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Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk

Human milk contains abundant oligosaccharides (OS) which are believed to have strong health benefits for neonates. OS are a minor component of bovine milk and little is known about how the production of OS is regulated in the bovine mammary gland. We have measured the abundance of 12 major OS in mil...

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Autores principales: Liu, Zhiqian, Wang, Tingting, Pryce, Jennie E., MacLeod, Iona M., Hayes, Ben J., Chamberlain, Amanda J., Jagt, Christy Vander, Reich, Coralie M., Mason, Brett A., Rochfort, Simone, Cocks, Benjamin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376028/
https://www.ncbi.nlm.nih.gov/pubmed/30765736
http://dx.doi.org/10.1038/s41598-019-38488-9
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author Liu, Zhiqian
Wang, Tingting
Pryce, Jennie E.
MacLeod, Iona M.
Hayes, Ben J.
Chamberlain, Amanda J.
Jagt, Christy Vander
Reich, Coralie M.
Mason, Brett A.
Rochfort, Simone
Cocks, Benjamin G.
author_facet Liu, Zhiqian
Wang, Tingting
Pryce, Jennie E.
MacLeod, Iona M.
Hayes, Ben J.
Chamberlain, Amanda J.
Jagt, Christy Vander
Reich, Coralie M.
Mason, Brett A.
Rochfort, Simone
Cocks, Benjamin G.
author_sort Liu, Zhiqian
collection PubMed
description Human milk contains abundant oligosaccharides (OS) which are believed to have strong health benefits for neonates. OS are a minor component of bovine milk and little is known about how the production of OS is regulated in the bovine mammary gland. We have measured the abundance of 12 major OS in milk of 360 cows, which had high density SNP marker genotypes. Most of the OS were found to be highly heritable (h(2) between 50 and 84%). A genome-wide association study allowed us to fine-map several QTL and identify candidate genes with major effects on five OS. Among them, a putative causal mutation close to the ABO gene on Chromosome 11 accounted for approximately 80% of genetic variance for two OS, N-acetylgalactosaminyllactose and lacto-N-neotetraose. This mutation lies very close to a variant associated with the expression levels of ABO. A third QTL mapped close to ST3GAL6 on Chromosome 1 explaining 33% of genetic variation of an abundant OS, 3′-sialyllactose. The presence of major gene effects suggests that targeted marker-assisted selection would lead to a significant increase in the level of these OS in milk. This is the first attempt to map candidate genes and causal mutations for bovine milk OS.
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spelling pubmed-63760282019-02-19 Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk Liu, Zhiqian Wang, Tingting Pryce, Jennie E. MacLeod, Iona M. Hayes, Ben J. Chamberlain, Amanda J. Jagt, Christy Vander Reich, Coralie M. Mason, Brett A. Rochfort, Simone Cocks, Benjamin G. Sci Rep Article Human milk contains abundant oligosaccharides (OS) which are believed to have strong health benefits for neonates. OS are a minor component of bovine milk and little is known about how the production of OS is regulated in the bovine mammary gland. We have measured the abundance of 12 major OS in milk of 360 cows, which had high density SNP marker genotypes. Most of the OS were found to be highly heritable (h(2) between 50 and 84%). A genome-wide association study allowed us to fine-map several QTL and identify candidate genes with major effects on five OS. Among them, a putative causal mutation close to the ABO gene on Chromosome 11 accounted for approximately 80% of genetic variance for two OS, N-acetylgalactosaminyllactose and lacto-N-neotetraose. This mutation lies very close to a variant associated with the expression levels of ABO. A third QTL mapped close to ST3GAL6 on Chromosome 1 explaining 33% of genetic variation of an abundant OS, 3′-sialyllactose. The presence of major gene effects suggests that targeted marker-assisted selection would lead to a significant increase in the level of these OS in milk. This is the first attempt to map candidate genes and causal mutations for bovine milk OS. Nature Publishing Group UK 2019-02-14 /pmc/articles/PMC6376028/ /pubmed/30765736 http://dx.doi.org/10.1038/s41598-019-38488-9 Text en © The Author(s) 2019 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/.
spellingShingle Article
Liu, Zhiqian
Wang, Tingting
Pryce, Jennie E.
MacLeod, Iona M.
Hayes, Ben J.
Chamberlain, Amanda J.
Jagt, Christy Vander
Reich, Coralie M.
Mason, Brett A.
Rochfort, Simone
Cocks, Benjamin G.
Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title_full Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title_fullStr Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title_full_unstemmed Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title_short Fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
title_sort fine-mapping sequence mutations with a major effect on oligosaccharide content in bovine milk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376028/
https://www.ncbi.nlm.nih.gov/pubmed/30765736
http://dx.doi.org/10.1038/s41598-019-38488-9
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