Burnside J, Darling D S, Carr F E, Chin W W
Division of Molecular Genetics, Brigham and Women's Hospital, Boston, Massachusetts.
J Biol Chem. 1989 Apr 25;264(12):6886-91.
An important physiological control of the glycoprotein hormone alpha-subunit is the negative feedback by thyroid hormones in the thyrotrope. A region of the rat glycoprotein hormone alpha-subunit gene that is involved in transcriptional regulation by thyroid hormone has been identified by transient transfection studies, and sequence-specific binding of the thyroid hormone receptor to a site within this region has been demonstrated. Deletion-mutation studies using plasmid expression vectors containing either 246, 170, or 80 base pairs of the 5'-flanking region of the rat alpha-subunit gene fused to the coding region of the bacterial chloramphenicol acetyltransferase gene demonstrate 3,5,3'-triiodo-L-thyronine (T3)-regulated expression in GH3 cells, a T3-responsive somatotrophic cell line. In order to investigate the possibility of thyroid hormone receptor interaction with this segment of the rat alpha-subunit gene, the binding of the thyroid hormone receptor to synthetic oligodeoxynucleotides was analyzed using an avidin-biotin complex DNA binding assay. An oligodeoxyribonucleotide representing a fragment of the alpha-subunit gene from -74 to -38, relative to the transcriptional start site, shows significant binding to [125I]T3-receptor complex present in nuclear extracts of GH3 cells. This fragment binds receptor to a degree similar to that seen with a fragment of the rat growth hormone gene which contains a putative thyroid hormone-responsive element. In addition, this fragment of the rat alpha-subunit gene binds to the in vitro synthesized human c-erbA beta protein, which has been identified as a member of the family of putative T3 receptors. These data demonstrate that a cis-active thyroid hormone-responsive element resides in the 5'-flanking region of the rat alpha-subunit gene and that the mechanism involved in the suppression of expression of this gene by T3 could involve specific binding of the thyroid hormone receptor to this region of the gene.
糖蛋白激素α亚基的一个重要生理调控机制是促甲状腺细胞中甲状腺激素的负反馈作用。通过瞬时转染研究,已确定大鼠糖蛋白激素α亚基基因中一个参与甲状腺激素转录调控的区域,并且已证实甲状腺激素受体与该区域内一个位点的序列特异性结合。使用含有大鼠α亚基基因5'侧翼区246、170或80个碱基对并与细菌氯霉素乙酰转移酶基因编码区融合的质粒表达载体进行缺失突变研究,结果表明在GH3细胞(一种对T3有反应的生长激素营养细胞系)中,3,5,3'-三碘-L-甲状腺原氨酸(T3)可调控其表达。为了研究甲状腺激素受体与大鼠α亚基基因这一片段相互作用的可能性,利用抗生物素蛋白-生物素复合物DNA结合分析法分析了甲状腺激素受体与合成寡脱氧核苷酸的结合情况。相对于转录起始位点,代表α亚基基因从-74至-38片段的寡脱氧核苷酸与GH3细胞核提取物中存在的[125I]T3-受体复合物有显著结合。该片段与受体的结合程度与含有假定甲状腺激素反应元件的大鼠生长激素基因片段相似。此外,大鼠α亚基基因的这一片段与体外合成的人c-erbAβ蛋白结合,该蛋白已被确定为假定的T3受体家族成员。这些数据表明,一个顺式作用的甲状腺激素反应元件位于大鼠α亚基基因的5'侧翼区,且T3抑制该基因表达所涉及的机制可能包括甲状腺激素受体与该基因这一区域的特异性结合。