Program in Molecular Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065
Program in Molecular Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065.
Proc Natl Acad Sci U S A. 2019 Mar 12;116(11):4973-4982. doi: 10.1073/pnas.1818680116. Epub 2019 Feb 4.
Each genomic locus in a eukaryotic cell has a distinct average time of replication during S phase that depends on the spatial and temporal pattern of replication initiation events. Replication timing can affect genomic integrity because late replication is associated with an increased mutation rate. For most eukaryotes, the features of the genome that specify the location and timing of initiation events are unknown. To investigate these features for the fission yeast, , we developed an integrative model to analyze large single-molecule and global genomic datasets. The model provides an accurate description of the complex dynamics of DNA replication at high resolution. We present evidence that there are many more potential initiation sites in the genome than previously identified and that the distribution of these sites is primarily determined by two factors: the sequence preferences of the origin recognition complex (ORC), and the interference of transcription with the assembly or stability of prereplication complexes (pre-RCs). We suggest that in addition to directly interfering with initiation, transcription has driven the evolution of the binding properties of ORC in and other eukaryotic species to target pre-RC assembly to regions of the genome that are less likely to be transcribed.
真核细胞中的每个基因组位点在 S 期都有一个独特的平均复制时间,这取决于复制起始事件的空间和时间模式。复制时间会影响基因组的完整性,因为晚期复制与更高的突变率有关。对于大多数真核生物来说,指定起始事件位置和时间的基因组特征是未知的。为了研究裂殖酵母的这些特征,我们开发了一个综合模型来分析大型单分子和全基因组数据集。该模型提供了对 DNA 复制复杂动力学的高分辨率准确描述。我们提供的证据表明, 基因组中有比以前鉴定出的更多的潜在起始位点,这些位点的分布主要由两个因素决定:起始识别复合物 (ORC) 的序列偏好,以及转录对前复制复合物 (pre-RC) 组装或稳定性的干扰。我们认为,转录除了直接干扰起始外,还推动了 ORC 在 和其他真核生物中的结合特性的进化,以使 pre-RC 组装靶向基因组中不太可能被转录的区域。