Stehle Isa M, Scinteie Monica F, Baiker Armin, Jenke Andreas C W, Lipps Hans J
Institute of Cell Biology, University Witten/Herdecke, Witten, FRG.
Chromosome Res. 2003;11(5):413-21. doi: 10.1023/a:1024962308071.
In order to analyze epigenetic factors involved in the regulation of DNA replication in higher eukaryotic cells, minimal systems have to be established. We have recently constructed a non-viral episomal vector system which replicates episomally in mammalian cells and is stably maintained in the cell in the absence of selection. The potential functional elements contained in this construct are an expression cassette upstream of a chromosomal S/MAR sequence and the SV40 origin of replication. In this report we describe that an active transcription upstream of the S/MAR running into this sequence is required and probably sufficient for episomal replication. We propose a model for the activation of replication in this system which may be the basis for further analysis of replication control in other systems.
为了分析参与高等真核细胞DNA复制调控的表观遗传因素,必须建立最小系统。我们最近构建了一种非病毒附加型载体系统,该系统在哺乳动物细胞中以附加型方式复制,并且在没有选择压力的情况下能在细胞中稳定维持。该构建体中包含的潜在功能元件是染色体S/MAR序列上游的一个表达盒和SV40复制起点。在本报告中,我们描述了S/MAR上游进入该序列的活跃转录是附加型复制所必需的,并且可能就足够了。我们提出了一个该系统中复制激活的模型,这可能是进一步分析其他系统中复制控制的基础。