Polyglutamylation of microtubules drives neuronal remodeling

A Antoneta Gavoci A Anxhela Zhiti M Michaela Rusková M Maria M. Magiera (Institut Curie, Université Paris Sciences et lettres, CNRS UMR3348) M Mengzhe Wang (The Education Ministry Key Laboratory of Resource Chemistry, Shanghai Engineering Research Center of Green Energy Chemical Engineering) K Karin A. Ziegler T Torben J. Hausrat A Anselm I. Ugwuja S Shreyangi Chakraborty S Stefan Engelhardt M Matthias Kneussel M Martin Balastik C Carsten Janke (Institut Curie, Université Paris Sciences et lettres, CNRS UMR3348) T Thomas Misgeld M Monika S. Brill

Abstract

Abstract Developmental remodeling shapes neural circuits via activity-dependent pruning of synapses and axons. Regulation of the cytoskeleton is critical for this process, as microtubule loss via enzymatic severing is an early step of pruning across many circuits and species. However, how microtubule-severing enzymes, such as spastin, are activated in specific neuronal compartments remains unknown. Here, we reveal that polyglutamylation, a post-translational tubulin modification enriched in neurons, plays an instructive role in developmental remodeling by tagging microtubules for severing. Motor neuron-specific gene deletion of enzymes that add or remove tubulin polyglutamylation—TTLL glutamylases vs. CCP deglutamylases—accelerates or delays neuromuscular synapse remodeling in a neurotransmission-dependent manner. This mechanism is not specific to peripheral synapses but also operates in central circuits, e.g., the hippocampus. Thus, tubulin polyglutamylation acts as a cytoskeletal rheostat of remodeling that shapes neuronal morphology and connectivity.

Article Details

Volume / Issue Vol. 16, Issue 1
Published June 25, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (15)

A

Antoneta Gavoci

A

Anxhela Zhiti

M

Michaela Rusková

M

Maria M. Magiera

Institut Curie, Université Paris Sciences et lettres, CNRS UMR3348

M

Mengzhe Wang

The Education Ministry Key Laboratory of Resource Chemistry, Shanghai Engineering Research Center of Green Energy Chemical Engineering

K

Karin A. Ziegler

T

Torben J. Hausrat

A

Anselm I. Ugwuja

S

Shreyangi Chakraborty

S

Stefan Engelhardt

M

Matthias Kneussel

M

Martin Balastik

C

Carsten Janke

Institut Curie, Université Paris Sciences et lettres, CNRS UMR3348

T

Thomas Misgeld

M

Monika S. Brill