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Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes
Loss of function (LoF) genetic variants are predicted to disrupt gene function, and are therefore expected to substantially reduce individual’s viability. Knowing the genetic burden of LoF variants in endangered species is of interest for a better understanding of the effects of declining population...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824148/ https://www.ncbi.nlm.nih.gov/pubmed/26912403 http://dx.doi.org/10.1093/gbe/evw040 |
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author | de Valles-Ibáñez, Guillem Hernandez-Rodriguez, Jessica Prado-Martinez, Javier Luisi, Pierre Marquès-Bonet, Tomàs Casals, Ferran |
author_facet | de Valles-Ibáñez, Guillem Hernandez-Rodriguez, Jessica Prado-Martinez, Javier Luisi, Pierre Marquès-Bonet, Tomàs Casals, Ferran |
author_sort | de Valles-Ibáñez, Guillem |
collection | PubMed |
description | Loss of function (LoF) genetic variants are predicted to disrupt gene function, and are therefore expected to substantially reduce individual’s viability. Knowing the genetic burden of LoF variants in endangered species is of interest for a better understanding of the effects of declining population sizes on species viability. In this study, we have estimated the number of LoF polymorphic variants in six great ape populations, based on whole-genome sequencing data in 79 individuals. Our results show that although the number of functional variants per individual is conditioned by the effective population size, the number of variants with a drastic phenotypic effect is very similar across species. We hypothesize that for those variants with high selection coefficients, differences in effective population size are not important enough to affect the efficiency of natural selection to remove them. We also describe that mostly CpG LoF mutations are shared across species, and an accumulation of LoF variants at olfactory receptor genes in agreement with its pseudogenization in humans and other primate species. |
format | Online Article Text |
id | pubmed-4824148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48241482016-04-08 Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes de Valles-Ibáñez, Guillem Hernandez-Rodriguez, Jessica Prado-Martinez, Javier Luisi, Pierre Marquès-Bonet, Tomàs Casals, Ferran Genome Biol Evol Letter Loss of function (LoF) genetic variants are predicted to disrupt gene function, and are therefore expected to substantially reduce individual’s viability. Knowing the genetic burden of LoF variants in endangered species is of interest for a better understanding of the effects of declining population sizes on species viability. In this study, we have estimated the number of LoF polymorphic variants in six great ape populations, based on whole-genome sequencing data in 79 individuals. Our results show that although the number of functional variants per individual is conditioned by the effective population size, the number of variants with a drastic phenotypic effect is very similar across species. We hypothesize that for those variants with high selection coefficients, differences in effective population size are not important enough to affect the efficiency of natural selection to remove them. We also describe that mostly CpG LoF mutations are shared across species, and an accumulation of LoF variants at olfactory receptor genes in agreement with its pseudogenization in humans and other primate species. Oxford University Press 2016-02-24 /pmc/articles/PMC4824148/ /pubmed/26912403 http://dx.doi.org/10.1093/gbe/evw040 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letter de Valles-Ibáñez, Guillem Hernandez-Rodriguez, Jessica Prado-Martinez, Javier Luisi, Pierre Marquès-Bonet, Tomàs Casals, Ferran Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title | Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title_full | Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title_fullStr | Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title_full_unstemmed | Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title_short | Genetic Load of Loss-of-Function Polymorphic Variants in Great Apes |
title_sort | genetic load of loss-of-function polymorphic variants in great apes |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824148/ https://www.ncbi.nlm.nih.gov/pubmed/26912403 http://dx.doi.org/10.1093/gbe/evw040 |
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