Abstract
Expression of a series of Ah receptor (AhR) deletion mutants in an in vitro translation system has been previously used to map several functional domains of the murine AhR (Dolwick et al. (1993) Proc. Natl. Acad. Sci. USA 90, 8566-8570). In this report, quantitative immunoprecipitation of 90-kDa heat shock protein (hsp90) from reticulocyte lysate allowed us to measure the level of the AhR and AhR deletion mutants complexed with hsp90. After translation of a series of deletion mutants it was determined that there are two distinct domains important in forming a stable AhR/hsp90 complex, corresponding to amino acid sequences 1-166 and 289-347 of the AhR. Neither ARNT, nor Per were able to stably interact with hsp90. Thus, the AhR appears to be a unique member of the PAS domain family of proteins that binds a known ligand and stably interacts with hsp90.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antibodies, Monoclonal / immunology
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Antibodies, Monoclonal / metabolism
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Aryl Hydrocarbon Receptor Nuclear Translocator
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Binding Sites / genetics
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DNA-Binding Proteins / chemistry
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Electrophoresis, Polyacrylamide Gel
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HSP90 Heat-Shock Proteins / immunology
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HSP90 Heat-Shock Proteins / metabolism*
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Helix-Loop-Helix Motifs / physiology
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Mice
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Mutation / genetics
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Precipitin Tests
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Protein Binding
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Protein Biosynthesis / genetics
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Receptors, Aryl Hydrocarbon / chemistry*
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Receptors, Aryl Hydrocarbon / genetics
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Receptors, Aryl Hydrocarbon / metabolism
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Sequence Deletion / genetics
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Transcription Factors / metabolism
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Transcription, Genetic / genetics
Substances
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Antibodies, Monoclonal
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Arnt protein, mouse
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DNA-Binding Proteins
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HSP90 Heat-Shock Proteins
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Receptors, Aryl Hydrocarbon
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Transcription Factors
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Aryl Hydrocarbon Receptor Nuclear Translocator