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First published online October 17, 2008; 10.1104/pp.108.130336

Plant Physiology 148:2083-2095 (2008)
© 2008 American Society of Plant Biologists

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BIOCHEMICAL PROCESSES AND MACROMOLECULAR STRUCTURES

A Genome-Wide and Metabolic Analysis Determined the Adaptive Response of Arabidopsis Cells to Folate Depletion Induced by Methotrexate1,[W]

Karen Loizeau, Veerle De Brouwer, Bernadette Gambonnet, Agnès Yu, Jean-Pierre Renou, Dominique Van Der Straeten, Willy E. Lambert, Fabrice Rébeillé and Stéphane Ravanel*

Laboratoire de Physiologie Cellulaire Végétale, UMR5168 CNRS-CEA-INRA-Université Joseph Fourier Grenoble I, Institut de Recherches en Technologies et Sciences pour le Vivant, CEA-Grenoble, F–38054 Grenoble cedex 9, France (K.L., B.G., F.R., S.R.); Laboratory of Toxicology (V.D.B., W.E.L.), and Unit Plant Hormone Signaling and Bio-imaging, Department of Molecular Genetics (D.V.D.S.), Ghent University, B–9000 Ghent, Belgium; and UMR INRA1165 CNRS8114 UEVE, Unité de Recherche en Génomique Végétale, CP5708, F–91057 Evry, France (A.Y., J.-P.R.)

Control of folate homeostasis is essential to sustain the demand for one-carbon (C1) units that are necessary for major biological functions, including nucleotide synthesis and methylation reactions. In this study, we analyzed the genome-wide and metabolic adaptive response of Arabidopsis (Arabidopsis thaliana) cells to folate depletion induced by the antifolate methotrexate. Drug treatment induced a response typical to xenobiotic stress and important changes in folate content and composition. This resulted in a reduction of cell division and primary energy metabolism that was likely associated with perturbation of nucleotide homeostasis. Through a modification of serine metabolism, folate depletion also induced O-acetylserine accumulation and mimicked sulfur deficiency response. The major adaptive response to folate limitation concerned the composition of the folate pool rather than the intracellular level of cofactors. Thus, no significant change in the expression of genes involved in cofactor synthesis, degradation, or trafficking was observed. However, changes in the distribution of C1 derivative pools and increased expression levels for transcripts coding enzymes manipulating C1 moieties in plastids suggested a reorientation of C1 units toward the synthesis of purine and thymidylate. Also, no genomic or metabolic adaptation was built up to counterbalance the major impairment of the methyl index, which controls the efficiency of methylation reactions in the cell. Together, these data suggested that the metabolic priority of Arabidopsis cells in response to folate limitation was to shuttle the available folate derivatives to the synthesis of nucleotides at the expense of methylation reactions.


1 This work was supported by the French Ministry of Research (a Ph.D. fellowship to K.L.). The folate analysis was supported by the Institute for the Promotion of Innovation through Science and Technology in Flanders (IWT Vlaanderen; grant no. GOA 1251204 [Bijzonder Onderzoeksfonds, UGent] to D.V.D.S. and W.L. and a bursary to V.D.B.).

The author responsible for the 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: Stéphane Ravanel (sravanel{at}cea.fr).

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

www.plantphysiol.org/cgi/doi/10.1104/pp.108.130336

* Corresponding author; e-mail sravanel{at}cea.fr.

Received September 25, 2008; accepted October 15, 2008; published October 17, 2008.




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