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Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution

Comparative genomic approaches have been used to identify sites where mutations are under purifying selection and of functional consequence by searching for sequences that are conserved across distantly related species. However, the performance of these approaches has not been rigorously evaluated u...

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Autores principales: Huber, Christian D., Kim, Bernard Y., Lohmueller, Kirk E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286533/
https://www.ncbi.nlm.nih.gov/pubmed/32469868
http://dx.doi.org/10.1371/journal.pgen.1008827
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author Huber, Christian D.
Kim, Bernard Y.
Lohmueller, Kirk E.
author_facet Huber, Christian D.
Kim, Bernard Y.
Lohmueller, Kirk E.
author_sort Huber, Christian D.
collection PubMed
description Comparative genomic approaches have been used to identify sites where mutations are under purifying selection and of functional consequence by searching for sequences that are conserved across distantly related species. However, the performance of these approaches has not been rigorously evaluated under population genetic models. Further, short-lived functional elements may not leave a footprint of sequence conservation across many species. We use simulations to study how one measure of conservation, the Genomic Evolutionary Rate Profiling (GERP) score, relates to the strength of selection (N(e)s). We show that the GERP score is related to the strength of purifying selection. However, changes in selection coefficients or functional elements over time (i.e. functional turnover) can strongly affect the GERP distribution, leading to unexpected relationships between GERP and N(e)s. Further, we show that for functional elements that have a high turnover rate, adding more species to the analysis does not necessarily increase statistical power. Finally, we use the distribution of GERP scores across the human genome to compare models with and without turnover of sites where mutations are under purifying selection. We show that mutations in 4.51% of the noncoding human genome are under purifying selection and that most of this sequence has likely experienced changes in selection coefficients throughout mammalian evolution. Our work reveals limitations to using comparative genomic approaches to identify deleterious mutations. Commonly used GERP score thresholds miss over half of the noncoding sites in the human genome where mutations are under purifying selection.
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spelling pubmed-72865332020-06-15 Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution Huber, Christian D. Kim, Bernard Y. Lohmueller, Kirk E. PLoS Genet Research Article Comparative genomic approaches have been used to identify sites where mutations are under purifying selection and of functional consequence by searching for sequences that are conserved across distantly related species. However, the performance of these approaches has not been rigorously evaluated under population genetic models. Further, short-lived functional elements may not leave a footprint of sequence conservation across many species. We use simulations to study how one measure of conservation, the Genomic Evolutionary Rate Profiling (GERP) score, relates to the strength of selection (N(e)s). We show that the GERP score is related to the strength of purifying selection. However, changes in selection coefficients or functional elements over time (i.e. functional turnover) can strongly affect the GERP distribution, leading to unexpected relationships between GERP and N(e)s. Further, we show that for functional elements that have a high turnover rate, adding more species to the analysis does not necessarily increase statistical power. Finally, we use the distribution of GERP scores across the human genome to compare models with and without turnover of sites where mutations are under purifying selection. We show that mutations in 4.51% of the noncoding human genome are under purifying selection and that most of this sequence has likely experienced changes in selection coefficients throughout mammalian evolution. Our work reveals limitations to using comparative genomic approaches to identify deleterious mutations. Commonly used GERP score thresholds miss over half of the noncoding sites in the human genome where mutations are under purifying selection. Public Library of Science 2020-05-29 /pmc/articles/PMC7286533/ /pubmed/32469868 http://dx.doi.org/10.1371/journal.pgen.1008827 Text en © 2020 Huber et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huber, Christian D.
Kim, Bernard Y.
Lohmueller, Kirk E.
Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title_full Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title_fullStr Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title_full_unstemmed Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title_short Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
title_sort population genetic models of gerp scores suggest pervasive turnover of constrained sites across mammalian evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7286533/
https://www.ncbi.nlm.nih.gov/pubmed/32469868
http://dx.doi.org/10.1371/journal.pgen.1008827
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