Translation and Folding Team, Université de Rennes 1, UMR CNRS 6290 IGDR, Campus de Beaulieu 35042 Rennes cedex, France.
Trends Biochem Sci. 2013 Aug;38(8):403-11. doi: 10.1016/j.tibs.2013.06.002. Epub 2013 Jun 30.
In bacteria, the main quality control mechanism for rescuing ribosomes that have arrested during translation is trans-translation, performed by transfer-mRNA (tmRNA) associated with small protein B (SmpB). Intriguingly, this very elegant mechanism is not always necessary to maintain cell viability, suggesting the existence of alternatives. Other rescue systems have recently been discovered, revealing a far more complicated story than expected. These include the alternative ribosome rescue factors ArfA and ArfB, the elongation factors EF4 and EF-P, the peptidyl-tRNA hydrolase Pth, and several protein synthesis factors. These discoveries make it possible to describe a large network of factors dedicated to ribosome rescue, thus ensuring cell survival during stresses that induce ribosome stalling.
在细菌中,拯救在翻译过程中停滞的核糖体的主要质量控制机制是转译,由与小蛋白 B(SmpB)相关的转移-mRNA(tmRNA)完成。有趣的是,这种非常优雅的机制并不总是维持细胞活力所必需的,这表明存在替代机制。最近发现了其他的拯救系统,揭示了一个比预期复杂得多的故事。这些包括替代核糖体拯救因子 ArfA 和 ArfB、延伸因子 EF4 和 EF-P、肽酰-tRNA 水解酶 Pth 和几个蛋白质合成因子。这些发现使得描述一个专门用于核糖体拯救的因子大网络成为可能,从而确保细胞在诱导核糖体停滞的压力下存活。