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First published online April 11, 2008; 10.1104/pp.108.117481

Plant Physiology 147:611-623 (2008)
© 2008 American Society of Plant Biologists

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CELL BIOLOGY AND SIGNAL TRANSDUCTION

Tobacco Mosaic Virus Movement Protein Interacts with Green Fluorescent Protein-Tagged Microtubule End-Binding Protein 11,[W]

Katrin Brandner2, Adrian Sambade2, Emmanuel Boutant, Pascal Didier, Yves Mély, Christophe Ritzenthaler and Manfred Heinlein*

Institut de Biologie Moléculaire des Plantes, laboratoire propre du CNRS (UPR 2357) conventionné avec l'Université Louis Pasteur, 67084 Strasbourg cedex, France (K.B., A.S., E.B., C.R. M.H.); and Institut Gilbert Laustriat, UMR CNRS 7034, Faculté de Pharmacie, Université Louis Pasteur, 67401 Illkirch, France (P.D., Y.M.)

The targeting of the movement protein (MP) of Tobacco mosaic virus to plasmodesmata involves the actin/endoplasmic reticulum network and does not require an intact microtubule cytoskeleton. Nevertheless, the ability of MP to facilitate the cell-to-cell spread of infection is tightly correlated with interactions of the protein with microtubules, indicating that the microtubule system is involved in the transport of viral RNA. While the MP acts like a microtubule-associated protein able to stabilize microtubules during late infection stages, the protein was also shown to cause the inactivation of the centrosome upon expression in mammalian cells, thus suggesting that MP may interact with factors involved in microtubule attachment, nucleation, or polymerization. To further investigate the interactions of MP with the microtubule system in planta, we expressed the MP in the presence of green fluorescent protein (GFP)-fused microtubule end-binding protein 1a (EB1a) of Arabidopsis (Arabidopsis thaliana; AtEB1a:GFP). The two proteins colocalize and interact in vivo as well as in vitro and exhibit mutual functional interference. These findings suggest that MP interacts with EB1 and that this interaction may play a role in the associations of MP with the microtubule system during infection.


1 This work was supported by the Deutscher Akademischer Austauschdienst, Germany (postdoctoral fellowship grant to K.B.), the Generalidad Valenciana, Spain (postdoctoral fellowship grants CTBPDC/2204/015 and BPOSTDOC06/072 to A.S.), le ministère délégué à la recherche, France (grant no. ACI BCMS187 to M.H.), and the CNRS, France. The fluorescence lifetime imaging microscopy setup was supported by the Association pour la Recherche contre le Cancer, France, the Association Française contre les Myopathies, the Fondation pour la Recherche Médicale, France, Sidaction, the program Physique-Chimie du Vivant of the CNRS, and the Réseau Technologique en microscopie photonique, France, through the Missions, Ressources et Compétences Technologiques of the CNRS.

2 These authors contributed equally to the article.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Manfred Heinlein (manfred.heinlein{at}ibmp-ulp.u-strasbg.fr).

[W] The online version of this article contains Web-only data.

www.plantphysiol.org/cgi/doi/10.1104/pp.108.117481

* Corresponding author; e-mail manfred.heinlein{at}ibmp-ulp.u-strasbg.fr.

Received February 8, 2008; accepted April 1, 2008; published April 11, 2008.




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