ArticleRNA (New York, N.Y.)2001
A mechanism for stop codon recognition by the ribosome: a bioinformatic approach.
Article in RNA (New York, N.Y.), 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
11 citing papers in PubMed, 23 citations in OpenAlex.
- Precision therapeutic tRNA rescue of nonsense mutation R166X inJournal of precision medicine (Amsterdam, Netherlands) · 2025Article
- Development of mammalian cell logic gates controlled by unnatural amino acids.Cell reports methods · 2021Article
- Termination of protein synthesis in mammalian mitochondria.The Journal of biological chemistry · 2011Review
- Structural aspects of translation termination on the ribosome.RNA (New York, N.Y.) · 2011Review
- The enigmatic mitochondrial genome of Rhabdopleura compacta (Pterobranchia) reveals insights into selection of an efficient tRNA system and supports monophyly of Ambulacraria.BMC evolutionary biology · 2011Article
- Recoding of translation in turtle mitochondrial genomes: programmed frameshift mutations and evidence of a modified genetic code.Journal of molecular evolution · 2008Article
- Parallel evolution of the genetic code in arthropod mitochondrial genomes.PLoS biology · 2006Article
- Are stop codons recognized by base triplets in the large ribosomal RNA subunit?RNA (New York, N.Y.) · 2005Article
- Invariant amino acids essential for decoding function of polypeptide release factor eRF1.Nucleic acids research · 2005Article
- Comparative study of translation termination sites and release factors (RF1 and RF2) in procaryotes.Journal of molecular evolution · 2003Article
- Termination of translation: interplay of mRNA, rRNAs and release factors?The EMBO journal · 2003Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
Protein synthesis in ribosomes requires two kinds of tRNAs: initiation and elongation. The former initiates the process (formylmethionine tRNA in prokaryotes and special methionine tRNA in eukaryotes). The latter participates in the synthesis proper, recognizing the sense codons. Synthesis is also assisted by special proteins: initiation, elongation, and termination factors. The termination factors are necessary to recognize stop codons (UAG, UGA, and UAA) and to release the complete protein chain from the elongation tRNA preceding a stop codon. No termination tRNA capable of recognizing stop codons by their anticodons is known. The termination factors are thought to do this. In the large ribosomal RNA, we found two sites that, like tRNAs, contain the anticodon hairpin but with triplets complementary to stop codons. One site is hairpin 69 from domain IV; the other site is hairpin 89, domain V. By analogy, we call them termination tRNAs: Ter-tRNA1 and Ter-tRNA2, respectively, even though they transport no amino acids, and suggest that they directly pair to stop codons. The termination factors only aid in this recognition, making it specific and reliable. A strong argument in favor of our hypothesis comes from vertebrate mitochondria. They are known to acquire two new stop codons, AGA and AGG. In the standard code, these are two out of six arginine codons. We revealed that the corresponding anticodons, UCU and CCU, have evolved in Ter-tRNA1 of these mitochondria.
Indexed as
Identifiers
11780625PMC1370208W2169847663What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.