Cargando…
Rare and population-specific functional variation across pig lines
BACKGROUND: It is expected that functional, mainly missense and loss-of-function (LOF), and regulatory variants are responsible for most phenotypic differences between breeds and genetic lines of livestock species that have undergone diverse selection histories. However, there is still limited knowl...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164375/ https://www.ncbi.nlm.nih.gov/pubmed/35659233 http://dx.doi.org/10.1186/s12711-022-00732-8 |
_version_ | 1784720120628641792 |
---|---|
author | Ros-Freixedes, Roger Valente, Bruno D. Chen, Ching-Yi Herring, William O. Gorjanc, Gregor Hickey, John M. Johnsson, Martin |
author_facet | Ros-Freixedes, Roger Valente, Bruno D. Chen, Ching-Yi Herring, William O. Gorjanc, Gregor Hickey, John M. Johnsson, Martin |
author_sort | Ros-Freixedes, Roger |
collection | PubMed |
description | BACKGROUND: It is expected that functional, mainly missense and loss-of-function (LOF), and regulatory variants are responsible for most phenotypic differences between breeds and genetic lines of livestock species that have undergone diverse selection histories. However, there is still limited knowledge about the existing missense and LOF variation in commercial livestock populations, in particular regarding population-specific variation and how it can affect applications such as across-breed genomic prediction. METHODS: We re-sequenced the whole genome of 7848 individuals from nine commercial pig lines (average sequencing coverage: 4.1×) and imputed whole-genome genotypes for 440,610 pedigree-related individuals. The called variants were categorized according to predicted functional annotation (from LOF to intergenic) and prevalence level (number of lines in which the variant segregated; from private to widespread). Variants in each category were examined in terms of their distribution along the genome, alternative allele frequency, per-site Wright’s fixation index (F(ST)), individual load, and association to production traits. RESULTS: Of the 46 million called variants, 28% were private (called in only one line) and 21% were widespread (called in all nine lines). Genomic regions with a low recombination rate were enriched with private variants. Low-prevalence variants (called in one or a few lines only) were enriched for lower allele frequencies, lower F(ST), and putatively functional and regulatory roles (including LOF and deleterious missense variants). On average, individuals carried fewer private deleterious missense alleles than expected compared to alleles with other predicted consequences. Only a small subset of the low-prevalence variants had intermediate allele frequencies and explained small fractions of phenotypic variance (up to 3.2%) of production traits. The significant low-prevalence variants had higher per-site F(ST) than the non-significant ones. These associated low-prevalence variants were tagged by other more widespread variants in high linkage disequilibrium, including intergenic variants. CONCLUSIONS: Most low-prevalence variants have low minor allele frequencies and only a small subset of low-prevalence variants contributed detectable fractions of phenotypic variance of production traits. Accounting for low-prevalence variants is therefore unlikely to noticeably benefit across-breed analyses, such as the prediction of genomic breeding values in a population using reference populations of a different genetic background. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12711-022-00732-8. |
format | Online Article Text |
id | pubmed-9164375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91643752022-06-05 Rare and population-specific functional variation across pig lines Ros-Freixedes, Roger Valente, Bruno D. Chen, Ching-Yi Herring, William O. Gorjanc, Gregor Hickey, John M. Johnsson, Martin Genet Sel Evol Research Article BACKGROUND: It is expected that functional, mainly missense and loss-of-function (LOF), and regulatory variants are responsible for most phenotypic differences between breeds and genetic lines of livestock species that have undergone diverse selection histories. However, there is still limited knowledge about the existing missense and LOF variation in commercial livestock populations, in particular regarding population-specific variation and how it can affect applications such as across-breed genomic prediction. METHODS: We re-sequenced the whole genome of 7848 individuals from nine commercial pig lines (average sequencing coverage: 4.1×) and imputed whole-genome genotypes for 440,610 pedigree-related individuals. The called variants were categorized according to predicted functional annotation (from LOF to intergenic) and prevalence level (number of lines in which the variant segregated; from private to widespread). Variants in each category were examined in terms of their distribution along the genome, alternative allele frequency, per-site Wright’s fixation index (F(ST)), individual load, and association to production traits. RESULTS: Of the 46 million called variants, 28% were private (called in only one line) and 21% were widespread (called in all nine lines). Genomic regions with a low recombination rate were enriched with private variants. Low-prevalence variants (called in one or a few lines only) were enriched for lower allele frequencies, lower F(ST), and putatively functional and regulatory roles (including LOF and deleterious missense variants). On average, individuals carried fewer private deleterious missense alleles than expected compared to alleles with other predicted consequences. Only a small subset of the low-prevalence variants had intermediate allele frequencies and explained small fractions of phenotypic variance (up to 3.2%) of production traits. The significant low-prevalence variants had higher per-site F(ST) than the non-significant ones. These associated low-prevalence variants were tagged by other more widespread variants in high linkage disequilibrium, including intergenic variants. CONCLUSIONS: Most low-prevalence variants have low minor allele frequencies and only a small subset of low-prevalence variants contributed detectable fractions of phenotypic variance of production traits. Accounting for low-prevalence variants is therefore unlikely to noticeably benefit across-breed analyses, such as the prediction of genomic breeding values in a population using reference populations of a different genetic background. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12711-022-00732-8. BioMed Central 2022-06-03 /pmc/articles/PMC9164375/ /pubmed/35659233 http://dx.doi.org/10.1186/s12711-022-00732-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Ros-Freixedes, Roger Valente, Bruno D. Chen, Ching-Yi Herring, William O. Gorjanc, Gregor Hickey, John M. Johnsson, Martin Rare and population-specific functional variation across pig lines |
title | Rare and population-specific functional variation across pig lines |
title_full | Rare and population-specific functional variation across pig lines |
title_fullStr | Rare and population-specific functional variation across pig lines |
title_full_unstemmed | Rare and population-specific functional variation across pig lines |
title_short | Rare and population-specific functional variation across pig lines |
title_sort | rare and population-specific functional variation across pig lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164375/ https://www.ncbi.nlm.nih.gov/pubmed/35659233 http://dx.doi.org/10.1186/s12711-022-00732-8 |
work_keys_str_mv | AT rosfreixedesroger rareandpopulationspecificfunctionalvariationacrosspiglines AT valentebrunod rareandpopulationspecificfunctionalvariationacrosspiglines AT chenchingyi rareandpopulationspecificfunctionalvariationacrosspiglines AT herringwilliamo rareandpopulationspecificfunctionalvariationacrosspiglines AT gorjancgregor rareandpopulationspecificfunctionalvariationacrosspiglines AT hickeyjohnm rareandpopulationspecificfunctionalvariationacrosspiglines AT johnssonmartin rareandpopulationspecificfunctionalvariationacrosspiglines |