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Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows

A better knowledge of the bovine milk proteome and its main drivers is a prerequisite for the modulation of bioactive proteins in milk for human nutrition, as well as for the discovery of biomarkers that are useful in husbandry and veterinary medicine. Milk composition is affected by lactation stage...

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Autores principales: Delosière, Mylène, Pires, José, Bernard, Laurence, Cassar-Malek, Isabelle, Bonnet, Muriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609625/
https://www.ncbi.nlm.nih.gov/pubmed/31273261
http://dx.doi.org/10.1038/s41598-019-46142-7
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author Delosière, Mylène
Pires, José
Bernard, Laurence
Cassar-Malek, Isabelle
Bonnet, Muriel
author_facet Delosière, Mylène
Pires, José
Bernard, Laurence
Cassar-Malek, Isabelle
Bonnet, Muriel
author_sort Delosière, Mylène
collection PubMed
description A better knowledge of the bovine milk proteome and its main drivers is a prerequisite for the modulation of bioactive proteins in milk for human nutrition, as well as for the discovery of biomarkers that are useful in husbandry and veterinary medicine. Milk composition is affected by lactation stage and reflects, in part, the energy balance of dairy cows. We aggregated the cow milk proteins reported in 20 recent proteomics publications to produce an atlas of 4654 unique proteins. A multistep assessment was applied to the milk proteome datasets according to lactation stages and milk fractions, including annotations, pathway analysis and literature mining. Fifty-nine proteins were exclusively detected in milk from early lactation. Among them, we propose six milk proteins as putative biomarkers of negative energy balance based on their implication in metabolic adaptative pathways. These proteins are PCK2, which is a gluconeogenic enzyme; ACAT1 and IVD, which are involved in ketone metabolism; SDHA and UQCRC1, which are related to mitochondrial oxidative metabolism; and LRRC59, which is linked to mammary gland cell proliferation. The cellular origin of these proteins warrants more in-depth research but may constitute part of a molecular signature for metabolic adaptations typical of early lactation.
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spelling pubmed-66096252019-07-14 Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows Delosière, Mylène Pires, José Bernard, Laurence Cassar-Malek, Isabelle Bonnet, Muriel Sci Rep Article A better knowledge of the bovine milk proteome and its main drivers is a prerequisite for the modulation of bioactive proteins in milk for human nutrition, as well as for the discovery of biomarkers that are useful in husbandry and veterinary medicine. Milk composition is affected by lactation stage and reflects, in part, the energy balance of dairy cows. We aggregated the cow milk proteins reported in 20 recent proteomics publications to produce an atlas of 4654 unique proteins. A multistep assessment was applied to the milk proteome datasets according to lactation stages and milk fractions, including annotations, pathway analysis and literature mining. Fifty-nine proteins were exclusively detected in milk from early lactation. Among them, we propose six milk proteins as putative biomarkers of negative energy balance based on their implication in metabolic adaptative pathways. These proteins are PCK2, which is a gluconeogenic enzyme; ACAT1 and IVD, which are involved in ketone metabolism; SDHA and UQCRC1, which are related to mitochondrial oxidative metabolism; and LRRC59, which is linked to mammary gland cell proliferation. The cellular origin of these proteins warrants more in-depth research but may constitute part of a molecular signature for metabolic adaptations typical of early lactation. Nature Publishing Group UK 2019-07-04 /pmc/articles/PMC6609625/ /pubmed/31273261 http://dx.doi.org/10.1038/s41598-019-46142-7 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
Delosière, Mylène
Pires, José
Bernard, Laurence
Cassar-Malek, Isabelle
Bonnet, Muriel
Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title_full Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title_fullStr Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title_full_unstemmed Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title_short Milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
title_sort milk proteome from in silico data aggregation allows the identification of putative biomarkers of negative energy balance in dairy cows
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609625/
https://www.ncbi.nlm.nih.gov/pubmed/31273261
http://dx.doi.org/10.1038/s41598-019-46142-7
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