Analysis of the coordinate expression of 3-hydroxy-3-methylglutaryl coenzyme A synthase and reductase activities in Chinese hamster ovary fibroblasts
| Autor: | Michael Sinensky, R Torget, Robin Schnitzer-Polokoff, Judy Logel |
|---|---|
| Rok vydání: | 1983 |
| Předmět: |
Hydroxymethylglutaryl-CoA Synthase
endocrine system Coenzyme A Biophysics Cycloheximide Reductase Naphthalenes Biochemistry Cell Line chemistry.chemical_compound Cricetulus Cricetinae Animals Lovastatin Molecular Biology Derepression ATP synthase biology Cholesterol Chinese hamster ovary cell Ovary Oxo-Acid-Lyases Fibroblasts Molecular biology chemistry Gene Expression Regulation HMG-CoA reductase Mutation biology.protein Female Hydroxymethylglutaryl CoA Reductases |
| Zdroj: | Archives of biochemistry and biophysics. 227(1) |
| ISSN: | 0003-9861 |
| Popis: | Decreased activities of both 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) synthase and HMG CoA reductase are observed in the presence of sterol in the Chinese hamster ovary (CHO) fibroblast. In three different genotypes of CHO cell mutants resistant to 25-hydroxycholesterol both enzyme activities exhibit a decreased response to 25-hydroxycholesterol compared to wild-type cells. Permanently repressed levels of both HMG CoA synthase and HMG CoA reductase activities are observed in another CHO mutant, phenotypically a mevalonate auxotroph. Mevinolin, a competitive inhibitor of HMG CoA reductase, has no effect on HMG CoA synthase activity measured in vitro. Incubation of CHO cells with sublethal concentrations of mevinolin produces an inhibition of the conversion of [14C]acetate to cholesterol and results in elevated levels of both HMG CoA synthase and HMG CoA reductase activities. Studies of CHO cells in sterol-free medium supplemented with cycloheximide indicate that continuous protein synthesis is not required for the maximal expression of HMG CoA synthase activity and provide an explanation for the lack of temporal similarity between HMG CoA synthase and reductase activities after derepression. These results support the hypothesis of a common mode of regulation for HMG CoA synthase and HMG CoA reductase activities in CHO fibroblasts. |
| Databáze: | OpenAIRE |
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