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Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf

Enhanced early life nutrition accelerates sexual development in the bull calf through neuroendocrine-signalling mediated via the hypothalamic–pituitary–testicular axis. Our aim was to assess the impact of contrasting feeding regimes in bull calves during the first 12 weeks of life on the testes tran...

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Autores principales: Coen, Stephen, Keogh, Kate, Lonergan, Pat, Fair, Sean, Kenny, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130005/
https://www.ncbi.nlm.nih.gov/pubmed/37185277
http://dx.doi.org/10.1038/s41598-022-23743-3
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author Coen, Stephen
Keogh, Kate
Lonergan, Pat
Fair, Sean
Kenny, David A.
author_facet Coen, Stephen
Keogh, Kate
Lonergan, Pat
Fair, Sean
Kenny, David A.
author_sort Coen, Stephen
collection PubMed
description Enhanced early life nutrition accelerates sexual development in the bull calf through neuroendocrine-signalling mediated via the hypothalamic–pituitary–testicular axis. Our aim was to assess the impact of contrasting feeding regimes in bull calves during the first 12 weeks of life on the testes transcriptome and proteome. Holstein–Friesian bull calves were offered either a high (HI) or moderate (MOD) plane of nutrition, designed to support target growth rates of 1.0 and 0.5 kg/day, respectively. At 12 weeks of age all calves were euthanized, testicular parenchyma sampled, and global transcriptome (miRNAseq and mRNAseq) and proteome analyses undertaken. Bioinformatic analyses revealed 7 differentially expressed (DE) miRNA and 20 DE mRNA. There were no differentially abundant proteins between the two dietary groups. Integration of omics results highlighted a potential role for the cadherin gene, CDH13, in earlier reproductive development. Furthermore, co-regulatory network analysis of the proteomic data revealed CDH13 as a hub protein within a network enriched for processes related to insulin, IGF-1, androgen and Sertoli cell junction signalling pathways as well as cholesterol biosynthesis. Overall, results highlight a potential role for CDH13 in mediating earlier reproductive development as a consequence of enhanced early life nutrition in the bull calf.
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spelling pubmed-101300052023-04-27 Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf Coen, Stephen Keogh, Kate Lonergan, Pat Fair, Sean Kenny, David A. Sci Rep Article Enhanced early life nutrition accelerates sexual development in the bull calf through neuroendocrine-signalling mediated via the hypothalamic–pituitary–testicular axis. Our aim was to assess the impact of contrasting feeding regimes in bull calves during the first 12 weeks of life on the testes transcriptome and proteome. Holstein–Friesian bull calves were offered either a high (HI) or moderate (MOD) plane of nutrition, designed to support target growth rates of 1.0 and 0.5 kg/day, respectively. At 12 weeks of age all calves were euthanized, testicular parenchyma sampled, and global transcriptome (miRNAseq and mRNAseq) and proteome analyses undertaken. Bioinformatic analyses revealed 7 differentially expressed (DE) miRNA and 20 DE mRNA. There were no differentially abundant proteins between the two dietary groups. Integration of omics results highlighted a potential role for the cadherin gene, CDH13, in earlier reproductive development. Furthermore, co-regulatory network analysis of the proteomic data revealed CDH13 as a hub protein within a network enriched for processes related to insulin, IGF-1, androgen and Sertoli cell junction signalling pathways as well as cholesterol biosynthesis. Overall, results highlight a potential role for CDH13 in mediating earlier reproductive development as a consequence of enhanced early life nutrition in the bull calf. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130005/ /pubmed/37185277 http://dx.doi.org/10.1038/s41598-022-23743-3 Text en © The Author(s) 2023 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 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/) .
spellingShingle Article
Coen, Stephen
Keogh, Kate
Lonergan, Pat
Fair, Sean
Kenny, David A.
Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title_full Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title_fullStr Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title_full_unstemmed Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title_short Early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
title_sort early life nutrition affects the molecular ontogeny of testicular development in the young bull calf
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130005/
https://www.ncbi.nlm.nih.gov/pubmed/37185277
http://dx.doi.org/10.1038/s41598-022-23743-3
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