In addition, a phylogenetic tree was constructed using the grouper β-HSD protein sequences to determine whether the exon-intron structure is consistent with the phylogenetic tree (Figure 2A). As expected, several genes with similar exon/intron structures were clustered together on the phylogenetic tree, such as hsd17b7 / hsd17b7l , hsd20b2 / hsd17b12a / hsd17b12b . However, due to large number of exon/intron structure types of the grouper β -hsd genes, only a few genes shared similar structures. The functional domains of grouper β-HSD were predicted by the CD-Search (Marchler-Bauer et al., 2017) based on their protein sequences (Figure 2C). As shown in Figure 2C, 18 of the 19 grouper β-HSDs possessed an SDR superfamily domain, except Hsdl2, indicating a high level of conservation of β -hsd genes belonging to the SDR superfamily. In addition to the SDR superfamily domain, Hsd17b4 also contained two other domains: PLN02864 superfamily domain and SCP2 superfamily domain. Notably, Hsdl2 was a member of the SDR superfamily, but no SDR superfamily domain existed in grouper Hsdl2, according to the CDD prediction.
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3β-HSD is potently inhibited by azastene, cyanoketone, epostane, and trilostane. [4] Medroxyprogesterone acetate and medrogestone are weak inhibitors of 3β-HSD which may substantially inhibit it at high dosages. Human steroidogenesis, showing reactions of 3β-HSD near-left in green box. Clinical significance Edit. The fetal adrenal cortex lacks expression of the enzyme early on, thus mineralocorticoids (e.g. aldosterone) and glucocorticoids (e.g. cortisol) cannot be synthesized. This is significant because cortisol induces type II pneumocytes of the lungs to synthesize and secrete pulmonary surfactant; without pulmonary surfactant to reduce the alveolar surface tension, premature neonates may die of neonatal respiratory distress syndrome. Claim jogo.
(1972) demonstrated that human amnion and chorion contain estrogen sulfatase and 17 β -dehydrogenase activities, whereas the chorion, but not the amnion, contain low levels of aromatase activity. Gant et al. (1977) carefully examined the biochemical properties of sulfatase activity with both DHEAS and P 5 S as substrates. Sulfatase activity was found in the microsomal fraction prepared from chorion but not amnion. Interestingly, activity was lower in week 10 than at term and three- to fourfold higher activity was observed with membranes from anencephalic fetuses. An early study by Jirásek et al . (1969) indicating 3 β -HSD/Δ 5 − 4 -isomerase activity in the chorion was also extended by Gant et al . (1977) . In addition, they observed low levels of steroid 5 α -reductase activity. More recently, Gibb et al .
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