Abstract
The precise mechanism of stop codon recognition in translation termination is still unclear. A previously published study by Ivanov and colleagues proposed a new model for stop codon recognition in which 3-nucleotide Ter-anticodons within the loops of hairpin helices 69 (domain IV) and 89 (domain V) in large ribosomal subunit (LSU) rRNA recognize stop codons to terminate protein translation in eubacteria and certain organelles. We evaluated this model by extensive bioinformatic analysis of stop codons and their putative corresponding Ter-anticodons across a much wider range of species, and found many cases for which it cannot explain the stop codon usage without requiring the involvement of one or more of the eight possible noncomplementary base pairs. Involvement of such base pairs may not be structurally or thermodynamically damaging to the model. However, if, according to the model, Ter-anticodon interaction with stop codons occurs within the ribosomal A-site, the structural stringency which that site imposes on sense codon·tRNA anticodon interaction should also extend to stop codon·Ter-anticodon interactions. Moreover, with Ter-tRNA in place of an aminoacyl-tRNA, for each of the various Ter-anticodons there is a sense codon that can interact with it preferentially by complementary and wobble base-pairing. Both these considerations considerably weaken the arguments put forth previously. Published by Cold Spring Harbor Laboratory Press.
Original language | English (US) |
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Pages (from-to) | 1478-1484 |
Number of pages | 7 |
Journal | RNA |
Volume | 11 |
Issue number | 10 |
DOIs | |
State | Published - Oct 2005 |
Externally published | Yes |
Keywords
- Mitochondrial genetic code
- Putative rRNA anticodons
- Stop codon recognition
- Stop codon usage
- Translation termination
ASJC Scopus subject areas
- Molecular Biology