Martin Luc J, Tremblay Jacques J
Ontogeny-Reproduction, Room T1-49, CHUL Research Center, 2705 Laurier Boulevard, Ste-Foy, Québec, Canada G1V 4G2.
Endocrinology. 2005 Feb;146(2):861-9. doi: 10.1210/en.2004-0859. Epub 2004 Oct 21.
The human (h) 3beta-hydroxysteroid dehydrogenase/Delta5-Delta4 isomerase type 2 (3beta-HSD2) enzyme, encoded by the hHSD3B2 gene, is mainly found in gonads and adrenals. This enzyme catalyzes an essential early step in the biosynthesis of all classes of steroid hormones. The critical nature of the enzyme is supported by the occurrence of human syndromes that are associated with insufficient 3beta-HSD2 expression and/or activity. Although the need for a functional 3beta-HSD2 enzyme is indisputable, the molecular mechanisms that regulate HSD3B2 expression (both basal and hormone-induced) in steroidogenic cells remain poorly understood. A role for the Nur77 family of immediate-early orphan nuclear receptors in steroidogenesis has received recent interest. For example, Nur77 is present in gonads and adrenals, where its expression is robustly and rapidly induced by hormones that stimulate steroidogenic gene expression. Moreover, the expression patterns of Nur77 and at least one key steroidogenic gene (hHSD3B2) closely parallel one another. We now report that the hHSD3B2 promoter is indeed a novel target for Nur77 in both testicular Leydig cells and adrenal cells. We have mapped a novel response element located at -130 bp specific for Nur77 and not other orphan nuclear receptors (steroidogenic factor-1 and liver receptor homolog-1) previously shown to regulate hHSD3B2 promoter activity. This Nur77 element is essential and sufficient to confer Nur77 responsiveness to the hHSD3B2 promoter, and its mutation blunts basal and hormone-induced hHSD3B2 promoter activity in steroidogenic cells. We also show that Nur77 synergizes with all members of the steroid receptor coactivator family of coactivators on the hHSD3B2 promoter. Taken together, our identification of Nur77 as an important regulator of HSD3B2 promoter activity helps us to better define the tissue-specific and hormonal regulation of the HSD3B2 gene in steroidogenic cells.
人(h)3β-羟基类固醇脱氢酶/Δ5-Δ4异构酶2型(3β-HSD2)由hHSD3B2基因编码,主要存在于性腺和肾上腺中。该酶催化各类甾体激素生物合成中一个至关重要的早期步骤。与3β-HSD2表达和/或活性不足相关的人类综合征的出现,支持了该酶的关键性质。尽管功能性3β-HSD2酶的必要性无可争议,但调节类固醇生成细胞中HSD3B2表达(基础表达和激素诱导表达)的分子机制仍知之甚少。Nur77家族即刻早期孤儿核受体在类固醇生成中的作用最近受到了关注。例如,Nur77存在于性腺和肾上腺中,在那里其表达受到刺激类固醇生成基因表达的激素的强烈且快速诱导。此外,Nur77和至少一种关键类固醇生成基因(hHSD3B2)的表达模式紧密平行。我们现在报告,hHSD3B2启动子确实是睾丸间质细胞和肾上腺细胞中Nur77的一个新靶点。我们已经定位了一个位于-130 bp处的新型反应元件,该元件对Nur77具有特异性,而对先前显示可调节hHSD3B2启动子活性的其他孤儿核受体(类固醇生成因子-1和肝脏受体同源物-1)不具有特异性。这个Nur77元件对于赋予hHSD3B2启动子对Nur77的反应性是必不可少且充分的,其突变会减弱类固醇生成细胞中基础和激素诱导的hHSD3B2启动子活性。我们还表明,Nur77与类固醇受体共激活因子家族的所有成员在hHSD3B2启动子上具有协同作用。综上所述,我们将Nur77鉴定为HSD3B2启动子活性的重要调节因子,这有助于我们更好地定义类固醇生成细胞中HSD3B2基因的组织特异性和激素调节。