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Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation

BACKGROUND: Skeletal muscle in livestock develops into meat, an important source of protein and other nutrients for human consumption. The muscle is largely composed of a fixed number of multinucleated myofibers determined during late gestation and remains constant postnatally. A population of postn...

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Autores principales: Sadkowski, Tomasz, Ciecierska, Anna, Oprządek, Jolanta, Balcerek, Edyta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793348/
https://www.ncbi.nlm.nih.gov/pubmed/29390965
http://dx.doi.org/10.1186/s12864-018-4492-5
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author Sadkowski, Tomasz
Ciecierska, Anna
Oprządek, Jolanta
Balcerek, Edyta
author_facet Sadkowski, Tomasz
Ciecierska, Anna
Oprządek, Jolanta
Balcerek, Edyta
author_sort Sadkowski, Tomasz
collection PubMed
description BACKGROUND: Skeletal muscle in livestock develops into meat, an important source of protein and other nutrients for human consumption. The muscle is largely composed of a fixed number of multinucleated myofibers determined during late gestation and remains constant postnatally. A population of postnatal muscle stem cells, called satellite cells, gives rise to myoblast cells that can fuse with the existing myofibers, thus increasing their size. This requires a delicate balance of transcription and growth factors and specific microRNA (miRNA) expressed by satellite cells and their supporting cells from the muscle stem cell niche. The role of transcription and growth factors in bovine myogenesis is well-characterized; however, very little is known about the miRNA activity during this process. We have hypothesized that the expression of miRNA can vary between primary cultures of skeletal muscle cells isolated from the semitendinosus muscles of different cattle breeds and subjected to myogenic differentiation. RESULTS: After a 6-day myogenic differentiation of cells isolated from the muscles of the examined cattle breeds, we found statistically significant differences in the number of myotubes between Hereford (HER)/Limousine (LIM) beef breeds and the Holstein-Friesian (HF) dairy breed (p ≤ 0.001). The microarray analysis revealed differences in the expression of 23 miRNA among the aforementioned primary cultures. On the basis of a functional analysis, we assigned 9 miRNA as molecules responsible for differentiation progression (miR-1, -128a, -133a, -133b, -139, -206, -222, -486, and -503). The target gene prediction and functional analysis revealed 59 miRNA-related genes belonging to the muscle organ development process. CONCLUSION: The number of myotubes and the miRNA expression in the primary cultures of skeletal muscle cells derived from the semitendinosus muscles of the HER/LIM beef cattle breeds and the HF dairy breed vary when cells are subjected to myogenic differentiation. The net effect of the identified miRNA and their target gene action should be considered the result of the breed-dependent activity of satellite cells and muscle stem cell niche cells and their mutual interactions, which putatively can be engaged in the formation of a larger number of myotubes in beef cattle-related cells (HER/LIM) during in vitro myogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4492-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-57933482018-02-12 Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation Sadkowski, Tomasz Ciecierska, Anna Oprządek, Jolanta Balcerek, Edyta BMC Genomics Research Article BACKGROUND: Skeletal muscle in livestock develops into meat, an important source of protein and other nutrients for human consumption. The muscle is largely composed of a fixed number of multinucleated myofibers determined during late gestation and remains constant postnatally. A population of postnatal muscle stem cells, called satellite cells, gives rise to myoblast cells that can fuse with the existing myofibers, thus increasing their size. This requires a delicate balance of transcription and growth factors and specific microRNA (miRNA) expressed by satellite cells and their supporting cells from the muscle stem cell niche. The role of transcription and growth factors in bovine myogenesis is well-characterized; however, very little is known about the miRNA activity during this process. We have hypothesized that the expression of miRNA can vary between primary cultures of skeletal muscle cells isolated from the semitendinosus muscles of different cattle breeds and subjected to myogenic differentiation. RESULTS: After a 6-day myogenic differentiation of cells isolated from the muscles of the examined cattle breeds, we found statistically significant differences in the number of myotubes between Hereford (HER)/Limousine (LIM) beef breeds and the Holstein-Friesian (HF) dairy breed (p ≤ 0.001). The microarray analysis revealed differences in the expression of 23 miRNA among the aforementioned primary cultures. On the basis of a functional analysis, we assigned 9 miRNA as molecules responsible for differentiation progression (miR-1, -128a, -133a, -133b, -139, -206, -222, -486, and -503). The target gene prediction and functional analysis revealed 59 miRNA-related genes belonging to the muscle organ development process. CONCLUSION: The number of myotubes and the miRNA expression in the primary cultures of skeletal muscle cells derived from the semitendinosus muscles of the HER/LIM beef cattle breeds and the HF dairy breed vary when cells are subjected to myogenic differentiation. The net effect of the identified miRNA and their target gene action should be considered the result of the breed-dependent activity of satellite cells and muscle stem cell niche cells and their mutual interactions, which putatively can be engaged in the formation of a larger number of myotubes in beef cattle-related cells (HER/LIM) during in vitro myogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4492-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-31 /pmc/articles/PMC5793348/ /pubmed/29390965 http://dx.doi.org/10.1186/s12864-018-4492-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sadkowski, Tomasz
Ciecierska, Anna
Oprządek, Jolanta
Balcerek, Edyta
Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title_full Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title_fullStr Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title_full_unstemmed Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title_short Breed-dependent microRNA expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
title_sort breed-dependent microrna expression in the primary culture of skeletal muscle cells subjected to myogenic differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793348/
https://www.ncbi.nlm.nih.gov/pubmed/29390965
http://dx.doi.org/10.1186/s12864-018-4492-5
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