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Genes to Cells (2008) 13, 181-197. doi:10.1111/j.1365-2443.2007.01157.x
© 2008 Blackwell Publishing or its licensors

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Dynamic events of sister chromosomes in the cell cycle of Escherichia coli

Shun Adachi, Toru Fukushimaa and Sota Hiraga*

Department of Radiation Genetics, Graduate School of Medicine, Kyoto University, Konoe-cho, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan

Various events involving partitioning of sister chromosomes were precisely analyzed in asynchronously growing Escherichia coli cells in various conditions. To examine the cohesion between sister chromosomes, we analyzed living cells growing under various conditions for the number of the replication origin (oriC) copies by flow cytometry and the foci of oriC by fluorescence microscopy. The average number of the oriC foci per cell was significantly smaller than the number of oriC copies per cell with few exceptions, suggesting cohesion of oriC sister copies. Cohesion phenomenon of oriC sister copies was also observed in a mukB null mutant cells under some growth conditions. Sister copies of the terminal region (ter) were also found to be cohesive. Immunofluorescence microscopy for nascent DNA pulse-labeled with 5-bromo-2'-deoxyuridine (BrdU) indicated that paired replication forks acting on bidirectional replication were able to migrate toward opposite directions during ongoing replication in poor medium; however, some of them were closely associated in rich media. Analysis of the foci of MukB–GFP indicates that the number of MukB foci was always larger than the number of replication forks. The number of MukB–GFP foci increased together with cell length. The sequence of these chromosomal events in the growing cells has been depicted.


Communicated by: Hiroji Aiba

aPresent address: Laboratory of Developmental Immunology, Graduate School of Frontier Biosciences, Graduate School of Medicine, Osaka University, 2–2 Yamada-oka, Suita, Osaka, 565-0871, Japan.

* Correspondence: E-mail: hiraga{at}rg.med.kyoto-u.ac.jp







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