Steinfelder H J, Hauser P, Nakayama Y, Radovick S, McClaskey J H, Taylor T, Weintraub B D, Wondisford F E
Molecular, Cellular and Nutritional Endocrinology Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3130-4. doi: 10.1073/pnas.88.8.3130.
Regulation of human thyrotropin beta subunit gene (TSHB) expression by thyrotropin-releasing hormone (TRH) was examined in a clonal rat pituitary-cell line (GH3). Transient expression studies were done with various 5'-flanking DNA sequences of TSHB coupled to reporter gene chloramphenicol acetyltransferase. Deletion analysis defined two discrete regions (-128 to -92 base pairs and -28 to +8 base pairs) that each mediated an approximately 2-fold TRH induction. The upstream site contains a DNA sequence with close homology to the DNA-binding site for a pituitary-specific transcriptional factor Pit-1/GHF-1. DNase I footprinting analysis of mouse thyrotropic tumor extract as well as DNA-transfection studies using an expression vector containing an N-terminal deletion of Pit-1/GHF-1 cDNA suggest that Pit-1/GHF-1 or a closely related protein in the thyrotroph mediates TRH responsiveness of this gene. In addition, the downstream site overlaps with the recently characterized thyroid hormone-inhibitory element of TSHB. In fact, deletion of DNA sequences important in thyroid hormone-receptor binding (c-erbAB/c-ERBA2) from +3 to +8 base pairs, significantly reduced (30%) TRH responsiveness. The location of a TRH-stimulatory element near a thyroid hormone-inhibitory element may allow for fine control of TSHB expression in vivo.
在克隆大鼠垂体细胞系(GH3)中研究了促甲状腺激素释放激素(TRH)对人促甲状腺激素β亚基基因(TSHB)表达的调控。使用与报告基因氯霉素乙酰转移酶偶联的TSHB的各种5'-侧翼DNA序列进行瞬时表达研究。缺失分析确定了两个离散区域(-128至-92碱基对和-28至+8碱基对),每个区域介导约2倍的TRH诱导。上游位点包含一个与垂体特异性转录因子Pit-1/GHF-1的DNA结合位点具有高度同源性的DNA序列。对小鼠促甲状腺肿瘤提取物的DNase I足迹分析以及使用含有Pit-1/GHF-1 cDNA N端缺失的表达载体的DNA转染研究表明,促甲状腺细胞中的Pit-1/GHF-1或密切相关的蛋白质介导了该基因的TRH反应性。此外,下游位点与最近鉴定的TSHB的甲状腺激素抑制元件重叠。事实上,从+3至+8碱基对删除在甲状腺激素受体结合中重要的DNA序列(c-erbAB/c-ERBA2),显著降低了(30%)TRH反应性。TRH刺激元件靠近甲状腺激素抑制元件的位置可能允许在体内对TSHB表达进行精细控制。