Kim M H, Peterson D O
Department of Biochemistry and Biophysics, Texas A & M University, College Station 77843-2128, USA.
J Biol Chem. 1995 Nov 17;270(46):27823-8.
The ubiquitous transcription factor Oct-1 stimulates basal transcription from the mouse mammary tumor virus (MMTV) promoter by binding to octamer-related sequences present in the proviral long terminal repeat. The mechanism of transcriptional activation by Oct-1 was investigated using in vitro transcription assays with a HeLa cell nuclear extract depleted of endogenous Oct-1. Oct-1-mediated transcriptional activation could be reconstituted by addition of bacterially expressed recombinant Oct-1 protein. The stimulatory effect of Oct-1 was observed only when the protein was present during formation of transcription preinitiation complexes and not when added to fully assembled complexes. Furthermore, assembled MMTV preinitiation complexes were resistant to inhibition by a competitor oligonucleotide containing MMTV octamer-related elements that could eliminate Oct-1-mediated stimulation when present during the assembly process. The time course of transcription complex assembly revealed that Oct-1 increases the number of templates on which functional transcription complexes form. Finally, experiments designed to exploit the sensitivity of discrete steps in transcription complex assembly to the anionic detergent Sarkosyl demonstrated that Oct-1 must be present during formation of an early intermediate in the assembly process.
普遍存在的转录因子Oct-1通过与前病毒长末端重复序列中存在的八聚体相关序列结合,刺激小鼠乳腺肿瘤病毒(MMTV)启动子的基础转录。利用不含内源性Oct-1的HeLa细胞核提取物进行体外转录分析,研究了Oct-1的转录激活机制。通过添加细菌表达的重组Oct-1蛋白,可以重建Oct-1介导的转录激活。仅当蛋白质在转录起始前复合物形成期间存在时,才观察到Oct-1的刺激作用,而在添加到完全组装的复合物时则未观察到。此外,组装好的MMTV起始前复合物对含有MMTV八聚体相关元件的竞争寡核苷酸的抑制具有抗性,该竞争寡核苷酸在组装过程中存在时可消除Oct-1介导的刺激。转录复合物组装的时间进程表明,Oct-1增加了形成功能性转录复合物的模板数量。最后,旨在利用转录复合物组装中离散步骤对阴离子去污剂 Sarkosyl 的敏感性进行的实验表明,Oct-1必须在组装过程中早期中间体形成期间存在。