# GCN2 is activated by methyl jasmonate through GCN1 and reactive oxygen species in Arabidopsis thaliana

**Authors:** Daniel Rincon Diaz, Morgan E. Wynn, Emmanuel Asiedu, Teressa K. Akuoko, Ansul Lokdarshi

PMC · DOI: 10.1038/s41598-025-32799-w · 2026-01-13

## TL;DR

This study explores how the protein GCN2 in Arabidopsis is activated by methyl jasmonate through GCN1 and reactive oxygen species, affecting plant stress responses.

## Contribution

The study reveals that GCN2 activation by methyl jasmonate in Arabidopsis depends on GCN1 and ROS, offering new insights into plant stress mitigation mechanisms.

## Key findings

- eIF2α phosphorylation under MeJA stress requires light and is suppressed by antioxidants and photosynthetic inhibitors.
- GCN1 is essential for GCN2 activation, as gcn1 mutants show reduced P-eIF2α in response to MeJA.
- gcn2 mutants maintain wild-type-like protein synthesis rates under MeJA stress despite impaired signaling.

## Abstract

Plant growth and productivity rely on rapid energy management strategies to adapt dynamic environments. Previous work in Arabidopsis thaliana identified a fast-regulatory switch linking cytosolic translation and reactive oxygen species (ROS) signaling, where the protein kinase general control of nonderepressible (GCN)2 is rapidly activated in response to ROS under numerous stresses and phosphorylates the eukaryotic translation initiation factor (eIF)2α as a potential stress mitigation mechanism. Here, we test the hypothesis that the Arabidopsis GCN2-eIF2α’s responses towards the plant defense hormone methyl jasmonate (MeJA) are regulated by light, ROS, and the conserved GCN2 activator protein, general control of non-derepressible 1 (GCN1). We show that eIF2α phosphorylation (P-eIF2α) under MeJA stress requires light and is suppressed by antioxidants and photosynthetic inhibitors. GCN1 is essential for this activation, as gcn1 mutant seedlings show reduced P-eIF2α in response to MeJA. Physiologically, both gcn1 and gcn2 mutants exhibit enhanced sensitivity to MeJA in a primary root growth assay. Surprisingly, despite impaired signaling, gcn2 mutants maintain wild-type-like protein synthesis rates under MeJA stress, as shown by polysome profiling and puromycin labeling. Combined, we provide fresh insights into the activation of the Arabidopsis GCN2-eIF2α module in response to MeJA stress by ROS and the GCN1 protein.

The online version contains supplementary material available at 10.1038/s41598-025-32799-w.

## Linked entities

- **Genes:** EIF2AK4 (eukaryotic translation initiation factor 2 alpha kinase 4) [NCBI Gene 440275], GCN1 (GCN1 activator of EIF2AK4) [NCBI Gene 10985], EIF2A (eukaryotic translation initiation factor 2A) [NCBI Gene 83939]
- **Proteins:** EIF2AK4 (eukaryotic translation initiation factor 2 alpha kinase 4), GCN1 (GCN1 activator of EIF2AK4), EIF2A (eukaryotic translation initiation factor 2A)
- **Chemicals:** methyl jasmonate (PubChem CID 62388), puromycin (PubChem CID 439530)
- **Species:** Arabidopsis thaliana (taxon 3702)

## Full-text entities

- **Genes:** EIF2 ALPHA (eukaryotic translation initiation factor 2 alpha subunit) [NCBI Gene 830430] {aka ATEIF2-A2, EIF2-A2, eukaryotic translation initiation factor 2 alpha subunit}, GCN1 (Gcn1p) [NCBI Gene 852680] {aka AAS103, NDR1}, GCN2 (protein kinase family protein) [NCBI Gene 825110] {aka ARABIDOPSIS THALIANA GENERAL CONTROL NON-REPRESSIBLE 2, ATGCN2, GENERAL CONTROL NON-REPRESSIBLE 2}, ABCF1 (ABC transporter family protein) [NCBI Gene 836200] {aka ARABIDOPSIS THALIANA GENERAL CONTROL NON-REPRESSIBLE 1, ATGCN1, ATP-binding cassette F1, GCN1, GENERAL CONTROL NON-REPRESSIBLE 1, MAE1.10}, GCN4 (amino acid starvation-responsive transcription factor GCN4) [NCBI Gene 856709] {aka AAS101, AAS3, ARG9}, MYB0 (myb domain protein 0) [NCBI Gene 822415] {aka ATGL1, ATMYB0, GL1, GLABRA 1, TRICHOME DIFFERENTIATION PROTEIN GL1, myb domain protein 0}, GCN2 (serine/threonine-protein kinase GCN2) [NCBI Gene 851877] {aka AAS1, AAS102, NDR2}
- **Diseases:** AL (MESH:D009101), growth retardation (MESH:D006130), DRD (MESH:C538007), retardation (MESH:D008607)
- **Chemicals:** abscisic acid (MESH:D000040), Methanol (MESH:D000432), chlorsulfuron (MESH:C037137), amino acid (MESH:D000596), agarose (MESH:D012685), salt (MESH:D012492), salicylic acid (MESH:D020156), 3-(3,4-dichlorophenyl)-1,1-dimethylurea (MESH:D004237), JA (MESH:C011006), Glutathione (MESH:D005978), Anthocyanin (MESH:D000872), N (MESH:D009584), PU (MESH:D011691), P (MESH:D010758), Polyvinylpyrrolidone (MESH:D011205), CSF (-), cadmium (MESH:D002104), acid (MESH:D000143), glycerol (MESH:D005990), Urea (MESH:D014508), Acetic acid (MESH:D019342), ROS (MESH:D017382), EGTA (MESH:D004533), auxin (MESH:D007210), Ponceau S (MESH:C032756), DMSO (MESH:D004121), EDTA (MESH:D004492), MeJA (MESH:C072239), water (MESH:D014867), H2O2 (MESH:D006861), NaCl (MESH:D012965), flavonoid (MESH:D005419), ethylene (MESH:C036216), DTT (MESH:D004229), AL (MESH:D000535)
- **Species:** Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]
- **Cell lines:** Col_0 — Homo sapiens (Human), Familial hypertrophic cardiomyopathy type 26, Induced pluripotent stem cell (CVCL_A6XE), ZT1.5 — Mus musculus (Mouse), Mouse lymphoma, Cancer cell line (CVCL_3839)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827998/full.md

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Source: https://tomesphere.com/paper/PMC12827998