Evidence map›Paper›PMID 36799927›Full record

ArticleGenetics2023

Genome-wide analysis reveals novel regulators of synaptic maintenance in Drosophila.

Jessica M Sidisky, Danielle de Paula Moreira, Meryem Okumus, Russell Caratenuto, Cassidy Drost, Bali Connors, Sarrah Hussain, Stephanie Alkhatib, Daniel T Babcock

Open access · hybridAbstract read
In one paragraph

Article in Genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Synaptic defects in a drosophila model of muscular dystrophy.Frontiers in cellular neuroscience · 2024
    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

9 authors at 1 institution in 1 country.

Jessica M SidiskyDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Danielle de Paula MoreiraDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Meryem OkumusDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Russell CaratenutoDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Cassidy DrostDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Bali ConnorsDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Sarrah HussainDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Stephanie AlkhatibDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.
Daniel T BabcockDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.ORCID 0000-0002-8102-9133
Lehigh University · US

Funding

Regulation of Synaptic Dysfunction and Maintenance with age using DrosophilaR01NS110727 · NINDS · LEHIGH UNIVERSITY · PI BABCOCK, DANIEL T. · 2019 to 2023
$1.7M
NINDS NIH HHS R01 NS110727
6 · The paper itself

Abstract

Maintaining synaptic communication is required to preserve nervous system function as an organism ages. While much work has been accomplished to understand synapse formation and development, we understand relatively little regarding maintaining synaptic integrity throughout aging. To better understand the mechanisms responsible for maintaining synaptic structure and function, we performed an unbiased forward genetic screen to identify genes required for synapse maintenance of adult Drosophila neuromuscular junctions. Using flight behavior as a screening tool, we evaluated flight ability in 198 lines from the Drosophila Genetic Reference Panel to identify single nucleotide polymorphisms (SNPs) that are associated with a progressive loss of flight ability with age. Among the many candidate genes identified from this screen, we focus here on 10 genes with clear human homologs harboring SNPs that are most highly associated with synaptic maintenance. Functional validation of these genes using mutant alleles revealed a progressive loss of synaptic structural integrity. Tissue-specific knockdown of these genes using RNA interference (RNAi) uncovered important roles for these genes in either presynaptic motor neurons, postsynaptic muscles, or associated glial cells, highlighting the importance of each component of tripartite synapses. These results offer greater insight into the mechanisms responsible for maintaining structural and functional integrity of synapses with age.

Indexed as

DrosophilaDrosophila ProteinsAnimalsHumansNeurogliaNeuromuscular JunctionSynapsesSynaptic TransmissionDrosophila ProteinsDrosophilaflightneuromuscular junctionsynapse

Identifiers

PMID36799927
PMCPMC10078915
OpenAlexW4321167278

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.