Laboratory of Yeast Genetics and Cell Biology, The Rockefeller University, 1230 York Avenue, Box 5, New York, NY 10065, USA.
J Cell Sci. 2010 Sep 15;123(Pt 18):3047-51. doi: 10.1242/jcs.067470. Epub 2010 Aug 24.
To ensure equal replication of the genome in every eukaryotic cell cycle, replication origins fire only once each S phase and do not fire after passive replication. Failure in these controls can lead to local amplification, contributing to genome instability and the development of cancer. To identify features of replication origins important for such amplification, we have investigated origin firing and local genome amplification in the presence of excess helicase loaders Cdc18 and Cdt1 in fission yeast. We find that S phase controls are attenuated and coordination of origin firing is lost, resulting in local amplification. Specific origins are necessary for amplification but act only within a permissive chromosomal context. Origins associated with amplification are highly AT-rich, fire efficiently and early during mitotic S phase, and are located in large intergenic regions. We propose that these features predispose replication origins to re-fire within a single S phase, or to remain active after passive replication.
为确保真核细胞周期中基因组的均等复制,复制原点在每个 S 期仅启动一次,且不会在被动复制后启动。这些控制的失败可能导致局部扩增,从而导致基因组不稳定和癌症的发生。为了确定复制原点对这种扩增重要的特征,我们研究了裂殖酵母中过量解旋酶加载蛋白 Cdc18 和 Cdt1 存在时的复制原点启动和局部基因组扩增。我们发现 S 期控制减弱,原点启动协调丢失,导致局部扩增。特定的原点对于扩增是必要的,但仅在允许的染色体环境中起作用。与扩增相关的原点富含 A-T,在有丝分裂 S 期早期高效启动,并且位于大的基因间区域。我们提出,这些特征使得复制原点易于在单个 S 期内重新启动,或者在被动复制后保持活性。