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The Ah Receptor: Adaptive Metabolism, Ligand Diversity, and the Xenokine Model.芳烃受体:适应性代谢、配体多样性与异种生物因子模型
Chem Res Toxicol. 2020 Apr 20;33(4):860-879. doi: 10.1021/acs.chemrestox.9b00476. Epub 2020 Apr 7.
2
CRISPR/Cas9 can mediate high-efficiency off-target mutations in mice in vivo.CRISPR/Cas9可在体内介导小鼠发生高效的脱靶突变。
Cell Death Dis. 2018 Oct 27;9(11):1099. doi: 10.1038/s41419-018-1146-0.
3
The Environmental Sensor AHR Protects from Inflammatory Damage by Maintaining Intestinal Stem Cell Homeostasis and Barrier Integrity.环境传感器 AHR 通过维持肠道干细胞稳态和屏障完整性来防止炎症损伤。
Immunity. 2018 Aug 21;49(2):353-362.e5. doi: 10.1016/j.immuni.2018.07.010. Epub 2018 Aug 14.
4
AhR signaling pathways and regulatory functions.芳香烃受体(AhR)信号通路与调控功能。
Biochim Open. 2018 Jun 11;7:1-9. doi: 10.1016/j.biopen.2018.05.001. eCollection 2018 Dec.
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The CRISPR tool kit for genome editing and beyond.CRISPR 工具包用于基因组编辑及其他领域。
Nat Commun. 2018 May 15;9(1):1911. doi: 10.1038/s41467-018-04252-2.
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Aryl hydrocarbon receptor (AHR): "pioneer member" of the basic-helix/loop/helix per-Arnt-sim (bHLH/PAS) family of "sensors" of foreign and endogenous signals.芳烃受体(AHR):外源性和内源性信号“传感器”的碱性螺旋/环/螺旋Per-Arnt-Sim(bHLH/PAS)家族的“先驱成员”。
Prog Lipid Res. 2017 Jul;67:38-57. doi: 10.1016/j.plipres.2017.06.001. Epub 2017 Jun 9.
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Cellular and Molecular Dynamics of Th17 Differentiation and its Developmental Plasticity in the Intestinal Immune Response.肠道免疫反应中Th17细胞分化的细胞与分子动力学及其发育可塑性
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Structural hierarchy controlling dimerization and target DNA recognition in the AHR transcriptional complex.结构层次控制 AHR 转录复合物中二聚化和靶 DNA 识别。
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9
Aryl hydrocarbon receptor is required for optimal B-cell proliferation.芳烃受体是B细胞最佳增殖所必需的。
EMBO J. 2017 Jan 4;36(1):116-128. doi: 10.15252/embj.201695027. Epub 2016 Nov 14.
10
Histological and Transcriptomic Changes in Male Zebrafish Testes Due to Early Life Exposure to Low Level 2,3,7,8-Tetrachlorodibenzo-p-Dioxin.幼年暴露于低水平2,3,7,8-四氯二苯并对二恶英对雄性斑马鱼睾丸的组织学和转录组学变化
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利用编辑重组方法在 Ahr 基因座上生成等位基因系列。

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

机构信息

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.

出版信息

Toxicol Sci. 2021 Apr 12;180(2):239-251. doi: 10.1093/toxsci/kfab005.

DOI:10.1093/toxsci/kfab005
PMID:33480436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8041461/
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.

摘要

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。