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Genome-wide Mapping of DNA Synthesis in Saccharomyces cerevisiae Reveals That Mechanisms Preventing Reinitiation of DNA Replication Are Not Redundant

机译:全基因组映射的酿酒酵母DNA合成揭示防止DNA复制的重新启动的机制不是多余的。

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摘要

To maintain genomic stability, reinitiation of eukaryotic DNA replication within a single cell cycle is blocked by multiple mechanisms that inactivate or remove replication proteins after G1 phase. Consistent with the prevailing notion that these mechanisms are redundant, we previously showed that simultaneous deregulation of three replication proteins, ORC, Cdc6, and Mcm2-7, was necessary to cause detectable bulk re-replication in G2/M phase in Saccharomyces cerevisiae. In this study, we used microarray comparative genomic hybridization (CGH) to provide a more comprehensive and detailed analysis of re-replication. This genome-wide analysis suggests that reinitiation in G2/M phase primarily occurs at a subset of both active and latent origins, but is independent of chromosomal determinants that specify the use and timing of these origins in S phase. We demonstrate that re-replication can be induced within S phase, but differs in amount and location from re-replication in G2/M phase, illustrating the dynamic nature of DNA replication controls. Finally, we show that very limited re-replication can be detected by microarray CGH when only two replication proteins are deregulated, suggesting that the mechanisms blocking re-replication are not redundant. Therefore we propose that eukaryotic re-replication at levels below current detection limits may be more prevalent and a greater source of genomic instability than previously appreciated.
机译:为了维持基因组稳定性,真核DNA复制在单个细胞周期内的重新启动受到多种机制的阻止,这些机制可在G1期后失活或去除复制蛋白。与这些机制是多余的普遍观念相一致,我们先前显示了三个复制蛋白,ORC,Cdc6和Mcm2-7的同时去调节,对于酿酒酵母在G2 / M期引起可检测的大量复制是必要的。在这项研究中,我们使用微阵列比较基因组杂交(CGH)提供了更全面和详细的重复分析。这种全基因组分析表明,G2 / M期的重新启动主要发生在活跃和潜在起源的子集中,但与染色体决定簇无关,后者决定了这些起源在S期的用途和时机。我们证明了复制可以在S期内被诱导,但是在G2 / M期的复制中其数量和位置有所不同,这说明了DNA复制控制的动态特性。最后,我们表明,只有两个复制蛋白被解除调控时,微阵列CGH可以检测到非常有限的复制,这表明阻止复制的机制不是多余的。因此,我们提出,在低于当前检测限的水平下,真核生物的复制可能比以前认识到的更为普遍,并且是更大的基因组不稳定性来源。

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