Evidence map›Paper›PMID 40975050›Full record

ArticleCurrent biology : CB2025

The kinesin motor Kif9 regulates centriolar satellite positioning during interphase.

Juan Jesus Vicente, Michael Wagenbach, Justin Decarreau, Alex Zelter, Michael J MacCoss, Trisha N Davis, Linda Wordeman

Abstract read
In one paragraph

Article in Current biology : CB, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. The Kinesin Motor Kif9 Disrupts Primary Cilia Length by Mispositioning Centriolar Satellites.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Juan Jesus VicenteDepartment of Neurobiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address: jjvr@uw.edu.
Michael WagenbachDepartment of Neurobiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195, USA.
Justin DecarreauDepartment of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA; Institute for Protein Design, University of Washington School of Medicine, Seattle, WA 98195, USA.
Alex ZelterDepartment of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Michael J MacCossDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Trisha N DavisDepartment of Biochemistry, University of Washington School of Medicine, Seattle, WA 98195, USA.
Linda WordemanDepartment of Neurobiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address: worde@uw.edu.

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI DAVIS, TRISHA N. · 2012 to 2021
$20.7M
Microtubule Dynamics and Chromosome SegregationR01GM069429 · NIGMS · UNIVERSITY OF WASHINGTON · PI WORDEMAN, LINDA · 2004 to 2020
$5.6M
Microtubule dynamics and error correctionR01GM145567 · NIGMS · UNIVERSITY OF WASHINGTON · PI WORDEMAN, LINDA · 2022 to 2025
$1.8M
DeltaVision OMX Blaze 3D Structured Illumination MicroscopeS10OD021490 · OD · UNIVERSITY OF WASHINGTON · PI WORDEMAN, LINDA · 2017 to 2017
$779k
NIGMS NIH HHS P41 GM103533NIGMS NIH HHS R01 GM069429NIGMS NIH HHS R01 GM145567NIH HHS S10 OD021490
6 · The paper itself

Abstract

Centrosomes are the principal microtubule-organizing centers of the cell, are cellular hubs for protein degradation, and play an essential role in mitotic spindle function that ultimately regulates chromosome segregation during mitosis. Centrosome maturation is achieved by strict control of protein acquisition and phosphorylation prior to mitosis. Defects in this process during interphase promote fragmentation of pericentriolar material once cells enter mitosis due to the increased forces exerted over the centrosome by the mitotic spindle, finally culminating in multipolar spindles and chromosome missegregation. Centriolar satellites, membrane-less assemblies of proteins involved in the trafficking of proteins toward and away from the centrosome, are thought to contribute to centrosome biogenesis. Moreover, centriolar satellites also regulate the quantity of proteolytic factors reaching the centrosome. Here, we show that the microtubule plus-end-directed kinesin motor Kif9 localizes to centriolar satellites and regulates their pericentrosomal localization during interphase. Lack of Kif9 leads to aggregation of satellites closer to the centrosome and increased centrosomal protein degradation that disrupts centrosome maturation and results in chromosome congression and segregation defects during mitosis. Our data show that the kinesin Kif9 controls the position of centriolar satellites relative to the centrosome and reveal roles for Kif9 and centriolar satellites in the regulation of cellular proteostasis and mitosis.

Indexed as

CentriolesInterphaseKinesinsCentrosomeChromosome SegregationHeLa CellsHumansMitosisKinesinscentriolar satellitescentrosomechromosome congressionchromosome missegregationKif9kinesinmicrotubulesmitosisPCM1pericentriolar material

Identifiers

PMID40975050
PMCPMC12629138

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.