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

In 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 perform...

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Autores principales: Cao, Jun, Wang, Xin, Advani, Vivek, Lu, Yao Wei, Malizia, Andrea P., Singh, Gurinder Bir, Huang, Zhan‐Peng, Liu, Jianming, Wang, Chunbo, Oliveira, Edilamar M., Mably, John D., Chen, Kaifu, Wang, Da‐Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392060/
https://www.ncbi.nlm.nih.gov/pubmed/36756712
http://dx.doi.org/10.1111/cpr.13416
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author Cao, Jun
Wang, Xin
Advani, Vivek
Lu, Yao Wei
Malizia, Andrea P.
Singh, Gurinder Bir
Huang, Zhan‐Peng
Liu, Jianming
Wang, Chunbo
Oliveira, Edilamar M.
Mably, John D.
Chen, Kaifu
Wang, Da‐Zhi
author_facet Cao, Jun
Wang, Xin
Advani, Vivek
Lu, Yao Wei
Malizia, Andrea P.
Singh, Gurinder Bir
Huang, Zhan‐Peng
Liu, Jianming
Wang, Chunbo
Oliveira, Edilamar M.
Mably, John D.
Chen, Kaifu
Wang, Da‐Zhi
author_sort Cao, Jun
collection PubMed
description In 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.
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spelling pubmed-103920602023-08-02 mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation Cao, Jun Wang, Xin Advani, Vivek Lu, Yao Wei Malizia, Andrea P. Singh, Gurinder Bir Huang, Zhan‐Peng Liu, Jianming Wang, Chunbo Oliveira, Edilamar M. Mably, John D. Chen, Kaifu Wang, Da‐Zhi Cell Prolif Original Articles In 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. John Wiley and Sons Inc. 2023-02-08 /pmc/articles/PMC10392060/ /pubmed/36756712 http://dx.doi.org/10.1111/cpr.13416 Text en © 2023 The Authors. Cell Proliferation published by Beijing Institute for Stem Cell and Regenerative Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Cao, Jun
Wang, Xin
Advani, Vivek
Lu, Yao Wei
Malizia, Andrea P.
Singh, Gurinder Bir
Huang, Zhan‐Peng
Liu, Jianming
Wang, Chunbo
Oliveira, Edilamar M.
Mably, John D.
Chen, Kaifu
Wang, Da‐Zhi
mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title_full mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title_fullStr mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title_full_unstemmed mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title_short mt‐Ty 5'tiRNA regulates skeletal muscle cell proliferation and differentiation
title_sort mt‐ty 5'tirna regulates skeletal muscle cell proliferation and differentiation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392060/
https://www.ncbi.nlm.nih.gov/pubmed/36756712
http://dx.doi.org/10.1111/cpr.13416
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