Evidence map›Paper›PMID 35319462›Full record

ArticleeLife2022

Evolutionary conservation of centriole rotational asymmetry in the human centrosome.

Noémie Gaudin, Paula Martin Gil, Meriem Boumendjel, Dmitry Ershov, Catherine Pioche-Durieu, Manon Bouix, Quentin Delobelle, Lucia Maniscalco, Than Bich Ngan Phan, Vincent Heyer and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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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

12 authors at 2 institutions in 2 countries.

Noémie GaudinUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Paula Martin GilUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Meriem BoumendjelUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Dmitry ErshovImage Analysis Hub, C2RT, Institut Pasteur, Paris, France.
Catherine Pioche-DurieuUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.ORCID 0000-0003-0988-1169
Manon BouixUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Quentin DelobelleUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Lucia ManiscalcoUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Than Bich Ngan PhanUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Vincent HeyerInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Ilkirch, France.
Bernardo Reina-San-MartinInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Ilkirch, France.
Juliette AzimzadehUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.ORCID 0000-0002-7292-9973
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Centrioles are formed by microtubule triplets in a ninefold symmetric arrangement. In flagellated protists and animal multiciliated cells, accessory structures tethered to specific triplets render the centrioles rotationally asymmetric, a property that is key to cytoskeletal and cellular organization in these contexts. In contrast, centrioles within the centrosome of animal cells display no conspicuous rotational asymmetry. Here, we uncover rotationally asymmetric molecular features in human centrioles. Using ultrastructure expansion microscopy, we show that LRRCC1, the ortholog of a protein originally characterized in flagellate green algae, associates preferentially to two consecutive triplets in the distal lumen of human centrioles. LRRCC1 partially co-localizes and affects the recruitment of another distal component, C2CD3, which also has an asymmetric localization pattern in the centriole lumen. Together, LRRCC1 and C2CD3 delineate a structure reminiscent of a filamentous density observed by electron microscopy in flagellates, termed the 'acorn.' Functionally, the depletion of LRRCC1 in human cells induced defects in centriole structure, ciliary assembly, and ciliary signaling, supporting that LRRCC1 cooperates with C2CD3 to organizing the distal region of centrioles. Since a mutation in the

Indexed as

Cell Cycle ProteinsCentriolesCiliopathiesMicrotubule-Associated ProteinsAnimalsCentrosomeCiliaHumansMicrotubulesC2cd3 protein, humanCell Cycle ProteinsLRRCC1 protein, humanMicrotubule-Associated ProteinsacornC2CD3cell biologycentriolecentriole rotational asymmetrycentrosomehumanJoubert syndromeLRRCC1primary ciliumVFL1

Identifiers

PMID35319462
PMCPMC8983040
OpenAlexW4220828016

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.