Evidence map›Paper›PMID 41526533›Full record

ArticleScientific reports2026

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

Daniel Rincon Diaz, Morgan E Wynn, Emmanuel Asiedu, Teressa K Akuoko, Ansul Lokdarshi

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daniel Rincon Diaz *Department of Biology, Valdosta State University, 1500 N Patterson St, Valdosta, GA, 31698, USA.ORCID http://orcid.org/0009-0000-1230-697X
Morgan E WynnDepartment of Biology, Valdosta State University, 1500 N Patterson St, Valdosta, GA, 31698, USA.ORCID http://orcid.org/0009-0003-1410-1590
Emmanuel AsieduDepartment of Biology, Valdosta State University, 1500 N Patterson St, Valdosta, GA, 31698, USA.ORCID http://orcid.org/0009-0004-9723-5259
Teressa K AkuokoDepartment of Biology, Valdosta State University, 1500 N Patterson St, Valdosta, GA, 31698, USA.ORCID http://orcid.org/0000-0001-9766-0782
Ansul Lokdarshi *Department of Biology, Valdosta State University, 1500 N Patterson St, Valdosta, GA, 31698, USA. alokdarshi@valdosta.edu.ORCID http://orcid.org/0000-0003-2264-2701

Funding

National Science Foundation 2334869
6 · The paper itself

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.

Indexed as

AcetatesArabidopsisArabidopsis ProteinsCyclopentanesOxylipinsProtein Serine-Threonine KinasesReactive Oxygen SpeciesEukaryotic Initiation Factor-2Gene Expression Regulation, PlantLightPhosphorylationProtein KinasesSignal TransductionAcetatesArabidopsis ProteinsCyclopentanesEukaryotic Initiation Factor-2GCN2 protein, ArabidopsisKIN10 protein, Arabidopsismethyl jasmonateOxylipinsProtein KinasesProtein Serine-Threonine KinasesReactive Oxygen SpeciesAbiotic stresseIF2αGCN1GCN2Methyl jasmonateTranslation

Identifiers

PMID41526533
PMCPMC12827998

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.