cDNA cloning and analysis of chick-embryo-liver cytochrome P-450 mRNA induced by porphyrinogenic drugs.
Hepatic microsomal cytochrome P-450 was elevated in 17-day chick embryos by combined administration of the porphyrinogenic drugs 2-allyl-2-isopropylacetamide and 3,5-diethoxycarbonyl-1,4-dihydrocollidine. Increased apoprotein levels were the result of de novo protein synthesis; in vitro obtained translation data suggested that cytochrome P-450 mRNA levels were elevated. A 1000-base cDNA sequence for the drug-induced cytochrome P-450 mRNA was isolated from a chick embryo cDNA 'library' and this was used as a specific probe to investigate drug-mediated induction of cytochrome P-450 mRNA. RNA-DNA 'dot' hybridisation studies demonstrated that drug treatment led to a 3-5-fold increase in the level of this mRNA and that the mRNA was predominantly associated with membrane-bound polyribosomes. Treatment of embryos with the drugs individually demonstrated that both of them induced synthesis of the same mRNA. These studies show directly that treatment of chick embryos with 2-allyl-2-isopropylacetamide or 3,5-diethoxycarbonyl-1,4-dihydrocollidine caused increased levels of cytochrome P-450 mRNA and suggest that this involved increased transcription of the gene.[1]References
- cDNA cloning and analysis of chick-embryo-liver cytochrome P-450 mRNA induced by porphyrinogenic drugs. Brooker, J.D., O'Connor, R. Eur. J. Biochem. (1982) [Pubmed]
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