Moreau Morgane J J, Schaeffer Patrick M
School of Pharmacy and Molecular Sciences, James Cook University, DB 21, James Cook Drive, Townsville, QLD 4811, Australia.
Mol Biosyst. 2012 Oct;8(10):2783-91. doi: 10.1039/c2mb25281c.
In E. coli, DNA replication termination occurs at Ter sites and is mediated by Tus. Two clusters of five Ter sites are located on each side of the terminus region and constrain replication forks in a polar manner. The polarity is due to the formation of the Tus-Ter-lock intermediate. Recently, it has been shown that DnaB helicase which unwinds DNA at the replication fork is preferentially stopped at the non-permissive face of a Tus-Ter complex without formation of the Tus-Ter-lock and that fork pausing efficiency is sequence dependent, raising two essential questions: Does the affinity of Tus for the different Ter sites correlate with fork pausing efficiency? Is formation of the Tus-Ter-lock the key factor in fork pausing? The combined use of surface plasmon resonance and GFP-Basta showed that Tus binds strongly to TerA-E and G, moderately to TerH-J and weakly to TerF. Out of these ten Ter sites only two, TerF and H, were not able to form significant Tus-Ter-locks. Finally, Tus's resistance to dissociation from Ter sites and the strength of the Tus-Ter-locks correlate with the differences in fork pausing efficiency observed for the different Ter sites by Duggin and Bell (2009).
在大肠杆菌中,DNA复制终止发生在Ter位点,由Tus介导。两组各含五个Ter位点的簇位于终止区两侧,以极性方式限制复制叉。这种极性是由于形成了Tus-Ter-lock中间体。最近的研究表明,在复制叉处解开DNA的DnaB解旋酶优先在Tus-Ter复合物的非允许面停止,且不形成Tus-Ter-lock,并且叉停顿效率取决于序列,这就提出了两个关键问题:Tus对不同Ter位点的亲和力与叉停顿效率相关吗?Tus-Ter-lock的形成是叉停顿的关键因素吗?表面等离子体共振和GFP-Basta的联合使用表明,Tus与TerA-E和G强烈结合,与TerH-J中度结合,与TerF弱结合。在这十个Ter位点中,只有TerF和H不能形成显著的Tus-Ter-lock。最后,Tus从Ter位点解离的抗性以及Tus-Ter-lock的强度与Duggin和Bell(2009年)观察到不同Ter位点的叉停顿效率差异相关。