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The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly
The molecular events that modulate chromatin structure during skeletal muscle differentiation are still poorly understood. We report in this paper that expression of the H3-K4 histone methyltransferase Set7 is increased when myoblasts differentiate into myotubes and is required for skeletal muscle d...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160588/ https://www.ncbi.nlm.nih.gov/pubmed/21859860 http://dx.doi.org/10.1083/jcb.201010090 |
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author | Tao, Yazhong Neppl, Ronald L. Huang, Zhan-Peng Chen, Jianfu Tang, Ru-Hang Cao, Ru Zhang, Yi Jin, Suk-Won Wang, Da-Zhi |
author_facet | Tao, Yazhong Neppl, Ronald L. Huang, Zhan-Peng Chen, Jianfu Tang, Ru-Hang Cao, Ru Zhang, Yi Jin, Suk-Won Wang, Da-Zhi |
author_sort | Tao, Yazhong |
collection | PubMed |
description | The molecular events that modulate chromatin structure during skeletal muscle differentiation are still poorly understood. We report in this paper that expression of the H3-K4 histone methyltransferase Set7 is increased when myoblasts differentiate into myotubes and is required for skeletal muscle development, expression of muscle contractile proteins, and myofibril assembly. Knockdown of Set7 or expression of a dominant-negative Set7 mutant impairs skeletal muscle differentiation, accompanied by a decrease in levels of histone monomethylation (H3-K4me1). Set7 directly interacts with MyoD to enhance expression of muscle differentiation genes. Expression of myocyte enhancer factor 2 and genes encoding contractile proteins is decreased in Set7 knockdown myocytes. Furthermore, we demonstrate that Set7 also activates muscle gene expression by precluding Suv39h1-mediated H3-K9 methylation on the promoters of myogenic differentiation genes. Together, our experiments define a biological function for Set7 in muscle differentiation and provide a molecular mechanism by which Set7 modulates myogenic transcription factors during muscle differentiation. |
format | Online Article Text |
id | pubmed-3160588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31605882012-02-22 The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly Tao, Yazhong Neppl, Ronald L. Huang, Zhan-Peng Chen, Jianfu Tang, Ru-Hang Cao, Ru Zhang, Yi Jin, Suk-Won Wang, Da-Zhi J Cell Biol Research Articles The molecular events that modulate chromatin structure during skeletal muscle differentiation are still poorly understood. We report in this paper that expression of the H3-K4 histone methyltransferase Set7 is increased when myoblasts differentiate into myotubes and is required for skeletal muscle development, expression of muscle contractile proteins, and myofibril assembly. Knockdown of Set7 or expression of a dominant-negative Set7 mutant impairs skeletal muscle differentiation, accompanied by a decrease in levels of histone monomethylation (H3-K4me1). Set7 directly interacts with MyoD to enhance expression of muscle differentiation genes. Expression of myocyte enhancer factor 2 and genes encoding contractile proteins is decreased in Set7 knockdown myocytes. Furthermore, we demonstrate that Set7 also activates muscle gene expression by precluding Suv39h1-mediated H3-K9 methylation on the promoters of myogenic differentiation genes. Together, our experiments define a biological function for Set7 in muscle differentiation and provide a molecular mechanism by which Set7 modulates myogenic transcription factors during muscle differentiation. The Rockefeller University Press 2011-08-22 /pmc/articles/PMC3160588/ /pubmed/21859860 http://dx.doi.org/10.1083/jcb.201010090 Text en © 2011 Tao et al. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/ (https://creativecommons.org/licenses/by-nc-sa/3.0/) ). |
spellingShingle | Research Articles Tao, Yazhong Neppl, Ronald L. Huang, Zhan-Peng Chen, Jianfu Tang, Ru-Hang Cao, Ru Zhang, Yi Jin, Suk-Won Wang, Da-Zhi The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title | The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title_full | The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title_fullStr | The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title_full_unstemmed | The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title_short | The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly |
title_sort | histone methyltransferase set7/9 promotes myoblast differentiation and myofibril assembly |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160588/ https://www.ncbi.nlm.nih.gov/pubmed/21859860 http://dx.doi.org/10.1083/jcb.201010090 |
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