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Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity

BACKGROUND: Healthy individuals on the lower end of the insulin sensitivity spectrum also have a reduced gene expression response to exercise for specific genes. The goal of this study was to determine the relationship between insulin sensitivity and exercise-induced gene expression in an unbiased,...

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Autores principales: McLean, Carrie S., Mielke, Clinton, Cordova, Jeanine M., Langlais, Paul R., Bowen, Benjamin, Miranda, Danielle, Coletta, Dawn K., Mandarino, Lawrence J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436215/
https://www.ncbi.nlm.nih.gov/pubmed/25984722
http://dx.doi.org/10.1371/journal.pone.0127089
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author McLean, Carrie S.
Mielke, Clinton
Cordova, Jeanine M.
Langlais, Paul R.
Bowen, Benjamin
Miranda, Danielle
Coletta, Dawn K.
Mandarino, Lawrence J.
author_facet McLean, Carrie S.
Mielke, Clinton
Cordova, Jeanine M.
Langlais, Paul R.
Bowen, Benjamin
Miranda, Danielle
Coletta, Dawn K.
Mandarino, Lawrence J.
author_sort McLean, Carrie S.
collection PubMed
description BACKGROUND: Healthy individuals on the lower end of the insulin sensitivity spectrum also have a reduced gene expression response to exercise for specific genes. The goal of this study was to determine the relationship between insulin sensitivity and exercise-induced gene expression in an unbiased, global manner. METHODS AND FINDINGS: Euglycemic clamps were used to measure insulin sensitivity and muscle biopsies were done at rest and 30 minutes after a single acute exercise bout in 14 healthy participants. Changes in mRNA expression were assessed using microarrays, and miRNA analysis was performed in a subset of 6 of the participants using sequencing techniques. Following exercise, 215 mRNAs were changed at the probe level (Bonferroni-corrected P<0.00000115). Pathway and Gene Ontology analysis showed enrichment in MAP kinase signaling, transcriptional regulation and DNA binding. Changes in several transcription factor mRNAs were correlated with insulin sensitivity, including MYC, r=0.71; SNF1LK, r=0.69; and ATF3, r= 0.61 (5 corrected for false discovery rate). Enrichment in the 5’-UTRs of exercise-responsive genes suggested regulation by common transcription factors, especially EGR1. miRNA species of interest that changed after exercise included miR-378, which is located in an intron of the PPARGC1B gene. CONCLUSIONS: These results indicate that transcription factor gene expression responses to exercise depend highly on insulin sensitivity in healthy people. The overall pattern suggests a coordinated cycle by which exercise and insulin sensitivity regulate gene expression in muscle.
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spelling pubmed-44362152015-05-27 Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity McLean, Carrie S. Mielke, Clinton Cordova, Jeanine M. Langlais, Paul R. Bowen, Benjamin Miranda, Danielle Coletta, Dawn K. Mandarino, Lawrence J. PLoS One Research Article BACKGROUND: Healthy individuals on the lower end of the insulin sensitivity spectrum also have a reduced gene expression response to exercise for specific genes. The goal of this study was to determine the relationship between insulin sensitivity and exercise-induced gene expression in an unbiased, global manner. METHODS AND FINDINGS: Euglycemic clamps were used to measure insulin sensitivity and muscle biopsies were done at rest and 30 minutes after a single acute exercise bout in 14 healthy participants. Changes in mRNA expression were assessed using microarrays, and miRNA analysis was performed in a subset of 6 of the participants using sequencing techniques. Following exercise, 215 mRNAs were changed at the probe level (Bonferroni-corrected P<0.00000115). Pathway and Gene Ontology analysis showed enrichment in MAP kinase signaling, transcriptional regulation and DNA binding. Changes in several transcription factor mRNAs were correlated with insulin sensitivity, including MYC, r=0.71; SNF1LK, r=0.69; and ATF3, r= 0.61 (5 corrected for false discovery rate). Enrichment in the 5’-UTRs of exercise-responsive genes suggested regulation by common transcription factors, especially EGR1. miRNA species of interest that changed after exercise included miR-378, which is located in an intron of the PPARGC1B gene. CONCLUSIONS: These results indicate that transcription factor gene expression responses to exercise depend highly on insulin sensitivity in healthy people. The overall pattern suggests a coordinated cycle by which exercise and insulin sensitivity regulate gene expression in muscle. Public Library of Science 2015-05-18 /pmc/articles/PMC4436215/ /pubmed/25984722 http://dx.doi.org/10.1371/journal.pone.0127089 Text en © 2015 McLean et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
McLean, Carrie S.
Mielke, Clinton
Cordova, Jeanine M.
Langlais, Paul R.
Bowen, Benjamin
Miranda, Danielle
Coletta, Dawn K.
Mandarino, Lawrence J.
Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title_full Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title_fullStr Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title_full_unstemmed Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title_short Gene and MicroRNA Expression Responses to Exercise; Relationship with Insulin Sensitivity
title_sort gene and microrna expression responses to exercise; relationship with insulin sensitivity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436215/
https://www.ncbi.nlm.nih.gov/pubmed/25984722
http://dx.doi.org/10.1371/journal.pone.0127089
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