Bingle Lewis E H, Macartney Donia P, Fantozzi Anaïs, Manzoor Susan E, Thomas Christopher M
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
J Mol Biol. 2005 Jun 3;349(2):302-16. doi: 10.1016/j.jmb.2005.03.062. Epub 2005 Apr 8.
KorB, encoded by plasmid RK2, belongs to the ParB family of active partitioning proteins. It binds to 12 operators on the RK2 genome and was previously known to repress promoters immediately adjacent to operators O(B)1, O(B)10 and O(B)12 (proximal) or up to 154 bp away (distal) from O(B)2, O(B)9 and O(B)11. To achieve strong repression, KorB requires a cooperative interaction with one of two other plasmid-encoded repressors, KorA or TrbA. Reporter gene assays were used in this study to test whether the additional KorB operators may influence transcription and to test how KorB acts at a distance. The distance between O(B)9 and trbBp could be increased to 1.6kb with little reduction in repression or cooperativity with TrbA. KorB was also able to repress the promoter and cooperate with TrbA when the O(B) site was placed downstream of trbBp. This suggested a potential regulatory role for O(B) sites located a long way from any known promoter on RK2. O(B)4, 1.9kb upstream of traGp, was shown to mediate TrbA-potentiated KorB repression of this promoter, but no effect on traJp upstream of O(B)4 was observed, which may be due to the roadblocking or topological influence of the nucleoprotein complex formed at the adjacent transfer origin, oriT. Repression and cooperativity were alleviated significantly when a lac operator was inserted between O(B)9 and trbBp in the context of a LacI+ host, a standard test for spreading of a DNA-binding protein. On the other hand, a standard test for DNA looping, movement of the operator to the opposite face of the DNA helix from the natural binding site, did not significantly affect KorB repression or cooperativity with TrbA and KorA over relatively short distances. While these results are more consistent with spreading as the mechanism by which KorB reaches its target, previous estimates of KorB molecules per cell are not consistent with there being enough to spread up to 1kb from each O(B). A plausible model is therefore that KorB can do both, spreading over relatively short distances and looping over longer distances.
由质粒RK2编码的KorB属于活性分配蛋白的ParB家族。它与RK2基因组上的12个操纵子结合,此前已知它能抑制紧邻操纵子O(B)1、O(B)10和O(B)12(近端)的启动子,或抑制距离O(B)2、O(B)9和O(B)11达154 bp远(远端)的启动子。为实现强效抑制,KorB需要与另外两个质粒编码的阻遏蛋白之一KorA或TrbA进行协同相互作用。本研究使用报告基因检测来测试额外的KorB操纵子是否可能影响转录,并测试KorB如何在远距离发挥作用。O(B)9与trbBp之间的距离可增加至1.6kb,而抑制作用或与TrbA的协同作用几乎没有降低。当O(B)位点位于trbBp下游时,KorB也能够抑制启动子并与TrbA协同作用。这表明位于距RK2上任何已知启动子很远位置的O(B)位点具有潜在的调控作用。位于traGp上游1.9kb处的O(B)4被证明介导TrbA增强的KorB对该启动子的抑制作用,但未观察到对O(B)4上游的traJp有影响,这可能是由于在相邻转移起始位点oriT形成的核蛋白复合物的路障效应或拓扑学影响。当在LacI+宿主背景下于O(B)9与trbBp之间插入一个lac操纵子时,抑制作用和协同作用显著减轻,这是对DNA结合蛋白扩散的标准测试。另一方面,对DNA环化的标准测试,即将操纵子从天然结合位点移至DNA螺旋的相对面,在相对较短距离内对KorB的抑制作用或与TrbA和KorA的协同作用没有显著影响。虽然这些结果与扩散作为KorB到达其靶标的机制更一致,但先前对每个细胞中KorB分子数量的估计与从每个O(B)扩散达1kb所需的数量不一致。因此,一个合理的模型是KorB既能在相对短的距离内扩散,也能在较长距离内形成环化。