| First Author | Iio H | Year | 2021 |
| Journal | Biochem Biophys Res Commun | Volume | 534 |
| Pages | 79-85 | PubMed ID | 33310192 |
| Mgi Jnum | J:305702 | Mgi Id | MGI:6705284 |
| Doi | 10.1016/j.bbrc.2020.11.116 | Citation | Iio H, et al. (2021) DNA maintenance methylation enzyme Dnmt1 in satellite cells is essential for muscle regeneration. Biochem Biophys Res Commun 534:79-85 |
| abstractText | Epigenetic transcriptional regulation is essential for the differentiation of various types of cells, including skeletal muscle cells. DNA methyltransferase 1 (Dnmt1) is responsible for maintenance of DNA methylation patterns via cell division. Here, we investigated the relationship between Dnmt1 and skeletal muscle regeneration. We found that Dnmt1 is upregulated in muscles during regeneration. To assess the role of Dnmt1 in satellite cells during regeneration, we performed conditional knockout (cKO) of Dnmt1 specifically in skeletal muscle satellite cells using Pax7(CreERT2) mice and Dnmt1 flox mice. Muscle weight and the cross-sectional area after injury were significantly lower in Dnmt1 cKO mice than in control mice. RNA sequencing analysis revealed upregulation of genes involved in cell adhesion and apoptosis in satellite cells from cKO mice. Moreover, satellite cells cultured from cKO mice exhibited a reduced number of cells. These results suggest that Dnmt1 is an essential factor for muscle regeneration and is involved in positive regulation of satellite cell number. |
