Abstract
Cyclophilin-40 (CyP40) promotes the formation of the gel shift complex that contains the aryl hydrocarbon receptor (AhR), AhR nuclear translocator (Arnt) and dioxin response element (DRE) using baculovirus expressed proteins. Here we reported that CyP40 plays a role in the AhR signaling. When the CyP40 content in MCF-7 cells is reduced, up-regulation of cyp1a1 and cyp1b1 by 3-methylchloranthrene (3MC) is also reduced, suggesting that CyP40 is essential for maximal AhR function. The CyP40 region containing amino acids 186-215, but not the peptidyl-prolyl cis-trans isomerase and tetratricopeptide repeat domains, is essential for forming the AhR/Arnt/DRE complex. CyP40 is found in the cell nucleus after 3MC treatment and appears to promote the DRE binding form of the AhR/Arnt heterodimer.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Amino Acid Sequence
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Animals
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Aryl Hydrocarbon Hydroxylases / genetics
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Aryl Hydrocarbon Receptor Nuclear Translocator / metabolism*
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Cell Line, Tumor
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Cell Nucleus / metabolism
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Cyclophilins / genetics
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Cyclophilins / metabolism*
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Cytochrome P-450 CYP1A1 / genetics
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Cytochrome P-450 CYP1B1
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Dimerization
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Dioxins / pharmacology
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Electrophoretic Mobility Shift Assay
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Humans
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Methylcholanthrene / pharmacology
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Peptidyl-Prolyl Isomerase F
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Receptors, Aryl Hydrocarbon / metabolism*
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Response Elements / drug effects
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Signal Transduction
Substances
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Peptidyl-Prolyl Isomerase F
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Dioxins
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Receptors, Aryl Hydrocarbon
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Aryl Hydrocarbon Receptor Nuclear Translocator
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Methylcholanthrene
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Aryl Hydrocarbon Hydroxylases
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CYP1B1 protein, human
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Cytochrome P-450 CYP1A1
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Cytochrome P-450 CYP1B1
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Cyclophilins