Conditional stability of HY5 through the ATE N-degron pathway regulates environmental responses in Arabidopsis thaliana

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Authors: Charlene Dambire, Isabel Manrique-Gil, Jorge Vicente, Carolina Farias Saad, Andreas Bachmair, Kris Gevaert, Frank Van Breusegem, Michael John Holdsworth
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Abstract

Abstract The N-degron pathways of ubiquitin mediated proteolysis target proteins for degradation dependent on their amino terminal residue, often produced after protease activity. Very few substrates have been identified in plants even though enzymes of these pathways are highly conserved in eukaryotes. Here we identify ELONGATED HYPOCOTYL5 (HY5), an important transcriptional regulator involved in many aspects of plant development, as a target for the endopeptidase METACASPASE (MC)9, producing the carboxy-terminal protein fragment (proteoform) E59-HY5. E59-HY5 is shown to be a substrate of the arginyl transferase (ATE) N-degron pathway, and influences physiological processes known to be controlled by HY5, including photomorphogenesis and the unfolded protein response. Conditional stability of E59-HY5 was shown to result from environmentally controlled ATE function, which may highlight a general mechanism for N-degron pathway regulation of proteoform and proteome function during growth and development.

Fields of Study & Subjects

Ubiquitin and proteasome pathways Light effects on plants Plant Molecular Biology Research

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publication date
11 February 2026
Language
EN
Document type
Preprint