Evidence map›Paper›PMID 29026105›Full record

ArticleScientific reports2017

MCPH1, mutated in primary microcephaly, is required for efficient chromosome alignment during mitosis.

M Arroyo, R Kuriyama, M Trimborn, D Keifenheim, A Cañuelo, A Sánchez, D J Clarke, J A Marchal

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  14. MCPH1 is essential for cellular adaptation to the GFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  15. Phosphorylation of MCPH1 isoforms during mitosis followed by isoform-specific degradation by APC/C-CDH1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  16. Article
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

8 authors at 3 institutions in 3 countries.

M ArroyoDepartamento de Biología Experimental, Universidad de Jaén, Jaen, Spain.
R KuriyamaDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, USA.
M TrimbornInstitute of Medical Genetics and Human Genetics, Charite Virchow-Klinikum Hospital, Berlin, Germany.
D KeifenheimDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, USA.
A CañueloDepartamento de Biología Experimental, Universidad de Jaén, Jaen, Spain.
A SánchezDepartamento de Biología Experimental, Universidad de Jaén, Jaen, Spain.
D J ClarkeDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, USA.
J A MarchalDepartamento de Biología Experimental, Universidad de Jaén, Jaen, Spain. jamaor@ujaen.es.
Universidad de Jaén · ESUniversity of Minnesota · USCharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MCPH1 gene, mutated in primary microcephaly, regulates cell progression into mitosis. While this role has been extensively investigated in the context of DNA damage, its function during unperturbed cell cycles has been given less attention. Here we have analyzed the dynamics of chromosome condensation and cell cycle progression in MCPH1 deficient cells under undamaging conditions. Our study demonstrates that chromosome condensation is uncoupled from cell cycle progression when MCPH1 function is lacking, resulting in cells that prematurely condense their chromosomes during mid G2-phase and delay decondensation at the completion of mitosis. However, mitosis onset occurs on schedule in MCPH1 deficient cells. We also revealed active Cdk1 to be mandatory for the premature onset of chromosome condensation during G2 and the maintenance of the condensed state thereafter. Interestingly, a novel cellular phenotype was observed while monitoring cell cycle progression in cells lacking MCPH1 function. Specifically, completion of chromosome alignment at the metaphase plate was significantly delayed. This deficiency reveals that MCPH1 is required for efficient chromosome biorientation during mitosis.

Indexed as

CDC2 Protein KinaseCell Cycle ProteinsChromosomes, HumanCytoskeletal ProteinsHeLa CellsHumansMicrocephalyMitosisMutationNerve Tissue ProteinsProphaseRNA, Small InterferingCDC2 Protein KinaseCell Cycle ProteinsCytoskeletal ProteinsMCPH1 protein, humanNerve Tissue ProteinsRNA, Small Interfering

Identifiers

PMID29026105
PMCPMC5638862
OpenAlexW2763668654

What OpenQuestion holds

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LicenceCC BY
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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.