Santamaría D, Hernández P, Martínez-Robles M L, Krimer D B, Schvartzman J B
Departamento de Biología Celular y del Desarrollo, CIB (CSIC), Velázquez 144, Madrid, 28006, Spain.
J Mol Biol. 2000 Jun 30;300(1):75-82. doi: 10.1006/jmbi.2000.3843.
In Escherichia coli plasmids carrying two inversely oriented ColE1 origins, DNA replication initiates at only one of the two potential origins. The other silent origin acts as a replication fork barrier. Whether this barrier is permanent or simply a pausing site remains unknown. Here, we used a repeated primer extension assay to map in vivo, at the nucleotide level, the 5' end of the nascent strand where initiation and blockage of replication forks occurs. Initiation occurred primarily at the previously defined origin, however, an alternative initiation site was detected 17 bp upstream. At the barrier, the lagging strand also terminated at the main initiation site. Therefore, the 5' end of the nascent strand at the barrier was identical to that generated during initiation. This observation strongly suggests that blockage of the replication fork at the silent origin is not just a pausing site but permanent, and leads to a premature termination event.
在携带两个反向排列的ColE1复制起点的大肠杆菌质粒中,DNA复制仅在两个潜在起点中的一个起始。另一个沉默起点充当复制叉屏障。这个屏障是永久性的还是仅仅是一个暂停位点仍然未知。在这里,我们使用重复引物延伸测定法在核苷酸水平上在体内绘制新生链的5'端,复制叉在此起始和受阻。起始主要发生在先前定义的起点,然而,在其上游17 bp处检测到一个替代起始位点。在屏障处,滞后链也在主要起始位点终止。因此,屏障处新生链的5'端与起始过程中产生的5'端相同。这一观察结果强烈表明,沉默起点处复制叉的阻断不仅仅是一个暂停位点,而是永久性的,并导致过早终止事件。