| Literature DB >> 15100436 |
Michael J Trimble1, Amy Minnicus, Kelly P Williams.
Abstract
UNLABELLED: The bacterial ribosome does not initiate translation on the mRNA portion of tmRNA; instead translation that had begun on a separate mRNA molecule resumes at a particular triplet on tmRNA (the resume codon). For at least two tRNAs that could pair with both the resume and -2 triplets on mutant tmRNAs, UAA (stop) as the second codon induced high-frequency -2 slippage on the resume codon in the P site. The frameshift product was not detected when the -2 base was altered. Deficiency for ribosomal L9 protein, which affects other cases of frameshifting, had no significant effect. A special feature of this frameshifting is its dependence on a particular context, that of the tmRNA resume codon; it failed on the same sequence in a regular mRNA, and, more strikingly, at the second tmRNA codon. This focuses attention on the peculiar features expected of the slippage-prone state, such as unusual E-site filling, that might make the P-site resume codon:anticodon interaction especially unstable. KEYWORDS: tmRNA; ribosome; frameshift; E site; translationMesh:
Substances:
Year: 2004 PMID: 15100436 PMCID: PMC1370571 DOI: 10.1261/rna.7010904
Source DB: PubMed Journal: RNA ISSN: 1355-8382 Impact factor: 4.942