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Mutant alleles differentially shape fitness and other complex traits in cattle

Mutant alleles (MAs) that have been classically recognised have large effects on phenotype and tend to be deleterious to traits and fitness. Is this the case for mutations with small effects? We infer MAs for 8 million sequence variants in 113k cattle and quantify the effects of MA on 37 complex tra...

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Autores principales: Xiang, Ruidong, Breen, Ed J., Bolormaa, Sunduimijid, Jagt, Christy J. Vander, Chamberlain, Amanda J., Macleod, Iona M., Goddard, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640064/
https://www.ncbi.nlm.nih.gov/pubmed/34857886
http://dx.doi.org/10.1038/s42003-021-02874-9
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author Xiang, Ruidong
Breen, Ed J.
Bolormaa, Sunduimijid
Jagt, Christy J. Vander
Chamberlain, Amanda J.
Macleod, Iona M.
Goddard, Michael E.
author_facet Xiang, Ruidong
Breen, Ed J.
Bolormaa, Sunduimijid
Jagt, Christy J. Vander
Chamberlain, Amanda J.
Macleod, Iona M.
Goddard, Michael E.
author_sort Xiang, Ruidong
collection PubMed
description Mutant alleles (MAs) that have been classically recognised have large effects on phenotype and tend to be deleterious to traits and fitness. Is this the case for mutations with small effects? We infer MAs for 8 million sequence variants in 113k cattle and quantify the effects of MA on 37 complex traits. Heterozygosity for variants at genomic sites conserved across 100 vertebrate species increase fertility, stature, and milk production, positively associating these traits with fitness. MAs decrease stature and fat and protein concentration in milk, but increase gestation length and somatic cell count in milk (the latter indicative of mastitis). However, the frequency of MAs decreasing stature and fat and protein concentration, increasing gestation length and somatic cell count were lower than the frequency of MAs with the opposite effect. These results suggest bias in the mutations direction of effect (e.g. towards reduced protein in milk), but selection operating to reduce the frequency of these MAs. Taken together, our results imply two classes of genomic sites subject to long-term selection: sites conserved across vertebrates show hybrid vigour while sites subject to less long-term selection show a bias in mutation towards undesirable alleles.
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spelling pubmed-86400642021-12-15 Mutant alleles differentially shape fitness and other complex traits in cattle Xiang, Ruidong Breen, Ed J. Bolormaa, Sunduimijid Jagt, Christy J. Vander Chamberlain, Amanda J. Macleod, Iona M. Goddard, Michael E. Commun Biol Article Mutant alleles (MAs) that have been classically recognised have large effects on phenotype and tend to be deleterious to traits and fitness. Is this the case for mutations with small effects? We infer MAs for 8 million sequence variants in 113k cattle and quantify the effects of MA on 37 complex traits. Heterozygosity for variants at genomic sites conserved across 100 vertebrate species increase fertility, stature, and milk production, positively associating these traits with fitness. MAs decrease stature and fat and protein concentration in milk, but increase gestation length and somatic cell count in milk (the latter indicative of mastitis). However, the frequency of MAs decreasing stature and fat and protein concentration, increasing gestation length and somatic cell count were lower than the frequency of MAs with the opposite effect. These results suggest bias in the mutations direction of effect (e.g. towards reduced protein in milk), but selection operating to reduce the frequency of these MAs. Taken together, our results imply two classes of genomic sites subject to long-term selection: sites conserved across vertebrates show hybrid vigour while sites subject to less long-term selection show a bias in mutation towards undesirable alleles. Nature Publishing Group UK 2021-12-02 /pmc/articles/PMC8640064/ /pubmed/34857886 http://dx.doi.org/10.1038/s42003-021-02874-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xiang, Ruidong
Breen, Ed J.
Bolormaa, Sunduimijid
Jagt, Christy J. Vander
Chamberlain, Amanda J.
Macleod, Iona M.
Goddard, Michael E.
Mutant alleles differentially shape fitness and other complex traits in cattle
title Mutant alleles differentially shape fitness and other complex traits in cattle
title_full Mutant alleles differentially shape fitness and other complex traits in cattle
title_fullStr Mutant alleles differentially shape fitness and other complex traits in cattle
title_full_unstemmed Mutant alleles differentially shape fitness and other complex traits in cattle
title_short Mutant alleles differentially shape fitness and other complex traits in cattle
title_sort mutant alleles differentially shape fitness and other complex traits in cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640064/
https://www.ncbi.nlm.nih.gov/pubmed/34857886
http://dx.doi.org/10.1038/s42003-021-02874-9
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