Wellinger R J, Wolf A J, Zakian V A
Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Mol Cell Biol. 1993 Jul;13(7):4057-65. doi: 10.1128/mcb.13.7.4057-4065.1993.
In order to understand the mechanisms leading to the complete duplication of linear eukaryotic chromosomes, the temporal order of the events involved in replication of a 7.5-kb Saccharomyces cerevisiae linear plasmid called YLpFAT10 was determined. Two-dimensional agarose gel electrophoresis was used to map the position of the replication origin and the direction of replication fork movement through the plasmid. Replication began near the center of YLpFAT10 at the site in the 2 microns sequences that corresponds to the 2 microns origin of DNA replication. Replication forks proceeded bidirectionally from the origin to the ends of YLpFAT10. Thus, yeast telomeres do not themselves act as origins of DNA replication. The time of origin utilization on YLpFAT10 and on circular 2 microns DNA in the same cells was determined both by two-dimensional gel electrophoresis and by density transfer experiments. As expected, 2 microns DNA replicated in early S phase. However, replication of YLpFAT10 occurred in late S phase. Thus, the time of activation of the 2 microns origin depended upon its physical context. Density transfer experiments established that the acquisition of telomeric TG1-3 single-strand tails, a predicted intermediate in telomere replication, occurred immediately after the replication forks approached the ends of YLpFAT10. Thus, telomere replication may be the very last step in S phase.
为了理解导致线性真核染色体完全复制的机制,我们确定了一个名为YLpFAT10的7.5 kb酿酒酵母线性质粒复制过程中所涉及事件的时间顺序。利用二维琼脂糖凝胶电泳来定位复制起点的位置以及复制叉通过质粒的移动方向。复制始于YLpFAT10中心附近,位于2微米序列中对应于2微米DNA复制起点的位点。复制叉从起点双向延伸至YLpFAT10的末端。因此,酵母端粒本身并不作为DNA复制的起点。通过二维凝胶电泳和密度转移实验,确定了同一细胞中YLpFAT10和环状2微米DNA上起点利用的时间。正如预期的那样,2微米DNA在S期早期复制。然而,YLpFAT10的复制发生在S期晚期。因此,2微米起点的激活时间取决于其物理环境。密度转移实验表明,端粒TG1-3单链尾巴(端粒复制中一个预测的中间体)的获得在复制叉接近YLpFAT10末端后立即发生。因此,端粒复制可能是S期的最后一步。