Phosphoproteome analyses pinpoint the F‐box protein SLOW MOTION as a regulator of warm temperature‐mediated hypocotyl growth in Arabidopsis

Author:

Zhu Shanshuo1234ORCID,Pan Lixia12ORCID,Vu Lam Dai1234ORCID,Xu Xiangyu12ORCID,Orosa‐Puente Beatriz56ORCID,Zhu Tingting12ORCID,Neyt Pia1,van de Cotte Brigitte12,Jacobs Thomas B.12ORCID,Gendron Joshua M.7,Spoel Steven H.5ORCID,Gevaert Kris34ORCID,De Smet Ive12ORCID

Affiliation:

1. Department of Plant Biotechnology and Bioinformatics Ghent University B‐9052 Ghent Belgium

2. VIB Center for Plant Systems Biology B‐9052 Ghent Belgium

3. VIB‐UGent Center for Medical Biotechnology, VIB B‐9000 Ghent Belgium

4. Department of Biomolecular Medicine Ghent University B‐9000 Ghent Belgium

5. Institute of Molecular Plant Sciences, School of Biological Sciences University of Edinburgh Edinburgh EH9 3BF UK

6. Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS) and Departamento de Química Orgánica Universidade de Santiago de Compostela 15782 Santiago de Compostela Spain

7. Department of Molecular, Cellular, and Developmental Biology Yale University New Haven CT 06511 USA

Abstract

Summary Hypocotyl elongation is controlled by several signals and is a major characteristic of plants growing in darkness or under warm temperature. While already several molecular mechanisms associated with this process are known, protein degradation and associated E3 ligases have hardly been studied in the context of warm temperature. In a time‐course phosphoproteome analysis on Arabidopsis seedlings exposed to control or warm ambient temperature, we observed reduced levels of diverse proteins over time, which could be due to transcription, translation, and/or degradation. In addition, we observed differential phosphorylation of the LRR F‐box protein SLOMO MOTION (SLOMO) at two serine residues. We demonstrate that SLOMO is a negative regulator of hypocotyl growth, also under warm temperature conditions, and protein–protein interaction studies revealed possible interactors of SLOMO, such as MKK5, DWF1, and NCED4. We identified DWF1 as a likely SLOMO substrate and a regulator of warm temperature‐mediated hypocotyl growth. We propose that warm temperature‐mediated regulation of SLOMO activity controls the abundance of hypocotyl growth regulators, such as DWF1, through ubiquitin‐mediated degradation.

Funder

Bijzonder Onderzoeksfonds UGent

Publisher

Wiley

Subject

Plant Science,Physiology

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