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首页> 外文期刊>Nature Communications >Long non-coding RNA Linc-RAM enhances myogenic differentiation by interacting with MyoD
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Long non-coding RNA Linc-RAM enhances myogenic differentiation by interacting with MyoD

机译:长的非编码RNA Linc-RAM通过与MyoD相互作用增强肌原性分化

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摘要

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.
机译:长的非编码RNA(lncRNA)是多种生物过程的重要调节剂。在这里我们报告了新型的长基因间非编码RNA的功能鉴定和表征,该基因具有MyoD调节和骨骼肌限制性表达,可促进成肌程序的激活,因此被称为Linc-RAM(成肌Linc-RNA激活剂)。 Linc-RAM从成肌细胞的基因间区域转录,其表达在成肌过程中被上调。值得注意的是,体内功能研究表明,由于卫星细胞的分化缺陷,Linc-RAM基因敲除小鼠的肌肉再生受损。从机理上讲,Linc-RAM通过直接结合MyoD来调节成肌基因的表达,进而促进MyoD–Baf60c–Brg1复合体在靶基因调控元件上的组装。总的来说,我们的发现揭示了谱系特异性Linc-RAM作为组织特异性染色质重塑和基因表达所需的调控性lncRNA的功能作用和分子机制。

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