Generation of an Allelic Series at the Ahr Locus Using an Edited Recombinant Approach.


Journal

Toxicological sciences : an official journal of the Society of Toxicology
ISSN: 1096-0929
Titre abrégé: Toxicol Sci
Pays: United States
ID NLM: 9805461

Informations de publication

Date de publication:
12 04 2021
Historique:
pubmed: 23 1 2021
medline: 19 8 2021
entrez: 22 1 2021
Statut: ppublish

Résumé

The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor and a member of the PER-ARNT-SIM (PAS) superfamily of environmental sensors. The AHR is involved in a series of biological processes including adaptive metabolism of xenobiotics, toxicity of certain environmental pollutants, vascular development, fertility, and immune function. Mouse models, including the Ahr null and Ahr conditional null (Ahrfx) mice, are widely used for the study of AHR-mediated biology and toxicity. The Ahr conditional null mouse harbors the low-affinity Ahrd allele that exhibits approximately a 10-fold lower binding affinity for certain xenobiotic AHR ligands than the widely used C57BL/6 mouse that harbors the higher affinity Ahrb1 allele. Here, we report a novel mouse model that introduces a V375A polymorphism that converts the low-affinity allele into a high-affinity allele, offering a more sensitive conditional model. In the generation of this novel conditional allele, two additional mutants arose, including a 3-bp deletion in the PAS-B domain (AhrNG367R) and an early termination codon in the PAS-B domain (AhrTer383). The AhrNG367R allele presents as a phenocopy of the null and the AhrTer383 allele presents as an antimorph when assessing for the ductus venosus and liver lobe weight endpoints. These new models represent a series of tools that will be useful in further characterizing AHR biology.

Identifiants

pubmed: 33480436
pii: 6106137
doi: 10.1093/toxsci/kfab005
pmc: PMC8041461
doi:

Substances chimiques

Ahr protein, mouse 0
Basic Helix-Loop-Helix Transcription Factors 0
Receptors, Aryl Hydrocarbon 0
Aryl Hydrocarbon Receptor Nuclear Translocator 138391-32-9

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

239-251

Subventions

Organisme : NIEHS NIH HHS
ID : R35 ES028377
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014520
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008692
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009135
Pays : United States
Organisme : NIEHS NIH HHS
ID : T32 ES007015
Pays : United States

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Rachel H Wilson (RH)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Patrick R Carney (PR)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Edward Glover (E)

Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Jessica C Parrott (JC)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Brenda L Rojas (BL)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Biotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Susan M Moran (SM)

Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Jeremiah S Yee (JS)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Manabu Nukaya (M)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Nicholas A Goetz (NA)

Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Clifford D Rubinstein (CD)

Biotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Kathy J Krentz (KJ)

Biotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Yongna Xing (Y)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

Christopher A Bradfield (CA)

Molecular and Environmental Toxicology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Department of Oncology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Biotechnology Center, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.

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