Evidence map›Paper›PMID 42094568›Full record

ArticlebioRxiv : the preprint server for biology2026

The cell cycle variant in multiciliated cells incorporates 2 centriole biogenesis cycles.

Amélie-Rose Boudjema, Rémi Balagué, Cayla E Jewett, Jacques Serizay, Gina M LoMastro, Olivier Mercey, Adel Al Jord, Adrien Candat, Marion Faucourt, Alexandre Schaeffer and 5 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Amélie-Rose BoudjemaInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.
Rémi BalaguéInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.
Cayla E JewettDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, United States.ORCID 0000-0002-8406-0814
Jacques SerizayInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.ORCID 0000-0002-4295-0624
Gina M LoMastroDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, United States.
Olivier MerceyDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.
Adel Al JordCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, Barcelona 08003, Spain.
Adrien CandatInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.
Marion FaucourtInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.
Alexandre SchaefferCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble France.
Camille NoûsCogitamus Laboratory, Paris, F-75005, France.
Nathalie DelgehyrInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.ORCID 0000-0001-9870-0475
Andrew J HollandDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, United States.ORCID 0000-0003-3728-6367
Nathalie SpasskyInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.
Alice MeunierInstitut de Biologie de l'École Normale Supérieure (IBENS), Paris Sciences et Lettres (PSL). Research University, Paris, F-75005, France. CNRS, umR 8197, Paris, F-75005, France. INSERM, U1024, Paris, F-75005, France.

Funding

Centrosome biogenesis and copy number controlR01GM114119 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2015 to 2023
$3.3M
The role of TRIM37 in driving tumorigenesis and cancer-specific vulnerability to PLK4 inhibitionR01CA266199 · NCI · JOHNS HOPKINS UNIVERSITY · PI Sergi Regot · 2022 to 2026
$2.7M
Molecular mechanism that suppresses the proliferation of cells with supernumerary centriolesR01GM133897 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2019 to 2022
$1.9M
NCI NIH HHS R01 CA266199NIGMS NIH HHS R01 GM114119NIGMS NIH HHS R01 GM133897
6 · The paper itself

Abstract

Multiciliated cell (MCC) differentiation is a calibrated version of the canonical cell cycle. The MCC cell cycle variant sustains amplification of centrioles for the nucleation of dozens of motile cilia, while avoiding cell division. In this study, we show that the MCC cell cycle variant is an accelerated version of the canonical cell cycle, which superposes two cycles of centriole biogenesis, in order to obtain multiple mature centrioles within a single -instead of double- cell cycle iteration. We further show that the precocious maturation of amplified procentrioles is even determinant for their spatial self-organization, disengagement and apical migration for cilia nucleation. Our findings collectively suggest that the decomposition of centriole biogenesis over two cycle iterations in dividing cells may have been adopted to ensure the growth of a solitary primary cilium, and exemplify how minimal deviations of the canonical cell cycle allow MCC progenitors to both amplify, and accelerate, centriole biogenesis for vital motile ciliogenesis.

Indexed as

basal bodycell cyclecentriole amplificationcentriole elongationcentriole maturationcentrosomecentrosome asymmetrydeuterosomesmicrotubulesmotile ciliaMulticiliated cellsprimary cilium

Identifiers

PMID42094568
PMCPMC13142301

What OpenQuestion holds

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Registered trials

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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.