Wu Yuting, Liu Xiao, Fan Yonghui, Zuo Hao, Niu Xiaoyu, Zuo Bo, Xu Zaiyan
Key Laboratory of Swine Genetics and Breeding of the Ministry of Agriculture and Rural Afairs, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Key Laboratory of Agriculture Animal Genetics, Breeding and Reproduction of the Ministry of Education, Huazhong Agricultural University, Wuhan 430070, China.
Cells. 2025 Mar 5;14(5):379. doi: 10.3390/cells14050379.
Non-coding genes, such as microRNA and lncRNA, which have been widely studied, play an important role in the regulatory network of skeletal muscle development. However, the functions and mechanisms of most non-coding RNAs in skeletal muscle regulatory networks are unclear. This study investigated the function and mechanism of in muscle growth and development. overexpression and interference tests were performed in C2C12 myoblasts and animal models. It was demonstrated that significantly promoted mouse muscle growth and development in vivo, while inhibited myoblast proliferation and promoted myoblast differentiation in vitro. Bioinformatics prediction using TargetScan for miRNA target identification and Bibiserv2 for potential miRNA-gene interaction analysis revealed a binding site in the sequence. The molecular mechanism of regulating muscle growth and development was studied by co-transfection experiment, luciferase reporter gene detection, RNA immunoprecipitation, and RNA pull-down. can directly bind to and AGO2 proteins and regulate the expression of target genes and by targeting , thereby regulating muscle growth and development. This study highlights that, as a novel regulator of myogenesis, regulates muscle growth and development by targeting .
非编码基因,如已被广泛研究的微小RNA(microRNA)和长链非编码RNA(lncRNA),在骨骼肌发育的调控网络中发挥着重要作用。然而,大多数非编码RNA在骨骼肌调控网络中的功能和机制尚不清楚。本研究调查了[具体基因名称]在肌肉生长发育中的功能和机制。在C2C12成肌细胞和动物模型中进行了[具体基因名称]的过表达和干扰试验。结果表明,[具体基因名称]在体内显著促进小鼠肌肉生长发育,而在体外抑制成肌细胞增殖并促进成肌细胞分化。使用TargetScan进行miRNA靶标鉴定以及使用Bibiserv2进行潜在的miRNA-基因相互作用分析的生物信息学预测揭示了[具体基因名称]序列中的一个[具体结合位点名称]结合位点。通过共转染实验、荧光素酶报告基因检测、RNA免疫沉淀和RNA下拉实验研究了[具体基因名称]调节肌肉生长发育的分子机制。[具体基因名称]可以直接与[具体蛋白质名称]和AGO2蛋白结合,并通过靶向[具体基因名称]调节[具体靶基因名称1]和[具体靶基因名称2]的表达,从而调节肌肉生长发育。本研究强调,作为一种新型的肌生成调节因子,[具体基因名称]通过靶向[具体基因名称]调节肌肉生长发育。