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Linc-YY1 promotes myogenic differentiation and muscle regeneration through an interaction with the transcription factor YY1

机译:Linc-YY1通过与转录因子YY1相互作用促进成肌分化和肌肉再生

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摘要

Little is known how lincRNAs are involved in skeletal myogenesis. Here we describe the discovery of Linc-YY1 from the promoter of the transcription factor (TF) Yin Yang 1 (YY1) gene. We demonstrate that Linc-YY1 is dynamically regulated during myogenesis in vitro and in vivo. Gain or loss of function of Linc-YY1 in C2C12 myoblasts or muscle satellite cells alters myogenic differentiation and in injured muscles has an impact on the course of regeneration. Linc-YY1 interacts with YY1 through its middle domain, to evict YY1/Polycomb repressive complex (PRC2) from target promoters, thus activating the gene expression in trans. In addition, Linc-YY1 also regulates PRC2-independent function of YY1. Finally, we identify a human Linc-YY1 orthologue with conserved function and show that many human and mouse TF genes are associated with lincRNAs that may modulate their activity. Altogether, we show that Linc-YY1 regulates skeletal myogenesis and uncover a previously unappreciated mechanism of gene regulation by lincRNA.
机译:lincRNAs如何参与骨骼肌发生机制还知之甚少。在这里,我们从转录因子(TF)阴阳1(YY1)基因的启动子描述了Linc-YY1的发现。我们证明Linc-YY1在体外和体内的成肌过程中被动态调节。 C2C12成肌细胞或肌肉卫星细胞中Linc-YY1功能的获得或丧失会改变成肌分化,并且在受伤的肌肉中会对再生过程产生影响。 Linc-YY1通过其中间结构域与YY1相互作用,以从靶标启动子中驱逐YY1 / Polycomb阻抑复合物(PRC2),从而激活反式基因表达。此外,Linc-YY1还调节YY1的PRC2独立功能。最后,我们确定了具有保守功能的人Linc-YY1直向同源物,并显示许多人和小鼠TF基因与可能调节其活性的lincRNA相关。总而言之,我们表明Linc-YY1调节骨骼肌的发生,并揭示出lincRNA调控基因的机制。

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