Evidence map›Paper›PMID 41721526›Full record

ArticlePlant physiology2026

Ethylene receptor gain- and loss-of-function mutants reveal an ETR1-dependent transcriptional network in Arabidopsis roots.

Maleana G White, Alexandria F Harkey, Joëlle K Mühlemann, Amy L Olex, Nathan J Pfeffer, Maarten Houben, Brad M Binder, Gloria K Muday

Abstract read
In one paragraph

Article in Plant physiology, 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

8 authors.

Maleana G WhiteWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0000-0001-9869-5688
Alexandria F HarkeyWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0000-0001-9250-9856
Joëlle K MühlemannWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0000-0003-2431-4357
Amy L OlexVirginia Commonwealth University, C. Kenneth and Dianne Wright Center for Clinical and Transtional Research, Richmond, VA, United States.ORCID 0000-0001-8064-521X
Nathan J PfefferWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0009-0005-2171-7355
Maarten HoubenWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0000-0003-4819-3158
Brad M BinderUniversity of Tennessee, Biochemistry & Cellular and Molecular Biology, Knoxville, TN, United States.
Gloria K MudayWake Forest University, Department of Biology and Center for Molecular Signaling, Winston-Salem, NC, United States.ORCID 0000-0002-0377-4517

Funding

Center for Molecular Signaling Graduate Research FellowshipNational Science Foundation Systems MCB-1716279WFU Provost's Pilot Research
6 · The paper itself

Abstract

In Arabidopsis (Arabidopsis thaliana), a family of 5 receptors mediates ethylene responses in roots, with Ethylene Response 1 (ETR1) controlling increases in root hair proliferation and decreases in lateral root formation. To define the ETR1-dependent gene regulatory network (GRN) controlling root development, we profiled the root transcriptome from Col-0 and the etr1-3 gain-of-function and etr1-7 loss-of-function mutants in the presence and absence of ethylene or the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC). We identified 4,522 differentially expressed (DE) transcripts in Col-0 roots that displayed altered abundance in response to ethylene and/or ACC treatment, with larger-magnitude changes induced by ethylene. These included 553 DE transcripts that were ETR1 dependent, defined by a lack of response to treatment with ethylene and/or ACC in ethylene-insensitive etr1-3 and constitutive alteration response in etr1-7 in the presence or absence of treatment relative to time-0 Col-0. These ETR1-dependent transcripts include transcripts from genes associated with ethylene biosynthesis and those encoding transcription factors (TFs). Reporter fusions driven by promoters from ACC OXIDASE 2 (ACO2) and ACO3, which convert ACC to ethylene, were regulated by ACC in root tissues in appropriate locations to control root development, with pACO5-driven GFP detected in root hairs. We examined the abundance of ETR1-dependent transcripts predicted to encode TFs and ACOs in Col-0 and an ein3 eil1 mutant, with and without ACC treatment. Our results suggested that the ETR1 and Ethylene Insensitive 3 (EIN3)/EIN3-like 1 (EIL1) canonical ethylene signaling pathway regulates some, but not all, of these transcriptional responses. Together, these findings reveal features of an ETR1-dependent GRN that controls both ethylene biosynthesis and root growth and development.

Indexed as

ArabidopsisArabidopsis ProteinsGene Regulatory NetworksLoss of Function MutationPlant RootsReceptors, Cell SurfaceAmino Acids, CyclicEthylenesGene Expression ProfilingGene Expression Regulation, PlantMutationSignal TransductionTranscription Factors1-aminocyclopropane-1-carboxylic acidAmino Acids, CyclicArabidopsis ProteinsethyleneEthylenesETR1 protein, ArabidopsisReceptors, Cell SurfaceTranscription Factors

Identifiers

PMID41721526
PMCPMC13023754

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LicenceCC BY-NC-ND
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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.