Inhibition of the JNK/MAPK signaling pathway by myogenesis-associated miRNAs is required for skeletal muscle development

Skeletal muscle differentiation is controlled by multiple cell signaling pathways, however, the JNK/MAPK signaling pathway dominating this process has not been fully elucidated. Here, we report that the JNK/MAPK pathway was significantly downregulated in the late stages of myogenesis, and in contras...

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Veröffentlicht in:Cell death and differentiation 2018-09, Vol.25 (9), p.1581-1597
Hauptverfasser: Xie, Shu-Juan, Li, Jun-Hao, Chen, Hua-Feng, Tan, Ye-Ya, Liu, Shu-Rong, Zhang, Yin, Xu, Hui, Yang, Jian-Hua, Liu, Shun, Zheng, Ling-Ling, Huang, Mian-Bo, Guo, Yan-Hua, Zhang, Qi, Zhou, Hui, Qu, Liang-Hu
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Sprache:eng
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Zusammenfassung:Skeletal muscle differentiation is controlled by multiple cell signaling pathways, however, the JNK/MAPK signaling pathway dominating this process has not been fully elucidated. Here, we report that the JNK/MAPK pathway was significantly downregulated in the late stages of myogenesis, and in contrast to P38/MAPK pathway, it negatively regulated skeletal muscle differentiation. Based on the PAR-CLIP-seq analysis, we identified six elevated miRNAs (miR-1a-3p, miR-133a-3p, miR-133b-3p, miR-206-3p, miR-128-3p, miR-351-5p), namely myogenesis-associated miRNAs (mamiRs), negatively controlled the JNK/MAPK pathway by repressing multiple factors for the phosphorylation of the JNK/MAPK pathway, including MEKK1, MEKK2, MKK7, and c-Jun but not JNK protein itself, and as a result, expression of transcriptional factor MyoD and mamiRs were further promoted. Our study revealed a novel double-negative feedback regulatory pattern of cell-specific miRNAs by targeting phosphorylation kinase signaling cascade responsible for skeletal muscle development.
ISSN:1350-9047
1476-5403
DOI:10.1038/s41418-018-0063-1