Evidence map›Paper›PMID 27304225›Full record

ArticleChannels (Austin, Tex.)2016

Specificity of the connexin W3/4 locus for functional gap junction formation.

Qin Xu, Xianming Lin, Arvydas Matiukas, Xian Zhang, Richard D Veenstra

Open access · goldAbstract read
In one paragraph

Article in Channels (Austin, Tex.), 2016. 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
–field-weighted citation impact, top 97% 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, 4 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 1 institution in 1 country.

Qin Xua Department of Pharmacology , SUNY Upstate Medical University , Syracuse , NY , USA.
Xianming Lina Department of Pharmacology , SUNY Upstate Medical University , Syracuse , NY , USA.
Arvydas Matiukasa Department of Pharmacology , SUNY Upstate Medical University , Syracuse , NY , USA.
Xian Zhanga Department of Pharmacology , SUNY Upstate Medical University , Syracuse , NY , USA.
Richard D Veenstraa Department of Pharmacology , SUNY Upstate Medical University , Syracuse , NY , USA.
SUNY Upstate Medical University · US

Funding

GAP JUNCTIONS AND IONIC CURRENTS IN DEVELOPING HEARTR01HL042220 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI VEENSTRA, RICHARD DAVID, YANG, JENNY J. · 1988 to 2013
$3.1M
NHLBI NIH HHS R01 HL042220
6 · The paper itself

Abstract

The N-terminal (NT) domain of the connexins forms an essential transjunctional voltage (Vj) sensor and pore-forming domain that when truncated, tagged, or mutated often leads to formation of a nonfunctional channel. The NT domain is relatively conserved among the connexins though the α- and δ-group connexins possess a G2 residue not found in the β- and γ-group connexins. Deletion of the connexin40 G2 residue (Cx40G2Δ) affected the Vj gating, increased the single channel conductance (γj), and decreased the relative K(+)/Cl(-) permeability (PK/PCl) ratio of the Cx40 gap junction channel. The conserved α/β-group connexin D2/3 and W3/4 loci are postulated to anchor the NT domain within the pore via hydrophilic and hydrophobic interactions with adjacent connexin T5 and M34 residues. Cx40D3N and D3R mutations produced limited function with progressive reductions in Vj gating and noisy low γj gap junction channels that reduced the γj of wild-type Cx40 channels from 150 pS to < 50 pS when coexpressed. Surprisingly, hydrophobic Cx40 W4F and W4Y substitution mutations were not compatible with function despite their ability to form gap junction plaques. These data are consistent with minor and major contributions of the G2 and D3 residues to the Cx40 channel pore structure, but not with the postulated hydrophobic W4 intermolecular interactions. Our results indicate an absolute requirement for an amphipathic W3/4 residue that is conserved among all α/β/δ/γ-group connexins. We alternatively hypothesize that the connexin D2/3-W3/4 locus interacts with the highly conserved FIFR M1 motif to stabilize the NT domain within the pore.

Indexed as

AnimalsCell LineConnexin 43ConnexinsElectrophysiological PhenomenaGap Junction alpha-5 ProteinGap JunctionsGenetic LociHumansIon ChannelsModels, MolecularMutationProtein ConformationProtein DomainsTransfectionConnexin 43ConnexinsGap Junction alpha-5 ProteinIon Channelschannel conductanceconnexin40connexin43gap junctionsheteromersmolecular modelmutations

Identifiers

PMID27304225
PMCPMC5034775
OpenAlexW2432681644

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.