Are minichromosomes valid model systems for DNA replication control?: Lessons learned from Escherichia coli

被引:16
作者
Asai, T
Bates, DB
Boye, E [1 ]
Kogoma, T
机构
[1] Univ New Mexico, Ctr Hlth Sci, Dept Cell Biol, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Ctr Hlth Sci, Dept Biol, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Ctr Hlth Sci, Ctr Canc, Albuquerque, NM 87131 USA
[4] Inst Canc Res, Dept Cell Biol, N-0310 Oslo, Norway
关键词
D O I
10.1046/j.1365-2958.1998.00901.x
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
Initiation of chromosome replication is a key event in the life cycle of any organism. Little is known, however, about the regulatory mechanisms of this vital process. Conventionally, the initiation mechanism of chromosome replication in microorganisms has been studied using plasmids in which an origin of chromosome replication has been cloned, rather than using the chromosome itself. The reason for this is that even bacterial chromosomes are so large that biochemical and genetic manipulations become difficult and cumbersome, Recently, the combination of flow cytometry and genetic methods, in which modifications of the replication origin are systematically introduced onto the chromosome, has made possible detailed studies of the molecular events involved in the control of replication initiation in Escherichia coli, The results indicate that requirements for initiation at the chromosomal origin, oriC, are drastically different from those for initiation at cloned oriC.
引用
收藏
页码:671 / 675
页数:5
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