miR-491 inhibits skeletal muscle differentiation through targeting myomaker

被引:21
|
作者
He, Jian [1 ]
Wang, Fei [2 ]
Zhang, Peng [1 ]
Li, Wenjiong [1 ]
Wang, Jing [1 ]
Li, Jinglong [1 ]
Liu, Hongju [1 ]
Chen, Xiaoping [1 ,2 ]
机构
[1] China Astronaut Res & Training Ctr, State Key Lab Space Med Fundamentals & Applicat, 26 Beiqing Rd, Beijing 100094, Peoples R China
[2] China Astronaut Res & Training Ctr, Natl Key Lab Human Factors Engn, 26 Beiqing Rd, Beijing 100094, Peoples R China
关键词
BCL-X-L; MYOBLAST FUSION; MOLECULAR REGULATION; MICRORNAS; EXPRESSION; CANCER; PROLIFERATION; REGENERATION; MYOGENESIS; APOPTOSIS;
D O I
10.1016/j.abb.2017.05.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The myogenesis of skeletal muscle has several stages, including satellite cell proliferation, differentiation, fusion and specific muscle formation. Recent studies have shown that myomaker, a muscle-specific transmembrane protein, was critical for myoblasts fusion. However, the regulatory mechanism of myomaker and its effects on myogenesis remain elusive. In this study, miR-491 was identified as a post transcriptional regulator of myomaker, which binds specifically to its 3' untranslated region leading to its down-regulation. At the end of myotube differentiation, the expression levels of miR-491 increased drastically, while myomaker was significantly down-regulated, which indicated that miR-491 shut down the expression of myomaker. Functional studies showed that miR-491 overexpression suppressed muscle cell differentiation and adult muscle regeneration, while the inhibition of miR-491 promoted myotube differentiation. Taken together, our findings identified miR-491 as a novel negative regulator of myogenic differentiation through targeting myomaker. (C) 2017 Published by Elsevier Inc.
引用
收藏
页码:30 / 38
页数:9
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