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AM1 is a potential ABA substitute for drought tolerance as revealed by physiological and ultra-structural responses of oilseed rape

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Abstract

Abscisic acid (ABA) is an important signaling molecule for plants under drought tolerance. However, ABA itself has many limitations to be used in agriculture practically. Recently, AM1 (ABA-mimicking ligand) has been found to replace ABA. In this study, we have investigated AM1’s potential role for drought tolerance by growing two contrasting rapeseed (Brassica napus L.) genotypes: Qinyou 8 (drought sensitive) and Q2 (drought resistant) with exogenous ABA or AM1 application under well-watered and drought-stressed conditions. Results demonstrate that drought stress has hampered plant growth (relative height growth rate, plant biomass, leaf area), plant water status (leaf relative water content, root moisture content, leaf water potential), photosynthetic gas exchange attributes like net photosynthesis rate (Pn), stomatal conductance (Gs), intercellular CO2 concentration (Ci), transpiration rate (E); chlorophyll fluorescence parameters like photosynthetic efficiency (Fv/Fm), effective quantum yield of PSII (Φ PSII ), photochemical quenching coefficient (qL), electron transport rate (ETR) and chlorophyll content, especially for Qinyou 8 significantly compared to well-watered plants. Whereas increased root/shoot ratio (R/S), water use efficiency (WUE) and non-photochemical quenching (NPQ) was recorded in both genotypes under drought stress. On the other hand, exogenous ABA or AM1 treatment has regulated all the above parameters in a rational way to avoid drought stress. Chloroplast transmission electron microscope images, especially for Qinyou8, have revealed that oxidative stress induced by drought has blurred the grana thylakoids, increased the size or number of plastoglobules due to lipid peroxidation, and the presence of starch granules depict weak capacity to convert them into simple sugars for osmotic adjustment. However, intact grana thylakoid, few plastoglobules with no or very few starch granules were observed in the chloroplast from ABA- or AM1-treated plants under drought. More importantly, AM1-treated plants under drought stress have responded in an extremely similar way like ABA-treated ones. Finally, it is suggested that AM1 is a potential ABA substitute for plant drought tolerance.

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References

  • An Y, Zhou P, Liang JF (2014) Effects of exogenous application of abscisic acid on membrane stability, osmotic adjustment, photosynthesis and hormonal status of two lucerne (Medicago sativa L.) genotypes under high temperature stress and drought stress. Crop Pasture Sci 65:274–286

    Article  CAS  Google Scholar 

  • Bosch SM, Alegre L (2004) Die and let live: leaf senescence contributes to plant survival under drought stress. Funct Plant Biol 31:203–216

    Article  Google Scholar 

  • Bray EA (2002) Abscisic acid regulation of gene expression during water-deficit stress in the era of the Arabidopsis genome. Plant Cell Environ 25:153–161

    Article  CAS  PubMed  Google Scholar 

  • Cao M, Liu X, Zhang Y, Xue X, Zhou XE et al (2013) ABA-mimicking ligand that reduces water loss and promotes drought resistance in plants. Cell Res 23:1043–1054

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dichio B, Romano M, Nuzzo V, Xiloyannis C (2002) Soil water availability and relationship between canopy and roots in young olive trees (cv Coratina). In: Vitagliano C, Martelli GP, editors. Proceedings of the 4th International symposium on olive growing, vol 1, pp 255–258

  • Dodd IC, Stikic R, Davies WJ (1996) Chemical regulation of gas exchange and growth of plants in drying soil in the field. J Exp Bot 47:1475–1490

    Article  CAS  Google Scholar 

  • Eckstein RL (2005) Differential effects of interspecific interactions and water availability on survival, growth and fecundity of three congeneric grassland herbs. New Phytol 166:525–535

