Gene Center, Department of Biochemistry and Center for Integrated Protein Science Munich (CiPSM), Feodor-Lynenstr. 25, 81377 München, Germany.
Gene Center, Department of Biochemistry and Center for Integrated Protein Science Munich (CiPSM), Feodor-Lynenstr. 25, 81377 München, Germany; Institute for Biochemistry and Molecular Biology, University of Hamburg, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany.
Trends Biochem Sci. 2017 Aug;42(8):669-680. doi: 10.1016/j.tibs.2017.05.009. Epub 2017 Jun 16.
Ribosomes that translate mRNAs lacking stop codons become stalled at the 3' end of the mRNA. Recycling of these stalled ribosomes is essential for cell viability. In bacteria three ribosome rescue systems have been identified so far, with the most ubiquitous and best characterized being the trans-translation system mediated by transfer-messenger RNA (tmRNA) and small protein B (SmpB). The two additional rescue systems present in some bacteria employ alternative rescue factor (Arf) A and release factor (RF) 2 or ArfB. Recent structures have revealed how ArfA mediates ribosome rescue by recruiting the canonical termination factor RF2 to ribosomes stalled on truncated mRNAs. This now provides us with the opportunity to compare and contrast the available structures of all three bacterial ribosome rescue systems.
核糖体翻译缺乏终止密码子的 mRNA 时会在 mRNA 的 3' 端停滞。这些停滞核糖体的循环回收对于细胞活力至关重要。到目前为止,已经在细菌中鉴定出三种核糖体救援系统,其中最普遍和特征最明显的是由转移信使 RNA(tmRNA)和小蛋白 B(SmpB)介导的转译转译系统。在一些细菌中存在的另外两种救援系统则使用替代救援因子(Arf)A 和释放因子(RF)2 或 ArfB。最近的结构揭示了 ArfA 如何通过招募典型的终止因子 RF2 到在截短的 mRNA 上停滞的核糖体上来介导核糖体救援。这为我们提供了比较和对比所有三种细菌核糖体救援系统的现有结构的机会。