Abeles A L, Austin S J
Laboratory of Chromosome Biology, National Cancer Institute-Frederick Cancer Research and Development Center, MD 21702-1201.
Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9011-5. doi: 10.1073/pnas.88.20.9011.
The copy number of the P1 plasmid replicon is stringently controlled, giving only one or two copies per newborn cell. Control is achieved by the action of the copy-control locus incA, which contains nine repeats of the 19-basepair binding site for the plasmid-encoded initiator protein RepA. A set of five similar repeats are present in the replication origin where RepA acts to trigger initiation. Using an in vitro replication system consisting of an Escherichia coli extract, the P1 origin as a template, and purified RepA protein, we show that supercoiled DNA circles containing the incA locus block origin function in trans. Shutdown becomes complete at a 1:1 ratio of origin to incA sequences. This is not due to titration of the RepA protein, as an excess of RepA can be added without restoring activity. Rather, the incA sequences appear to block the origin by direct contact in a plasmid-plasmid pairing event. When both the origin and the incA locus are present on one plasmid, trans contacts with daughter molecules appear to predominate over cis looping. The results are consistent with a model for replication control where daughter plasmids block their own replication by a pairing in which each origin is in contact with the incA locus of its partner.
P1质粒复制子的拷贝数受到严格控制,每个新生细胞仅产生一到两个拷贝。这种控制是通过复制控制位点incA的作用实现的,该位点包含质粒编码的起始蛋白RepA的19个碱基对结合位点的九个重复序列。在RepA触发起始作用的复制起点存在一组五个相似的重复序列。利用由大肠杆菌提取物、作为模板的P1起点和纯化的RepA蛋白组成的体外复制系统,我们发现含有incA位点的超螺旋DNA环在反式作用中阻断起点功能。当起点与incA序列的比例为1:1时,关闭作用完全完成。这不是由于RepA蛋白的滴定,因为添加过量的RepA并不能恢复活性。相反,incA序列似乎通过质粒-质粒配对事件中的直接接触来阻断起点。当起点和incA位点都存在于一个质粒上时,与子代分子的反式接触似乎比顺式环化更占优势。这些结果与一种复制控制模型一致,即子代质粒通过一种配对来阻断自身复制,在这种配对中,每个起点都与其伙伴的incA位点接触。