Jazwinski S M, Edelman G M
Proc Natl Acad Sci U S A. 1979 Mar;76(3):1223-7. doi: 10.1073/pnas.76.3.1223.
Cell-free extracts prepared from growing cells of the budding yeast Saccharomyces stimulated DNA synthesis directed by the supercoiled 2-micrometer yeast DNA plasmid. The major products of the reaction were open-circular daughter molecules possessing newly synthesized full-length linear DNA strands. Some of these were ligated and supertwisted by the extracts to yield a supercoiled DNA product. Both of the complementary DNA strands of the template were replicated. In addition, the extracts induced the appearance of theta-forms of the plasmid DNA, which are presumed to be replicative intermediates. The results of experiments utilizing BrdUTP incorporation indicated that DNA repair did not contribute significantly to the overall reaction. Extracts prepared from the cell division cycle mutants cdc7 and cdc8, held in culture at the nonpermissive temperature, possessed diminished activity. Because these mutants define a dependent sequence of events leading from the start of the cell cycle through G1 to S phase, this result suggests that the activity that stimulates 2-micrometer DNA replication in vitro is subject to control in the yeast cell cycle.
从出芽酵母酿酒酵母生长细胞制备的无细胞提取物刺激了由超螺旋2微米酵母DNA质粒指导的DNA合成。反应的主要产物是具有新合成的全长线性DNA链的开环子代分子。其中一些被提取物连接并超螺旋化,产生超螺旋DNA产物。模板的两条互补DNA链都被复制。此外,提取物诱导了质粒DNA的θ形式的出现,推测其为复制中间体。利用BrdUTP掺入的实验结果表明,DNA修复对整体反应的贡献不大。在非允许温度下培养的细胞分裂周期突变体cdc7和cdc8制备的提取物活性降低。由于这些突变体定义了从细胞周期开始到G1期再到S期的一系列依赖事件,该结果表明在体外刺激2微米DNA复制的活性在酵母细胞周期中受到调控。