Evidence map›Paper›PMID 30392158›Full record

ArticlePlant molecular biology2018

Transient induction of a subset of ethylene biosynthesis genes is potentially involved in regulation of grapevine bud dormancy release.

Zhaowan Shi, Tamar Halaly-Basha, Chuanlin Zheng, Mira Weissberg, Ron Ophir, David W Galbraith, Xuequn Pang, Etti Or

Abstract read
PubMed Publisher
In one paragraph

Article in Plant molecular biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Zhaowan ShiInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel.
Tamar Halaly-BashaInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel.
Chuanlin ZhengInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel.
Mira WeissbergInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel.
Ron OphirInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel.
David W GalbraithSchool of Plant Sciences and Bio5 Institute, University of Arizona, Tucson, AZ, 85721, USA.
Xuequn PangCollege of Life Sciences, South China Agricultural University, Guangzhou, 510642, China.
Etti OrInstitute of Plant Sciences, Department of Fruit Tree Sciences, Agricultural Research Organization, Volcani Center, 7528809, Rishon LeZion, Israel. vhettior@agri.gov.il.
Agricultural Research Organization · ILSouth China Agricultural University · CNUniversity of Arizona · US

Funding

United States-Israel Binational Agricultural Research and Development Fund IS-4639-13
6 · The paper itself

Abstract

key messageTransient 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. 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.

Indexed as

Gene Expression Regulation, PlantAmino Acid OxidoreductasesEthylenesLyasesPlant DormancyPlant Growth RegulatorsPlant ProteinsVitis1-aminocyclopropane-1-carboxylic acid oxidase1-aminocyclopropanecarboxylate synthaseAmino Acid OxidoreductasesethyleneEthylenesLyasesPlant Growth RegulatorsPlant ProteinsACC oxidase (ACO)ACC synthase (ACS)BudDormancyEthyleneGrapevineVitis vinifera

Identifiers

PMID30392158
OpenAlexW2899052599

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.