    Article  PubMed  Google Scholar 

  • Fjelldal PG, Lock EJ, Hansen T, Waagbø R, Wargelius A, Martens LG, El-Mowafi A, Ørnsrud R (2012) Continuous light induces bone resorption and affects vertebral morphology in Atlantic salmon (Salmo salar L.) fed a phosphorous deficient diet. Aquac Nutr 18:610–619

    Article  CAS  Google Scholar 

  • Griffiths H, Parry MAJ (2002) Plant responses to water stress. Ann Bot 89:801–802

    Article  PubMed  PubMed Central  Google Scholar 

  • Han Y, Wang L, Zhang X, Korpelainen H, Li C (2013) Sexual differences in photosynthetic activity, ultrastructure and phytoremediation potential of Populus cathayana exposed to lead and drought. Tree Physiol 33:1043–1060

    Article  CAS  PubMed  Google Scholar 

  • Hartung W, Sauter A, Hose E (2002) Abscisic acid in the xylem: where does it come from, where does it go to? J Exp Bot 53:27–32

    Article  CAS  PubMed  Google Scholar 

  • Hull HM, Morton HL, Wharrie JR (1975) Environmental influence on cuticle development and resultant foliar penetration. Bot Rev 41:421–451

    Article  Google Scholar 

  • Iyer NJ, Tang Y, Mahalingam R (2013) Physiological, biochemical and molecular responses to a combination of drought and ozone in Medicago truncatula. Plant Cell Environ 36:706–720

    Article  CAS  PubMed  Google Scholar 

  • Jimenez S, Dridi J, Gutierrez D, Moret D, Irigoyen JJ, Moreno MA, Gogorcena Y (2013) Physiological, biochemical and molecular responses in four Prunus rootstocks submitted to drought stress. Tree Physiol 33:1061–1075

    Article  CAS  PubMed  Google Scholar 

  • Li Y, Zhao H, Duan B, Korpelainen H, Li C (2011) Effect of drought and ABA on growth, photosynthesis and antioxidant system of Cotinus coggygria seedlings under two different light conditions. Environ Exp Bot 71:107–113

    Article  CAS  Google Scholar 

  • Liu FL, Shahnazari A, Andersen MN, Jacobsen SE, Jensen CR (2006) Physiological responses of potato (Solanum tuberosum L.) to partial root-zone drying: ABA signalling, leaf gas exchange, and water use efficiency. J Exp Bot 57:3727–3735

    Article  CAS  PubMed  Google Scholar 

  • Lovisolo C, Perrone I, Carra A, Ferrandino A, Flexas J, Medrano H, Schubert A (2010) Drought-induced changes in development and function of grapevine (Vitis spp.) organs and in their hydraulic and non-hydraulic interactions at the whole-plant level: a physiological and molecular update. Funct Plant Biol 37:98–116

    Article  CAS  Google Scholar 

  • Mahdid M, Kameli A, Ehlert C, Simonneau T (2011) Rapid changes in leaf elongation, ABA and water status during the recovery phase following application of water stress in two durum wheat varieties differing in drought tolerance. Plant Physiol Biochem 49:1077–1083

    Article  CAS  PubMed  Google Scholar 

  • Maxwell K, Johnson GN (2000) Chlorophyll fluorescence—a practical guide. J Exp Bot 51:659–668

    Article  CAS  PubMed  Google Scholar 

  • Mayaba N, Beckett RP, Csintalan Z, Tuba Z (2001) ABA increases the desiccation tolerance of photosynthesis in the afromontane understorey moss Atrichum androgynum. Ann Bot 88:1093–1100

    Article  CAS  Google Scholar 

  • Melcher K, Ng LM, Zhou XE, Soon FF, Xu Y et al (2009) A gate-latch-lock mechanism for hormone signalling by abscisic acid receptors. Nature 462:602–608

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410

    Article  CAS  PubMed  Google Scholar 

  • Naeem MS, Warusawitharana H, Liu HB, Liu D, Ahmad R, Waraich EA, Xu L, Zhou WJ (2012) 5-aminolevulinic acid alleviates the salinity-induced changes in Brassica napus as revealed by the ultrastructural study of chloroplast. Plant Physiol Biochem 57:84–92

