Identification and functional characterization of the Arabidopsis Snf1‐related protein kinase SnRK2.4 phosphatidic acid‐binding domain |
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Authors: | MAGDALENA M. JULKOWSKA FIONN MCLOUGHLIN CARLOS S. GALVAN‐AMPUDIA JOHANNA M. RANKENBERG DOROTA KAWA MARIA KLIMECKA MICHEL A. HARING TEUN MUNNIK EDGAR E. KOOIJMAN CHRISTA TESTERINK |
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Affiliation: | 1. Plant Physiology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands;2. Department of Biological Sciences, Kent State University, Kent, OH, USA;3. International Institute for Complex Adaptive Matter, University of California, Davis, CA, USA;4. Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland |
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Abstract: | ![]() Phosphatidic acid (PA) is an important signalling lipid involved in various stress‐induced signalling cascades. Two SnRK2 protein kinases (SnRK2.4 and SnRK2.10), previously identified as PA‐binding proteins, are shown here to prefer binding to PA over other anionic phospholipids and to associate with cellular membranes in response to salt stress in Arabidopsis roots. A 42 amino acid sequence was identified as the primary PA‐binding domain (PABD) of SnRK2.4. Unlike the full‐length SnRK2.4, neither the PABD‐YFP fusion protein nor the SnRK2.10 re‐localized into punctate structures upon salt stress treatment, showing that additional domains of the SnRK2.4 protein are required for its re‐localization during salt stress. Within the PABD, five basic amino acids, conserved in class 1 SnRK2s, were found to be necessary for PA binding. Remarkably, plants overexpressing the PABD, but not a non‐PA‐binding mutant version, showed a severe reduction in root growth. Together, this study biochemically characterizes the PA–SnRK2.4 interaction and shows that functionality of the SnRK2.4 PABD affects root development. |
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Keywords: | phosphatidic acid phospholipid binding root system architecture SnRK2.10 |
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