Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Endogenous auxin regulates the sensitivity of Dendrobium (cv. Miss Teen) flower pedicel abscission to ethylene

Karnchana Rungruchkanont A , Saichol Ketsa A D , Orawan Chatchawankanphanich B and Wouter G. van Doorn C
+ Author Affiliations
- Author Affiliations

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

B National Center for Genetic Engineering and Biotechnology (BIOTEC), Kasetsart University, Kamphaengsaen Campus, Nakhon Pathom 73140, Thailand.

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

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

Functional Plant Biology 34(10) 885-894 https://doi.org/10.1071/FP07146
Submitted: 12 June 2007  Accepted: 24 July 2007   Published: 13 September 2007

Abstract

Dendrobium flower buds and flowers have an abscission zone at the base of the pedicel (flower stalk). Ethylene treatment of cv. Miss Teen inflorescences induced high rates of abscission in flower buds but did not affect abscission once the flowers had opened. It is not known if auxin is a regulator of the abscission of floral buds and open flowers. The hypotheses that auxin is such a regulator and is responsible for the decrease in ethylene sensitivity were tested. Severed inflorescences bearing 4–8 floral buds and 4–6 open flowers were used in all tests. The auxin antagonists 2,3,5-triiodobenzoic acid (TIBA, an inhibitor of auxin transport) or 2-(4-chlorophenoxy)-2-methyl propionic acid (CMPA, an inhibitor of auxin action) were applied to the stigma of open flowers. Both chemicals induced high flower abscission rates, even if the inflorescences were not treated with ethylene. The effects of these auxin antagonists virtually disappeared when the inflorescences were treated with 1-methylcyclopropene (1-MCP), indicating that the abscission induced by the auxin antagonists was due to ethylene. Removal of the open flowers at the distal end of the pedicel hastened the time to abscission of the remaining pedicel, and also resulted in an increase in ethylene sensitivity. Indole-3-acetic acid (IAA) in lanolin, placed on the cut surface of the pedicel, replaced the effect of the removed flower. Treatments that promoted abscission of open flowers up-regulated a gene encoding a β-1,4-glucanase (Den-Cel1) in the abscission zone (AZ). The abundance of Den-Cel1 mRNA was highly correlated with β-1,4-glucanase activity in the AZ. The results show that auxin is an endogenous regulator of floral bud and flower abscission and suggest that auxin might explain, at least partially, why pedicel abscission of Dendrobium cv. Miss Teen changes from very ethylene-sensitive to ethylene-insensitive.

Additional keywords: abscission, abscission zone, auxin, auxin inhibitor, ethylene, 1-MCP.


Acknowledgements

This research was financially supported by the Thailand Research Fund (TRF), the Graduate School at Kasetsart University, and the Postgraduate Education and Research Development Project in Postharvest Technology.


References


Abu-Goukh AA, Bashir HA (2003) Changes in pectic enzymes and cellulase activity during guava fruit ripening. Food Chemistry 83, 213–218.
Crossref | GoogleScholarGoogle Scholar | open url image1

Aneja M, Gianfana T, Ng E (1999) The roles of abscisic acid and ethylene in the abscission and senescence of cocoa flowers. Plant Growth Regulation 27, 149–155.
Crossref | GoogleScholarGoogle Scholar | open url image1

Anthon GE, Barrett DM (2002) Determination of reducing sugars with 3-methyl-2-benzothiazolinonehydrazone. Analytical Biochemistry 305, 287–289.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Awad M, Young RE (1979) Postharvest variation in cellulase, polygalacturonase and pectinmethylesterase in avocado (Persea americana Mill. cv. Fuerte) fruit in relation to respiration and ethylene production. Plant Physiology 64, 306–308.
PubMed |
open url image1

Blankenship SM, Dole JM (2003) 1-Methylcyclopropene: a review. Postharvest Biology and Technology 28, 1–25.
Crossref | GoogleScholarGoogle Scholar | open url image1

Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248–254.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Bunya-atichart K, Ketsa S, van Doorn WG (2006) High floral bud abscission and lack of open flower abscission in Dendrobium cv. Miss Teen: rapid reduction of ethylene sensitivity in the abscission zone. Functional Plant Biology 33, 539–546.
Crossref | GoogleScholarGoogle Scholar | open url image1

Chang S, Puryear J, Cairney J (1993) A simple and efficient method for isolating RNA from pines trees. Plant Molecular Biology Reporter 11, 113–116. open url image1

