Kadesch T, Berg P
Mol Cell Biol. 1986 Jul;6(7):2593-601. doi: 10.1128/mcb.6.7.2593-2601.1986.
We have examined the ability of the simian virus 40 72-base pair enhancer segment to simultaneously activate multiple transcription units with plasmids that contain one, two, or three simian virus 40-based transcription units in various arrangements. After transfection into CV1 cells, the expression of a marker gene, Ecogpt, was determined as a function of the position of that marker gene relative to the other transcription units and the position of the marker gene relative to enhancer elements on the plasmids. Two types of position effects were revealed by that analysis. The first, promoter occlusion, causes reduced transcription at a downstream promoter if transcription is initiated at a nearby upstream promoter. This effect does not involve enhancer elements directly, even though the effect is most pronounced when the downstream promoter lacks an enhancer element. The second effect stems from the ability of promoter sequences to reduce the effect of a single enhancer element on other promoters in the same plasmid. This latter effect is mediated by either promoters adjacent to the enhancer element or promoters interposed between the enhancer element and the other promoters on the plasmid.
我们利用含有一个、两个或三个以猿猴病毒40为基础的转录单位且排列方式各异的质粒,研究了猿猴病毒40 72碱基对增强子片段同时激活多个转录单位的能力。将这些质粒转染到CV1细胞后,根据标记基因Ecogpt相对于其他转录单位的位置以及该标记基因相对于质粒上增强子元件的位置,来确定其表达情况。该分析揭示了两种类型的位置效应。第一种是启动子阻遏,如果转录在附近的上游启动子处起始,会导致下游启动子的转录减少。即使当下游启动子缺乏增强子元件时这种效应最为明显,该效应也并不直接涉及增强子元件。第二种效应源于启动子序列降低同一质粒中单个增强子元件对其他启动子作用的能力。后一种效应是由与增强子元件相邻的启动子或位于增强子元件与质粒上其他启动子之间的启动子介导的。