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Dynamically regulated miRNA-mRNA networks revealed by exercise

BACKGROUND: MiRNAs are essential mediators of many biological processes. The aim of this study was to investigate the dynamics of miRNA-mRNA regulatory networks during exercise and the subsequent recovery period. RESULTS: Here we monitored the transcriptome changes using microarray analysis of the w...

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Autores principales: Tonevitsky, Alexander G, Maltseva, Diana V, Abbasi, Asghar, Samatov, Timur R, Sakharov, Dmitry A, Shkurnikov, Maxim U, Lebedev, Alexey E, Galatenko, Vladimir V, Grigoriev, Anatoly I, Northoff, Hinnak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681679/
https://www.ncbi.nlm.nih.gov/pubmed/24219008
http://dx.doi.org/10.1186/1472-6793-13-9
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author Tonevitsky, Alexander G
Maltseva, Diana V
Abbasi, Asghar
Samatov, Timur R
Sakharov, Dmitry A
Shkurnikov, Maxim U
Lebedev, Alexey E
Galatenko, Vladimir V
Grigoriev, Anatoly I
Northoff, Hinnak
author_facet Tonevitsky, Alexander G
Maltseva, Diana V
Abbasi, Asghar
Samatov, Timur R
Sakharov, Dmitry A
Shkurnikov, Maxim U
Lebedev, Alexey E
Galatenko, Vladimir V
Grigoriev, Anatoly I
Northoff, Hinnak
author_sort Tonevitsky, Alexander G
collection PubMed
description BACKGROUND: MiRNAs are essential mediators of many biological processes. The aim of this study was to investigate the dynamics of miRNA-mRNA regulatory networks during exercise and the subsequent recovery period. RESULTS: Here we monitored the transcriptome changes using microarray analysis of the whole blood of eight highly trained athletes before and after 30 min of moderate exercise followed by 30 min and 60 min of recovery period. We combined expression profiling and bioinformatics and analysed metabolic pathways enriched with differentially expressed mRNAs and mRNAs which are known to be validated targets of differentially expressed miRNAs. Finally we revealed four dynamically regulated networks comprising differentially expressed miRNAs and their known target mRNAs with anti-correlated expression profiles over time. The data suggest that hsa-miR-21-5p regulated TGFBR3, PDGFD and PPM1L mRNAs. Hsa-miR-24-2-5p was likely to be responsible for MYC and KCNJ2 genes and hsa-miR-27a-5p for ST3GAL6. The targets of hsa-miR-181a-5p included ROPN1L and SLC37A3. All these mRNAs are involved in processes highly relevant to exercise response, including immune function, apoptosis, membrane traffic of proteins and transcription regulation. CONCLUSIONS: We have identified metabolic pathways involved in response to exercise and revealed four miRNA-mRNA networks dynamically regulated following exercise. This work is the first study to monitor miRNAs and mRNAs in parallel into the recovery period. The results provide a novel insight into the regulatory role of miRNAs in stress adaptation.
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spelling pubmed-36816792013-06-14 Dynamically regulated miRNA-mRNA networks revealed by exercise Tonevitsky, Alexander G Maltseva, Diana V Abbasi, Asghar Samatov, Timur R Sakharov, Dmitry A Shkurnikov, Maxim U Lebedev, Alexey E Galatenko, Vladimir V Grigoriev, Anatoly I Northoff, Hinnak BMC Physiol Research Article BACKGROUND: MiRNAs are essential mediators of many biological processes. The aim of this study was to investigate the dynamics of miRNA-mRNA regulatory networks during exercise and the subsequent recovery period. RESULTS: Here we monitored the transcriptome changes using microarray analysis of the whole blood of eight highly trained athletes before and after 30 min of moderate exercise followed by 30 min and 60 min of recovery period. We combined expression profiling and bioinformatics and analysed metabolic pathways enriched with differentially expressed mRNAs and mRNAs which are known to be validated targets of differentially expressed miRNAs. Finally we revealed four dynamically regulated networks comprising differentially expressed miRNAs and their known target mRNAs with anti-correlated expression profiles over time. The data suggest that hsa-miR-21-5p regulated TGFBR3, PDGFD and PPM1L mRNAs. Hsa-miR-24-2-5p was likely to be responsible for MYC and KCNJ2 genes and hsa-miR-27a-5p for ST3GAL6. The targets of hsa-miR-181a-5p included ROPN1L and SLC37A3. All these mRNAs are involved in processes highly relevant to exercise response, including immune function, apoptosis, membrane traffic of proteins and transcription regulation. CONCLUSIONS: We have identified metabolic pathways involved in response to exercise and revealed four miRNA-mRNA networks dynamically regulated following exercise. This work is the first study to monitor miRNAs and mRNAs in parallel into the recovery period. The results provide a novel insight into the regulatory role of miRNAs in stress adaptation. BioMed Central 2013-06-07 /pmc/articles/PMC3681679/ /pubmed/24219008 http://dx.doi.org/10.1186/1472-6793-13-9 Text en Copyright © 2013 Tonevitsky et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tonevitsky, Alexander G
Maltseva, Diana V
Abbasi, Asghar
Samatov, Timur R
Sakharov, Dmitry A
Shkurnikov, Maxim U
Lebedev, Alexey E
Galatenko, Vladimir V
Grigoriev, Anatoly I
Northoff, Hinnak
Dynamically regulated miRNA-mRNA networks revealed by exercise
title Dynamically regulated miRNA-mRNA networks revealed by exercise
title_full Dynamically regulated miRNA-mRNA networks revealed by exercise
title_fullStr Dynamically regulated miRNA-mRNA networks revealed by exercise
title_full_unstemmed Dynamically regulated miRNA-mRNA networks revealed by exercise
title_short Dynamically regulated miRNA-mRNA networks revealed by exercise
title_sort dynamically regulated mirna-mrna networks revealed by exercise
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681679/
https://www.ncbi.nlm.nih.gov/pubmed/24219008
http://dx.doi.org/10.1186/1472-6793-13-9
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