, Prinsen E et al (2014) Cadmium-induced ethylene production and responses in Arabidopsis thaliana rely on ACS2 and ACS6 gene expression. BMC Plant Biol 14:214

    PubMed Central  PubMed  Google Scholar 

  • Schmülling T (2004) Cytokinin. In: Lennarz W, Lane MD (eds) Encyclopedia of biological chemistry. Academic Press/Elsevier Science

  • Shan C, Mei Z, Duan J, Chen H, Feng H, Cai W (2014) OsGA2ox5, a gibberellin metabolism enzyme, is involved in plant growth, the root gravity response and salt stress. PLoS ONE 9:e87110

    PubMed Central  PubMed  Google Scholar 

  • Sharma P, Bhardwaj R (2007) Effects of 24-epibrassinolide on growth and metal uptake Brassica juncea L. under copper metal stress. Acta Physiol Plant 29:259–263

    CAS  Google Scholar 

  • Shi GR, Cai QS, Liu QQ, Wu L (2009) Salicylic acid-mediated alleviation of cadmium toxicity in hemp plants in relation to cadmium uptake, photosynthesis, and antioxidant enzymes. Acta Physiol Plant 31:969–977

    CAS  Google Scholar 

  • Silva PO, Medina EF, Barros RS, Ribeiro DM (2014) Germination of salt-stressed seeds as related to the ethylene biosynthesis ability in three Stylosanthes species. J Plant Physiol 171:14–22

    CAS  PubMed  Google Scholar 

  • Singh S, Prasad SM (2014) Growth, photosynthesis and oxidative responses of Solanum melongena L. Seedlings to cadmium stress: mechanism of toxicity amelioration by kinetin. Sci Hort 176:1–10

    CAS  Google Scholar 

  • Song L, Ding W, Zhao M, Sun B, Zhang L (2006) Nitric oxide protects against oxidative stress under heat stress in the calluses from two ecotypes of reed. Plant Sci 171:449–458

    CAS  PubMed  Google Scholar 

  • Spollen WG, LeNoble ME, Samuels TD et al (2000) Abscisic acid accumulation maintains maize primary root elongation at low water potentials by restricting ethylene production. Plant Physiol 122:967–976

    PubMed Central  CAS  PubMed  Google Scholar 

  • Srivastava AK, Venkatachalam P, Raghothama KG, Sahi SV (2007) Identification of lead-regulated genes by suppression subtractive hybridization in the heavy metal accumulator Sesbania drummondii. Planta 225:1353–1365

    CAS  PubMed  Google Scholar 

  • Stroiński A, Chadzinikolau T, Giżewska K, Zielezińska M (2010) ABA or cadmium induced phytochelatin synthesis in potato tubers. Biol Plant 54:117–120

    Google Scholar 

  • Stroiński A, Giżewska K, Zielezińska M (2013) Abscisic acid is required in transduction of cadmium signal to potato roots. Biol Plant 57:121–127

    Google Scholar 

  • Sun X, Guo L (2013) Relationship between cadmium-induced root subapical hair development and ethylene biosynthesis in oilseed rape seedlings. Acta Biol Cracov Ser Bot 55:68–75

    CAS  Google Scholar 

  • Swamy PM, Smith B (1999) Role of abscisic acid in plant stress tolerance. Curr Sci 76:1220–1227

    CAS  Google Scholar 

  • Tanaka Y, Sano T, Tamaoki M, Nakajima N et al (2005) Ethylene inhibits abscisic acid-induced stomatal closure in Arabidopsis. Plant Physiol 138:2337–2343

    PubMed Central  CAS  PubMed  Google Scholar 

  • Tang CF, Liu YG, Zeng GM, Li X et al (2005) Effects of exogenous spermidine on antioxidant system responses of Typha latifolia L. under Cd2+ stress. J Intl Plant Biol 47:428–434

    CAS  Google Scholar 

  • Toth T, Zsiros O, Kis M, Garab G, Kovacs L (2012) Cadmium exerts its toxic effects on photosynthesis via a cascade mechanism in the cyanobacterium, Synechocystis PCC 6803. Plant Cell Environ 35:2075–2086

    CAS  PubMed  Google Scholar 

  • Tudoreanu L, Phillips CJC (2004) Modelling cadmium uptake and accumulation in plants. Adv Agron 84:121–157

    CAS  Google Scholar 

  • Tuteja N (2007) Abscisic acid and abiotic stress signalling. Plant Signal Behav 2:135–138

