Evidence map›Paper›PMID 30680309›Full record

ArticleeNeuro

Neuron-Specific Gene 2 (NSG2) Encodes an AMPA Receptor Interacting Protein That Modulates Excitatory Neurotransmission.

Praveen Chander, Matthew J Kennedy, Bettina Winckler, Jason P Weick

Open access · goldAbstract read
In one paragraph

Article in eNeuro. 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
1.8field-weighted citation impact, top 17% 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, 41 citations in OpenAlex.

  1. Article
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  5. The protein interactome of the Neuron Specific Gene family (NSG1-3).bioRxiv : the preprint server for biology · 2025
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  11. Nutrients · 2024
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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 3 institutions in 1 country.

Praveen ChanderDepartment of Neurosciences, University of New Mexico-Health Science Center, Albuquerque, NM 87131.
Matthew J KennedyDepartment of Pharmacology, University of Colorado-Denver, Aurora, CO 80045.ORCID 0000-0002-7029-7802
Bettina WincklerDepartment of Cell Biology, University of Virginia, Charlottesville, VA 22908.ORCID 0000-0002-7924-9313
Jason P WeickDepartment of Neurosciences, University of New Mexico-Health Science Center, Albuquerque, NM 87131.ORCID 0000-0003-3135-9860
University of New Mexico · USUniversity of Colorado Denver · USUniversity of Virginia · US

Funding

University of New Mexico (UNM) Center for Brain Recovery and RepairP20GM109089 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI SHUTTLEWORTH, CLAUDE W · 2015 to 2024
$22.7M
Mechanisms of dendritic exocytosisR01NS082271 · NINDS · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2013 to 2017
$1.7M
Light-based regulation of autophagy processing to target pathological forms of tauR21NS093442 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BHASKAR, KIRAN, WEICK, JASON P · 2016 to 2017
$417k
NIGMS NIH HHS P20 GM109089NINDS NIH HHS R01 NS082271
6 · The paper itself

Abstract

Neurons have evolved a number of unique protein-coding genes that regulate trafficking of protein complexes within small organelles throughout dendrites and axons. Neuron-specific gene 2 (NSG2) encodes for one of the most abundant proteins in the nervous system during perinatal development. NSG2 belongs to a family of small neuronal endosomal proteins but its function has remained uncharacterized to date. Here, we show that NSG2 is found in discrete punctae restricted to the somatodendritic arbors of developing mouse and human neurons, and a significant proportion of NSG2 punctae colocalize with postsynaptic HOMER1 and surface-expressed AMPA-type glutamate receptors (AMPARs) at excitatory synapses. Immunoprecipitation revealed that NSG2 physically interacts with both the GluA1 and GluA2 AMPAR subunits in mouse brain. Knock-out of NSG2 in mouse hippocampal neurons selectively impaired the frequency of miniature EPSCs (mEPSCs) and caused alterations in PSD95 expression at postsynaptic densities (PSDs). In contrast, NSG2 overexpression caused a significant increase in the amplitude of mEPSCs as well as GluA2 surface expression. Thus, NSG2 functions as an AMPAR-binding protein that is required for normal synapse formation and/or maintenance, and has unique functions compared with other NSG family members.

Indexed as

AnimalsCarrier ProteinsCell Line, TumorGene ExpressionGene Knockout TechniquesHEK293 CellsHippocampusHomer Scaffolding ProteinsHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsMice, Inbred C57BLNerve Tissue ProteinsNeuronsPatch-Clamp TechniquesReceptors, AMPACarrier ProteinsHomer1 protein, mouseHomer Scaffolding ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsNerve Tissue ProteinsNSG2 protein, humanNsg2 protein, mouseReceptors, AMPAAMPARendosomeHMP19humansynaptogenesistrafficking

Identifiers

PMID30680309
PMCPMC6345199
OpenAlexW2907888820

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.