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An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake

The selection of cattle with enhanced feed efficiency is of importance with regard to reducing feed costs in the beef industry. Global transcriptome profiling was undertaken on liver and skeletal muscle biopsies from Simmental heifers and bulls divergent for residual feed intake (RFI), a widely ackn...

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Autores principales: McKenna, Clare, Keogh, Kate, Porter, Richard K., Waters, Sinead M., Cormican, Paul, Kenny, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076192/
https://www.ncbi.nlm.nih.gov/pubmed/33903612
http://dx.doi.org/10.1038/s41598-021-87842-3
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author McKenna, Clare
Keogh, Kate
Porter, Richard K.
Waters, Sinead M.
Cormican, Paul
Kenny, David A.
author_facet McKenna, Clare
Keogh, Kate
Porter, Richard K.
Waters, Sinead M.
Cormican, Paul
Kenny, David A.
author_sort McKenna, Clare
collection PubMed
description The selection of cattle with enhanced feed efficiency is of importance with regard to reducing feed costs in the beef industry. Global transcriptome profiling was undertaken on liver and skeletal muscle biopsies from Simmental heifers and bulls divergent for residual feed intake (RFI), a widely acknowledged feed efficiency phenotype, in order to identify genes that may be associated with this trait. We identified 5 genes (adj. p < 0.1) to be differentially expressed in skeletal muscle between high and low RFI heifers with all transcripts involved in oxidative phosphorylation and mitochondrial homeostasis. A total of 11 genes (adj. p < 0. 1) were differentially expressed in liver tissue between high and low RFI bulls with differentially expressed genes related to amino and nucleotide metabolism as well as endoplasmic reticulum protein processing. No genes were identified as differentially expressed in either heifer liver or bull muscle analyses. Results from this study show that the molecular control of RFI in young cattle is modified according to gender, which may be attributable to differences in physiological maturity between heifers and bulls of the same age. Despite this we have highlighted a number of genes that may hold potential as molecular biomarkers for RFI cattle.
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spelling pubmed-80761922021-04-27 An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake McKenna, Clare Keogh, Kate Porter, Richard K. Waters, Sinead M. Cormican, Paul Kenny, David A. Sci Rep Article The selection of cattle with enhanced feed efficiency is of importance with regard to reducing feed costs in the beef industry. Global transcriptome profiling was undertaken on liver and skeletal muscle biopsies from Simmental heifers and bulls divergent for residual feed intake (RFI), a widely acknowledged feed efficiency phenotype, in order to identify genes that may be associated with this trait. We identified 5 genes (adj. p < 0.1) to be differentially expressed in skeletal muscle between high and low RFI heifers with all transcripts involved in oxidative phosphorylation and mitochondrial homeostasis. A total of 11 genes (adj. p < 0. 1) were differentially expressed in liver tissue between high and low RFI bulls with differentially expressed genes related to amino and nucleotide metabolism as well as endoplasmic reticulum protein processing. No genes were identified as differentially expressed in either heifer liver or bull muscle analyses. Results from this study show that the molecular control of RFI in young cattle is modified according to gender, which may be attributable to differences in physiological maturity between heifers and bulls of the same age. Despite this we have highlighted a number of genes that may hold potential as molecular biomarkers for RFI cattle. Nature Publishing Group UK 2021-04-26 /pmc/articles/PMC8076192/ /pubmed/33903612 http://dx.doi.org/10.1038/s41598-021-87842-3 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 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
McKenna, Clare
Keogh, Kate
Porter, Richard K.
Waters, Sinead M.
Cormican, Paul
Kenny, David A.
An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title_full An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title_fullStr An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title_full_unstemmed An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title_short An examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
title_sort examination of skeletal muscle and hepatic tissue transcriptomes from beef cattle divergent for residual feed intake
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076192/
https://www.ncbi.nlm.nih.gov/pubmed/33903612
http://dx.doi.org/10.1038/s41598-021-87842-3
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