Author:
TRIMBLE MICHAEL J.,MINNICUS AMY,WILLIAMS KELLY P.
Abstract
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; translation
Publisher
Cold Spring Harbor Laboratory
Cited by
17 articles.
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