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Study on the Relationship between the miRNA-centered ceRNA Regulatory Network and Fatigue.

Authors
  • Yang, Xingzhe1
  • Li, Feng2
  • Ma, Jie1
  • Liu, Yan1
  • Wang, Xuejiao1
  • Wang, Ruochong1
  • Zhang, Yifei1
  • Zhang, Wei1
  • He, Qingyun1
  • Song, Dandan1
  • Yu, Jiaojiao1
  • 1 College of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. , (China)
  • 2 College of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China. [email protected] , (China)
Type
Published Article
Journal
Journal of Molecular Neuroscience
Publisher
Springer-Verlag
Publication Date
Oct 01, 2021
Volume
71
Issue
10
Pages
1967–1974
Identifiers
DOI: 10.1007/s12031-021-01845-3
PMID: 33993410
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

In recent years, the incidence of fatigue has been increasing, and the effective prevention and treatment of fatigue has become an urgent problem. As a result, the genetic research of fatigue has become a hot spot. Transcriptome-level regulation is the key link in the gene regulatory network. The transcriptome includes messenger RNAs (mRNAs) and noncoding RNAs (ncRNAs). MRNAs are common research targets in gene expression profiling. Noncoding RNAs, including miRNAs, lncRNAs, circRNAs and so on, have been developed rapidly. Studies have shown that miRNAs are closely related to the occurrence and development of fatigue. MiRNAs can regulate the immune inflammatory reaction in the central nervous system (CNS), regulate the transmission of nerve impulses and gene expression, regulate brain development and brain function, and participate in the occurrence and development of fatigue by regulating mitochondrial function and energy metabolism. LncRNAs can regulate dopaminergic neurons to participate in the occurrence and development of fatigue. This has certain value in the diagnosis of chronic fatigue syndrome (CFS). CircRNAs can participate in the occurrence and development of fatigue by regulating the NF-κB pathway, TNF-α and IL-1β. The ceRNA hypothesis posits that in addition to the function of miRNAs in unidirectional regulation, mRNAs, lncRNAs and circRNAs can regulate gene expression by competitive binding with miRNAs, forming a ceRNA regulatory network with miRNAs. Therefore, we suggest that the miRNA-centered ceRNA regulatory network is closely related to fatigue. At present, there are few studies on fatigue-related ncRNA genes, and most of these limited studies are on miRNAs in ncRNAs. However, there are a few studies on the relationship between lncRNAs, cirRNAs and fatigue. Less research is available on the pathogenesis of fatigue based on the ceRNA regulatory network. Therefore, exploring the complex mechanism of fatigue based on the ceRNA regulatory network is of great significance. In this review, we summarize the relationship between miRNAs, lncRNAs and circRNAs in ncRNAs and fatigue, and focus on exploring the regulatory role of the miRNA-centered ceRNA regulatory network in the occurrence and development of fatigue, in order to gain a comprehensive, in-depth and new understanding of the essence of the fatigue gene regulatory network. © 2021. The Author(s).

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