Evidence map›Paper›PMID 9362510›Full record

ArticleThe Journal of cell biology1997

Targeting of the synaptic vesicle protein synaptobrevin in the axon of cultured hippocampal neurons: evidence for two distinct sorting steps.

A E West, R L Neve, K M Buckley

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-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

21 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
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  9. Article
  10. Polarized targeting of ion channels in neurons.Pflugers Archiv : European journal of physiology · 2007
    Review
  11. Factors regulating the abundance and localization of synaptobrevin in the plasma membrane.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  12. Targeting mechanisms of high voltage-activated Ca2+ channels.Journal of bioenergetics and biomembranes · 2003
    Review
  13. Article
  14. Review
  15. Alternative splicing unmasks dendritic and axonal targeting signals in metabotropic glutamate receptor 1.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  16. Article
  17. A conserved mechanism of synaptogyrin localization.Molecular biology of the cell · 2001
    Article
  18. Clinical mutations in the L1 neural cell adhesion molecule affect cell-surface expression.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
    Article
  19. Review
  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

3 authors at 2 institutions in 1 country.

A E WestDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.
R L Neve
K M Buckley
McLean Hospital · USHarvard University · US

Funding

EXPRESSION OF SYNAPTIC VESICLE PROTEINSR01NS027536 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BUCKLEY, KATHLEEN M · 1991 to 1999
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DEVELOPMENTAL NEUROLOGYT32NS007009 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BUCKLEY, KATHLEEN M · 1985 to 1999
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NINDS NIH HHS 2 T32 NS07009-21NINDS NIH HHS NS27536NINDS NIH HHS T32 NS007009
6 · The paper itself

Abstract

Synaptic vesicles are concentrated in the distal axon, far from the site of protein synthesis. Integral membrane proteins destined for this organelle must therefore make complex targeting decisions. Short amino acid sequences have been shown to act as targeting signals directing proteins to a variety of intracellular locations. To identify synaptic vesicle targeting sequences and to follow the path that proteins travel en route to the synaptic vesicle, we have used a defective herpes virus amplicon expression system to study the targeting of a synaptobrevin-transferrin receptor (SB-TfR) chimera in cultured hippocampal neurons. Addition of the cytoplasmic domain of synaptobrevin onto human transferrin receptor was sufficient to retarget the transferrin receptor from the dendrites to presynaptic sites in the axon. At the synapse, the SB-TfR chimera did not localize to synaptic vesicles, but was instead found in an organelle with biochemical and functional characteristics of an endosome. The chimera recycled in parallel with synaptic vesicle proteins demonstrating that the nerve terminal efficiently sorts transmembrane proteins into different pathways. The synaptobrevin sequence that controls targeting to the presynaptic endosome was not localized to a single, 10- amino acid region of the molecule, indicating that this targeting signal may be encoded by a more distributed structural conformation. However, the chimera could be shifted to synaptic vesicles by deletion of amino acids 61-70 in synaptobrevin, suggesting that separate signals encode the localization of synaptobrevin to the synapse and to the synaptic vesicle.

Indexed as

AnimalsAxonsCell CompartmentationCell PolarityCells, CulturedEndosomesHippocampusMembrane ProteinsRatsReceptors, TransferrinRecombinant Fusion ProteinsR-SNARE ProteinsSynapsesSynaptic VesiclesMembrane ProteinsReceptors, TransferrinRecombinant Fusion ProteinsR-SNARE Proteins

Identifiers

PMID9362510
PMCPMC2139969
OpenAlexW1980548298

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.