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复制起点:我们为何需要这么多?

Replication origins: why do we need so many?

作者信息

Bielinsky Anja-Katrin

机构信息

Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Molecular and Cellular Biology Building, Room 6-106, 420 Washington Ave SE, Minneapolis, Minnesota 55455, USA.

出版信息

Cell Cycle. 2003 Jul-Aug;2(4):307-9.

Abstract

During the G1 phase of the cell cycle, replication origins are prepared to fire, a process that is referred to as origin licensing. It was often pondered what a cell's fate would be if not all of its replication origins were licensed and subsequently activated during S phase. One obvious prediction was that S phase would simply be prolonged. As it turns out, however, the consequences are much more complex. A short G1 phase enforced by premature entry into S phase, or other events that negatively affect origin licensing, will ultimately compromise the cell's ability to complete DNA replication before entering mitosis. As a result, the cell becomes genomically unstable when it attempts to repair unreplicated DNA during anaphase. Thus, the density of active replication origins in the chromosomes of eukaryotic cells determines S phase dynamics and chromosome stability during mitosis.

摘要

在细胞周期的G1期,复制起点准备启动,这一过程被称为起点许可。人们常常思考,如果细胞的所有复制起点在S期没有全部获得许可并随后被激活,细胞的命运将会如何。一个明显的预测是S期会简单地延长。然而,事实证明,后果要复杂得多。过早进入S期导致的短G1期,或其他对起点许可产生负面影响的事件,最终会损害细胞在进入有丝分裂之前完成DNA复制的能力。结果,当细胞在后期试图修复未复制的DNA时,它会变得基因组不稳定。因此,真核细胞染色体中活跃复制起点的密度决定了有丝分裂期间的S期动态和染色体稳定性。

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