Arabidopsis nonresponding to oxylipins locus NOXY7 encodes a yeast GCN1 homolog that mediates noncanonical translation regulation and stress adaptation

Plant Cell Environ. 2018 Jun;41(6):1438-1452. doi: 10.1111/pce.13182. Epub 2018 Mar 30.

Abstract

Stress adaptation and translational regulation was studied using noxy7 (nonresponding to oxylipins7) from a series of Arabidopsis thaliana mutants. We identified the noxy7 mutation in At1g64790, which encodes a homolog of the yeast translational regulator General Control Nonderepressible1 (GCN1) that activates the GCN2 kinase; GCN2 in turn phosphorylates the α subunit of the translation initiation factor eIF2. This regulatory circuit is conserved in yeast and mammals, in which phosphorylated eIF2α (P-eIF2α) facilitates stress adaptation by inhibiting protein synthesis. In phenotypic and de novo protein synthesis studies with Arabidopsis mutants, we found that NOXY7/GCN1 and GCN2 mediate P-eIF2α formation and adaptation to amino acid deprivation; however, P-eIF2α formation is not linked to general protein synthesis arrest. Additional evidence suggested that NOXY7/GCN1 but not GCN2 regulates adaptation to mitochondrial dysfunction, high boron concentration, and activation of plant immunity to infection by Pseudomonas syringae pv tomato (Pst). In these responses, NOXY7/GCN1 acts with GCN20 to regulate translation in a noncanonical pathway independently of GCN2 and P-eIF2α. These results show the lesser functional relevance of GCN2 and P-eIF2α in plants relative to other eukaryotes and highlight the prominent role of NOXY7/GCN1 and GCN20 in regulation of translation and stress adaptation in plants.

Keywords: Arabidopsis; eIF2α phosphorylation; regulation of translation; stress adaptation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological* / drug effects
  • Alleles
  • Arabidopsis / metabolism*
  • Arabidopsis / microbiology
  • Arabidopsis / physiology*
  • Arabidopsis Proteins / metabolism*
  • Eukaryotic Initiation Factor-2 / metabolism
  • Genetic Loci
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mutation / genetics
  • Peptide Elongation Factors / chemistry*
  • Phenotype
  • Phosphorylation / drug effects
  • Plant Roots / drug effects
  • Plant Roots / physiology
  • Plant Stomata / drug effects
  • Plant Stomata / physiology
  • Protein Biosynthesis* / drug effects
  • Protein Synthesis Inhibitors / pharmacology
  • Pseudomonas / physiology
  • Saccharomyces cerevisiae Proteins / chemistry*
  • Sequence Homology, Amino Acid*
  • Stress, Physiological* / drug effects

Substances

  • Arabidopsis Proteins
  • At1g64790 protein, Arabidopsis
  • Eukaryotic Initiation Factor-2
  • GCN1 protein, S cerevisiae
  • Intracellular Signaling Peptides and Proteins
  • Peptide Elongation Factors
  • Protein Synthesis Inhibitors
  • Saccharomyces cerevisiae Proteins