Imai T, Kawaguchi H, Wada T, Handa H
Department of Bacteriology, Faculty of Medicine, University of Tokyo, Japan.
Virus Genes. 1991 Jan;5(1):47-55. doi: 10.1007/BF00571730.
A cell-free transcription system using nuclear extracts prepared from adenovirus type 5 (Ad5)-infected and mock-infected cells were utilized to study the E1A-mediated transactivation of transcription from the Ad5 early region 4 (E4) promoter. The transcription activity of Ad-infected cell extracts was several times higher than that of mock-infected cell extracts when the E4 wild-type (WT) promoter was used. The increased activity required expression of E1A proteins. However, the transcription activities of both cell extracts were not different when the mutant promoter containing only the E4 TATA box was used. The formation of a stable preinitiation complex at the E4 WT promoter was facilitated by expression of E1A, whereas it was not facilitated at the mutant promoter. The results suggested that the E1A proteins stimulated transcription from the E4 promoter by enhancing the formation of a stable preinitiation complex through the upstream elements, together with the TATA box.
利用从感染5型腺病毒(Ad5)和模拟感染的细胞中制备的核提取物建立的无细胞转录系统,来研究E1A介导的Ad5早期区域4(E4)启动子的转录激活。当使用E4野生型(WT)启动子时,感染Ad的细胞提取物的转录活性比模拟感染的细胞提取物高几倍。这种活性增加需要E1A蛋白的表达。然而,当使用仅包含E4 TATA框的突变启动子时,两种细胞提取物的转录活性没有差异。E1A的表达促进了在E4 WT启动子处稳定预起始复合物的形成,而在突变启动子处则没有促进作用。结果表明,E1A蛋白通过与TATA框一起增强上游元件介导的稳定预起始复合物的形成,从而刺激E4启动子的转录。