Evidence map›Paper›PMID 42228718›Full record

ArticlePloS one2026

A Lipoxygenase 3 mutation reverses growth phenotypes in an Arabidopsis Plastid Lipase 3 overexpression line.

Yosia Mugume, Ron Cook, Breana Hagerty, Jinjie Liu, Zachary B Alvord, Linda Danhof, John E Froehlich, Josh V Vermaas, Christoph Benning

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yosia MugumeMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.ORCID https://orcid.org/0000-0003-3340-9622
Ron CookMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.
Breana HagertyMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.
Jinjie LiuMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.ORCID https://orcid.org/0000-0002-1827-411X
Zachary B AlvordMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.
Linda DanhofMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.
John E FroehlichMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.
Josh V VermaasMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.ORCID https://orcid.org/0000-0003-3139-6469
Christoph BenningMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plastid Lipase 3 (PLIP3) is a chloroplast phospholipase A that cleaves linolenic acid, a polyunsaturated fatty acid, from the sn-1 position of the chloroplast membrane lipid monogalactosyldiacylglycerol. Linolenic acid is subsequently converted by enzymes in the chloroplast and the peroxisome to jasmonic acid (JA) requiring transport between the organelles. Overexpression of a cDNA encoding PLIP3 resulted in stunted plant growth with altered leaf morphology caused by accumulation of JA and other oxylipin metabolites redirecting the metabolism from growth to defense. We conducted a genetic suppressor screen in the PLIP3-OX (PLIP3 overexpression) line to query the entire pathway from the start of JA biosynthesis to its perception, transduction, and modification by other signaling pathways. We identified a mutant allele of the 13-lipoxgenase LOX3, lox3-4, that is causal to the attenuation of the PLIP3-OX phenotype with reduced dwarfism and decreased production of JA and other oxylipins. The responsible G776E point mutation is in the C terminal catalytic domain in proximity to the non heme iron binding site of LOX3. The point mutation likely inhibits the oxidation of α-linolenic acid demonstrating its importance for general JA biosynthesis as its activity cannot be compensated for by other 13-lipoxygenases.

Indexed as

ArabidopsisArabidopsis ProteinsLipoxygenaseMutationPlastidsalpha-Linolenic AcidCyclopentanesGene Expression Regulation, PlantOxylipinsPhenotypePoint Mutation13-lipoxygenasealpha-Linolenic AcidArabidopsis ProteinsCyclopentanesjasmonic acidLipoxygenaseOxylipins

Identifiers

PMID42228718
PMCPMC13229349

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.