Evidence map›Paper›PMID 25905467›Full record

ArticlePLoS genetics2015

Neto-mediated intracellular interactions shape postsynaptic composition at the Drosophila neuromuscular junction.

Cathy I Ramos, Oghomwen Igiesuorobo, Qi Wang, Mihaela Serpe

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. 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
1.0field-weighted citation impact, top 29% 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. Article
  2. Nonionic signaling rapidly remodels postsynaptic DLG to induce retrograde homeostatic plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Neto proteins differentially modulate the gating properties ofbioRxiv : the preprint server for biology · 2024
    Article
  7. Rapid homeostatic modulation of transsynaptic nanocolumn rings.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. The auxiliary glutamate receptor subunit dSol-1 promotes presynaptic neurotransmitter release and homeostatic potentiation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Vps54 regulatesBiology open · 2020
    Article
  17. Review
  18. Article
  19. Article
  20. 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 1 institution in 1 country.

Cathy I RamosProgram in Cellular Regulation and Metabolism, NICHD, NIH, Bethesda, Maryland, United States of America.
Oghomwen IgiesuoroboProgram in Cellular Regulation and Metabolism, NICHD, NIH, Bethesda, Maryland, United States of America.
Qi WangProgram in Cellular Regulation and Metabolism, NICHD, NIH, Bethesda, Maryland, United States of America.
Mihaela SerpeProgram in Cellular Regulation and Metabolism, NICHD, NIH, Bethesda, Maryland, United States of America.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Mechanisms of synapse developmentZIAHD008914 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI SERPE, MIHAELA · 2011 to 2025
$16.4M
Modulation of TGF-beta signalingZIAHD008869 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI SERPE, MIHAELA · 2009 to 2025
$8.0M
Intramural NIH HHS ZIA HD008869Intramural NIH HHS ZIA HD008914NICHD NIH HHS HD008869 05NICHD NIH HHS HD008914 03
6 · The paper itself

Abstract

The molecular mechanisms controlling the subunit composition of glutamate receptors are crucial for the formation of neural circuits and for the long-term plasticity underlying learning and memory. Here we use the Drosophila neuromuscular junction (NMJ) to examine how specific receptor subtypes are recruited and stabilized at synaptic locations. In flies, clustering of ionotropic glutamate receptors (iGluRs) requires Neto (Neuropillin and Tolloid-like), a highly conserved auxiliary subunit that is essential for NMJ assembly and development. Drosophila neto encodes two isoforms, Neto-α and Neto-β, with common extracellular parts and distinct cytoplasmic domains. Mutations that specifically eliminate Neto-β or its intracellular domain were generated. When Neto-β is missing or is truncated, the larval NMJs show profound changes in the subtype composition of iGluRs due to reduced synaptic accumulation of the GluRIIA subunit. Furthermore, neto-β mutant NMJs fail to accumulate p21-activated kinase (PAK), a critical postsynaptic component implicated in the synaptic stabilization of GluRIIA. Muscle expression of either Neto-α or Neto-β rescued the synaptic transmission at neto null NMJs, indicating that Neto conserved domains mediate iGluRs clustering. However, only Neto-β restored PAK synaptic accumulation at neto null NMJs. Thus, Neto engages in intracellular interactions that regulate the iGluR subtype composition by preferentially recruiting and/or stabilizing selective receptor subtypes.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsGene Expression Regulation, DevelopmentalLarvaMembrane ProteinsNeuromuscular Junctionp21-Activated KinasesProtein IsoformsReceptors, Ionotropic GlutamateSynapsesSynaptic TransmissionDrosophila ProteinsMembrane ProteinsNeto protein, Drosophilap21-Activated KinasesPak protein, DrosophilaProtein IsoformsReceptors, Ionotropic Glutamate

Identifiers

PMID25905467
PMCPMC4408064
OpenAlexW2009458678

What OpenQuestion holds

Textmetadata
LicenceCC0
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.