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Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness

There is now considerable evidence supporting the view that codon usage is frequently under selection for translational accuracy. There are, however, multiple forms of inaccuracy (missense, premature termination, and frameshifting errors) and pinpointing a particular error process behind apparently...

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Autores principales: Warnecke, Tobias, Huang, Yang, Przytycka, Teresa M., Hurst, Laurence D.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941156/
https://www.ncbi.nlm.nih.gov/pubmed/20688751
http://dx.doi.org/10.1093/gbe/evq049
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author Warnecke, Tobias
Huang, Yang
Przytycka, Teresa M.
Hurst, Laurence D.
author_facet Warnecke, Tobias
Huang, Yang
Przytycka, Teresa M.
Hurst, Laurence D.
author_sort Warnecke, Tobias
collection PubMed
description There is now considerable evidence supporting the view that codon usage is frequently under selection for translational accuracy. There are, however, multiple forms of inaccuracy (missense, premature termination, and frameshifting errors) and pinpointing a particular error process behind apparently adaptive mRNA anatomy is rarely straightforward. Understanding differences in the fitness costs associated with different types of translational error can help us devise critical tests that can implicate one error process to the exclusion of others. To this end, we present a model that captures distinct features of frameshifting cost and apply this to 641 prokaryotic genomes. We demonstrate that, although it is commonly assumed that the ribosome encounters an off-frame stop codon soon after the frameshift and costs of mis-elongation are therefore limited, genomes with high GC content typically incur much larger per-error costs. We go on to derive the prediction, unique to frameshifting errors, that differences in translational robustness between the 5′ and 3′ ends of genes should be less pronounced in genomes with higher GC content. This prediction we show to be correct. Surprisingly, this does not mean that GC-rich organisms necessarily carry a greater fitness burden as a consequence of accidental frameshifting. Indeed, increased per-error costs are often more than counterbalanced by lower predicted error rates owing to more diverse anticodon repertoires in GC-rich genomes. We therefore propose that selection on tRNA repertoires may operate to reduce frameshifting errors.
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spelling pubmed-29411562010-09-17 Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness Warnecke, Tobias Huang, Yang Przytycka, Teresa M. Hurst, Laurence D. Genome Biol Evol Research Articles There is now considerable evidence supporting the view that codon usage is frequently under selection for translational accuracy. There are, however, multiple forms of inaccuracy (missense, premature termination, and frameshifting errors) and pinpointing a particular error process behind apparently adaptive mRNA anatomy is rarely straightforward. Understanding differences in the fitness costs associated with different types of translational error can help us devise critical tests that can implicate one error process to the exclusion of others. To this end, we present a model that captures distinct features of frameshifting cost and apply this to 641 prokaryotic genomes. We demonstrate that, although it is commonly assumed that the ribosome encounters an off-frame stop codon soon after the frameshift and costs of mis-elongation are therefore limited, genomes with high GC content typically incur much larger per-error costs. We go on to derive the prediction, unique to frameshifting errors, that differences in translational robustness between the 5′ and 3′ ends of genes should be less pronounced in genomes with higher GC content. This prediction we show to be correct. Surprisingly, this does not mean that GC-rich organisms necessarily carry a greater fitness burden as a consequence of accidental frameshifting. Indeed, increased per-error costs are often more than counterbalanced by lower predicted error rates owing to more diverse anticodon repertoires in GC-rich genomes. We therefore propose that selection on tRNA repertoires may operate to reduce frameshifting errors. Oxford University Press 2010 2010-08-05 /pmc/articles/PMC2941156/ /pubmed/20688751 http://dx.doi.org/10.1093/gbe/evq049 Text en © The Author(s) 2010. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Warnecke, Tobias
Huang, Yang
Przytycka, Teresa M.
Hurst, Laurence D.
Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title_full Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title_fullStr Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title_full_unstemmed Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title_short Unique Cost Dynamics Elucidate the Role of Frameshifting Errors in Promoting Translational Robustness
title_sort unique cost dynamics elucidate the role of frameshifting errors in promoting translational robustness
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941156/
https://www.ncbi.nlm.nih.gov/pubmed/20688751
http://dx.doi.org/10.1093/gbe/evq049
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