Involvement of heme in the transcriptional activation of CYPIIB1/B2 gene by phenobarbitone in rat liver—Studies with succinylacetone
Autor: | Govindarajan Padmanaban, Venkataraman Venkateswar |
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Rok vydání: | 1991 |
Předmět: |
Male
Transcription Genetic Biophysics Heme In Vitro Techniques Biology Biochemistry chemistry.chemical_compound Cytochrome P-450 Enzyme System Transcription (biology) Animals RNA Messenger Molecular Biology Gene chemistry.chemical_classification Molecular Reproduction Development & Genetics ATP synthase Porphobilinogen Synthase Molecular biology Heptanoates Rats Heme oxygenase Enzyme Gene Expression Regulation Liver chemistry Phenobarbital Rat liver biology.protein Thioacetamide |
Zdroj: | Archives of Biochemistry and Biophysics. 290:167-172 |
ISSN: | 0003-9861 |
DOI: | 10.1016/0003-9861(91)90603-g |
Popis: | Earlier studies in this laboratory had implicated heme to function as a positive modulator of phenobarbitone-mediated activation of CYPIIB1/B2 gene transcription in rat liver. However, recent reports have indicated that succinylacetone, a specific inhibitor of delta-aminolevulinate dehydrase, does not affect this process. The present studies indicate that succinylacetone does inhibit the phenobarbitone-mediated increase in CYPIIB1/B2 mRNAs and their transcription in rat liver at early time points (45 min to 3 h), but the inhibition is not pronounced at later time points (16 h). Succinylacetone is a weaker inhibitor of heme biosynthesis than CoCl2, 3-amino-1,2,4-triazole, or thioacetamide used earlier in this laboratory. Succinylacetone induces delta-aminolevulinate synthase, whereas the other compounds depress the levels of the enzyme. There is a good correlation between the amount of freshly synthesized nuclear heme pool and the activation of CYPIIB1/B2 transcription by phenobarbitone. A model implicating a nuclear heme pool regulating the transcription of delta-aminolevulinate synthase, CYPIIB1/B2, and heme oxygenase genes is proposed. |
Databáze: | OpenAIRE |
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