Literature DB >> 30371853

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

Roger Lille-Langøy1, Odd André Karlsen1, Line Merethe Myklebust1, Jared V Goldstone2, Astrid Mork-Jansson1,3, Rune Male1, Bruce Blumberg4, John J Stegeman2, Anders Goksøyr1.   

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.
© The Author(s) 2018. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  genetic variation; interspecies variation; pregnane X receptor; risk assessment; zebrafish

Mesh:

Substances:

Year:  2019        PMID: 30371853      PMCID: PMC6390661          DOI: 10.1093/toxsci/kfy269

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  62 in total

1.  Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion.

Authors:  J T den Dunnen; S E Antonarakis
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

2.  Dimerizing the estrogen receptor DNA binding domain enhances binding to estrogen response elements.

Authors:  M A Kuntz; D J Shapiro
Journal:  J Biol Chem       Date:  1997-10-31       Impact factor: 5.157

3.  The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variants.

Authors:  J Zhang; P Kuehl; E D Green; J W Touchman; P B Watkins; A Daly; S D Hall; P Maurel; M Relling; C Brimer; K Yasuda; S A Wrighton; M Hancock; R B Kim; S Strom; K Thummel; C G Russell; J R Hudson; E G Schuetz; M S Boguski
Journal:  Pharmacogenetics       Date:  2001-10

4.  Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group.

Authors:  S E Antonarakis
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

5.  Expression of PXR, CYP3A and MDR1 genes in liver of zebrafish.

Authors:  Taise Bresolin; Mauro de Freitas Rebelo; Afonso Celso Dias Bainy
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2005 Mar-Apr       Impact factor: 3.228

6.  2.1 A crystal structure of human PXR in complex with the St. John's wort compound hyperforin.

Authors:  Ryan E Watkins; Jodi M Maglich; Linda B Moore; G Bruce Wisely; Schroeder M Noble; Paula R Davis-Searles; Mill H Lambert; Steven A Kliewer; Matthew R Redinbo
Journal:  Biochemistry       Date:  2003-02-18       Impact factor: 3.162

7.  Structure of the intact PPAR-gamma-RXR- nuclear receptor complex on DNA.

Authors:  Vikas Chandra; Pengxiang Huang; Yoshitomo Hamuro; Srilatha Raghuram; Yongjun Wang; Thomas P Burris; Fraydoon Rastinejad
Journal:  Nature       Date:  2008-11-20       Impact factor: 49.962

8.  A simple and fast secondary structure prediction method using hidden neural networks.

Authors:  Kuang Lin; Victor A Simossis; Willam R Taylor; Jaap Heringa
Journal:  Bioinformatics       Date:  2004-09-17       Impact factor: 6.937

9.  Genenames.org: the HGNC resources in 2013.

Authors:  Kristian A Gray; Louise C Daugherty; Susan M Gordon; Ruth L Seal; Mathew W Wright; Elspeth A Bruford
Journal:  Nucleic Acids Res       Date:  2012-11-17       Impact factor: 16.971

10.  SIFT web server: predicting effects of amino acid substitutions on proteins.

Authors:  Ngak-Leng Sim; Prateek Kumar; Jing Hu; Steven Henikoff; Georg Schneider; Pauline C Ng
Journal:  Nucleic Acids Res       Date:  2012-06-11       Impact factor: 16.971

View more
  3 in total

1.  The chemical defensome of five model teleost fish.

Authors:  Marta Eide; Xiaokang Zhang; Odd André Karlsen; Jared V Goldstone; John Stegeman; Inge Jonassen; Anders Goksøyr
Journal:  Sci Rep       Date:  2021-05-18       Impact factor: 4.379

Review 2.  The role of pregnane X receptor (PXR) in substance metabolism.

Authors:  Ye Lv; Yi-Yang Luo; Hui-Wen Ren; Cheng-Jie Li; Zhi-Xin Xiang; Zhi-Lin Luan
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-16       Impact factor: 6.055

3.  CRISPR-Cas9-Mutated Pregnane X Receptor (pxr) Retains Pregnenolone-induced Expression of cyp3a65 in Zebrafish (Danio rerio) Larvae.

Authors:  Matthew C Salanga; Nadja R Brun; Rene D Francolini; John J Stegeman; Jared V Goldstone
Journal:  Toxicol Sci       Date:  2020-03-01       Impact factor: 4.849

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.