Wu Pei-Yun Jenny, Nurse Paul
The Rockefeller University, New York, NY 10065, USA.
Cell. 2009 Mar 6;136(5):852-64. doi: 10.1016/j.cell.2009.01.017.
Initiation of eukaryotic DNA synthesis occurs at origins of replication that are utilized with characteristic times and frequencies during S phase. We have investigated origin usage by evaluating the kinetics of replication factor binding in fission yeast and show that similar to metazoa, ORC binding is periodic during the cell cycle, increasing during mitosis and peaking at M/G1. At an origin, the timing of ORC binding in M and pre-RC assembly in G1 correlates with the timing of firing during S, and the level of pre-IC formation reflects origin efficiency. Extending mitosis allows ORC to become more equally associated with origins and leads to genome-wide changes in origin usage, while overproduction of pre-IC factors increases replication of both efficient and inefficient origins. We propose that differential recruitment of ORC to origins during mitosis followed by competition among origins for limiting replication factors establishes the timing and efficiency of origin firing.
真核生物DNA合成的起始发生在复制起点,这些起点在S期以特定的时间和频率被利用。我们通过评估裂殖酵母中复制因子结合的动力学来研究复制起点的使用情况,结果表明,与后生动物类似,ORC结合在细胞周期中是周期性的,在有丝分裂期间增加,并在M/G1期达到峰值。在一个复制起点,ORC在M期的结合时间和G1期前复制复合体(pre-RC)的组装时间与S期的起始时间相关,并且前起始复合体(pre-IC)形成的水平反映了复制起点的效率。延长有丝分裂时间会使ORC与复制起点的结合更加均匀,并导致全基因组范围内复制起点使用情况的变化,而pre-IC因子的过量表达会增加高效和低效复制起点的复制。我们提出,有丝分裂期间ORC向复制起点的差异募集,随后复制起点之间对有限复制因子的竞争,决定了复制起点起始的时间和效率。