Shimizu Yoshihiro
Laboratory for Cell-Free Protein Synthesis, Quantitative Biology Center - RIKEN Kobe, Hyogo, Japan.
Front Microbiol. 2014 Apr 10;5:170. doi: 10.3389/fmicb.2014.00170. eCollection 2014.
During protein synthesis in cells, translating ribosomes may encounter abnormal situations that lead to retention of immature peptidyl-tRNA on the ribosome due to failure of suitable termination processes. Bacterial cells handle such situations by employing three systems that rescue the stalled translation machinery. The transfer messenger RNA/small protein B (tmRNA/SmpB) system, also called the trans-translation system, rescues stalled ribosomes by initiating template switching from the incomplete mRNA to the short open reading frame of tmRNA, leading to the production of a protein containing a C-terminal tag that renders it susceptible to proteolysis. The ArfA/RF2 and ArfB systems rescue stalled ribosomes directly by hydrolyzing the immature peptidyl-tRNA remaining on the ribosome. Here, the biochemical aspects of these systems, as clarified by recent studies, are reviewed.
在细胞内蛋白质合成过程中,正在进行翻译的核糖体可能会遇到异常情况,由于合适的终止过程失败,导致未成熟的肽基 - tRNA滞留在核糖体上。细菌细胞通过采用三种系统来处理这种情况,以拯救停滞的翻译机制。转移信使RNA/小蛋白B(tmRNA/SmpB)系统,也称为反式翻译系统,通过启动从不完整的mRNA到tmRNA的短开放阅读框的模板切换来拯救停滞的核糖体,从而产生一种含有C末端标签的蛋白质,使其易于被蛋白酶水解。ArfA/RF2和ArfB系统通过水解核糖体上残留的未成熟肽基 - tRNA直接拯救停滞的核糖体。在此,对这些系统的生化方面进行综述,这些方面已由最近的研究所阐明。