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CPK13, a Noncanonical Ca2+-Dependent Protein Kinase, Specifically Inhibits KAT2 and KAT1 Shaker K+ Channels and Reduces Stomatal Opening

Authors: Ronzier, Elsa; Corratgé-Faillie, Claire; Sanchez, Frédéric; Prado, Karine; Brière, Christian; Leonhardt, Nathalie; Thibaud, Jean-Baptiste; +1 Authors

CPK13, a Noncanonical Ca2+-Dependent Protein Kinase, Specifically Inhibits KAT2 and KAT1 Shaker K+ Channels and Reduces Stomatal Opening

Abstract

Abstract Ca2 +-dependent protein kinases (CPKs) form a large family of 34 genes in Arabidopsis (Arabidopsis thaliana). Based on their dependence on Ca2+, CPKs can be sorted into three types: strictly Ca2+-dependent CPKs, Ca2+-stimulated CPKs (with a significant basal activity in the absence of Ca2+), and essentially calcium-insensitive CPKs. Here, we report on the third type of CPK, CPK13, which is expressed in guard cells but whose role is still unknown. We confirm the expression of CPK13 in Arabidopsis guard cells, and we show that its overexpression inhibits light-induced stomatal opening. We combine several approaches to identify a guard cell-expressed target. We provide evidence that CPK13 (1) specifically phosphorylates peptide arrays featuring Arabidopsis K+ Channel KAT2 and KAT1 polypeptides, (2) inhibits KAT2 and/or KAT1 when expressed in Xenopus laevis oocytes, and (3) closely interacts in plant cells with KAT2 channels (Förster resonance energy transfer-fluorescence lifetime imaging microscopy). We propose that CPK13 reduces stomatal aperture through its inhibition of the guard cell-expressed KAT2 and KAT1 channels.

Keywords

570, KAT2 channels, Patch-Clamp Techniques, Arabidopsis, KAT1, Ca 2+-dependent, CPKs, Xenopus laevis, [SDV.BV]Life Sciences [q-bio]/Vegetal Biology, Animals, [SDV.BV] Life Sciences [q-bio]/Vegetal Biology, Phosphorylation, Potassium Channels, Inwardly Rectifying, Xenopus oocytes, 580, Arabidopsis Proteins, protein kinase, Microscopy, Fluorescence, Potassium Channels, Voltage-Gated, Plant Stomata, Calcium, Protein Kinases

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
106
Top 1%
Top 10%
Top 10%
hybrid