Evidence map›Paper›PMID 35817504›Full record

ArticleCurrent topics in developmental biology2022

Receptor control by membrane-tethered ubiquitin ligases in development and tissue homeostasis.

Andres M Lebensohn, J Fernando Bazan, Rajat Rohatgi

Open access · greenAbstract read
In one paragraph

Article in Current topics in developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
7.0field-weighted citation impact, top 2% of its field
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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Lgr6Genes & diseases · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. "Design principles of a membrane-spanning ubiquitin ligase".bioRxiv : the preprint server for biology · 2025
    Article
  7. Wnt signalosomes: What we know that we do not know.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  8. Article
  9. Article
  10. Review
  11. 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

3 authors at 2 institutions in 1 country.

Andres M LebensohnLaboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States. Electronic address: andres.lebensohn@nih.gov.
J Fernando Bazanħ bioconsulting llc, Stillwater, MN, United States. Electronic address: jfbazan@gmail.com.
Rajat RohatgiDepartment of Biochemistry, Stanford University School of Medicine, Stanford, CA, United States; Department of Medicine, Stanford University School of Medicine, Stanford, CA, United States. Electronic address: rrohatgi@stanford.edu.
National Cancer Institute · USStanford University · US

Funding

New regulatory mechanisms of WNT signaling in development, stem cells and cancerZIABC011901 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEBENSOHN, ANDRES · 2019 to 2025
$8.4M
Supplement application for an Olympus automated microscopeR35GM118082 · NIGMS · STANFORD UNIVERSITY · PI RAJAT ROHATGI · 2016 to 2026
$7.6M
A protein traffic control system that regulates left-right patterning and heart developmentR01HL157103 · NHLBI · STANFORD UNIVERSITY · PI GUNN, TERESA M, LO, CECILIA W. · 2021 to 2024
$2.9M
Unconventional signaling by the R-spondin family of WNT regulatorsR21HD101980 · NICHD · STANFORD UNIVERSITY · PI ROHATGI, RAJAT · 2020 to 2021
$435k
NHLBI NIH HHS R01 HL157103NICHD NIH HHS R21 HD101980NIGMS NIH HHS R35 GM118082
6 · The paper itself

Abstract

Paracrine cell-cell communication is central to all developmental processes, ranging from cell diversification to patterning and morphogenesis. Precise calibration of signaling strength is essential for the fidelity of tissue formation during embryogenesis and tissue maintenance in adults. Membrane-tethered ubiquitin ligases can control the sensitivity of target cells to secreted ligands by regulating the abundance of signaling receptors at the cell surface. We discuss two examples of this emerging concept in signaling: (1) the transmembrane ubiquitin ligases ZNRF3 and RNF43 that regulate WNT and bone morphogenetic protein receptor abundance in response to R-spondin ligands and (2) the membrane-recruited ubiquitin ligase MGRN1 that controls Hedgehog and melanocortin receptor abundance. We focus on the mechanistic logic of these systems, illustrated by structural and protein interaction models enabled by AlphaFold. We suggest that membrane-tethered ubiquitin ligases play a widespread role in remodeling the cell surface proteome to control responses to extracellular ligands in diverse biological processes.

Indexed as

ThrombospondinsWnt Signaling PathwayHedgehog ProteinsHomeostasisLigandsUbiquitinUbiquitin-Protein LigasesHedgehog ProteinsLigandsThrombospondinsUbiquitinUbiquitin-Protein LigasesATRNBMPBMPR1ACancerCell surface receptorDevelopmentDVLE3EndocytosisFrizzledFZDHedgehogHeparan sulfate proteoglycanHSPGLGRLRP6MARCHMEGF8MelanocortinMembrane-tetheredMGRN1MMMMorphogenMOSMOPatterningPrimary ciliumPROTACProtein degradationRegenerationRINGRNF43RSPOR-spondinSignalingSmoothenedStem cellsTissue homeostasisUbiquitin ligaseUbiquitylationWNTZNRF3

Identifiers

PMID35817504
PMCPMC10231660
OpenAlexW4285078835

What OpenQuestion holds

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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.