4.8 Article

Adenylates regulate Arabidopsis plastidial thioredoxin activities through the binding of a CBS domain protein

Journal

PLANT PHYSIOLOGY
Volume 189, Issue 4, Pages 2298-2314

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plphys/kiac199

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Funding

  1. Ministe`re de la Recherche et de l'Enseignement Superieur
  2. French State grant (Saclay Plant Sciences) [ANR-17-EUR-0007, ANR-11-IDEX-0003-02]
  3. Labex Saclay Plant Sciences-SPS [ANR-17-EUR-0007]
  4. French Infrastructure for Integrated Structural Biology [ANR-10-INSB-05]

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This study reveals the role of CBSX proteins in regulating thioredoxins (TRXs) and plant stress adaptation. CBSX2 specifically inhibits the activities of m-type TRXs, and this inhibition can be alleviated in the presence of AMP or ATP.
Cystathionine-beta-synthase (CBS) domains are found in proteins of all living organisms and have been proposed to play a role as energy sensors regulating protein activities through their adenosyl ligand binding capacity. In plants, members of the CBSX protein family carry a stand-alone pair of CBS domains. In Arabidopsis (Arabidopsis thaliana), CBSX1 and CBSX2 are targeted to plastids where they have been proposed to regulate thioredoxins (TRXs). TRXs are ubiquitous cysteine thiol oxido-reductases involved in the redox-based regulation of numerous enzymatic activities as well as in the regeneration of thiol-dependent peroxidases. In Arabidopsis, 10 TRX isoforms have been identified in plastids and divided into five sub-types. Here, we show that CBSX2 specifically inhibits the activities of m-type TRXs toward two chloroplast TRX-related targets. By testing activation of NADP-malate dehydrogenase and reduction of 2-Cys peroxiredoxin, we found that TRXm1/2 inhibition by CBSX2 was alleviated in the presence of AMP or ATP. We also determined, by pull-down assays, a direct interaction of CBSX2 with reduced TRXm1 and m2 that was abolished in the presence of adenosyl ligands. In addition, we report that, compared with wild-type plants, the Arabidopsis T-DNA double mutant cbsx1 cbsx2 exhibits growth and chlorophyll accumulation defects in cold conditions, suggesting a function of plastidial CBSX proteins in plant stress adaptation. Together, our results show an energy-sensing regulation of plastid TRX m activities by CBSX, possibly allowing a feedback regulation of ATP homeostasis via activation of cyclic electron flow in the chloroplast, to maintain a high energy level for optimal growth. A cystathionine-beta-synthase protein inhibits m-type thioredoxin activities toward NADP-malate dehydrogenase and 2-Cys peroxiredoxin in an adenylate-dependent manner.

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