Roberts R C, Burioni R, Helinski D R
Department of Biology, University of California, San Diego, La Jolla 92093.
J Bacteriol. 1990 Nov;172(11):6204-16. doi: 10.1128/jb.172.11.6204-6216.1990.
One of the regions responsible for the stable inheritance of the broad-host-range plasmid RK2 is contained within the PstI C fragment, located from coordinates 30.8 to 37.0 kb (P.N. Saurugger, O. Hrabak, H. Schwab, and R.M. Lafferty, J. Biotechnol. 4:333-343, 1986). Genetic analysis of this 6.2-kb region demonstrated that no function was present that stabilized by selectively killing plasmid-free segregants. The sequence from 36.0 to 37.0 kb mediated a twofold increase in plasmid copy number, but this region was not required for stabilization activity. The PstI C fragment was shown to encode a multimer resolution system from 33.1 to 35.3 kb. The resolution cis-acting site was mapped to 140 bp, sequenced, and observed to contain two directly repeated sequences of 6 and 7 bases and two perfect inverted repeats of 6 and 8 bases. The trans-acting factor(s) was mapped and functionally determined to encode a resolvase capable of catalyzing recombination at high frequency between cis-acting sites in either direct or inverted orientation. Multimer resolution alone did not account for complete plasmid stabilization by the PstI C fragment, since removal of regions adjacent to the 35.3-kb border of the minimal mrs locus dramatically reduced stabilization. The minimal region required for complete stabilization, from 32.8 to 35.9 kb, was capable of fully stabilizing plasmids independently of the replicon or the recA proficiency of the host. Stabilization activity was also fully expressed in several diverse gram-negative bacteria, whereas the F plasmid par locus functioned only in Escherichia coli. On the basis of these observations, we conclude that under the growth conditions used, the minimal stabilization locus encodes both an mrs activity and a stabilization activity that has the properties of a par locus.
广宿主范围质粒RK2稳定遗传所涉及的区域之一包含在PstI C片段内,该片段位于坐标30.8至37.0 kb之间(P.N. Saurugger、O. Hrabak、H. Schwab和R.M. Lafferty,《生物技术杂志》4:333 - 343,1986年)。对这个6.2 kb区域的遗传分析表明,不存在通过选择性杀死无质粒分离物来实现稳定的功能。36.0至37.0 kb的序列介导了质粒拷贝数两倍的增加,但该区域对于稳定活性并非必需。PstI C片段被证明在33.1至35.3 kb编码一个多聚体解离系统。解离顺式作用位点被定位到140 bp,进行了测序,并观察到其包含两个6个和7个碱基的直接重复序列以及两个6个和8个碱基的完美反向重复序列。反式作用因子被定位并在功能上确定为编码一种解离酶,能够在顺式作用位点之间以高频催化正向或反向排列的重组。仅多聚体解离并不能解释PstI C片段对质粒的完全稳定作用,因为去除最小mrs基因座35.3 kb边界附近的区域会显著降低稳定性。完全稳定所需的最小区域,从32.8至35.9 kb,能够独立于宿主的复制子或recA能力完全稳定质粒。稳定活性在几种不同的革兰氏阴性细菌中也能完全表达,而F质粒par基因座仅在大肠杆菌中起作用。基于这些观察结果,我们得出结论,在所使用的生长条件下,最小稳定基因座编码一种mrs活性和一种具有par基因座特性的稳定活性。