Farrell F X, Sax C M, Zehner Z E
Department of Biochemistry and Molecular Biophysics, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298.
Mol Cell Biol. 1990 May;10(5):2349-58. doi: 10.1128/mcb.10.5.2349-2358.1990.
Vimentin is one member of the intermediate filament multigene family which exhibits both tissue- and developmental stage-specific expression. In vivo, vimentin is expressed in cells of mesenchymal origin. Previously, we identified both enhancer and promoter elements in the chicken vimentin gene which regulate gene expression in a positive manner. In this report, we have identified a 40-base-pair region at -568 base pairs between the proximal and distal enhancer elements which represses transcriptional activity. This silencer region can also repress the heterologous herpes simplex virus thymidine kinase promoter, which is comparable to the vimentin promoter. In addition, the element is able to function in a position- and orientation-independent manner, and the amount of repression is increased by multiple copies. Here we show by gel retardation assays and DNase I footprinting that this region binds a protein in nuclear extracts from HeLa cells. Southwestern (DNA-protein) blot analysis indicates this protein is approximately 95 kilodaltons in size. Moreover, protein distribution and activity mimic the expression pattern of vimentin during myogenesis, i.e., protein binding increases as vimentin gene expression decreases. The silencer region shares strong sequence similarity with 5'-flanking sequences found in both the human and hamster vimentin genes and with other characterized silencer elements, including the human immunodeficiency virus long terminal repeat, rat growth hormone, chicken lysozyme, and rat insulin genes. Thus, a negative element appears to bind a 95-kilodalton protein involved in regulating the tissue-specific expression of the chicken vimentin gene.
波形蛋白是中间丝多基因家族的成员之一,其表达具有组织特异性和发育阶段特异性。在体内,波形蛋白在间充质起源的细胞中表达。此前,我们在鸡波形蛋白基因中鉴定出了增强子和启动子元件,它们以正向方式调节基因表达。在本报告中,我们在近端和远端增强子元件之间的-568碱基对处鉴定出一个40碱基对的区域,该区域可抑制转录活性。这个沉默子区域也能抑制异源单纯疱疹病毒胸苷激酶启动子,该启动子与波形蛋白启动子类似。此外,该元件能够以位置和方向独立的方式发挥作用,多个拷贝会增加抑制量。在这里,我们通过凝胶阻滞试验和DNase I足迹法表明,该区域与HeLa细胞核提取物中的一种蛋白质结合。蛋白质免疫印迹(DNA-蛋白质)分析表明,这种蛋白质的大小约为95千道尔顿。此外,蛋白质的分布和活性模仿了波形蛋白在肌生成过程中的表达模式,即随着波形蛋白基因表达的降低,蛋白质结合增加。该沉默子区域与人类和仓鼠波形蛋白基因的5'侧翼序列以及其他已鉴定的沉默子元件具有很强的序列相似性,包括人类免疫缺陷病毒长末端重复序列、大鼠生长激素、鸡溶菌酶和大鼠胰岛素基因。因此,一个负调控元件似乎结合了一种95千道尔顿的蛋白质,该蛋白质参与调节鸡波形蛋白基因的组织特异性表达。