Evidence map›Paper›PMID 29509805›Full record

ArticlePloS one2018

CENP-C/H/I/K/M/T/W/N/L and hMis12 but not CENP-S/X participate in complex formation in the nucleoplasm of living human interphase cells outside centromeres.

Christian Hoischen, Sibel Yavas, Thorsten Wohland, Stephan Diekmann

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  4. Centromeric protein K (CENPK) promotes gastric cancer proliferation and migration via interacting with XRCC5.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2022
    Article
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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

4 authors at 2 institutions in 2 countries.

Christian HoischenMolecular Biology, Leibniz Institute on Aging-Friz-Lipmann-Institute (FLI), Jena, Germany.ORCID 0000-0003-2817-1752
Sibel YavasDepartments of Biological Sciences and Chemistry and Centre of Bioimaging Sciences, Lee Wee Kheng Buildung, National University of Singapore, Singapore, Singapore.
Thorsten WohlandDepartments of Biological Sciences and Chemistry and Centre of Bioimaging Sciences, Lee Wee Kheng Buildung, National University of Singapore, Singapore, Singapore.
Stephan DiekmannMolecular Biology, Leibniz Institute on Aging-Friz-Lipmann-Institute (FLI), Jena, Germany.
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DENational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kinetochore proteins assemble onto centromeric chromatin and regulate DNA segregation during cell division. The inner kinetochore proteins bind centromeres while most outer kinetochore proteins assemble at centromeres during mitosis, connecting the complex to microtubules. Here, we measured the co-migration between protein pairs of the constitutive centromere associated network (CCAN) and hMis12 complexes by fluorescence cross-correlation spectroscopy (FCCS) in the nucleoplasm outside centromeres in living human interphase cells. FCCS is a method that can tell if in living cells two differently fluorescently labelled molecules migrate independently, or co-migrate and thus are part of one and the same soluble complex. We also determined the apparent dissociation constants (Kd) of the hetero-dimers CENP-T/W and CENP-S/X. We measured co-migration between CENP-K and CENP-T as well as between CENP-M and CENP-T but not between CENP-T/W and CENP-S/X. Furthermore, CENP-C co-migrated with CENP-H, and CENP-K with CENP-N as well as with CENP-L. Thus, in the nucleoplasm outside centromeres, a large fraction of the CENP-H/I/K/M proteins interact with CENP-C, CENP-N/L and CENP-T/W but not with CENP-S/X. Our FCCS analysis of the Mis12 complex showed that hMis12, Nsl1, Dsn1 and Nnf1 also form a complex outside centromeres of which at least hMis12 associated with the CENP-C/H/I/K/M/T/W/N/L complex.

Indexed as

InterphaseApoptosis Regulatory ProteinsCell Cycle ProteinsCell Line, TumorCentromereChromosomal Proteins, Non-HistoneDNA-Binding ProteinsHumansMicrotubule-Associated ProteinsNeoplasm ProteinsNeoplasmsNuclear ProteinsTumor Suppressor ProteinsApoptosis Regulatory ProteinsCell Cycle ProteinsCENPH protein, humanCENPI protein, humanCENPK protein, humanCENPL protein, humanCENPM protein, humanCENPN protein, humanCENPS protein, humanCENPW protein, humanCENPX protein, humancentromere protein CChromosomal Proteins, Non-HistoneDNA-Binding ProteinsMicrotubule-Associated ProteinsMIS12 protein, humanNeoplasm ProteinsNuclear ProteinsTumor Suppressor Proteins

Identifiers

PMID29509805
PMCPMC5839545
OpenAlexW2789719196

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.