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Plant function and evolutionary biology
RESEARCH ARTICLE

Auxin is required for pollination-induced ovary growth in Dendrobium orchids

Saichol Ketsa A C , Apinya Wisutiamonkul A and Wouter G. van Doorn B
+ Author Affiliations
- Author Affiliations

A Department of Horticulture, Faculty of Agriculture, Kasetsart University, Bangkok 10900, Thailand.

B Wageningen University and Research Centre, PO Box 17, 6700AA Wageningen, The Netherlands.

C Corresponding author. Email: agrsck@ku.ac.th

Functional Plant Biology 33(9) 887-892 https://doi.org/10.1071/FP06034
Submitted: 15 February 2006  Accepted: 18 May 2006   Published: 1 September 2006

Abstract

In Dendrobium and other orchids the ovule becomes mature long after pollination, whereas the ovary starts growing within two days of pollination. The signalling pathway that induces rapid ovary growth after pollination has remained elusive. We placed the auxin antagonist α-(p-chlorophenoxy) isobutyric acid (PCIB) or the auxin transport inhibitor 2,3,5-triiodobenzoic acid (TIBA) on the stigma, before pollination. Both treatments nullified pollination-induced ovary growth. The ovaries also did not grow after similar stigma treatment with 1-methylcyclopropene (1-MCP), AgNO3 (both inhibitors of ethylene action), aminooxyacetic acid (AOA) or CoCl2 (which both inhibit ethylene synthesis), before pollination. Pollination could be replaced by placement of the auxin naphthylacetic acid (NAA) on the stigma. All mentioned inhibitors nullified the effect of NAA, indicating that if auxin is the initiator of ovary growth, it acts through ethylene. The results suggest that the pollination effect on ovary growth requires auxin (at least auxin transport and maybe also auxin signalling), and both ethylene synthesis and ethylene action.

Keywords: auxin, Dendrobium flower, ethylene action, ethylene production, ovary growth.


Acknowledgments

The research was financially supported by the Thailand Research Fund (TRF).


References


Abeles FB , Morgan PW , Saltveit ME (1992) ‘Ethylene in plant biology.’ (Academic Press: New York)

Al-Hammadi ASA, Sreelakshmi Y, Negi S, Siddiqi I, Sharma R (2003) The polycotyledon mutant of tomato shows enhanced polar auxin transport. Plant Physiology 133, 113–125.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Arditti J, Jeffrey DC, Flick BH (1971) Post-pollination phenomena in orchid flowers. III. Effect and interactions of auxin, kinetin or gibberellin. New Phytologist 70, 1125–1141.
Crossref | GoogleScholarGoogle Scholar | open url image1

Cox CM, Swain SM (2006) Localised and non-localised promotion of fruit development by seeds in Arabidopsis. Functional Plant Biology 33, 1–8.
Crossref | GoogleScholarGoogle Scholar | open url image1

Duncan RE, Curtis JT (1942) Intermittent growth of fruits of Phalaenopsis. A correlation of the growth phases of an orchid fruit with internal development. Bulletin of the Torrey Botanical Club 69, 167–183.
Crossref | GoogleScholarGoogle Scholar | open url image1

Fitting H (1909) Die Beeinflussung der Orchideenblüten durch die Bestäubung und durch andere Umstände. Zeitschrift für Botanik 1, 1–86. open url image1

Fitting H (1910) Weitere entwicklungsphysiologische Untersuchungen an Orchideenblüten. Zeitschrift für Botanik 2, 225–267. open url image1

Frenkel C, Haard NF (1973) Initiation of ripening in Bartlett pears with an antiauxin α-(p-chlorophenoxy) isobutyric acid. Plant Physiology 52, 380–384.
PubMed |
open url image1

Guo H, Ecker JR (2004) The ethylene signaling pathway: new insights. Current Opinion in Plant Biology 7, 40–49.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Heslop-Harrison J (1957) The physiology of reproduction in Dactylorchis. I. Auxin and the control of meiosis, ovule formation and ovary growth. Botaniska Notiser 110, 28–50. open url image1

Hildebrand F (1863) Die Fruchtbildung der Orchideen, ein Beweis für die doppelte Wirkung des Pollens. Botanische Zeitung 21, 329–333. open url image1

Ketsa S, Luangsuwalai K (1996) The relationship between 1-aminocyclopropane-1-carboxylic acid content in pollinia, ethylene production and senescence of pollinated Dendrobium orchid flowers. Postharvest Biology and Technology 8, 57–64.
Crossref | GoogleScholarGoogle Scholar | open url image1

Ketsa S, Rugkong A (2000) The role of ethylene in enhancing the initial ovary growth of Dendrobium ‘Pompadour’ following pollination. Journal of Horticultural Science & Biotechnology 75, 451–454. open url image1

Ketsa S, Bunya-atichart K, van Doorn WG (2001) Ethylene production and post-pollination development in Dendrobium flowers treated with foreign pollen. Australian Journal of Plant Physiology 28, 409–415. open url image1

Laibach F, Maschmann E (1933) Über den Wuchsstoff der Orchideenpollinien. Jahrbücher für wissenschaftliche Botanik 78, 399–430. open url image1

Müller R (1953) Zur quantitativen Bestimmung von Indolylessigsäure mittels Papierchromatographie und Papierelektrophorese. Beiträge zur Biologie der Pflanzen 30, 1–32. open url image1

O’Neill S (1997) Pollination regulation of flower development. Annual Review of Plant Physiology and Plant Molecular Biology 48, 547–574.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

O’Neill S, Nadeau JA, Zhang XS, Bui AQ, Halevy AH (1993) Interorgan regulation of ethylene biosynthetic genes by pollination. The Plant Cell 5, 419–432.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Oono Y, Chiharu O, Rahman A, Aspuria ET, Hayashi K, Tanaka A, Uchimiya H (2003) p-Chlorophenoxyisobutyric acid impairs auxin response in Arabidopsis root. Plant Physiology 133, 1135–1147.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Porat R, Nadeau JA, Kirby JA, Sutter EG, O’Neill SD (1998) Characterization of the primary pollen signal in the postpollination syndrome of Phalaenopsis flowers. Plant Growth Regulation 24, 109–117.
Crossref | GoogleScholarGoogle Scholar | open url image1

Strauss MS, Arditti J (1982) Postpollination phenomena in orchid flowers X. Transport and fate of auxin. Botanical Gazette 143, 286–293.
Crossref | GoogleScholarGoogle Scholar | open url image1

Tudela D, Primo-Millo E (1992) 1-Aminocyclopropane-1-carboxylic acid transported from roots to shoots promotes leaf abscission in cleopatra mandarin (Citrus reshni Hort, ex tan.) seedlings rehydrated after water stress. Plant Physiology 100, 131–137.
PubMed |
open url image1

Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Annual Review of Plant Physiololgy 35, 155–189. open url image1

Zhang XS, O’Neill SD (1993) Ovary and gametophyte development are coordinately regulated following pollination by auxin and ethylene. The Plant Cell 5, 403–418.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1