Evidence map›Paper›PMID 26949251›Full record

ArticleeLife2016

The cell proliferation antigen Ki-67 organises heterochromatin.

Michal Sobecki, Karim Mrouj, Alain Camasses, Nikolaos Parisis, Emilien Nicolas, David Llères, François Gerbe, Susana Prieto, Liliana Krasinska, Alexandre David and 11 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 199 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed, 2 pooled it
12.9field-weighted citation impact, top 1% 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

199 citing papers in PubMed, 2 syntheses or guidelines pooled it, 372 citations in OpenAlex.

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139 more citing papers are in PubMed but not listed here.

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

21 authors at 5 institutions in 3 countries.

Michal SobeckiMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Karim MroujMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Alain CamassesMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Nikolaos ParisisMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.ORCID http://orcid.org/0000-0002-5706-0122
Emilien NicolasRNA Molecular Biology, Center for Microscopy and Molecular Imaging, Fonds de la Recherche Nationale, Université Libre de Bruxelles, Charleroi-Gosselies, Belgium.
David LlèresMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
François GerbeFaculty of Sciences, University of Montpellier, Montpellier, France.
Susana PrietoMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Liliana KrasinskaMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Alexandre DavidFaculty of Sciences, University of Montpellier, Montpellier, France.
Manuel EgurenSpanish National Cancer Research Centre, Madrid, Spain.ORCID http://orcid.org/0000-0003-0850-939X
Marie-Christine BirlingICS, Mouse Clinical Institute, Illkirch-Graffenstaden, France.
Serge UrbachFaculty of Sciences, University of Montpellier, Montpellier, France.
Sonia HemMass Spectrometry Platform MSPP, SupAgro, Montpellier, France.
Jérôme DéjardinFaculty of Sciences, University of Montpellier, Montpellier, France.
Marcos MalumbresSpanish National Cancer Research Centre, Madrid, Spain.ORCID http://orcid.org/0000-0002-0829-6315
Philippe JayFaculty of Sciences, University of Montpellier, Montpellier, France.
Vjekoslav DulicMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.
Denis Lj LafontaineRNA Molecular Biology, Center for Microscopy and Molecular Imaging, Fonds de la Recherche Nationale, Université Libre de Bruxelles, Charleroi-Gosselies, Belgium.
Robert FeilMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.ORCID http://orcid.org/0000-0002-5671-5860
Daniel FisherMontpellier Institute of Molecular Genetics (IGMM) CNRS UMR 5535, Centre National de la Recherche Scientifique (CNRS), Montpellier, France.ORCID http://orcid.org/0000-0002-0822-3482
Centre National de la Recherche Scientifique · FRSpanish National Cancer Research Centre · ESUniversité Libre de Bruxelles · BEInstitut Agro Montpellier · FRInstitut Clinique de la Souris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigen Ki-67 is a nuclear protein expressed in proliferating mammalian cells. It is widely used in cancer histopathology but its functions remain unclear. Here, we show that Ki-67 controls heterochromatin organisation. Altering Ki-67 expression levels did not significantly affect cell proliferation in vivo. Ki-67 mutant mice developed normally and cells lacking Ki-67 proliferated efficiently. Conversely, upregulation of Ki-67 expression in differentiated tissues did not prevent cell cycle arrest. Ki-67 interactors included proteins involved in nucleolar processes and chromatin regulators. Ki-67 depletion disrupted nucleologenesis but did not inhibit pre-rRNA processing. In contrast, it altered gene expression. Ki-67 silencing also had wide-ranging effects on chromatin organisation, disrupting heterochromatin compaction and long-range genomic interactions. Trimethylation of histone H3K9 and H4K20 was relocalised within the nucleus. Finally, overexpression of human or Xenopus Ki-67 induced ectopic heterochromatin formation. Altogether, our results suggest that Ki-67 expression in proliferating cells spatially organises heterochromatin, thereby controlling gene expression.

Indexed as

Cell ProliferationAnimalsGene ExpressionGene Knockdown TechniquesHeterochromatinHumansKi-67 AntigenMiceXenopusHeterochromatinKi-67 Antigencell biologycell proliferationheterochromatinhumanKi-67mouse

Identifiers

PMID26949251
PMCPMC4841783
OpenAlexW2297680570

What OpenQuestion holds

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LicenceCC BY
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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.