Céspedes, Miguel Angel, Galindo, Maximo Ibo and Couso, Juan Pablo (2010) Dioxin Toxicity In Vivo Results from an Increase in the Dioxin-Independent Transcriptional Activity of the Aryl Hydrocarbon Receptor. PLoS ONE, 5 (11). ISSN 1932-6203
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Abstract
The Aryl hydrocarbon receptor (Ahr) is the nuclear receptor mediating the toxicity of dioxins -widespread and persistent pollutants whose toxic effects include tumor promotion, teratogenesis, wasting syndrome and chloracne. Elimination of Ahr in mice eliminates dioxin toxicity but also produces adverse effects, some seemingly unrelated to dioxin. Thus the relationship between the toxic and dioxin-independent functions of Ahr is not clear, which hampers understanding and treatment of dioxin toxicity. Here we develop a Drosophila model to show that dioxin actually increases the in vivo dioxin-independent activity of Ahr. This hyperactivation resembles the effects caused by an increase in the amount of its dimerisation partner Ahr nuclear translocator (Arnt) and entails an increased transcriptional potency of Ahr, in addition to the previously described effect on nuclear translocation. Thus the two apparently different functions of Ahr, dioxin-mediated and dioxin-independent, are in fact two different levels (hyperactivated and basal, respectively) of a single function.
Item Type: | Article |
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Additional Information: | Article Number: e15382 |
Schools and Departments: | School of Life Sciences > Biochemistry Brighton and Sussex Medical School > Clinical and Experimental Medicine |
Depositing User: | Miguel Cespedes |
Date Deposited: | 06 Feb 2012 19:19 |
Last Modified: | 02 Jul 2019 18:05 |
URI: | http://sro.sussex.ac.uk/id/eprint/20081 |
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