Wang Xin-Ping, Zhang Yan-Jin, Deng Jian-Hong, Pan Hong-Yi, Zhou Fu-Chun, Gao Shou-Jiang
Departments of Pediatrics and Microbiology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900, USA.
J Biol Chem. 2002 Apr 5;277(14):12023-31. doi: 10.1074/jbc.M108026200. Epub 2002 Jan 30.
Viral interferon regulatory factor (vIRF) encoded by Kaposi's sarcoma-associated herpesvirus (KSHV) has been shown to transform NIH3T3 and Rat-1 cells, inhibit interferon signal transduction, and regulate the expression of KSHV genes. We had previously characterized the vIRF core promoter and defined a 12-O-tetradecanoylphorbol-13-acetate (TPA)-responsive region in the upstream regulatory sequence of vIRF gene. Here, we have further identified a novel transcriptional silencer, named Tis in this region. Tis represses the promoter activities of vIRF and heterologous herpes simplex virus thymidine kinase genes in both position- and orientation-independent manners. Deletion analysis has identified a cis-element of 23 nucleotides that is essential for the negative regulation. Two Tis-binding protein complexes, named vR1 and vR2, were observed by electrophoretic mobility shift assays using nuclear extracts from both KSHV-negative and -positive cell lines. A sequence fragment GAGTTAATAGGTAGAG in the cis-element was shown to be required for the DNA-protein interactions as well as the repression of vIRF promoter activity. Point-mutation analysis identified TTAAT and GTTAATAG as the core sequence motifs for the binding of vR1 and vR2, respectively. These results define the function of a novel transcriptional silencer in the regulation of vIRF gene expression.
卡波西肉瘤相关疱疹病毒(KSHV)编码的病毒干扰素调节因子(vIRF)已被证明可转化NIH3T3和Rat-1细胞、抑制干扰素信号转导并调节KSHV基因的表达。我们之前已对vIRF核心启动子进行了特征分析,并在vIRF基因的上游调控序列中确定了一个佛波酯(TPA)反应区域。在此,我们在该区域进一步鉴定出一种新型转录沉默子,命名为Tis。Tis以位置和方向独立的方式抑制vIRF和异源单纯疱疹病毒胸苷激酶基因的启动子活性。缺失分析确定了一个23个核苷酸的顺式元件,它对负调控至关重要。使用来自KSHV阴性和阳性细胞系的核提取物进行电泳迁移率变动分析,观察到两种Tis结合蛋白复合物,命名为vR1和vR2。顺式元件中的序列片段GAGTTAATAGGTAGAG被证明是DNA-蛋白质相互作用以及抑制vIRF启动子活性所必需的。点突变分析确定TTAAT和GTTAATAG分别为vR1和vR2结合的核心序列基序。这些结果确定了一种新型转录沉默子在调节vIRF基因表达中的功能。