Lane D, Hill D, Caughey P, Gunn P
J Mol Biol. 1984 Dec 5;180(2):267-82. doi: 10.1016/s0022-2836(84)80004-2.
The sequence of an 897 base-pair fragment (42.1 to 43.0 kilobase co-ordinates on the F genetic map) containing the primary origin (ori-1) of mini-F replication has been determined. It contains one significant open reading frame, which probably codes for part of the C protein thought to be necessary for ori-1 replication activity. Tests of the ability of the sequenced ori-1 region to direct replication of DNA polymerase I-dependent replicons revealed that ori-1 replication requires adjacent mini-F sequences, 43.0 to 43.9 kilobase co-ordinates on the F genetic map in cis as well as a trans-acting gene product, probably the E protein, from the essential replication region of mini-F. In addition, a sequence required for control of pif gene expression has been mapped to a 160 base-pair region immediately upstream from the C (pifC) gene, and the crossover site of a specific recA-independent recombination mechanism has been mapped to a 220 base-pair region on the side of the pif control sequence distal to the C gene.
已确定了一个包含微小F复制的主要起始点(ori - 1)的897个碱基对片段的序列(在F基因图谱上的坐标为42.1至43.0千碱基)。它包含一个重要的开放阅读框,可能编码被认为是ori - 1复制活性所必需的C蛋白的一部分。对测序的ori - 1区域指导依赖DNA聚合酶I的复制子进行复制的能力测试表明,ori - 1复制需要相邻的微小F序列,即在F基因图谱上顺式的43.0至43.9千碱基坐标,以及一个反式作用基因产物,可能是来自微小F必需复制区域的E蛋白。此外,已将控制pif基因表达所需的序列定位到紧接C(pifC)基因上游的一个160个碱基对区域,并且已将一种特定的不依赖recA的重组机制的交叉位点定位到pif控制序列中远离C基因一侧的一个220个碱基对区域。