Ma Zhiyuan, Sun Xiaorui, Xu Dequan, Xiong Yuanzhu, Zuo Bo
Key Laboratory of Swine Genetics and Breeding of the Ministry of Agriculture, College of Animal Sciences, Huazhong Agricultural University, Wuhan 430070, China.
Key Laboratory of Swine Genetics and Breeding of the Ministry of Agriculture, College of Animal Sciences, Huazhong Agricultural University, Wuhan 430070, China.
Biochem Biophys Res Commun. 2015 Nov 27;467(4):670-5. doi: 10.1016/j.bbrc.2015.10.086. Epub 2015 Oct 21.
Myogenesis is a complex process including myoblast proliferation, differentiation and myotube formation and is controlled by myogenic regulatory factors (MRFs), MyoD, MyoG, Myf5 and Myf6 (also known as MRF4). MicroRNA is a kind of ∼22 nt-long non-coding small RNAs, and act as key transcriptional or post-transcriptional regulators of gene expression. Identification of miRNAs involved in the regulation of muscle genes could improve our understanding of myogenesis process. In this study, we investigated the regulation of Myf6 gene by miRNAs. We showed that miR-374b specifically bound to the 3'untranslated region (UTR) of Myf6 and down-regulated the expression of Myf6 gene at both mRNA and protein level. Furthermore, miR-374b is ubiquitously expressed in the tissues of adult C57BL6 mouse, and the mRNA abundance increases first and then decreases during C2C12 myoblasts differentiation. Over-expression of miR-374b impaired C2C12 cell differentiation, while inhibiting miR-374b expression by 2'-O-methyl antisense oligonucleotides promoted C2C12 cell differentiation. Taken together, our findings identified miR-374b directly targets Myf6 and negatively regulates myogenesis.
成肌作用是一个复杂的过程,包括成肌细胞增殖、分化和肌管形成,并受成肌调节因子(MRFs)、肌分化抗原(MyoD)、肌细胞生成素(MyoG)、肌原性决定因子5(Myf5)和肌原性决定因子6(也称为MRF4)的控制。微小RNA是一类长度约为22个核苷酸的非编码小RNA,是基因表达的关键转录或转录后调节因子。鉴定参与肌肉基因调控的微小RNA可以增进我们对成肌过程的理解。在本研究中,我们研究了微小RNA对Myf6基因的调控作用。我们发现,miR-374b特异性结合Myf6的3'非翻译区(UTR),并在mRNA和蛋白质水平下调Myf6基因的表达。此外,miR-374b在成年C57BL6小鼠组织中广泛表达,且在C2C12成肌细胞分化过程中mRNA丰度先升高后降低。过表达miR-374b会损害C2C12细胞分化,而用2'-O-甲基反义寡核苷酸抑制miR-374b表达则会促进C2C12细胞分化。综上所述,我们的研究结果表明miR-374b直接靶向Myf6并对成肌作用起负调控作用。
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