Evidence map›Paper›PMID 25329901›Full record

ArticlePLoS genetics2014

The vesicle protein SAM-4 regulates the processivity of synaptic vesicle transport.

Qun Zheng, Shikha Ahlawat, Anneliese Schaefer, Tim Mahoney, Sandhya P Koushika, Michael L Nonet

Abstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
  2. Kinesins inOpen biology · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
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  14. Review
  15. Imaging Intracellular Trafficking in Neurons of C. elegans.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  16. Article
  17. Article
  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

6 authors.

Qun ZhengDepartment of Anatomy and Neurobiology, Washington University Medical School, St. Louis, Missouri, United States of America.
Shikha AhlawatNational Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, India.
Anneliese SchaeferDepartment of Anatomy and Neurobiology, Washington University Medical School, St. Louis, Missouri, United States of America; Department of Neurology, Washington University Medical School, St. Louis, Missouri, United States of America.
Tim MahoneyDepartment of Anatomy and Neurobiology, Washington University Medical School, St. Louis, Missouri, United States of America; Huffington Center On Aging, Baylor College of Medicine, Houston, Texas, United States of America.
Sandhya P KoushikaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Colaba, Mumbai, India.
Michael L NonetDepartment of Anatomy and Neurobiology, Washington University Medical School, St. Louis, Missouri, United States of America.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
MOLECULAR GENETIC ANALYSIS OF DEVELOPING SYNAPSESR01NS040094 · NINDS · WASHINGTON UNIVERSITY · PI NONET, MICHAEL L · 2000 to 2018
$4.0M
MOLECULAR GENETIC ANALYSIS OF DEVELOPING SYNAPSESR56NS040094 · NINDS · WASHINGTON UNIVERSITY · PI NONET, MICHAEL L · 2012 to 2012
$380k
Howard Hughes Medical InstituteNIH HHS P40 OD010440NINDS NIH HHS NS 040094NINDS NIH HHS R01 NS040094NINDS NIH HHS R56 NS040094
6 · The paper itself

Abstract

Axonal transport of synaptic vesicles (SVs) is a KIF1A/UNC-104 mediated process critical for synapse development and maintenance yet little is known of how SV transport is regulated. Using C. elegans as an in vivo model, we identified SAM-4 as a novel conserved vesicular component regulating SV transport. Processivity, but not velocity, of SV transport was reduced in sam-4 mutants. sam-4 displayed strong genetic interactions with mutations in the cargo binding but not the motor domain of unc-104. Gain-of-function mutations in the unc-104 motor domain, identified in this study, suppress the sam-4 defects by increasing processivity of the SV transport. Genetic analyses suggest that SAM-4, SYD-2/liprin-α and the KIF1A/UNC-104 motor function in the same pathway to regulate SV transport. Our data support a model in which the SV protein SAM-4 regulates the processivity of SV transport.

Indexed as

AnimalsAnimals, Genetically ModifiedAxonal TransportBinding SitesCaenorhabditis elegansCaenorhabditis elegans ProteinsIntercellular Signaling Peptides and ProteinsMembrane ProteinsMutationNerve Tissue ProteinsNeuritesNeuronsPhosphoproteinsSynaptic VesiclesCaenorhabditis elegans ProteinsIntercellular Signaling Peptides and ProteinsMembrane ProteinsNerve Tissue ProteinsPhosphoproteinsSAM-4 protein, C elegansSYD-2 protein, C elegansUNC-104 protein, C elegans

Identifiers

PMID25329901
PMCPMC4199485

What OpenQuestion holds

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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 OpenQuestion graph.