Wold S, Crooke E, Skarstad K
Department of Biophysics, Institute for Cancer Research, Montebello, Oslo, Norway.
Nucleic Acids Res. 1996 Sep 15;24(18):3527-32. doi: 10.1093/nar/24.18.3527.
Fis protein participates in the normal control of chromosomal replication in Escherichia coli. However, the mechanism by which it executes its effect is largely unknown. We demonstrate an inhibitory influence of purified Fis protein on replication from oriC in vitro. Fis inhibits DNA synthesis equally well in replication systems either dependent upon or independent of RNA polymerase, even when the latter is stimulated by the presence of HU or IHF. The extent of inhibition by Fis is modulated by the concentrations of DnaA protein and RNA polymerase; the more limiting the amounts of these, the more severe the inhibition by Fis. Thus, the level of inhibition seems to depend on the ease with which the open complex can be formed. Fis-mediated inhibition of DNA replication does not depend on a functional primary Fis binding site between DnaA boxes R2 and R3 in oriC, as mutations that cause reduced binding of Fis to this site do not affect the degree of inhibition. The data presented suggest that Fis prevents formation of an initiation-proficient structure at oriC by forming an alternative, initiation-preventive complex. This indicates a negative role for Fis in the regulation of replication initiation.
Fis蛋白参与大肠杆菌染色体复制的正常调控。然而,其发挥作用的机制在很大程度上尚不清楚。我们证明了纯化的Fis蛋白在体外对oriC复制具有抑制作用。Fis在依赖或不依赖RNA聚合酶的复制系统中对DNA合成的抑制效果相同,即使后者受到HU或IHF存在的刺激。Fis的抑制程度受DnaA蛋白和RNA聚合酶浓度的调节;这些物质的量越少,Fis的抑制作用就越严重。因此,抑制水平似乎取决于开放复合物形成的难易程度。Fis介导的DNA复制抑制并不依赖于oriC中DnaA框R2和R3之间的功能性主要Fis结合位点,因为导致Fis与该位点结合减少的突变并不影响抑制程度。所呈现的数据表明,Fis通过形成一种替代的、阻止起始的复合物来阻止oriC处形成起始能力强的结构。这表明Fis在复制起始调控中起负向作用。