4.7 Article

The Possible Role of Complete Loss of Myostatin in Limiting Excessive Proliferation of Muscle Cells (C2C12) via Activation of MicroRNAs

Journal

Publisher

MDPI
DOI: 10.3390/ijms20030643

Keywords

MSTN; RNA-seq; miRNA-seq; transcriptomics; C2C12; RMS

Funding

  1. Special Funds for the Cultivation and Breeding of New Transgenic Organisms [2016ZX08006001]
  2. Program for Changjiang Scholars and the Innovative Research Team in University [IRT_16R32]
  3. Program for the JLU Science and Technology Innovative Research Team [2017TD-28]

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Myostatin (MSTN) is a member of the TGF- superfamily that negatively regulates skeletal muscle growth and differentiation. However, the mechanism by which complete MSTN deletion limits excessive proliferation of muscle cells remains unclear. In this study, we knocked out MSTN in mouse myoblast lines using a Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9) system and sequenced the mRNA and miRNA transcriptomes. The results show that complete loss of MSTN upregulates seven miRNAs targeting an interaction network composed of 28 downregulated genes, including TGFB1, FOS and RB1. These genes are closely associated with tumorigenesis and cell proliferation. Our study suggests that complete loss of MSTN may limit excessive cell proliferation via activation of miRNAs. These data will contribute to the treatment of rhabdomyosarcoma (RMS).

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