Davidson Iain F, Li Anatoliy, Blow J Julian
School of Life Sciences, University of Dundee, Dundee DD1 5EH, United Kingdom.
Mol Cell. 2006 Nov 3;24(3):433-43. doi: 10.1016/j.molcel.2006.09.010.
Correct regulation of the replication licensing system ensures that no DNA is rereplicated in a single cell cycle. When the licensing protein Cdt1 is overexpressed in G2 phase of the cell cycle, replication origins are relicensed and the DNA is rereplicated. At the same time, checkpoint pathways are activated that block further cell cycle progression. We have studied the consequence of deregulating the licensing system by adding recombinant Cdt1 to Xenopus egg extracts. We show that Cdt1 induces checkpoint activation and the appearance of small fragments of double-stranded DNA. DNA fragmentation and strong checkpoint activation are dependent on uncontrolled rereplication and do not occur after a single coordinated round of rereplication. The DNA fragments are composed exclusively of rereplicated DNA. The unusual characteristics of these fragments suggest that they result from head-to-tail collision (rear ending) of replication forks chasing one another along the same DNA template.
复制许可系统的正确调控可确保在单个细胞周期内不会再次复制DNA。当许可蛋白Cdt1在细胞周期的G2期过度表达时,复制起点会被重新许可,DNA会再次复制。与此同时,检查点通路被激活,阻止细胞周期进一步推进。我们通过向非洲爪蟾卵提取物中添加重组Cdt1来研究解除许可系统调控的后果。我们发现Cdt1会诱导检查点激活以及双链DNA小片段的出现。DNA片段化和强烈的检查点激活依赖于不受控制的再次复制,在单次协调的再次复制后不会发生。这些DNA片段仅由再次复制的DNA组成。这些片段的异常特征表明它们是由沿着同一DNA模板相互追逐的复制叉的头对头碰撞(追尾)导致的。