Evidence map›Paper›PMID 40834096›Full record

ArticleScience advances2025

Mechanistic insights into TTLL11 polyglutamylase-mediated primary tubulin chain elongation.

Jana Campbell, Miroslava Vosahlikova, Samar Ismail, Margareta Volnikova, Lucia Motlova, Julia Kudlacova, Kseniya Ustinova, Ivan Snajdr, Zora Novakova, Miroslav Basta and 4 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
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

14 authors.

Jana CampbellInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0001-5761-0764
Miroslava VosahlikovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0003-4832-7953
Samar IsmailGrenoble Institute Neurosciences, University Grenoble Alpes, Inserm U1216, CNRS, 38000 Grenoble, France.ORCID 0009-0001-8316-4654
Margareta VolnikovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0009-0000-4589-1802
Lucia MotlovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0002-5581-8737
Julia KudlacovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0001-7100-4162
Kseniya UstinovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0001-6632-5850
Ivan SnajdrInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo n. 2, Prague, Czech Republic.ORCID 0000-0002-0831-4034
Zora NovakovaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0001-9804-6346
Miroslav BastaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0009-0007-3874-248X
Irina GutscheInstitut de Biologie Structurale, Université Grenoble Alpes, CEA, CNRS (IBS), 38044 Grenoble, France.ORCID 0000-0002-1908-3921
Marie-Jo MoutinGrenoble Institute Neurosciences, University Grenoble Alpes, Inserm U1216, CNRS, 38000 Grenoble, France.ORCID 0000-0003-2681-9818
Ambroise DesfossesInstitut de Biologie Structurale, Université Grenoble Alpes, CEA, CNRS (IBS), 38044 Grenoble, France.ORCID 0000-0002-6525-5042
Cyril BarinkaInstitute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Prumyslova 595, Vestec, Czech Republic.ORCID 0000-0003-2751-3060

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules (MTs) undergo diverse posttranslational modifications that regulate their structural and functional properties. Among these, polyglutamylation-a dominant and conserved modification targeting unstructured tubulin C-terminal tails-plays a pivotal role in defining the tubulin code. Here, we describe a mechanism by which tubulin tyrosine ligase-like 11 (TTLL11) expands and diversifies the code. Cryo-electron microscopy revealed a unique bipartite MT recognition strategy wherein TTLL11 binding and catalytic domains engage adjacent MT protofilaments. Biochemical and cellular assays identified previously uncharacterized polyglutamylation patterns, showing that TTLL11 directly extends the primary polypeptide chains of α- and β-tubulin in vitro, challenging the prevailing paradigms emphasizing lateral branching. Moreover, cell-based and in vivo data suggest a cross-talk between polyglutamylation and the detyrosination/tyrosination cycle likely linked to the TTLL11-mediated elongation of the primary α-tubulin chain. These findings unveil an unrecognized layer of complexity within the tubulin code and offer mechanistic insights into the molecular basis of functional specialization of MT cytoskeleton.

Indexed as

Peptide SynthasesTubulinCryoelectron MicroscopyHumansMicrotubulesModels, MolecularProtein BindingProtein Processing, Post-TranslationalPeptide SynthasesTubulintubulin polyglutamylase

Identifiers

PMID40834096
PMCPMC12366701

What OpenQuestion holds

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LicenceCC BY
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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.