Lee H J, Chang C
Department of Human Oncology, University of Wisconsin, Madison 53792.
J Biol Chem. 1995 Mar 10;270(10):5434-40. doi: 10.1074/jbc.270.10.5434.
A DNA response element (TR2RE-SV40) for the TR2 orphan receptor, a member of the steroid-thyroid hormone receptor superfamily, has been identified in the simian virus 40 (SV40) +55 region (nucleotide numbers 368-389, 5'-GTTAAGGTTCGTAGGTCATGGA-3'). Electrophoretic mobility shift assay, using in vitro translated TR2 orphan receptor with a molecular mass of 67 kilodaltons, showed a specific binding with high affinity (dissociation constant = 9 nM) for this DNA sequence. DNA-swap experiments using chloramphenicol acetyl-transferase assay demonstrated that androgen can suppress the transcriptional activities of SV40 early promoter via the interaction between this TR2RE-SV40 and the chimeric receptor AR/TR2/AR with the DNA-binding domain of the TR2 orphan receptor flanked by the N-terminal and androgen-binding domains of the androgen receptor. In addition, this TR2RE-SV40 can function as a repressor to suppress the transcriptional activities of both SV40 early and late promoters. Together, these data suggest the TR2RE-SV40 may represent the first identified natural DNA response element for the TR2 orphan receptor that may function as a repressor for the SV40 gene expression.
类固醇 - 甲状腺激素受体超家族成员TR2孤儿受体的DNA反应元件(TR2RE - SV40)已在猿猴病毒40(SV40)的+55区域(核苷酸编号368 - 389,5'-GTTAAGGTTCGTAGGTCATGGA-3')中被鉴定出来。使用体外翻译的分子量为67千道尔顿的TR2孤儿受体进行的电泳迁移率变动分析表明,该DNA序列与之具有高亲和力的特异性结合(解离常数 = 9 nM)。使用氯霉素乙酰转移酶测定的DNA交换实验表明,雄激素可通过该TR2RE - SV40与嵌合受体AR/TR2/AR之间的相互作用抑制SV40早期启动子的转录活性,其中TR2孤儿受体的DNA结合结构域两侧分别是雄激素受体的N端和雄激素结合结构域。此外,该TR2RE - SV40可作为阻遏物抑制SV40早期和晚期启动子的转录活性。总之,这些数据表明TR2RE - SV40可能是首次鉴定出的TR2孤儿受体的天然DNA反应元件,它可能作为SV40基因表达的阻遏物发挥作用。