Evidence map›Paper›PMID 29941476›Full record

ArticleThe Journal of cell biology2018

Spindle rotation in human cells is reliant on a MARK2-mediated equatorial spindle-centering mechanism.

Ihsan Zulkipli, Joanna Clark, Madeleine Hart, Roshan L Shrestha, Parveen Gul, David Dang, Tami Kasichiwin, Izabela Kujawiak, Nishanth Sastry, Viji M Draviam

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. TEX38 localizes ZDHHC19 to the plasma membrane and regulates sperm head morphogenesis in mice.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  13. AnBio-protocol · 2018
    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

10 authors at 3 institutions in 1 country.

Ihsan ZulkipliDepartment of Genetics, University of Cambridge, Cambridge, England, UK.ORCID 0000-0002-6426-5126
Joanna ClarkDepartment of Genetics, University of Cambridge, Cambridge, England, UK.
Madeleine HartSchool of Biological and Chemical Sciences, Queen Mary University of London, London, England, UK.
Roshan L ShresthaDepartment of Genetics, University of Cambridge, Cambridge, England, UK.ORCID 0000-0001-5093-9460
Parveen GulSchool of Biological and Chemical Sciences, Queen Mary University of London, London, England, UK.
David DangSchool of Biological and Chemical Sciences, Queen Mary University of London, London, England, UK.
Tami KasichiwinSchool of Biological and Chemical Sciences, Queen Mary University of London, London, England, UK.
Izabela KujawiakDepartment of Genetics, University of Cambridge, Cambridge, England, UK.ORCID 0000-0002-9770-5722
Nishanth SastryDepartment of Informatics, King's College, London, England, UK.
Viji M DraviamSchool of Biological and Chemical Sciences, Queen Mary University of London, London, England, UK v.draviam@qmul.ac.uk.ORCID 0000-0001-8295-3689
Queen Mary University of London · GBUniversity of Cambridge · GBKing's College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M009513/1Biotechnology and Biological Sciences Research Council BB/R01003X/1Cancer Research UK 9787Cancer Research UK C28598/A9787
6 · The paper itself

Abstract

The plane of cell division is defined by the final position of the mitotic spindle. The spindle is pulled and rotated to the correct position by cortical dynein. However, it is unclear how the spindle's rotational center is maintained and what the consequences of an equatorially off centered spindle are in human cells. We analyzed spindle movements in 100s of cells exposed to protein depletions or drug treatments and uncovered a novel role for MARK2 in maintaining the spindle at the cell's geometric center. Following MARK2 depletion, spindles glide along the cell cortex, leading to a failure in identifying the correct division plane. Surprisingly, spindle off centering in MARK2-depleted cells is not caused by excessive pull by dynein. We show that MARK2 modulates mitotic microtubule growth and length and that codepleting mitotic centromere-associated protein (MCAK), a microtubule destabilizer, rescues spindle off centering in MARK2-depleted cells. Thus, we provide the first insight into a spindle-centering mechanism needed for proper spindle rotation and, in turn, the correct division plane in human cells.

Indexed as

Cell Line, TumorDyneinsHeLa CellsHumansMicrotubulesMitosisProtein Serine-Threonine KinasesRNA InterferenceRNA, Small InterferingSpindle ApparatusDyneinsMARK2 protein, humanProtein Serine-Threonine KinasesRNA, Small Interfering

Identifiers

PMID29941476
PMCPMC6122980
OpenAlexW2810947364

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.