Chang Dong-Eun, Smalley Darren J, Conway Tyrrell
Advanced Center for Genome Technology, The University of Oklahoma, Norman, OK 73019-0245, USA.
Mol Microbiol. 2002 Jul;45(2):289-306. doi: 10.1046/j.1365-2958.2002.03001.x.
When conditions cause bacterial growth to stop, extensive reprogramming of physiology and gene expression allows for the cell's survival. We used whole-genome DNA arrays to determine the system response in Escherichia coli cells experiencing transient growth arrest caused by glucose-lactose diauxie and H2O2 treatment, and also entry into stationary phase. The results show that growth-arrested cells induce stringent control of several gene systems. The vast majority of genes encoding the transcription and translation apparatus immediately downregulate, followed by a global return to steady state when growth resumes. Approximately one-half of the amino acid biosynthesis genes downregulate during growth arrest, with the notable exception of the his operon, which transiently upregulates in the diauxie experiment. Nucleotide biosynthesis downregulates, a result that is again consistent with the stringent response. Likewise, aerobic metabolism downregulates during growth arrest, and the results led us to suggest a model for stringent control of the ArcA regulon. The stationary phase stress response fully induces during growth arrest, whether transient or permanent, in a manner consistent with known mechanisms related to stringent control. Cells similarly induce the addiction module anti-toxin and toxin genes during growth arrest; the latter are known to inhibit translation and DNA replication. The results indicate that in all aspects of the response cells do not distinguish between transient and potentially permanent growth arrest (stationary phase). We introduce an expanded model for the stringent response that integrates induction of stationary phase survival genes and inhibition of transcription, translation and DNA replication. Central to the model is the reprogramming of transcription by guanosine tetraphosphate (ppGpp), which provides for the cell's rapid response to growth arrest and, by virtue of its brief half-life, the ability to quickly resume growth as changing conditions allow.
当环境条件导致细菌生长停止时,生理和基因表达的广泛重编程有助于细胞存活。我们使用全基因组DNA阵列来确定大肠杆菌细胞在经历由葡萄糖-乳糖双相生长和H2O2处理导致的短暂生长停滞以及进入稳定期时的系统反应。结果表明,生长停滞的细胞会诱导对多个基因系统的严格调控。绝大多数编码转录和翻译装置的基因会立即下调,随后在生长恢复时整体恢复到稳态。大约一半的氨基酸生物合成基因在生长停滞期间下调,但组氨酸操纵子是个显著例外,它在双相生长实验中短暂上调。核苷酸生物合成下调,这一结果再次与严格反应一致。同样,有氧代谢在生长停滞期间下调,这些结果使我们提出了一个关于ArcA调控子严格控制的模型。无论生长停滞是短暂的还是永久的(稳定期),稳定期应激反应都会以与已知严格控制机制一致的方式完全诱导。细胞在生长停滞期间同样会诱导成瘾模块的抗毒素和毒素基因;后者已知会抑制翻译和DNA复制。结果表明,在反应的各个方面,细胞无法区分短暂的和潜在的永久生长停滞(稳定期)。我们引入了一个扩展的严格反应模型,该模型整合了稳定期存活基因的诱导以及转录、翻译和DNA复制的抑制。该模型的核心是鸟苷四磷酸(ppGpp)对转录的重编程,它使细胞能够对生长停滞做出快速反应,并且由于其短暂的半衰期,能够在条件变化允许时迅速恢复生长。