Department of Developmental Biology, Stanford University School of Medicine, Stanford, California, United States of America.
PLoS One. 2011 Apr 11;6(4):e18179. doi: 10.1371/journal.pone.0018179.
Bacteria adapt to shifts from rapid to slow growth, and have developed strategies for long-term survival during prolonged starvation and stress conditions. We report the regulatory response of C. crescentus to carbon starvation, based on combined high-throughput proteome and transcriptome analyses. Our results identify cell cycle changes in gene expression in response to carbon starvation that involve the prominent role of the FixK FNR/CAP family transcription factor and the CtrA cell cycle regulator. Notably, the SigT ECF sigma factor mediates the carbon starvation-induced degradation of CtrA, while activating a core set of general starvation-stress genes that respond to carbon starvation, osmotic stress, and exposure to heavy metals. Comparison of the response of swarmer cells and stalked cells to carbon starvation revealed four groups of genes that exhibit different expression profiles. Also, cell pole morphogenesis and initiation of chromosome replication normally occurring at the swarmer-to-stalked cell transition are uncoupled in carbon-starved cells.
细菌适应从快速生长到缓慢生长的转变,并已制定出在长期饥饿和压力条件下长期生存的策略。我们根据高通量蛋白质组学和转录组学分析的综合结果,报告了 C. crescentus 对碳饥饿的调控反应。我们的结果确定了细胞周期在基因表达上对碳饥饿的反应,涉及到 FixK FNR/CAP 家族转录因子和 CtrA 细胞周期调节剂的突出作用。值得注意的是,SigT ECF sigma 因子介导 CtrA 的碳饥饿诱导降解,同时激活一组核心的普遍饥饿应激基因,这些基因对碳饥饿、渗透压应激和重金属暴露有响应。对游动细胞和柄细胞对碳饥饿的反应进行比较,揭示了四组表现出不同表达谱的基因。此外,在游动细胞到柄细胞的转变中正常发生的细胞极形态发生和染色体复制的起始在碳饥饿的细胞中被解耦。