Evidence map›Paper›PMID 26987116›Full record

ArticlePloS one2016

The Extracellular and Cytoplasmic Domains of Syndecan Cooperate Postsynaptically to Promote Synapse Growth at the Drosophila Neuromuscular Junction.

Margaret U Nguyen, Jereen Kwong, Julia Chang, Victoria G Gillet, Rachel M Lee, Karl Gregory Johnson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Type IIa RPTPs and Glycans: Roles in Axon Regeneration and Synaptogenesis.International journal of molecular sciences · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Diverse roles for glycosaminoglycans in neural patterning.Developmental dynamics : an official publication of the American Association of Anatomists · 2018
    Review
  11. Review
  12. 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 1 institution in 1 country.

Margaret U NguyenNeuroscience Department, Pomona College, Claremont, California, United States of America.
Jereen KwongMolecular Biology Program, Pomona College, Claremont, California, United States of America.
Julia ChangMolecular Biology Program, Pomona College, Claremont, California, United States of America.
Victoria G GilletNeuroscience Department, Pomona College, Claremont, California, United States of America.
Rachel M LeeNeuroscience Department, Pomona College, Claremont, California, United States of America.
Karl Gregory JohnsonMolecular Biology Program, Pomona College, Claremont, California, United States of America.
Pomona College · US

Funding

Characterizing the function of Syndecan during CNS developmentR15NS065433 · NINDS · POMONA COLLEGE · PI JOHNSON, KARL GREGORY · 2009 to 2009
$51k
NINDS NIH HHS 1R15NS065433-01NINDS NIH HHS R15 NS065433
6 · The paper itself

Abstract

The heparan sulfate proteoglycan (HSPG) Syndecan (Sdc) is a crucial regulator of synapse development and growth in both vertebrates and invertebrates. In Drosophila, Sdc binds via its extracellular heparan sulfate (HS) sidechains to the receptor protein tyrosine phosphatase LAR to promote the morphological growth of the neuromuscular junction (NMJ). To date, however, little else is known about the molecular mechanisms by which Sdc functions to promote synapse growth. Here we show that all detectable Sdc found at the NMJ is provided by the muscle, strongly suggesting a post-synaptic role for Sdc. We also show that both the cytoplasmic and extracellular domains of Sdc are required to promote synapse growth or to rescue Sdc loss of function. We report the results of a yeast two-hybrid screen using the cytoplasmic domains of Sdc as bait, and identify several novel candidate binding partners for the cytoplasmic domains of Sdc. Together, these studies provide new insight into the mechanism of Sdc function at the NMJ, and provide enticing future directions for further exploring how Sdc promotes synapse growth.

Indexed as

AnimalsDrosophilaDrosophila ProteinsMuscle, SkeletalNeuromuscular JunctionSynapsesSynaptic TransmissionSyndecansDrosophila ProteinsSyndecans

Identifiers

PMID26987116
PMCPMC4795781
OpenAlexW2309560234

What OpenQuestion 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 OpenQuestion graph.