Evidence map›Paper›PMID 26359495›Full record

ArticleThe Journal of biological chemistry2015

The Q-soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Q-SNARE) SNAP-47 Regulates Trafficking of Selected Vesicle-associated Membrane Proteins (VAMPs).

Aurelia Kuster, Sebastien Nola, Florent Dingli, Barbara Vacca, Christian Gauchy, Jean-Claude Beaujouan, Marcela Nunez, Thomas Moncion, Damarys Loew, Etienne Formstecher and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  10. siRNA screening reveals that SNAP29 contributes to exosome release.Cellular and molecular life sciences : CMLS · 2023
    Article
  11. Intercellular transfer of miR-200c-3p impairs the angiogenic capacity of cardiac endothelial cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
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  19. Soluble syntaxin 3 functions as a transcriptional regulator.The Journal of biological chemistry · 2018
    Article
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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

12 authors at 6 institutions in 1 country.

Aurelia KusterMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Sebastien NolaMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Florent DingliProtein Mass Spectrometry Laboratory, Institut Curie, 75005 Paris.
Barbara VaccaMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Christian GauchyMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Jean-Claude BeaujouanMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Marcela NunezHybrigenics, 3-5 Impasse Reille, 75014 Paris, France.
Thomas MoncionHybrigenics, 3-5 Impasse Reille, 75014 Paris, France.
Damarys LoewProtein Mass Spectrometry Laboratory, Institut Curie, 75005 Paris.
Etienne FormstecherHybrigenics, 3-5 Impasse Reille, 75014 Paris, France.
Thierry GalliMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris. Electronic address: thierry.galli@inserm.fr.
Veronique Proux-GillardeauxMembrane Traffic in Health and Disease, INSERM U950, CNRS, UMR 7592, Institut Jacques Monod, Université Paris Diderot, Sorbonne Paris Cité, F-75013 Paris.
Université Paris Cité · FRHybrigenics (France) · FRInserm · FRInstitut Curie · FRInstitut Jacques Monod · FRProtéomique, Réponse Inflammatoire et Spectrométrie de Masse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SNAREs constitute the core machinery of intracellular membrane fusion, but vesicular SNAREs localize to specific compartments via largely unknown mechanisms. Here, we identified an interaction between VAMP7 and SNAP-47 using a proteomics approach. We found that SNAP-47 mainly localized to cytoplasm, the endoplasmic reticulum (ER), and ERGIC and could also shuttle between the cytoplasm and the nucleus. SNAP-47 preferentially interacted with the trans-Golgi network VAMP4 and post-Golgi VAMP7 and -8. SNAP-47 also interacted with ER and Golgi syntaxin 5 and with syntaxin 1 in the absence of Munc18a, when syntaxin 1 is retained in the ER. A C-terminally truncated SNAP-47 was impaired in interaction with VAMPs and affected their subcellular distribution. SNAP-47 silencing further shifted the subcellular localization of VAMP4 from the Golgi apparatus to the ER. WT and mutant SNAP-47 overexpression impaired VAMP7 exocytic activity. We conclude that SNAP-47 plays a role in the proper localization and function of a subset of VAMPs likely via regulation of their transport through the early secretory pathway.

Indexed as

AnimalsDogsMadin Darby Canine Kidney CellsProtein TransportQ-SNARE ProteinsR-SNARE ProteinsSubcellular FractionsQ-SNARE ProteinsR-SNARE ProteinsERGICmembrane fusionmembrane traffickingnuclear translocationprotein secretionSNAP-47SNARE proteinsVAMPvesicles

Identifiers

PMID26359495
PMCPMC4653666
OpenAlexW1839422703

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.