Benech P, Vigneron M, Peretz D, Revel M, Chebath J
Department of Virology, Weizmann Institute of Science, Rehovot, Israel.
Mol Cell Biol. 1987 Dec;7(12):4498-504. doi: 10.1128/mcb.7.12.4498-4504.1987.
The interferon (IFN)-activated human 2',5'-oligo(A) synthetase E gene contains 11 RNA starts and lacks TATA and CAAT signals. DNA sequences around the promoter make the expression of the chloramphenicol acetyltransferase gene (CAT) inducible over 20-fold by IFN. A 72-base-pair segment (E-IRS) immediately upstream of the RNA starts was defined as being required for IFN-activated expression of the E-gene promoter-CAT constructs and acts in a position-independent manner. It also confers IFN-activated enhancement to the herpes simplex virus thymidine kinase promoter. On this promoter, the 5' part of the E-IRS functions as a constitutive enhancer, while the last 16 base pairs of the E-IRS is sufficient to give IFN-induced expression. On the E-gene promoter, the constitutive enhancer and the IFN-activated sequence are both needed but can be separated. In addition, promoter competition experiments indicate a third regulatory region which helps to repress expression of the E gene in uninduced cells.
干扰素(IFN)激活的人2',5'-寡腺苷酸合成酶E基因包含11个RNA起始位点,且缺乏TATA和CAAT信号。启动子周围的DNA序列使氯霉素乙酰转移酶基因(CAT)的表达在IFN作用下可诱导增加20倍以上。RNA起始位点上游紧邻的一个72碱基对片段(E-IRS)被确定为E基因启动子-CAT构建体IFN激活表达所必需的,并且以位置独立的方式起作用。它还赋予单纯疱疹病毒胸苷激酶启动子IFN激活增强作用。在该启动子上,E-IRS的5'部分作为组成型增强子起作用,而E-IRS的最后16个碱基对足以产生IFN诱导的表达。在E基因启动子上,组成型增强子和IFN激活序列都需要,但可以分开。此外,启动子竞争实验表明存在第三个调节区域,该区域有助于抑制未诱导细胞中E基因的表达。