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HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs

Fiber type-specific programs controlled by the transcription factor MEF2 dictate muscle functionality. Here, we show that HDAC4, a potent MEF2 inhibitor, is predominantly localized to the nuclei in fast/glycolytic fibers in contrast to the sarcoplasm in slow/oxidative fibers. The cytoplasmic localiz...

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Autores principales: Cohen, Todd J., Choi, Moon-Chang, Kapur, Meghan, Lira, Vitor A., Yan, Zhen, Yao, Tso-Pang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400309/
https://www.ncbi.nlm.nih.gov/pubmed/25728750
http://dx.doi.org/10.14348/molcells.2015.2278
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author Cohen, Todd J.
Choi, Moon-Chang
Kapur, Meghan
Lira, Vitor A.
Yan, Zhen
Yao, Tso-Pang
author_facet Cohen, Todd J.
Choi, Moon-Chang
Kapur, Meghan
Lira, Vitor A.
Yan, Zhen
Yao, Tso-Pang
author_sort Cohen, Todd J.
collection PubMed
description Fiber type-specific programs controlled by the transcription factor MEF2 dictate muscle functionality. Here, we show that HDAC4, a potent MEF2 inhibitor, is predominantly localized to the nuclei in fast/glycolytic fibers in contrast to the sarcoplasm in slow/oxidative fibers. The cytoplasmic localization is associated with HDAC4 hyper-phosphorylation in slow/oxidative-fibers. Genetic reprogramming of fast/glycolytic fibers to oxidative fibers by active CaMKII or calcineurin leads to increased HDAC4 phosphorylation, HDAC4 nuclear export, and an increase in markers associated with oxidative fibers. Indeed, HDAC4 represses the MEF2-dependent, PGC-1α-mediated oxidative metabolic gene program. Thus differential phosphorylation and localization of HDAC4 contributes to establishing fiber type-specific transcriptional programs.
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spelling pubmed-44003092015-04-24 HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs Cohen, Todd J. Choi, Moon-Chang Kapur, Meghan Lira, Vitor A. Yan, Zhen Yao, Tso-Pang Mol Cells Articles Fiber type-specific programs controlled by the transcription factor MEF2 dictate muscle functionality. Here, we show that HDAC4, a potent MEF2 inhibitor, is predominantly localized to the nuclei in fast/glycolytic fibers in contrast to the sarcoplasm in slow/oxidative fibers. The cytoplasmic localization is associated with HDAC4 hyper-phosphorylation in slow/oxidative-fibers. Genetic reprogramming of fast/glycolytic fibers to oxidative fibers by active CaMKII or calcineurin leads to increased HDAC4 phosphorylation, HDAC4 nuclear export, and an increase in markers associated with oxidative fibers. Indeed, HDAC4 represses the MEF2-dependent, PGC-1α-mediated oxidative metabolic gene program. Thus differential phosphorylation and localization of HDAC4 contributes to establishing fiber type-specific transcriptional programs. Korean Society for Molecular and Cellular Biology 2015-04 2015-02-25 /pmc/articles/PMC4400309/ /pubmed/25728750 http://dx.doi.org/10.14348/molcells.2015.2278 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Articles
Cohen, Todd J.
Choi, Moon-Chang
Kapur, Meghan
Lira, Vitor A.
Yan, Zhen
Yao, Tso-Pang
HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title_full HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title_fullStr HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title_full_unstemmed HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title_short HDAC4 Regulates Muscle Fiber Type-Specific Gene Expression Programs
title_sort hdac4 regulates muscle fiber type-specific gene expression programs
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400309/
https://www.ncbi.nlm.nih.gov/pubmed/25728750
http://dx.doi.org/10.14348/molcells.2015.2278
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