Department of Biological Science, Florida State University, Tallahassee, FL 32306, USA.
J Cell Biol. 2010 Jun 14;189(6):967-80. doi: 10.1083/jcb.201002002. Epub 2010 Jun 7.
DNA replication in all eukaryotes follows a defined replication timing program, the molecular mechanism of which remains elusive. Using a Xenopus laevis egg extract replication system, we previously demonstrated that replication timing is established during early G1 phase of the cell cycle (timing decision point [TDP]), which is coincident with the repositioning and anchorage of chromatin in the newly formed nucleus. In this study, we use this same system to show that G2 phase chromatin lacks determinants of replication timing but maintains the overall spatial organization of chromatin domains, and we confirm this finding by genome-wide analysis of rereplication in vivo. In contrast, chromatin from quiescent cells retains replication timing but exhibits disrupted spatial organization. These data support a model in which events at the TDP, facilitated by chromatin spatial organization, establish determinants of replication timing that persist independent of spatial organization until the process of chromatin replication during S phase erases those determinants.
所有真核生物的 DNA 复制都遵循一个明确的复制时间程序,但其分子机制仍难以捉摸。我们之前使用非洲爪蟾卵提取物复制系统证明,复制时间是在细胞周期的早期 G1 期(定时决策点 [TDP])确定的,此时染色质在新形成的核中重新定位和锚定。在这项研究中,我们使用相同的系统表明 G2 期染色质缺乏复制时间的决定因素,但维持染色质域的整体空间组织,并且我们通过体内重新复制的全基因组分析证实了这一发现。相比之下,静止细胞的染色质保留复制时间,但表现出空间组织的破坏。这些数据支持这样一种模型,即 TDP 处的事件通过染色质空间组织促进了复制时间决定因素的建立,这些决定因素在 S 期的染色质复制过程消除这些决定因素之前独立于空间组织而持续存在。