Haring V, Scholz P, Scherzinger E, Frey J, Derbyshire K, Hatfull G, Willetts N S, Bagdasarian M
Proc Natl Acad Sci U S A. 1985 Sep;82(18):6090-4. doi: 10.1073/pnas.82.18.6090.
Essential replication (rep) genes of the broad host range plasmid RSF1010 have been cloned onto controlled expression vectors and their protein products have been visualized, after induction, by NaDodSO4/polyacrylamide gel electrophoresis of whole cell lysates. During this induction the replication of a coresident RSF1010 replicon, pKT210, was analyzed by quantitative DNA X DNA hybridization. The initiation of pKT210 replication was stimulated 6-fold by a simultaneous overproduction of the RepA and RepC proteins compared to cells in which only the RepA protein was overproduced. An enhanced synthesis of the RepB protein resulted in a 1.6-fold stimulation of pKT210 replication, whereas an overproduction of the RepA protein alone had no effect. Purified RepC protein has been shown to bind preferentially to DNA carrying the replication origin of RSF1010. Within this segment it was bound specifically to those DNA fragments that contained the 20-base-pair direct repeats of the origin region. These results suggest that RepC protein acts as a positive replication regulator, that its concentration is rate-limiting, and that the replication rate of RSF1010 is controlled, at least in part, at the level of RepC synthesis.
广宿主范围质粒RSF1010的必需复制(rep)基因已被克隆到可控表达载体上,其蛋白质产物在诱导后通过全细胞裂解物的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳进行可视化。在该诱导过程中,通过定量DNA×DNA杂交分析了共存在的RSF1010复制子pKT210的复制情况。与仅过量表达RepA蛋白的细胞相比,RepA和RepC蛋白同时过量表达时,pKT210复制的起始受到6倍的刺激。RepB蛋白合成增强导致pKT210复制受到1.6倍的刺激,而单独过量表达RepA蛋白则没有影响。已证明纯化的RepC蛋白优先结合携带RSF1010复制起点的DNA。在该片段内,它特异性结合那些含有起点区域20个碱基对直接重复序列的DNA片段。这些结果表明,RepC蛋白作为一种正向复制调节因子,其浓度是限速的,并且RSF1010的复制速率至少部分在RepC合成水平受到控制。