Kinetics of Paused Ribosome Recycling in Escherichia coli

The bacterial tmRNA-SmpB system recycles stalled translation complexes in a process termed 'ribosome rescue.' tmRNA-SmpB specifically recognizes ribosomes that are paused at or near the 3' end of truncated mRNA; therefore, nucleolytic mRNA processing is required before paused ribosomes can be rescued from full-length transcripts. Here, we examine the recycling of ribosomes paused on both full-length and truncated mRNAs. Peptidyl-tRNAs corresponding to each paused translation complex were identified, and their turnover kinetics was used to estimate the half-lives of paused ribosomes in vivo. Ribosomes were paused at stop codons on full-length mRNA using a nascent peptide motif that interferes with translation termination and elicits tmRNA-SmpB activity. Peptidyl-tRNA turnover from these termination-paused ribosomes was slightly more rapid in tmRNA(+) cells (T-1/2=22 +/- 2.2 s) than in Delta tmRNA cells (T-1/2=32 +/- 1.6 s). Overexpression of release factor (RF) 1 greatly accelerated peptidyl-tRNA turnover from termination-paused ribosomes in both tmRNA(+) and Delta tmLRNA cells, whereas other termination factors had little or no effect on recycling. In contrast to inefficient translation termination, ribosome recycling from truncated transcripts lacking in-frame stop codons was dramatically accelerated by tmRNA-SmpB. However, peptidyl-tRNA still turned over from nonstop-paused ribosomes at a significant rate (t(1/2)=61 +/- 7.3 s) in Delta tmRNA cells. Overexpression of RF-1, RF-3, and ribosome recycling factor in Delta tmRNA cells failed to accelerate ribosome recycling from nonstop mRNA. These results indicate that tmRNA-SmpB activity is rate limited by mRNA cleavage, and that RF-3 and ribosome recycling factor do not constitute a tmRNA-independent rescue pathway, as previously suggested. Peptidyl-tRNA turnover from nonstop-paused ribosomes in Delta tmRNA cells suggests the existence of another uncharacterized ribosome rescue pathway. (C) 2009 Elsevier Ltd. All rights reserved.