Evidence map›Paper›PMID 28954866›Full record

ArticleMolecular biology of the cell2017

Two mechanisms coordinate the recruitment of the chromosomal passenger complex to the plane of cell division.

Jennifer Landino, Stephen R Norris, Muyi Li, Edward R Ballister, Michael A Lampson, Ryoma Ohi

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

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  5. Aurora kinases: Generators of spatial control during mitosis.Frontiers in cell and developmental biology · 2023
    Review
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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

6 authors at 3 institutions in 1 country.

Jennifer LandinoDepartment of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232.
Stephen R NorrisDepartment of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232.
Muyi LiDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104.
Edward R BallisterDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104.
Michael A LampsonDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104.
Ryoma OhiDepartment of Cell and Developmental Biology, Vanderbilt University Medical Center, Nashville, TN 37232 oryoma@umich.edu.
University of Pennsylvania · USVanderbilt University Medical Center · USUniversity of Michigan · US

Funding

Regulation of microtubule dynamics during cell divisionR01GM086610 · NIGMS · VANDERBILT UNIVERSITY · PI OHI, RYOMA · 2010 to 2023
$4.5M
Regulation of cell division by mitotic kinasesR01GM083988 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GRISHCHUK, EKATERINA L, LAMPSON, MICHAEL · 2008 to 2017
$3.2M
NIGMS NIH HHS R01 GM083988NIGMS NIH HHS R01 GM086610
6 · The paper itself

Abstract

During cytokinesis, the chromosomal passenger complex (CPC) promotes midzone organization, specifies the cleavage plane, and regulates furrow contractility. The localizations of the CPC are coupled to its cytokinetic functions. At the metaphase-to-anaphase transition, the CPC dissociates from centromeres and localizes to midzone microtubules and the equatorial cortex. CPC relocalization to the cell middle is thought to depend on MKlp2-driven, plus end-directed transport. In support of this idea, MKlp2 depletion impairs cytokinesis; however, cytokinesis failure stems from furrow regression rather than failed initiation of furrowing. This suggests that an alternative mechanism(s) may concentrate the CPC at the division plane. We show here that direct actin binding, via the inner centromere protein (INCENP), enhances CPC enrichment at the equatorial cortex, thus acting in tandem with MKlp2. INCENP overexpression rescues furrowing in MKlp2-depleted cells in an INCENP-actin binding-dependent manner. Using live-cell imaging, we also find that MKlp2-dependent targeting of the CPC is biphasic. MKlp2 targets the CPC to the anti-parallel microtubule overlap of the midzone, after which the MKlp2-CPC complex moves in a nondirected manner. Collectively, our work suggests that both actin binding and MKlp2-dependent midzone targeting cooperate to precisely position the CPC during mitotic exit, and that these pathways converge to ensure successful cleavage furrow ingression.

Indexed as

AnaphaseAurora Kinase BCell DivisionCentromereChromosomal Proteins, Non-HistoneChromosomesChromosome SegregationCytokinesisDNA-Binding ProteinsHeLa CellsHumansKinesinsMetaphaseMicrofilament ProteinsMicrotubulesSpindle ApparatusAurora Kinase BChromosomal Proteins, Non-HistoneDNA-Binding ProteinsINCENP protein, humanKIF20A protein, humanKinesinsMicrofilament Proteins

Identifiers

PMID28954866
PMCPMC5706991
OpenAlexW2759295823

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.