Evidence map›Paper›PMID 33507632›Full record

ArticleMolecular genetics & genomic medicine2021

Functional analysis of the F337C mutation in the CLCN1 gene associated with dominant myotonia congenita reveals an alteration of the macroscopic conductance and voltage dependence.

Kevin Jehasse, Kathleen Jacquerie, Alice de Froidmont, Camille Lemoine, Thierry Grisar, Katrien Stouffs, Bernard Lakaye, Vincent Seutin

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Kevin JehasseLaboratory of Neurophysiology, GIGA Institute, Liege, Belgium.ORCID 0000-0001-8845-6595
Kathleen JacquerieDepartment of Electrical Engineering and Computer Science, Liège University, Liège, Belgium.ORCID 0000-0002-4435-3057
Alice de FroidmontLaboratory of Neurophysiology, GIGA Institute, Liege, Belgium.
Camille LemoineLaboratory of Neurophysiology, GIGA Institute, Liege, Belgium.
Thierry GrisarLaboratory of Molecular Regulation of Neurogenesis, GIGA Institute, Liège, Belgium.
Katrien StouffsNeurogenetics Research Group, Vrije Universiteit Brussel (VUB, Universitair Ziekenhuis Brussel (UZ Brussel), Reproduction and Genetics, Brussels, Belgium.ORCID 0000-0001-8164-5692
Bernard LakayeLaboratory of Molecular Regulation of Neurogenesis, GIGA Institute, Liège, Belgium.
Vincent SeutinLaboratory of Neurophysiology, GIGA Institute, Liege, Belgium.ORCID 0000-0002-8046-8142
University of Liège · BEVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyotonia congenita (MC) is a common channelopathy affecting skeletal muscle and which is due to pathogenic variants within the CLCN1 gene. Various alterations in the function of the channel have been reported and we here illustrate a novel one.

methodsA patient presenting the symptoms of myotonia congenita was shown to bear a new heterozygous missense variant in exon 9 of the CLCN1 gene (c.1010 T > G, p.(Phe337Cys)). Confocal imaging and patch clamp recordings of transiently transfected HEK293 cells were used to functionally analyze the effect of this variant on channel properties.

resultsConfocal imaging showed that the F337C mutant incorporated as well as the WT channel into the plasma membrane. However, in patch clamp, we observed a smaller conductance for F337C at -80 mV. We also found a marked reduction of the fast gating component in the mutant channels, as well as an overall reduced voltage dependence.

conclusionTo our knowledge, this is the first report of a mixed alteration in the biophysical properties of hClC-1 consisting of a reduced conductance at resting potential and an almost abolished voltage dependence.

Indexed as

Mutation, MissenseAction PotentialsCell MembraneChloride ChannelsHEK293 CellsHumansIon Channel GatingMyotonia CongenitaProtein TransportChloride ChannelsCLC-1 channelchannel gatingCLCN1microscopymyotoniapatch clamp

Identifiers

PMID33507632
PMCPMC8077071
OpenAlexW3123108536

What OpenQuestion holds

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LicenceCC BY
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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.