    PubMed Central  PubMed  Google Scholar 

  • United Nations Environment Programme (2008) Draft final review of scientific information on cadmium. http://www.chem.unep.ch/pb_and_cd/SR/Draft_final_reviews_Nov2008.htm. Accessed 20th Sep. 2014

  • Uraguchi S, Mori S, Kuramata M, Kawasaki A, Arao T, Ishikawa S (2009) Root-to-shoot Cd translocation via the xylem is the major process determining shoot and grain cadmium accumulation in rice. J Exp Bot 60:2677–2688

    PubMed Central  CAS  PubMed  Google Scholar 

  • Van de Mortel JE, Schat H, Moerland PD, Ver Loren van Themaat E et al (2008) Expression differences for genes involved in lignin, glutathione and sulphate metabolism in response to cadmium in Arabidopsis thaliana and the related Zn/Cd-hyperaccumulator Thlaspi caerulescens. Plant Cell Environ 31:301–324

    PubMed  Google Scholar 

  • Vázquez MN, Guerrero YR, González LM, de la Nova WT (2013) Brassinosteroids and plant responses to heavy metal stress. An overview. Open J Metal 3:34–41

    Google Scholar 

  • Velitcukova M, Fedina I (1998) Response of photosynthesis of Pisum sativum to salt stress as affected by methyl jasmonate. Photosynthetica 35:89–97

    Google Scholar 

  • Verbruggen N, Hermans C, Schat H (2009) Mechanisms to cope with arsenic or cadmium excess in plants. Curr Opin Plant Biol 12:364–372

    CAS  PubMed  Google Scholar 

  • Verma K, Mehta SK, Shekhawat GS (2013) Nitric oxide (NO) counteracts cadmium induced cytotoxic processes mediated by reactive oxygen species (ROS) in Brassica juncea: cross-talk between ROS, NO and antioxidant responses. Biometals 26:255–269

    CAS  PubMed  Google Scholar 

  • Villiers F, Jourdain A, Bastien O, Leonhardt N et al (2012) Evidence for functional interaction between brassinosteroids and cadmium response in Arabidopsis thaliana. J Exp Bot 63:1185–1200

    CAS  PubMed  Google Scholar 

  • Vitti A, Nuzzaci M, Scopa A, Tataranni G, Remans T et al (2013) Auxin and cytokinin metabolism and root morphological modifications in Arabidopsis thaliana seedlings infected with cucumber mosaic virus (CMV) or exposed to cadmium. Int J Mol Sci 14:6889–6902

    PubMed Central  CAS  PubMed  Google Scholar 

  • Wang B, Du Y (2013) Cadmium and its neurotoxic effects. In: Oxidative medicine and cellular longevity, vol. 2013, article ID 898034, doi:10.1155/2013/898034

  • Wang B, Zhang J, Xia X, Zhang WH (2011) Ameliorative effect of brassinosteroid and ethylene on germination of cucumber seeds in the presence of sodium chloride. Plant Growth Regul 65:407–413

    CAS  Google Scholar 

  • Wang ZY, Bai MY, Oh E, Zhu JY (2012) Brassinosteroid signaling network and regulation of photomorphogenesis. Annu Rev Genet 46:701–724

    CAS  PubMed  Google Scholar 

  • Wang Q, Liang X, Dong Y, Xu L et al (2013) Effects of exogenous salicylic acid and nitric oxide on physiological characteristics of perennial ryegrass under cadmium stress. J Plant Growth Regul 32:721–731

    CAS  Google Scholar 

  • Weber M, Trampczynska A, Clemens S (2006) Comparative transcriptome analysis of toxic metal responses in Arabidopsis thaliana and the Cd2+-hypertolerant facultative metallophyte Arabidopsis halleri. Plant Cell Environ 29:950–963

    CAS  PubMed  Google Scholar 

  • White PJ, Broadley MR (2003) Calcium in plants. Ann Bot 92:487–511

    PubMed Central  CAS  PubMed  Google Scholar 

  • WHO (2007) Health risks of heavy metals from long-range transboundary air pollution. World Health Organization 2007. WHO Regional Office for Europe, Copenhagen

    Google Scholar 

  • Wilen RW, Ewan BE, Gusta LV (1994) Interaction of abscisic acid and jasmonic acid on the inhibition of seed germination and the induction of freezing tolerance. Can J Bot 72:1009–1017

