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RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids

MicroRNAs (miRNAs) are indispensable for the regulation of skeletal muscle. We performed RNA sequencing (RNA-seq) to establish a comprehensive miRNA profiling of goats in seven stages, namely, 45- (F45), 65- (F65), 90- (F90), 120- (F120), and 135-day (F135) fetuses, newborn (B1), and 90-day-old (B90...

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Autores principales: Ling, Yinghui, Zheng, Qi, Jing, Jing, Sui, Menghua, Zhu, Lu, Li, Yunsheng, Zhang, Yunhai, Liu, Ya, Fang, Fugui, Zhang, Xiaorong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358459/
https://www.ncbi.nlm.nih.gov/pubmed/32733538
http://dx.doi.org/10.3389/fgene.2020.00684
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author Ling, Yinghui
Zheng, Qi
Jing, Jing
Sui, Menghua
Zhu, Lu
Li, Yunsheng
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Zhang, Xiaorong
author_facet Ling, Yinghui
Zheng, Qi
Jing, Jing
Sui, Menghua
Zhu, Lu
Li, Yunsheng
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Zhang, Xiaorong
author_sort Ling, Yinghui
collection PubMed
description MicroRNAs (miRNAs) are indispensable for the regulation of skeletal muscle. We performed RNA sequencing (RNA-seq) to establish a comprehensive miRNA profiling of goats in seven stages, namely, 45- (F45), 65- (F65), 90- (F90), 120- (F120), and 135-day (F135) fetuses, newborn (B1), and 90-day-old (B90) kids. In total, 421 known miRNAs and 228 goat novel miRNAs were identified in the data, and the average abundance of 19 miRNAs in seven stages exceeds 10,000 reads per million. Furthermore, 420 differentially expressed miRNAs (DEmiRNAs) were identified in all comparison group at seven stages, 80 of which were uniquely differentially expressed in the B1 and B90 comparison groups. Pathway analysis indicated that this group was associated with the release of muscle hypertrophy and regulation of myoblast proliferation. Besides, 305 DEmiRNAs were clustered into three significantly enriched profiles (profiles 11, 16, and 19). Function analysis revealed that profile 16 was related to muscle hypertrophy and differentiation. Profile 11 was involved in multiple enzyme activities and metabolic processes in muscle cells. And profile 19 was involved in material transport and structural stability. Two highly expressed miRNAs and three key miRNAs (chi-miR-328-3p, chi-miR-767, and chi-miR-150) of these profiles were verified to be consistent with the data by quantitative real-time PCR. These results provided a catalog of goat muscle-associated miRNAs, allowing us to better understand the transformation of miRNA roles during mammalian muscle development.
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spelling pubmed-73584592020-07-29 RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids Ling, Yinghui Zheng, Qi Jing, Jing Sui, Menghua Zhu, Lu Li, Yunsheng Zhang, Yunhai Liu, Ya Fang, Fugui Zhang, Xiaorong Front Genet Genetics MicroRNAs (miRNAs) are indispensable for the regulation of skeletal muscle. We performed RNA sequencing (RNA-seq) to establish a comprehensive miRNA profiling of goats in seven stages, namely, 45- (F45), 65- (F65), 90- (F90), 120- (F120), and 135-day (F135) fetuses, newborn (B1), and 90-day-old (B90) kids. In total, 421 known miRNAs and 228 goat novel miRNAs were identified in the data, and the average abundance of 19 miRNAs in seven stages exceeds 10,000 reads per million. Furthermore, 420 differentially expressed miRNAs (DEmiRNAs) were identified in all comparison group at seven stages, 80 of which were uniquely differentially expressed in the B1 and B90 comparison groups. Pathway analysis indicated that this group was associated with the release of muscle hypertrophy and regulation of myoblast proliferation. Besides, 305 DEmiRNAs were clustered into three significantly enriched profiles (profiles 11, 16, and 19). Function analysis revealed that profile 16 was related to muscle hypertrophy and differentiation. Profile 11 was involved in multiple enzyme activities and metabolic processes in muscle cells. And profile 19 was involved in material transport and structural stability. Two highly expressed miRNAs and three key miRNAs (chi-miR-328-3p, chi-miR-767, and chi-miR-150) of these profiles were verified to be consistent with the data by quantitative real-time PCR. These results provided a catalog of goat muscle-associated miRNAs, allowing us to better understand the transformation of miRNA roles during mammalian muscle development. Frontiers Media S.A. 2020-07-07 /pmc/articles/PMC7358459/ /pubmed/32733538 http://dx.doi.org/10.3389/fgene.2020.00684 Text en Copyright © 2020 Ling, Zheng, Jing, Sui, Zhu, Li, Zhang, Liu, Fang and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ling, Yinghui
Zheng, Qi
Jing, Jing
Sui, Menghua
Zhu, Lu
Li, Yunsheng
Zhang, Yunhai
Liu, Ya
Fang, Fugui
Zhang, Xiaorong
RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title_full RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title_fullStr RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title_full_unstemmed RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title_short RNA-Seq Reveals miRNA Role Shifts in Seven Stages of Skeletal Muscles in Goat Fetuses and Kids
title_sort rna-seq reveals mirna role shifts in seven stages of skeletal muscles in goat fetuses and kids
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358459/
https://www.ncbi.nlm.nih.gov/pubmed/32733538
http://dx.doi.org/10.3389/fgene.2020.00684
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