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Abscisic Acid and Ethylene Interact in Rice Spikelets in Response to Water Stress During Meiosis

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Abstract

This study investigated whether and how the interaction between abscisic acid (ABA) and ethylene is involved in the regulation of rice (Oryza sativa L.) spikelet sterility when subjected to water stress during meiosis. Two rice cultivars, HA-3 (drought-resistant) and WY-7 (drought-susceptible), were used and subjected to well-watered and water-stressed (WS) treatments during meiosis (15–2 days before heading). Leaf water potentials of both cultivars markedly decreased during the day as a result of the WS treatment, but panicle water potentials remained constant. The percentage of sterile spikelets in WS plants was increased by 49.7% for WJ-7 but only 12.7% for HA-3. ABA, ethylene, and 1-aminocyclopropane-1-carboxylic acid were all enhanced in spikelets by the water stress, but ethylene was enhanced more than ABA in WY-7 when compared with that in HA-3. Spikelet sterility was significantly reduced when ABA or amino-ethoxyvinylglycine, an inhibitor of ethylene synthesis, was applied to the panicles of WS plants at the early meiosis stage. Application of ethephon, an ethylene-releasing agent, or fluridone, an inhibitor of ABA synthesis, had the opposite effect, and sterility was increased. The results suggest that antagonistic interactions between ABA and ethylene may be involved in mediating the effect of water stress on spikelet fertility. A higher ratio of ABA to ethylene would be a physiologic trait of rice adaptation to water stress.

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References

  • Andersen MN, Asch F, Wu F, Jensen CR, Naested H, Mogensen VO, Koch KE (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  PubMed  CAS  Google Scholar 

  • Belder P, Bouman BAM, Cabangon R, Guoan L, Quilang EJP, Li Y, Spiertz JHJ, Tuong TP (2004) Effect of water-saving irrigation on rice yield and water use in typical lowland conditions in Asia. Agric Water Manag 65:193–210

    Article  Google Scholar 

  • Bellarire BA, Carmody J, Braud J, Gossett DR, Banks SW, Lucas TE, Fowler TE (2000) Involvement of abscisic acid-dependent and independent pathways in the upregulation of antioxidant enzyme activity during NaCl stress in cotton callus tissue. Free Radic Res 33:531–545

    Article  Google Scholar 

  • Beltrano J, Carbone A, Montaldi ER, Guiamet JJ (1994) Ethylene as promoter of wheat grain maturation and ear senescence. Plant Growth Regul 15:107–112

    Article  CAS  Google Scholar 

  • Bollmark M, Kubat B, Eliasson L (1988) Variations in endogenous cytokinin content during adventitious root formation in pea cuttings. J Plant Physiol 132:262–265

    CAS  Google Scholar 

  • Boyer JS, Westgate ME (2004) Grain yield with limited water. J Exp Bot 55:2385–2349

    Article  PubMed  CAS  Google Scholar 

  • Cheng CY, Lur HS (1996) Ethylene may be involved in abortion of the maize caryopsis. Physiol Plant 98:245–252

    Article  CAS  Google Scholar 

  • Davies PJ (1995) Introduction. In: Davies PJ (ed), Plant hormones, physiology, biochemistry and molecular biology. Dordrecht, The Netherlands: Kluwer Academic Publishers, pp 1–12

    Google Scholar 

  • Davies PJ (2004) The plant hormones: their nature, occurrence and function. In: Davies PJ (ed), Plant Hormones, biosynthesis, signal transduction, action! Dordrecht, The Netherlands: Kluwer Academic Publishers, pp 1–15

    Google Scholar 

  • Debata A, Murty KS (1983) Endogenous ethylene content in rice leaves during senescence. Indian J Plant Physiol 26:425–427

    Google Scholar 

  • Dembinska O, Lalonde S, Saini HS (1992) Evidence against the regulation of grain set by spikelet abscisic acid levels in water-stressed wheat. Plant Physiol 100:1599–1602

    Article  PubMed  CAS  Google Scholar 

  • Gazzarrini S, McCourt P (2001) Genetic interactions between ABA, ethylene and sugar signaling pathways. Curr Opin Plant Biol 4:387–391

    Article  PubMed  CAS  Google Scholar 

  • Guan LQ, Scandalios JG (1998) Effects of the plant growth regulator abscisic acid and high osmoticum on the developmental expression of the maize catalase genes. Physiol Plant 104:413–422

