Sleigh M J
CSIRO Division of Molecular Biology, North Ryde, NSW, Australia.
Nucleic Acids Res. 1987 Nov 25;15(22):9379-95. doi: 10.1093/nar/15.22.9379.
Expression of genes driven by the SV40 promoter/enhancer appears to be under net negative regulatory control in undifferentiated F9 cells, but not in their differentiated derivatives. In cells containing integrated copies of an SV40 promoter-driven marker gene, induction of differentiation by retinoic acid treatment produced a modest increase in transcription from the viral promoter. A much greater increase was observed when differentiated or undifferentiated cells were treated with the protein synthesis inhibitor, cycloheximide. If cycloheximide acts through removal of negative-regulatory molecule(s), then it is apparent that these molecules are present in both differentiated and undifferentiated cells, and that retinoic acid treatment removes only a portion of the total transcriptional repression. RNA levels from a variety of cellular genes activated during F9 cell differentiation were either unaffected or only slightly increased by cycloheximide treatment. This suggests important qualitative or quantitative differences in the regulation mechanism for viral and cellular genes in differentiating F9 cells.
由SV40启动子/增强子驱动的基因表达在未分化的F9细胞中似乎受到净负调控,但在其分化衍生物中则不然。在含有SV40启动子驱动的标记基因整合拷贝的细胞中,用视黄酸处理诱导分化会使病毒启动子的转录适度增加。当用蛋白质合成抑制剂环己酰亚胺处理分化或未分化细胞时,观察到的增加幅度要大得多。如果环己酰亚胺通过去除负调控分子起作用,那么很明显这些分子存在于分化和未分化细胞中,并且视黄酸处理仅去除了总转录抑制的一部分。在F9细胞分化过程中被激活的多种细胞基因的RNA水平,要么不受环己酰亚胺处理的影响,要么仅略有增加。这表明在分化的F9细胞中,病毒基因和细胞基因的调控机制存在重要的定性或定量差异。