Dewar James M, Budzowska Magda, Walter Johannes C
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Howard Hughes Medical Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Nature. 2015 Sep 17;525(7569):345-50. doi: 10.1038/nature14887. Epub 2015 Aug 31.
Eukaryotic DNA replication terminates when replisomes from adjacent replication origins converge. Termination involves local completion of DNA synthesis, decatenation of daughter molecules and replisome disassembly. Termination has been difficult to study because termination events are generally asynchronous and sequence nonspecific. To overcome these challenges, we paused converging replisomes with a site-specific barrier in Xenopus egg extracts. Upon removal of the barrier, forks underwent synchronous and site-specific termination, allowing mechanistic dissection of this process. We show that DNA synthesis does not slow detectably as forks approach each other, and that leading strands pass each other unhindered before undergoing ligation to downstream lagging strands. Dissociation of the replicative CMG helicase (comprising CDC45, MCM2-7 and GINS) occurs only after the final ligation step, and is not required for completion of DNA synthesis, strongly suggesting that converging CMGs pass one another and dissociate from double-stranded DNA. This termination mechanism allows rapid completion of DNA synthesis while avoiding premature replisome disassembly.
当真核生物中来自相邻复制起点的复制体汇聚时,DNA复制终止。终止过程涉及DNA合成的局部完成、子代分子的解连环以及复制体的解体。由于终止事件通常是异步的且不具有序列特异性,因此很难对其进行研究。为了克服这些挑战,我们在非洲爪蟾卵提取物中利用位点特异性屏障使汇聚的复制体暂停。去除屏障后,复制叉进行同步且位点特异性的终止,从而能够对这一过程进行机制剖析。我们发现,当复制叉相互靠近时,DNA合成没有明显减慢,并且前导链在与下游滞后链连接之前不受阻碍地相互穿过。复制型CMG解旋酶(由CDC45、MCM2-7和GINS组成)仅在最后的连接步骤之后才发生解离,并且DNA合成的完成并不需要它,这有力地表明汇聚的CMG相互穿过并从双链DNA上解离。这种终止机制能够在避免复制体过早解体的同时快速完成DNA合成。