    Article  CAS  Google Scholar 

  • Guan LM, Zhao J, Scandalios JG (2000) Cis-elements and trans-factors that regulate expression of maize Catl antioxidant gene in response to ABA and osmotic stress: H2O2 is the likely intermediary signaling molecule for response. Plant J 22:87–95

    Article  PubMed  CAS  Google Scholar 

  • Guinn G (1976) Water stress and ethylene evolution by young cotton bolls. Plant Physiol 57:403–405

    PubMed  CAS  Google Scholar 

  • Hanson AD, Peacock WJ, Evans LT, Arntzen CJ, Khush GS (1990) Drought resistance in rice. Nature 345:26–27

    Article  Google Scholar 

  • He Z (1993) Method for an indirect enzyme-linked immunosorbent asssay. In: He ZP (ed), Guidance to experiment on chemical control in crop plants. Beijing, China: Beijing Agricultural University Publishers, pp 60–68

    Google Scholar 

  • Inthapan P, Fukai S (1988) Growth and yield of rice cultivars under sprinkler irrigation in south-eastern Queensland. 2. Comparison with maize and grain sorghum under wet and dry conditions. Aust J Exp Agric 28:243–248

    Article  Google Scholar 

  • Khan RI, Choudhury MA (1992) Role of endogenous hormones in the regulation of whole plant senescence in rice. Indian J Exp Biol 30:131–134

    CAS  Google Scholar 

  • LeNoble ME, Spollen WG, Sharp RE (2004) Maintenance of shoot growth by endogenous ABA: genetic assessment of the involvement of ethylene suppression. J Exp Bot 55:237–245

    Article  PubMed  CAS  Google Scholar 

  • Ling Q, Su Z, Chang H, Cai J, Ho J (1983) The leaf-age model of development process in different varieties of rice. Sci Agric Sin 16:9–18

    Google Scholar 

  • Mohapatra PK, Naik PK, Patel R (2000) Ethylene inhibitors improve dry matter partitioning and development of late flowering spikelets on rice panicles. Aust J Plant Physiol 27:311–323

    CAS  Google Scholar 

  • Morgan JM (1980) Possible role of abscisic acid in reducing seed set in water-stressed wheat plants. Nature 285:655–657

    Article  CAS  Google Scholar 

  • Morgan JM, King RW (1984) Association between loss of leaf turgor, abscisic acid levels and seed set in two wheat cultivars. Aust J Plant Physiol 11:143–150

    CAS  Google Scholar 

  • Morgan PW, Drew MC (1997) Ethylene and plant responses to stress. Physiol Plant 100:620–630

    Article  CAS  Google Scholar 

  • Naik PK, Mohapatra PK (1999) Ethylene inhibitors promote male gametophyte survival in rice. Plant Growth Regul 28:29–39

    Article  CAS  Google Scholar 

  • Naik PK, Mohapatra PK (2000) Ethylene inhibitors enhanced sucrose synthase activity and promoted grain filling of basal rice kernels. Aust J Plant Physiol 27:997–1008

    CAS  Google Scholar 

  • Namuco OS, O’Toole JC (1986) Reproductive stage water-stress and sterility. 1. Effect of stress during meiosis. Crop Sci 26:317–321

    Article  Google Scholar 

  • Narayana I, Lalonde S, Saini HS (1991) Water-stress-induced ethylene production in wheat. Plant Physiol 96:406–410

    PubMed  CAS  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. Plant Physiol 105:981–987

    PubMed  CAS  Google Scholar 

  • Ober ES, Setter TL, Madison JT, Thompson JF, Shapiro PS (1991) Influence of water deficit on maize endosperm development. Enzyme activities and RNA transcripts of starch and zein synthesis, abscisic acid, and cell division. Plant Physiol 97:154–164

    PubMed  CAS  Google Scholar 

  • Overmyer K, Tuominen H, Kettunen R, Betz C, Langebartels C, Sandermann H Jr, Kangasjarvi J (2000) Ozone-sensitive Arabidopsis rcdl mutant reveals opposite roles for ethylene and jasmonate signaling pathways in regulating superoxide-dependent cell death. Plant Cell 12:1849–1862

    Article  PubMed  CAS  Google Scholar 

  • Rajasekaran LR, Blake TJ (1999) New plant growth regulators protect photosynthesis and enhance growth under drought of jack pine seedlings. J Plant Growth Regul 18:175–181

    Article  PubMed  CAS  Google Scholar 

  • Saini HS (1997) Effects of water stress on male gametophyte development in plants. Sex Plant Reprod 10:67–73

    Article  Google Scholar 

  • Saini HS, Aspinall D (1981) Effect of water deficit on sporogenesis in wheat (Triticum aestivum L.). Ann Bot 48:623–633

