Evidence map›Paper›PMID 17363264›Full record

ArticleMolecular and cellular neurosciences2007

The ubiquitin-proteasome system postsynaptically regulates glutamatergic synaptic function.

Kevin F Haas, Stephanie L H Miller, David B Friedman, Kendal Broadie

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Identification of secretory autophagy as a mechanism modulating activity-induced synaptic remodeling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Review
  4. Article
  5. Cell Clearing Systems Bridging Neuro-Immunity and Synaptic Plasticity.International journal of molecular sciences · 2019
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Drosophila-Cdh1 (Rap/Fzr) a regulatory subunit of APC/C is required for synaptic morphology, synaptic transmission and locomotion.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2013
    Article
  12. Review
  13. Article
  14. Proteasome inhibition leads to early loss of synaptic proteins in neuronal culture.Journal of neural transmission (Vienna, Austria : 1996) · 2012
    Article
  15. Article
  16. Article
  17. Article
  18. Ubiquitination in postsynaptic function and plasticity.Annual review of cell and developmental biology · 2010
    Review
  19. Article
  20. Na,K-ATPase activity regulates AMPA receptor turnover through proteasome-mediated proteolysis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    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

4 authors at 2 institutions in 1 country.

Kevin F HaasDepartment of Neurology, Vanderbilt University, Nashville, TN 37235-1634, USA. kevin.haas@vanderbilt.edu
Stephanie L H Miller
David B Friedman
Kendal Broadie
Vanderbilt University · USJohn F. Kennedy Center for the Performing Arts · US

Funding

Synaptic Mechnisms in Drosophila Neurodegeneration ModelR01NS041740 · NINDS · VANDERBILT UNIVERSITY · PI BROADIE, KENDAL · 2001 to 2009
$3.2M
Ubiquitin proteasome sytem regulation of synaptic fuctionK08NS048882 · NINDS · VANDERBILT UNIVERSITY · PI HAAS, KEVIN F · 2006 to 2010
$826k
NINDS NIH HHS K08 NS048882NINDS NIH HHS NS048882-01NINDS NIH HHS NS41740NINDS NIH HHS R01 NS041740
6 · The paper itself

Abstract

The ubiquitin-proteasome system (UPS) actively controls protein dynamics and local abundance via regulated protein degradation. This study investigates UPS' roles in the regulation of postsynaptic function and molecular composition in the Drosophila neuromuscular junction (NMJ) genetic system. To specifically impair UPS function postsynaptically, the UAS/GAL4 transgenic method was employed to drive postsynaptic expression of proteasome beta2 and beta6 subunit mutant proteins, which operate through a dominant negative mechanism to block proteasome function. When proteasome mutant subunits were constitutively expressed, excitatory junctional current (EJC) amplitudes were increased, demonstrating that postsynaptic proteasome function limits neurotransmission strength. Interestingly, the alteration in synaptic strength was calcium-dependent and miniature EJCs had significantly smaller mean amplitudes and more rapid mean decay rates. Postsynaptic levels of the Drosophila PSD-95/SAP97 homologue, discs large (DLG), and the GluRIIB-containing glutamate receptor were increased, but GluRIIA-containing receptors were unaltered. With acute postsynaptic proteasome inhibition using an inducible transgenic system, neurotransmission was similarly elevated with the same specific increase in postsynaptic GluRIIB abundance. These findings demonstrate postsynaptic proteasome regulation of glutamatergic synaptic function that is mediated through specific regulation of GluRIIB-containing glutamate receptors.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsDiscs Large Homolog 1 ProteinDrosophilaDrosophila ProteinsGlutamic AcidMembrane ProteinsNeuromuscular JunctionProteasome Endopeptidase ComplexProteomicsReceptors, GlutamateSynapsesTumor Suppressor ProteinsUbiquitinAdaptor Proteins, Signal TransducingDiscs Large Homolog 1 Proteindlg1 protein, DrosophilaDLG1 protein, humanDrosophila ProteinsGlutamic AcidMembrane ProteinsProteasome Endopeptidase ComplexReceptors, GlutamateTumor Suppressor ProteinsUbiquitin

Identifiers

PMID17363264
PMCPMC1936977
OpenAlexW2037017587

What OpenQuestion holds

Textmetadata
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.