Weeks D L, Jones N C
Nucleic Acids Res. 1985 Jul 25;13(14):5389-402. doi: 10.1093/nar/13.14.5389.
To identify sequences within the adenovirus-5 E3 promoter necessary for E1A trans-activation, a series of promoter deletion mutants were constructed and analysed. A region between positions -82 and -105 was shown to be critical both for E1A induced expression as well as uninduced expression. The importance of this region was confirmed by constructing hybrid promoters consisting of E3 and Herpes simplex virus thymidine kinase sequences. The E1A insensitive tk promoter could be converted to an E1A sensitive promoter by replacing sequences upstream of position -79 with the corresponding region of the E3 promoter. This critical region of the E3 promoter contains a sequence 5' AGATGACTA3' which is also present in important upstream regions of the E2A and E4 promoters.
为了鉴定腺病毒5型E3启动子中E1A反式激活所必需的序列,构建并分析了一系列启动子缺失突变体。已表明-82至-105位之间的区域对于E1A诱导的表达以及未诱导的表达均至关重要。通过构建由E3和单纯疱疹病毒胸苷激酶序列组成的杂合启动子,证实了该区域的重要性。通过用E3启动子的相应区域替换-79位上游的序列,可将对E1A不敏感的tk启动子转化为对E1A敏感的启动子。E3启动子的这一关键区域包含序列5'AGATGACTA3',该序列也存在于E2A和E4启动子的重要上游区域中。