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Abscisic Acid Decreases Leaf Na+ Exclusion in Salt-Treated Phaseolus vulgaris L.

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Abstract

Previous results showed that in short-term NaCl-treated beans increased leaf abscisic acid (ABA) concentration was triggered by Na+ but not by Cl-. In this work, the specificity of ABA signaling for Na+ homeostasis was studied by comparing the plant’s responses to solutions that modified accumulation of ABA and/or Na+ uptake and distribution, such as supplemental Ca2+, increased nutrient strength, different isosmotic composition, application of exogenous ABA, fluridone (an ABA inhibitor) and aminooxiacetic acid (AOA, an ethylene inhibitor). After fluridone pretreatment, salt-treated beans had lower Na+ uptake and higher leaf Na+ exclusion capacity than non-pretreated plants. Moreover, Na+ uptake was increased and leaf Na+ exclusion was decreased by AOA and ABA. NaCl and KCl similarly increased leaf ABA and decreased transpiration rates, whereas supplemental Ca2+ and increased strength nutrient solution decreased leaf ABA and leaf Na+. These results show (1) a non-ion-specific increase in ABA that probably signaled the osmotic component of salt, and (2) increased ABA levels that resulted in higher leaf Na+ concentrations due to lower Na+ exclusion or increased root-shoot Na+ translocation.

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References

  • Abeles FB, Morgan PW, Saltveit M E Jr (1992) Ethylene in plant biology, 2nd edn. Academic Press, San Diego, CA, p 414

    Google Scholar 

  • Borel C, Audran C, Frey A, Marion-Poll A, Tardieu F, Simonneau T (2000) N. plumbaginifolia zeaxanthin epoxidase transgenic lines have unaltered baseline ABA accumulation in roots and xylem sap, but contrasting sensitivities of ABA accumulation to water deficit. J Exp Bot 52:427–434

    Google Scholar 

  • Chinnusamy V, Schumaker K, Zhu JK (2004) Molecular genetic perspectives on cross-talk and specificity in abiotic stress signalling in plants. J Exp Bot 55:225–236

    Article  PubMed  CAS  Google Scholar 

  • Cramer GR (2002) Sodium-calcium interactions under salinity stress. In: Laüchli A, Luttge U (eds) Salinity: Environment-Plants-Molecules. Kluwer Academic Publishers, Dordrecht, pp 205–229

    Google Scholar 

  • Jacoby B (1999) Mechanisms involved in salt tolerance of plants. In: Pessarakli M (ed) Handbook of plant and crop stress. Marcel Dekker, New York, pp 97–123

    Google Scholar 

  • LaHaye PA, Epstein E (1971) Calcium and salt toleration by bean plants. Physiol Plant 25:213–218

    Article  CAS  Google Scholar 

  • Maathuis FJM (2006) The role of monovalent cation transporters in plant responses to salinity. J Exp Bot 57:1137–1147

    Article  PubMed  CAS  Google Scholar 

  • Montero E, Cabot C, Barceló J, Ch Poschenrieder (1997) Endogenous abscisic acid levels are linked to decreased growth of bush bean plants treated with NaCl. Physiol Plant 101:17–22

    Article  CAS  Google Scholar 

  • Montero E, Cabot C, Poschenrieder Ch, Barceló J (1998) Relative importance of osmotic-stress and ion-specific effects on ABA-mediated inhibition of leaf expansion growth in Phaseolus vulgaris. Plant Cell Environ 21:54–62

    Article  CAS  Google Scholar 

  • Morgan PW, He CJ, De Greef JA, De Proft MP (1990) Does water deficit stress promote ethylene synthesis by intact plants? Plant Physiol 94:1616–1624

    Article  PubMed  CAS  Google Scholar 

  • Mustili AC, Merlot S, Vavasseur A, Fenzi F, Giraudat J (2002) Arabidopsis OST1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production. Plant Cell 14:3089–3099

    Article  Google Scholar 

  • Ober ES, Sharp RE (1994) Proline accumulation in maize (Zea mays L.) primary roots at low water potentials. I. Requirement for increased levels of abscisic acid. J Exp Bot 37:535–541

    Google Scholar 

  • Plaut Z, Grieve CM (1988) Photosynthesis of salt-stressed maize as influenced by Ca:Na ratios in the nutrient solution. Plant Soil 105:283–286

    Article  CAS  Google Scholar 

  • Popova LP, Outlaw WH, Aghoram K, Hite DRC (2000) Abscisic acid–an intraleaf water-stress signal. Physiol Plant 108:376–387

    CAS  Google Scholar 

  • Quarrie SA, Whitfford PN, Appleford NEJ, Wang TL, Cook SK, Henson IE, Loveys BR (1988) A monoclonal antibody to (S)-abscisic acid: its characterisation and use in a radioimmunoassay for measuring abscisic acid in crude extracts of cereals and lupin leaves. Planta 173:330–339

    Article  CAS  Google Scholar 

  • Roberts SK, Snowman BN (2000) The effects of ABA on channel-mediated K+ transport across higher plant roots. J Exp Bot 51:1585–1594

    Article  PubMed  CAS  Google Scholar 

  • Sibole JV, Montero E, Cabot C, Ch Poschenrieder, Barceló J (1998) Role of sodium in the ABA-mediated long-term growth response of bean to salt stress. Physiol Plant 104:299–305

    Article  CAS  Google Scholar 

  • Trejo CL, Davies WJ (1991) Drought-induced closure of Phaseolus vulgaris L. stomata precedes leaf water deficit and any increase in xylem ABA concentration. J Exp Bot 42:1507–1515

    Article  CAS  Google Scholar 

  • Voisin AS, Reidy B, Parent B, Rolland G, Redondo E, Gerentes D, Tardieu F, Muller B (2006) Are ABA, ethylene or their interaction involved in the response of leaf growth to soil water deficit? An analysis using naturally occurring variation or genetic transformation of ABA production in maize. Plant Cell Environ 29:1829–1840

    Article  PubMed  CAS  Google Scholar 

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Acknowledgment

This work was supported by DGCIYT projects BFU2004-02237-C02-01 and BFU2007-6032/BFI.

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Correspondence to Catalina Cabot.

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Cabot, C., Sibole, J.V., Barceló, J. et al. Abscisic Acid Decreases Leaf Na+ Exclusion in Salt-Treated Phaseolus vulgaris L.. J Plant Growth Regul 28, 187–192 (2009). https://doi.org/10.1007/s00344-009-9088-5

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  • DOI: https://doi.org/10.1007/s00344-009-9088-5

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