Identification of novel plant cysteine oxidase inhibitors from a yeast chemical genetic screen

Symplectic ID
1552599
Source
Ora (Hyrax)
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Saturday, 29 August, 2026 - 06:13
DOI
10.1016/j.jbc.2023.105366
Publication Date
Thursday, 19 October, 2023
Keywords
plant
Saccharomyces cerevisiae
Arabidopsis proteins
cysteine dioxygenase
hypoxia
oxygen
Arabidopsis
cysteine
gene expression regulation
Authors
Lavilla-Puerta, M
Latter, R
Bellè, F
Cervelli, T
Galli, A
Perata, P
Chini, A
Flashman, E
Giuntoli, B
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Abstract
<p>Hypoxic responses in plants involve Plant Cysteine Oxidases (PCOs). They catalyze the N-terminal cysteine oxidation of Ethylene Response Factors VII (ERF-VII) in an oxygen-dependent manner, leading to their degradation&nbsp;<em>via</em>&nbsp;the cysteine N-degron pathway (Cys-NDP) in normoxia. In hypoxia, PCO activity drops, leading to the stabilization of ERF-VIIs and subsequent hypoxic gene upregulation. Thus far, no chemicals have been described to specifically inhibit PCO enzymes. In this work, we devised an&nbsp;<em>in&nbsp;vivo</em>&nbsp;pipeline to discover Cys-NDP effector molecules. Budding yeast expressing AtPCO4 and plant-based ERF-VII reporters was deployed to screen a library of natural-like chemical scaffolds and was further combined with an Arabidopsis Cys-NDP reporter line. This strategy allowed us to identify three PCO inhibitors, two of which were shown to affect PCO activity&nbsp;<em>in&nbsp;vitro</em>. Application of these molecules to Arabidopsis seedlings led to an increase in ERF-VII stability, induction of anaerobic gene expression, and improvement of tolerance to anoxia. By combining a high-throughput heterologous platform and the plant model Arabidopsis, our synthetic pipeline provides a versatile system to study how the Cys-NDP is modulated. Its first application here led to the discovery of at least two hypoxia-mimicking molecules with the potential to impact plant tolerance to low oxygen stress.</p>
Publisher
Elsevier
ISSN
0021-9258
Journal Title
Journal of Biological Chemistry
eISSN
1083-351X
Volume
299
Issue
12
ID at Source
uuid_5476fc8e-b4fc-48e3-8374-42692b445f3f
Publication Status
Published
Open access
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