High Transcriptional Error Rates Vary as a Function of Gene Expression Level
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Univ Arizona, Dept Ecol & Evolutionary BiolUniv Arizona, Dept Mol & Cellular Biol
Issue Date
2020-01
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OXFORD UNIV PRESSCitation
Kendra M Meer, Paul G Nelson, Kun Xiong, Joanna Masel, High Transcriptional Error Rates Vary as a Function of Gene Expression Level, Genome Biology and Evolution, Volume 12, Issue 1, January 2020, Pages 3754–3761, https://doi.org/10.1093/gbe/evz275Journal
GENOME BIOLOGY AND EVOLUTIONRights
© The Author(s) 2019. 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 License (http://creativecommons.org/licenses/by/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Errors in gene transcription can be costly, and organisms have evolved to prevent their occurrence or mitigate their costs. The simplest interpretation of the drift barrier hypothesis suggests that species with larger population sizes would have lower transcriptional error rates. However, Escherichia coil seems to have a higher transcriptional error rate than species with lower effective population sizes, for example Saccharomyces cerevisiae. This could be explained if selection in E. coli were strong enough to maintain adaptations that mitigate the consequences of transcriptional errors through robustness, on a gene by gene basis, obviating the need for low transcriptional error rates and associated costs of global proofreading. Here, we note that if selection is powerful enough to evolve local robustness, selection should also be powerful enough to locally reduce error rates. We therefore predict that transcriptional error rates will be lower in highly abundant proteins on which selection is strongest. However, we only expect this result when error rates are high enough to significantly impact fitness. As expected, we find such a relationship between expression and transcriptional error rate for non-C -> U errors in E. coli (especially G -> A), but not in S. cerevisiae. We do not find this pattern for C -> U changes in E. coli, presumably because most deamination events occurred during sample preparation, but do for C -> U changes in S. cerevisiae, supporting the interpretation that C -> U error rates estimated with an improved protocol, and which occur at rates comparable with E. coli non-C -> U errors, are biological.Note
Open access journalISSN
1759-6653EISSN
1759-6653PubMed ID
31841128Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1093/gbe/evz275
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Except where otherwise noted, this item's license is described as © The Author(s) 2019. 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 License (http://creativecommons.org/licenses/by/4.0/).
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