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Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle
Enhanced coverage and sensitivity of next-generation ‘omic’ platforms has allowed the characterization of gene, metabolite and protein responses in highly metabolic tissues, such as, skeletal muscle. A limitation, however, is the capability to determine interaction between dynamic biological network...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647435/ https://www.ncbi.nlm.nih.gov/pubmed/29044196 http://dx.doi.org/10.1038/s41598-017-14081-w |
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author | Pérez-Schindler, Joaquín Kanhere, Aditi Edwards, Lindsay Allwood, J. William Dunn, Warwick B. Schenk, Simon Philp, Andrew |
author_facet | Pérez-Schindler, Joaquín Kanhere, Aditi Edwards, Lindsay Allwood, J. William Dunn, Warwick B. Schenk, Simon Philp, Andrew |
author_sort | Pérez-Schindler, Joaquín |
collection | PubMed |
description | Enhanced coverage and sensitivity of next-generation ‘omic’ platforms has allowed the characterization of gene, metabolite and protein responses in highly metabolic tissues, such as, skeletal muscle. A limitation, however, is the capability to determine interaction between dynamic biological networks. To address this limitation, we applied Weighted Analyte Correlation Network Analysis (WACNA) to RNA-seq and metabolomic datasets to identify correlated subnetworks of transcripts and metabolites in response to a high-fat diet (HFD)-induced obesity and/or exercise. HFD altered skeletal muscle lipid profiles and up-regulated genes involved in lipid catabolism, while decreasing 241 exercise-responsive genes related to skeletal muscle plasticity. WACNA identified the interplay between transcript and metabolite subnetworks linked to lipid metabolism, inflammation and glycerophospholipid metabolism that were associated with IL6, AMPK and PPAR signal pathways. Collectively, this novel experimental approach provides an integrative resource to study transcriptional and metabolic networks in skeletal muscle in the context of health and disease. |
format | Online Article Text |
id | pubmed-5647435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56474352017-10-26 Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle Pérez-Schindler, Joaquín Kanhere, Aditi Edwards, Lindsay Allwood, J. William Dunn, Warwick B. Schenk, Simon Philp, Andrew Sci Rep Article Enhanced coverage and sensitivity of next-generation ‘omic’ platforms has allowed the characterization of gene, metabolite and protein responses in highly metabolic tissues, such as, skeletal muscle. A limitation, however, is the capability to determine interaction between dynamic biological networks. To address this limitation, we applied Weighted Analyte Correlation Network Analysis (WACNA) to RNA-seq and metabolomic datasets to identify correlated subnetworks of transcripts and metabolites in response to a high-fat diet (HFD)-induced obesity and/or exercise. HFD altered skeletal muscle lipid profiles and up-regulated genes involved in lipid catabolism, while decreasing 241 exercise-responsive genes related to skeletal muscle plasticity. WACNA identified the interplay between transcript and metabolite subnetworks linked to lipid metabolism, inflammation and glycerophospholipid metabolism that were associated with IL6, AMPK and PPAR signal pathways. Collectively, this novel experimental approach provides an integrative resource to study transcriptional and metabolic networks in skeletal muscle in the context of health and disease. Nature Publishing Group UK 2017-10-18 /pmc/articles/PMC5647435/ /pubmed/29044196 http://dx.doi.org/10.1038/s41598-017-14081-w Text en © The Author(s) 2017 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 Pérez-Schindler, Joaquín Kanhere, Aditi Edwards, Lindsay Allwood, J. William Dunn, Warwick B. Schenk, Simon Philp, Andrew Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title | Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title_full | Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title_fullStr | Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title_full_unstemmed | Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title_short | Exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
title_sort | exercise and high-fat feeding remodel transcript-metabolite interactive networks in mouse skeletal muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647435/ https://www.ncbi.nlm.nih.gov/pubmed/29044196 http://dx.doi.org/10.1038/s41598-017-14081-w |
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