Danesch U, Gloss B, Schmid W, Schütz G, Schüle R, Renkawitz R
EMBO J. 1987 Mar;6(3):625-30. doi: 10.1002/j.1460-2075.1987.tb04800.x.
Transcription of the gene coding for tryptophan oxygenase (TO) in rat liver is induced 10-fold by glucocorticoids. To identify DNA elements mediating the glucocorticoid-regulated expression of the TO gene we transfected mouse L cells with a fusion gene consisting of 1.95 kb TO 5'-flanking sequences linked to the coding sequence of the gene for chloramphenicol acetyltransferase (CAT). CAT assay and RNA mapping experiments demonstrate that both transient and stable expression of the TO-CAT fusion gene are inducible by dexamethasone. Analysis of transcripts from 5'-deletion mutants identifies two glucocorticoid-responsive elements (GRE), located 450 bp and 1.2 kb upstream of the cap site. The purified rat glucocorticoid receptor binds to the sequence of each GRE as evidenced from footprinting experiments. Interestingly the protected sequence of the proximal footprint is by itself not sufficient for sequence induction, but requires sequences located immediately upstream.
大鼠肝脏中编码色氨酸加氧酶(TO)的基因转录受糖皮质激素诱导,可增加10倍。为了鉴定介导糖皮质激素调节TO基因表达的DNA元件,我们用一个融合基因转染了小鼠L细胞,该融合基因由1.95 kb的TO 5'侧翼序列与氯霉素乙酰转移酶(CAT)基因的编码序列相连组成。CAT分析和RNA定位实验表明,TO-CAT融合基因的瞬时表达和稳定表达均可被地塞米松诱导。对5'缺失突变体转录本的分析确定了两个糖皮质激素反应元件(GRE),位于帽位点上游450 bp和1.2 kb处。足迹实验证明,纯化的大鼠糖皮质激素受体与每个GRE的序列结合。有趣的是,近端足迹的保护序列本身不足以诱导序列,而是需要紧邻上游的序列。