Evidence map›Paper›PMID 38378792›Full record

ArticleCommunications biology2024

The exocyst complex and intracellular vesicles mediate soluble protein trafficking to the primary cilium.

S M Niedziółka, S Datta, T Uśpieński, B Baran, W Skarżyńska, E W Humke, R Rohatgi, P Niewiadomski

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Preassembly and independent trafficking of the exocyst complex inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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 at 3 institutions in 2 countries.

S M NiedziółkaCentre of New Technologies, University of Warsaw, Warsaw, Poland.
S DattaCentre of New Technologies, University of Warsaw, Warsaw, Poland.
T UśpieńskiCentre of New Technologies, University of Warsaw, Warsaw, Poland.
B BaranCentre of New Technologies, University of Warsaw, Warsaw, Poland.
W SkarżyńskaCentre of New Technologies, University of Warsaw, Warsaw, Poland.
E W HumkeDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
R RohatgiDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0001-7609-8858
P NiewiadomskiCentre of New Technologies, University of Warsaw, Warsaw, Poland. p.niewiadomski@cent.uw.edu.pl.ORCID 0000-0001-6254-6162
University of Warsaw · PLIGM Biosciences (United States) · USStanford University · US

Funding

Supplement application for an Olympus automated microscopeR35GM118082 · NIGMS · STANFORD UNIVERSITY · PI RAJAT ROHATGI · 2016 to 2026
$7.6M
Molecular dissection of signal transduction at primary ciliaR01GM112988 · NIGMS · STANFORD UNIVERSITY · PI ROHATGI, RAJAT · 2015 to 2016
$618k
NIGMS NIH HHS R01 GM112988NIGMS NIH HHS R35 GM118082
6 · The paper itself

Abstract

The efficient transport of proteins into the primary cilium is a crucial step for many signaling pathways. Dysfunction of this process can lead to the disruption of signaling cascades or cilium assembly, resulting in developmental disorders and cancer. Previous studies on the protein delivery to the cilium were mostly focused on the membrane-embedded receptors. In contrast, how soluble proteins are delivered into the cilium is poorly understood. In our work, we identify the exocyst complex as a key player in the ciliary trafficking of soluble Gli transcription factors. In line with the known function of the exocyst in intracellular vesicle transport, we demonstrate that soluble proteins, including Gli2/3 and Lkb1, can use the endosome recycling machinery for their delivery to the primary cilium. Finally, we identify GTPases: Rab14, Rab18, Rab23, and Arf4 that are involved in vesicle-mediated Gli protein ciliary trafficking. Our data pave the way for a better understanding of ciliary transport and uncover transport mechanisms inside the cell.

Indexed as

CiliaSignal TransductionBiological TransportCytoplasmProtein Transport

Identifiers

PMID38378792
PMCPMC10879184
OpenAlexW4392002121

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.