Transgenic overexpression of miR-133a in skeletal muscle

<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of non-coding regulatory RNAs of ~22 nucleotides in length. miRNAs regulate gene expression post-transcriptionally, primarily by associating with the 3' untranslated region (UTR) of their regulator...

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Main Authors: Chen Jian-Fu, Deng Zhongliang, Wang Da-Zhi
Format: Article
Language:English
Published: BMC 2011-05-01
Series:BMC Musculoskeletal Disorders
Subjects:
Online Access:http://www.biomedcentral.com/1471-2474/12/115
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spelling doaj-955a7bd44fc34dc8b4b1d6bb3a3717132020-11-25T01:32:31ZengBMCBMC Musculoskeletal Disorders1471-24742011-05-0112111510.1186/1471-2474-12-115Transgenic overexpression of miR-133a in skeletal muscleChen Jian-FuDeng ZhongliangWang Da-Zhi<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of non-coding regulatory RNAs of ~22 nucleotides in length. miRNAs regulate gene expression post-transcriptionally, primarily by associating with the 3' untranslated region (UTR) of their regulatory target mRNAs. Recent work has begun to reveal roles for miRNAs in a wide range of biological processes, including cell proliferation, differentiation and apoptosis. Many miRNAs are expressed in cardiac and skeletal muscle, and dysregulated miRNA expression has been correlated with muscle-related disorders. We have previously reported that the expression of muscle-specific miR-1 and miR-133 is induced during skeletal muscle differentiation and miR-1 and miR-133 play central regulatory roles in myoblast proliferation and differentiation in vitro.</p> <p>Methods</p> <p>In this study, we measured the expression of miRNAs in the skeletal muscle of mdx mice, an animal model for human muscular dystrophy. We also generated transgenic mice to overexpress miR-133a in skeletal muscle.</p> <p>Results</p> <p>We examined the expression of miRNAs in the skeletal muscle of <it>mdx </it>mice. We found that the expression of muscle miRNAs, including miR-1a, miR-133a and miR-206, was up-regulated in the skeletal muscle of <it>mdx </it>mice. In order to further investigate the function of miR-133a in skeletal muscle in vivo, we have created several independent transgenic founder lines. Surprisingly, skeletal muscle development and function appear to be unaffected in miR-133a transgenic mice.</p> <p>Conclusions</p> <p>Our results indicate that miR-133a is dispensable for the normal development and function of skeletal muscle.</p> http://www.biomedcentral.com/1471-2474/12/115microRNA-133askeletal muscletransgenicdifferentiation
collection DOAJ
language English
format Article
sources DOAJ
author Chen Jian-Fu
Deng Zhongliang
Wang Da-Zhi
spellingShingle Chen Jian-Fu
Deng Zhongliang
Wang Da-Zhi
Transgenic overexpression of miR-133a in skeletal muscle
BMC Musculoskeletal Disorders
microRNA-133a
skeletal muscle
transgenic
differentiation
author_facet Chen Jian-Fu
Deng Zhongliang
Wang Da-Zhi
author_sort Chen Jian-Fu
title Transgenic overexpression of miR-133a in skeletal muscle
title_short Transgenic overexpression of miR-133a in skeletal muscle
title_full Transgenic overexpression of miR-133a in skeletal muscle
title_fullStr Transgenic overexpression of miR-133a in skeletal muscle
title_full_unstemmed Transgenic overexpression of miR-133a in skeletal muscle
title_sort transgenic overexpression of mir-133a in skeletal muscle
publisher BMC
series BMC Musculoskeletal Disorders
issn 1471-2474
publishDate 2011-05-01
description <p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are a class of non-coding regulatory RNAs of ~22 nucleotides in length. miRNAs regulate gene expression post-transcriptionally, primarily by associating with the 3' untranslated region (UTR) of their regulatory target mRNAs. Recent work has begun to reveal roles for miRNAs in a wide range of biological processes, including cell proliferation, differentiation and apoptosis. Many miRNAs are expressed in cardiac and skeletal muscle, and dysregulated miRNA expression has been correlated with muscle-related disorders. We have previously reported that the expression of muscle-specific miR-1 and miR-133 is induced during skeletal muscle differentiation and miR-1 and miR-133 play central regulatory roles in myoblast proliferation and differentiation in vitro.</p> <p>Methods</p> <p>In this study, we measured the expression of miRNAs in the skeletal muscle of mdx mice, an animal model for human muscular dystrophy. We also generated transgenic mice to overexpress miR-133a in skeletal muscle.</p> <p>Results</p> <p>We examined the expression of miRNAs in the skeletal muscle of <it>mdx </it>mice. We found that the expression of muscle miRNAs, including miR-1a, miR-133a and miR-206, was up-regulated in the skeletal muscle of <it>mdx </it>mice. In order to further investigate the function of miR-133a in skeletal muscle in vivo, we have created several independent transgenic founder lines. Surprisingly, skeletal muscle development and function appear to be unaffected in miR-133a transgenic mice.</p> <p>Conclusions</p> <p>Our results indicate that miR-133a is dispensable for the normal development and function of skeletal muscle.</p>
topic microRNA-133a
skeletal muscle
transgenic
differentiation
url http://www.biomedcentral.com/1471-2474/12/115
work_keys_str_mv AT chenjianfu transgenicoverexpressionofmir133ainskeletalmuscle
AT dengzhongliang transgenicoverexpressionofmir133ainskeletalmuscle
AT wangdazhi transgenicoverexpressionofmir133ainskeletalmuscle
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