Winklehner-Jennewein P, Geymayer S, Lechner J, Welte T, Hansson L, Geley S, Doppler W
Institut für Medizinische Chemie und Biochemie, Universität Innsbruck, A-6020, Innsbruck, Austria.
Gene. 1998 Sep 14;217(1-2):127-39. doi: 10.1016/s0378-1119(98)00380-1.
The 5' flanking region of the human beta-casein gene was investigated for the presence of regulatory sequences mediating the action of the lactogenic hormones prolactin and dexamethasone. DNA encompassing 9389 base pairs of the flanking region was isolated and a sequence comparison performed with regulatory regions previously identified in the beta-casein gene of rodents and ruminants. The analysis revealed the presence of a distal region between -4700 and -4550 with a high percentage of identity to the bovine beta-casein enhancer region, and a proximal region between -1 and -200 similar to the proximal promoter regions found in rodents and ruminants. Reporter gene constructs under the control of the distal or the proximal region of the human beta-casein gene were tested for their responsiveness to prolactin and dexamethasone. In transfection experiments, the distal region functioned as a lactogenic hormone inducible enhancer, whereas the proximal region exhibited low activity. In electromobility shift assays, multiple binding sites for Stat5, CCAAT/enhancer-binding proteins, and Ets domain proteins were identified in the distal human enhancer. These transcription factors have already been demonstrated as important regulators of the transcription of milk protein genes in rodents. Thus, a common set of transcription factors appears to be required for the expression of the human beta-casein gene and of milk protein genes in other species.
对人β-酪蛋白基因的5'侧翼区域进行了研究,以寻找介导催乳素和地塞米松等泌乳激素作用的调控序列。分离出包含9389个碱基对侧翼区域的DNA,并与先前在啮齿动物和反刍动物的β-酪蛋白基因中鉴定出的调控区域进行了序列比较。分析发现,在-4700至-4550之间存在一个远端区域,与牛β-酪蛋白增强子区域具有高度同源性,在-1至-200之间存在一个近端区域,类似于在啮齿动物和反刍动物中发现的近端启动子区域。测试了在人β-酪蛋白基因远端或近端区域控制下的报告基因构建体对催乳素和地塞米松的反应性。在转染实验中,远端区域起泌乳激素诱导增强子的作用,而近端区域活性较低。在电泳迁移率变动分析中,在人远端增强子中鉴定出多个Stat5、CCAAT/增强子结合蛋白和Ets结构域蛋白的结合位点。这些转录因子已被证明是啮齿动物中乳蛋白基因转录的重要调节因子。因此,人β-酪蛋白基因和其他物种中乳蛋白基因的表达似乎需要一组共同的转录因子。