Department of Biology, University of Copenhagen, DK-2200 Copenhagen, Denmark; email:
Annu Rev Genet. 2018 Nov 23;52:321-348. doi: 10.1146/annurev-genet-120215-035130.
Protein synthesis consumes a large fraction of available resources in the cell. When bacteria encounter unfavorable conditions and cease to grow, specialized mechanisms are in place to ensure the overall reduction of costly protein synthesis while maintaining a basal level of translation. A number of ribosome-associated factors are involved in this regulation; some confer an inactive, hibernating state of the ribosome in the form of 70S monomers (RaiA; this and the following are based on Escherichia coli nomenclature) or 100S dimers (RMF and HPF homologs), and others inhibit translation at different stages in the translation cycle (RsfS, YqjD and paralogs, SRA, and EttA). Stationary phase cells therefore exhibit a complex array of different ribosome subpopulations that adjusts the translational capacity of the cell to the encountered conditions and ensures efficient reactivation of translation when conditions improve. Here, we review the current state of research regarding stationary phase-specific translation factors, in particular ribosome hibernation factors and other forms of translational regulation in response to stress conditions.
蛋白质合成在细胞中消耗大量可用资源。当细菌遇到不利条件并停止生长时,会有专门的机制确保全面减少昂贵的蛋白质合成,同时保持基本的翻译水平。许多与核糖体相关的因素参与了这种调节;有些因素以 70S 单体(RaiA;这和下面的内容基于大肠杆菌命名法)或 100S 二聚体(RMF 和 HPF 同源物)的形式赋予核糖体休眠的非活性状态,而其他因素则在翻译周期的不同阶段抑制翻译(RsfS、YqjD 和其等位基因、SRA 和 EttA)。因此,静止期细胞表现出一系列复杂的不同核糖体亚群,这些亚群根据所遇到的条件调整细胞的翻译能力,并确保在条件改善时有效地重新激活翻译。在这里,我们综述了关于特定于静止期的翻译因子的最新研究进展,特别是核糖体休眠因子和其他形式的应激条件下的翻译调控。