Mueller C R, Muller W J, Hassell J A
Department of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
J Virol. 1988 May;62(5):1667-78. doi: 10.1128/JVI.62.5.1667-1678.1988.
The polyomavirus enhancer occupies 244 base pairs within noncoding sequences between the early and late transcription units. To define more precisely the DNA sequences that make up the enhancer, we cloned it together with the viral early promoter upstream of a reporter gene, isolated mutants bearing deletions introduced in vitro in the enhancer, and measured the capacity of the various mutant genomes to express the cat gene after transient transfection into mouse 3T3 cells. Analysis of a large number of deletion mutants revealed that the enhancer is between 102 and 172 base pairs long and can be divided into at least three functional elements. Relative to the entire enhancer, individual elements possessed little or no enhancer activity. However, pairs of elements enhanced transcription to levels much higher than the sum of individual elements approximating the activity of the complete enhancer. These findings support the view that the polyomavirus enhancer is composed of multiple sequence elements that function combinatorily and imply that a measure of cooperation exists in the interaction between cellular protein factors bound to their cognate sites in the enhancer and the transcriptional machinery of the cell.
多瘤病毒增强子位于早期和晚期转录单元之间的非编码序列内,占据244个碱基对。为了更精确地确定构成增强子的DNA序列,我们将其与病毒早期启动子一起克隆到报告基因的上游,分离出在体外对增强子进行缺失突变的突变体,并在将各种突变基因组瞬时转染到小鼠3T3细胞后,测量其表达cat基因的能力。对大量缺失突变体的分析表明,增强子长度在102至172个碱基对之间,可分为至少三个功能元件。相对于整个增强子,单个元件几乎没有或完全没有增强子活性。然而,元件对可将转录增强到比单个元件之和高得多的水平,接近完整增强子的活性。这些发现支持了多瘤病毒增强子由多个序列元件组成且协同发挥作用的观点,并暗示在与增强子中其同源位点结合的细胞蛋白因子与细胞转录机制之间的相互作用中存在一定程度的协同作用。