Evidence map›Paper›PMID 19433455›Full record

ArticleThe Journal of cell biology2009

Regulation of glutamate receptor subunit availability by microRNAs.

Julie Karr, Vasia Vagin, Kaiyun Chen, Subhashree Ganesan, Oxana Olenkina, Vladimir Gvozdev, David E Featherstone

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.5field-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

34 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Human Brain Injury and miRNAs: An Experimental Study.International journal of molecular sciences · 2019
    Article
  5. Article
  6. Cereblon Maintains Synaptic and Cognitive Function by Regulating BK Channel.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  7. Article
  8. The interplay of microRNAs and post-ischemic glutamate excitotoxicity: an emergent research field in stroke medicine.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2016
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. MicroRNAs in neuronal communication.Molecular neurobiology · 2014
    Review
  19. Review
  20. Review
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

7 authors at 2 institutions in 2 countries.

Julie KarrBiological Sciences, University of Illinois at Chicago, Chicago, IL 60607, USA.
Vasia Vagin
Kaiyun Chen
Subhashree Ganesan
Oxana Olenkina
Vladimir Gvozdev
David E Featherstone
University of Illinois Chicago · USInstitute of Molecular Genetics · RU

Funding

Molecular basis of glutamate receptor field formationR01NS045628 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FEATHERSTONE, DAVID E · 2003 to 2006
$1.3M
NINDS NIH HHS R01 NS045628NINDS NIH HHS R01NS045628
6 · The paper itself

Abstract

The efficacy of synaptic transmission depends, to a large extent, on postsynaptic receptor abundance. The molecular mechanisms controlling receptor abundance are poorly understood. We tested whether abundance of postsynaptic glutamate receptors (GluRs) in Drosophila neuromuscular junctions is controlled by microRNAs, and provide evidence that it is. We show here that postsynaptic knockdown of dicer-1, the endoribonuclease necessary for microRNA synthesis, leads to large increases in postsynaptic GluR subunit messenger RNA and protein. Specifically, we measured increases in GluRIIA and GluRIIB but not GluRIIC. Further, knockout of MiR-284, a microRNA predicted to bind to GluRIIA and GluRIIB but not GluRIIC, increases expression of GluRIIA and GluRIIB but not GluRIIC proportional to the number of predicted binding sites in each transcript. Most of the de-repressed GluR protein, however, does not appear to be incorporated into functional receptors, and only minor changes in synaptic strength are observed, which suggests that microRNAs primarily regulate Drosophila receptor subunit composition rather than overall receptor abundance or synaptic strength.

Indexed as

AnimalsDrosophilaDrosophila ProteinsMicroRNAsProtein SubunitsReceptors, GlutamateRibonuclease IIIRNA HelicasesRNA, MessengerSynapsesDcr-1 protein, DrosophilaDrosophila ProteinsMicroRNAsProtein SubunitsReceptors, GlutamateRibonuclease IIIRNA HelicasesRNA, Messenger

Identifiers

PMID19433455
PMCPMC2711579
OpenAlexW2071588351

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.