Literature DB >> 10448124

Transactivation activity of human, zebrafish, and rainbow trout aryl hydrocarbon receptors expressed in COS-7 cells: greater insight into species differences in toxic potency of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners.

C C Abnet1, R L Tanguay, W Heideman, R E Peterson.   

Abstract

Transactivation assays were used to compare the potency and efficacy of polychlorinated dibenzo-p-dioxin (PCDD), dibenzofuran (PCDF), and biphenyl (PCB) congeners in activating aryl hydrocarbon receptors (AhRs) from rainbow trout (rtAhR2alpha and rtAhR2beta), zebrafish (zfAhR2), and human (huAhR), respectively. All AhRs were expressed with their species-specific AhR nuclear translocator (ARNT) in COS-7 cells. Transactivation activity was determined for two PCDD, two PCDF, and seven PCB congeners with each of the four AhR/ARNT pairs using prt1Aluc, a luciferase reporter driven by two dioxin-responsive enhancer elements (DREs) from the rainbow trout cyp1A gene. Maximal-fold induction, EC50, and relative potency values were calculated for congeners that exhibited dose-related activity in the assay. Of the four AhR/ARNT pairs tested with PCDD, PCDF, and non-ortho PCB congeners, three exhibited high activity (rainbow trout AhR2alpha, zebrafish AhR2, and human AhR), while rainbow trout AhR2beta had very weak or no activity. Comparisons between these AhRs showed that while mono-ortho PCBs were able to activate the human AhR, they were generally ineffective in activating rainbow trout and zebrafish AhR2s. This supports the hypothesis that structural differences between mammalian and fish AhRs may account for differences in relative potencies of the mono-ortho PCBs between mammals and fish. Another important finding was a significant difference in transactivation activity between the two rainbow trout AhR2 isoforms despite the fact that they are 95% identical at the amino acid level. For all PCDD, PCDF, and PCB agonists tested, rainbow trout AhR2alpha was significantly more active than AhR2beta. However, rainbow trout AhR2beta is active as a 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-activated transcription factor, with enhancer elements from the mouse cyp1A gene. This suggests that AhR2beta may have evolved to serve a different physiological function than AhR2alpha in salmonid fish species. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10448124     DOI: 10.1006/taap.1999.8719

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  20 in total

1.  AHR1B, a new functional aryl hydrocarbon receptor in zebrafish: tandem arrangement of ahr1b and ahr2 genes.

Authors:  Sibel I Karchner; Diana G Franks; Mark E Hahn
Journal:  Biochem J       Date:  2005-11-15       Impact factor: 3.857

2.  Aryl hydrocarbon receptors in the frog Xenopus laevis: two AhR1 paralogs exhibit low affinity for 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD).

Authors:  Jeremy A Lavine; Ashley J Rowatt; Tatyana Klimova; Aric J Whitington; Emelyne Dengler; Catherine Beck; Wade H Powell
Journal:  Toxicol Sci       Date:  2005-06-15       Impact factor: 4.849

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.  Distinct response to dioxin in an arylhydrocarbon receptor (AHR)-humanized mouse.

Authors:  Takashi Moriguchi; Hozumi Motohashi; Tomonori Hosoya; Osamu Nakajima; Satoru Takahashi; Seiichiroh Ohsako; Yasunobu Aoki; Noriko Nishimura; Chiharu Tohyama; Yoshiaki Fujii-Kuriyama; Masayuki Yamamoto
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-01       Impact factor: 11.205

5.  Ligand selectivity and gene regulation by the human aryl hydrocarbon receptor in transgenic mice.

Authors:  Colin A Flaveny; Iain A Murray; Chris R Chiaro; Gary H Perdew
Journal:  Mol Pharmacol       Date:  2009-03-19       Impact factor: 4.436

6.  Atranorin and lecanoric acid antagonize TCDD-induced xenobiotic response element-driven activity, but not xenobiotic response element-independent activity.

Authors:  Ken-Ichi Nakashima; Hiroki Tanabe; Yoshiaki Fujii-Kuriyama; Hidetoshi Hayashi; Makoto Inoue
Journal:  J Nat Med       Date:  2016-03-15       Impact factor: 2.343

7.  Optimizing multi-dimensional high throughput screening using zebrafish.

Authors:  Lisa Truong; Sean M Bugel; Anna Chlebowski; Crystal Y Usenko; Michael T Simonich; Staci L Massey Simonich; Robert L Tanguay
Journal:  Reprod Toxicol       Date:  2016-07-21       Impact factor: 3.143

8.  Cardiac myocyte-specific AHR activation phenocopies TCDD-induced toxicity in zebrafish.

Authors:  Kevin A Lanham; Jessica Plavicki; Richard E Peterson; Warren Heideman
Journal:  Toxicol Sci       Date:  2014-07-18       Impact factor: 4.849

9.  Functional properties of the four Atlantic salmon (Salmo salar) aryl hydrocarbon receptor type 2 (AHR2) isoforms.

Authors:  Maria C Hansson; Mark E Hahn
Journal:  Aquat Toxicol       Date:  2007-11-01       Impact factor: 4.964

10.  Biological responses of midge (Chironomus riparius) and lamprey (Lampetra fluviatilis) larvae in ecotoxicity assessment of PCDD/F-, PCB- and Hg-contaminated river sediments.

Authors:  J Salmelin; A K Karjalainen; H Hämäläinen; M T Leppänen; H Kiviranta; J V K Kukkonen; K M Vuori
Journal:  Environ Sci Pollut Res Int       Date:  2016-06-09       Impact factor: 4.223

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