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Molecular and Cellular Biology, August 2000, p. 6095-6104, Vol. 20, No. 16
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Analysis of the Complex Relationship between
Nuclear Export and Aryl Hydrocarbon Receptor-Mediated Gene
Regulation
Richard S.
Pollenz* and
E. Rick
Barbour
Department of Biochemistry and Molecular
Biology, Medical University of South Carolina, Charleston, South
Carolina
Received 10 February 2000/Returned for modification 29 March
2000/Accepted 22 May 2000
The aryl hydrocarbon receptor (AHR) contains signals for both
nuclear import and nuclear export (NES). The purpose of the studies in
this report was to determine the relationship between the nuclear
export of the AHR and AHR-mediated gene regulation. Blockage of nuclear
export in HepG2 cells with leptomycin B (LMB) resulted in increased
levels of AHR-AHR nuclear translocator (ARNT) complex in the nucleus
and correlative reductions in agonist-stimulated AHR degradation.
However, LMB exposure inhibited agonist-mediated induction of numerous
AHR-responsive reporter genes by 75 to 89% and also inhibited
induction of endogenous CYP1A1. LMB did not transform the
AHR to a ligand binding species or affect activation by TCDD
(2,3,7,8-tetrachlorodibenzo-p-dioxin). Mutagenesis of leucines 66 and 71 of the putative AHR NES resulted in a protein with
reduced function in dimerization to ARNT and binding to DNA, while
alanine substitution at leucine 69 (AHRA69) resulted in an
AHR that bound with ARNT and associated with DNA. AHRA69
protein injected directly into the nuclei of E36 cells remained nuclear following 6 h of agonist stimulation. In transient-transfection assays, AHRA69 accumulated within the nucleus was not
degraded efficiently following agonist exposure. Finally,
AHRA69 supported induction of AHR-responsive reporter genes
in an agonist-dependent manner. These findings show that it is possible
to generate an AHR protein defective in nuclear export that is
functional in agonist-mediated gene induction. This implies that the
negative effect of LMB on agonist-mediated gene induction is
independent of the nuclear export of the AHR.
*
Corresponding author. Present address: Department of
Biology, University of South Florida, 4204 E. Fowler Ave., SCA 110, Tampa, FL 33620-5200. Phone: (813) 974-3250. Fax: (813) 974-3263. E-mail: rpollen{at}chuma.cas.usf.edu.
Molecular and Cellular Biology, August 2000, p. 6095-6104, Vol. 20, No. 16
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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