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

Harpster MH, Brummell DA, Dunsmuir P (1998) Expression analysis of a ripening-specific, auxin-repressed endo-β-1,4-glucanase gene in strawberry. Plant Physiology 118, 1307–1316.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Henderson J, Osborne DJ (1994) Intertissue signalling during the 2-phase abscission of oil palm fruit. Journal of Experimental Botany 45, 943–951.
Crossref | GoogleScholarGoogle Scholar | open url image1

Iannetta PPM, Wyman M, Neelam A, Jones C, Taylor MA, Davies HV, Sexton R (2000) A causal role for ethylene and endo-β-1,4-glucanase in the abscission of red-raspberry (Rubus idaeus) drupelets. Physiologia Plantarum 110, 535–543.
Crossref | GoogleScholarGoogle Scholar | open url image1

Kalaitzis P, Hong SB, Solomos T, Tucker ML (1999) Molecular characterization of a tomato endo-β-1,4-glucanase gene expressed in mature pistils, abscission zones and fruit. Plant & Cell Physiology 40, 905–908.
PubMed |
open url image1

Mandels M, Sternberg D (1976) Recent advances in cellulase technology. Journal of Fermentation and Technology 54, 267–286. open url image1

McKay MJ, Ross JJ, Lawrence NL, Cramp RE, Beveridge CA, Reid JB (1994) Control of internode length in Pisum sativum. Plant Physiology 106, 1521–1526.
PubMed |
open url image1

Meir S, Hunter DA, Chen JC, Halaly V, Reid MS (2006) Molecular changes occurring during acquisition of abscission competence following auxin depletion in Mirabilis jalapa. Plant Physiology 141, 1604–1616.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Morgan PW, Durham JI (1972) Abscission: potentiating action of auxin transport inhibitors. Plant Physiology 50, 313–318.
PubMed |
open url image1

Oono Y, Ooura C, 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

Patterson SE, Bleecker AB (2004) Ethylene-dependent and independent processes associated with floral organ abscission in Arabidopsis. Plant Physiology 134, 194–203.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Roberts JA, Elliott KA, Gonzalez-Carranza ZH (2002) Abscission, dehiscence and other cell separation processes. Annual Review of Plant Biology 53, 131–158.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Sargent JA, Osborne DJ, Dunford SM (1984) Cell separation and its hormonal control during fruit abscission in the Graminae. Journal of Experimental Botany 35, 1663–1674. open url image1

Sekai WS (1973) Simple method for differential staining of paraffin embedded plant materials using toluidine blue O. stain. Stain Technology 48, 247–249.
PubMed |
open url image1

Sexton R 2002. Abscission. In ‘Handbook of Plant and Crop Physiology’. (Ed. M. Pessaraki) pp. 205–227. (Marcel Dekker: New York.).

Sexton R, Laird G, van Doorn WG (2000) Lack of ethylene involvement in tulip tepal abscission. Physiologia Plantarum 108, 321–329.
Crossref | GoogleScholarGoogle Scholar | open url image1

Sussman MR, Goldsmith MHM (1981) The action of specific inhibitors of auxin transport on uptake of auxin and binding of N-1-naphthylphtahlamic acid to membrane site in maize coleoptiles. Planta 152, 13–18.
Crossref | GoogleScholarGoogle Scholar | open url image1

Taylor JE, Coupe SA, Picton S, Roberts JA (1994) Characterization and accumulation pattern of an mRNA encoding an abscission-related β-1,4-glucanase from leaflets of Sambucus nigra. Plant Molecular Biology 24, 961–964.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Trainotti L, Spolaore S, Pavanello A, Baldan B, Casadoro G (1999) A novel E-type endo-β-1,4-glucanase with a putative cellulose-binding domain is highly expressed in ripening strawberry fruits. Plant Molecular Biology 40, 323–332.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Tucker ML, Whitelaw CA, Lyssenko NN, Nath P (2002) Functional analysis of regulatory elements in the gene promoter for an abscission-specific cellulase from bean and isolation, expression, and binding affinity to three TGA-type basic leucine zipper transcription factors. Plant Physiology 130, 1487–1496.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Turner AD, Wien HC (1994) Dry matter assimilation and partitioning in pepper cultivars differing in susceptibility to stress-induced bud and flower abscission. Annals of Botany 73, 617–622.
Crossref | GoogleScholarGoogle Scholar | open url image1

van Doorn WG (2002) Effect of ethylene on flower abscission: a survey. Annals of Botany 89, 689–693.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

van Doorn WG, Stead AD (1997) Abscission of flowers and floral parts. Journal of Experimental Botany 48, 821–837.
Crossref | GoogleScholarGoogle Scholar | open url image1

Woodward AW, Bartel B (2005) Auxin: regulation, action, and interaction. Annals of Botany 95, 707–735.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1