mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation

Author:

Cao Jun12,Wang Xin1ORCID,Advani Vivek13,Lu Yao Wei14ORCID,Malizia Andrea P.1,Singh Gurinder Bir13,Huang Zhan‐Peng1,Liu Jianming1,Wang Chunbo5,Oliveira Edilamar M.36,Mably John D.3ORCID,Chen Kaifu1,Wang Da‐Zhi13ORCID

Affiliation:

1. Department of Cardiology, Boston Children's Hospital Harvard Medical School Boston Massachusetts USA

2. Faculty of Environment and Life Beijing University of Technology Beijing P. R. China

3. Departments of Internal Medicine, Molecular Pharmacology & Physiology, Center for Regenerative Medicine, USF Health Heart Institute, Morsani College of Medicine University of South Florida Tampa Florida USA

4. Vascular Biology Program, Department of Surgery, Boston Children's Hospital Harvard Medical School Boston Massachusetts USA

5. UNC McAllister Heart Institute University of North Carolina Chapel Hill North Carolina USA

6. School of Physical Education and Sport University of Sao Paulo Sao Paulo Brazil

Abstract

AbstractIn this study, we sought to determine the role of tRNA‐derived fragments in the regulation of gene expression during skeletal muscle cell proliferation and differentiation. We employed cell culture to examine the function of mt‐Ty 5’ tiRNAs. Northern blotting, RT‐PCR as well as RNA‐Seq, were performed to determine the effects of mt‐Ty 5’ tiRNA loss and gain on gene expression. Standard and transmission electron microscopy (TEM) were used to characterize cell and sub‐cellular structures. mt‐Ty 5’tiRNAs were found to be enriched in mouse skeletal muscle, showing increased levels in later developmental stages. Gapmer‐mediated inhibition of tiRNAs in skeletal muscle C2C12 myoblasts resulted in decreased cell proliferation and myogenic differentiation; consistent with this observation, RNA‐Seq, transcriptome analyses, and RT‐PCR revealed that skeletal muscle cell differentiation and cell proliferation pathways were also downregulated. Conversely, overexpression of mt‐Ty 5’tiRNAs in C2C12 cells led to a reversal of these transcriptional trends. These data reveal that mt‐Ty 5’tiRNAs are enriched in skeletal muscle and play an important role in myoblast proliferation and differentiation. Our study also highlights the potential for the development of tiRNAs as novel therapeutic targets for muscle‐related diseases.

Funder

American Heart Association

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Cell Biology,General Medicine

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