Publication details

Redox regulation of plant S-nitrosoglutathione reductase activity through post-translational modifications of cysteine residues

Authors

TICHA Tereza LOCHMAN Jan ČINČALOVÁ Lucie LUHOVÁ Lenka PETŘIVALSKÝ Marek

Year of publication 2017
Type Article in Periodical
Magazine / Source Biochemical and biophysical research communications
MU Faculty or unit

Faculty of Science

Citation
Doi http://dx.doi.org/10.1016/j.bbrc.2017.10.090
Keywords Nitric oxide; Post-translational modifications; Redox regulation; S-nitrosoglutathione reductase; S-nitrosation
Description Nitric oxide (NO) is considered as a signalling molecule involved in a variety of important physiological and pathological processes in plant and animal systems. The major pathway of NO reactions in vivo represents S-nitrosation of thiols to form S-nitrosothiols. S-nitrosoglutathione reductase (GSNOR) is the key enzyme in the degradation pathway of S-nitrosoglutathione (GSNO), a low-molecular weight adduct of NO and glutathione. GSNOR indirectly regulates the level of protein S-nitrosothiol in the cells. This study was focused on the dynamic regulation of the activity of plant GSNORs through reversible S-nitrosation and/or oxidative modifications of target cysteine residues. Pre-incubation with NO/NO- donors or hydrogen peroxide resulted in a decreased reductase and dehydrogenase activity of all studied plant GSNORs. Incubation with thiol reducing agent completely reversed inhibitory effects of nitrosative modifications and partially also oxidative inhibition. In biotin-labelled samples, S-nitrosation of plant GSNORs was confirmed after immunodetection and using mass spectrometry S-nitrosation of conserved Cys271 was identified in tomato GSNOR. Negative regulation of constitutive GSNOR activity in vivo by nitrosative or oxidative modifications might present an important mechanism to control GSNO levels, a critical mediator of the downstream signalling effects of NO, as well as for formaldehyde detoxification in dehydrogenase reaction mode. (C) 2017 Elsevier Inc. All rights reserved.

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