Haase S B, Heinzel S S, Calos M P
Department of Genetics, Stanford University School of Medicine, California 94305.
Mol Cell Biol. 1994 Apr;14(4):2516-24. doi: 10.1128/mcb.14.4.2516-2524.1994.
This study addresses the effect of transcription on replication, using a system based on autonomously replicating plasmids in human cells. We added transcriptional elements from the human cytomegalovirus promoter/enhancer and the human beta-actin promoter to autonomously replicating plasmids based on human sequences and found that the transcriptional elements inhibited plasmid replication. Furthermore, conditional inhibition of plasmid replication was demonstrated by using a tetracycline-responsive promoter. We found that replication activity of plasmids carrying this promoter was inversely correlated with promoter activity. Replication activity was partially restored on plasmids when a transcriptional termination sequence was placed directly downstream of the promoter element. Transcriptional activity of the promoters and the efficacy of the terminator sequence were confirmed by using steady-state RNA analysis. These experiments suggest that transcription inhibits DNA replication on these plasmids and that the degree of inhibition is dependent on transcription strength. The possible significance of these results for chromosomal DNA replication are discussed.
本研究利用基于人类细胞中自主复制质粒的系统,探讨转录对复制的影响。我们将来自人类巨细胞病毒启动子/增强子和人类β-肌动蛋白启动子的转录元件添加到基于人类序列的自主复制质粒中,发现这些转录元件抑制了质粒复制。此外,通过使用四环素响应启动子证明了质粒复制的条件性抑制。我们发现携带该启动子的质粒的复制活性与启动子活性呈负相关。当转录终止序列直接置于启动子元件下游时,质粒的复制活性部分恢复。通过使用稳态RNA分析证实了启动子的转录活性和终止序列的功效。这些实验表明转录抑制了这些质粒上的DNA复制,并且抑制程度取决于转录强度。讨论了这些结果对染色体DNA复制可能具有的意义。