Fabre S, Manin M, Pailhoux E, Veyssière G, Jean C
Laboratoire de Physiologie Comparée et Endocrinologie, Centre National de la Recherche Scientifique Unité de Recherche Associée 360, Université Blaise Pascal-Clermont Ferrand II, Aubière, France.
J Biol Chem. 1994 Feb 25;269(8):5857-64.
Mouse vas deferens protein (MVDP), a member of the aldo-keto reductase superfamily, is exclusively produced in the epithelial cells of the deferent duct under androgenic regulation. To better understand androgenregulated MVDP gene expression, the location and sequences of androgen response elements (AREs) in the 5'-flanking DNA were determined. Sequence analysis revealed two putative AREs as follows: one between positions -1186 and -1171 (distal ARE) and the other between -111 and -97 (proximal ARE). To study hormonal regulation, fragments of the MVDP promoter region, extending from residue -1804 to +41, were linked to the chloramphenicol acetyltransferase (CAT) reporter gene and cotransfected with a human androgen receptor expression vector into T47D cells in a transient expression assay. A minimal region (-121 to +41) was identified as being sufficient for androgen-regulated gene expression. A mutation in proximal ARE almost completely abolished androgen induction of CAT. One copy of the sequence TGAAGT tcc TGTTCT, cloned in the opposite orientation in front of the thymidine kinase promoter, confers androgen responsiveness to the CAT reporter gene. Androgen transcriptional activity was not detected with the distal ARE. The data provide strong evidence that transcriptional regulation of the MVDP gene occurs via the sequence TGAAGT tcc TGTTCT.
小鼠输精管蛋白(MVDP)是醛糖还原酶超家族的成员之一,在雄激素调控下由输精管上皮细胞特异性产生。为了更好地理解雄激素调控的MVDP基因表达,我们确定了5'-侧翼DNA中雄激素反应元件(AREs)的位置和序列。序列分析揭示了两个假定的AREs,如下所示:一个位于-1186至-1171位之间(远端ARE),另一个位于-111至-97位之间(近端ARE)。为了研究激素调控,将从-1804至+41位的MVDP启动子区域片段与氯霉素乙酰转移酶(CAT)报告基因连接,并在瞬时表达实验中与人类雄激素受体表达载体共转染到T47D细胞中。一个最小区域(-121至+41)被确定为足以进行雄激素调控的基因表达。近端ARE中的一个突变几乎完全消除了雄激素对CAT的诱导作用。在胸苷激酶启动子前以相反方向克隆的TGAAGT tcc TGTTCT序列的一个拷贝赋予了CAT报告基因雄激素反应性。远端ARE未检测到雄激素转录活性。这些数据提供了强有力的证据,表明MVDP基因的转录调控是通过TGAAGT tcc TGTTCT序列发生的。