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miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells

BACKGROUND: Skeletal muscle differentiation is a multistep, complex pathway in which several important signaling molecules are involved. Recently, microRNAs (miRNAs), endogenous non-coding small RNAs that regulate mRNAs, have been proposed to be involved in skeletal muscle differentiation. In this s...

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Autores principales: Katase, Naoki, Terada, Kumiko, Suzuki, Takahiro, Nishimatsu, Shin-ichiro, Nohno, Tsutomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433089/
https://www.ncbi.nlm.nih.gov/pubmed/25925429
http://dx.doi.org/10.1186/s12860-015-0061-9
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author Katase, Naoki
Terada, Kumiko
Suzuki, Takahiro
Nishimatsu, Shin-ichiro
Nohno, Tsutomu
author_facet Katase, Naoki
Terada, Kumiko
Suzuki, Takahiro
Nishimatsu, Shin-ichiro
Nohno, Tsutomu
author_sort Katase, Naoki
collection PubMed
description BACKGROUND: Skeletal muscle differentiation is a multistep, complex pathway in which several important signaling molecules are involved. Recently, microRNAs (miRNAs), endogenous non-coding small RNAs that regulate mRNAs, have been proposed to be involved in skeletal muscle differentiation. In this study, we identified skeletal muscle differentiation-associated miRNAs by comparing miRNA expression profiles between C2C12 cells and Wnt4 over-expressing C2C12 cells (W4-08), which can spontaneously differentiate into myotubes. RESULTS: We identified miR-206, miR-133a, and miR-133b as up-regulated miRNAs and miR-487b, miR-3963 and miR-6412 as down-regulated miRNAs in differentiating cells. We focused on the down-regulated miRNAs because their functions were largely unknown. Transfection of mimics of these miRNAs into C2C12 cells resulted in significantly reduced expression of myogenic differentiation markers, including troponin T and myosin heavy chain fast type and slow type, but did not affect the expression of the myogenic transcription factors, MyoD and myogenin. CONCLUSIONS: These miRNAs were characterized as new myogenic differentiation-associated miRNAs which may delay late myogenic differentiation or maturation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-015-0061-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-44330892015-05-16 miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells Katase, Naoki Terada, Kumiko Suzuki, Takahiro Nishimatsu, Shin-ichiro Nohno, Tsutomu BMC Cell Biol Research Article BACKGROUND: Skeletal muscle differentiation is a multistep, complex pathway in which several important signaling molecules are involved. Recently, microRNAs (miRNAs), endogenous non-coding small RNAs that regulate mRNAs, have been proposed to be involved in skeletal muscle differentiation. In this study, we identified skeletal muscle differentiation-associated miRNAs by comparing miRNA expression profiles between C2C12 cells and Wnt4 over-expressing C2C12 cells (W4-08), which can spontaneously differentiate into myotubes. RESULTS: We identified miR-206, miR-133a, and miR-133b as up-regulated miRNAs and miR-487b, miR-3963 and miR-6412 as down-regulated miRNAs in differentiating cells. We focused on the down-regulated miRNAs because their functions were largely unknown. Transfection of mimics of these miRNAs into C2C12 cells resulted in significantly reduced expression of myogenic differentiation markers, including troponin T and myosin heavy chain fast type and slow type, but did not affect the expression of the myogenic transcription factors, MyoD and myogenin. CONCLUSIONS: These miRNAs were characterized as new myogenic differentiation-associated miRNAs which may delay late myogenic differentiation or maturation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-015-0061-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-30 /pmc/articles/PMC4433089/ /pubmed/25925429 http://dx.doi.org/10.1186/s12860-015-0061-9 Text en © Katase et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Katase, Naoki
Terada, Kumiko
Suzuki, Takahiro
Nishimatsu, Shin-ichiro
Nohno, Tsutomu
miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title_full miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title_fullStr miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title_full_unstemmed miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title_short miR-487b, miR-3963 and miR-6412 delay myogenic differentiation in mouse myoblast-derived C2C12 cells
title_sort mir-487b, mir-3963 and mir-6412 delay myogenic differentiation in mouse myoblast-derived c2c12 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433089/
https://www.ncbi.nlm.nih.gov/pubmed/25925429
http://dx.doi.org/10.1186/s12860-015-0061-9
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