Evidence map›Paper›PMID 26912793›Full record

ArticleMolecular biology of the cell2016

Divergent microtubule assembly rates after short- versus long-term loss of end-modulating kinesins.

Linda Wordeman, Justin Decarreau, Juan Jesus Vicente, Michael Wagenbach

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

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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 1 institution in 1 country.

Linda WordemanDepartment of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195 worde@uw.edu.
Justin DecarreauDepartment of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195.
Juan Jesus VicenteDepartment of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195.
Michael WagenbachDepartment of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195.
University of Washington · US

Funding

Microtubule Dynamics and Chromosome SegregationR01GM069429 · NIGMS · UNIVERSITY OF WASHINGTON · PI WORDEMAN, LINDA · 2004 to 2020
$5.6M
Microtuble-dependent markers for chromosome instabilityR21CA174527 · NCI · UNIVERSITY OF WASHINGTON · PI WORDEMAN, LINDA · 2014 to 2015
$370k
Identification and characterization of a novel mitotic kinesin Kif25F32GM105099 · NIGMS · UNIVERSITY OF WASHINGTON · PI DECARREAU, JUSTIN · 2013 to 2013
$52k
NCI NIH HHS R21 CA174527NIGMS NIH HHS F32 GM105099NIGMS NIH HHS F32GM105099NIGMS NIH HHS GM69429NIGMS NIH HHS R01 GM069429
6 · The paper itself

Abstract

Depletion of microtubule (MT) regulators can initiate stable alterations in MT assembly rates that affect chromosome instability and mitotic spindle function, but the manner by which cellular MT assembly rates can stably increase or decrease is not understood. To investigate this phenomenon, we measured the response of microtubule assembly to both rapid and long-term loss of MT regulators MCAK/Kif2C and Kif18A. Depletion of MCAK/Kif2C by siRNA stably decreases MT assembly rates in mitotic spindles, whereas depletion of Kif18A stably increases rates of assembly. Surprisingly, this is not phenocopied by rapid rapamycin-dependent relocalization of MCAK/Kif2C and Kif18A to the plasma membrane. Instead, this treatment yields opposite affects on MT assembly. Rapidly increased MT assembly rates are balanced by a decrease in nucleated microtubules, whereas nucleation appears to be maximal and limiting for decreased MT assembly rates and also for long-term treatments. We measured amplified tubulin synthesis during long-term depletion of MT regulators and hypothesize that this is the basis for different phenotypes arising from long-term versus rapid depletion of MT regulators.

Indexed as

Cell MembraneHCT116 CellsHeLa CellsHumansKinesinsMicrotubule-Associated ProteinsMicrotubulesRecombinant Fusion ProteinsRNA, Small InterferingSirolimusSpindle ApparatusTacrolimus Binding ProteinsKIF18A protein, humanKIF2C protein, humanKinesinsMAPRE1 protein, humanMicrotubule-Associated ProteinsRecombinant Fusion ProteinsRNA, Small InterferingSirolimusTacrolimus Binding Proteins

Identifiers

PMID26912793
PMCPMC4831883
OpenAlexW2314252412

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.