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Abstract: Zinc (Zn) is an essential micronutrient for plants, but accumulation of excess Zn causes oxidative stress, even though the element is not redox-active. An oxidative stress signature, consisting of multiple oxidative stress related parameters, is indicative of disturbance of redox homeostasis and signaling, but has not been determined after exposure to excess Zn. To reveal general and Zn-specific effects, changes in oxidative stress related gene expression, enzyme activities and metabolites were determined after 24h exposure of Arabidopsis thaliana plants to a concentration range of 0, 100, 250 or 500μM excess ZnSO4, and the oxidative stress signature compared to the ones reported previously for cadmium or copper exposure in the same experimental system. Zn accumulated in both roots and leaves, which led to a disturbed redox homeostasis as evident from increased H2O2 levels and altered glutathione redox state. In roots, magnesium uptake was affected and glutathione levels decreased due to reduced glutathione reductase activity and increased phytochelatin production. In leaves, mRNA levels of all chloroplast-localized superoxide dismutases (SOD) were downregulated, indicating that the converse regulation by Cu availability of FeSOD (FSD) and Cu/ZnSOD genes (CSDs) was disturbed. Furthermore, an opposite stress-dependent transcriptional regulation of the different loci of a miRNA species was observed: excess Zn repressed primary transcripts of the MIR398a gene, but increased MIR398b and MIR398c transcription. Also, accumulation of mRNA was inhibited for CSD2, but stimulated for CSD1. MiR398 has been reported to downregulate CSD1 and CSD2 mRNA. Here, the opposite effect on CSD1 and CSD2 mRNA accumulation under Zn stress in the leaves could be explained if CSD1 in the leaves would be regulated exclusively by miR398a, and not by miR398b/c under these conditions. The results support the existence of Zn-specific signal transduction pathways influencing anti-oxidative responses and are useful as a starting point for genetic screens identifying upstream metal-specific sensing and signaling mechanisms. [Copyright &y& Elsevier]

Abstract: Metals, like cadmium (Cd) and copper (Cu), have the ability to induce the production of reactive oxygen species (ROS) at the cellular level. It is widely known that these ROS can cause irreversible damage to cellular components, like DNA, proteins and lipids. On the other hand, ROS can also act as signaling molecules and in this way they play an essential role in many normal physiological processes, but also in defense responses against stress. ROS signaling in plants uses mitogen-activated protein kinase (MAPK) pathways leading to the transcriptional control of target genes involved in the scavenging or production of ROS. Here, oxidative signaling induced by exposure to excess Cd or Cu was investigated in relation to anti-oxidative defense responses to these metals. Three-week-old Arabidopsis thaliana plants were exposed to environmentally realistic concentrations of Cu and Cd and immediate responses were measured at the level of hydrogen peroxide (H2O2) content, lipid peroxidation and transcript levels of genes involved in ROS homeostasis and signaling. Our findings show immediate (after 2h exposure) effects in the roots following Cu exposure, whereas effects in the leaves were generally more delayed. Effects of Cd exposure in leaves and roots were observed only after 24h exposure. On one hand, exposure of roots to Cu leads via activation of NADPH oxidases and Fenton reactions to H2O2 production that can induce MAPK and oxylipin signaling to control the cellular redox status. On the other hand, conversion of H2O2 to the more damaging hydroxyl radical by Fenton and Haber–Weiss reactions can initiate lipid peroxidation leading to membrane damage. In roots exposed to elevated Cd concentrations only oxidative signaling was initiated, possibly via NADPH oxidase-mediated ROS production. In leaves, time-dependent activation of MAPK and oxylipin signaling was seen after exposure to both metals, Cu or Cd, independent of changes in H2O2 content. [Copyright &y& Elsevier]