Leza M A, Hearing P
Department of Microbiology, State University of New York, Stony Brook 11794-8621.
J Virol. 1988 Aug;62(8):3003-13. doi: 10.1128/JVI.62.8.3003-3013.1988.
We have analyzed the sequences that regulate the transcription of adenovirus type 5 early region 4 (E4). A region located immediately upstream of the E4 TATA box is required for efficient E4 transcription in vitro and in vivo. A cellular transcription factor, termed ETF-A, binds to this region. ETF-A also binds to additional sites in the E4 5'-flanking region, including the adenovirus terminal repeat, as well as to the adenovirus early region 2 promoter region and the adeno-associated virus early promoter region. A repeated sequence motif is found in each binding domain. The same factor binds to a region upstream of a cellular gene that contains a cyclic AMP response element. Consistent with this result, E4 expression is induced in vivo by cyclic AMP. Two other regions further upstream of the E4 initiation site also contribute to efficient E4 expression. These domains are functionally redundant and contain binding sites for ETF-A. One domain is the adenovirus terminal repeat, which has strong promoter activity in vitro and in vivo.
我们分析了调控腺病毒5型早期区域4(E4)转录的序列。E4 TATA框紧邻上游的一个区域对于体外和体内的高效E4转录是必需的。一种称为ETF-A的细胞转录因子与该区域结合。ETF-A还与E4 5'侧翼区域的其他位点结合,包括腺病毒末端重复序列,以及腺病毒早期区域2启动子区域和腺相关病毒早期启动子区域。在每个结合结构域中发现了一个重复序列基序。同一因子与含有环磷酸腺苷反应元件的细胞基因上游区域结合。与该结果一致,环磷酸腺苷在体内诱导E4表达。E4起始位点上游更远的另外两个区域也有助于高效的E4表达。这些结构域在功能上是冗余的,并且含有ETF-A的结合位点。一个结构域是腺病毒末端重复序列,其在体外和体内具有很强的启动子活性。