Celniker S E, Campbell J L
Cell. 1982 Nov;31(1):201-13. doi: 10.1016/0092-8674(82)90420-2.
An enzyme system prepared from Saccharomyces cerevisiae carries out the replication of exogenous yeast plasmid DNA. Replication in vitro mimics that in vivo in that DNA synthesis in extracts of strain cdc8, a temperature-sensitive DNA replication mutant, is thermolabile relative to the wild-type, and in that aphidicolin inhibits replication in vitro. Furthermore, only plasmids containing a functional yeast replicator, ARS, initiate replication at a specific site in vitro. Analysis of replicative intermediates shows that plasmid YRp7, which contains the chromosomal replicator ARS1, initiates bidirectional replication in a 100 bp region within the sequence required for autonomous replication in vivo. Plasmids containing ARS2, another chromosomal replicator, and the ARS region of the endogenous yeast plasmid 2 microns circle give similar results, suggesting that ARS sequences are specific origins of chromosomal replication. Used in conjunction with deletion mapping, the in vitro system allows definition of the minimal sequences required for the initiation of replication.
从酿酒酵母制备的一种酶系统可实现外源酵母质粒DNA的复制。体外复制模拟体内复制,即温度敏感型DNA复制突变体cdc8菌株提取物中的DNA合成相对于野生型是热不稳定的,而且阿非科林可抑制体外复制。此外,只有含有功能性酵母复制子ARS的质粒才能在体外特定位点起始复制。对复制中间体的分析表明,含有染色体复制子ARS1的质粒YRp7在体内自主复制所需序列内的一个100 bp区域起始双向复制。含有另一个染色体复制子ARS2以及内源性酵母质粒2μm环的ARS区域的质粒也给出类似结果,这表明ARS序列是染色体复制的特定起始位点。与缺失作图结合使用时,该体外系统可确定复制起始所需的最小序列。