Ingmer H, Cohen S N
Department of Genetics, Stanford University School of Medicine, California 94305.
J Bacteriol. 1993 Sep;175(18):6046-8. doi: 10.1128/jb.175.18.6046-6048.1993.
We report here direct evidence that mutations in the par locus affect protein-DNA interactions in vivo at the replication origin of plasmid pSC101. Concomitant with par-mediated plasmid stabilization, two sites in the origin region show an altered methylation pattern as detected by in vivo footprinting with dimethyl sulfate. One site is located near an integration host factor-binding sequence adjacent to the first of three direct repeats known to be involved in the initiation of pSC101 replication; the second site is within the third direct repeat.
我们在此报告直接证据,表明par位点的突变在体内影响质粒pSC101复制起点处的蛋白质-DNA相互作用。与par介导的质粒稳定性相伴的是,通过硫酸二甲酯体内足迹法检测发现,起点区域的两个位点呈现出改变的甲基化模式。一个位点位于与已知参与pSC101复制起始的三个直接重复序列中的第一个相邻的整合宿主因子结合序列附近;第二个位点位于第三个直接重复序列内。