Garwood J, Kohiyama M
Biochemical Genetics Group, Institut Jacques Monod, Université Paris, France.
J Biol Chem. 1996 Mar 29;271(13):7404-11. doi: 10.1074/jbc.271.13.7404.
Using hemimethylated, fully methylated, and unmethylated oligonucleotide probes corresponding to part of the origin of Escherichia coli DNA replication, oriC (+81-136), we have characterized a novel hemimethylated DNA-specific protein binding activity. This activity appears to be located in the cytoplasm rather than in membrane fractions. It has been partially purified and, in DNase footprinting analysis, found to preferentially protect only a subset of the hemimethylated GATC sites present in the minimal oriC. These sites are found adjacent to the DnaA binding box, R1, and overlap the integration host factor binding site. The activity does not correspond to known hemimethylated binding proteins, although in the seqA deletion mutant, there is a 3-fold reduction of the activity. The stage of the cell cycle in synchronized PC2 cultures does not seem to significantly affect thte relative levels of this binding activity. A possible role in sequestration of the newly replicated hemimethylated origin is discussed.
我们使用与大肠杆菌DNA复制起点oriC(+81 - 136)部分序列对应的半甲基化、全甲基化和未甲基化的寡核苷酸探针,鉴定出一种新型的半甲基化DNA特异性蛋白结合活性。这种活性似乎位于细胞质中,而非膜组分中。它已得到部分纯化,并且在DNA酶足迹分析中发现,它仅优先保护最小oriC中存在的半甲基化GATC位点的一个子集。这些位点位于DnaA结合框R1附近,并与整合宿主因子结合位点重叠。尽管在seqA缺失突变体中该活性降低了3倍,但该活性并不对应于已知的半甲基化结合蛋白。同步化PC2培养物中的细胞周期阶段似乎并未显著影响这种结合活性的相对水平。文中讨论了其在隔离新复制的半甲基化起点方面可能发挥的作用。