Evidence map›Paper›PMID 24523912›Full record

ArticlePloS one2014

Subcellular sorting of the G-protein coupled mouse somatostatin receptor 5 by a network of PDZ-domain containing proteins.

Carola Bauch, Judith Koliwer, Friedrich Buck, Hans-Hinrich Hönck, Hans-Jürgen Kreienkamp

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Spatial encoding of GPCR signaling in the nervous system.Current opinion in cell biology · 2019
    Review
  8. GIRK currents in VTA dopamine neurons control the sensitivity of mice to cocaine-induced locomotor sensitization.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  9. Review
  10. Article
  11. G Protein-Gated Potassium Channels: A Link to Drug Addiction.Trends in pharmacological sciences · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. VPS26A-SNX27 Interaction-Dependent mGluR5 Recycling in Dorsal Horn Neurons Mediates Neuropathic Pain in Rats.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. A unique PDZ domain and arrestin-like fold interaction reveals mechanistic details of endocytic recycling by SNX27-retromer.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

5 authors at 2 institutions in 1 country.

Carola BauchInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Judith KoliwerInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Friedrich BuckInstitut für klinische Chemie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Hans-Hinrich HönckInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Hans-Jürgen KreienkampInstitut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Universität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PSD-95/discs large/ZO-1 (PDZ) domain proteins integrate many G-protein coupled receptors (GPCRs) into membrane associated signalling complexes. Additional PDZ proteins are involved in intracellular receptor trafficking. We show that three PDZ proteins (SNX27, PIST and NHERF1/3) regulate the mouse somatostatin receptor subtype 5 (SSTR5). Whereas the PDZ ligand motif of SSTR5 is not necessary for plasma membrane targeting or internalization, it protects the SSTR5 from postendocytic degradation. Under conditions of lysosomal inhibition, recycling of the SSTR5 to the plasma membrane does not depend on the PDZ ligand. However, recycling of the wild type receptor carrying the PDZ binding motif depends on SNX27 which interacts and colocalizes with the receptor in endosomal compartments. PIST, implicated in lysosomal targeting of some membrane proteins, does not lead to degradation of the SSTR5. Instead, overexpressed PIST retains the SSTR5 at the Golgi. NHERF family members release SSTR5 from retention by PIST, allowing for plasma membrane insertion. Our data suggest that PDZ proteins act sequentially on the GPCR at different stages of its subcellular trafficking.

Indexed as

Gene Expression RegulationAdaptor Proteins, Signal TransducingAmino Acid MotifsAnimalsBiotinylationCarrier ProteinsCell MembraneEndocytosisEndosomesGolgi ApparatusGolgi Matrix ProteinsHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsLigandsMiceAdaptor Proteins, Signal TransducingCarrier ProteinsGolgi Matrix ProteinsGopc protein, mouseIntracellular Signaling Peptides and ProteinsLigandsPhosphoproteinsReceptors, SomatostatinSnx27 protein, mousesodium-hydrogen exchanger regulatory factorSodium-Hydrogen Exchangerssomatostatin receptor 5Sorting Nexins

Identifiers

PMID24523912
PMCPMC3921201
OpenAlexW2061004371

What Socratic 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 Socratic graph.