Blanchard Pierre-Gilles, Luu-The Van
Oncology and Molecular Endocrinology Research Center, Laval University Hospital Research Center (CRCHUL) and Laval University, 2705 Laurier Boulevard, Quebec, Canada.
J Endocrinol. 2007 Aug;194(2):449-55. doi: 10.1677/JOE-07-0144.
Recently, we have shown that human and monkey type 12 17beta-hydroxysteroid dehydrogenases (17beta-HSD12) are estrogen-specific enzymes catalyzing the transformation of estrone (E(1)) into estradiol (E(2)). To further characterize this novel steroidogenic enzyme in an animal model, we have isolated a cDNA fragment encoding mouse 17beta-HSD12 and characterized its enzymatic activity. Using human embryonic kidney cells (HEK)-293 cells stably expressing mouse 17beta-HSD12, we found that in contrast with the human and monkey enzymes, which are specific for the transformation of E(1) to E(2), mouse 17beta-HSD12 also catalyzes the transformation of 4-androstenedione into testosterone (T), dehydroepiandroster-one (DHEA) into 5-androstene-3beta,17beta-diol (5-diol), as well as androsterone into 5alpha-androstane-3alpha,17beta-diol (3alpha-diol). Previously, we have shown that the specificity of human and monkey 17beta-HSD12s for C18-steroid is due to the presence of a bulky phenylalanine (F) at position 234 creating steric hindrance, preventing the entrance of C19-steroids into the active site. To determine whether the smaller size of the corresponding leucine (L) in the mouse sequence is responsible for the entrance of androgenic substrates, we performed site-directed mutagenesis to substitute Leu 234 for Phe in the mouse enzyme. In agreement with our hypothesis, the mutated enzyme has a highly reduced ability to metabolize androgens. mRNA quantification in several mouse tissues using real-time PCR shows that mouse 17beta-HSD12 mRNA is highly expressed in the female clitoral gland, male preputial gland, as well as in retroperitoneal fat and adrenal of both sexes. The differential androgenic/estrogenic substrate specificity of type 12 17beta-HSD in the mouse and primates seems to agree with the observation that androgen and estrogen in the mouse are provided almost exclusively by gonads, while in primates an important part of these steroid hormones are produced locally from adrenal precursors.
最近,我们已经表明,人和猴的12型17β-羟基类固醇脱氢酶(17β-HSD12)是雌激素特异性酶,可催化雌酮(E1)转化为雌二醇(E2)。为了在动物模型中进一步表征这种新型类固醇生成酶,我们分离了编码小鼠17β-HSD12的cDNA片段并表征了其酶活性。使用稳定表达小鼠17β-HSD12的人胚肾细胞(HEK)-293细胞,我们发现,与特异性将E1转化为E2的人和猴酶不同,小鼠17β-HSD12还催化4-雄烯二酮转化为睾酮(T)、脱氢表雄酮(DHEA)转化为5-雄烯-3β,17β-二醇(5-二醇),以及雄甾酮转化为5α-雄烷-3α,17β-二醇(3α-二醇)。此前,我们已经表明,人和猴17β-HSD12对C18-类固醇的特异性是由于234位存在一个庞大的苯丙氨酸(F),产生空间位阻,阻止C19-类固醇进入活性位点。为了确定小鼠序列中相应亮氨酸(L)的较小尺寸是否是雄激素底物进入的原因,我们进行了定点诱变,将小鼠酶中的Leu 234替换为Phe。与我们的假设一致,突变酶代谢雄激素的能力大大降低。使用实时PCR对几种小鼠组织进行mRNA定量分析表明,小鼠17β-HSD12 mRNA在雌性阴蒂腺、雄性包皮腺以及两性的腹膜后脂肪和肾上腺中高表达。小鼠和灵长类动物中12型17β-HSD的雄激素/雌激素底物特异性差异似乎与以下观察结果一致:小鼠中的雄激素和雌激素几乎完全由性腺提供,而在灵长类动物中,这些类固醇激素的重要部分是由肾上腺前体在局部产生的。