Sanchez-Pacheco A, Palomino T, Aranda A
Instituto de Investigaciones Biomédicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Mol Cell Biol. 1995 Nov;15(11):6322-30. doi: 10.1128/MCB.15.11.6322.
Expression of the growth hormone gene is due to the presence of the pituitary-specific transcription factor GHF-1/Pit-1. The action of the thyroid hormone T3 is mediated by nuclear receptors that regulate transcription by interaction with DNA elements located near promoters of the regulated genes. In this study, we show that T3 inhibits expression of the GHF-1/Pit-1 gene in rat pituitary GH4C1 cells by a novel mechanism that involves transcriptional interference with other regulatory elements of the promoter. Sequences between bp -90 and -200 of the rat GHF-1/Pit-1 gene which do not contain a hormone response element but contain two cyclic AMP-responsive elements mediate most of the repressive effect of T3. The hormone reduces basal levels of GHF-1/Pit-1 promoter activity and antagonizes its response to cyclic AMP and the tumor promoter TPA (12-O-tetradecanoylphorbol-13-acetate). A similar repression is found with a heterologous promoter that contains four copies of the cyclic AMP-responsive element motif. This regulation provides a novel example of the cross-talk between the thyroid hormone receptor and the signal transduction pathways used by different hormones and growth factors. Additionally, T3 interferes with in vitro binding of GHF-1/Pit-1 to a positive autoregulatory element located at bp -45 to -63 and has a detectable inhibitory effect on the activity of a promoter construct which extends to bp -90 of 5'-flanking DNA. The regulation of the transcription factor provides a novel example of negative transcriptional regulation by thyroid hormones.
生长激素基因的表达归因于垂体特异性转录因子GHF-1/Pit-1的存在。甲状腺激素T3的作用由核受体介导,这些核受体通过与位于受调控基因启动子附近的DNA元件相互作用来调节转录。在本研究中,我们表明T3通过一种新机制抑制大鼠垂体GH4C1细胞中GHF-1/Pit-1基因的表达,该机制涉及对启动子其他调控元件的转录干扰。大鼠GHF-1/Pit-1基因-90至-200碱基对之间的序列不包含激素反应元件,但包含两个环磷酸腺苷反应元件,介导了T3的大部分抑制作用。该激素降低了GHF-1/Pit-启动子活性的基础水平,并拮抗其对环磷酸腺苷和肿瘤启动子TPA(12-O-十四烷酰佛波醇-13-乙酸酯)的反应。在含有四个环磷酸腺苷反应元件基序拷贝的异源启动子中也发现了类似的抑制作用。这种调节为甲状腺激素受体与不同激素和生长因子所使用的信号转导途径之间的相互作用提供了一个新的例子。此外,T3干扰GHF-1/Pit-1与位于-45至-63碱基对处的正向自调节元件的体外结合,并对延伸至5'-侧翼DNA -90碱基对的启动子构建体的活性具有可检测的抑制作用。转录因子的这种调节为甲状腺激素的负转录调节提供了一个新的例子。