Jin R, Novick R P
Molecular Pathogenesis Program, Skirball Institute, New York University School of Medicine, New York, NY 10016, USA.
Plasmid. 2001 Sep;46(2):95-105. doi: 10.1006/plas.2001.1535.
pT181 is a small rolling-circle plasmid from Staphylococcus aureus whose initiator protein, RepC, melts the plasmid's double-strand origin (DSO) and extrudes a cruciform involving IR II, a palindrome flanking the initiation nick site. We have hypothesized that the cruciform is required for initiation, providing a single-stranded region for the assembly of the replisome (R. Jin et al., 1997, EMBO J. 16, 4456-4566). In this study, we have tested the requirement for cruciform extrusion by disrupting the symmetry of the IR II palindrome or by increasing its length. The modified DSOs were tested for replication with RepC in trans. Rather surprisingly, disruption of the IR II symmetry had no detectable effect on replication or on competitivity of the modified DSO, though plasmids with IR II disrupted were less efficiently relaxed than the wild type by RepC. However, in conjunction with IR II disruption, modification of the tight RepC binding site IR III blocked replication. These results define two key elements of the pT181 initiation mechanism--the IR II conformation and the RepC binding site (IR III)--and they indicate that pT181 replication initiation is sufficiently robust to be able to compensate for significant modifications in the configuration of the DSO.
pT181是一种来自金黄色葡萄球菌的小型滚环质粒,其引发蛋白RepC使质粒的双链复制起点(DSO)解链,并挤出一个包含IR II的十字形结构,IR II是起始切口位点侧翼的一个回文序列。我们推测十字形结构是起始所必需的,为复制体的组装提供一个单链区域(R. Jin等人,1997年,《欧洲分子生物学组织杂志》16卷,4456 - 4566页)。在本研究中,我们通过破坏IR II回文序列的对称性或增加其长度来测试对十字形结构挤出的需求。用RepC在反式条件下测试修饰后的DSO的复制情况。相当令人惊讶的是,IR II对称性的破坏对复制或修饰后的DSO的竞争力没有可检测到的影响,尽管IR II被破坏的质粒被RepC松弛的效率比野生型低。然而,与IR II破坏相结合,紧密的RepC结合位点IR III的修饰会阻断复制。这些结果定义了pT181起始机制的两个关键要素——IR II构象和RepC结合位点(IR III)——并且它们表明pT181复制起始足够稳健,能够补偿DSO构型的显著修饰。