Brent G A, Williams G R, Harney J W, Forman B M, Samuels H H, Moore D D, Larsen P R
Thyroid Division, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Mol Endocrinol. 1991 Apr;5(4):542-8. doi: 10.1210/mend-5-4-542.
The thyroid hormone response element (T3RE) of the rat GH (rGH) promoter is located at -188 to -165 relative to the mRNA start site (TSS). Similar sites have been identified in other genes regulated by T3. We have investigated some of these T3REs in positions within the rGH promoter to assess the relative influences of DNA-binding site and position on positive and negative regulation by T3. Synthetic oligonucleotides were used with sequences from the rGH T3RE and proposed negative T3REs (nT3RE) from the rat and human alpha-subunit and rat beta TSH genes. The nT3REs were placed in the background of the wild-type rGH promoter in two positions, at -55 and down-stream of the TSS, with up- and down-mutations of the rGH T3RE. Rat GH T3RE elements were placed 700 basepairs up-stream of a basal rGH promoter and some also at the -55 and TSS positions. Constructions were tested in a transient transfection assay in rat pituitary tumor cells. Two copies of the rGHPAL (palindromic T3RE) placed 700 basepairs up-stream of the rGH promoter conferred 10-fold T3 induction. In the -55 position, the rGHPAL increased T3 induction compared to that in controls, whereas a fragment from the rat and human alpha-subunit gene in the same position reduced induction. Negative T3REs from rat beta TSH and human alpha-subunit reduced T3 induction 50% when placed at the TSS position of a rGH promoter containing an up-mutant T3RE. The T3REPAL placed at the same site increased T3 induction.(ABSTRACT TRUNCATED AT 250 WORDS)
大鼠生长激素(rGH)启动子的甲状腺激素反应元件(T3RE)相对于mRNA起始位点(TSS)位于-188至-165处。在其他受T3调控的基因中也发现了类似的位点。我们研究了rGH启动子内这些T3RE中的一些,以评估DNA结合位点和位置对T3正负调控的相对影响。使用了合成寡核苷酸,其序列来自rGH T3RE以及大鼠和人类α亚基及大鼠β促甲状腺激素基因中提议的负性T3RE(nT3RE)。将nT3RE置于野生型rGH启动子的背景中,分别位于-55和TSS下游两个位置,并对rGH T3RE进行了正向和反向突变。将大鼠GH T3RE元件置于基础rGH启动子上游700个碱基对处,有些还置于-55和TSS位置。构建体在大鼠垂体肿瘤细胞的瞬时转染试验中进行了测试。在rGH启动子上游700个碱基对处放置两个拷贝的rGHPAL(回文T3RE)可使T3诱导增加10倍。在-55位置,与对照组相比,rGHPAL增加了T3诱导,而同一位置来自大鼠和人类α亚基基因的片段则降低了诱导。当置于含有正向突变T3RE的rGH启动子的TSS位置时,大鼠β促甲状腺激素和人类α亚基的负性T3RE使T3诱导降低了50%。置于同一位置的T3REPAL增加了T3诱导。(摘要截短于250字)