Identification of MyoD-Responsive Transcripts Reveals a Novel Long Non-coding RNA (lncRNA-AK143003) that Negatively Regulates Myoblast Differentiation.

Sci Rep

Key Laboratory of Swine Genetics and Breeding of Ministry of Agriculture & Key Laboratory of Agriculture Animal Genetics, Breeding and Reproduction of Ministry of Education, College of Animal Science, Huazhong Agricultural University, Wuhan, 430070, Hubei, P.R. China.

Published: June 2017

AI Article Synopsis

  • Myogenic differentiation factor (MyoD) is essential for muscle development, and this study aimed to uncover previously unexplored long non-coding RNAs (lncRNAs) that are regulated by MyoD in muscle cells.
  • A microarray analysis revealed 997 lncRNAs and 1,817 mRNAs that were differentially expressed when MyoD was knocked down in C2C12 muscle cells, indicating their potential role in muscle differentiation and cell cycle processes.
  • Specifically, the study identified lnc-AK143003, which is regulated by MyoD, and demonstrated that silencing this lncRNA promotes myogenic marker gene expression, while its overexpression inhibits it.

Article Abstract

Myogenic differentiation factor (MyoD) is a master transcription factor in muscle development and differentiation. Although several long non-coding RNAs (lncRNAs) linked to MyoD have been found to influence muscle development, the functions of many lncRNAs have not been explored. Here we utilized lncRNA and mRNA microarray analysis to identify potential lncRNAs regulated by MyoD in muscle cells. A total of 997 differentially expressed lncRNAs (335 up-regulated and 662 down-regulated) and 1,817 differentially expressed mRNAs (148 up-regulated and 1,669 down-regulated) were identified after MyoD knockdown in C2C12 cells. Functional predictions suggested that most lncRNAs are involved in the biological pathways related to muscle differentiation and cell cycle with co-expressed genes. To gain further insight into the MyoD-mediated lncRNA expression in muscle differentiation, tissue expression profiles and MyoD overexpression were performed, and we found one of the candidate lncRNAs-AK143003 was significantly regulated by MyoD. Further analyses showed its noncoding ability and cytoplasmic localisation. Silencing of AK143003 stimulated the accumulation of myogenic marker genes, whereas AK143003 overexpression led to their decreased synthesis. This study identified a multitude of MyoD-mediated lncRNAs for further investigation and identified a novel lncRNA, lnc-AK143003, which plays a role in controlling muscle differentiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460278PMC
http://dx.doi.org/10.1038/s41598-017-03071-7DOI Listing

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