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Pollen tube growth is affected by exogenous hormones and correlated with hormone changes in styles in Torenia fournieri L.

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Abstract

In the present report, we described the effects of indole-3-acetic acid (IAA), zeatin (ZT), gibberellin (GA3), and abscisic acid (ABA) on in vitro pollen germination and pollen tube growth in Torenia fournieri L. The results showed that IAA and GA3 stimulated in vitro pollen tube growth, ABA inhibited pollen tube growth, and ZT had no significant effect on the process. The stimulating effect of exogenous IAA was particularly distinct, and led to synchronous growth of straighter and more slender pollen tubes compared with the controls. However, no significant changes were found in the germination of the treated pollen. The auxin efflux inhibitor, 10 μM 1-N-naphthylphthalamic acid (NPA), was also found to stimulate pollen tube growth. We measured the content of hormones (free IAA, ZT, GA3, and ABA) in the stigmas and styles before and after pollination. The hormone contents of stigmas measured 0.5 h after pollination (0.5 HAP) showed that ABA content decreased, whereas the content of IAA, ZT, or GA3 did not change significantly. The hormone level in pollinated styles (4 HAP) when pollen tubes had grown into the middle part of style was characterized by an increase in free IAA and GA3 and a decrease in ABA, which was in agreement with the results that IAA and GA3 promoted but ABA inhibited pollen tube growth in vitro. Furthermore, the change of IAA level in styles was most notable, which was accordant to the fact that auxin stimulated significantly pollen tube growth in vitro. Using immunoenzyme and immunogold labeling techniques and an anti-IAA monoclonal antibody, we confirmed that free IAA was present throughout style tissues, and distributed in the nucleus and cytoplasm of style cells. All these results suggested that hormones, especially IAA, play important roles in pollen tube growth of T. fournieri.

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Abbreviations

ABA:

Abscisic acid

EDAC:

1-Ethyl-3-(3-dimethyllaminopropyl) carbodiimide hydrochloride

ELISA:

Enzyme linked immunosorbent assay

GA3 :

Gibberellic acid

HAP:

Hours after pollination

IAA:

Indole-3-acetic acid

NPA:

1-N-naphthylphthalamic acid

SABC:

Streptayidin and biotinylated horseradish peroxidase complex

STT:

Stylar transmitting tissue

ZT:

Zeatin

References

  • Aloni R, Aloni E, Langhans M, Ullrich CI (2006) Role of auxin in regulating Arabidopsis flower development. Planta 223:315–328

    Article  PubMed  CAS  Google Scholar 

  • Avsian-Kretchmer O, Cheng JC, Chen LJ, Moctezuma E, Sung ZR (2002) Indole acetic acid distribution coincides with vascular differentiation pattern during Arabidopsis leaf ontogeny. Plant Physiol 130:199–209

    Article  PubMed  CAS  Google Scholar 

  • Burg SP, Dijkman MJ (1967) Ethylene and auxin participation in pollen induced fading of Vanda Orchid blossoms. Plant Physiol 42:1648–1650

    PubMed  CAS  Google Scholar 

  • Catala C, Rose JKC, York WS, Albersheim P, Darvill AG, Bennett AB (2001) Characterization of a tomato xyloglucan endotransglycosylase gene that is down-regulated by auxin in etiolated hypocotyls. Plant Physiol 127:1180–1192

    Article  PubMed  CAS  Google Scholar 

  • Chauhan YS, Katiyar SR (1998) Effects of radiation and growth hormones on pollen germination, pollen tube growth and modulation of radiation responses of Pinus kesiya Royle ex Gord. Cytologia 63:341–348

    CAS  Google Scholar 

  • Cheung AY, Wang H, Wu HM (1995) A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth. Cell 82:383–393

    Article  PubMed  CAS  Google Scholar 

  • De Martinis D, Cotti G, te Lintel HS, Harren FJ, Mariani C (2002) Ethylene response to pollen tube growth in Nicotiana tabacum flowers. Planta 214:806–812

    Article  PubMed  CAS  Google Scholar 

  • Dhawan K, Malik CP (1981) Effect of growth regulators and light on pollen germination and pollen tube growth in Pinus roxburghii Sarg. Ann Bot 47:239–248

    CAS  Google Scholar 

  • Elleman CJ, Dickinson HG (1999) Commonalities between pollen/stigma and host/pathogen interactions: calcium accumulation during stigmatic penetration by Brassica oleracea pollen tubes. Sex Plant Reprod 12:194–202

    Article  CAS  Google Scholar 

  • Holdaway-Clarke TL, Hepler PK (2003) Control of pollen tube growth: role of ion gradients and fluxes. New Phytol 159:539–563

    Article  CAS  Google Scholar 

  • Holden MJ, Marty JA, Singh-Cundy A (2003) Pollination-induced ethylene promotes the early phase of pollen tube growth in Petunia inflate. J Plant Physiol 160:261–269

