Evidence map›Paper›PMID 35100385›Full record

ArticleG3 (Bethesda, Md.)2022

A conditional glutamatergic synaptic vesicle marker for Drosophila.

Sarah J Certel, Evelyne Ruchti, Brian D McCabe, R Steven Stowers

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. 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
1.2field-weighted citation impact, top 25% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Constitutive and Conditional Epitope Tagging of Endogenous G-Protein-Coupled Receptors inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
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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

4 authors at 3 institutions in 2 countries.

Sarah J CertelDivision of Biological Sciences, Center for Structural and Functional Neuroscience, The University of Montana, Missoula, MT 59812, USA.ORCID 0000-0003-2039-2657
Evelyne RuchtiBrain Mind Institute, Swiss Federal Institute of Technology (EPFL), Lausanne VD 1015, Switzerland.ORCID 0000-0003-1211-2336
Brian D McCabeBrain Mind Institute, Swiss Federal Institute of Technology (EPFL), Lausanne VD 1015, Switzerland.ORCID 0000-0003-1620-0501
R Steven StowersDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, MT 59717, USA.ORCID 0000-0002-1473-2478
École Polytechnique Fédérale de Lausanne · CHMontana State University · USUniversity of Montana · US

Funding

Functional role of dual neurotransmitter usage in aggressionR01GM115510 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI Sarah J Certel, Karla R. Kaun · 2015 to 2026
$3.1M
NIGMS NIH HHS R01 GM115510
6 · The paper itself

Abstract

Glutamate is a principal neurotransmitter used extensively by the nervous systems of all vertebrate and invertebrate animals. It is primarily an excitatory neurotransmitter that has been implicated in nervous system development, as well as a myriad of brain functions from the simple transmission of information between neurons to more complex aspects of nervous system function including synaptic plasticity, learning, and memory. Identification of glutamatergic neurons and their sites of glutamate release are thus essential for understanding the mechanisms of neural circuit function and how information is processed to generate behavior. Here, we describe and characterize smFLAG-vGlut, a conditional marker of glutamatergic synaptic vesicles for the Drosophila model system. smFLAG-vGlut is validated for functionality, conditional expression, and specificity for glutamatergic neurons and synaptic vesicles. The utility of smFLAG-vGlut is demonstrated by glutamatergic neurotransmitter phenotyping of 26 different central complex neuron types of which nine were established to be glutamatergic. This illumination of glutamate neurotransmitter usage will enhance the modeling of central complex neural circuitry and thereby our understanding of information processing by this region of the fly brain. The use of smFLAG for glutamatergic neurotransmitter phenotyping and identification of glutamate release sites can be extended to any Drosophila neuron(s) represented by a binary transcription system driver.

Indexed as

DrosophilaSynaptic VesiclesAnimalsCentral Nervous SystemGlutamic AcidNeuronsSynaptic TransmissionGlutamic AcidDrosophilaepitope tagglutamatergicsynaptic vesiclevGlut

Identifiers

PMID35100385
PMCPMC8895992
OpenAlexW4206049860

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.