Evidence map›Paper›PMID 24934224›Full record

ArticleGenes & development2014

Multicilin drives centriole biogenesis via E2f proteins.

Lina Ma, Ian Quigley, Heymut Omran, Chris Kintner

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
–field-weighted citation impact
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

95 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
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  5. Genome Wide Identification and Characterization ofInternational journal of genomics · 2026
    Article
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  16. Formation and function of multiciliated cells.The Journal of cell biology · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Lina MaThe Salk Institute for Biological Studies, La Jolla 92037, California, USA;
Ian QuigleyThe Salk Institute for Biological Studies, La Jolla 92037, California, USA;
Heymut OmranDepartment of Pediatrics, University Hospital Muenster, 48149 Muenster; Germany.
Chris KintnerThe Salk Institute for Biological Studies, La Jolla 92037, California, USA;
Salk Institute for Biological Studies · USUniversity Hospital Münster · DE

Funding

Transcriptional regulation of multiciliate cell differentiationR01GM096021 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI KINTNER, CHRISTOPHER ROBERT · 2010 to 2013
$1.5M
The transcriptional control and function of proton-secreting cellsF32DK084706 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI QUIGLEY, IAN K. · 2011 to 2013
$161k
NIDDK NIH HHS F32 DK084706NIGMS NIH HHS GM96021NIGMS NIH HHS R01 GM096021
6 · The paper itself

Abstract

Multiciliate cells employ hundreds of motile cilia to produce fluid flow, which they nucleate and extend by first assembling hundreds of centrioles. In most cells, entry into the cell cycle allows centrioles to undergo a single round of duplication, but in differentiating multiciliate cells, massive centriole assembly occurs in G0 by a process initiated by a small coiled-coil protein, Multicilin. Here we show that Multicilin acts by forming a ternary complex with E2f4 or E2f5 and Dp1 that binds and activates most of the genes required for centriole biogenesis, while other cell cycle genes remain off. This complex also promotes the deuterosome pathway of centriole biogenesis by activating the expression of deup1 but not its paralog, cep63. Finally, we show that this complex is disabled by mutations in human Multicilin that cause a severe congenital mucociliary clearance disorder due to reduced generation of multiple cilia. By coopting the E2f regulation of cell cycle genes, Multicilin drives massive centriole assembly in epithelial progenitors in a manner required for multiciliate cell differentiation.

Indexed as

AnimalsCentriolesE2F Transcription FactorsGene Expression Regulation, DevelopmentalMiceMutationProtein BindingSkinTranscription Factor DP1Xenopus laevisXenopus ProteinsE2F Transcription Factorsmulticilin, XenopusTranscription Factor DP1Xenopus Proteinscentriolese2f4multiciliate cells

Identifiers

PMID24934224
PMCPMC4083089
OpenAlexW2083516106

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.