Evidence map›Paper›PMID 17658257›Full record

ArticleCurrent biology : CB2007

UNC-1 regulates gap junctions important to locomotion in C. elegans.

Bojun Chen, Qiang Liu, Qian Ge, Jia Xie, Zhao-Wen Wang

Abstract read
In one paragraph

Article in Current biology : CB, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
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

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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

52 citing papers in PubMed.

  1. Defining the electrical synapse.Nature reviews. Neuroscience · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Bojun ChenDepartment of Neuroscience, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, Connecticut 06030.
Qiang Liu
Qian Ge
Jia Xie
Zhao-Wen Wang

Funding

GDP/GTP Exchange Factors: Nucleus Accumbens PlasticityR01DA015464 · NIDA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI EIPPER, ELIZABETH ANNE · 2004 to 2008
$1.6M
Mutants Showing SLO-1 Synaptic MislocalizationR21MH070739 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI WANG, ZHAO-WEN · 2004 to 2005
$359k
NIDA NIH HHS DA 015464NIDA NIH HHS R01 DA015464NIMH NIH HHS R21 MH070739
6 · The paper itself

Abstract

In C. elegans, loss-of-function (lf) mutations of the stomatin-like protein (SLP) UNC-1 and the innexin UNC-9 inhibit locomotion [1, 2] and modulate sensitivity to volatile anesthetics [3, 4]. It was unknown why unc-1(lf) and unc-9(lf) mutants have similar phenotypes. We tested the hypothesis that UNC-1 is a regulator of gap junctions formed by UNC-9. Analyses of junctional currents between body-wall muscle cells showed that electrical coupling was inhibited to a similar degree in unc-1(lf), unc-9(lf), and unc-1(lf);unc-9(lf) double mutants, suggesting that UNC-1 and UNC-9 function together. Expression of Punc-1::DsRED2 and Punc-9::GFP transcriptional fusions suggests that unc-1 and unc-9 are coexpressed in neurons and body-wall muscle cells. Immunohistochemistry showed that UNC-1 and UNC-9 colocalized at intercellular junctions and that unc-1(lf) did not alter UNC-9 expression or subcellular localization. Bimolecular fluorescence complementation (BiFC) assays suggest that UNC-1 and UNC-9 are physically very close at intercellular junctions. Targeted rescue experiments suggest that UNC-9 and UNC-1 function predominantly in neurons to control locomotion. Thus, in addition to the recently reported function of regulating mechanosensitive ion channels [5, 6], SLPs might have a novel function of regulating gap junctions.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsGap JunctionsLocomotionMembrane ProteinsMolecular Sequence DataMuscle CellsNeuronsCaenorhabditis elegans ProteinsMembrane ProteinsUnc-1 protein, C elegansUnc-9 protein, C elegans

Identifiers

PMID17658257
PMCPMC1976340

What OpenQuestion holds

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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.