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Long non-coding RNA Linc-RAM enhances myogenic differentiation by interacting with MyoD.
- Source :
-
Nature communications [Nat Commun] 2017 Jan 16; Vol. 8, pp. 14016. Date of Electronic Publication: 2017 Jan 16. - Publication Year :
- 2017
-
Abstract
- Long non-coding RNAs (lncRNAs) are important regulators of diverse biological processes. Here we report on functional identification and characterization of a novel long intergenic non-coding RNA with MyoD-regulated and skeletal muscle-restricted expression that promotes the activation of the myogenic program, and is therefore termed Linc-RAM (Linc-RNA Activator of Myogenesis). Linc-RAM is transcribed from an intergenic region of myogenic cells and its expression is upregulated during myogenesis. Notably, in vivo functional studies show that Linc-RAM knockout mice display impaired muscle regeneration due to the differentiation defect of satellite cells. Mechanistically, Linc-RAM regulates expression of myogenic genes by directly binding MyoD, which in turn promotes the assembly of the MyoD-Baf60c-Brg1 complex on the regulatory elements of target genes. Collectively, our findings reveal the functional role and molecular mechanism of a lineage-specific Linc-RAM as a regulatory lncRNA required for tissues-specific chromatin remodelling and gene expression.
- Subjects :
- Animals
Chromosomal Proteins, Non-Histone genetics
Chromosomal Proteins, Non-Histone metabolism
DNA Helicases genetics
DNA Helicases metabolism
Mice
Mice, Knockout
Muscle Proteins genetics
Muscle Proteins metabolism
Muscle, Skeletal growth & development
Muscle, Skeletal metabolism
MyoD Protein genetics
Myoblasts cytology
Nuclear Proteins genetics
Nuclear Proteins metabolism
Protein Binding
RNA, Long Noncoding genetics
Transcription Factors genetics
Transcription Factors metabolism
Muscle Development
MyoD Protein metabolism
Myoblasts metabolism
RNA, Long Noncoding metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 28091529
- Full Text :
- https://doi.org/10.1038/ncomms14016