Evidence map›Paper›PMID 26393506›Full record

ArticlePloS one2015

Tricornered Kinase Regulates Synapse Development by Regulating the Levels of Wiskott-Aldrich Syndrome Protein.

Rajalaxmi Natarajan, Kara Barber, Amanda Buckley, Phillip Cho, Anuoluwapo Egbejimi, Yogesh P Wairkar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 86% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. The NDR family of kinases: essential regulators of aging.Frontiers in molecular neuroscience · 2024
    Review
  4. 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

6 authors at 1 institution in 1 country.

Rajalaxmi NatarajanDepartment of Neurology and Mitchell Center for Neurodegenerative Diseases, University of Texas Medical Branch, Galveston, Texas, United States of America.
Kara BarberNeuroscience Graduate Program, University of Texas Medical Branch, Galveston, Texas, United States of America.
Amanda BuckleyDepartment of Neurology and Mitchell Center for Neurodegenerative Diseases, University of Texas Medical Branch, Galveston, Texas, United States of America.
Phillip ChoSummer Undergraduate Research Program, University of Texas Medical Branch, Galveston, Texas, United States of America.
Anuoluwapo EgbejimiDepartment of Neurology, University of Texas Medical Branch, Galveston, Texas, United States of America; Neuroscience Graduate Program, University of Texas Medical Branch, Galveston, Texas, United States of America.
Yogesh P WairkarDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, Texas, United States of America; Department of Neurology and Mitchell Center for Neurodegenerative Diseases, University of Texas Medical Branch, Galveston, Texas, United States of America.
The University of Texas Medical Branch at Galveston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise regulation of synapses during development is essential to ensure accurate neural connectivity and function of nervous system. Many signaling pathways, including the mTOR (mechanical Target of Rapamycin) pathway operate in neurons to maintain genetically determined number of synapses during development. mTOR, a kinase, is shared between two functionally distinct multi-protein complexes- mTORC1 and mTORC2, that act downstream of Tuberous Sclerosis Complex (TSC). We and others have suggested an important role for TSC in synapse development at the Drosophila neuromuscular junction (NMJ) synapses. In addition, our data suggested that the regulation of the NMJ synapse numbers in Drosophila largely depends on signaling via mTORC2. In the present study, we further this observation by identifying Tricornered (Trc) kinase, a serine/threonine kinase as a likely mediator of TSC signaling. trc genetically interacts with Tsc2 to regulate the number of synapses. In addition, Tsc2 and trc mutants exhibit a dramatic reduction in synaptic levels of WASP, an important regulator of actin polymerization. We show that Trc regulates the WASP levels largely, by regulating the transcription of WASP. Finally, we show that overexpression of WASP (Wiskott-Aldrich Syndrome Protein) in trc mutants can suppress the increase in the number of synapses observed in trc mutants, suggesting that WASP regulates synapses downstream of Trc. Thus, our data provide a novel insight into how Trc may regulate the genetic program that controls the number of synapses during development.

Indexed as

AnimalsAnimals, Genetically ModifiedCell Cycle ProteinsDrosophila melanogasterDrosophila ProteinsEpistasis, GeneticGene Expression Regulation, DevelopmentalMechanistic Target of Rapamycin Complex 2Microscopy, ConfocalModels, GeneticMultiprotein ComplexesMutationNerve Tissue ProteinsNeuromuscular JunctionProtein Serine-Threonine KinasesReverse Transcriptase Polymerase Chain ReactionCell Cycle ProteinsDrosophila Proteinsgig protein, DrosophilaHIW protein, DrosophilaMechanistic Target of Rapamycin Complex 2Multiprotein ComplexesNerve Tissue ProteinsProtein Serine-Threonine KinasesTOR Serine-Threonine Kinasestrc protein, DrosophilaTSC1 protein, DrosophilaWASp protein, DrosophilaWiskott-Aldrich Syndrome Protein

Identifiers

PMID26393506
PMCPMC4578898
OpenAlexW2338932640

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.