miR-377 Inhibits Proliferation and Differentiation of Bovine Skeletal Muscle Satellite Cells by Targeting FHL2

被引:9
|
作者
Zhu, Yun [1 ]
Li, Peng [1 ]
Dan, Xingang [1 ]
Kang, Xiaolong [1 ]
Ma, Yun [1 ]
Shi, Yuangang [1 ]
机构
[1] Ningxia Univ, Sch Agr, Helan Mt West Rd 489, Yinchuan 750021, Ningxia, Peoples R China
关键词
miR-377; skeletal muscle satellite cells; proliferation; differentiation; wnt/beta-catenin signaling; FHL2; LIM-ONLY PROTEIN; BETA-CATENIN; INTERACTS; PROGENITORS; ACTIVATION; EXPRESSION; GROWTH;
D O I
10.3390/genes13060947
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Non-coding RNAs, especially microRNAs (miRNAs), play an important role in skeletal muscle growth and development. miR-377 regulates many basic biological processes and plays a key role in tumor cell proliferation, migration and apoptosis. Nevertheless, the function of miR-377 during skeletal muscle development and how it regulates skeletal muscle satellite cells (SMSCs) remains unclear. In the present study, we proposed to elucidate the regulatory mechanism of miR-377 in the proliferation and differentiation of bovine primary SMSCs. Our results showed that miR-377 can significantly inhibit the proliferation of SMSCs. In addition, we found that miR-377 can reduce myotube formation and restrain skeletal myogenic differentiation. Moreover, the results obtained from the biosynthesis and dual luciferase experiments showed that FHL2 was the target gene of miR-377. We further probed the function of FHL2 in muscle development and found that FHL2 silencing significantly suppressed the proliferation and differentiation of SMSCS, which is contrary to the role of miR-377. Furthermore, FHL2 interacts with Dishevelled-2 (Dv12) to enable Wnt/beta-catenin signaling pathway, consequently regulating skeletal muscle development. miR-377 negatively regulates the Wnt/beta-catenin signaling pathway by targeting FHL2-mediated Dv12. Overall, these findings demonstrated that miR-377 regulates the bovine SMSCs proliferation and differentiation by targeting FHL2 and attenuating the Wnt/beta-catenin signaling pathway.
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页数:14
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