| Literature DB >> 25686699 |
Lijun Wang1, Yu Zhao2, Xichen Bao3, Xihua Zhu3, Yvonne Ka-Yin Kwok2, Kun Sun4, Xiaona Chen2, Yongheng Huang5, Ralf Jauch5, Miguel A Esteban3, Hao Sun4, Huating Wang1.
Abstract
Emerging studies document the roles of long non-coding RNAs (LncRNAs) in regulating gene expression at chromatin level but relatively less is known how they regulate DNA methylation. Here we identify an lncRNA, Dum (developmental pluripotency-associated 2 (Dppa2) Upstream binding Muscle lncRNA) in skeletal myoblast cells. The expression of Dum is dynamically regulated during myogenesis in vitro and in vivo. It is also transcriptionally induced by MyoD binding upon myoblast differentiation. Functional analyses show that it promotes myoblast differentiation and damage-induced muscle regeneration. Mechanistically, Dum was found to silence its neighboring gene, Dppa2, in cis through recruiting Dnmt1, Dnmt3a and Dnmt3b. Furthermore, intrachromosomal looping between Dum locus and Dppa2 promoter is necessary for Dum/Dppa2 interaction. Collectively, we have identified a novel lncRNA that interacts with Dnmts to regulate myogenesis.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25686699 PMCID: PMC4349245 DOI: 10.1038/cr.2015.21
Source DB: PubMed Journal: Cell Res ISSN: 1001-0602 Impact factor: 25.617