Evidence map›Paper›PMID 15470145›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Developmentally regulated switch in alternatively spliced SNAP-25 isoforms alters facilitation of synaptic transmission.

Christina Bark, Frederick P Bellinger, Ashutosh Kaushal, James R Mathews, L Donald Partridge, Michael C Wilson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 12% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Isoswitching drives the aging process in human brains.bioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Article
  5. Understanding the molecular diversity of synapses.Nature reviews. Neuroscience · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. GPCR regulation of secretion.Pharmacology & therapeutics · 2018
    Review
  14. Review
  15. Review
  16. A Multilevel Functional Study of aThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  17. Article
  18. Article
  19. The neurogenetics of alternative splicing.Nature reviews. Neuroscience · 2016
    Review
  20. Membrane Trafficking in Neuronal Development: Ins and Outs of Neural Connectivity.International review of cell and molecular biology · 2016
    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

6 authors at 2 institutions in 2 countries.

Christina BarkDepartment of Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, SE-171 76 Stockholm, Sweden.
Frederick P Bellinger
Ashutosh Kaushal
James R Mathews
L Donald Partridge
Michael C Wilson
University of New Mexico · USKarolinska University Hospital · SE

Funding

SNAP-25 EXPRESSION AND HYPERACTIVITY IN COLOBOMA MICER01MH048989 · NIMH · UNIVERSITY OF NEW MEXICO · PI WILSON, MICHAEL COLIN · 1992 to 2008
$2.7M
NIMH NIH HHS MH48989NIMH NIH HHS R01 MH048989
6 · The paper itself

Abstract

Although the basic molecular components that promote regulated neurotransmitter release are well established, the contribution of these proteins as regulators of the plasticity of neurotransmission and refinement of synaptic connectivity during development is elaborated less fully. For example, during the period of synaptic growth and maturation in brain, the expression of synaptosomal protein 25 kDa (SNAP-25), a neuronal t-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) essential for action potential-dependent neuroexocytosis, is altered through alternative splicing of pre-mRNA transcripts. We addressed the role of the two splice-variant isoforms of SNAP-25 with a targeted mouse mutation that impairs the shift from SNAP-25a to SNAP-25b. Most of these mutant mice die between 3 and 5 weeks of age, which coincides with the time when SNAP-25b expression normally reaches mature levels in brain and synapse formation is essentially completed. The altered expression of these SNAP-25 isoforms influences short-term synaptic function by affecting facilitation but not the initial probability of release. This suggests that mechanisms controlling alternative splicing between SNAP-25 isoforms contribute to a molecular switch important for survival that helps to guide the transition from immature to mature synaptic connections, as well as synapse regrowth and remodeling after neural injury.

Indexed as

Alternative SplicingSynaptic TransmissionAnimalsGene Expression Regulation, DevelopmentalGene TargetingHippocampusIntegrasesMembrane ProteinsMiceMice, Mutant StrainsNerve Tissue ProteinsNeuronal PlasticityNeuronsPatch-Clamp TechniquesPhenotypeProtein IsoformsIntegrasesMembrane ProteinsNerve Tissue ProteinsProtein IsoformsSnap25 protein, mouseSynaptosomal-Associated Protein 25

Identifiers

PMID15470145
PMCPMC6729955
OpenAlexW1967517418

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.