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CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding
The proliferation and differentiation of mammalian skeletal muscle satellite cells (MuSCs) are highly complicated. Apart from the regulatory signaling cascade driven by the protein-coding genes, non-coding RNAs such as microRNAs (miRNA) and circular RNAs (circRNAs) play essential roles in this biolo...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657166/ https://www.ncbi.nlm.nih.gov/pubmed/36361663 http://dx.doi.org/10.3390/ijms232112868 |
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author | Zheng, Shuailong Li, Li Zhou, Helin Zhang, Xujia Xu, Xiaoli Dai, Dinghui Zhan, Siyuan Cao, Jiaxue Guo, Jiazhong Zhong, Tao Wang, Linjie Zhang, Hongping |
author_facet | Zheng, Shuailong Li, Li Zhou, Helin Zhang, Xujia Xu, Xiaoli Dai, Dinghui Zhan, Siyuan Cao, Jiaxue Guo, Jiazhong Zhong, Tao Wang, Linjie Zhang, Hongping |
author_sort | Zheng, Shuailong |
collection | PubMed |
description | The proliferation and differentiation of mammalian skeletal muscle satellite cells (MuSCs) are highly complicated. Apart from the regulatory signaling cascade driven by the protein-coding genes, non-coding RNAs such as microRNAs (miRNA) and circular RNAs (circRNAs) play essential roles in this biological process. However, circRNA functions in MuSCs proliferation and differentiation remain largely to be elucidated. Here, we screened for an exonic circTCF4 based on our previous RNA-Seq data, specifically expressed during the development of the longest dorsal muscle in goats. Subsequently, the circular structure and whole sequence of circTCF4 were verified using Sanger sequencing. Besides, circTCF4 was spatiotemporally expressed in multiple tissues from goats but strikingly enriched in muscles. Furthermore, circTCF4 suppressed MuSCs proliferation and differentiation, independent of AGO2 binding. Finally, we conducted Poly(A) RNA-Seq using cells treated with small interfering RNA targeting circTCF4 and found that circTCF4 would affect multiple signaling pathways, including the insulin signaling pathway and AMPK signaling pathway related to muscle differentiation. Our results provide additional solid evidence for circRNA regulating skeletal muscle formation. |
format | Online Article Text |
id | pubmed-9657166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96571662022-11-15 CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding Zheng, Shuailong Li, Li Zhou, Helin Zhang, Xujia Xu, Xiaoli Dai, Dinghui Zhan, Siyuan Cao, Jiaxue Guo, Jiazhong Zhong, Tao Wang, Linjie Zhang, Hongping Int J Mol Sci Article The proliferation and differentiation of mammalian skeletal muscle satellite cells (MuSCs) are highly complicated. Apart from the regulatory signaling cascade driven by the protein-coding genes, non-coding RNAs such as microRNAs (miRNA) and circular RNAs (circRNAs) play essential roles in this biological process. However, circRNA functions in MuSCs proliferation and differentiation remain largely to be elucidated. Here, we screened for an exonic circTCF4 based on our previous RNA-Seq data, specifically expressed during the development of the longest dorsal muscle in goats. Subsequently, the circular structure and whole sequence of circTCF4 were verified using Sanger sequencing. Besides, circTCF4 was spatiotemporally expressed in multiple tissues from goats but strikingly enriched in muscles. Furthermore, circTCF4 suppressed MuSCs proliferation and differentiation, independent of AGO2 binding. Finally, we conducted Poly(A) RNA-Seq using cells treated with small interfering RNA targeting circTCF4 and found that circTCF4 would affect multiple signaling pathways, including the insulin signaling pathway and AMPK signaling pathway related to muscle differentiation. Our results provide additional solid evidence for circRNA regulating skeletal muscle formation. MDPI 2022-10-25 /pmc/articles/PMC9657166/ /pubmed/36361663 http://dx.doi.org/10.3390/ijms232112868 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zheng, Shuailong Li, Li Zhou, Helin Zhang, Xujia Xu, Xiaoli Dai, Dinghui Zhan, Siyuan Cao, Jiaxue Guo, Jiazhong Zhong, Tao Wang, Linjie Zhang, Hongping CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title | CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title_full | CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title_fullStr | CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title_full_unstemmed | CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title_short | CircTCF4 Suppresses Proliferation and Differentiation of Goat Skeletal Muscle Satellite Cells Independent from AGO2 Binding |
title_sort | circtcf4 suppresses proliferation and differentiation of goat skeletal muscle satellite cells independent from ago2 binding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657166/ https://www.ncbi.nlm.nih.gov/pubmed/36361663 http://dx.doi.org/10.3390/ijms232112868 |
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