Reyes-Lamothe Rodrigo, Possoz Christophe, Danilova Olessia, Sherratt David J
Department of Biochemistry, University of Oxford, Oxford OX1 3 QU, UK.
Cell. 2008 Apr 4;133(1):90-102. doi: 10.1016/j.cell.2008.01.044.
A prevalent view of DNA replication has been that it is carried out in fixed "replication factories." By tracking the progression of sister replication forks with respect to genetic loci in live Escherichia coli, we show that at initiation replisomes assemble at replication origins irrespective of where the origins are positioned within the cell. Sister replisomes separate and move to opposite cell halves shortly after initiation, migrating outwards as replication proceeds and both returning to midcell as replication termination approaches. DNA polymerase is maintained at stalled replication forks, and over short intervals of time replisomes are more dynamic than genetic loci. The data are inconsistent with models in which replisomes associated with sister forks act within a fixed replication factory. We conclude that independent replication forks follow the path of the compacted chromosomal DNA, with no structure other than DNA anchoring the replisome to any particular cellular region.
关于DNA复制,一种普遍的观点认为它是在固定的“复制工厂”中进行的。通过追踪活的大肠杆菌中姐妹复制叉相对于基因座的进展情况,我们发现,在起始阶段,复制体在复制起点处组装,而不管起点在细胞内的位置如何。姐妹复制体在起始后不久分离并移动到细胞的相对两半,随着复制的进行向外迁移,并且在复制终止接近时都回到细胞中部。DNA聚合酶维持在停滞的复制叉处,并且在短时间间隔内,复制体比基因座更具动态性。这些数据与姐妹叉相关的复制体在固定复制工厂内起作用的模型不一致。我们得出结论,独立的复制叉沿着压缩的染色体DNA的路径移动,除了DNA之外没有其他结构将复制体锚定到任何特定的细胞区域。
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