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Circular code motifs in the ribosome: a missing link in the evolution of translation?
The origin of the genetic code remains enigmatic five decades after it was elucidated, although there is growing evidence that the code coevolved progressively with the ribosome. A number of primordial codes were proposed as ancestors of the modern genetic code, including comma-free codes such as th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859856/ https://www.ncbi.nlm.nih.gov/pubmed/31506380 http://dx.doi.org/10.1261/rna.072074.119 |
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author | Dila, Gopal Ripp, Raymond Mayer, Claudine Poch, Olivier Michel, Christian J. Thompson, Julie D. |
author_facet | Dila, Gopal Ripp, Raymond Mayer, Claudine Poch, Olivier Michel, Christian J. Thompson, Julie D. |
author_sort | Dila, Gopal |
collection | PubMed |
description | The origin of the genetic code remains enigmatic five decades after it was elucidated, although there is growing evidence that the code coevolved progressively with the ribosome. A number of primordial codes were proposed as ancestors of the modern genetic code, including comma-free codes such as the RRY, RNY, or GNC codes (R = G or A, Y = C or T, N = any nucleotide), and the X circular code, an error-correcting code that also allows identification and maintenance of the reading frame. It was demonstrated previously that motifs of the X circular code are significantly enriched in the protein-coding genes of most organisms, from bacteria to eukaryotes. Here, we show that imprints of this code also exist in the ribosomal RNA (rRNA). In a large-scale study involving 133 organisms representative of the three domains of life, we identified 32 universal X motifs that are conserved in the rRNA of >90% of the organisms. Intriguingly, most of the universal X motifs are located in rRNA regions involved in important ribosome functions, notably in the peptidyl transferase center and the decoding center that form the original “proto-ribosome.” Building on the existing accretion models for ribosome evolution, we propose that error-correcting circular codes represented an important step in the emergence of the modern genetic code. Thus, circular codes would have allowed the simultaneous coding of amino acids and synchronization of the reading frame in primitive translation systems, prior to the emergence of more sophisticated start codon recognition and translation initiation mechanisms. |
format | Online Article Text |
id | pubmed-6859856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68598562020-12-01 Circular code motifs in the ribosome: a missing link in the evolution of translation? Dila, Gopal Ripp, Raymond Mayer, Claudine Poch, Olivier Michel, Christian J. Thompson, Julie D. RNA Article The origin of the genetic code remains enigmatic five decades after it was elucidated, although there is growing evidence that the code coevolved progressively with the ribosome. A number of primordial codes were proposed as ancestors of the modern genetic code, including comma-free codes such as the RRY, RNY, or GNC codes (R = G or A, Y = C or T, N = any nucleotide), and the X circular code, an error-correcting code that also allows identification and maintenance of the reading frame. It was demonstrated previously that motifs of the X circular code are significantly enriched in the protein-coding genes of most organisms, from bacteria to eukaryotes. Here, we show that imprints of this code also exist in the ribosomal RNA (rRNA). In a large-scale study involving 133 organisms representative of the three domains of life, we identified 32 universal X motifs that are conserved in the rRNA of >90% of the organisms. Intriguingly, most of the universal X motifs are located in rRNA regions involved in important ribosome functions, notably in the peptidyl transferase center and the decoding center that form the original “proto-ribosome.” Building on the existing accretion models for ribosome evolution, we propose that error-correcting circular codes represented an important step in the emergence of the modern genetic code. Thus, circular codes would have allowed the simultaneous coding of amino acids and synchronization of the reading frame in primitive translation systems, prior to the emergence of more sophisticated start codon recognition and translation initiation mechanisms. Cold Spring Harbor Laboratory Press 2019-12 /pmc/articles/PMC6859856/ /pubmed/31506380 http://dx.doi.org/10.1261/rna.072074.119 Text en © 2019 Dila et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Article Dila, Gopal Ripp, Raymond Mayer, Claudine Poch, Olivier Michel, Christian J. Thompson, Julie D. Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title | Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title_full | Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title_fullStr | Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title_full_unstemmed | Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title_short | Circular code motifs in the ribosome: a missing link in the evolution of translation? |
title_sort | circular code motifs in the ribosome: a missing link in the evolution of translation? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859856/ https://www.ncbi.nlm.nih.gov/pubmed/31506380 http://dx.doi.org/10.1261/rna.072074.119 |
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