Evidence map›Paper›PMID 32348467›Full record

ArticleThe Journal of cell biology2020

KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling.

Petra Pejskova, Madeline Louise Reilly, Lucia Bino, Ondrej Bernatik, Linda Dolanska, Ranjani Sri Ganji, Zbynek Zdrahal, Alexandre Benmerah, Lukas Cajanek

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Primary Cilia Formation Does Not Rely on WNT/β-Catenin Signaling.Frontiers in cell and developmental biology · 2021
    Article
  18. Article
  19. Histone DemethylaseOncoTargets and therapy · 2020
    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

9 authors at 3 institutions in 2 countries.

Petra PejskovaDepartment of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Madeline Louise ReillyLaboratory of Hereditary Kidney Diseases, Institut National de la Santé et de la Recherche Médicale UMR 1163, Paris University, Imagine Institute, Paris, France.
Lucia BinoDepartment of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Ondrej BernatikDepartment of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Linda DolanskaDepartment of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Ranjani Sri GanjiCentral European Institute of Technology, Brno, Czech Republic.
Zbynek ZdrahalCentral European Institute of Technology, Brno, Czech Republic.
Alexandre BenmerahLaboratory of Hereditary Kidney Diseases, Institut National de la Santé et de la Recherche Médicale UMR 1163, Paris University, Imagine Institute, Paris, France.
Lukas CajanekDepartment of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Masaryk University · CZCentral European Institute of Technology · CZInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cilia play critical roles in development and disease. Their assembly and disassembly are tightly coupled to cell cycle progression. Here, we present data identifying KIF14 as a regulator of cilia formation and Hedgehog (HH) signaling. We show that RNAi depletion of KIF14 specifically leads to defects in ciliogenesis and basal body (BB) biogenesis, as its absence hampers the efficiency of primary cilium formation and the dynamics of primary cilium elongation, and disrupts the localization of the distal appendage proteins SCLT1 and FBF1 and components of the IFT-B complex. We identify deregulated Aurora A activity as a mechanism contributing to the primary cilium and BB formation defects seen after KIF14 depletion. In addition, we show that primary cilia in KIF14-depleted cells are defective in response to HH pathway activation, independently of the effects of Aurora A. In sum, our data point to KIF14 as a critical node connecting cell cycle machinery, effective ciliogenesis, and HH signaling.

Indexed as

Adaptor Proteins, Signal TransducingAurora Kinase ABasal BodiesCell CycleChromatography, LiquidCiliaHedgehog ProteinsHEK293 CellsHumansInterphaseIntracellular Signaling Peptides and ProteinsKinesinsMitosisOncogene ProteinsProtein Serine-Threonine KinasesRNA InterferenceAdaptor Proteins, Signal TransducingAURKA protein, humanAurora Kinase Acitron-kinaseFBF1 protein, humanHedgehog ProteinsIntracellular Signaling Peptides and ProteinsKIF14 protein, humanKinesinsOncogene ProteinsProtein Serine-Threonine KinasesSCLT1 protein, humanSodium Channels

Identifiers

PMID32348467
PMCPMC7265313
OpenAlexW3017738201

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.