Cheatham B, Carmichael D, Peterson R, Pan L, Koontz J W
Department of Biochemistry, University of Tennessee, Knoxville 37996-0840.
Arch Biochem Biophys. 1992 Nov 1;298(2):522-6. doi: 10.1016/0003-9861(92)90444-2.
Insulin-mediated regulation of glucocorticoid-induced expression of the liver-specific gene tyrosine aminotransferase was studied in a clone of the Reuber rat hepatoma cells. Insulin inhibited dexamethasone-induced chloramphenicol acetyltransferase expression from approximately 4 kb of TAT 5' flanking sequence. The degree of this inhibition was comparable to the response of the endogenous gene. A construct of approximately 3 kbp of 5' flanking sequence exhibited no significant basal expression but retained sensitivity to glucocorticoids and to insulin inhibition of the glucocorticoid response. Results of further analysis of the insulin response in deletion constructs and constructs containing glucocorticoid responsive elements ligated to a heterologous promoter suggest that in addition to the glucocorticoid response elements a region close to the start site in the TAT promoter is necessary for insulin to inhibit glucocorticoid-mediated induction of expression.
在鲁伯大鼠肝癌细胞系的一个克隆中,研究了胰岛素介导的对糖皮质激素诱导的肝脏特异性基因酪氨酸转氨酶表达的调控。胰岛素抑制了地塞米松诱导的氯霉素乙酰转移酶从约4kb的酪氨酸转氨酶5'侧翼序列的表达。这种抑制程度与内源性基因的反应相当。一个约3kbp的5'侧翼序列构建体没有显著的基础表达,但对糖皮质激素和胰岛素对糖皮质激素反应的抑制仍保持敏感性。对缺失构建体和含有与异源启动子连接的糖皮质激素反应元件的构建体中胰岛素反应的进一步分析结果表明,除了糖皮质激素反应元件外,酪氨酸转氨酶启动子中靠近起始位点的一个区域对于胰岛素抑制糖皮质激素介导的表达诱导也是必需的。