ArticleJournal of experimental botany2017
Regulation of ethylene-related gene expression by indole-3-acetic acid and 4-chloroindole-3-acetic acid in relation to pea fruit and seed development.
Article in Journal of experimental botany, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
9 citing papers in PubMed, 15 citations in OpenAlex.
- Molecular mechanisms of seed dormancy release in Paeonia lactiflora revealed through transcriptomic and metabolomic analysis.BMC plant biology · 2026Article
- The Complex Roles of Plant Hormones During Clubroot Disease Development in the Brassicaceae.Journal of plant growth regulation · 2025Review
- Auxins in the right space and time regulate pea fruit development.Journal of experimental botany · 2022Article
- The role of indole derivative in the growth of plants: A review.Frontiers in plant science · 2022Review
- Review
- Sedentary Plant-Parasitic Nematodes Alter Auxin Homeostasis via Multiple Strategies.Frontiers in plant science · 2021Review
- TIR1 auxin receptors are implicated in the differential response to 4-Cl-IAA and IAA in developing pea fruit.Journal of experimental botany · 2019Article
- Heat stress differentially modifies ethylene biosynthesis and signaling in pea floral and fruit tissues.Plant molecular biology · 2017Article
- Auxin Gradients Determine Reproductive Development in Pea (Pisum sativum).Physiologia plantarumArticle
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In pea, the auxins 4-chloroindole-3-acetic acid (4-Cl-IAA) and indole-3-acetic acid (IAA) occur naturally; however, only 4-Cl-IAA stimulates pericarp growth and gibberellin (GA) biosynthesis, and inhibits the ethylene response in deseeded ovaries (pericarps), mimicking the presence of seeds. Expression of ovary ethylene biosynthesis genes was regulated similarly in most cases by the presence of 4-Cl-IAA or seeds. PsACS1 [which encodes an enzyme that synthesizes 1-aminocyclopropane-1-carboxylic acid (ACC)] transcript abundance was high in pericarp tissue adjacent to developing seeds following pollination. ACC accumulation in 4-Cl-IAA-treated deseeded pericarps was driven by high PsASC1 expression (1800-fold). 4-Cl-IAA, but not IAA, also suppressed the pericarp transcript levels of PsACS4. 4-Cl-IAA increased PsACO1 and decreased PsACO2 and PsACO3 expression (enzymes that convert ACC to ethylene) but did not change ACO enzyme activity. Increased ethylene was countered by a 4-Cl-IAA-specific decrease in ethylene responsiveness potentially via modulation of pericarp ethylene receptor and signaling gene expression. This pattern did not occur in IAA-treated pericarps. Overall, the effect of 4-Cl-IAA and IAA on ethylene biosynthesis gene expression generally explains the ethylene evolution patterns, and their effects on GA biosynthesis and ethylene signaling gene expression explain the tissue response patterns in young pea ovaries.
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