Evidence map›Paper›PMID 26133798›Full record

ArticleJournal of neurophysiology2015

pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability.

V Carmean, M A Yonkers, M B Tellez, J R Willer, G B Willer, R G Gregg, R Geisler, S C Neuhauss, A B Ribera

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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  7. Defects of the Glycinergic Synapse in Zebrafish.Frontiers in molecular neuroscience · 2016
    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

9 authors at 3 institutions in 2 countries.

V CarmeanNeuroscience Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado;
M A YonkersNeuroscience Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado;
M B TellezDepartment of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado;
J R WillerDepartment of Biochemistry and Molecular Biology, University of Louisville, Louisville, Kentucky; Zebrafish Mutant Mapping Facility, University of Louisville, Louisville, Kentucky; and.
G B WillerDepartment of Biochemistry and Molecular Biology, University of Louisville, Louisville, Kentucky; Zebrafish Mutant Mapping Facility, University of Louisville, Louisville, Kentucky; and.
R G GreggDepartment of Biochemistry and Molecular Biology, University of Louisville, Louisville, Kentucky; Zebrafish Mutant Mapping Facility, University of Louisville, Louisville, Kentucky; and.
R GeislerMax-Planck-Institut für Entwicklungsbiologie, Tübingen, Germany.
S C NeuhaussMax-Planck-Institut für Entwicklungsbiologie, Tübingen, Germany.
A B RiberaNeuroscience Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado; Department of Physiology and Biophysics, University of Colorado Anschutz Medical Campus, Aurora, Colorado; angie.ribera@ucdenver.edu.
University of Colorado Anschutz Medical Campus · USUniversity of Louisville · USMax Planck Institute for Developmental Biology · DE

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
MOLECULAR ANALYSIS OF K+CURRENTS IN DEVELOPING NEURONSR01NS025217 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 1993 to 2014
$3.9M
NEURONAL EXCITABILITY IN WILD TYPE AND MUTANT ZEBRAFISHR01NS038937 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2000 to 2010
$2.4M
NEUROSCIENCE TRAINING GRANTT32HD041697 · NICHD · UNIVERSITY OF COLORADO DENVER · PI RESTREPO, DIEGO · 2001 to 2015
$2.4M
Neuronal Transdifferention in vivo: Mechanism and PotentialR01NS086839 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2014 to 2018
$1.7M
NCATS NIH HHS UL1 TR001082NCRR NIH HHS UL1-RR-025780NICHD NIH HHS T32 HD041697NINDS NIH HHS P30 NS048154NINDS NIH HHS P30-NS-048154NINDS NIH HHS R01 NS025217NINDS NIH HHS R01-NS-025217NINDS NIH HHS R01 NS038937NINDS NIH HHS R01-NS-038937NINDS NIH HHS R01 NS086839
6 · The paper itself

Abstract

The study of touch-evoked behavior allows investigation of both the cells and circuits that generate a response to tactile stimulation. We investigate a touch-insensitive zebrafish mutant, macho (maco), previously shown to have reduced sodium current amplitude and lack of action potential firing in sensory neurons. In the genomes of mutant but not wild-type embryos, we identify a mutation in the pigk gene. The encoded protein, PigK, functions in attachment of glycophosphatidylinositol anchors to precursor proteins. In wild-type embryos, pigk mRNA is present at times when mutant embryos display behavioral phenotypes. Consistent with the predicted loss of function induced by the mutation, knock-down of PigK phenocopies maco touch insensitivity and leads to reduced sodium current (INa) amplitudes in sensory neurons. We further test whether the genetic defect in pigk underlies the maco phenotype by overexpressing wild-type pigk in mutant embryos. We find that ubiquitous expression of wild-type pigk rescues the touch response in maco mutants. In addition, for maco mutants, expression of wild-type pigk restricted to sensory neurons rescues sodium current amplitudes and action potential firing in sensory neurons. However, expression of wild-type pigk limited to sensory cells of mutant embryos does not allow rescue of the behavioral touch response. Our results demonstrate an essential role for pigk in generation of the touch response beyond that required for maintenance of proper INa density and action potential firing in sensory neurons.

Indexed as

Action PotentialsAnimalsAnimals, Genetically ModifiedCell Adhesion MoleculesGene Knockdown TechniquesGenotyping TechniquesMutationPatch-Clamp TechniquesPhenotypePolymerase Chain ReactionRNA, MessengerSensory Receptor CellsSodiumTouch PerceptionZebrafishZebrafish ProteinsCell Adhesion MoleculesPigK protein, zebrafishRNA, MessengerSodiumZebrafish Proteinsglycophosphatidylinositol-anchored proteinNavPigkRohon-Beard cellstouch response

Identifiers

PMID26133798
PMCPMC4541141
OpenAlexW2285884421

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.