Romero Julia, Lee Hoyun
Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario K1H 8M5, Canada.
Nat Struct Mol Biol. 2008 Jul;15(7):722-9. doi: 10.1038/nsmb.1439. Epub 2008 Jun 8.
Faithful replication of the entire genome once per cell cycle is essential for maintaining genetic integrity, and the origin of DNA replication is key in this regulation. Unlike that in unicellular organisms, the replication initiation mechanism in mammalian cells is not well understood. We have identified a strong origin of replication at the DBF4 promoter locus, which contains two initiation zones, two origin recognition complex (ORC) binding sites and two DNase I-hypersensitive regions within approximately 1.5 kb. Notably, similar to the Escherichia coli oriC, replication at the DBF4 locus starts from initiation zone I, which contains an ORC-binding site, and progresses in the direction of transcription toward initiation zone II, located approximately 0.4 kb downstream. Replication on the opposite strand from zone II, which contains another ORC-binding site, may be activated or facilitated by replication from zone I. We term this new mammalian replication mode 'asymmetric bidirectional replication'.
每个细胞周期对整个基因组进行一次忠实复制对于维持遗传完整性至关重要,而DNA复制起点是这一调控过程的关键。与单细胞生物不同,哺乳动物细胞中的复制起始机制尚不清楚。我们在DBF4启动子位点鉴定出一个强大的复制起点,该位点在约1.5 kb范围内包含两个起始区、两个复制起点识别复合体(ORC)结合位点和两个DNase I超敏区域。值得注意的是,与大肠杆菌oriC相似,DBF4位点的复制从包含一个ORC结合位点的起始区I开始,并朝着转录方向向位于下游约0.4 kb处的起始区II推进。包含另一个ORC结合位点的起始区II的互补链上的复制可能会被起始区I的复制激活或促进。我们将这种新的哺乳动物复制模式称为“不对称双向复制”。