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.
Toxicol Sci. 2021 Apr 12;180(2):239-251. doi: 10.1093/toxsci/kfab005.
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.
芳香烃受体 (AHR) 是一种配体激活的转录因子,也是环境传感器 PER-ARNT-SIM (PAS) 超家族的成员。AHR 参与一系列生物学过程,包括外源性物质的适应性代谢、某些环境污染物的毒性、血管发育、生育能力和免疫功能。包括 Ahr 缺失和 Ahr 条件性缺失 (Ahrfx) 小鼠在内的小鼠模型广泛用于研究 AHR 介导的生物学和毒性。Ahr 条件性缺失小鼠携带低亲和力 Ahrd 等位基因,与广泛使用的携带高亲和力 Ahrb1 等位基因的 C57BL/6 小鼠相比,对某些外源性 AHR 配体的结合亲和力低约 10 倍。在这里,我们报告了一种新型小鼠模型,该模型引入了 V375A 多态性,将低亲和力等位基因转化为高亲和力等位基因,提供了一种更敏感的条件性模型。在这种新型条件性等位基因的产生过程中,还出现了另外两种突变体,包括 PAS-B 结构域中的 3 个碱基缺失 (AhrNG367R) 和 PAS-B 结构域中的提前终止密码子 (AhrTer383)。AhrNG367R 等位基因表现为缺失表型,而 AhrTer383 等位基因在评估静脉导管和肝叶重量终点时表现为反突变体。这些新模型代表了一系列工具,将有助于进一步表征 AHR 生物学。