Matsumoto Akino, Daigaku Yasukazu, Tsubouchi Tomomi
Laboratory of Stem Cell Biology, National Institute for Basic Biology, National Institutes of Natural Sciences, 38 Nishigonaka, Myodaiji, Okazaki, Aichi 444-8585, Japan.
Department of Basic Biology, the Graduate University for Advanced Studies, SOKENDAI, 38 Nishigonaka, Myodaiji, Okazaki, Aichi 444-8585, Japan.
J Biochem. 2025 Mar 4;177(3):213-223. doi: 10.1093/jb/mvae097.
Various methods have been developed to map replication initiation zones (IZs) genome-wide, often finding far fewer IZs than expected. In particular, IZs corresponding to later stages of S phase are under-represented. Here, we reanalysed IZs with respect to replication timing in mouse ES cells. These datasets identified over five times as many early IZs compared to late IZs. In addition, we have set up a polymerase-usage sequencing (Pu-seq) system in mouse ES cells to map IZs genome-wide. Pu-seq showed less bias towards early IZs, potentially indicating better sensitivity for identifying IZs in late S phase.
已经开发出各种方法来在全基因组范围内绘制复制起始区域(IZs),但通常发现IZs的数量比预期少得多。特别是,与S期后期相对应的IZs代表性不足。在这里,我们重新分析了小鼠胚胎干细胞中与复制时间相关的IZs。这些数据集显示,早期IZs的数量是晚期IZs的五倍多。此外,我们在小鼠胚胎干细胞中建立了一种聚合酶使用测序(Pu-seq)系统,以在全基因组范围内绘制IZs。Pu-seq对早期IZs的偏向性较小,这可能表明在识别S期后期的IZs方面具有更好的灵敏度。