Spatial H2O2 signaling specificity: H2O2 from chloroplasts and peroxisomes modulates the plant transcriptome differentially
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24908268
DOI
10.1093/mp/ssu070
PII: S1674-2052(14)60819-4
Knihovny.cz E-resources
- Keywords
- catalase, glycolate oxidase, hydrogen peroxide, oxidative signaling., photorespiration, reactive oxygen species,
- MeSH
- Arabidopsis cytology drug effects genetics metabolism MeSH
- Chloroplasts drug effects metabolism MeSH
- Plants, Genetically Modified MeSH
- Genome, Plant genetics MeSH
- Kinetics MeSH
- Metabolomics MeSH
- Carbon Dioxide pharmacology MeSH
- Hydrogen Peroxide metabolism MeSH
- Peroxisomes drug effects metabolism MeSH
- Stigmasterol metabolism MeSH
- Transcriptome * drug effects MeSH
- Tryptophan metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Carbon Dioxide MeSH
- Hydrogen Peroxide MeSH
- Stigmasterol MeSH
- Tryptophan MeSH
Hydrogen peroxide (H2O2) operates as a signaling molecule in eukaryotes, but the specificity of its signaling capacities remains largely unrevealed. Here, we analyzed whether a moderate production of H2O2 from two different plant cellular compartments has divergent effects on the plant transcriptome. Arabidopsis thaliana overexpressing glycolate oxidase in the chloroplast (Fahnenstich et al., 2008; Balazadeh et al., 2012) and plants deficient in peroxisomal catalase (Queval et al., 2007; Inzé et al., 2012) were grown under non-photorespiratory conditions and then transferred to photorespiratory conditions to foster the production of H2O2 in both organelles. We show that H2O2 originating in a specific organelle induces two types of responses: one that integrates signals independently from the subcellular site of H2O2 production and another that is dependent on the H2O2 production site. H2O2 produced in peroxisomes induces transcripts involved in protein repair responses, while H2O2 produced in chloroplasts induces early signaling responses, including transcription factors and biosynthetic genes involved in production of secondary signaling messengers. There is a significant bias towards the induction of genes involved in responses to wounding and pathogen attack by chloroplastic-produced H2O2, including indolic glucosinolates-, camalexin-, and stigmasterol-biosynthetic genes. These transcriptional responses were accompanied by the accumulation of 4-methoxy-indol-3-ylmethyl glucosinolate and stigmasterol.
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