Epigenetic regulation of satellite cell activation during muscle regeneration

被引:53
作者
Dilworth, F. Jeffrey [1 ,2 ]
Blais, Alexandre [3 ,4 ]
机构
[1] Ottawa Hosp Res Inst, Regenerat Med Program, Sprott Ctr Stem Cell Res, Ottawa, ON K1H 8L6, Canada
[2] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON K1H 8M5, Canada
[3] Ottawa Inst Syst Biol, Ottawa, ON K1H 8M5, Canada
[4] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
HISTONE H3 LYSINE-27; DNA METHYLATION; TRANSCRIPTION FACTORS; LINKS INFLAMMATION; GENE-EXPRESSION; STEM-CELL; CHROMATIN; RECRUITMENT; BINDING; PAX7;
D O I
10.1186/scrt59
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Satellite cells are a population of adult muscle stem cells that play a key role in mediating muscle regeneration. Activation of these quiescent stem cells in response to muscle injury involves modulating expression of multiple developmentally regulated genes, including mediators of the muscle-specific transcription program: Pax7, Myf5, MyoD and myogenin. Here we present evidence suggesting an essential role for the antagonistic Polycomb group and Trithorax group proteins in the epigenetic marking of muscle-specific genes to ensure proper temporal and spatial expression during muscle regeneration. The importance of Polycomb group and Trithorax group proteins in establishing chromatin structure at muscle-specific genes suggests that therapeutic modulation of their activity in satellite cells could represent a viable approach for repairing damaged muscle in muscular dystrophy.
引用
收藏
页数:8
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