    Google Scholar 

  • Saini HS, Westgate ME (2000) Reproductive development in grain crops during drought. Adv Agron 68:59–96

    Google Scholar 

  • Saini HS, Sedgley M, Aspinall D (1984) Developmental anatomy in wheat of male sterility induced by heat stress, water deficit or abscisic acid. Aust J Plant Physiol 11:243–253

    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  PubMed  CAS  Google Scholar 

  • Sharp RE, Poroyko V, Hejlek LG, Spollen WG, Springer GK, Bohnert HJ, Nguyen HT (2004) Root growth maintenance during water deficits: Physiology to functional genomics. J Exp Bot 55:2343–2351

    Article  PubMed  CAS  Google Scholar 

  • Sheoran IS, Saini HS (1996) Drought-induced male sterility in rice: Changes in carbohydrate levels and enzyme activities associated with the inhibition of starch accumulation in pollen. Sex Plant Reprod 9:161–169

    Article  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • Tambussi EA, Bartoli CG, Beltrano J, Guiamet JJ, Araus JL (2000) Oxidative damage to thylakoid proteins in water stressed leaves of wheat (Triticum asetivum). Physiol Plant 108:398–404

    Article  CAS  Google Scholar 

  • Tao H, Brueck H, Dittert K, Kreye C, Lin S, Sattelmacher B (2006) Growth and yield formation for rice (Oryza sativa L.) in the water-saving ground cover rice production system (GCRPS). Field Crops Res 95:1–12

    Article  Google Scholar 

  • Tsuda M, Takami S (1993) Changes of water potential in rice panicle under increasing drought stress at various stages. Jpn J Crop Sci 62:41–46

    Google Scholar 

  • Waters SP, Martin P, Lee BT (1984) Influence of sucrose and abscisic acid on the determination of grain number in wheat. J Exp Bot 35:829–840

    Article  CAS  Google Scholar 

  • Wilkinson S, Davies WJ (2002) ABA-based chemical signaling: the co-ordination of responses to stress in plants. Plant Cell Environ 25:195–210

    Article  PubMed  CAS  Google Scholar 

  • Xie ZJ, Jiang D, Cao WX, Dai TB, Jing Q (2003) Relationships of endogenous plant hormones to accumulation of grain protein and starch in winter wheat under different post-anthesis soil water statuses. Plant Growth Regul 41:117–127

    Article  CAS  Google Scholar 

  • Yang J, Zhang J (2006) Grain filling of cereals under soil drying. New Phytol 169:223–236

    Article  PubMed  CAS  Google Scholar 

  • Yang J, Zhang J, Wang Z, Zhu Q, Wang W (2001) Hormonal changes in the grains of rice subjected to water stress during grain filling. Plant Physiol 127:315–323

    Article  PubMed  CAS  Google Scholar 

  • Yang J, Zhang J, Wang Z, Zhu Q, Liu L (2003) Involvement of abscisic acid and cytokinins in the senescence and remobilization of carbon reserves in wheat subjected to water stress during grain filling. Plant Cell Environ 26:1621–1631

    Article  CAS  Google Scholar 

  • Yang J, Zhang J, Ye Y, Wang Z, Zhu Q, Liu L (2004) Involvement of abscisic acid and ethylene in the responses of rice grains to water stress during filling. Plant Cell Environ 27:1055–1064

    Article  CAS  Google Scholar 

  • Zee SY, O’Brien (1970) A special type of tracheary element associated with ‘xylem discontinuity’ in the floral axis of wheat. Aust J Biol Sci 23:783–791

  • Zeng ZR, Morgan JM, King RW (1985) Regulation of grain number in wheat: geneotypic difference and response to applied abscisic acid and to high temperature. Aust J Plant Physiol 13:347–352

    Article  Google Scholar 

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

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The authors gratefully acknowledge the grants from the National Natural Science Foundation of China (Project No. 30671225), the Natural Science Foundation of Jiangsu Province (BK2006069), Hong Kong Research Grants Council (Project No. HKBU 2165/05M), and Hong Kong University Grant Committee (AOE/B-07/99).

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Correspondence to Jianhua Zhang.

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Yang, J., Zhang, J., Liu, K. et al. Abscisic Acid and Ethylene Interact in Rice Spikelets in Response to Water Stress During Meiosis. J Plant Growth Regul 26, 318–328 (2007). https://doi.org/10.1007/s00344-007-9013-8

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  • DOI: https://doi.org/10.1007/s00344-007-9013-8

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