Transient induction of a subset of ethylene biosynthesis genes is potentially involved in regulation of grapevine bud dormancy release
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Author
Shi, ZhaowanHalaly-Basha, Tamar
Zheng, Chuanlin
Weissberg, Mira
Ophir, Ron
Galbraith, David W.
Pang, Xuequn
Or, Etti
Affiliation
Univ Arizona, Sch Plant SciUniv Arizona, Inst Bio5
Issue Date
2018-12
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SPRINGERCitation
Shi, Z., Halaly-Basha, T., Zheng, C. et al. Plant Mol Biol (2018) 98: 507. https://doi.org/10.1007/s11103-018-0793-yJournal
PLANT MOLECULAR BIOLOGYRights
© Springer Nature B.V. 2018.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Key message Transient increases in ethylene biosynthesis, achieved by tight regulation of transcription of specific ACC oxidase and ACC synthase genes, play a role in activation of grapevine bud dormancy release. Abstract The molecular mechanisms regulating dormancy release in grapevine buds are as yet unclear. It has been hypothesized that its core involves perturbation of respiration which induces an interplay between ethylene and ABA metabolism that removes repression and allows regrowth. Roles for hypoxia and ABA metabolism in this process have been previously supported. The potential involvement of ethylene biosynthesis in regulation of dormancy release, which has received little attention so far, is now explored. Our results indicate that (1) ethylene biosynthesis is induced by hydrogen cyanamide (HC) and azide (AZ), known artificial stimuli of dormancy release, (2) inhibitors of ethylene biosynthesis and signalling antagonize dormancy release by HC/AZ treatments, (3) ethylene application induces dormancy release, (4) there are two sets of bud-expressed ethylene biosynthesis genes which are differentially regulated, (5) only one set is transiently upregulated by HC/AZ and during the natural dormancy cycle, concomitant with changes in ethylene levels, and (6) levels of ACC oxidase transcripts and ethylene sharply decrease during natural dormancy release, whereas ACC accumulates. Given these results, we propose that transient increases in ethylene biosynthesis prior to dormancy release, achieved primarily by regulation of transcription of specific ACC oxidase genes, play a role in activation of dormancy release.Note
12 month embargo; published online: 03 November 2018ISSN
0167-44121573-5028
PubMed ID
30392158Version
Final accepted manuscriptSponsors
United States-Israel Binational Agricultural Research and Development Fund (BARD) [IS-4639-13]; China Scholarship CouncilAdditional Links
http://link.springer.com/10.1007/s11103-018-0793-yae974a485f413a2113503eed53cd6c53
10.1007/s11103-018-0793-y
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