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

机译:与肌发生相关的miRNA抑制JNK / MAPK信号通路是骨骼肌发育所必需的

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摘要

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.
机译:骨骼肌的分化受多种细胞信号通路的控制,但是,尚未完全阐明主导该过程的JNK / MAPK信号通路。在这里,我们报道JNK / MAPK通路在成肌的后期显着下调,与P38 / MAPK通路相反,它负向调节骨骼肌的分化。根据PAR-CLIP-seq分析,我们鉴定了六个升高的miRNA(miR-1a-3p,miR-133a-3p,miR-133b-3p,miR-206-3p,miR-128-3p,miR-351- 5p),即与肌发生相关的miRNA(mamiRs),通过抑制JNK / MAPK途径磷酸化的多种因子(包括MEKK1,MEKK2,MKK7和c-Jun)抑制JNK / MAPK途径的负向调控,但不抑制JNK蛋白本身,结果,进一步促进了转录因子MyoD和mamiR的表达。我们的研究通过靶向负责骨骼肌发育的磷酸化激酶信号级联,揭示了细胞特异性miRNA的新型双阴性反馈调控模式。

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