Evidence map›Paper›PMID 33899739›Full record

ArticleeLife2021

DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction.

Eva On-Chai Lau, Devid Damiani, Georges Chehade, Nuria Ruiz-Reig, Rana Saade, Yves Jossin, Mohamed Aittaleb, Olivier Schakman, Nicolas Tajeddine, Philippe Gailly and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 45 citations in OpenAlex.

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  16. DIAPH3 predicts survival of patients withFrontiers in oncology · 2024
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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 2 countries.

Eva On-Chai LauUniversité catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.
Devid Damiani *Université catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.
Georges Chehade *Université catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.
Nuria Ruiz-ReigUniversité catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.ORCID 0000-0001-7008-7920
Rana SaadeUniversité catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.
Yves JossinUniversité catholique de Louvain, Institute of Neuroscience, Mammalian Development and Cell Biology, Brussels, Belgium.ORCID 0000-0001-8466-7432
Mohamed AittalebCollege of Health and Life Sciences, HBKU, Doha, Qatar.
Olivier SchakmanUniversité catholique de Louvain, Institute of Neuroscience, Cell Physiology, Brussels, Belgium.
Nicolas TajeddineUniversité catholique de Louvain, Institute of Neuroscience, Cell Physiology, Brussels, Belgium.
Philippe GaillyUniversité catholique de Louvain, Institute of Neuroscience, Cell Physiology, Brussels, Belgium.
Fadel TissirUniversité catholique de Louvain, Institute of Neuroscience, Developmental Neurobiology, Brussels, Belgium.ORCID 0000-0002-9292-6622
UCLouvain · BEHamad bin Khalifa University · QA

Funding

Wellcome Trust
6 · The paper itself

Abstract

Diaphanous (DIAPH) three (DIAPH3) is a member of the formin proteins that have the capacity to nucleate and elongate actin filaments and, therefore, to remodel the cytoskeleton. DIAPH3 is essential for cytokinesis as its dysfunction impairs the contractile ring and produces multinucleated cells. Here, we report that DIAPH3 localizes at the centrosome during mitosis and regulates the assembly and bipolarity of the mitotic spindle. DIAPH3-deficient cells display disorganized cytoskeleton and multipolar spindles. DIAPH3 deficiency disrupts the expression and/or stability of several proteins including the kinetochore-associated protein SPAG5. DIAPH3 and SPAG5 have similar expression patterns in the developing brain and overlapping subcellular localization during mitosis. Knockdown of SPAG5 phenocopies DIAPH3 deficiency, whereas its overexpression rescues the DIAHP3 knockdown phenotype. Conditional inactivation of

Indexed as

Behavior, AnimalMitosisNeurogenesisAnimalsCell Cycle ProteinsCell Line, TumorCerebral CortexFeeding BehaviorForminsGene Expression Regulation, DevelopmentalGenotypeHumansLocomotionMaze LearningMiceMice, KnockoutCell Cycle ProteinsForminsSpag5 protein, mouseAstrinmalformation of cortical developmentmDia2mouseMTOCneuroscience

Identifiers

PMID33899739
PMCPMC8102060
OpenAlexW3157106888

What OpenQuestion holds

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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.