4.7 Article

EDL3 is an F-box protein involved in the regulation of abscisic acid signalling in Arabidopsis thaliana

期刊

JOURNAL OF EXPERIMENTAL BOTANY
卷 62, 期 15, 页码 5547-5560

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jxb/err236

关键词

ABA; anthocyanin; Arabidopsis; de-etiolation; EDL3; F-box protein; flowering; germination induction; root growth; water stress

资金

  1. Deutsche Forschungsgemeinschaft [KR 2020/1-3, 1-4]
  2. DFG [KR2020/2-3]
  3. European Union [HPRN-CT-2002-00333]
  4. Freiburg Institute for Advanced Studies (FRIAS), School of Life Sciences

向作者/读者索取更多资源

The EID1-like protein 3 (EDL3) shows high similarity to EID1 (Empfindlicher im dunkelroten Licht 1), an F-box protein that functions as a negative regulator in the signalling cascade downstream of the phytochrome A photoreceptor in Arabidopsis thaliana. Analyses revealed a strong and rapid induction of EDL3 gene expression under osmotic stress, high salinity, and upon abscisic acid (ABA) application. Therefore, it was speculated that EDL3 is involved in the regulation of responses controlled by this plant hormone, which not only regulates many aspects of plant development but also integrates responses towards temperature, drought, osmotic, and salt stresses. Physiological data obtained with over-expresser lines and a conditional knock-down mutant demonstrated that EDL3 functions as a positive regulator in ABA-dependent signalling cascades that control seed germination, root growth, greening of etiolated seedlings, and transition to flowering. Results further demonstrate that EDL3 regulates anthocyanin accumulation under drought stress. The observed effects on physiological responses fit to tissue-specific expression patterns obtained with EDL3-promoter:GUS lines. Bimolecular Fluorescence Complementation assays and yeast two-hybrid analyses showed that EDL3 carries a functional F-box domain. Thus, the protein is presumed to act as a component of a ubiquitin ligase complex that specifically directs negatively acting factors in ABA signalling to degradation via the proteasome.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据