Devaraj Aishwarya, Shoji Shinichiro, Holbrook Eric D, Fredrick Kurt
Ohio State Biochemistry Program, The Ohio State University, Columbus, 43210, USA.
RNA. 2009 Feb;15(2):255-65. doi: 10.1261/rna.1320109. Epub 2008 Dec 17.
The exit (E) site has been implicated in several ribosomal activities, including translocation, decoding, and maintenance of the translational reading frame. Here, we target the 30S subunit E site by introducing a deletion in rpsG that truncates the beta-hairpin of ribosomal protein S7. This mutation (S7DeltaR77-Y84) increases both -1 and +1 frameshifting but does not increase miscoding, providing evidence that the 30S E site plays a specific role in frame maintenance. Mutation S7DeltaR77-Y84 also stimulates +1 programmed frameshifting during prfB'-lacZ translation in many synthetic contexts. However, no effect is seen when the E codon of the frameshift site corresponds to those found in nature, suggesting that E-tRNA release does not normally limit the rate of prfB frameshifting. Ribosomes containing S7DeltaR77-Y84 exhibit an elevated rate of spontaneous reverse translocation and an increased K (1/2) for E-tRNA. These effects are of similar magnitude, suggesting that both result from destabilization of E-tRNA. Finally, this mutation of the 30S E site does not inhibit EF-G-dependent translocation, consistent with a primary role for the 50S E site in the mechanism.
核糖体E位点与多种核糖体活动有关,包括转位、解码以及维持翻译阅读框。在此,我们通过在rpsG基因中引入缺失来靶向30S亚基的E位点,该缺失会截断核糖体蛋白S7的β-发夹结构。此突变(S7DeltaR77-Y84)增加了-1和+1移码,但并未增加错义编码,这表明30S E位点在阅读框维持中发挥着特定作用。在许多合成环境中,突变S7DeltaR77-Y84在prfB'-lacZ翻译过程中也会刺激+1程序性移码。然而,当移码位点的E密码子与天然存在的密码子相同时,未观察到任何影响,这表明E-tRNA的释放通常不会限制prfB移码的速率。含有S7DeltaR77-Y84的核糖体表现出自发反向转位的速率升高以及E-tRNA的K(1/2)增加。这些效应的幅度相似,表明两者均源于E-tRNA的不稳定。最后,30S E位点的这种突变并不抑制EF-G依赖的转位,这与50S E位点在该机制中的主要作用一致。