Arrest of cell division and nucleoid partition by genetic alterations in the sliding clamp of the replicase and in DnaA

被引:17
作者
Kawakami, H
Iwura, T
Takata, M
Sekimizu, K
Hiraga, S
Katayama, T
机构
[1] Kyushu Univ, Grad Sch Pharmaceut Sci, Dept Mol Microbiol, Higashi Ku, Fukuoka 8128582, Japan
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Dev Biochem, Bunkyo Ku, Tokyo 1130033, Japan
[3] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Mol Cell Biol, Kumamoto 8620976, Japan
基金
日本学术振兴会;
关键词
cell cycle; DnaA; FtsZ; nucleoid; sliding clamp;
D O I
10.1007/s004380100546
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In Escherichia coli, an interaction between the replication initiator DnaA and the sliding clamp protein, the beta subunit (DnaN) of DNA polymerase III, is required to regulate the chromosomal replication cycle. We report here that colony formation by, and cell division of, the temperature (42 degreesC)-sensitive dnaN59 mutant are inhibited at 34-35 degreesC when DnaA is moderately (4-to 8-fold) overexpressed, although chromosomal replication and the beta subunit-dependent regulation of DnaA activity are not significantly inhibited. Immunoblotting analysis revealed that the beta subunit is abundant (present at a level of about 5000 dimers per cell) at 34 degreesC, and its concentration per unit cell volume was practically unaffected in the dnaN59 mutant by the overexpression of DnaA. The dnaN mutant cells that overexpress DnaA become filamentous at 34 degreesC via an sfiA-independent pathway, different from that activated by the SOS response. This filamentation is accompanied by inhibition of nucleoid partition and FtsZ ring formation. In the dnaN59 mutant, oversupply of DnaA may disturb the coordinated action of cell cycle-regulating molecules, thus leading to the inhibition of these events.
引用
收藏
页码:167 / 179
页数:13
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