Lesley Joseph A, Shapiro Lucy
Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
J Bacteriol. 2008 Oct;190(20):6867-80. doi: 10.1128/JB.00700-08. Epub 2008 Aug 22.
Cell cycle progression and polar differentiation are temporally coordinated in Caulobacter crescentus. This oligotrophic bacterium divides asymmetrically to produce a motile swarmer cell that represses DNA replication and a sessile stalked cell that replicates its DNA. The initiation of DNA replication coincides with the proteolysis of the CtrA replication inhibitor and the accumulation of DnaA, the replication initiator, upon differentiation of the swarmer cell into a stalked cell. We analyzed the adaptive response of C. crescentus swarmer cells to carbon starvation and found that there was a block in both the swarmer-to-stalked cell polar differentiation program and the initiation of DNA replication. SpoT is a bifunctional synthase/hydrolase that controls the steady-state level of the stress-signaling nucleotide (p)ppGpp, and carbon starvation caused a SpoT-dependent increase in (p)ppGpp concentration. Carbon starvation activates DnaA proteolysis (B. Gorbatyuk and G. T. Marczynski, Mol. Microbiol. 55:1233-1245, 2005). We observed that SpoT is required for this phenomenon in swarmer cells, and in the absence of SpoT, carbon-starved swarmer cells inappropriately initiated DNA replication. Since SpoT controls (p)ppGpp abundance, we propose that this nucleotide relays carbon starvation signals to the cellular factors responsible for activating DnaA proteolysis, thereby inhibiting the initiation of DNA replication. SpoT, however, was not required for the carbon starvation block of the swarmer-to-stalked cell polar differentiation program. Thus, swarmer cells utilize at least two independent signaling pathways to relay carbon starvation signals: a SpoT-dependent pathway mediating the inhibition of DNA replication initiation, and a SpoT-independent pathway(s) that blocks morphological differentiation.
新月柄杆菌的细胞周期进程和极性分化在时间上是协调的。这种贫营养细菌进行不对称分裂,产生一个抑制DNA复制的游动细胞和一个复制其DNA的固着柄细胞。DNA复制的起始与CtrA复制抑制剂的蛋白水解以及游动细胞分化为柄细胞时复制起始因子DnaA的积累同时发生。我们分析了新月柄杆菌游动细胞对碳饥饿的适应性反应,发现游动细胞到柄细胞的极性分化程序和DNA复制的起始均受阻。SpoT是一种双功能合成酶/水解酶,可控制应激信号核苷酸(p)ppGpp的稳态水平,碳饥饿导致SpoT依赖的(p)ppGpp浓度增加。碳饥饿激活DnaA蛋白水解(B. Gorbatyuk和G. T. Marczynski,《分子微生物学》55:1233 - 1245,2005)。我们观察到SpoT是游动细胞中这一现象所必需的,在没有SpoT的情况下,碳饥饿的游动细胞会不恰当地起始DNA复制。由于SpoT控制(p)ppGpp的丰度,我们提出这种核苷酸将碳饥饿信号传递给负责激活DnaA蛋白水解的细胞因子,从而抑制DNA复制的起始。然而,SpoT对于游动细胞到柄细胞极性分化程序的碳饥饿阻断并非必需。因此,游动细胞利用至少两条独立的信号通路来传递碳饥饿信号:一条依赖SpoT的通路介导对DNA复制起始的抑制,以及一条不依赖SpoT的通路阻断形态分化。