Heme is a positive regulator of cytochrome P-450 gene transcription

Arch Biochem Biophys. 1988 Aug 1;264(2):584-90. doi: 10.1016/0003-9861(88)90324-4.

Abstract

Inhibitors of heme biosynthesis such as CoCl2, 3-amino-1,2,4-triazole, and thioacetamide block the 3-methylcholanthrene-mediated induction of cytochrome P-450 (c + d) messenger RNAs and their transcription in rat liver. This effect is specific, since the messenger RNA levels for albumin and glutathione transferase (Ya + Yc) and their transcription are not significantly influenced under conditions of heme depletion. Exogenous administration of heme at very low doses (50 micrograms/100 g body wt) is able to completely counteract the effects of the heme biosynthetic inhibitors on cytochrome P-450 (c + d) messenger RNA levels and their transcription. This constitutes a direct proof for the role of heme as a positive regulator of cytochrome P-450 gene transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amitrole / pharmacology
  • Animals
  • Base Sequence
  • Cobalt / pharmacology
  • Cytochrome P-450 Enzyme System / genetics*
  • DNA / genetics
  • DNA, Recombinant
  • Heme / antagonists & inhibitors
  • Heme / biosynthesis
  • Heme / physiology*
  • Male
  • Methylcholanthrene / pharmacology
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • RNA, Messenger / biosynthesis
  • Rats
  • Thioacetamide / pharmacology
  • Transcription, Genetic* / drug effects

Substances

  • DNA, Recombinant
  • RNA, Messenger
  • Thioacetamide
  • Cobalt
  • Heme
  • Methylcholanthrene
  • DNA
  • Cytochrome P-450 Enzyme System
  • cobaltous chloride
  • Amitrole