Evidence map›Paper›PMID 40743395›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

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

Claudia M Fusco, Anja Staab, Ashley M Bourke, Georgi Tushev, Kristina Desch, Erico Moreto Lins, Elena Ciirdaeva, Susanne Tom Dieck, Nina Kaltenschnee, Alexander Heckel and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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. Review
  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

12 authors.

Claudia M FuscoDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Anja StaabDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Ashley M BourkeDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.ORCID 0000-0003-2482-4963
Georgi TushevDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.ORCID 0000-0002-3340-9422
Kristina DeschDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Erico Moreto LinsDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Elena CiirdaevaDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Susanne Tom DieckDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Nina KaltenschneeInstitute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt, Frankfurt 60438, Germany.
Alexander HeckelInstitute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt, Frankfurt 60438, Germany.
Julian D LangerDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.
Erin M SchumanDepartment of Synaptic Plasticity, Max Planck Institute for Brain Research, Frankfurt 60438, Germany.

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) DiverseSynapse 101054512European Molecular Biology Organization (EMBO) ALTF 238-2021
6 · The paper itself

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.

Indexed as

NeuronsRibosomesAnimalsDendritesOrganelle BiogenesisProtein BiosynthesisRatsRNA, RibosomalRNA, Ribosomallocal translationprotein synthesisribosomesynapses

Identifiers

PMID40743395
PMCPMC12337303

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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.