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调节肌肉特异性微小RNA表达的生肌因子。

Myogenic factors that regulate expression of muscle-specific microRNAs.

作者信息

Rao Prakash K, Kumar Roshan M, Farkhondeh Mina, Baskerville Scott, Lodish Harvey F

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Jun 6;103(23):8721-6. doi: 10.1073/pnas.0602831103. Epub 2006 May 26.

Abstract

Since their discovery as key regulators of early animal development, microRNAs now are recognized as widespread regulators of gene expression. Despite their abundance, little is known regarding the regulation of microRNA biogenesis. We show that three highly conserved muscle-specific microRNAs, miR-1, miR-133 and miR-206, are robustly induced during the myoblast-myotube transition, both in primary human myoblasts and in the mouse mesenchymal C2C12 stem cell line. These microRNAs were not induced during osteogenic conversion of C2C12 cells. Moreover, both loci encoding miR-1, miR-1-1, and miR-1-2, and two of the three encoding miR-133, miR-133a-1 and miR-133a-2, are strongly induced during myogenesis. Some of the induced microRNAs are in intergenic regions, whereas two are transcribed in the opposite direction to the nonmuscle-specific gene in which they are embedded. By using CHIP analysis, we demonstrate that the myogenic factors Myogenin and MyoD bind to regions upstream of these microRNAs and, therefore, are likely to regulate their expression. Because miR-1 and miR-206 are predicted to repress similar mRNA targets, our work suggests that induction of these microRNAs is important in regulating the expression of muscle-specific proteins.

摘要

自被发现作为动物早期发育的关键调节因子以来,微小RNA如今被公认为是广泛存在的基因表达调节因子。尽管它们数量众多,但关于微小RNA生物合成的调节却知之甚少。我们发现,在原代人成肌细胞和小鼠间充质C2C12干细胞系的成肌细胞-肌管转变过程中,三种高度保守的肌肉特异性微小RNA,即miR-1、miR-133和miR-206,均被强烈诱导。在C2C12细胞向成骨细胞转化的过程中,这些微小RNA并未被诱导。此外,编码miR-1的两个基因座,即miR-1-1和miR-1-2,以及编码miR-133的三个基因座中的两个,即miR-133a-1和miR-133a-2,在肌肉生成过程中均被强烈诱导。一些被诱导的微小RNA位于基因间区域,而另外两个则以与其所嵌入的非肌肉特异性基因相反的方向转录。通过染色质免疫沉淀(CHIP)分析,我们证明了成肌因子肌细胞生成素(Myogenin)和肌分化抗原(MyoD)与这些微小RNA上游区域结合,因此可能调节它们的表达。由于预测miR-1和miR-206会抑制相似的mRNA靶点,我们的研究表明,这些微小RNA的诱导在调节肌肉特异性蛋白的表达中具有重要作用。

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