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Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis

The molecular mechanism of muscle atrophy has been studied a lot, but there is no comprehensive analysis focusing on the denervated muscle atrophy. The gene network that controls the development of denervated muscle atrophy needs further elucidation. We examined differentially expressed genes (DEGs)...

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Autores principales: Gu, Xinyi, Jin, Bo, Qi, Zhidan, Yin, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245453/
https://www.ncbi.nlm.nih.gov/pubmed/34193880
http://dx.doi.org/10.1038/s41598-021-92489-1
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author Gu, Xinyi
Jin, Bo
Qi, Zhidan
Yin, Xiaofeng
author_facet Gu, Xinyi
Jin, Bo
Qi, Zhidan
Yin, Xiaofeng
author_sort Gu, Xinyi
collection PubMed
description The molecular mechanism of muscle atrophy has been studied a lot, but there is no comprehensive analysis focusing on the denervated muscle atrophy. The gene network that controls the development of denervated muscle atrophy needs further elucidation. We examined differentially expressed genes (DEGs) from five denervated muscle atrophy microarray datasets and predicted microRNAs that target these DEGs. We also included the differentially expressed microRNAs datasets of denervated muscle atrophy in previous studies as background information to identify potential key microRNAs. Finally, we compared denervated muscle atrophy with disuse muscle atrophy caused by other reasons, and obtained the Den-genes which only differentially expressed in denervated muscle atrophy. In this meta-analysis, we obtained 429 up-regulated genes, 525 down-regulated genes and a batch of key microRNAs in denervated muscle atrophy. We found eight important microRNA-mRNA interactions (miR-1/Jun, miR-1/Vegfa, miR-497/Vegfa, miR-23a/Vegfa, miR-206/Vegfa, miR-497/Suclg1, miR-27a/Suclg1, miR-27a/Mapk14). The top five KEGG pathways enriched by Den-genes are Insulin signaling pathway, T cell receptor signaling pathway, MAPK signaling pathway, Toll-like receptor signaling pathway and B cell receptor signaling pathway. Our research has delineated the RNA regulatory network of denervated muscle atrophy, and uncovered the specific genes and terms in denervated muscle atrophy.
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spelling pubmed-82454532021-07-06 Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis Gu, Xinyi Jin, Bo Qi, Zhidan Yin, Xiaofeng Sci Rep Article The molecular mechanism of muscle atrophy has been studied a lot, but there is no comprehensive analysis focusing on the denervated muscle atrophy. The gene network that controls the development of denervated muscle atrophy needs further elucidation. We examined differentially expressed genes (DEGs) from five denervated muscle atrophy microarray datasets and predicted microRNAs that target these DEGs. We also included the differentially expressed microRNAs datasets of denervated muscle atrophy in previous studies as background information to identify potential key microRNAs. Finally, we compared denervated muscle atrophy with disuse muscle atrophy caused by other reasons, and obtained the Den-genes which only differentially expressed in denervated muscle atrophy. In this meta-analysis, we obtained 429 up-regulated genes, 525 down-regulated genes and a batch of key microRNAs in denervated muscle atrophy. We found eight important microRNA-mRNA interactions (miR-1/Jun, miR-1/Vegfa, miR-497/Vegfa, miR-23a/Vegfa, miR-206/Vegfa, miR-497/Suclg1, miR-27a/Suclg1, miR-27a/Mapk14). The top five KEGG pathways enriched by Den-genes are Insulin signaling pathway, T cell receptor signaling pathway, MAPK signaling pathway, Toll-like receptor signaling pathway and B cell receptor signaling pathway. Our research has delineated the RNA regulatory network of denervated muscle atrophy, and uncovered the specific genes and terms in denervated muscle atrophy. Nature Publishing Group UK 2021-06-30 /pmc/articles/PMC8245453/ /pubmed/34193880 http://dx.doi.org/10.1038/s41598-021-92489-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gu, Xinyi
Jin, Bo
Qi, Zhidan
Yin, Xiaofeng
Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title_full Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title_fullStr Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title_full_unstemmed Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title_short Identification of potential microRNAs and KEGG pathways in denervation muscle atrophy based on meta-analysis
title_sort identification of potential micrornas and kegg pathways in denervation muscle atrophy based on meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245453/
https://www.ncbi.nlm.nih.gov/pubmed/34193880
http://dx.doi.org/10.1038/s41598-021-92489-1
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