A 1169 base pair fragment of bovine 3β-hydroxysteroid dehydrogenase/Δ64 isomerase (3β-HSD) cDNA was used to quantitate 3β-HSD messenger RNA (mRNA) levels in the bovine ovary during the estrous cycle. The content of 3β- HSD protein was measured by immunoblot analysis using an antiserum developed in rabbits against human 3β-HSD, whereas 3β-HSD activity was measured using [3H]pregnenolone, [3H] dehydroepiandrosterone, and [3H]androst-5-ene-3β,17β-diol as substrates. There was a parallel increase in 3β-HSD mRNA, protein content, and enzymatic activity levels from days 1–3 after estrus to maximal values at 50–100% above control on days 8–11 after estrus. Thereafter, all values decreased progressively until days 16–17 before a dramatic fall to 5% or less than maximal values on days 18–20 after estrus. Almost superimposable results of enzymatic activity were obtained with the three substrates, thus suggesting a unique 3β-HSD or parallel changes in the activity of multiple 3β-HSDs. The above-described changes observed during the luteal phase are almost exclusively due to variations in corpora lutea. In fact, 3β-HSD activity in ovarian follicles was approximately 10,000 lower than that measured in corpora lutea. The close correlation observed over a wide range of 3β-HSD mRNA, protein content, and activity levels suggests that changes of ovarian 3β-HSD activity are controlled at the level of 3β-HSD gene expression and/or 3β-HSD mRNA stability. (Endocrinology127: 2141–2148, 199)

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