Evidence map›Paper›PMID 21602795›Full record

ArticleNature cell biology2011

Control of vertebrate multiciliogenesis by miR-449 through direct repression of the Delta/Notch pathway.

Brice Marcet, Benoît Chevalier, Guillaume Luxardi, Christelle Coraux, Laure-Emmanuelle Zaragosi, Marie Cibois, Karine Robbe-Sermesant, Thomas Jolly, Bruno Cardinaud, Chimène Moreilhon and 6 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 174 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
174citing papers in PubMed, 1 pooled it
16.8field-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, 1 synthesis or guideline pooled it, 288 citations in OpenAlex.

  1. Pooled it
  2. Airway epithelial miRNA expression is altered in asthma.American journal of respiratory and critical care medicine · 2012
    Trial
  3. Article
  4. Article
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  7. Article
  8. Review
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  10. Article
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  15. Article
  16. Formation and function of multiciliated cells.The Journal of cell biology · 2024
    Review
  17. Article
  18. A role for mutations inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Review
  20. Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

16 authors at 8 institutions in 1 country.

Brice MarcetCNRS, Institut de Pharmacologie Moléculaire et Cellulaire, F06560 Sophia Antipolis, France.
Benoît Chevalier
Guillaume Luxardi
Christelle Coraux
Laure-Emmanuelle Zaragosi
Marie Cibois
Karine Robbe-Sermesant
Thomas Jolly
Bruno Cardinaud
Chimène Moreilhon
Lisa Giovannini-Chami
Béatrice Nawrocki-Raby
Philippe Birembaut
Rainer Waldmann
Laurent Kodjabachian
Pascal Barbry
Centre National de la Recherche Scientifique · FRInserm · FRInstitut de Pharmacologie Moléculaire et Cellulaire · FRCentre Hospitalier Universitaire de Nice · FRInstitut de Biologie du Développement Marseille · FRInstitut de Neurobiologie de la Méditerranée · FRUniversité Côte d'Azur · FRUniversité de Reims Champagne-Ardenne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiciliated cells lining the surface of some vertebrate epithelia are essential for various physiological processes, such as airway cleansing. However, the mechanisms governing motile cilia biosynthesis remain poorly elucidated. We identify miR-449 microRNAs as evolutionarily conserved key regulators of vertebrate multiciliogenesis. In human airway epithelium and Xenopus laevis embryonic epidermis, miR-449 microRNAs strongly accumulated in multiciliated cells. In both models, we show that miR-449 microRNAs promote centriole multiplication and multiciliogenesis by directly repressing the Delta/Notch pathway. We established Notch1 and its ligand Delta-like 1(DLL1) as miR-449 bona fide targets. Human DLL1 and NOTCH1 protein levels were lower in multiciliated cells than in surrounding cells, decreased after miR-449 overexpression and increased after miR-449 inhibition. In frog, miR-449 silencing led to increased Dll1 expression. Consistently, overexpression of Dll1 mRNA lacking miR-449 target sites repressed multiciliogenesis, whereas both Dll1 and Notch1 knockdown rescued multiciliogenesis in miR-449-deficient cells. Antisense-mediated protection of miR-449-binding sites of endogenous human Notch1 or frog Dll1 strongly repressed multiciliogenesis. Our results unravel a conserved mechanism whereby Notch signalling must undergo miR-449-mediated inhibition to permit differentiation of ciliated cell progenitors.

Indexed as

Gene Expression Regulation, DevelopmentalSignal TransductionAnimalsCalcium-Binding ProteinsCells, CulturedCell SurvivalCiliaConserved SequenceEpidermisFemaleFlow CytometryGene Knockdown TechniquesHumansIntercellular Signaling Peptides and ProteinsMembrane ProteinsMicroRNAsCalcium-Binding ProteinsDLK1 protein, humanDLL1 protein, XenopusIntercellular Signaling Peptides and ProteinsMembrane ProteinsMicroRNAsMIRN449 microRNA, humanReceptor, Notch1Xenopus Proteins

Identifiers

PMID21602795
OpenAlexW2012319310

What OpenQuestion holds

Textmetadata
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.