Evidence map›Paper›PMID 29203870›Full record

ArticleNature communications2017

IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning.

Nicolas Taulet, Benjamin Vitre, Christelle Anguille, Audrey Douanier, Murielle Rocancourt, Michael Taschner, Esben Lorentzen, Arnaud Echard, Benedicte Delaval

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The intraflagellar transport cycle.Nature reviews. Molecular cell biology · 2025
    Review
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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

9 authors at 2 institutions in 2 countries.

Nicolas TauletCRBM, CNRS, Univ. Montpellier, Centrosome, Cilia and Pathology Lab, 1919 Route de Mende, 34293, Montpellier, France.
Benjamin VitreCRBM, CNRS, Univ. Montpellier, Centrosome, Cilia and Pathology Lab, 1919 Route de Mende, 34293, Montpellier, France.
Christelle AnguilleCRBM, CNRS, Univ. Montpellier, Centrosome, Cilia and Pathology Lab, 1919 Route de Mende, 34293, Montpellier, France.
Audrey DouanierCRBM, CNRS, Univ. Montpellier, Centrosome, Cilia and Pathology Lab, 1919 Route de Mende, 34293, Montpellier, France.
Murielle RocancourtInstitut PASTEUR, CNRS UMR 3691 Membrane Traffic and Cell Division Lab, Cell Biology and Infection Department, 25-28 rue du Dr Roux, 75015, Paris, France.
Michael TaschnerDepartment of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10c, DK-8000, Aarhus C, Denmark.
Esben LorentzenDepartment of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10c, DK-8000, Aarhus C, Denmark.
Arnaud EchardInstitut PASTEUR, CNRS UMR 3691 Membrane Traffic and Cell Division Lab, Cell Biology and Infection Department, 25-28 rue du Dr Roux, 75015, Paris, France.ORCID http://orcid.org/0000-0001-7402-1398
Benedicte DelavalCRBM, CNRS, Univ. Montpellier, Centrosome, Cilia and Pathology Lab, 1919 Route de Mende, 34293, Montpellier, France. benedicte.delaval@crbm.cnrs.fr.ORCID http://orcid.org/0000-0003-0274-185X
Centre National de la Recherche Scientifique · FRAarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokinesis mediates the physical separation of dividing cells and, in 3D epithelia, provides a spatial landmark for lumen formation. Here, we unravel an unexpected role in cytokinesis for proteins of the intraflagellar transport (IFT) machinery, initially characterized for their ciliary role and their link to polycystic kidney disease. Using 2D and 3D cultures of renal cells, we show that IFT proteins are required to correctly shape the central spindle, to control symmetric cleavage furrow ingression and to ensure central lumen positioning. Mechanistically, IFT88 directly interacts with the kinesin MKLP2 and is essential for the correct relocalization of the Aurora B/MKLP2 complex to the central spindle. IFT88 is thus required for proper centralspindlin distribution and central spindle microtubule organization. Overall, this work unravels a novel non-ciliary mechanism for IFT proteins at the central spindle, which could contribute to kidney cyst formation by affecting lumen positioning.

Indexed as

AnimalsAurora Kinase BCells, CulturedCytokinesisHCT116 CellsHeLa CellsHumansKidneyKidney TubulesKinesinsMicrotubulesPolycystic Kidney DiseasesSpindle ApparatusSus scrofaTumor Suppressor ProteinsAurora Kinase BKinesinsTumor Suppressor Proteins

Identifiers

PMID29203870
PMCPMC5715026
OpenAlexW2768449157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.