    Article  PubMed  CAS  Google Scholar 

  • Kim S, Mollet JC, Dong J, Zhang K, Park SY, Lord EM (2003) Chemocyanin, a small basic protein from the lily stigma, induces pollen tube chemotropism. Proc Natl Acad Sci USA 100:16125–16130

    Article  PubMed  CAS  Google Scholar 

  • Knox RB (1984) Pollen–pistil interactions. In: Linskens HF, Heslop-Harrison J (eds) Cellular interactions, encyclopedia of plant physiology. New series. Springer-Verlag, Berlin, pp 508–608

    Google Scholar 

  • Kovaleva L, Zakharova E (2003) Hormonal status of the pollen–pistil system at the progamic phase of fertilization after compatible and incompatible pollination in Petunia hybrida L. Sex Plant Reprod 16:191–196

    Article  CAS  Google Scholar 

  • Kovaleva LV, Zakharova EV, Minkina YuV, Timofeeva GV, Andreev IM (2005) Germination and in vitro growth of petunia male gametophyte are affected by exogenous hormones and involve the changes in the endogenous hormone level. Russ J Plant Physiol 52:521–526

    Article  CAS  Google Scholar 

  • Leung J, Bouvier-Durand M, Morris PC, Guerrier D, Chefdor F, Giraudat J (1994) Arabidopsis ABA response gene ABI1: features of a calcium-modulated protein phosphatase. Science 264:1448–1452

    Article  PubMed  CAS  Google Scholar 

  • Lomax TL, Muday GK, Rubery PH (1995) Auxin transport. In: Davies PJ (ed) Plant hormones and their role in plant growth and development. Kluwer Academic Publishers, Boston Dordrecht (Netherlands), pp 509–530

    Google Scholar 

  • Ma LG, Xu XD, Cui SJ, Sun DY (1999) The presence of a heterotrimeric G protein and its role in signal transduction of extracellular calmodulin in pollen germination and tube growth. Plant Cell 11(7):1351–1364

    Article  PubMed  CAS  Google Scholar 

  • Madhu A, Thomas G, Edward N (1999) The roles of abscisic acid and ethylene in the abscission and senescence of cocoa flowers. Plant Growth Regul 27:149–155

    Article  Google Scholar 

  • Mol R, Filek M, Machackova I, Matthys-Rochon E (2004) Ethylene synthesis and auxin augmentation in pistil tissues are important for egg cell differentiation after pollination in maize. Plant Cell Physiol 45:1396–1405

    Article  PubMed  CAS  Google Scholar 

  • Nemhauser JL, Feldman LJ, Zambryski PC (2000) Auxin and ETTIN in Arabidopsis gynoecium morphogenesis. Development 127:3877–3888

    PubMed  CAS  Google Scholar 

  • Ohmiya A, Hayashi T (1992). Immuno-gold localization of IAA in leaf cells of Prunus persica at different stages of development. Physiol Plantarum 85:439–445

    Article  CAS  Google Scholar 

  • O’Neill SD (1997) Pollination regulation of flower development. Annu Rev Plant Physiol Plant Mol Biol 48:547–574

    Article  PubMed  CAS  Google Scholar 

  • Palanivelu R, Brass L, Edlund AF, Preuss D (2003) Pollen tube growth and guidance is regulated by POP2, an Arabidopsis gene that controls GABA levels. Cell 114:47–59

    Article  PubMed  CAS  Google Scholar 

  • Park JE, Kim YS, Yoon HK, Yun J, Park CM (2007) Functional characterization of a small auxin-up RNA gene in apical hook development in Arabidopsis. Plant Sci 172:150–157

    Google Scholar 

  • Petrásek J, Cerná A, Schwarzerová K, Elkner M, Morris DA, Zazímalová E (2003) Do phytotropins inhibit auxin efflux by impairing vesicle traffic. Plant Physiol 131:254–263

    Article  PubMed  CAS  Google Scholar 

  • Qin Y, Zhao J (2006) Localization of arabinogalactan proteins in egg cells, zygotes, and two-celled proembryos and effects of β-D-glucosyl Yariv reagent on egg cell fertilization and zygote division in Nicotiana tabacum L. J Exp Bot 57:2061–2074

    Article  PubMed  CAS  Google Scholar 

  • Raghavan V, Baruah HK (1959) Effect of time factor on the stimulation of pollen germination and pollen tube growth by certain auxin, vitamins, and trace elements. Physiol Plantarum 12:441–451

    Article  Google Scholar 

  • Rakitin VYu, Rakitin LYu (1986) Determination of gas exchange and the content of ethylene, carbon dioxide, and oxygen in plant tissues of higher plants. Fiziol Rast 33:403–413

    CAS  Google Scholar 

  • Reddy VS, Ali GS, Reddy ASN (2002) Genes encoding calmodulin-binding proteins in the Arabidopsis genome. J Biol Chem 277:9840–9852

