PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2019 | 41 | 11 |

Tytuł artykułu

Cross-priming accentuates key biochemical and molecular indicators of defense and improves cold tolerance in chickpea (Cicer arietinum L.)

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Cold environment favors long vegetative phase but also impose substantial loss by damaging reproductive functioning in chickpea. Field temperature below 10 °C is even more detrimental for reproductive development, enhances floral and pod abortion. In this study, contrasting chickpea varieties PDG3 and GPF2 were exposed to drought, recovered, and subsequently exposed to lethal cold stress ~ 4–5 °C with an aim to induce defense response against cold shock. Physiological, biochemical, and molecular signatures related to damage and defense, i.e., membrane damage, antioxidative enzymes, fatty acid desaturase (CaFAD2.1), and small HSPs (CaHSP18.5 and CaHSP22.7), were analyzed. Drought pretreatment/preconditioning maintained the membrane stability in the cold by managing malondialdehyde (MDA) content and lipoxygenase (LOX) activity. Improved mitochondrial functioning (TTC reduction), increased activity of catalase (CAT), ascorbate peroxidase (APX), and glutathione reductase (GR) proved better cellular functioning during cold exposure. The expression and activity of superoxide dismutase (CaSOD) were down-regulated in both varieties, but CaCAT, CaAPX, CaGR, and CaFAD2.1 expressions were up-regulated in GPF2. Small heat shock protein CaHSP22.7 was also up-regulated in drought preconditioned PDG3 and GPF2 and after cold shock. Drought pretreatment/preconditioning significantly improved membrane damage during cold exposure, induced antioxidative system, and up-regulated FAD2. This study also pointed the possible role of CaHSP22.7 in cold tolerance and CaHSP18.5 in drought stress. The sensitive variety (GPF2) was positively responsive to preconditioning as this variety showed improvement in defense-related parameters; however, genotypic variations were observed in PDG3.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

41

Numer

11

Opis fizyczny

Article 181 [13p.], fig.,ref.

Twórcy

autor
  • Centre for Biosciences, School of Basic and Applied Sciences, Central University of Punjab, Bathinda 151001, India
autor
  • Centre for Biosciences, School of Basic and Applied Sciences, Central University of Punjab, Bathinda 151001, India
autor
  • Department of Botany, Panjab University, Chandigarh 160014, India
autor
  • Centre for Biosciences, School of Basic and Applied Sciences, Central University of Punjab, Bathinda 151001, India
  • Department of Plant Sciences, School of Basic and Applied Sciences, Central University of Punjab, Bathinda 151001, India

