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Expression profiling and functional characterization of miR-192 throughout sheep skeletal muscle development

机译:整个绵羊骨骼肌发育过程中miR-192的表达谱和功能表征

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MicroRNAs (miRNAs) are evolutionarily conserved, small, non-coding RNAs that have emerged as key regulators of myogenesis. Here, we examined the miRNA expression profiles of developing sheep skeletal muscle using a deep sequencing approach. We detected 2,396 miRNAs in the sheep skeletal muscle tissues. Of these, miR-192 was found to be up-regulated in prenatal skeletal muscle, but was down-regulated postnatally. MiR-192 expression also decreased during the myogenic differentiation of sheep satellite cells (SCs). MiR-192 overexpression significantly attenuated SCs myogenic differentiation but promoted SCs proliferation, whereas miR-192 inhibition enhanced SCs differentiation but suppressed SCs proliferation. We found that miR-192 targeted retinoblastoma 1 (RB1), a known regulator of myogenesis. Furthermore, knockdown of RB1 in cultured cells significantly inhibited SCs myogenic differentiation but accelerated SCs proliferation, confirming the role of RB1 in myogenesis. Taken together, our findings enrich the ovine miRNA database, and outline the miRNA transcriptome of sheep during skeletal muscle development. Moreover, we show that miR-192 affects SCs proliferation and myogenic differentiation via down-regulation of RB1.
机译:MicroRNA(miRNA)是进化保守的小非编码RNA,已成为肌生成的关键调节因子。在这里,我们使用深度测序方法检查了发育中的绵羊骨骼肌的miRNA表达谱。我们在绵羊骨骼肌组织中检测到2396个miRNA。其中,发现miR-192在产前骨骼肌中被上调,但在产后却被下调。在绵羊卫星细胞(SCs)的成肌分化过程中,MiR-192表达也降低。 MiR-192的过表达显着减弱了SC的肌源性分化,但促进了SC的增殖,而miR-192的抑制作用则增强了SC的分化,但抑制了SC的增殖。我们发现miR-192靶向成视网膜细胞瘤1(RB1),是已知的肌生成调节剂。此外,在培养细胞中敲低RB1可以显着抑制SCs的成肌分化,但可以促进SCs的增殖,从而证实RB1在肌发生中的作用。综上所述,我们的发现丰富了绵羊miRNA数据库,并概述了骨骼肌发育过程中绵羊的miRNA转录组。此外,我们表明miR-192通过下调RB1影响SC的增殖和肌源性分化。

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