Skarstad Kirsten, Løbner-Olesen Anders
Department of Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, 0310 Oslo, Norway.
EMBO J. 2003 Jan 2;22(1):140-50. doi: 10.1093/emboj/cdg003.
DNA replication in most organisms is regulated such that all chromosomes are replicated once, and only once, per cell cycle. In rapidly growing Escherichia coli, replication of eight identical chromosomes is initiated essentially simultanously, each from the same origin, oriC. Plasmid-borne oriC sequences (minichromosomes) are also initiated in synchrony with the eight chromosomal origins. We demonstrate that specific inactivation of newly formed, hemimethylated origins (sequestration) was required for the stable co-existence of oriC-dependent replicons. Cells in which initiations were not confined to a short interval in the cell cycle (carrying mutations in sequestration or initiation genes or expressing excess initiator protein) could not support stable co-existence of several oriC-dependent replicons. The results show that such stable co-existence of oriC-dependent replicons is dependent on both a period of sequestration that is longer than the initiation interval and a reduction of the initiation potential during the sequestration period. These regulatory requirements are the same as those required to confine initiation of each replicon to once, and only once, per cell cycle.
大多数生物体中的DNA复制受到调控,使得每个细胞周期中所有染色体都只复制一次,且仅复制一次。在快速生长的大肠杆菌中,八个相同染色体的复制基本上是同时启动的,每个染色体都从同一个原点oriC开始。携带oriC序列的质粒(微型染色体)也与八个染色体原点同步启动。我们证明,新形成的半甲基化原点的特异性失活(隔离)是oriC依赖性复制子稳定共存所必需的。在细胞周期中起始不局限于短时间间隔的细胞(携带隔离或起始基因突变或表达过量起始蛋白)无法支持多个oriC依赖性复制子的稳定共存。结果表明,oriC依赖性复制子的这种稳定共存既依赖于比起始间隔更长的隔离期,也依赖于隔离期内起始潜能的降低。这些调控要求与将每个复制子的起始限制在每个细胞周期仅一次且仅一次所需的要求相同。