Bibliografia

  • Aroca R, Irigoyen JJ, Sánchez-Díaz M (2003) Drought enhances maize chilling tolerance. II. Photosynthetic traits and protective mechanisms against oxidative stress. Physiol Plant 117:540–549
  • Banzet N, Richaud C, Deveaux Y, Kazmaier M, Gagnon J, Triantaphylidès C (1998) Accumulation of small heat shock proteins, including mitochondrial HSP22, induced by oxidative stress and adaptive response in tomato cells. Plant J 13:519–527
  • Beck EH, Fettig S, Knake C, Hartig K, Bhattarai T (2007) Specific and unspecific responses of plants to cold and drought stress. J Biosci 32:501–510
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
  • Cao S, Zheng Y, Wang K, Jin P, Rui H (2009) Methyl jasmonate reduces chilling injury and enhances antioxidant enzyme activity in postharvest loquat fruit. Food Chem 115:1458–1463
  • Cayuela E, Muñoz-Mayor A, Vicente-Agulló F, Moyano E, Garcia-Abellan JO, Estañ MT, Bolarín MC (2007) Drought pretreatment increases the salinity resistance of tomato plants. J Plant Nutr Soil Sci 170:479–484
  • Chakrabarty D, Verma AK, Datta SK (2009) Oxidative stress and antioxidant activity as the basis of senescence in Hemerocallis (day lily) flowers. J Hortic For 1:113–119
  • Cloutier Y, Siminovitch D (1982) Correlation between cold-and drought-induced frost hardiness in winter wheat and rye varieties. Plant Physiol 69:256–258
  • Dong X, Bi H, Wu G, Ai X (2013) Drought-induced chilling tolerance in cucumber involves membrane stabilisation improved by antioxidant system. Int J Plant Prod 7:67–80
  • Feussner I, Wasternack C (2002) The lipoxygenase pathway. Annu Rev Plant Biol 53:275–297
  • Garcı́a-Limones C, Hervás A, Navas Cortés JA, Jiménez Dı́az RM, Tena M (2002) Induction of an antioxidant enzyme system and other oxidative stress markers associated with compatible and incompatible interactions between chickpea (Cicer arietinum L.) and Fusarium oxysporum f. sp. ciceris. Physiol Mol Plant Pathol 61:325–337
  • 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 28:1091–1101
  • Hamilton EW, Heckathorn SA (2001) Mitochondrial adaptations to NaCl. Complex I is protected by anti-oxidants and small heat shock proteins, whereas complex II is protected by proline and betaine. Plant Physiol 126:1266–1274
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hernandez J, Jimenez A, Mullineaux P, Sevilia F (2000) Tolerance of pea (Pisum sativum L.) to long-term salt stress is associated with induction of antioxidant defences. Plant Cell Environ 23:853–862
  • Hoffman L, DaCosta M, Ebdon JS, Zhao J (2012) Effects of drought preconditioning on freezing tolerance of perennial ryegrass. Enviro Exp Bot 79:11–20
  • Kargiotidou A, Deli D, Galanopoulou D, Tsaftaris A, Farmaki T (2008) Low temperature and light regulate delta 12 fatty acid desaturases (FAD2) at a transcriptional level in cotton (Gossypium hirsutum). J Exp Bot 59:2043–2056
  • Kaur S, Jairath A, Singh I, Nayyar H, Kumar S (2016) Alternate mild drought stress (− 0.1 MPa PEG) immunizes sensitive chickpea cultivar against lethal chilling by accentuating the defense mechanisms. Acta Physiol Plant 38:189
  • Krasensky J, Jonak C (2012) Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J Exp Bot 63:1593–1608
  • Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1998) Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought-and low-temperature-responsive gene expression, respectively, in Arabidopsis. Plant Cell 10:1391–1406
  • Lutts S, Kinet J, Bouharmont J (1996) NaCl-induced senescence in leaves of rice (Oryza sativa L.) cultivars differing in salinity resistance. Ann Bot 78:389–398
  • Mantyla E, Lang V, Palva ET (1995) Role of abscisic acid in drought-induced freezing tolerance, cold acclimation, and accumulation of LT178 and RAB18 proteins in Arabidopsis thaliana. Plant Physiol 107:141–148
  • Miquel M, James D, Dooner H (1993) Arabidopsis requires polyunsaturated lipids for low-temperature survival. Proc Natl Acad Sci 90:6208–6212
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Murata N, Los DA (1997) Membrane fluidity and temperature perception. Plant Physiol 115:875
  • Nayyar H, Bains T, Kumar S (2005a) Chilling stressed chickpea seedlings: effect of cold acclimation, calcium and abscisic acid on cryoprotective solutes and oxidative damage. Environ Exp Bot 54:275–285
  • Nayyar H, Bains TS, Kumar S, Kaur G (2005b) Chilling effects during seed filling on accumulation of seed reserves and yield of chickpea. J Sci Food Agric 85:1925–1930
  • Palma F, López Gómez M, Tejera N, Lluch C (2013) Salicylic acid improves the salinity tolerance of Medicago sativa in symbiosis with Sinorhizobium meliloti by preventing nitrogen fixation inhibition. Plant Sci 208:75–82
  • Pirzadah TB, Malik B, Rehman RU, Hakeem KR, Qureshi MI (2014) Signaling in response to cold stress. Plant signaling: understanding the molecular crosstalk. Springer, New York, pp 193–226
  • Poorter H, Bühler J, van Dusschoten D, Climent J, Postma JA (2012) Pot size matters: a meta-analysis of the effects of rooting volume on plant growth. Funct Plant Biol 39:839–850
  • Porta H et al (1999) Analysis of lipoxygenase mRNA accumulation in the common bean (Phaseolus vulgaris L.) during development and under stress conditions. Plant Cell Physiol 40:850–858
  • Rejeb IB, Pastor V, Mauch-Mani B (2014) Plant responses to simultaneous biotic and abiotic stress: molecular mechanisms. Plants 3:458–475
  • Saini R, Kumar S (2019) Genome-wide identification, characterization and in silico profiling of genes encoding FAD (fatty acid desaturase) proteins in chickpea (Cicer arietinum L.). Plant Gene 18:100180
  • Sun W, Van Montagu M, Verbruggen N (2002) Small heat shock proteins and stress tolerance in plants. Biochim Biophys Acta Gene Struct Expr 1577:1–9
  • Theocharis A, Clément C, Barka EA (2012) Physiological and molecular changes in plants grown at low temperatures. Planta 235:1091–1105
  • Upchurch RG (2008) Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress. Biotechnol Lett 30:967–977
  • Verma S, Dubey R (2003) Lead toxicity induces lipid peroxidation and alters the activities of antioxidant enzymes in growing rice plants. Plant Sci 164:645–655
  • Wang X, Vignjevic M, Liu F, Jacobsen S, Jiang D, Wollenweber B (2015) Drought priming at vegetative growth stages improves tolerance to drought and heat stresses occurring during grain filling in spring wheat. Plant Growth Regul 75:677–687
  • Zhang J-H, Wang L-J, Pan Q-H, Wang Y-Z, Zhan J-C, Huang W-D (2008) Accumulation and subcellular localization of heat shock proteins in young grape leaves during cross-adaptation to temperature stresses. Sci Hortic 117:231–240
  • Zou J, Liu A, Chen X, Zhou X, Gao G, Wang W, Zhang X (2009) Expression analysis of nine rice heat shock protein genes under abiotic stresses and ABA treatment. J Plant Physiol 166:851–861

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-a04acc48-acc3-462f-b9f5-4e508b839093
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.