Yang W L, Lim R W
Department of Pharmacology, University of Missouri-Columbia 65212, USA.
Biochem J. 1997 Jan 15;321 ( Pt 2)(Pt 2):281-7. doi: 10.1042/bj3210281.
TIS1, an inducible orphan nuclear receptor, was originally isolated as a tumour-promoter-inducible gene in mouse 3T3 cells and later shown to be induced by growth factors and other extracellular stimuli. We show here that TIS1 mRNA was expressed in proliferating C2C12 mouse skeletal muscle cells out that the level of TIS1 expression increased during muscle differentiation. Overexpression of TIS1 transactivated muscle creatine kinase (MCK) reporter genes containing as little as 80 bp of the proximal 5' flanking region. In contrast, a promoterless TIS1 construct and a frameshift mutant TIS1 construct were unable to transactivate the MCK reporter gene. Moreover, the effect exerted by TIS1 appeared to be selective for the MCK promoter. Treatment of C2C12 cells with forskolin, which is known to induce TIS1 expression, also stimulated MCK reporter gene activity. Interestingly, in vitro translated TIS1 protein failed to bind to the MCK promoter region, suggesting that the transactivation effect of TIS1 may be mediated without direct interaction of the protein with the MCK promoter DNA. Collectively, these results suggest that changing levels of TIS1 may help to modulate the expression of MCK, and perhaps other muscle-specific genes, in response to physiological changes.
TIS1是一种可诱导的孤儿核受体,最初是作为肿瘤促进剂诱导基因在小鼠3T3细胞中分离出来的,后来发现它可被生长因子和其他细胞外刺激诱导。我们在此表明,TIS1 mRNA在增殖的C2C12小鼠骨骼肌细胞中表达,并且在肌肉分化过程中TIS1的表达水平增加。TIS1的过表达可激活肌肉肌酸激酶(MCK)报告基因,该报告基因仅含有近端5'侧翼区域的80 bp。相比之下,无启动子的TIS1构建体和移码突变的TIS1构建体无法激活MCK报告基因。此外,TIS1发挥的作用似乎对MCK启动子具有选择性。用已知可诱导TIS1表达的福斯可林处理C2C12细胞,也可刺激MCK报告基因的活性。有趣的是,体外翻译的TIS1蛋白未能与MCK启动子区域结合,这表明TIS1的反式激活作用可能是在该蛋白与MCK启动子DNA没有直接相互作用的情况下介导的。总的来说,这些结果表明,TIS1水平的变化可能有助于调节MCK以及可能其他肌肉特异性基因的表达,以响应生理变化。