A simplify scheme depicting the interactions between cellular redox state and participation in ROS scavenging mechanisms.
Oxidative stress is an unavoidable consequence of environmental stresses. ROS accumulation begins in chloroplasts and then it spreads throughout the whole cell. Activation of a secondary ROS sources e.g. NADPH oxidase complexes or photorespiration resulted in substantial H2O2 accumulation in cytosol. To avoid deleterious effects of ROS several compartment-specific mechanisms evolved, including accumulation of low-molecular-weight antioxidants (glutathione, ascorbate), scavenging enzymes (catalases CAT, ascorbate peroxidases APX, and sodium dismutases SOD) and protein thiols (peroxiredoxins PRX, glutaredoxins GRX, and thioredoxins TRX) that undergoes a reversible cycles the thiol-disulphide exchange. The redox-sensitive proteins sense, transduce, and translate ROS signals into appropriate cellular responses. Thus, precise regulation of size and redox status of the thiol pool is of essential importance for induction of appropriate responses. In plant cells glutathione is present in different compartments in milimolar concentrations and in quiescence it maintained largely in reduced state due to activity of glutathione reductases (GR) at expense of NADPH. Stress-induced ROS accumulation stimulates oxidation of glutathione (GSSG) and in the same time de novo synthesis of GSH. Disturbances in GSH/GSSG ratio might non-specifically influence several downstream pathways, e.g. by induction of thiol-disulfide exchange on target proteins. Cellular redox potential depends primarily on the total concentration of the total glutathione and the extend of its oxidation. GSSG accumulation did not disturb the redox potential if it is compensated by increasing the total glutathione concentration. However, if size of total pool remains unchanged when the GSH:GSSG ratio increased the cell redox potential in the cytosol become more positive. We propose that the improved stress tolerance of annexin STANN1-overexpressing potato plants results from amelioration of oxidative shift of the cytosolic glutathione redox potential. Elevation of STANN1 level had a pleiotropic effect on plant metabolism and physiology what suggested that not one specific but several downstream signaling pathways were touched. Disruption of the glutathione redox potential is sufficient to induce such effect; e.g., in transgenic tobacco with constitutive up-regulation of glutathione content MAPK and SA signaling pathways were modified. Annexin posses oxidation-sensitive cysteines and can act as a reductant influencing thus the redox potential. During stress in transgenic plants the capacity of cytosol redox buffer was more reducing compared to WT what prevents oxidation of downstream targets and modulate timing as well as magnitude of stress response. It had a beneficial effect on cell survival, photosynthesis and delay senescence. Similar effects were observed in tobacco and Arabidopsis plants and over-expressing particular elements of antioxidant systems.

A simplify scheme depicting the interactions between cellular redox state and participation in ROS scavenging mechanisms. Oxidative stress is an unavoidable consequence of environmental stresses. ROS accumulation begins in chloroplasts and then it spreads throughout the whole cell. Activation of a secondary ROS sources e.g. NADPH oxidase complexes or photorespiration resulted in substantial H2O2 accumulation in cytosol. To avoid deleterious effects of ROS several compartment-specific mechanisms evolved, including accumulation of low-molecular-weight antioxidants (glutathione, ascorbate), scavenging enzymes (catalases CAT, ascorbate peroxidases APX, and sodium dismutases SOD) and protein thiols (peroxiredoxins PRX, glutaredoxins GRX, and thioredoxins TRX) that undergoes a reversible cycles the thiol-disulphide exchange. The redox-sensitive proteins sense, transduce, and translate ROS signals into appropriate cellular responses. Thus, precise regulation of size and redox status of the thiol pool is of essential importance for induction of appropriate responses. In plant cells glutathione is present in different compartments in milimolar concentrations and in quiescence it maintained largely in reduced state due to activity of glutathione reductases (GR) at expense of NADPH. Stress-induced ROS accumulation stimulates oxidation of glutathione (GSSG) and in the same time de novo synthesis of GSH. Disturbances in GSH/GSSG ratio might non-specifically influence several downstream pathways, e.g. by induction of thiol-disulfide exchange on target proteins. Cellular redox potential depends primarily on the total concentration of the total glutathione and the extend of its oxidation. GSSG accumulation did not disturb the redox potential if it is compensated by increasing the total glutathione concentration. However, if size of total pool remains unchanged when the GSH:GSSG ratio increased the cell redox potential in the cytosol become more positive. We propose that the improved stress tolerance of annexin STANN1-overexpressing potato plants results from amelioration of oxidative shift of the cytosolic glutathione redox potential. Elevation of STANN1 level had a pleiotropic effect on plant metabolism and physiology what suggested that not one specific but several downstream signaling pathways were touched. Disruption of the glutathione redox potential is sufficient to induce such effect; e.g., in transgenic tobacco with constitutive up-regulation of glutathione content MAPK and SA signaling pathways were modified. Annexin posses oxidation-sensitive cysteines and can act as a reductant influencing thus the redox potential. During stress in transgenic plants the capacity of cytosol redox buffer was more reducing compared to WT what prevents oxidation of downstream targets and modulate timing as well as magnitude of stress response. It had a beneficial effect on cell survival, photosynthesis and delay senescence. Similar effects were observed in tobacco and Arabidopsis plants and over-expressing particular elements of antioxidant systems.

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Annexins are a family of calcium- and membrane-binding proteins that are important for plant tolerance to adverse environmental conditions. Annexins function to counteract oxidative stress, maintain cell redox homeostasis, and enhance drought tolerance. In the present study, an endogenous annexin, STANN1, was overexpressed to determine whether crop...

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... Moreover, these stress response mechanisms can be interconnected, and specific proteins may also provide photoprotection in potato plants under drought stress such as a recent report reviewed a likely light and ABA crosstalk during drought response in Arabidopsis (Mukherjee et al., 2023;Szalonek et al., 2015;Wang et al., 2023). ...
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