Protein kinase C modulates regulation of the CYP1A1 gene by the aryl hydrocarbon receptor

Yue-Hwa Chen, Robert H. Tukey

Research output: Contribution to journalArticle

125 Citations (Scopus)

Abstract

Transcriptional activation of the human CYPIA1 gene by halogenated and polycyclic aromatic hydrocarbons is mediated by the aryl hydrocarbon receptor (AhR) complex, a ligand-dependent transcription factor. A competent AhR comprises at least two components following nuclear translocation and DNA binding, the AhR and the AhR nuclear translocator (Arnt) protein, whose combined action on human CYP1A1 gene transcription is shown to be dependent upon functional protein kinase C (PKC). In the present study, we examined the effects of phorbol 12-myristate 13-acetate, a potent PKC activator, on the ligand-induced transcriptional activation of the CYPIA1 gene and cellular function of the AhR in human HepG2 101L cells. The 101L cells carry a stable transgene consisting of 1800 bases of 5'-flanking DNA and the promoter of the human CYPIA1 gene linked to the firefly luciferase structural gene (Postlind, H., Vu, T. P., Tukey, R. H. and Quattrochi, L. C. (1993) Toxicol. Appl. Pharmacol. 118, 255-262). Pretreatment of cells with 12-myristate 13-acetate enhanced ligand-induced CYPIA1 gene expression 2-3-fold. Inhibition of PKC activity blocked directly the transcriptional activation and the transactivation of the CYPIA1 gene, indicating a role for PKC in the AhR- mediated transcriptional activation process. However, the DNA binding activities of the in vitro activated and the induced nuclear AhR as measured by electrophoretic mobility shift analysis were not affected when CYPIA1 transcription was inhibited, indicating the actions of PKC to be a nuclear event that works in concert with or precedes AhR binding to the gene. These results illustrate that PKC is absolutely essential for the cellular and molecular events that control induction of CYPIA1 gene transcription.

Original languageEnglish
Pages (from-to)26261-26266
Number of pages6
JournalJournal of Biological Chemistry
Volume271
Issue number42
DOIs
Publication statusPublished - 1996
Externally publishedYes

Fingerprint

Aryl Hydrocarbon Receptors
Cytochrome P-450 CYP1A1
Protein Kinase C
Genes
Transcriptional Activation
Transcription
Chemical activation
Ligands
DNA
Acetates
Aryl Hydrocarbon Receptor Nuclear Translocator
Firefly Luciferases
Electrophoretic mobility
Polycyclic Aromatic Hydrocarbons
Hep G2 Cells
Myristic Acid
Nuclear Proteins
Transgenes
Gene expression
Transcription Factors

ASJC Scopus subject areas

  • Biochemistry

Cite this

Protein kinase C modulates regulation of the CYP1A1 gene by the aryl hydrocarbon receptor. / Chen, Yue-Hwa; Tukey, Robert H.

In: Journal of Biological Chemistry, Vol. 271, No. 42, 1996, p. 26261-26266.

Research output: Contribution to journalArticle

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