    Article  PubMed  CAS  Google Scholar 

  • Rober-Kleber N, Albrechtova JTP, Fleig S, Huck N, Michalke W, Wagner E, Speth V, Neuhaus G, Fischer-Iglesias C (2003) Plasma membrane H+-ATPase is involved in auxin-mediated cell elongation during wheat embryo development. Plant Physiol 131:1302–1312

    Article  PubMed  CAS  Google Scholar 

  • Ross JJ, O’Neill DP, Smith JJ, Kerckhoffs LH, Elliott RC (2000) Evidence that auxin promotes gibberellin A1 biosynthesis in pea. Plant J 21:547–552

    Article  PubMed  CAS  Google Scholar 

  • Sidhu RK, Basra AS, Malik CP (1986) Hormonal effects on tube elongation, 14CO2 fixation and phosphoenolpyruvate carboxylase activity in Amaryllis pollen: promotion by abscisic acid. Plant Growth Regul 4(3):293–298

    Article  CAS  Google Scholar 

  • Singh DP, Jermakow AM, Swain SM (2002) Gibberellins are required for seed development and pollen tube growth in Arabidopsis. Plant Cell 14:3133–3147

    Article  PubMed  CAS  Google Scholar 

  • Tanimoto E (2005) Regulation of root growth by plant hormones-roles for auxin and gibberellin. Crit Rev Plant Sci 24:249–265

    Article  CAS  Google Scholar 

  • Tao W, Verbelen JP (1996) Switching on and off cell division and cell expansion in cultured mesophyll protoplasts from tobacco. Plant Sci 116:107–115

    Article  CAS  Google Scholar 

  • Teng NJ, Wang J, Chen T, Wu XQ, Wang YH, Lin JX (2006) Elevated CO2 induces physiological, biochemical and structural changes in leaves of Arabidopsis thaliana. New Phytol 172:92–103

    Article  PubMed  CAS  Google Scholar 

  • Van Staden J, Cook EL, Nooden LD (1988) Cytokinins and senescence. In: Nooden LD, Leopold AC (eds) Senescence and aging in plants. Academic Press, San Diego, pp 281–328

    Google Scholar 

  • Wang H, Wu HM, Cheung AY (1996) Pollination induces mRNA poly(A) tail-shortening and cell deterioration in flower transmitting tissue. Plant J 9:715–727

    Article  PubMed  CAS  Google Scholar 

  • Wolbang CM, Ross JJ (2001) Auxin promotes gibberellin biosynthesis in decapitated tobacco plants. Planta 214:153–157

    Article  PubMed  CAS  Google Scholar 

  • Wolbang CM, Chandler PM, Smith JJ, Ross JJ (2004) Auxin from the developing inflorescence is required for the biosynthesis of active gibberellins in barley stems. Plant Physiol 134:769–776

    Article  PubMed  CAS  Google Scholar 

  • Yamaguchi S, Smith MW, Brown RG, Kamiya Y, Sun T (1998) Phytochrome regulation and differential expression of gibberellin 3-beta-hydroxylase genes in germinating Arabidopsis seeds. Plant Cell 10:2115–2126

    Article  PubMed  CAS  Google Scholar 

  • Yang SF, Hoffman N (1984) Ethylene biosynthesis and its regulation in higher plants. Annu Rev Plant Physiol 35:155–189

    Article  CAS  Google Scholar 

  • Yang T, Poovaiah BW (2000) Molecular and biochemical evidence for the involvement of calcium/calmodulin in auxin action. J Biol Chem 275:3137–3143

    Article  PubMed  CAS  Google Scholar 

  • Yoon IS, Mori H, Kim JH, Kang BG, Imaseki H (1997) VR-ACS6 is an auxin-inducible 1-aminocyclopropane-1-carboxylate synthase gene in mungbean (Vigna radiata). Plant Cell Physiol 38:217–224

    PubMed  CAS  Google Scholar 

  • Zhang XS, O’Neill DS (1993) Ovary and gametophyte development are coordinately regulated following pollination by auxin and ethylene. Plant Cell 5:403–418

    Article  PubMed  CAS  Google Scholar 

  • Zhao J, Yang HY, Lord EM (2004) Calcium levels increase in the lily stylar transmitting tract after pollination. Sex Plant Reprod 16:259–263

    Article  CAS  Google Scholar 

  • Zhu SF, Gao F, Cao XS, Chen M, Ye GY, Wei CH, Li Y (2005) The rice dwarf virus P2 protein interacts with ent-kaurene oxidases in vivo, leading to reduced biosynthesis of gibberellins and rice dwarf symptoms. Plant Physiol 139:1935–1945

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This study was supported by the National Natural Science Foundation of China (30521004) and the Key Grant Project of Chinese Ministry of Education (307018).

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Correspondence to Jie Zhao.

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Wu, J., Qin, Y. & Zhao, J. Pollen tube growth is affected by exogenous hormones and correlated with hormone changes in styles in Torenia fournieri L.. Plant Growth Regul 55, 137–148 (2008). https://doi.org/10.1007/s10725-008-9268-5

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