Evidence map›Paper›PMID 30371853›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2019

Sequence Variations in pxr (nr1i2) From Zebrafish (Danio rerio) Strains Affect Nuclear Receptor Function.

Roger Lille-Langøy, Odd André Karlsen, Line Merethe Myklebust, Jared V Goldstone, Astrid Mork-Jansson, Rune Male, Bruce Blumberg, John J Stegeman, Anders Goksøyr

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 3 institutions in 2 countries.

Roger Lille-LangøyDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
Odd André KarlsenDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
Line Merethe MyklebustDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
Jared V GoldstoneBiology Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, U. S. A.
Astrid Mork-JanssonDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
Rune MaleDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
Bruce BlumbergDepartment of Developmental and Cell Biology, University of California, Irvine, CA 92697, U. S. A.
John J StegemanBiology Department, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, U. S. A.
Anders GoksøyrDepartment of Biological Sciences, University of Bergen, N-5006 Bergen, Norway.
University of Bergen · NOWoods Hole Oceanographic Institution · USUniversity of California, Irvine · US

Funding

Training CoreP42ES007381 · NIEHS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SHERR, DAVID H · 1995 to 2019
$46.1M
Nomenclature of Human and Vertebrate GenesU41HG003345 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI BIRNEY, EWAN, BRUFORD, ELSPETH · 2013 to 2017
$2.4M
TALENs-based PXR Knockout and Humanized ZebrafishR21HD073805 · NICHD · WOODS HOLE OCEANOGRAPHIC INSTITUTION · PI GOLDSTONE, JARED VERRILL · 2013 to 2014
$454k
NHGRI NIH HHS U41 HG003345NICHD NIH HHS R21 HD073805NIEHS NIH HHS P42 ES007381
6 · The paper itself

Abstract

Regulators of biotransformation are of particular interest in pharmacology and toxicology, determining in part the metabolism, disposition, and toxicity of chemicals. The nuclear receptor NR1I2 (pregnane X receptor, PXR) is a prominent xenosensor that regulates the expression of biotransformation enzymes governing elimination of many exogenous as well as endogenous compounds. Zebrafish (Danio rerio) has only one gene locus for pxr, but different genetic variants have been identified in zebrafish. However, the prevalence and significance of these variants are unknown. We hypothesize that sequence variation occurring in the Pxr gene of zebrafish may affect the action and fate of many chemicals in this species, a key model organism in various fields of research, including environmental toxicology. Here, we examine variation in Pxr sequences from four different strains of zebrafish and assess the responses of each Pxr to clotrimazole and butyl-4-aminobenzoate. The Pxr variants differed in both their ability to bind these structurally different ligands and to regulate reporter gene expression in vitro. We infer that the observed sequence variations in zebrafish Pxrs likely affect the response to putative Pxr agonists in vivo and potentially cause strain-specific biotransformation of xenobiotics in zebrafish. Thus, the choice of zebrafish strain could affect the outcome of downstream toxicological studies.

Indexed as

Amino Acid SequenceAnimalsChlorocebus aethiopsCOS CellsGenes, ReporterLigandsMolecular Docking SimulationPregnane X ReceptorSequence AnalysisStructure-Activity RelationshipZebrafishLigandsPregnane X Receptorgenetic variationinterspecies variationpregnane X receptorrisk assessmentzebrafish

Identifiers

PMID30371853
PMCPMC6390661
OpenAlexW2917780499

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.