Cargando…
Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse
Although skeletal muscle metabolism is a well-studied physiological process, little is known about how it is regulated at the transcriptional level. The myogenic transcription factor myogenin is required for skeletal muscle development during embryonic and fetal life, but myogenin's role in adu...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962629/ https://www.ncbi.nlm.nih.gov/pubmed/21042574 http://dx.doi.org/10.1371/journal.pone.0013535 |
_version_ | 1782189195949768704 |
---|---|
author | Flynn, Jesse M. Meadows, Eric Fiorotto, Marta Klein, William H. |
author_facet | Flynn, Jesse M. Meadows, Eric Fiorotto, Marta Klein, William H. |
author_sort | Flynn, Jesse M. |
collection | PubMed |
description | Although skeletal muscle metabolism is a well-studied physiological process, little is known about how it is regulated at the transcriptional level. The myogenic transcription factor myogenin is required for skeletal muscle development during embryonic and fetal life, but myogenin's role in adult skeletal muscle is unclear. We sought to determine myogenin's function in adult muscle metabolism. A Myog conditional allele and Cre-ER transgene were used to delete Myog in adult mice. Mice were analyzed for exercise capacity by involuntary treadmill running. To assess oxidative and glycolytic metabolism, we performed indirect calorimetry, monitored blood glucose and lactate levels, and performed histochemical analyses on muscle fibers. Surprisingly, we found that Myog-deleted mice performed significantly better than controls in high- and low-intensity treadmill running. This enhanced exercise capacity was due to more efficient oxidative metabolism during low- and high-intensity exercise and more efficient glycolytic metabolism during high-intensity exercise. Furthermore, Myog-deleted mice had an enhanced response to long-term voluntary exercise training on running wheels. We identified several candidate genes whose expression was altered in exercise-stressed muscle of mice lacking myogenin. The results suggest that myogenin plays a critical role as a high-level transcriptional regulator to control the energy balance between aerobic and anaerobic metabolism in adult skeletal muscle. |
format | Text |
id | pubmed-2962629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29626292010-11-01 Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse Flynn, Jesse M. Meadows, Eric Fiorotto, Marta Klein, William H. PLoS One Research Article Although skeletal muscle metabolism is a well-studied physiological process, little is known about how it is regulated at the transcriptional level. The myogenic transcription factor myogenin is required for skeletal muscle development during embryonic and fetal life, but myogenin's role in adult skeletal muscle is unclear. We sought to determine myogenin's function in adult muscle metabolism. A Myog conditional allele and Cre-ER transgene were used to delete Myog in adult mice. Mice were analyzed for exercise capacity by involuntary treadmill running. To assess oxidative and glycolytic metabolism, we performed indirect calorimetry, monitored blood glucose and lactate levels, and performed histochemical analyses on muscle fibers. Surprisingly, we found that Myog-deleted mice performed significantly better than controls in high- and low-intensity treadmill running. This enhanced exercise capacity was due to more efficient oxidative metabolism during low- and high-intensity exercise and more efficient glycolytic metabolism during high-intensity exercise. Furthermore, Myog-deleted mice had an enhanced response to long-term voluntary exercise training on running wheels. We identified several candidate genes whose expression was altered in exercise-stressed muscle of mice lacking myogenin. The results suggest that myogenin plays a critical role as a high-level transcriptional regulator to control the energy balance between aerobic and anaerobic metabolism in adult skeletal muscle. Public Library of Science 2010-10-22 /pmc/articles/PMC2962629/ /pubmed/21042574 http://dx.doi.org/10.1371/journal.pone.0013535 Text en Flynn 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 Flynn, Jesse M. Meadows, Eric Fiorotto, Marta Klein, William H. Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title | Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title_full | Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title_fullStr | Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title_full_unstemmed | Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title_short | Myogenin Regulates Exercise Capacity and Skeletal Muscle Metabolism in the Adult Mouse |
title_sort | myogenin regulates exercise capacity and skeletal muscle metabolism in the adult mouse |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962629/ https://www.ncbi.nlm.nih.gov/pubmed/21042574 http://dx.doi.org/10.1371/journal.pone.0013535 |
work_keys_str_mv | AT flynnjessem myogeninregulatesexercisecapacityandskeletalmusclemetabolismintheadultmouse AT meadowseric myogeninregulatesexercisecapacityandskeletalmusclemetabolismintheadultmouse AT fiorottomarta myogeninregulatesexercisecapacityandskeletalmusclemetabolismintheadultmouse AT kleinwilliamh myogeninregulatesexercisecapacityandskeletalmusclemetabolismintheadultmouse |