Evidence map›Paper›PMID 27022091›Full record

ArticleThe Journal of cell biology2016

The proteasome controls presynaptic differentiation through modulation of an on-site pool of polyubiquitinated conjugates.

Maria J Pinto, Pedro L Alves, Luís Martins, Joana R Pedro, Hyun R Ryu, Noo Li Jeon, Anne M Taylor, Ramiro D Almeida

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. The tyrosine phosphatase STEP is a developmental suppressor of synaptogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  8. The Ubiquitinated Axon: Local Control of Axon Development and Function by Ubiquitin.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Maria J PintoCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal PhD Program in Experimental Biology and Biomedicine, Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal.
Pedro L AlvesInstituto de Educação e Cidadania, 3770-033 Mamarrosa, Portugal.
Luís MartinsCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal.
Joana R PedroCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal.
Hyun R RyuInstitute of Advanced Machinery and Design, Seoul National University, Seoul 151-744, Korea.
Noo Li JeonInstitute of Advanced Machinery and Design, Seoul National University, Seoul 151-744, Korea Department of Mechanical and Aerospace Engineering, Seoul National University, Seoul 151-744, Korea.
Anne M TaylorJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill, NC 27599.
Ramiro D AlmeidaCNC - Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal Institute for Interdisciplinary Research, University of Coimbra, 3004-517 Coimbra, Portugal School of Allied Health Technologies, Polytechnic Institute of Porto, 4400-330 Vila Nova de Gaia, Portugal ramirodalmeida@gmail.com.
University of Coimbra · PTSeoul National University · KRInstituto Superior de Educação e Ciências · PTNorth Carolina State University · US

Funding

UNC Neuroscience Center Research Cores: MicroscopyP30NS045892 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZYLKA, MARK J. · 2003 to 2022
$11.5M
A user-friendly scalable microfluidic platform for enhanced neuron-cell cultureR42MH097377 · NIMH · XONA MICROFLUIDICS, LLC · PI TAYLOR, ANNE MARION · 2016 to 2018
$2.0M
A user-friendly scalable microfluidic platform for enhanced neuron-cell cultureR41MH097377 · NIMH · XONA MICROFLUIDICS, LLC · PI TAYLOR, ANNE MARION · 2013 to 2014
$679k
NIMH NIH HHS R41 MH097377NIMH NIH HHS R42 MH097377NINDS NIH HHS P30 NS045892
6 · The paper itself

Abstract

Differentiation of the presynaptic terminal is a complex and rapid event that normally occurs in spatially specific axonal regions distant from the soma; thus, it is believed to be dependent on intra-axonal mechanisms. However, the full nature of the local events governing presynaptic assembly remains unknown. Herein, we investigated the involvement of the ubiquitin-proteasome system (UPS), the major degradative pathway, in the local modulation of presynaptic differentiation. We found that proteasome inhibition has a synaptogenic effect on isolated axons. In addition, formation of a stable cluster of synaptic vesicles onto a postsynaptic partner occurs in parallel to an on-site decrease in proteasome degradation. Accumulation of ubiquitinated proteins at nascent sites is a local trigger for presynaptic clustering. Finally, proteasome-related ubiquitin chains (K11 and K48) function as signals for the assembly of presynaptic terminals. Collectively, we propose a new axon-intrinsic mechanism for presynaptic assembly through local UPS inhibition. Subsequent on-site accumulation of proteins in their polyubiquitinated state triggers formation of presynapses.

Indexed as

Cell DifferentiationHippocampusPolyubiquitinPresynaptic TerminalsProteasome Endopeptidase ComplexUbiquitinated ProteinsAnimalsAxonsCells, CulturedLuminescent ProteinsMicroscopy, FluorescenceProteasome InhibitorsProteolysisRats, WistarRecombinant Fusion ProteinsSignal TransductionLuminescent ProteinsPolyubiquitinProteasome Endopeptidase ComplexProteasome InhibitorsRecombinant Fusion ProteinsUbiquitinated Proteins

Identifiers

PMID27022091
PMCPMC4810304
OpenAlexW2329349916

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.