Helmstetter C E, Leonard A C
Department of Experimental Biology, Roswell Park Memorial Institute, Buffalo, NY 14263.
J Mol Biol. 1987 Sep 20;197(2):195-204. doi: 10.1016/0022-2836(87)90118-5.
A mechanism for the segregation of chromosomes and minichromosomes into daughter cells during division of Escherichia coli is presented. It is based on the idea that the cell envelope contains a large number of sites capable of binding to the chromosomal replication origin, oriC, and that a polymerizing DNA strand becomes attached to one of the sites at initiation of a round of replication. The attachment sites are distributed throughout the actively growing cell envelope, i.e. lateral envelope and septum, but not in the existing cell poles. This asymmetric distribution of oriC attachment sites accounts for the experimentally observed non-random chromosome and minichromosome segregation, and for the variation in the degree of non-random segregation with cell strain and growth rate. The multi-site attachment concept also accounts for the unstable maintenance of minichromosomes.
本文提出了一种在大肠杆菌分裂过程中染色体和微型染色体向子细胞分离的机制。该机制基于这样一种观点,即细胞膜含有大量能够与染色体复制起点oriC结合的位点,并且在一轮复制起始时,聚合的DNA链会附着到其中一个位点上。附着位点分布在整个活跃生长的细胞膜上,即侧膜和隔膜,但不存在于现有的细胞极中。oriC附着位点的这种不对称分布解释了实验观察到的非随机染色体和微型染色体分离现象,以及非随机分离程度随细胞菌株和生长速率的变化。多位点附着概念也解释了微型染色体的不稳定维持。