Evidence map›Paper›PMID 39841143›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Preventing inappropriate signals pre- and post-ligand perception by a toggle switch mechanism of ERECTA.

Liangliang Chen, Michal Maes, Alicia M Cochran, Julian R Avila, Paul Derbyshire, Jan Sklenar, Kelsey M Haas, Judit Villén, Frank L H Menke, Keiko U Torii

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. ERECTA-family receptor kinases: versatile regulators of plant developmental signaling.The Plant journal : for cell and molecular biology · 2026
    Review
  4. Clathrin-mediated endocytosis of ERECTA family receptors is essential for proper stomatal development inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Preventing inappropriate signals pre- and post-ligand perception by a toggle switch mechanism of ERECTA.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Liangliang ChenHHMI, The University of Texas at Austin, Austin, TX 78712.
Michal MaesHHMI, University of Washington, Seattle, WA 98195.
Alicia M CochranHHMI, The University of Texas at Austin, Austin, TX 78712.
Julian R AvilaHHMI, University of Washington, Seattle, WA 98195.
Paul DerbyshireThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Jan SklenarThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, United Kingdom.ORCID 0000-0003-1858-2574
Kelsey M HaasDepartment of Genome Sciences, University of Washington, Seattle, WA 98195.
Judit VillénDepartment of Genome Sciences, University of Washington, Seattle, WA 98195.
Frank L H MenkeThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich NR4 7UH, United Kingdom.ORCID 0000-0003-2490-4824
Keiko U ToriiHHMI, The University of Texas at Austin, Austin, TX 78712.ORCID 0000-0002-6168-427X

Funding

Towards a comprehensive roadmap of cellular signaling.R35GM119536 · NIGMS · UNIVERSITY OF WASHINGTON · PI VILLEN, JUDIT · 2016 to 2020
$2.2M
The role of phosphorylation in the cellular organization of the proteomeR35GM152061 · NIGMS · UNIVERSITY OF WASHINGTON · PI Judit Villen · 2024 to 2026
$1.3M
Gordon and Betty Moore Foundation (GBMF) GBMF3035HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM119536National Science Foundation (NSF) IOS-0744892NIGMS NIH HHS R35 GM119536NIGMS NIH HHS R35 GM152061
6 · The paper itself

Abstract

Dynamic control of signaling events requires swift regulation of receptors at an active state. By focusing on the Arabidopsis ERECTA (ER) receptor kinase, which perceives peptide ligands to control multiple developmental processes, we report a mechanism preventing inappropriate receptor activity. The ER C-terminal tail (ER_CT) functions as an autoinhibitory domain: Its removal confers higher kinase activity and hyperactivity during inflorescence and stomatal development. ER_CT is required for the binding of a receptor kinase inhibitor, BKI1, and two U-box E3 ligases, PUB30 and PUB31, that trigger activated ER to degradation through ubiquitination. We further identify ER_CT as a phosphodomain transphosphorylated by the coreceptor BAK1. The phosphorylation impacts the tail structure, likely releasing ER from autoinhibition. The phosphonull version enhances BKI1 association, whereas the phosphomimetic version promotes PUB30/31 association. Thus, ER_CT acts as an off-on-off toggle switch, facilitating the release of BKI1 inhibition, enabling signal activation, and swiftly turning over the receptors afterward. Our results elucidate a mechanism that fine-tunes receptor signaling via a phosphoswitch module, maintaining the receptor at a low basal state while ensuring robust yet transient activation upon ligand perception.

Indexed as

ArabidopsisArabidopsis ProteinsProtein Serine-Threonine KinasesReceptors, Cell SurfaceSignal TransductionLigandsPhosphorylationUbiquitinationUbiquitin-Protein LigasesArabidopsis ProteinsBAK1 protein, ArabidopsisLigandsProtein Serine-Threonine KinasesReceptors, Cell SurfaceUbiquitin-Protein Ligasesinflorescence growthpeptide hormonephosphoswitchreceptor kinasestomatal development

Identifiers

PMID39841143
PMCPMC11789017

What OpenQuestion 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 OpenQuestion graph.