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  4. Decoys provide a scalable platform for the identification of plant E3 ubiquitin ligases that regulate circadian function
 
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Decoys provide a scalable platform for the identification of plant E3 ubiquitin ligases that regulate circadian function

Journal
eLife
Journal Volume
8
Date Issued
2019
Author(s)
Feke, Ann
Liu, Wei
Hong, Jing
Li, Man-Wah
CHIN-MEI LEE  
Zhou, Elton K.
Gendron, Joshua M.
DOI
10.7554/eLife.44558
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/469898
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85065217486&doi=10.7554%2feLife.44558&partnerID=40&md5=b581bcac26ed299f3e323539c5d87948
Abstract
The circadian clock relies on regulated degradation of clock proteins to maintain rhythmicity. Despite this, we know few components that mediate protein degradation. This is due to high levels of functional redundancy within plant E3 ubiquitin ligase families. In order to overcome this issue and discover E3 ubiquitin ligases that control circadian function, we generated a library of transgenic Arabidopsis plants expressing dominant-negative ‘decoy’ E3 ubiquitin ligases. We determined their effects on the circadian clock and identified dozens of new potential regulators of circadian function. To demonstrate the potency of the decoy screening methodology to overcome redundancy and identify bona fide clock regulators, we performed follow-up studies on MAC3A (PUB59) and MAC3B (PUB60). We show that they redundantly control circadian period by regulating splicing. This work demonstrates the viability of ubiquitin ligase decoys as a screening platform to overcome genetic challenges and discover E3 ubiquitin ligases that regulate plant development.
Type
journal article

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