Skip to main content
Log in

Identification of different ABA biosynthesis sites at seedling and fruiting stages in Arachis hypogaea L. following water stress

  • Original Paper
  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Abscisic acid (ABA) is one of the most important phytohormones involved in abiotic stress responses. ABA transport in plants is important in determining endogenous ABA levels and their resulting physiological responses. However, the regulation of ABA transport remains unclear. In this study, we compared the ABA concentrations and AhNCED1 levels at seedling and fruiting stages in peanut (Arachis hypogaea L.), in response to water stress. At the seedling stage, ABA initially accumulated in roots (1 h), followed by the lower stem (2 h) and finally in the upper stem (4 h). The expression/activity of an ABA biosynthesis rate-limiting enzyme, AhNCED1, showed the same accumulation patterns. In contrast, during the fruiting stage, ABA and AhNCED1 increases were initially detected in the first apical leaf of main stem, followed by the stem, and finally in the root. These results imply that biosynthesis of ABA in peanut plants subject to water deficiency could be dependent on developmental stage with the roots being the initial site of ABA biosynthesis during the seedling stage, whereas during the fruiting stage ABA biosynthesis occurs initially in the leaf. The distribution patterns of ABA in seedling stage peanuts in response to water stress were: root-stem-leaf, while in fruiting stage peanuts the distribution patterns of ABA were: leaf-stem-root. These findings will help to understand plant regulatory water deficit resistance mechanisms at seedling and fruiting stages and to advance our total understanding of the regulation of ABA transport.

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
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Americo R, Santiago J, Silvia R, Angela S, Karen S, Jose G, Christian S, Pedro L (2009) The short-rooted phenotype of the Brevis radix mutant partly reflects root abscisic acid hypersensitivity. Plant Physiol 149:1917–1928

    Article  Google Scholar 

  • Christmann A, Hoffmann T, Teplova I, Grill E, Mu¨ller A (2005) Generation of active pools of abscisic acid revealed by in vivo imaging of water-stressed Arabidopsis. Plant Physiol 137:209–219

    Article  PubMed  CAS  Google Scholar 

  • Christmann A, Weiler E, Steudle E, Grill E (2007) A hydraulic signal in root-to-shoot signalling of water shortage. Plant J 52:167–174

    Article  PubMed  CAS  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • Davies WJ, Kudoyarova G, Hartung W (2005) Long-distance ABA signaling and its relation to other signaling pathways in the detection of soil drying and the mediation of the plant’s response to drought. J Plant Growth Regul 24:285–295

    Article  CAS  Google Scholar 

  • Dodd I, Egea G, Davies W (2008) Accounting for sap flow from different parts of the root system improves the prediction of xylem ABA concentration in plants grown with heterogeneous soil moisture. J Exp Bot 21:695–707

    Google Scholar 

  • Endo A, Sawada Y, Takahashi H, Okamoto M, Ikegami K, Koiwai H, Seo M, Toyomasu T, Mitsuhashi W, Shinozaki K, Nakazono M, Kamiya Y, Koshiba T, Nambara E (2008) Drought induction of Arabidopsis 9-cis-epoxycarotenoid dioxygenase occurs in vascular parenchyma cells. Plant Physiol 147:1984–1993

    Article  PubMed  CAS  Google Scholar 

  • FAO Statistical Yearbook (2004). http://www.fao.org/statistics/yearbook/vol 11/

  • Fryer M, 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

    Article  PubMed  CAS  Google Scholar 

  • Geetha G, Harshavardhan V, Thamme G, Patricia J, Dhanalakshmi R, Sreenivasulu N, Udaya K (2009) Identification and functional validation of a unique set of drought induced genes preferentially expressed in response to gradual water stress in peanut. Mol Genet Genomics 281:591–605

    Article  Google Scholar 

  • Govind G, ThammeGowde HV, Lyser DR, Muthapa SK, Nese S, Makarla UK (2009) Identification and functional validation of a unique set of drought induced genes preferentially expressed in response to gradual water stress in peanut. Mol Genet Genomics 281:591–605

    Article  PubMed  CAS  Google Scholar 

  • Holbrook NM, Shashidhar VR, James RA, Munns R (2002) Stomatal control in tomato with ABA-deficient roots: response of grafted plants to soil drying. J Exp Bot 53:1503–1514

    Article  PubMed  CAS  Google Scholar 

  • Hu B, Liu X, Hong L, Li L, Luo G (2010a) Expression of Arachis hypogaea 9-cis epoxycarotenoid dioxygenase 1 (AhNCED1) in different organs of peanut and localization in Arabidopsis. Biotechnol Biotechnol EQ 24:1–7

    Google Scholar 

  • Hu B, Wan X, Liu X, Guo D, Li L (2010b) Abscisic acid-mediated inhibition of seed germination involves a positive feedback regulation of ABA biosynthesis in Arachis hypogaea L. Afr J Biotechnol 9:1578–1586

    CAS  Google Scholar 

  • Hu B, Hong L, Liu X, Xiao S, Lv Y, Li L (2012) Compartive study of the tissye specific distribution of ABA form Arachis hyopgaea L. and expression of the 9-cis epoxycarotenoid dioxygenase 1 (AhNCED1) during plant development. Biotechl Biotechnol EQ DOi: 10.5504/bbeq.2012.0060

