Evidence map›Paper›PMID 10531442›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Targeted expression of truncated glued disrupts giant fiber synapse formation in Drosophila.

M J Allen, X Shan, P Caruccio, S J Froggett, K G Moffat, R K Murphey

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

56 citing papers in PubMed, 104 citations in OpenAlex.

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  8. A Role forFrontiers in cellular neuroscience · 2019
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  18. The Krüppel-Like Factor Dar1 Determines Multipolar Neuron Morphology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  19. Article
  20. Engrailed alters the specificity of synaptic connections of Drosophila auditory neurons with the giant fiber.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    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 2 institutions in 2 countries.

M J AllenDepartment of Biology, Morrill Science Center, University of Massachusetts, Amherst, Massachusetts 01003, USA. mjallen@bio.umass.edu
X Shan
P Caruccio
S J Froggett
K G Moffat
R K Murphey
University of Massachusetts Amherst · USUniversity of Warwick · GB

Funding

ORIGINS OF NEURONAL SPECIFICITYR01NS015571 · NINDS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MURPHEY, RODNEY K · 1985 to 1999
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NINDS NIH HHS NS15571
6 · The paper itself

Abstract

Glued(1) (Gl(1)) mutants produce a truncated protein that acts as a poison subunit and disables the cytoplasmic retrograde motor dynein. Heterozygous mutants have axonal defects in the adult eye and the nervous system. Here we show that selective expression of the poison subunit in neurons of the giant fiber (GF) system disrupts synaptogenesis between the GF and one of its targets, the tergotrochanteral motorneuron (TTMn). Growth and pathfinding by the GF axon and the TTMn dendrite are normal, but the terminal of the GF axon fails to develop normally and becomes swollen with large vesicles. This is a presynaptic defect because expression of truncated Glued restricted to the GF results in the same defect. When tested electrophysiologically, the flies with abnormal axons show a weakened or absent GF-TTMn connection. In Glued(1) heterozygotes, GF-TTMn synapse formation appears morphologically normal, but adult flies show abnormal responses to repetitive stimuli. This physiological effect is also observed when tetanus toxin is expressed in the GFs. Because the GF-TTMn is thought to be a mixed electrochemical synapse, the results show that Glued has a role in assembling both the chemical and electrical components. We speculate that disrupting transport of a retrograde signal disrupts synapse formation and maturation.

Indexed as

Sequence DeletionAnimalsAxonsDendritesDrosophila melanogasterDrosophila ProteinsElectric StimulationEnhancer Elements, GeneticGene Expression Regulation, DevelopmentalGenotypeMicrotubule-Associated ProteinsMotor NeuronsMutagenesisNerve FibersNervous SystemNervous System Physiological PhenomenaDCTN1-p150 protein, DrosophilaDrosophila ProteinsMicrotubule-Associated Proteins

Identifiers

PMID10531442
PMCPMC6782895
OpenAlexW1856652139

What OpenQuestion holds

Textmetadata
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.