4.6 Article

Interaction of karrikinolide and ethylene in controlling germination of dormant Avena fatua L. caryopses

Journal

PLANT GROWTH REGULATION
Volume 67, Issue 2, Pages 185-190

Publisher

SPRINGER
DOI: 10.1007/s10725-012-9675-5

Keywords

Avena fatua L.; Butenolide; Caryopses; Ethylene; Karrikinolide; Primary dormancy; Germination

Categories

Funding

  1. Ministry of Science and Higher Education [NN310151935, NN726340]

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Caryopses of L. are dormant after harvest and germinate poorly at 20 A degrees C. Dormancy was released by after-ripening the dry caryopses in the dark at 25 A degrees C for 3 months. Karrikinolide (butenolide, 3-methyl-2-furo[2,3-]pyran-2-one, KAR(1)), in contrast to exogenous ethylene and the precursor of ethylene biosynthesis 1-aminocyclopropane-1-carboxylic acid (ACC), completely overcame dormancy. The effect of KAR(1) was not affected by aminoethoxyvinylglycine (AVG), alpha-aminoisobutyric acid (AIB) and CoCl2, inhibitors of ACC synthase and oxidase, respectively. 2,5-Norbornadiene (NBD), a reversible inhibitor of ethylene binding to its receptor, counteracted the stimulatory effect of KAR(1). Ethylene, ethephon and ACC counteracted and AVG reinforced inhibition caused by norbornadiene. Inhibition due to norbornadiene, applied during the first 3 days of imbibition in the presence of KAR(1), disappeared after transfer to air or ethylene. The obtained results confirm that KAR(1) breaks dormancy and indicate that ethylene alone plays no role in releasing dormancy of caryopses. KAR(1) probably did not relieve dormancy via the stimulation of ethylene biosynthesis. Some level of endogenous ethylene is probably required for ethylene action, which might be required for releasing dormancy by KAR(1) or for subsequent germination of caryopses after removing dormancy.

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