Zhang Xueping, Diab Iman H, Zehner Zendra E
Department of Biochemistry and the Massey Cancer Center, Medical College of Virginia Campus of Virginia Commonwealth University, Richmond, VA 23298-0614, USA.
Nucleic Acids Res. 2003 Jun 1;31(11):2900-14. doi: 10.1093/nar/gkg380.
Vimentin, a member of the intermediate filament protein family, is regulated both developmentally and tissue specifically. It is also a marker of the metastatic potential of many tumor cells. Pre viously, the human vimentin promoter has been shown to contain multiple elements for the binding of both positive- and negative-acting regulatory factors. Transient transfection analysis of various vimentin 5'-end promoter sequences and mutants thereof fused to a reporter gene further defined two regulatory elements, a positive element that binds Sp1 and a negative element that binds the protein ZBP-89. ZBP-89 has been shown to be either a repressor or an activator of gene expression, depending on the promoter. Here, we show that for vimentin, both ZBP-89 and ZBP-99 repress reporter gene expression in Schneider (S2) cells. Deletion constructs confirm that the glutamine-rich region of Sp1 is required to enhance vimentin transcription, whereas the N-terminus of ZBP-89 is required to interact with Sp1 and repress gene expression. The overexpression of hTAF(II)130 can alleviate ZBP-89 repression in S2 cells, suggesting how ZBP-89 might serve to block gene expression.
波形蛋白是中间丝蛋白家族的成员之一,其表达在发育过程和组织中具有特异性调控。它也是许多肿瘤细胞转移潜能的标志物。此前,已证明人类波形蛋白启动子含有多个可与正负调控因子结合的元件。对与报告基因融合的各种波形蛋白5'端启动子序列及其突变体进行瞬时转染分析,进一步确定了两个调控元件,一个是与Sp1结合的正向元件,另一个是与蛋白ZBP-89结合的负向元件。根据启动子的不同,ZBP-89已被证明是基因表达的抑制因子或激活因子。在此,我们表明,对于波形蛋白,ZBP-89和ZBP-99均可抑制施耐德(S2)细胞中的报告基因表达。缺失构建体证实,Sp1富含谷氨酰胺的区域是增强波形蛋白转录所必需的,而ZBP-89的N端是与Sp1相互作用并抑制基因表达所必需的。hTAF(II)130的过表达可减轻S2细胞中ZBP-89的抑制作用,提示了ZBP-89可能阻断基因表达的机制。