Evidence map›Paper›PMID 29483145›Full record

ArticleThe Journal of cell biology2018

BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone.

Fan Ye, Andrew R Nager, Maxence V Nachury

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 174 papers.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed
25.3field-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

174 citing papers in PubMed, 268 citations in OpenAlex.

  1. Article
  2. Review
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  5. Review
  6. Article
  7. Article
  8. Primary cilia and neural computation.Journal of biomedical science · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Proteome-widebioRxiv : the preprint server for biology · 2025
    Article
  16. Article
  17. Design principles of ciliary signaling.Journal of cell science · 2025
    Review
  18. Review
  19. Review
  20. Identification of New Ciliary Signaling Pathways in the Brain and Insights into Neurological Disorders.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article

114 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

3 authors at 2 institutions in 1 country.

Fan YeDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA.
Andrew R NagerDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA.
Maxence V NachuryDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA maxence.nachury@ucsf.edu.ORCID 0000-0003-4918-1562
University of California, San Francisco · USStanford University · US

Funding

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
NICHD NIH HHS R21 HD087126NIGMS NIH HHS R01 GM089933
6 · The paper itself

Abstract

A diffusion barrier at the transition zone enables the compartmentalization of signaling molecules by cilia. The BBSome and the small guanosine triphosphatase Arl6, which triggers BBSome coat polymerization, are required for the exit of activated signaling receptors from cilia, but how diffusion barriers are crossed when membrane proteins exit cilia remains to be determined. In this study, we found that activation of the ciliary G protein-coupled receptors (GPCRs) Smoothened and SSTR3 drove the Arl6-dependent assembly of large, highly processive, and cargo-laden retrograde BBSome trains. Single-molecule imaging revealed that the assembly of BBSome trains enables the lateral transport of ciliary GPCRs across the transition zone. However, the removal of activated GPCRs from cilia was inefficient because a second periciliary diffusion barrier was infrequently crossed. We conclude that exit from cilia is a two-step process in which BBSome/Arl6 trains first move activated GPCRs through the transition zone before a periciliary barrier can be crossed.

Indexed as

ADP-Ribosylation FactorsAnimalsCell LineCiliaCyclic AMP-Dependent Protein KinasesMiceMultiprotein ComplexesReceptors, G-Protein-CoupledReceptors, SomatostatinSignal TransductionADP-Ribosylation FactorsArl6 protein, mouseCyclic AMP-Dependent Protein KinasesGPR161 protein, mouseMultiprotein ComplexesReceptors, G-Protein-CoupledReceptors, Somatostatinsomatostatin receptor 3

Identifiers

PMID29483145
PMCPMC5940304
OpenAlexW2949451105

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.