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miR-30-5p Regulates Muscle Differentiation and Alternative Splicing of Muscle-Related Genes by Targeting MBNL.

Authors :
Bo-Wen Zhang
Han-Fang Cai
Xue-Feng Wei
Jia-Jie Sun
Xian-Yong Lan
Chu-Zhao Lei
Feng-Peng Lin
Xing-Lei Qi
Plath, Martin
Hong Chen
Source :
International Journal of Molecular Sciences. 2016, Vol. 17 Issue 2, p182. 16p. 1 Black and White Photograph, 1 Diagram, 4 Graphs.
Publication Year :
2016

Abstract

MicroRNAs (miRNAs), a class of single stranded, small (∼22 nucleotides), non-coding RNAs, play an important role in muscle development. We focused on the role of the miR-30-5p family during bovine muscle development from previous high-throughput sequencing results and analyzed their expression profiles. MHC and MyoG mRNAs expression as well as their proteins were suppressed in differentiated C2C12 cells, suggesting the importance of miR-30-5p in muscle development. MBNL, the candidate target of miR-30-5p, is an alternative splicing regulation factor. MBNL1 and MBNL3 have opposite effects on muscle differentiation. Our results confirmed that miR-30a-5p and miR-30e-5p repress the expression of MBNL1, MBNL2 and MBNL3, whereas miR-30b-5p inhibits MBNL1 and MBNL2 expression. This provides direct evidence that MBNL expression can be flexibly regulated by miR-30-5p. Previous studies showed that MBNL1 promotes exon inclusion of two muscle-related genes (Trim55 and INSR). Through RNA splicing studies, we found that miR-30-5p had an effect on their alternative splicing, which means miR-30-5p via MBNL1 could be integrated into muscle signaling pathways in which INSR or Trim55 are located. In conclusion, miR-30-5p could inhibit muscle cell differentiation and regulate the alternative splicing of Trim55 and INSR by targeting MBNL. These results promote the understanding of the function of miRNAs in muscle development. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
17
Issue :
2
Database :
Academic Search Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
113337134
Full Text :
https://doi.org/10.3390/ijms17020182