Evidence map›Paper›PMID 33238150›Full record

ArticleDevelopmental cell2020

NLR-1/CASPR Anchors F-Actin to Promote Gap Junction Formation.

Lingfeng Meng, Dong Yan

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Defining the electrical synapse.Nature reviews. Neuroscience · 2026
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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

2 authors at 1 institution in 1 country.

Lingfeng MengDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Dong YanDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA; Department of Neurobiology, Regeneration Next, and Duke Institute for Brain Sciences, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: dong.yan@duke.edu.
Duke University Hospital · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Genetic study of gap junction formation and regulation in C. elegans neuronsR01NS105638 · NINDS · DUKE UNIVERSITY · PI YAN, DONG · 2018 to 2022
$1.8M
Mechanisms of neural circuit formation in C. elegansR01NS094171 · NINDS · DUKE UNIVERSITY · PI YAN, DONG · 2015 to 2019
$1.5M
NIH HHS P40 OD010440NINDS NIH HHS R01 NS094171NINDS NIH HHS R01 NS105638
6 · The paper itself

Abstract

Gap junctions are present in most tissues and play essential roles in various biological processes. However, we know surprisingly little about the molecular mechanisms underlying gap junction formation. Here, we uncover the essential role of a conserved EGF- and laminin-G-domain-containing protein nlr-1/CASPR in the regulation of gap junction formation in multiple tissues across different developmental stages in C. elegans. NLR-1 is located in the gap junction perinexus, a region adjacent to but not overlapping with gap junctions, and forms puncta before the clusters of gap junction channels appear on the membrane. We show that NLR-1 can directly bind to actin to recruit F-actin networks at the gap junction formation plaque, and the formation of F-actin patches plays a critical role in the assembly of gap junction channels. Our findings demonstrate that nlr-1/CASPR acts as an early stage signal for gap junction formation through anchoring of F-actin networks.

Indexed as

ActinsAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalcium-Binding ProteinsCell Adhesion Molecules, NeuronalEmbryo, NonmammalianGap JunctionsMembrane ProteinsModels, BiologicalMusclesNeuronsPharynxProtein BindingActinsCaenorhabditis elegans ProteinsCalcium-Binding ProteinsCell Adhesion Molecules, NeuronalCNTNAP1 protein, humanMembrane Proteinsnlr-1 protein, C elegansC. eleganscontactin-associated proteinF-actinGap junction

Identifiers

PMID33238150
PMCPMC7725993
OpenAlexW3108618324

What OpenQuestion holds

Textmetadata
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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.