  • Ikegami K, Okamoto M, Seo M, Koshiba T (2009) Activation of abscisic acid biosynthesis in the leaves of Arabidopsis thaliana in response to water deficit. J Plant Res 122:235–243

    Article  PubMed  CAS  Google Scholar 

  • Jiang F, Hartung W (2008) Long-distance signalling of abscisic acid (ABA): the factors regulating the intensity of the ABA signal. J Exp Bot 59:37–43

    Article  PubMed  CAS  Google Scholar 

  • Kandasamy MK, McKinney EC, Meaghe RB (2002) Functional nonequivalency of actin isovariants in arabidopsis. Mol Biol Cell 13:251–261

    Article  PubMed  CAS  Google Scholar 

  • Koiwai H, Nakaminami K, Seo M, Mitsuhashi W, Toyomasu T, Koshiba T (2004) Tissue-specific localization of an abscisic acid biosynthetic enzyme, AAO3, in Arabidopsis. Plant Physiol 134:1697–1707

    Article  PubMed  CAS  Google Scholar 

  • Masanori O, Yoko T, Suzanne R, Yuji K, Motoaki S, Eiji N (2009) High humidity induces abscisic acid 8′-hydroxylase in stomata and vasculature to regulate local and systemic abscisic acid responses in Arabidopsis. Plant Physiol 149:825–834

    Google Scholar 

  • Melhorn V, Matsumi K, Koiwai H, Ikegami K, Okamoto M, Nambara E, Bittner F, Koshiba T (2008) Transient expression of AtNCED3 and AAO3 genes in guard cells causes stomatal closure in Vicia faba. J Plant Res 121:125–131

    Article  PubMed  CAS  Google Scholar 

  • Neumann A, Folkard A, Yong W, Christian RJ, Nd Henrik, Vagn OM, Karen EK (2002) Soluble invertase expression is an early target of drought stress during the critical, abortion-sensitive phase of young ovary development in Maize. Plant Physiol 130:591–604

    Article  Google Scholar 

  • Schachtman DP, Goodger JQD (2008) Chemical root to shoot signaling under drought. Trends Plant Sci 13:281–287

    Article  PubMed  CAS  Google Scholar 

  • Schraut D, Ullrich CI, Hartung W (2004) Lateral ABA transport in maize roots (Zea mays): visualization by immunolocalization. J Exp Bot 55:1635–1641

    Article  PubMed  CAS  Google Scholar 

  • Soar C, Speirs J, Maffei S, Loveys B (2004) Gradients in stomatal conductance, xylem sap ABA and bulk leaf ABA along canes of Vitis vinifera cv Shiraz: biochemical and molecular biological evidence indicating their source. Func Plant Bio 31:659–669

    Article  CAS  Google Scholar 

  • Tan B, Schwartz S, Zeevaart J, McCarty D (1997) Genetic control of abscisic acid biosynthesis in Maize. Proc Natl Acad Sci 94:1235–1240

    Article  Google Scholar 

  • Wan X, Li L (2005) Molecular cloning and characterization of a dehydration- inducible cDNA encoding a putative 9-cis-epoxycarotenoid dioxygenase in Arachis hypogaea L. DNA Seq 16:217–223

    PubMed  CAS  Google Scholar 

  • Wan X, Li L (2006) Regulation of ABA level and water-stress tolerance of Arabidopsis by ectopic expression of a peanut 9-cis-epoxycarotenoid dioxygenase gene. Biochem Biophysiol Res Commun 347:1030–1038

    Article  CAS  Google Scholar 

  • Wu F, Qi X, Cao Z, Liu Z, Du S, Mei C, Zhao C, Wang X, Shang Y, Tao J, Zhang X, Lu Y, Zhao R, Zhang D (2009) The magnesium-chelatase H subunit binds abscisic acid and functions in abscisic acid signaling: new evidence in Arabidopsis. Plant Physiol 150:1940–1954

    Article  PubMed  CAS  Google Scholar 

  • Xiong L, Lee H, Ishitani M, Zhu J (2002) Regulation of osmotic stress responsive gene expression by the LOS6/ABA1 locus in Arabidopsis. J Bio Chem 277:8588–8596

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We are very grateful to Dr. Nicole Grant at University of Technology, Sydney for critical reading of the manuscript. This work was supported by Natural Science Foundation of China (30971715 to Ling Li), Guangdong Natural Science Foundation (915106310100001 and 10251063101000010 to Ling Li), China Postdoctoral Science Foundation (20110490907 to Dr. Bo Hu) and Science and Technology Planning Project of Guangdong Province (2011B020301009 to Dr. Bo Hu).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. Li.

Additional information

Bo Hu and Lan Hong contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hu, B., Hong, L., Liu, X. et al. Identification of different ABA biosynthesis sites at seedling and fruiting stages in Arachis hypogaea L. following water stress. Plant Growth Regul 70, 131–140 (2013). https://doi.org/10.1007/s10725-013-9785-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10725-013-9785-8

Keywords

Navigation