tRNA slippage at the tmRNA resume codon
Author(s) -
Michael J. Trimble,
AMY MINNICUS,
Kelly P. Williams
Publication year - 2004
Publication title -
rna
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.037
H-Index - 171
eISSN - 1469-9001
pISSN - 1355-8382
DOI - 10.1261/rna.7010904
Subject(s) - biology , transfer rna , codon usage bias , computational biology , genetics , rna , genome , gene
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
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