Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration

Satellite stem cell availability and high regenerative capacity have made them an ideal therapeutic approach for muscular dystrophies and neuromuscular diseases. Adult satellite stem cells remain in a quiescent state and become activated upon muscular injury. A series of molecular mechanisms succeed...

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Autores principales: Magdaleena Naemi Mbadhi, Jun-ming Tang, Jing-xuan Zhang
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/2ceae69514a34778bb049b0324633a9c
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spelling oai:doaj.org-article:2ceae69514a34778bb049b0324633a9c2021-12-03T05:49:00ZHistone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration2296-634X10.3389/fcell.2021.759237https://doaj.org/article/2ceae69514a34778bb049b0324633a9c2021-12-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.759237/fullhttps://doaj.org/toc/2296-634XSatellite stem cell availability and high regenerative capacity have made them an ideal therapeutic approach for muscular dystrophies and neuromuscular diseases. Adult satellite stem cells remain in a quiescent state and become activated upon muscular injury. A series of molecular mechanisms succeed under the control of epigenetic regulation and various myogenic regulatory transcription factors myogenic regulatory factors, leading to their differentiation into skeletal muscles. The regulation of MRFs via various epigenetic factors, including DNA methylation, histone modification, and non-coding RNA, determine the fate of myogenesis. Furthermore, the development of histone deacetylation inhibitors (HDACi) has shown promising benefits in their use in clinical trials of muscular diseases. However, the complete application of using satellite stem cells in the clinic is still not achieved. While therapeutic advancements in the use of HDACi in clinical trials have emerged, histone methylation modulations and the long non-coding RNA (lncRNA) are still under study. A comprehensive understanding of these other significant epigenetic modulations is still incomplete. This review aims to discuss some of the current studies on these two significant epigenetic modulations, histone methylation and lncRNA, as potential epigenetic targets in skeletal muscle regeneration. Understanding the mechanisms that initiate myoblast differentiation from its proliferative state to generate new muscle fibres will provide valuable information to advance the field of regenerative medicine and stem cell transplant.Magdaleena Naemi MbadhiJun-ming TangJing-xuan ZhangFrontiers Media S.A.articleepigeneticsskeletal muscleskeletal muscle regenerationhistone methylationlncRNAssatellite stem cellsBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic epigenetics
skeletal muscle
skeletal muscle regeneration
histone methylation
lncRNAs
satellite stem cells
Biology (General)
QH301-705.5
spellingShingle epigenetics
skeletal muscle
skeletal muscle regeneration
histone methylation
lncRNAs
satellite stem cells
Biology (General)
QH301-705.5
Magdaleena Naemi Mbadhi
Jun-ming Tang
Jing-xuan Zhang
Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
description Satellite stem cell availability and high regenerative capacity have made them an ideal therapeutic approach for muscular dystrophies and neuromuscular diseases. Adult satellite stem cells remain in a quiescent state and become activated upon muscular injury. A series of molecular mechanisms succeed under the control of epigenetic regulation and various myogenic regulatory transcription factors myogenic regulatory factors, leading to their differentiation into skeletal muscles. The regulation of MRFs via various epigenetic factors, including DNA methylation, histone modification, and non-coding RNA, determine the fate of myogenesis. Furthermore, the development of histone deacetylation inhibitors (HDACi) has shown promising benefits in their use in clinical trials of muscular diseases. However, the complete application of using satellite stem cells in the clinic is still not achieved. While therapeutic advancements in the use of HDACi in clinical trials have emerged, histone methylation modulations and the long non-coding RNA (lncRNA) are still under study. A comprehensive understanding of these other significant epigenetic modulations is still incomplete. This review aims to discuss some of the current studies on these two significant epigenetic modulations, histone methylation and lncRNA, as potential epigenetic targets in skeletal muscle regeneration. Understanding the mechanisms that initiate myoblast differentiation from its proliferative state to generate new muscle fibres will provide valuable information to advance the field of regenerative medicine and stem cell transplant.
format article
author Magdaleena Naemi Mbadhi
Jun-ming Tang
Jing-xuan Zhang
author_facet Magdaleena Naemi Mbadhi
Jun-ming Tang
Jing-xuan Zhang
author_sort Magdaleena Naemi Mbadhi
title Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
title_short Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
title_full Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
title_fullStr Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
title_full_unstemmed Histone Lysine Methylation and Long Non-Coding RNA: The New Target Players in Skeletal Muscle Cell Regeneration
title_sort histone lysine methylation and long non-coding rna: the new target players in skeletal muscle cell regeneration
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/2ceae69514a34778bb049b0324633a9c
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AT junmingtang histonelysinemethylationandlongnoncodingrnathenewtargetplayersinskeletalmusclecellregeneration
AT jingxuanzhang histonelysinemethylationandlongnoncodingrnathenewtargetplayersinskeletalmusclecellregeneration
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