    Article  CAS  PubMed  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

    Article  Google Scholar 

  • Quarrie SA (1980) Genotypic differences in leaf water potential, abscisic acid and proline concentrations in spring wheat during drought stress. Ann Bot 46:383–394

    CAS  Google Scholar 

  • Rohacek K (2002) Chlorophyll fluorescence parameters: the definitions, photosynthetic meaning and mutual relationships. Photosynthetica 40:13–29

    Article  CAS  Google Scholar 

  • Sengupta D, Guha A, Reddy AR (2013) Interdependence of plant water status with photosynthetic performance and root defense responses in Vigna radiata (L.) Wilczek under progressive drought stress and recovery. J Photochem Photobiol B 127:170–181

    Article  CAS  PubMed  Google Scholar 

  • Sharp RE, LeNoble ME, Else MA, Thorne ET, Gherardi F (2000) Endogenous ABA maintains shoot growth in tomato independently of effects on plant water balance: evidence for an interaction with ethylene. J Exp Bot 51:1575–1584

    Article  CAS  PubMed  Google Scholar 

  • Shukla N, Awasthi RP, Rawat L, Kumar J (2012) Biochemical and physiological responses of rice (Oryza sativa L.) as influenced by Trichoderma harzianum under drought stress. Plant Physiol Biochem 54:78–88

    Article  CAS  PubMed  Google Scholar 

  • Snel JFH, Kooten VO (1990) The use of chlorophyll fluorescence and other non-invasive spectroscopic techniques in plant stress physiology. Wageningen University and Research Centre

  • Subrahmanyam D, Rathore VS (2000) Influence of manganese toxicity on photosynthesis in ricebean (Vigna umbellata) seedlings. Photosynthetica 38:449–453

    Article  CAS  Google Scholar 

  • Tatar O, Gevrek MN (2008) Influence of water stress on proline accumulation, lipid peroxidation and water content of wheat. Asian J Plant Sci 7:409–412

    Article  CAS  Google Scholar 

  • Vranová E, Inzé D, Van Breusegem F (2002) Signal transduction during oxidative stress. J Exp Bot 53:1227–1236

    Article  PubMed  Google Scholar 

  • Wang ZL, Huang BR, Xu QZ (2003) Effects of abscisic acid on drought responses of Kentucky bluegrass. J Am Soc Hortic Sci 128:36–419

    CAS  Google Scholar 

  • Xing J, Fei JJ (2004) The main meteorological disasters and defense technology of rapeseed in Anhui province. Anhui Agri Sci Bull 10:28–46

    Google Scholar 

  • Zhang RH, Zheng YJ, Ma GS, Zhang XH, Lu HD, Xue JQ et al (2011) Effects of drought stress on the photosynthesis and protective enzymes of the leaves of Maize during Seedling Stage. Acta Botanica Sinica 31:1303–1311

    CAS  Google Scholar 

  • Zhu JK (2002) Salt and drought stress signal transduction in plants. Annu Rev Plant Biol 53:247–273

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

This study was supported by Special Fund for Agro-scientific Research in the Public Interest (201203096), 12th Five-Year Plan of National Science and Technology Program (2014BAD11B00), National Natural Science Foundation of China (31101124), and PhD Research Startup Fund, Chinese Academy of Agricultural Sciences (CAAS).

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Correspondence to Chunlei Zhang.

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Communicated by H. Li.

M. S. Naeem and L. Dai contributed equally to this work.

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Naeem, M.S., Dai, L., Ahmad, F. et al. AM1 is a potential ABA substitute for drought tolerance as revealed by physiological and ultra-structural responses of oilseed rape. Acta Physiol Plant 38, 183 (2016). https://doi.org/10.1007/s11738-016-2190-y

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  • DOI: https://doi.org/10.1007/s11738-016-2190-y

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