Journal of Biological Chemistry
Volume 294, Issue 46, 15 November 2019, Pages 17543-17554
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Plant Biology
Calmodulin is involved in the dual subcellular location of two chloroplast proteinsCalmodulin control of cellular location

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Cell compartmentalization is an essential process by which eukaryotic cells separate and control biological processes. Although calmodulins are well-known to regulate catalytic properties of their targets, we show here their involvement in the subcellular location of two plant proteins. Both proteins exhibit a dual location, namely in the cytosol in addition to their association to plastids (where they are known to fulfil their role). One of these proteins, ceQORH, a long-chain fatty acid reductase, was analyzed in more detail, and its calmodulin-binding site was identified by specific mutations. Such a mutated form is predominantly targeted to plastids at the expense of its cytosolic location. The second protein, TIC32, was also shown to be dependent on its calmodulin-binding site for retention in the cytosol. Complementary approaches (bimolecular fluorescence complementation and reverse genetics) demonstrated that the calmodulin isoform CAM5 is specifically involved in the retention of ceQORH in the cytosol. This study identifies a new role for calmodulin and sheds new light on the intriguing CaM-binding properties of hundreds of plastid proteins, despite the fact that no CaM or CaM-like proteins were identified in plastids.

chloroplast
subcellular fractionation
subcellular organelle
calmodulin (CaM)
plant molecular biology
plant biochemistry
Chloroplast envelope
Subcellular location

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This work was supported by the French National Research Agency. This work was supported in part by Fellowships ANR-06-GPLA-0003, ANR Génomique Végétale–Genoplante 2010 Glyco-chloroplast; ANR-2010-BLAN-1610-01, ANR Blanc Chloro-Pro; and ANR-10-LABX-49-01, Labex GRAL from the French National Research Agency (to L. M.). This work was also supported in part by Ph.D. Fellowship ANR-10-LABX-49-01 (Labex GRAL) from the INRA Plant Biology and Breeding Division and from the French National Research Agency (to I. B.) and by a Ph.D. fellowship from the CEA (to S. M.). We also acknowledge ANR Project Grant ANR-15-IDEX-02. Additional support was provided by specific ANR Labex GRAL, CNRS, and INRA funding and by access to the local IRIG–CEA facilities for confocal microscopy. The authors declare that they have no conflicts of interest with the contents of this article.

This article contains Figs. S1–S5.

1

These authors contributed equally to this work.

2

Present address: Cornell University, Ithaca, NY 14853.

3

Present address: Kelly Scientific, 1204 Geneva, Switzerland.

4

Present address: Génétique et Amélioration des Fruits et Légumes, INRA, 84140 Montfavet, France.

5

Present address: Institut pour l'Avancée des Biosciences, Université Grenoble Alpes, CNRS, INSERM, La Tronche, France.

7

The abbreviations used are:

    CaM

    calmodulin

    BiFC

    bimolecular fluorescence complementation

    LHCP

    light-harvesting complex protein

    HRP

    horseradish peroxidase

    YFP

    yellow fluorescent protein.