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microRNA‐151–3p Regulates Slow Muscle Gene Expression by Targeting ATP2a2 in Skeletal Muscle Cells
Author(s) -
Wei Huan,
Li Zhongwen,
Wang Xiaobin,
Wang Jie,
Pang Weijun,
Yang Gongshe,
Shen Qingwu W.
Publication year - 2015
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.24793
Subject(s) - myogenesis , skeletal muscle , biology , myocyte , microbiology and biotechnology , microrna , gene expression , regulation of gene expression , c2c12 , gene , genetics , endocrinology
MicroRNAs (miRNAs) are a group of small noncoding RNAs that regulate the stability or translation of cognate mRNAs at the post‐transcriptional level. Accumulating evidence indicates that miRNAs play important roles in many aspects of muscle function, including muscle growth and development, regeneration, contractility, and muscle fiber type plasticity. In the current study, we examined the function of miR‐151–3p in myoblast proliferation and differentiation. Results show that overexpression of miR‐151–3p not only upregulates myoblast proliferation, but also decreases slow muscle gene expression (such as MHC‐β/slow and slow muscle troponin I) in both C2C12 myotubes and in primary cultures. Alternatively, inhibition of miR‐151–3p by antisense RNA was found to upregulate MHC‐β/slow expression, indicating that miR‐151–3p plays a role in muscle fiber type determination. Further investigation into the underlying mechanisms revealed for the first time that miR‐151–3p directly targets ATP2a2, a gene encoding for a slow skeletal and cardiac muscle specific Ca 2+ ATPase, SERCA2 thus downregulating slow muscle gene expression. Mechanisms by which the alteration in SERCA2 expression induces changes in other slow muscle gene expression levels needs to be defined in future research. J. Cell. Physiol. 230: 1003–1012, 2015. © 2014 Wiley Periodicals, Inc., A Wiley Company