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A systematic survey to identify lethal recessive variation in highly managed pig populations
BACKGROUND: Lethal recessive variation can cause prenatal death of homozygous offspring. Although usually present at low-frequency in populations, the impact on individual fitness can be substantial. Until recently, the presence of recessive embryonic lethal variation could only be measured indirect...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5680825/ https://www.ncbi.nlm.nih.gov/pubmed/29121877 http://dx.doi.org/10.1186/s12864-017-4278-1 |
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author | Derks, Martijn F. L. Megens, Hendrik-Jan Bosse, Mirte Lopes, Marcos S. Harlizius, Barbara Groenen, Martien A. M. |
author_facet | Derks, Martijn F. L. Megens, Hendrik-Jan Bosse, Mirte Lopes, Marcos S. Harlizius, Barbara Groenen, Martien A. M. |
author_sort | Derks, Martijn F. L. |
collection | PubMed |
description | BACKGROUND: Lethal recessive variation can cause prenatal death of homozygous offspring. Although usually present at low-frequency in populations, the impact on individual fitness can be substantial. Until recently, the presence of recessive embryonic lethal variation could only be measured indirectly through reduced fertility. In this study, we estimate the presence of genetic loci associated with both early and late termination of development during gestation in pigs from the wealth of genome data routinely generated by a commercial breeding company. RESULTS: We examined three commercial pig (Sus scrofa) populations for potentially deleterious genetic variation based on 80 K SNP-chip genotypes, and estimate the effects on reproductive traits. 24,000 pigs from three populations were analyzed for missing or depletion of homozygous haplotypes. We identified 145 haplotypes (ranging from 0.5–4 Mb in size) in the genome with complete absence or depletion of homozygous animals. Thirty-five haplotypes show a negative effect on at least one of the analysed reproductive traits (total number born, number of stillborn, and number of mummified piglets). One variant in particular appeared to result in relative late termination of development of fetuses, responsible for a significant fraction of observed stillborn piglets (‘mummies’), as they die mid-gestation. Moreover, we identified the BMPER gene as a likely candidate underlying this phenomenon. CONCLUSIONS: Our study shows that although lethal recessive variation is present, the frequency of these alleles is invariably low in these highly managed populations. Nevertheless, due to cumulative effects of deleterious variants, large numbers of affected offspring are produced. Furthermore, our study demonstrates the use of a large-scale commercial genetic experiment to systematically screen for ‘natural knockouts’ that can increase understanding of gene function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4278-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5680825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56808252017-11-17 A systematic survey to identify lethal recessive variation in highly managed pig populations Derks, Martijn F. L. Megens, Hendrik-Jan Bosse, Mirte Lopes, Marcos S. Harlizius, Barbara Groenen, Martien A. M. BMC Genomics Research Article BACKGROUND: Lethal recessive variation can cause prenatal death of homozygous offspring. Although usually present at low-frequency in populations, the impact on individual fitness can be substantial. Until recently, the presence of recessive embryonic lethal variation could only be measured indirectly through reduced fertility. In this study, we estimate the presence of genetic loci associated with both early and late termination of development during gestation in pigs from the wealth of genome data routinely generated by a commercial breeding company. RESULTS: We examined three commercial pig (Sus scrofa) populations for potentially deleterious genetic variation based on 80 K SNP-chip genotypes, and estimate the effects on reproductive traits. 24,000 pigs from three populations were analyzed for missing or depletion of homozygous haplotypes. We identified 145 haplotypes (ranging from 0.5–4 Mb in size) in the genome with complete absence or depletion of homozygous animals. Thirty-five haplotypes show a negative effect on at least one of the analysed reproductive traits (total number born, number of stillborn, and number of mummified piglets). One variant in particular appeared to result in relative late termination of development of fetuses, responsible for a significant fraction of observed stillborn piglets (‘mummies’), as they die mid-gestation. Moreover, we identified the BMPER gene as a likely candidate underlying this phenomenon. CONCLUSIONS: Our study shows that although lethal recessive variation is present, the frequency of these alleles is invariably low in these highly managed populations. Nevertheless, due to cumulative effects of deleterious variants, large numbers of affected offspring are produced. Furthermore, our study demonstrates the use of a large-scale commercial genetic experiment to systematically screen for ‘natural knockouts’ that can increase understanding of gene function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4278-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-09 /pmc/articles/PMC5680825/ /pubmed/29121877 http://dx.doi.org/10.1186/s12864-017-4278-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Derks, Martijn F. L. Megens, Hendrik-Jan Bosse, Mirte Lopes, Marcos S. Harlizius, Barbara Groenen, Martien A. M. A systematic survey to identify lethal recessive variation in highly managed pig populations |
title | A systematic survey to identify lethal recessive variation in highly managed pig populations |
title_full | A systematic survey to identify lethal recessive variation in highly managed pig populations |
title_fullStr | A systematic survey to identify lethal recessive variation in highly managed pig populations |
title_full_unstemmed | A systematic survey to identify lethal recessive variation in highly managed pig populations |
title_short | A systematic survey to identify lethal recessive variation in highly managed pig populations |
title_sort | systematic survey to identify lethal recessive variation in highly managed pig populations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5680825/ https://www.ncbi.nlm.nih.gov/pubmed/29121877 http://dx.doi.org/10.1186/s12864-017-4278-1 |
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