Evidence map›Paper›PMID 27432995›Full record

ArticleThe Journal of general physiology2016

Biophysical characterization of the honeybee DSC1 orthologue reveals a novel voltage-dependent Ca2+ channel subfamily: CaV4.

Pascal Gosselin-Badaroudine, Adrien Moreau, Louis Simard, Thierry Cens, Matthieu Rousset, Claude Collet, Pierre Charnet, Mohamed Chahine

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2016. 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
4.0field-weighted citation impact, top 7% 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, 18 citations in OpenAlex.

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  4. Electrophysiology of Ctenophore Smooth Muscle.Methods in molecular biology (Clifton, N.J.) · 2024
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  11. What makes a sodium channel?The Journal of general physiology · 2016
    Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Pascal Gosselin-BadaroudineCentre de Recherche, Institut Universitaire en Santé Mentale de Québec, Quebec City, Quebec G1J 2G3, Canada.
Adrien MoreauCentre de Recherche, Institut Universitaire en Santé Mentale de Québec, Quebec City, Quebec G1J 2G3, Canada.
Louis SimardCentre de Recherche, Institut Universitaire en Santé Mentale de Québec, Quebec City, Quebec G1J 2G3, Canada.
Thierry CensInstitut des Biomolécules Max Mousseron, Centre National de la Recherche Scientifique UMR 5247, 1919 Montpellier, France.
Matthieu RoussetInstitut des Biomolécules Max Mousseron, Centre National de la Recherche Scientifique UMR 5247, 1919 Montpellier, France.
Claude ColletINRA UR 406, Abeilles et Environnement, Domaine Saint Paul - Site Agroparc, 84914 Avignon, France.
Pierre CharnetInstitut des Biomolécules Max Mousseron, Centre National de la Recherche Scientifique UMR 5247, 1919 Montpellier, France.
Mohamed ChahineCentre de Recherche, Institut Universitaire en Santé Mentale de Québec, Quebec City, Quebec G1J 2G3, Canada Department of Medicine, Université Laval, Quebec City, Quebec G1K 7P4, Canada mohamed.chahine@phc.ulaval.ca.ORCID 0000-0002-9500-2839
Institut Universitaire en Santé Mentale de Québec · CACentre National de la Recherche Scientifique · FRAgroParisTech · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bilaterian voltage-gated Na(+) channels (NaV) evolved from voltage-gated Ca(2+) channels (CaV). The Drosophila melanogaster Na(+) channel 1 (DSC1), which features a D-E-E-A selectivity filter sequence that is intermediate between CaV and NaV channels, is evidence of this evolution. Phylogenetic analysis has classified DSC1 as a Ca(2+)-permeable Na(+) channel belonging to the NaV2 family because of its sequence similarity with NaV channels. This is despite insect NaV2 channels (DSC1 and its orthologue in Blatella germanica, BSC1) being more permeable to Ca(2+) than Na(+) In this study, we report the cloning and molecular characterization of the honeybee (Apis mellifera) DSC1 orthologue. We reveal several sequence variations caused by alternative splicing, RNA editing, and genomic variations. Using the Xenopus oocyte heterologous expression system and the two-microelectrode voltage-clamp technique, we find that the channel exhibits slow activation and inactivation kinetics, insensitivity to tetrodotoxin, and block by Cd(2+) and Zn(2+) These characteristics are reminiscent of CaV channels. We also show a strong selectivity for Ca(2+) and Ba(2+) ions, marginal permeability to Li(+), and impermeability to Mg(2+) and Na(+) ions. Based on current ion channel nomenclature, the D-E-E-A selectivity filter, and the properties we have uncovered, we propose that DSC1 homologues should be classified as CaV4 rather than NaV2. Indeed, channels that contain the D-E-E-A selectivity sequence are likely to feature the same properties as the honeybee's channel, namely slow activation and inactivation kinetics and strong selectivity for Ca(2+) ions.

Indexed as

Alternative SplicingAnimalsBeesCalcium ChannelsCloning, MolecularPatch-Clamp TechniquesPhylogenyCalcium Channels

Identifiers

PMID27432995
PMCPMC4969797
OpenAlexW2493891178

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.