Evidence map›Paper›PMID 20714347›Full record

ArticlePLoS genetics2010

Conserved role of unc-79 in ethanol responses in lightweight mutant mice.

David J Speca, Daisuke Chihara, Amir M Ashique, M Scott Bowers, Jonathan T Pierce-Shimomura, Jungsoo Lee, Nusrat Rabbee, Terence P Speed, Rodrigo J Gularte, James Chitwood and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

34 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  9. Forward genetic approach for behavioral neuroscience using animal models.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Phenotypic evolution of UNC80 loss of function.American journal of medical genetics. Part A · 2016
    Article
  14. Article
  15. Article
  16. Review
  17. Genes and Alcohol Consumption: Studies with Mutant Mice.International review of neurobiology · 2016
    Review
  18. Review
  19. Article
  20. Article
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

16 authors at 4 institutions in 2 countries.

David J SpecaDepartment of Neurology and the Ernest Gallo Clinic and Research Center, University of California San Francisco, Emeryville, California, United States of America. dave.speca@gmail.com
Daisuke Chihara
Amir M Ashique
M Scott Bowers
Jonathan T Pierce-Shimomura
Jungsoo Lee
Nusrat Rabbee
Terence P Speed
Rodrigo J Gularte
James Chitwood
Juan F Medrano
Mark Liao
James M Sonner
Edmond I Eger
Andrew S Peterson
Steven L McIntire
University of California, San Francisco · USUniversity of California, Davis · USUniversity of California, Berkeley · USErnest Gallo Clinic and Research Center · US

Funding

SITES AND MECHANISMS OF INHALED ANESTHETIC ACTIONSP01GM047818 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SONNER, JAMES MICHAEL · 1994 to 2008
$11.0M
NIAAA NIH HHS P50AA01772NIGMS NIH HHS P01 GM047818NIGMS NIH HHS P01GM47818
6 · The paper itself

Abstract

The mechanisms by which ethanol and inhaled anesthetics influence the nervous system are poorly understood. Here we describe the positional cloning and characterization of a new mouse mutation isolated in an N-ethyl-N-nitrosourea (ENU) forward mutagenesis screen for animals with enhanced locomotor activity. This allele, Lightweight (Lwt), disrupts the homolog of the Caenorhabditis elegans (C. elegans) unc-79 gene. While Lwt/Lwt homozygotes are perinatal lethal, Lightweight heterozygotes are dramatically hypersensitive to acute ethanol exposure. Experiments in C. elegans demonstrate a conserved hypersensitivity to ethanol in unc-79 mutants and extend this observation to the related unc-80 mutant and nca-1;nca-2 double mutants. Lightweight heterozygotes also exhibit an altered response to the anesthetic isoflurane, reminiscent of unc-79 invertebrate mutant phenotypes. Consistent with our initial mapping results, Lightweight heterozygotes are mildly hyperactive when exposed to a novel environment and are smaller than wild-type animals. In addition, Lightweight heterozygotes exhibit increased food consumption yet have a leaner body composition. Interestingly, Lightweight heterozygotes voluntarily consume more ethanol than wild-type littermates. The acute hypersensitivity to and increased voluntary consumption of ethanol observed in Lightweight heterozygous mice in combination with the observed hypersensitivity to ethanol in C. elegans unc-79, unc-80, and nca-1;nca-2 double mutants suggests a novel conserved pathway that might influence alcohol-related behaviors in humans.

Indexed as

Body WeightMutationAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsEthanolFemaleIon ChannelsMaleMembrane ProteinsMiceMice, Inbred C57BLMotor ActivityNerve Tissue ProteinsCaenorhabditis elegans ProteinsEthanolIon ChannelsMembrane ProteinsNALCN protein, mouseNerve Tissue ProteinsUnc-79 protein, C elegansUNC-79 protein, mouse

Identifiers

PMID20714347
PMCPMC2920847
OpenAlexW2054906824

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.