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Thioredoxin m4 Controls Photosynthetic Alternative Electron Pathways in Arabidopsis
Author(s) -
Agathe Courteille,
Simona Vesa,
Ruth SanzBarrio,
Anne-Claire Noel,
Nolle Becuwe-Linka,
Inmaculada Farrán,
Michel Havaux,
Pascal Rey,
Dominique Rumeau
Publication year - 2012
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.112.207019
Subject(s) - plastoquinone , arabidopsis , biology , chloroplast , photosystem i , biochemistry , photosynthesis , arabidopsis thaliana , photoprotection , thylakoid , electron transport chain , nicotiana tabacum , thioredoxin , photoinhibition , microbiology and biotechnology , cytochrome b6f complex , mutant , electrochemical gradient , photosystem ii , biophysics , enzyme , gene , membrane
In addition to the linear electron flow, a cyclic electron flow (CEF) around photosystem I occurs in chloroplasts. In CEF, electrons flow back from the donor site of photosystem I to the plastoquinone pool via two main routes: one that involves the Proton Gradient Regulation5 (PGR5)/PGRL1 complex (PGR) and one that is dependent of the NADH dehydrogenase-like complex. While the importance of CEF in photosynthesis and photoprotection has been clearly established, little is known about its regulation. We worked on the assumption of a redox regulation and surveyed the putative role of chloroplastic thioredoxins (TRX). Using Arabidopsis (Arabidopsis thaliana) mutants lacking different TRX isoforms, we demonstrated in vivo that TRXm4 specifically plays a role in the down-regulation of the NADH dehydrogenase-like complex-dependent plastoquinone reduction pathway. This result was confirmed in tobacco (Nicotiana tabacum) plants overexpressing the TRXm4 orthologous gene. In vitro assays performed with isolated chloroplasts and purified TRXm4 indicated that TRXm4 negatively controls the PGR pathway as well. The physiological significance of this regulation was investigated under steady-state photosynthesis and in the pgr5 mutant background. Lack of TRXm4 reversed the growth phenotype of the pgr5 mutant, but it did not compensate for the impaired photosynthesis and photoinhibition sensitivity. This suggests that the physiological role of TRXm4 occurs in vivo via a mechanism distinct from direct up-regulation of CEF.

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