Yamaguchi M, Obata Y, Matsukage A
Laboratory of Cell Biology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Nucleic Acids Res. 1989 May 25;17(10):3725-34. doi: 10.1093/nar/17.10.3725.
Simian virus (SV) 40 enhancer (nucleotide position 108 to 294) was combined with chloramphenicol acetyltransferase (CAT) plasmid whose expression is under control of mouse DNA polymerase beta gene promoter. Although the SV40 enhancer stimulated the transient CAT-expression directed by the DNA polymerase beta gene promoter two to three fold in human HeLa cells, it repressed the CAT-expression by 50 to 60% in mouse NIH/3T3 cells. The repression was observed relatively independently on the orientation of the insertion and the distance from the promoter. These properties of the enhancer are very similar to those of so-called transcriptional silencer element. In both HeLa and NIH/3T3 cells, the SV40 enhancer stimulated effectively its own early gene promoter-directed CAT-expression. In mouse immature T-cell line RV-1 in which the SV40 promoter-enhancer did not function, no effect of the SV40 enhancer sequence on the DNA polymerase beta promoter-directed CAT-expression was observed. Thus, it is suggested that both cell type-specific trans-acting factor(s) and the specific combination with the promoter sequence turn the properties of the SV40 enhancer into those of a silencer.
将猿猴病毒(SV)40增强子(核苷酸位置108至294)与氯霉素乙酰转移酶(CAT)质粒相结合,该质粒的表达受小鼠DNA聚合酶β基因启动子的控制。尽管SV40增强子在人HeLa细胞中可使由DNA聚合酶β基因启动子指导的瞬时CAT表达增强2至3倍,但在小鼠NIH/3T3细胞中却使CAT表达降低了50%至60%。这种抑制作用在相对独立于插入方向和与启动子距离的情况下被观察到。增强子的这些特性与所谓的转录沉默元件非常相似。在HeLa细胞和NIH/3T3细胞中,SV40增强子均能有效刺激其自身早期基因启动子指导的CAT表达。在SV40启动子-增强子不起作用的小鼠未成熟T细胞系RV-1中,未观察到SV40增强子序列对DNA聚合酶β启动子指导的CAT表达有任何影响。因此,提示细胞类型特异性反式作用因子以及与启动子序列的特定组合将SV40增强子的特性转变为沉默子的特性。