Dong Bing, Zhao Feng-Qi
Lactation and Mammary Gland Biology Group, Department of Animal Science, University of Vermont, Burlington, VT 05405, USA.
Biochem J. 2007 Jan 1;401(1):57-64. doi: 10.1042/BJ20060570.
Transcription of the milk protein beta-casein gene is induced by the lactogenic hormones Prl (prolactin) and glucocorticoids. Multiple transcription factors involved in this induction have been identified, including the STAT5 (signal transducer and activator of transcription 5) and the GR (glucocorticoid receptor). Our previous studies have identified a binding site for the ubiquitous Oct-1 (octamer-binding transcription factor 1) protein in the lactogenic hormonal regulatory region of the mouse beta-casein promoter. In the present study, we report that Oct-1 is indeed expressed and binds to the beta-casein promoter in mammary epithelial cells. Oct-1 activates hormonally induced beta-casein promoter activity in a dose-dependent manner. Hormonal induction of promoter activity was decreased not only by mutating the Oct-1-binding site from ATTAGCAT to GCTAGCAT, which abolishes Oct-1 binding (50% decrease, P<0.01), but also by changing the site to the consensus Oct-1-binding motif ATTTGCAT (40% decrease, P<0.01). Reversing the Oct-1-binding site reduced hormonal induction by 70% (P<0.01), showing that orientation of Oct-1 binding is also critical in hormonal action. In transient transfection experiments, Oct-1 collaboratively transactivated the beta-casein gene promoter with STAT5 and/or GR in the presence of Prl receptor in cells treated with the lactogenic hormones. The C-terminus of Oct-1 was not essential to its function. The results of the present study provide biochemical evidence that the ubiquitous Oct-1 transcription factor may be involved in hormonally regulated, tissue-specific beta-casein gene expression.
乳蛋白β-酪蛋白基因的转录由催乳激素Prl(催乳素)和糖皮质激素诱导。已鉴定出参与这种诱导作用的多种转录因子,包括信号转导及转录激活因子5(STAT5)和糖皮质激素受体(GR)。我们之前的研究在小鼠β-酪蛋白启动子的催乳激素调节区域中鉴定出了普遍存在的八聚体结合转录因子1(Oct-1)蛋白的一个结合位点。在本研究中,我们报告Oct-1确实在乳腺上皮细胞中表达并与β-酪蛋白启动子结合。Oct-1以剂量依赖的方式激活激素诱导的β-酪蛋白启动子活性。启动子活性的激素诱导不仅通过将Oct-1结合位点从ATTAGCAT突变为GCTAGCAT(消除Oct-1结合,降低50%,P<0.01)而降低,还通过将该位点改变为共有Oct-1结合基序ATTTGCAT(降低40%,P<0.01)而降低。颠倒Oct-1结合位点使激素诱导降低70%(P<0.01),表明Oct-1结合的方向在激素作用中也至关重要。在瞬时转染实验中,在经催乳激素处理的细胞中,Oct-1在存在Prl受体的情况下与STAT5和/或GR协同反式激活β-酪蛋白基因启动子。Oct-1的C末端对其功能并非必需。本研究结果提供了生化证据,表明普遍存在的Oct-1转录因子可能参与激素调节的、组织特异性的β-酪蛋白基因表达。