Muramatsu M, Okuda A, Morimura S, Osada S, Diccianni M B, Imagawa M
Department of Biochemistry, University of Tokyo Faculty of Medicine, Japan.
Princess Takamatsu Symp. 1990;21:189-98.
The mechanism of specific expression of glutathione transferase P gene during hepatocarcinogenesis of the rat has been investigated by cloning the gene and determining the upstream regulatory sequences. Two enhancers and a silencer are located within 3 kb upstream of the promoter. The stronger enhancer designated GPEI has two TPA (12-O-tetradecanoyl phorbol 13-acetate)-response element (TRE)-like sequences arranged in a palindrome at a 3 base pairs spacing. This special combination was found to form a very strong enhancer which could act efficiently even in F9 cells where the collagenase enhancer with a singlet TRE cannot work due to the low c-jun content. Whether this structure is operating with a very low concentration of c-jun/c-fos heterodimer or with any other proteins remains to be determined. These findings suggest that new and more efficient enhancers evolve by a combination of basic enhancer elements. The silencer region consists of several sequences that can bind specific protein(s) and works cooperatively.
通过克隆谷胱甘肽转移酶P基因并确定其上游调控序列,对大鼠肝癌发生过程中该基因特异性表达的机制进行了研究。在启动子上游3 kb范围内定位到两个增强子和一个沉默子。较强的增强子命名为GPEI,有两个佛波酯(12 - O - 十四烷酰佛波醇13 - 乙酸酯)反应元件(TRE)样序列,以回文形式排列,间隔3个碱基对。发现这种特殊组合形成了一个非常强的增强子,即使在F9细胞中也能有效发挥作用,在F9细胞中,由于c - jun含量低,具有单个TRE的胶原酶增强子无法发挥作用。这种结构是通过极低浓度的c - jun/c - fos异二聚体还是与其他任何蛋白质一起发挥作用,仍有待确定。这些发现表明,新的、更有效的增强子是由基本增强子元件组合进化而来的。沉默子区域由几个能结合特定蛋白质的序列组成,并协同发挥作用。