Literature DB >> 18171593

The integration of glutathione homeostasis and redox signaling.

Andreas J Meyer1.   

Abstract

Formation of reactive oxygen species (ROS) is a common feature of abiotic and biotic stress reactions. ROS need to be detoxified to avoid deleterious reactions, but at the same time, the increased formation of ROS can also be exploited for redox signaling. Glutathione, as the most abundant low-molecular weight thiol in the cellular redox system, is used for both detoxification of ROS and transmission of redox signals. Detoxification of H(2)O(2) through the glutathione-ascorbate cycle leads to a transient change in the degree of oxidation of the cellular glutathione pool, and thus a change in the glutathione redox potential. The shift in the glutathione redox potential can be sensed by glutaredoxins (GRXs), small ubiquitous oxidoreductases, which reversibly transfer electrons between the glutathione redox buffer and thiol groups of target proteins. While very little is known about native GRX target proteins and their behavior in vivo, it is shown here that reduction-oxidation-sensitive GFP (roGFP), when expressed in plants, is an artificial target protein of GRXs. The specific interaction of roGFP with GRX results in continuous formation and release of the roGFP disulfide bridge depending on the actual redox potential of the cellular glutathione buffer. Ratiometric analysis of redox-dependent fluorescence allows dynamic imaging of the glutathione redox potential. It was hypothesized that a similar equilibration occurs between the glutathione buffer and native target proteins of GRXs. As a consequence, even minor deviations in the glutathione redox potential due to either depletion of reduced glutathione (GSH) or increasing oxidation can be exploited for fine tuning the activity of target proteins. The integration of the glutathione buffer with redox-active target proteins is a local reaction in specific subcellular compartments. This observation emphasizes the importance of subcellular compartmentalization in understanding the biology of the cellular redox system in plants.

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Year:  2008        PMID: 18171593     DOI: 10.1016/j.jplph.2007.10.015

Source DB:  PubMed          Journal:  J Plant Physiol        ISSN: 0176-1617            Impact factor:   3.549


  62 in total

1.  Glutathione.

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2.  Molecular Biology, Biochemistry and Cellular Physiology of Cysteine Metabolism in Arabidopsis thaliana.

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4.  Light-dependent single-cell heterogeneity in the chloroplast redox state regulates cell fate in a marine diatom.

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5.  Signaling molecules and cell death in Melissa officinalis plants exposed to ozone.

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6.  Glutamate receptor-like channel3.3 is involved in mediating glutathione-triggered cytosolic calcium transients, transcriptional changes, and innate immunity responses in Arabidopsis.

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7.  Redox states of glutathione and ascorbate in root tips of poplar (Populus tremula X P. alba) depend on phloem transport from the shoot to the roots.

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Review 8.  The oxidative protein folding machinery in plant cells.

Authors:  Isabel Aller; Andreas J Meyer
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9.  Transcriptional profiling of an Fd-GOGAT1/GLU1 mutant in Arabidopsis thaliana reveals a multiple stress response and extensive reprogramming of the transcriptome.

Authors:  Ralph Kissen; Per Winge; Diem Hong Thi Tran; Tommy S Jørstad; Trond R Størseth; Tone Christensen; Atle M Bones
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10.  Sulphur flux through the sulphate assimilation pathway is differently controlled by adenosine 5'-phosphosulphate reductase under stress and in transgenic poplar plants overexpressing gamma-ECS, SO, or APR.

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Journal:  J Exp Bot       Date:  2009-11-18       Impact factor: 6.992

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