Evidence map›Paper›PMID 24867636›Full record

ArticleeLife2014

Ki-67 is a PP1-interacting protein that organises the mitotic chromosome periphery.

Daniel G Booth, Masatoshi Takagi, Luis Sanchez-Pulido, Elizabeth Petfalski, Giulia Vargiu, Kumiko Samejima, Naoko Imamoto, Chris P Ponting, David Tollervey, William C Earnshaw and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

125 citing papers in PubMed, 242 citations in OpenAlex.

  1. Article
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  6. Review
  7. Sustainable integrative cell biology: CENP-C is guilty by association.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
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  16. Human REXO4 is Required for Cell Cycle Progression.bioRxiv : the preprint server for biology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Review

65 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

11 authors at 5 institutions in 2 countries.

Daniel G BoothWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Masatoshi TakagiCellular Dynamics Laboratory, Riken Advanced Science Institute, Wako Saitama, Japan.
Luis Sanchez-PulidoMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
Elizabeth PetfalskiWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Giulia VargiuWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Kumiko SamejimaWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Naoko ImamotoCellular Dynamics Laboratory, Riken Advanced Science Institute, Wako Saitama, Japan.
Chris P PontingMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom.
David TollerveyWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
William C EarnshawWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom bill.earnshaw@ed.ac.uk.
Paola VagnarelliBiosciences, Brunel University, London, United Kingdom Paola.Vagnarelli@brunel.ac.uk.
University of Edinburgh · GBGenomics (United Kingdom) · GBRIKEN Advanced Science Institute · JPWellcome Centre for Cell Biology · GBBrunel University of London · GB

Funding

Medical Research Council MC_U137761446Medical Research Council MC_UU_12021/1Wellcome Trust 073915Wellcome Trust 077248Wellcome Trust 092076
6 · The paper itself

Abstract

When the nucleolus disassembles during open mitosis, many nucleolar proteins and RNAs associate with chromosomes, establishing a perichromosomal compartment coating the chromosome periphery. At present nothing is known about the function of this poorly characterised compartment. In this study, we report that the nucleolar protein Ki-67 is required for the assembly of the perichromosomal compartment in human cells. Ki-67 is a cell-cycle regulated protein phosphatase 1-binding protein that is involved in phospho-regulation of the nucleolar protein B23/nucleophosmin. Following siRNA depletion of Ki-67, NIFK, B23, nucleolin, and four novel chromosome periphery proteins all fail to associate with the periphery of human chromosomes. Correlative light and electron microscopy (CLEM) images suggest a near-complete loss of the entire perichromosomal compartment. Mitotic chromosome condensation and intrinsic structure appear normal in the absence of the perichromosomal compartment but significant differences in nucleolar reassembly and nuclear organisation are observed in post-mitotic cells.DOI: http://dx.doi.org/10.7554/eLife.01641.001.

Indexed as

MitosisCell NucleolusChromosomes, HumanHeLa CellsHumansIntracellular Signaling Peptides and ProteinsKi-67 AntigenMicroscopy, ElectronMolecular Sequence DataNuclear ProteinsNucleolinNucleophosminPhosphoproteinsPhosphorylationProtein Phosphatase 1RNA-Binding ProteinsIntracellular Signaling Peptides and ProteinsKi-67 AntigenNIFK protein, humanNPM1 protein, humanNuclear ProteinsNucleolinNucleophosminPhosphoproteinsProtein Phosphatase 1RNA-Binding Proteinschromosomesmitosisnucleolusphosphatases

Identifiers

PMID24867636
PMCPMC4032110
OpenAlexW2069938004

What OpenQuestion holds

Textmetadata
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.