Modulation of mitochondrial activity by S-nitrosoglutathione reductase in Arabidopsis thaliana transgenic cell lines

Biochim Biophys Acta. 2013 Mar;1827(3):239-47. doi: 10.1016/j.bbabio.2012.11.011. Epub 2012 Nov 29.

Abstract

The enzyme S-nitrosoglutathione reductase (GSNOR) has an important role in the metabolism of S-nitrosothiols (SNO) and, consequently, in the modulation of nitric oxide (NO)-mediated processes. Although the mitochondrial electron transport chain is an important target of NO, the role of GSNOR in the functionality of plant mitochondria has not been addressed. Here, we measured SNO content and NO emission in Arabidopsis thaliana cell suspension cultures of wild-type (WT) and GSNOR overexpressing (GSNOR(OE)) or antisense (GSNOR(AS)) transgenic lines, grown under optimal conditions and under nutritional stress. Respiratory activity of isolated mitochondria and expression of genes encoding for mitochondrial proteins were also analyzed. Under optimal growth conditions, GSNOR(OE) had the lowest SNO and NO levels and GSNOR(AS) the highest, as expected by the GSNO-consuming activity of GSNOR. Under stress, this pattern was reversed. Analysis of oxygen uptake by isolated mitochondria showed that complex I and external NADH dehydrogenase activities were inhibited in GSNOR(OE) cells grown under nutritional stress. Moreover, GSNOR(OE) could not increase alternative oxidase (AOX) activity under nutritional stress. GSNOR(AS) showed constitutively high activity of external NADH dehydrogenase, and maintained the activity of the uncoupling protein (UCP) under stress. The alterations observed in mitochondrial protein activities were not strictly correlated to changes in gene expression, but instead seemed to be related with the SNO/NO content, suggesting a post-transcriptional regulation. Overall, our results highlight the importance of GSNOR in modulating SNO and NO homeostasis as well mitochondrial functionality, both under normal and adverse conditions in A. thaliana cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Oxidoreductases / metabolism*
  • Arabidopsis / genetics
  • Arabidopsis / growth & development
  • Arabidopsis / metabolism*
  • Cell Line
  • Electron Transport Complex I / metabolism
  • Mitochondria / metabolism*
  • Mitochondrial Proteins / metabolism
  • NADH Dehydrogenase / metabolism
  • Nitric Oxide / metabolism
  • Oxidoreductases / metabolism
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • S-Nitrosothiols / analysis

Substances

  • Mitochondrial Proteins
  • Plant Proteins
  • S-Nitrosothiols
  • Nitric Oxide
  • Oxidoreductases
  • alternative oxidase
  • Aldehyde Oxidoreductases
  • formaldehyde dehydrogenase, glutathione-independent
  • NADH Dehydrogenase
  • Electron Transport Complex I