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

Authors: Wilson, Rachel H; Carney, Patrick R; Glover, Edward; Parrott, Jessica C; Rojas, Brenda L; Moran, Susan M; Yee, Jeremiah S; Nukaya, Manabu; Goetz, Nicholas A; Rubinstein, Clifford D; Krentz, Kathy J; Xing, Yongna; Bradfield, Christopher A

Published In Toxicol Sci, (2021 04 12)

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.

PubMed ID: 33480436

MeSH Terms: Alleles; Animals; Aryl Hydrocarbon Receptor Nuclear Translocator/genetics; Basic Helix-Loop-Helix Transcription Factors; Liver*/metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Receptors, Aryl Hydrocarbon*/genetics; Receptors, Aryl Hydrocarbon*/metabolism