Evidence map›Paper›PMID 35058575›Full record

ArticleCell death and differentiation2022

Genetic interaction between PLK1 and downstream MCPH proteins in the control of centrosome asymmetry and cell fate during neural progenitor division.

José González-Martínez, Andrzej W Cwetsch, Javier Gilabert-Juan, Jesús Gómez, Guillermo Garaulet, Paulina Schneider, Guillermo de Cárcer, Francisca Mulero, Eduardo Caleiras, Diego Megías and 2 more

Open access · bronzeAbstract read
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Article in Cell death and differentiation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 9 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 3 institutions in 2 countries.

José González-MartínezCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0002-3850-6803
Andrzej W CwetschCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Javier Gilabert-JuanCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0001-5187-3942
Jesús GómezConfocal Microscopy Core Unit, CNIO, Madrid, Spain.ORCID http://orcid.org/0000-0002-8567-8907
Guillermo GarauletMolecular Imaging Core Unit, CNIO, Madrid, Spain.
Paulina SchneiderCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Guillermo de CárcerCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0002-3220-1785
Francisca MuleroMolecular Imaging Core Unit, CNIO, Madrid, Spain.
Eduardo CaleirasHistopathology Core Unit, CNIO, Madrid, Spain.
Diego MegíasConfocal Microscopy Core Unit, CNIO, Madrid, Spain.
Eva PorlanCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Marcos MalumbresCell Division and Cancer group, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. malumbres@cnio.es.ORCID http://orcid.org/0000-0002-0829-6315
Spanish National Cancer Research Centre · ESCentro Nacional de Epidemiología · ESConsejo Superior de Investigaciones Científicas · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alteration of centrosome function and dynamics results in major defects during chromosome segregation and is associated with primary autosomal microcephaly (MCPH). Despite the knowledge accumulated in the last few years, why some centrosomal defects specifically affect neural progenitors is not clear. We describe here that the centrosomal kinase PLK1 controls centrosome asymmetry and cell fate in neural progenitors during development. Gain- or loss-of-function mutations in Plk1, as well as deficiencies in the MCPH genes Cdk5rap2 (MCPH3) and Cep135 (MCPH8), lead to abnormal asymmetry in the centrosomes carrying the mother and daughter centriole in neural progenitors. However, whereas loss of MCPH proteins leads to increased centrosome asymmetry and microcephaly, deficient PLK1 activity results in reduced asymmetry and increased expansion of neural progenitors and cortical growth during mid-gestation. The combination of PLK1 and MCPH mutations results in increased microcephaly accompanied by more aggressive centrosomal and mitotic abnormalities. In addition to highlighting the delicate balance in the level and activity of centrosomal regulators, these data suggest that human PLK1, which maps to 16p12.1, may contribute to the neurodevelopmental defects associated with 16p11.2-p12.2 microdeletions and microduplications in children with developmental delay and dysmorphic features.

Indexed as

Cell Cycle ProteinsMicrocephalyNeural Stem CellsProtein Serine-Threonine KinasesProto-Oncogene ProteinsCell DifferentiationCentrosomeChildChromosome SegregationHumansMutationNerve Tissue ProteinsPolo-Like Kinase 1CDK5RAP2 protein, humanCell Cycle ProteinsNerve Tissue ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID35058575
PMCPMC9345906
OpenAlexW4206243539

What OpenQuestion holds

Textmetadata
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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.