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

Authors :
Jeremiah S. Yee
Rachel H Wilson
Clifford Dustin Rubinstein
Nicholas A Goetz
Jessica C. Parrott
Manabu Nukaya
Susan M. Moran
E.W.N. Glover
Brenda L Rojas
Kathy J. Krentz
Christopher A. Bradfield
Yongna Xing
Patrick R. Carney
Source :
Toxicol Sci
Publication Year :
2021

Abstract

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.

Details

ISSN :
10960929
Volume :
180
Issue :
2
Database :
OpenAIRE
Journal :
Toxicological sciences : an official journal of the Society of Toxicology
Accession number :
edsair.doi.dedup.....b6495cb26c6b27a21188fb4bb35ec4db