Evidence map›Paper›PMID 41872551›Full record

ArticleEMBO reports2026

TPGS1 regulates central spindle microtubule glutamylation and remodeling during telophase and abscission.

Rachel Sachs, Yusuke Ogi, Rytis Prekeris

Abstract read
In one paragraph

Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Rachel SachsDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Yusuke OgiDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Rytis PrekerisDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. rytis.prekeris@ucdenver.edu.ORCID 0000-0003-3393-1963

Funding

Molecular Mechanisms Regulating Epithelial Cell Apical Polarity and CiliogenesisR01DK064380 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Rytis Prekeris · 2004 to 2026
$7.1M
Predoctoral Training Program in Molecular and Cellular Biology (Supplement: Mentoring in the Research Environment)T32GM136444 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI MICHAEL A MCMURRAY, Rytis Prekeris · 2020 to 2026
$3.7M
The roles of midbody associated mRNAs in regulating cell proliferation and differentiationR01GM143774 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI PREKERIS, RYTIS, RAPOSO, GRACA GRACA · 2021 to 2024
$1.7M
HHS | National Institutes of Health (NIH) T32 GM136444-S3NIDDK NIH HHS R01 DK064380NIGMS NIH HHS R01 GM143774NIGMS NIH HHS T32 GM136444
6 · The paper itself

Abstract

Microtubules perform a variety of cellular functions, including regulation of mitotic cell division, cilia formation, and neurite extension. Post-translational modifications controlled by the TTLL-family of enzymes confer a host of properties that affect microtubule dynamics and function. Specifically, polyglutamylation of tubulin C-terminal tails plays an important role in regulating microtubule dynamics and function within specific cellular contexts. In this study, we examined contributions from and potential regulators of polyglutamylation during mitosis, focusing on the microtubule remodeling that occurs in telophase once the mitotic spindle has completed chromosome separation. We demonstrate that the anaphase-to-telophase transition is accompanied by an increase in short-chain polyglutamylation of central spindle microtubules. We also show that TTLL1 and TPGS1, subunits of the tubulin polyglutamylation complex, are targeted to the intracellular bridge and midbody during cell progression through telophase. Finally, we demonstrate that loss of TPGS1 leads to defects in remodeling of the central spindle during telophase and impacts the cell's ability to complete mitotic cell division.

Indexed as

MicrotubulesPeptide SynthasesSpindle ApparatusTelophaseCytokinesisHeLa CellsHumansMitosisProtein Processing, Post-TranslationalTubulinPeptide SynthasesTubulintubulin polyglutamylaseCytokinesisGlutamylationMicrotubulesRemodelingTelophase

Identifiers

PMID41872551
PMCPMC13121839

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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.