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miR-155 通过抑制 MEF2A 蛋白的表达来抑制骨骼肌分化。

miR-155 inhibits expression of the MEF2A protein to repress skeletal muscle differentiation.

机构信息

Department of Cardiology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115; Department of Cell and Developmental Biology, University of North Carolina, Chapel Hill, North Carolina 27599.

Department of Cardiology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Biol Chem. 2011 Oct 14;286(41):35339-35346. doi: 10.1074/jbc.M111.273276. Epub 2011 Aug 25.

Abstract

microRNAs (miRNAs) are 21-23-nucleotide non-coding RNAs. It has become more and more evident that this class of small RNAs plays critical roles in the regulation of gene expression at the post-transcriptional level. MEF2A is a member of the MEF2 (myogenic enhancer factor 2) family of transcription factors. Prior report showed that the 3'-untranslated region (3'-UTR) of the Mef2A gene mediated its repression; however, the molecular mechanism underlying this intriguing observation was unknown. Here, we report that MEF2A is repressed by miRNAs. We identify miR-155 as one of the primary miRNAs that significantly represses the expression of MEF2A. We show that knockdown of the Mef2A gene by siRNA impairs myoblast differentiation. Similarly, overexpression of miR-155 leads to the repression of endogenous MEF2A expression and the inhibition of myoblast differentiation. Most importantly, reintroduction of MEF2A in miR-155 overexpressed myoblasts was able to partially rescue the miR-155-induced myoblast differentiation defect. Our data therefore establish miR-155 as an important regulator of MEF2A expression and uncover its function in muscle gene expression and myogenic differentiation.

摘要

microRNAs (miRNAs) 是 21-23 个核苷酸的非编码 RNA。越来越明显的是,这类小 RNA 在转录后水平上对基因表达的调控起着关键作用。MEF2A 是 MEF2(肌增强因子 2)家族转录因子的成员。先前的报告表明,Mef2A 基因的 3'-非翻译区(3'-UTR)介导其抑制;然而,这一有趣观察结果背后的分子机制尚不清楚。在这里,我们报告 MEF2A 受到 miRNAs 的抑制。我们鉴定出 miR-155 是显著抑制 MEF2A 表达的主要 miRNAs 之一。我们表明,通过 siRNA 敲低 Mef2A 基因会损害成肌细胞分化。类似地,miR-155 的过表达导致内源性 MEF2A 表达的抑制和成肌细胞分化的抑制。最重要的是,在 miR-155 过表达的成肌细胞中重新引入 MEF2A 能够部分挽救 miR-155 诱导的成肌细胞分化缺陷。因此,我们的数据确立了 miR-155 作为 MEF2A 表达的重要调节剂,并揭示了它在肌肉基因表达和肌生成分化中的功能。

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