Evidence map›Paper›PMID 29153323›Full record

ArticleCurrent biology : CB2017

Microtubule Tip Tracking by the Spindle and Kinetochore Protein Ska1 Requires Diverse Tubulin-Interacting Surfaces.

Julie K Monda, Ian P Whitney, Ekaterina V Tarasovetc, Elizabeth Wilson-Kubalek, Ronald A Milligan, Ekaterina L Grishchuk, Iain M Cheeseman

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  11. Ultrafast Force-Clamp Spectroscopy of Microtubule-Binding Proteins.Methods in molecular biology (Clifton, N.J.) · 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

7 authors at 3 institutions in 2 countries.

Julie K MondaWhitehead Institute for Biomedical Research, 455 Main Street, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Ian P WhitneyWhitehead Institute for Biomedical Research, 455 Main Street, Cambridge, MA 02142, USA.
Ekaterina V TarasovetcDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Center for Theoretical Problems of Physicochemical Pharmacology, Russian Academy of Sciences, Moscow, Russia.
Elizabeth Wilson-KubalekDepartment of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Ronald A MilliganDepartment of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Ekaterina L GrishchukDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Iain M CheesemanWhitehead Institute for Biomedical Research, 455 Main Street, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA. Electronic address: icheese@wi.mit.edu.
Whitehead Institute for Biomedical Research · USScripps Research Institute · USUniversity of Pennsylvania · US

Funding

Studies on Microtubule Binding ProteinsR37GM052468 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI MILLIGAN, RONALD A, WILSON-KUBALEK, ELIZABETH M · 2011 to 2020
$6.9M
STUDIES ON MICROTUBULE BINDING PROTEINSR01GM052468 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI MILLIGAN, RONALD A · 1995 to 2010
$5.0M
Molecular Analysis of the Kinetochore-Microtubule InterfaceR01GM088313 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI CHEESEMAN, IAIN MCPHERSON · 2009 to 2017
$3.6M
Coupling kinetochore microtubule dynamics to chromosome motionR01GM098389 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GRISHCHUK, EKATERINA L · 2012 to 2020
$3.1M
NIGMS NIH HHS R01 GM052468NIGMS NIH HHS R01 GM088313NIGMS NIH HHS R01 GM098389NIGMS NIH HHS R37 GM052468
6 · The paper itself

Abstract

The macromolecular kinetochore functions to generate interactions between chromosomal DNA and spindle microtubules [1]. To facilitate chromosome movement and segregation, kinetochores must maintain associations with both growing and shrinking microtubule ends. It is critical to define the proteins and their properties that allow kinetochores to associate with dynamic microtubules. The kinetochore-localized human Ska1 complex binds to microtubules and tracks with depolymerizing microtubule ends [2]. We now demonstrate that the Ska1 complex also autonomously tracks with growing microtubule ends in vitro, a key property that would allow this complex to act at kinetochores to mediate persistent associations with dynamic microtubules. To define the basis for Ska1 complex interactions with dynamic microtubules, we investigated the tubulin-binding properties of the Ska1 microtubule binding domain. In addition to binding to the microtubule lattice and dolastatin-induced protofilament-like structures, we demonstrate that the Ska1 microtubule binding domain can associate with soluble tubulin heterodimers and promote assembly of oligomeric ring-like tubulin structures. We generated mutations on distinct surfaces of the Ska1 microtubule binding domain that disrupt binding to soluble tubulin but do not prevent microtubule binding. These mutants display compromised microtubule tracking activity in vitro and result in defective chromosome alignment and mitotic progression in cells using a CRISPR/Cas9-based replacement assay. Our work supports a model in which multiple surfaces of Ska1 interact with diverse tubulin substrates to associate with dynamic microtubule polymers and facilitate optimal chromosome segregation.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosomal Proteins, Non-HistoneChromosome SegregationKinetochoresMicrotubulesSpindle ApparatusTubulinCaenorhabditis elegans ProteinsChromosomal Proteins, Non-Histoneska-1 protein, C elegansTubulinchromosome segregationkinetochoremicrotubulemitosistubulin

Identifiers

PMID29153323
PMCPMC5726585
OpenAlexW2769904743

What OpenQuestion holds

Textmetadata
LicenceTDM
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.