Neuronal processes contain the essential components for the late steps of ribosome biogenesis

C Claudia M. Fusco (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) A Anja Staab (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) A Ashley M. Bourke (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) G Georgi Tushev K Kristina Desch (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) E Erico Moreto Lins (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) E Elena Ciirdaeva (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) S Susanne tom Dieck (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) N Nina Kaltenschnee (Institute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt) A Alexander Heckel (Institute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt) J Julian D. Langer (Department of Synaptic Plasticity, Max Planck Institute for Brain Research) E Erin M. Schuman (Department of Synaptic Plasticity, Max Planck Institute for Brain Research)

Abstract

Neurons rely on spatial and temporal control of protein synthesis to respond rapidly and locally to external stimuli, a process facilitated by the dynamic localization and modification of ribosomes. While previous research has shown that neuronal activity can regulate ribosome localization and modify translation rates, little is known about ribosomal assembly within neuronal processes. Here, we investigated the potential for local ribosome maturation in rat neurons using proteomics, RNA sequencing, and imaging methods. We detected an abundance of ribosome biogenesis factors in distal neuronal compartments, particularly those associated with the late stages of ribosome assembly. Moreover, we detected cytosolic pre-ribosomal RNA species in dendrites, as well as the enzymes necessary for their processing, suggesting that local ribosome maturation can occur far from the nucleus. These findings challenge conventional models that confine ribosome biogenesis to nuclear and perinuclear regions and suggest that neurons may fine-tune local protein synthesis by regulating ribosome assembly near synaptic sites. This mechanism may enable rapid modulation of the translational capacity in response to physiological changes, regulating synaptic plasticity and local protein synthesis in neurons.

Article Details

Volume / Issue Vol. 122, Issue 31
Published August 05, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (12)

C

Claudia M. Fusco

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

A

Anja Staab

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

A

Ashley M. Bourke

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

G

Georgi Tushev

K

Kristina Desch

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

E

Erico Moreto Lins

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

E

Elena Ciirdaeva

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

S

Susanne tom Dieck

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

N

Nina Kaltenschnee

Institute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt

A

Alexander Heckel

Institute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt

J

Julian D. Langer

Department of Synaptic Plasticity, Max Planck Institute for Brain Research

E

Erin M. Schuman

Department of Synaptic Plasticity, Max Planck Institute for Brain Research