Parks C L, Banerjee S, Spector D J
Department of Microbiology, College of Medicine, Pennsylvania State University, Hershey 17033.
J Virol. 1988 Jan;62(1):54-67. doi: 10.1128/JVI.62.1.54-67.1988.
Genetic analysis of the transcriptional control sequences of the E1b gene of adenovirus type 5 identified two regions that stimulated specific transcription by whole cell extracts from uninfected cells. The first region, located within 50 nucleotides (position -50) 5' to the transcription initiation (cap) site, contains a G+C-rich consensus-binding site (GC box) for the transcription factor Sp1 and a TATA box. Unambiguous stimulatory activity of the second region, between positions -358 and -127, was observed only in the absence of the GC box. DNase I protection experiments (footprinting) with crude nuclear extracts from uninfected cells revealed multiple DNA-protein interactions at the control region. Proximal to the initiation site, both the GC box and the cap site were protected; however, protection of the TATA box was not observed. In the distal region, four protein-binding sites, designated I through IV, were located between positions -250 and -120. Three of the four mapped in protein-coding sequences of the adjacent E1a gene. Sites I and II were 5' to position -218 whereas sites III and IV were 3' to position -218. This finding was consistent with results of the transcriptional analysis indicating that subsets of the distal region were sufficient for stimulation of transcription in vitro in the absence of the GC box. Within the boundaries of site I, a 10-base-pair protected sequence was similar to one located 5' to the adenovirus E1a, E2a, E3, E4, E2 late, and polypeptide IX transcription initiation sites. Sequences within the boundaries of the other three sites were similar to those within other viral and cellular enhancers.
对5型腺病毒E1b基因转录控制序列的遗传分析确定了两个区域,它们可被未感染细胞的全细胞提取物刺激产生特异性转录。第一个区域位于转录起始(帽)位点5'端的50个核苷酸(-50位)内,包含转录因子Sp1的富含G+C的共有结合位点(GC盒)和一个TATA盒。仅在没有GC盒的情况下,才观察到第二个区域(-358至-127位之间)明确的刺激活性。用未感染细胞的粗核提取物进行的DNase I保护实验(足迹法)揭示了控制区域存在多个DNA-蛋白质相互作用。在起始位点附近,GC盒和帽位点均受到保护;然而,未观察到TATA盒受到保护。在远端区域,四个蛋白质结合位点(分别命名为I至IV)位于-250至-120位之间。四个位点中的三个位于相邻E1a基因的蛋白质编码序列中。位点I和II在-218位的5'端,而位点III和IV在-218位的3'端。这一发现与转录分析结果一致,表明在没有GC盒的情况下,远端区域的亚组足以在体外刺激转录。在位点I的边界内,一个10个碱基对的受保护序列类似于位于腺病毒E1a、E2a、E3、E4、E2晚期和多肽IX转录起始位点5'端的序列。其他三个位点边界内的序列与其他病毒和细胞增强子内的序列相似。