Gorman C M, Rigby P W, Lane D P
Cell. 1985 Sep;42(2):519-26. doi: 10.1016/0092-8674(85)90109-6.
Many viral genomes, including those of SV40 and MuLV, are not efficiently expressed in undifferentiated embryonal carcinoma (EC) cells but are expressed in differentiated derivatives. This regulation appears to be at the level of transcription. We have used DNA-mediated gene transfer to analyze the function of several viral promoters in EC cells. We show that the SV40 early promoter works efficiently in an enhancer-independent fashion following transfection into undifferentiated cells. Strikingly, the promoter in the LTR of MSV does not function in such cells; but when upstream sequences, including the enhancer, are deleted expression ensues. Replacement of the SV40 enhancer by that of MSV results in inactivation of the SV40 early promoter in these cells. We propose that the undifferentiated cells contain a trans-acting regulatory factor (or factors) that reduces transcription by interacting with viral enhancers.
许多病毒基因组,包括猴空泡病毒40(SV40)和鼠白血病病毒(MuLV)的基因组,在未分化的胚胎癌细胞(EC)中不能有效表达,但在其分化衍生物中可以表达。这种调控似乎发生在转录水平。我们利用DNA介导的基因转移来分析几种病毒启动子在EC细胞中的功能。我们发现,将SV40早期启动子转染到未分化细胞后,它能以不依赖增强子的方式高效发挥作用。令人惊讶的是,莫洛尼氏肉瘤病毒(MSV)长末端重复序列(LTR)中的启动子在这类细胞中不起作用;但当缺失包括增强子在内的上游序列时,表达就会出现。用MSV的增强子替换SV40的增强子会导致这些细胞中SV40早期启动子失活。我们推测,未分化细胞含有一种反式作用调节因子,它通过与病毒增强子相互作用来降低转录水平。