Bach Trond, Skarstad Kirsten
Department of Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital HF, 0310 Oslo, Norway.
J Mol Biol. 2005 Jul 1;350(1):7-11. doi: 10.1016/j.jmb.2005.04.055.
Sequestration of newly replicated origins is one of the mechanisms required to limit initiation of Escherichia coli chromosome replication to once per generation. Origin sequestration lasts for a considerably longer period of time than the sequestration of other newly replicated regions of the chromosome. The reason for this may be the high number of GATC sites present in the origin. Alternatively, other sequence elements in the origin region may be important for its prolonged sequestration. To distinguish between these possibilities we constructed a DNA fragment containing ten GATC sites distributed with the same spacing as the ten GATC sites in the left half of oriC, but with random sequence between the GATC sites, and inserted it at a non-sequestered chromosome location. Sequestration of this GATC-cluster lasted as long as that of oriC, or even longer. The result shows that the presence of ten GATC sites, distributed as in oriC, is sufficient to cause full sequestration, and that other sequence elements most likely do not contribute to sequestration.
将新复制的复制起点隔离是将大肠杆菌染色体复制起始限制为每代一次所需的机制之一。起点隔离持续的时间比染色体其他新复制区域的隔离长得多。其原因可能是起点中存在大量的GATC位点。或者,起点区域中的其他序列元件可能对其延长的隔离很重要。为了区分这些可能性,我们构建了一个DNA片段,其中包含十个GATC位点,其分布间距与oriC左半部分的十个GATC位点相同,但GATC位点之间为随机序列,并将其插入到非隔离的染色体位置。这个GATC簇的隔离持续时间与oriC相同,甚至更长。结果表明,如oriC中那样分布的十个GATC位点的存在足以导致完全隔离,并且其他序列元件很可能对隔离没有贡献。