    CAS  Google Scholar 

  • Xiang C, Oliver DJ (1998) Glutathione metabolic genes coordinately respond to heavy metals and jasmonic acid in Arabidopsis. Plant Cell 10:1539–1550

    PubMed Central  CAS  PubMed  Google Scholar 

  • Xu J, Wang W, Yin H, Liu X et al (2010) Exogenous nitric oxide improves antioxidative capacity and reduces auxin degradation in roots of Medicago truncatula seedlings under cadmium stress. Plant Soil 326:321–330

    CAS  Google Scholar 

  • Yakimova ET, Kapchina-Toteva VM, Laarhoven LJ et al (2006) Involvement of ethylene and lipid signalling in cadmium-induced programmed cell death in tomato suspension cells. Plant Physiol Biochem 44:581–589

    CAS  PubMed  Google Scholar 

  • Yan Z, Chen J, Li X (2013) Methyl jasmonate as modulator of Cd toxicity in Capsicum frutescens var. fasciculatum seedlings. Ecotoxicol Environ Saf 98:203–209

    CAS  PubMed  Google Scholar 

  • Yang XE, Long XX, Ye HB, He ZL et al (2004) Cadmium tolerance and hyperaccumulation in a new Zn hyperaccumulating plant species (Sedum alfredii Hance). Plant Soil 259:181–189

    CAS  Google Scholar 

  • Ye Y, Li Z, Xing D (2013) Nitric oxide promotes MPK6-mediated caspase-3-like activation in cadmium-induced Arabidopsis thaliana programmed cell death. Plant Cell Environ 36:1–15

    CAS  PubMed  Google Scholar 

  • Yuan GF, Jia CG, Li Z, Sun B et al (2010) Effect of brassinosteroids on drought resistance and abscisic acid concentration in tomato under water stress. Sci Hort 126:103–108

    CAS  Google Scholar 

  • Zawaski C, Busov VB (2014) Roles of gibberellin catabolism and signaling in growth and physiological response to drought and short-day photoperiods in Populus trees. PLoS ONE 9:e86217

    PubMed Central  PubMed  Google Scholar 

  • Zhang F, Zhang H, Xia Y, Wang G et al (2011) Exogenous application of salicylic acid alleviates cadmium toxicity and reduces hydrogen peroxide accumulation in root apoplasts of Phaseolus aureus and Vicia sativa. Plant Cell Rep 30:1475–1483

    CAS  PubMed  Google Scholar 

  • Zhao H, Yang H (2008) Exogenous polyamines alleviate the lipid peroxidation induced by cadmium chloride stress in Malus hupehensis Rehd. Sci Hortic 116:442–447

    CAS  Google Scholar 

  • Zhao FY, Hu F, Zhang SY, Wang K et al (2013) MAPKs regulate root growth by influencing auxin signaling and cell cycle-related gene expression in cadmium-stressed rice. Environ Sci Pollut Res 20:5449–5460

    CAS  Google Scholar 

  • Zhu XF, Jiang T, Wang ZW, Lei GJ et al (2012) Gibberellic acid alleviates cadmium toxicity by reducing nitric oxide accumulation and expression of IRT1 in Arabidopsis thaliana. J Hazard Mater 239:302–307

    PubMed  Google Scholar 

  • Zhu JY, Sae-Seaw J, Wang ZY (2013a) Brassinosteroid signalling. Development 140:1615–1620

    PubMed Central  CAS  PubMed  Google Scholar 

  • Zhu XF, Wang ZW, Dong F, Lei GJ et al (2013b) Exogenous auxin alleviates cadmium toxicity in Arabidopsis thaliana by stimulating synthesis of hemicellulose 1 and increasing the cadmium fixation capacity of root cell walls. J Hazard Mater 263:398–403

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

MA, MIRK and NAK are grateful to the University Grants Commission (UGC) and Department of Biotechnology (DBT), New Delhi (India) for partial financial support. NAA is grateful to the Portuguese Foundation for Science and Technology (FCT) for post-doctoral fellowship (SFRH/BPD/84671/2012).

Conflicts of interest

The authors declare that there are no conflicts of interest.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Naser A. Anjum or Nafees A. Khan.

Additional information

Handling Editor: Peter Nick

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Asgher, M., Khan, M.I.R., Anjum, N.A. et al. Minimising toxicity of cadmium in plants—role of plant growth regulators. Protoplasma 252, 399–413 (2015). https://doi.org/10.1007/s00709-014-0710-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00709-014-0710-4

Keywords

Navigation