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Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation.

Publication ,  Journal Article
Loizeau, K; Gambonnet, B; Zhang, G-F; Curien, G; Jabrin, S; Van Der Straeten, D; Lambert, WE; Rébeillé, F; Ravanel, S
Published in: Plant Physiol
October 2007

In all organisms, control of folate homeostasis is of vital importance to sustain the demand for one-carbon (C1) units that are essential in major metabolic pathways. In this study we induced folate deficiency in Arabidopsis (Arabidopsis thaliana) cells by using two antifolate inhibitors. This treatment triggered a rapid and important decrease in the pool of folates with significant modification in the distribution of C1-substituted folate coenzymes, suggesting an adaptive response to favor a preferential shuttling of the flux of C1 units to the synthesis of nucleotides over the synthesis of methionine (Met). Metabolic profiling of folate-deficient cells indicated important perturbation of the activated methyl cycle because of the impairment of Met synthases that are deprived of their substrate 5-methyl-tetrahydrofolate. Intriguingly, S-adenosyl-Met and Met pools declined during the initial period of folate starvation but were further restored to typical levels. Reestablishment of Met and S-adenosyl-Met homeostasis was concomitant with a previously unknown posttranslational modification that consists in the removal of 92 amino acids at the N terminus of cystathionine gamma-synthase (CGS), the first specific enzyme for Met synthesis. Rescue experiments and analysis of different stresses indicated that CGS processing is specifically associated with perturbation of the folates pool. Also, CGS processing involves chloroplastic serine-type proteases that are expressed in various plant species subjected to folate starvation. We suggest that a metabolic effector, to date unidentified, can modulate CGS activity in vivo through an interaction with the N-terminal domain of the enzyme and that removal of this domain can suppress this regulation.

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Published In

Plant Physiol

DOI

ISSN

0032-0889

Publication Date

October 2007

Volume

145

Issue

2

Start / End Page

491 / 503

Location

United States

Related Subject Headings

  • Plant Biology & Botany
  • Molecular Sequence Data
  • Methionine
  • Gene Expression Regulation, Plant
  • Folic Acid Antagonists
  • Folic Acid
  • Cells, Cultured
  • Carbon-Sulfur Lyases
  • Carbon-Oxygen Lyases
  • Carbon
 

Citation

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Loizeau, K., Gambonnet, B., Zhang, G.-F., Curien, G., Jabrin, S., Van Der Straeten, D., … Ravanel, S. (2007). Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation. Plant Physiol, 145(2), 491–503. https://doi.org/10.1104/pp.107.105379
Loizeau, Karen, Bernadette Gambonnet, Guo-Fang Zhang, Gilles Curien, Samuel Jabrin, Dominique Van Der Straeten, Willy E. Lambert, Fabrice Rébeillé, and Stéphane Ravanel. “Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation.Plant Physiol 145, no. 2 (October 2007): 491–503. https://doi.org/10.1104/pp.107.105379.
Loizeau K, Gambonnet B, Zhang G-F, Curien G, Jabrin S, Van Der Straeten D, et al. Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation. Plant Physiol. 2007 Oct;145(2):491–503.
Loizeau, Karen, et al. “Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation.Plant Physiol, vol. 145, no. 2, Oct. 2007, pp. 491–503. Pubmed, doi:10.1104/pp.107.105379.
Loizeau K, Gambonnet B, Zhang G-F, Curien G, Jabrin S, Van Der Straeten D, Lambert WE, Rébeillé F, Ravanel S. Regulation of one-carbon metabolism in Arabidopsis: the N-terminal regulatory domain of cystathionine gamma-synthase is cleaved in response to folate starvation. Plant Physiol. 2007 Oct;145(2):491–503.

Published In

Plant Physiol

DOI

ISSN

0032-0889

Publication Date

October 2007

Volume

145

Issue

2

Start / End Page

491 / 503

Location

United States

Related Subject Headings

  • Plant Biology & Botany
  • Molecular Sequence Data
  • Methionine
  • Gene Expression Regulation, Plant
  • Folic Acid Antagonists
  • Folic Acid
  • Cells, Cultured
  • Carbon-Sulfur Lyases
  • Carbon-Oxygen Lyases
  • Carbon