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柄杆菌染色体复制起点的比较分析。

Comparative analysis of Caulobacter chromosome replication origins.

作者信息

Shaheen S M, Ouimet Marie-Claude, Marczynski Gregory T

机构信息

McGill University, Department of Microbiology and Immunology, 3775 University Street, Room 506, Montreal, QC H3A 2B4, Canada.

出版信息

Microbiology (Reading). 2009 Apr;155(Pt 4):1215-1225. doi: 10.1099/mic.0.025528-0.

Abstract

Caulobacter crescentus (CB15) initiates chromosome replication only in stalked cells and not in swarmers. To better understand this dimorphic control of chromosome replication, we isolated replication origins (oris) from freshwater Caulobacter (FWC) and marine Caulobacter (MCS) species. Previous studies implicated integration host factor (IHF) and CcrM DNA methylation sites in replication control. However, ori IHF and CcrM sites identified in the model FWC CB15 were only conserved among closely related FWCs. DnaA boxes and CtrA binding sites are established CB15 ori components. CtrA is a two-component regulator that blocks chromosome replication selectively in CB15 swarmers. DnaA boxes and CtrA sites were found in five FWC and three MCS oris. Usually, a DnaA box and a CtrA site were paired, suggesting that CtrA binding regulates DnaA activity. We tested this hypothesis by site-directed mutagenesis of an MCS10 ori which contains only one CtrA binding site overlapping a critical DnaA box. This overlapping site is unique in the whole MCS10 genome. Selective DnaA box mutations decreased replication, while selective CtrA binding site mutations increased replication of MCS10 ori plasmids. Therefore, both FWC and MCS oris use CtrA to repress replication. Despite this similarity, phylogenetic analysis unexpectedly shows that CtrA usage evolved separately among these Caulobacter oris. We discuss consensus oris and convergent ori evolution in differentiating bacteria.

摘要

新月柄杆菌(CB15)仅在柄细胞中启动染色体复制,而在游动细胞中则不会。为了更好地理解这种对染色体复制的二态性控制,我们从淡水柄杆菌(FWC)和海洋柄杆菌(MCS)物种中分离出了复制起点(ori)。先前的研究表明整合宿主因子(IHF)和CcrM DNA甲基化位点参与复制控制。然而,在模式FWC CB15中鉴定出的ori IHF和CcrM位点仅在密切相关的FWC中保守。DnaA框和CtrA结合位点是已确定的CB15 ori组件。CtrA是一种双组分调节因子,可在CB15游动细胞中选择性地阻断染色体复制。在五个FWC和三个MCS ori中发现了DnaA框和CtrA位点。通常,一个DnaA框和一个CtrA位点配对,这表明CtrA结合调节DnaA活性。我们通过对仅包含一个与关键DnaA框重叠的CtrA结合位点的MCS10 ori进行定点诱变来验证这一假设。这个重叠位点在整个MCS10基因组中是独一无二的。选择性DnaA框突变会降低复制,而选择性CtrA结合位点突变会增加MCS10 ori质粒的复制。因此,FWC和MCS ori都利用CtrA来抑制复制。尽管有这种相似性,但系统发育分析意外地表明,CtrA的使用在这些柄杆菌ori中是独立进化的。我们讨论了区分细菌中的共有ori和趋同ori进化。

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