Literature DB >> 20231332

Amino acid substitutions in the aryl hydrocarbon receptor ligand binding domain reveal YH439 as an atypical AhR activator.

Fiona Whelan1, Nan Hao, Sebastian G B Furness, Murray L Whitelaw, Anne Chapman-Smith.   

Abstract

The aryl hydrocarbon receptor (AhR) is traditionally defined as a transcription factor activated by exogenous polyaromatic and halogenated aromatic hydrocarbon (PAH/HAH) ligands. Active AhR induces genes involved in xenobiotic metabolism, including cytochrome P4501A1, which function to metabolize activating ligands. However, recent studies implicate AhR in biological events that are apparently unrelated to the xenobiotic response, implying that endogenous activation mechanisms exist. Three AhR genes in zebrafish (Danio rerio) encode proteins that demonstrate differential activation in response to PAH/HAHs, with the nonresponsive drAhR1a having some sequence divergence from the PAH/HAH-responsive AhRs in the ligand binding domain (LBD). We used these differences to guide the mutagenesis of mouse AhR (mAhR), aiming to generate variants that functionally discriminate between activation mechanisms. We found substitution of histidine 285 in the LBD with tyrosine gave a receptor that could be activated by isopropyl-2-(1,3-dithietane-2-ylidene)-2-[N-(4-methylthiazol-2-yl)carbamoyl]acetate (YH439), a potential AhR ligand chemically distinct from classic PAH/HAH-type ligands, but prevented activation by both exogenous PAH/HAH ligands and the endogenous activation mimics of suspension culture and application of shear-stressed serum. The differential response of H285Y mAhR to YH439 suggests that this activator has a novel mode of interaction that tolerates tyrosine at position 285 in the LBD and is distinct from the binding mode of the well characterized PAH/HAH ligands. In support of this, the PAH-type antagonist 3',4'-dimethoxyflavone blocked mAhR activation by 2,3,7,8-tetrachlorodibenzo-p-dioxin but not YH439. Furthermore, the strict correlation between response to exogenous PAH/HAH ligands and mimics of endogenous activation suggests that a PAH-type ligand may underpin endogenous mechanisms of activation.

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Year:  2010        PMID: 20231332     DOI: 10.1124/mol.109.062927

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  9 in total

1.  And Now for Something Completely Different: Diversity in Ligand-Dependent Activation of Ah Receptor Responses.

Authors:  Michael S Denison; Samantha C Faber
Journal:  Curr Opin Toxicol       Date:  2017-02

2.  Development of novel CH223191-based antagonists of the aryl hydrocarbon receptor.

Authors:  Eun-Young Choi; Hyosung Lee; R W Cameron Dingle; Kyung Bo Kim; Hollie I Swanson
Journal:  Mol Pharmacol       Date:  2011-10-03       Impact factor: 4.436

Review 3.  Exactly the same but different: promiscuity and diversity in the molecular mechanisms of action of the aryl hydrocarbon (dioxin) receptor.

Authors:  Michael S Denison; Anatoly A Soshilov; Guochun He; Danica E DeGroot; Bin Zhao
Journal:  Toxicol Sci       Date:  2011-09-09       Impact factor: 4.849

4.  CH223191 is a ligand-selective antagonist of the Ah (Dioxin) receptor.

Authors:  Bin Zhao; Danica E Degroot; Ai Hayashi; Guochun He; Michael S Denison
Journal:  Toxicol Sci       Date:  2010-07-15       Impact factor: 4.849

5.  Comparative analysis of homology models of the AH receptor ligand binding domain: verification of structure-function predictions by site-directed mutagenesis of a nonfunctional receptor.

Authors:  Domenico Fraccalvieri; Anatoly A Soshilov; Sibel I Karchner; Diana G Franks; Alessandro Pandini; Laura Bonati; Mark E Hahn; Michael S Denison
Journal:  Biochemistry       Date:  2013-01-14       Impact factor: 3.162

6.  Ligand promiscuity of aryl hydrocarbon receptor agonists and antagonists revealed by site-directed mutagenesis.

Authors:  Anatoly A Soshilov; Michael S Denison
Journal:  Mol Cell Biol       Date:  2014-03-03       Impact factor: 4.272

7.  Nucleotide specificity of DNA binding of the aryl hydrocarbon receptor:ARNT complex is unaffected by ligand structure.

Authors:  Danica E DeGroot; Michael S Denison
Journal:  Toxicol Sci       Date:  2013-10-17       Impact factor: 4.849

8.  Identification of residues in the N-terminal PAS domains important for dimerization of Arnt and AhR.

Authors:  Nan Hao; Murray L Whitelaw; Keith E Shearwin; Ian B Dodd; Anne Chapman-Smith
Journal:  Nucleic Acids Res       Date:  2011-01-17       Impact factor: 16.971

9.  Comparative In Vitro and In Silico Analysis of the Selectivity of Indirubin as a Human Ah Receptor Agonist.

Authors:  Samantha C Faber; Anatoly A Soshilov; Sara Giani Tagliabue; Laura Bonati; Michael S Denison
Journal:  Int J Mol Sci       Date:  2018-09-10       Impact factor: 5.923

  9 in total

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