Evidence map›Paper›PMID 34417301›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Wnt signaling recruits KIF2A to the spindle to ensure chromosome congression and alignment during mitosis.

Anja Bufe, Ana García Del Arco, Magdalena Hennecke, Anchel de Jaime-Soguero, Matthias Ostermaier, Yu-Chih Lin, Anja Ciprianidis, Janina Hattemer, Ulrike Engel, Petra Beli and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Morphogen Gradients as Drivers of Mosaicism During Early Human Development.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  11. Article
  12. Mitotic WNT: aligning chromosomes through KIF2A.Molecular & cellular oncology · 2021
    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

12 authors at 4 institutions in 1 country.

Anja BufeCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.ORCID 0000-0003-3427-3413
Ana García Del ArcoCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.ORCID 0000-0001-9030-5964
Magdalena HenneckeSection for Cellular Oncology, Institute of Molecular Oncology, Göttingen Center for Molecular Biosciences and University Medical Center Göttingen, Georg-August University Göttingen, D-37077 Göttingen, Germany.
Anchel de Jaime-SogueroCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.ORCID 0000-0002-9358-3676
Matthias OstermaierInstitute for Molecular Biology (IMB), D-55128 Mainz, Germany.ORCID 0000-0002-4290-9410
Yu-Chih LinSection for Cellular Oncology, Institute of Molecular Oncology, Göttingen Center for Molecular Biosciences and University Medical Center Göttingen, Georg-August University Göttingen, D-37077 Göttingen, Germany.
Anja CiprianidisCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.
Janina HattemerCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.
Ulrike EngelCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany.
Petra BeliInstitute for Molecular Biology (IMB), D-55128 Mainz, Germany.ORCID 0000-0001-9507-9820
Holger BastiansSection for Cellular Oncology, Institute of Molecular Oncology, Göttingen Center for Molecular Biosciences and University Medical Center Göttingen, Georg-August University Göttingen, D-37077 Göttingen, Germany.
Sergio P AcebrónCentre for Organismal Studies, Heidelberg University, D-69120 Heidelberg, Germany; sergio.acebron@cos.uni-heidelberg.de.ORCID 0000-0002-7694-2497
Heidelberg University · DEUniversitätsmedizin Göttingen · DEInstitute of Molecular Biology · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Canonical Wnt signaling plays critical roles in development and tissue renewal by regulating β-catenin target genes. Recent evidence showed that β-catenin-independent Wnt signaling is also required for faithful execution of mitosis. However, the targets and specific functions of mitotic Wnt signaling still remain uncharacterized. Using phosphoproteomics, we identified that Wnt signaling regulates the microtubule depolymerase KIF2A during mitosis. We found that Dishevelled recruits KIF2A via its N-terminal and motor domains, which is further promoted upon LRP6 signalosome formation during cell division. We show that Wnt signaling modulates KIF2A interaction with PLK1, which is critical for KIF2A localization at the spindle. Accordingly, inhibition of basal Wnt signaling leads to chromosome misalignment in somatic cells and pluripotent stem cells. We propose that Wnt signaling monitors KIF2A activity at the spindle poles during mitosis to ensure timely chromosome alignment. Our findings highlight a function of Wnt signaling during cell division, which could have important implications for genome maintenance, notably in stem cells.

Indexed as

Chromosome SegregationMitosisWnt Signaling PathwayChromosome PositioningChromosomes, HumanHumansKinesinsSpindle ApparatusKIF2A protein, humanKinesinschromosome alignmentDishevelledKinesin-13mitosisWnt signaling

Identifiers

PMID34417301
PMCPMC8403935
OpenAlexW3194376223

What OpenQuestion holds

Textmetadata
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.