Evidence map›Paper›PMID 23227189›Full record

ArticlePloS one2012

JNK pathway activation is controlled by Tao/TAOK3 to modulate ethanol sensitivity.

David Kapfhamer, Ian King, Mimi E Zou, Jana P Lim, Ulrike Heberlein, Fred W Wolf

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. JNK Signaling Positively Regulates Acute Ethanol Tolerance inInternational journal of molecular sciences · 2024
    Article
  5. The role of TAOK3 in cancer progression and development as a prognostic marker: A pan-cancer analysis study.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Genome-wide Mendelian randomization identifies actionable novel drug targets for psychiatric disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  10. Article
  11. Article
  12. TAOK3 is a MAP3K contributing to osteoblast differentiation and skeletal mineralization.Biochemical and biophysical research communications · 2020
    Article
  13. The Diverse Roles of TAO Kinases in Health and Diseases.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Conserved Tao Kinase Activity Regulates Dendritic Arborization, Cytoskeletal Dynamics, and Sensory Function inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  16. Article
  17. Article
  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

6 authors at 2 institutions in 1 country.

David KapfhamerThe Ernest Gallo Clinic and Research Center, University of California San Francisco, Emeryville, California, United States of America.
Ian King
Mimi E Zou
Jana P Lim
Ulrike Heberlein
Fred W Wolf
University of California, San Francisco · USErnest Gallo Clinic and Research Center · US

Funding

Vector, Transgenic, and Imaging CoreP50AA017072 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RON, DORIT · 2008 to 2017
$13.9M
GENES THAT REGULATE ETHANOL RESPONSES IN DROSOPHILAR01AA010035 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHAH, NIRAO MAHESH · 1995 to 2014
$4.4M
NIAAA NIH HHS P50 AA017072NIAAA NIH HHS R01 AA010035
6 · The paper itself

Abstract

Neuronal signal transduction by the JNK MAP kinase pathway is altered by a broad array of stimuli including exposure to the widely abused drug ethanol, but the behavioral relevance and the regulation of JNK signaling is unclear. Here we demonstrate that JNK signaling functions downstream of the Sterile20 kinase family gene tao/Taok3 to regulate the behavioral effects of acute ethanol exposure in both the fruit fly Drosophila and mice. In flies tao is required in neurons to promote sensitivity to the locomotor stimulant effects of acute ethanol exposure and to establish specific brain structures. Reduced expression of key JNK pathway genes substantially rescued the structural and behavioral phenotypes of tao mutants. Decreasing and increasing JNK pathway activity resulted in increased and decreased sensitivity to the locomotor stimulant properties of acute ethanol exposure, respectively. Further, JNK expression in a limited pattern of neurons that included brain regions implicated in ethanol responses was sufficient to restore normal behavior. Mice heterozygous for a disrupted allele of the homologous Taok3 gene (Taok3Gt) were resistant to the acute sedative effects of ethanol. JNK activity was constitutively increased in brains of Taok3Gt/+ mice, and acute induction of phospho-JNK in brain tissue by ethanol was occluded in Taok3Gt/+ mice. Finally, acute administration of a JNK inhibitor conferred resistance to the sedative effects of ethanol in wild-type but not Taok3Gt/+ mice. Taken together, these data support a role of a TAO/TAOK3-JNK neuronal signaling pathway in regulating sensitivity to acute ethanol exposure in flies and in mice.

Indexed as

AnimalsBase SequenceBehavior, AnimalDNA PrimersDrosophilaDrosophila ProteinsEthanolImmunohistochemistryMAP Kinase Kinase 4MiceMice, Inbred C57BLMutationProtein Serine-Threonine KinasesReverse Transcriptase Polymerase Chain ReactionDNA PrimersDrosophila ProteinsEthanolMAP Kinase Kinase 4Protein Serine-Threonine KinasesTao protein, Drosophila

Identifiers

PMID23227189
PMCPMC3515618
OpenAlexW2029573742

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.