Evidence map›Paper›PMID 36125182›Full record

ArticleThe EMBO journal2022

Human SFI1 and Centrin form a complex critical for centriole architecture and ciliogenesis.

Marine H Laporte, Imène B Bouhlel, Eloïse Bertiaux, Ciaran G Morrison, Alexia Giroud, Susanne Borgers, Juliette Azimzadeh, Michel Bornens, Paul Guichard, Anne Paoletti and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2022. 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
4.1field-weighted citation impact, top 5% 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, 36 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

11 authors at 2 institutions in 3 countries.

Marine H LaporteDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.ORCID 0000-0002-7856-6763
Imène B BouhlelInstitut Curie, UMR 144, CNRS, PSL University, Paris, France.
Eloïse BertiauxDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.
Ciaran G MorrisonDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.ORCID 0000-0003-2401-7029
Alexia GiroudDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.ORCID 0000-0003-2389-5858
Susanne BorgersDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.
Juliette AzimzadehUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Michel Bornens *Institut Curie, UMR 144, CNRS, PSL University, Paris, France.
Paul GuichardDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.ORCID 0000-0002-0363-1049
Anne PaolettiInstitut Curie, UMR 144, CNRS, PSL University, Paris, France.ORCID 0000-0002-9004-559X
Virginie HamelDepartment of Molecular and Cellular Biology, University of Geneva, Geneva, Switzerland.ORCID 0000-0001-5092-2343
University of Geneva · CHCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the course of evolution, the centrosome function has been conserved in most eukaryotes, but its core architecture has evolved differently in some clades, with the presence of centrioles in humans and a spindle pole body (SPB) in yeast. Similarly, the composition of these two core elements has diverged, with the exception of Centrin and SFI1, which form a complex in yeast to initiate SPB duplication. However, it remains unclear whether this complex exists at centrioles and whether its function has been conserved. Here, using expansion microscopy, we demonstrate that human SFI1 is a centriolar protein that associates with a pool of Centrin at the distal end of the centriole. We also find that both proteins are recruited early during procentriole assembly and that depletion of SFI1 results in the loss of the distal pool of Centrin, without altering centriole duplication. Instead, we show that SFI1/Centrin complex is essential for centriolar architecture, CEP164 distribution, and CP110 removal during ciliogenesis. Together, our work reveals a conserved SFI1/Centrin module displaying divergent functions between mammals and yeast.

Indexed as

Calcium-Binding ProteinsCell Cycle ProteinsCentriolesAnimalsHumansRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle Pole BodiesCalcium-Binding ProteinsCell Cycle ProteinsCETN1 protein, humanRepressor ProteinsSaccharomyces cerevisiae ProteinsSfi1 protein, humanSFI1 protein, S cerevisiaecentriolescentrosomeciliogenesisexpansion microscopyhuman cells

Identifiers

PMID36125182
PMCPMC9627676
OpenAlexW4296788965

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.