Kambe F, Seo H
Department of Endocrinology and Metabolism, Nagoya University, Japan.
J Endocrinol. 1996 Aug;150(2):287-98. doi: 10.1677/joe.0.1500287.
The molecular mechanism for hormone- and serum-dependent regulation of thyroglobulin (TG) gene expression was studied. A construct of rat TG promoter (-178 to -3) linked to a luciferase gene was transfected into TSH-, insulin- and serum-deprived FRTL-5 cells. Addition of TSH, insulin or serum augmented the luciferase activity. The endogenous TG mRNA level was also increased, indicating that the promoter used confers responsiveness of TG gene to these additives. The possible involvement of thyroid-transcription factors, TTF-1, TTF-2 and Pax-8, in the induction of TG gene transcription was studied using an electrophoretic mobility shift assay. Since the protein/DNA ratio in FRTL-5 cell extracts was significantly increased by these additives, binding activities of these factors per unit of DNA were examined. It was demonstrated that TSH, insulin or serum increased not only TTF-2 binding activity but also the binding activities of TTF-1 and Pax-8. However, the magnitude of the increase in TTF-1 and Pax-8 mRNA levels per unit of DNA was less than that of the binding activity. Taken together, our results suggest that TSH, insulin and serum increase the binding activities of TTF-1 and Pax-8 to the TG promoter presumably through the posttranslational modification of the factors, thereby enhancing TG gene transcription.
研究了甲状腺球蛋白(TG)基因表达的激素和血清依赖性调节的分子机制。将与荧光素酶基因相连的大鼠TG启动子(-178至-3)构建体转染到促甲状腺激素(TSH)、胰岛素和血清剥夺的FRTL-5细胞中。添加TSH、胰岛素或血清可增强荧光素酶活性。内源性TG mRNA水平也升高,表明所使用的启动子赋予TG基因对这些添加剂的反应性。使用电泳迁移率变动分析研究了甲状腺转录因子TTF-1、TTF-2和Pax-8在TG基因转录诱导中的可能作用。由于这些添加剂显著增加了FRTL-5细胞提取物中的蛋白质/DNA比率,因此检测了每单位DNA这些因子的结合活性。结果表明,TSH、胰岛素或血清不仅增加了TTF-2的结合活性,还增加了TTF-1和Pax-8的结合活性。然而,每单位DNA的TTF-1和Pax-8 mRNA水平增加的幅度小于结合活性增加的幅度。综上所述,我们的结果表明,TSH、胰岛素和血清可能通过这些因子的翻译后修饰增加TTF-1和Pax-8与TG启动子的结合活性,从而增强TG基因转录。