Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.

Myostatin (MSTN) has been shown to be a negative regulator of skeletal muscle development and growth. MSTN dysfunction therefore offers a strategy for promoting animal growth performance in livestock production. In this study, we investigated the possibility of using RNAi-based technology to generat...

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Main Authors: Shengwei Hu, Wei Ni, Wujiafu Sai, Ha Zi, Jun Qiao, Pengyang Wang, Jinliang Sheng, Chuangfu Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3603981?pdf=render
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spelling doaj-833ffc0e124940f2af7ad36ca90af9052020-11-25T00:53:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5852110.1371/journal.pone.0058521Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.Shengwei HuWei NiWujiafu SaiHa ZiJun QiaoPengyang WangJinliang ShengChuangfu ChenMyostatin (MSTN) has been shown to be a negative regulator of skeletal muscle development and growth. MSTN dysfunction therefore offers a strategy for promoting animal growth performance in livestock production. In this study, we investigated the possibility of using RNAi-based technology to generate transgenic sheep with a double-muscle phenotype. A shRNA expression cassette targeting sheep MSTN was used to generate stable shRNA-expressing fibroblast clones. Transgenic sheep were further produced by somatic cell nuclear transfer (SCNT) technology. Five lambs developed to term and three live lambs were obtained. Integration of shRNA expression cassette in three live lambs was confirmed by PCR. RNase protection assay showed that the shRNAs targeting MSTN were expressed in muscle tissues of three transgenic sheep. MSTN expression was significantly inhibited in muscle tissues of transgenic sheep when compared with control sheep. Moreover, transgenic sheep showed a tendency to faster increase in body weight than control sheep. Histological analysis showed that myofiber diameter of transgenic sheep M17 were bigger than that of control sheep. Our findings demonstrate a promising approach to promoting muscle growth in livestock production.http://europepmc.org/articles/PMC3603981?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Shengwei Hu
Wei Ni
Wujiafu Sai
Ha Zi
Jun Qiao
Pengyang Wang
Jinliang Sheng
Chuangfu Chen
spellingShingle Shengwei Hu
Wei Ni
Wujiafu Sai
Ha Zi
Jun Qiao
Pengyang Wang
Jinliang Sheng
Chuangfu Chen
Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
PLoS ONE
author_facet Shengwei Hu
Wei Ni
Wujiafu Sai
Ha Zi
Jun Qiao
Pengyang Wang
Jinliang Sheng
Chuangfu Chen
author_sort Shengwei Hu
title Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
title_short Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
title_full Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
title_fullStr Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
title_full_unstemmed Knockdown of myostatin expression by RNAi enhances muscle growth in transgenic sheep.
title_sort knockdown of myostatin expression by rnai enhances muscle growth in transgenic sheep.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Myostatin (MSTN) has been shown to be a negative regulator of skeletal muscle development and growth. MSTN dysfunction therefore offers a strategy for promoting animal growth performance in livestock production. In this study, we investigated the possibility of using RNAi-based technology to generate transgenic sheep with a double-muscle phenotype. A shRNA expression cassette targeting sheep MSTN was used to generate stable shRNA-expressing fibroblast clones. Transgenic sheep were further produced by somatic cell nuclear transfer (SCNT) technology. Five lambs developed to term and three live lambs were obtained. Integration of shRNA expression cassette in three live lambs was confirmed by PCR. RNase protection assay showed that the shRNAs targeting MSTN were expressed in muscle tissues of three transgenic sheep. MSTN expression was significantly inhibited in muscle tissues of transgenic sheep when compared with control sheep. Moreover, transgenic sheep showed a tendency to faster increase in body weight than control sheep. Histological analysis showed that myofiber diameter of transgenic sheep M17 were bigger than that of control sheep. Our findings demonstrate a promising approach to promoting muscle growth in livestock production.
url http://europepmc.org/articles/PMC3603981?pdf=render
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