Evidence map›Paper›PMID 33856408›Full record

ArticleThe Journal of cell biology2021

Time-resolved proteomics profiling of the ciliary Hedgehog response.

Elena A May, Marian Kalocsay, Inès Galtier D'Auriac, Patrick S Schuster, Steven P Gygi, Maxence V Nachury, David U Mick

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
12.1field-weighted citation impact, top 1% 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

63 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
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  8. Stereotypical interciliary contacts in abioRxiv : the preprint server for biology · 2026
    Article
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  14. Review
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  19. BMP4 regulates asymmetric Pkd2 distribution in mouse nodal immotile cilia and ciliary mechanosensing required for left-right determination.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 2 countries.

Elena A May *Center of Human and Molecular Biology, Saarland University School of Medicine, Homburg, Germany.
Marian Kalocsay *Department of Systems Biology, Laboratory of Systems Pharmacology, Harvard Medical School, Boston, MA.
Inès Galtier D'AuriacDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA.
Patrick S SchusterCenter of Human and Molecular Biology, Saarland University School of Medicine, Homburg, Germany.
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA.
Maxence V NachuryDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA.
David U MickCenter of Human and Molecular Biology, Saarland University School of Medicine, Homburg, Germany.
Saarland University · DEHarvard University · USUniversity of California, San Francisco · US

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
Quality control of the primary cilium proteomeR01GM089933 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Maxence V Nachury · 2010 to 2026
$5.8M
Proteomics of Primary Cilia through Proximity LabelingR21HD087126 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI NACHURY, MAXENCE V · 2016 to 2017
$435k
NEI NIH HHS P30 EY002162NICHD NIH HHS R21 HD087126NIGMS NIH HHS R01 GM067945NIGMS NIH HHS R01 GM089933
6 · The paper itself

Abstract

The primary cilium is a signaling compartment that interprets Hedgehog signals through changes of its protein, lipid, and second messenger compositions. Here, we combine proximity labeling of cilia with quantitative mass spectrometry to unbiasedly profile the time-dependent alterations of the ciliary proteome in response to Hedgehog. This approach correctly identifies the three factors known to undergo Hedgehog-regulated ciliary redistribution and reveals two such additional proteins. First, we find that a regulatory subunit of the cAMP-dependent protein kinase (PKA) rapidly exits cilia together with the G protein-coupled receptor GPR161 in response to Hedgehog, and we propose that the GPR161/PKA module senses and amplifies cAMP signals to modulate ciliary PKA activity. Second, we identify the phosphatase Paladin as a cell type-specific regulator of Hedgehog signaling that enters primary cilia upon pathway activation. The broad applicability of quantitative ciliary proteome profiling promises a rapid characterization of ciliopathies and their underlying signaling malfunctions.

Indexed as

AnimalsCell LineCiliaCyclic AMPCyclic AMP-Dependent Protein KinasesFibroblastsHedgehog ProteinsHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsMiceNIH 3T3 CellsProteomicsReceptors, G-Protein-CoupledSignal TransductionCyclic AMPCyclic AMP-Dependent Protein KinasesHedgehog ProteinsIntracellular Signaling Peptides and Proteinsprotein kinase modulatorReceptors, G-Protein-Coupled

Identifiers

PMID33856408
PMCPMC8054476
OpenAlexW3153776555

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.