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Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs

Feed efficiency (FE) is a highly important economic trait in pig production. Investigating the molecular mechanisms of FE is essential for trait improvement. In this study, the skeletal muscle proteome of high-FE and low-FE pigs were investigated by the iTRAQ approach. A total of 1780 proteins were...

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Autores principales: Fu, Liangliang, Xu, Yueyuan, Hou, Ye, Qi, Xiaolong, Zhou, Lian, Liu, Huiying, Luan, Yu, Jing, Lu, Miao, Yuanxin, Zhao, Shuhong, Liu, Huazhen, Li, Xinyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366906/
https://www.ncbi.nlm.nih.gov/pubmed/28345649
http://dx.doi.org/10.1038/srep45291
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author Fu, Liangliang
Xu, Yueyuan
Hou, Ye
Qi, Xiaolong
Zhou, Lian
Liu, Huiying
Luan, Yu
Jing, Lu
Miao, Yuanxin
Zhao, Shuhong
Liu, Huazhen
Li, Xinyun
author_facet Fu, Liangliang
Xu, Yueyuan
Hou, Ye
Qi, Xiaolong
Zhou, Lian
Liu, Huiying
Luan, Yu
Jing, Lu
Miao, Yuanxin
Zhao, Shuhong
Liu, Huazhen
Li, Xinyun
author_sort Fu, Liangliang
collection PubMed
description Feed efficiency (FE) is a highly important economic trait in pig production. Investigating the molecular mechanisms of FE is essential for trait improvement. In this study, the skeletal muscle proteome of high-FE and low-FE pigs were investigated by the iTRAQ approach. A total of 1780 proteins were identified, among which 124 proteins were differentially expressed between the high- and low-FE pigs, with 74 up-regulated and 50 down-regulated in the high-FE pigs. Ten randomly selected differentially expressed proteins (DEPs) were validated by Western blotting and quantitative PCR (qPCR). Gene ontology (GO) analysis showed that all the 25 DEPs located in mitochondria were down-regulated in the high-FE pigs. Furthermore, the glucose-pyruvate-tricarboxylic acid (TCA)-oxidative phosphorylation energy metabolism signaling pathway was found to differ between high- and low-FE pigs. The key enzymes involved in the conversion of glucose to pyruvate were up-regulated in the high-FE pigs. Thus, our results suggested mitochondrial energy metabolism in the skeletal muscle tissue was negatively correlated with FE in pigs, and glucose utilization to generate ATP was more efficient in the skeletal muscle tissue of high-FE pigs. This study offered new targets and pathways for improvement of FE in pigs.
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spelling pubmed-53669062017-03-28 Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs Fu, Liangliang Xu, Yueyuan Hou, Ye Qi, Xiaolong Zhou, Lian Liu, Huiying Luan, Yu Jing, Lu Miao, Yuanxin Zhao, Shuhong Liu, Huazhen Li, Xinyun Sci Rep Article Feed efficiency (FE) is a highly important economic trait in pig production. Investigating the molecular mechanisms of FE is essential for trait improvement. In this study, the skeletal muscle proteome of high-FE and low-FE pigs were investigated by the iTRAQ approach. A total of 1780 proteins were identified, among which 124 proteins were differentially expressed between the high- and low-FE pigs, with 74 up-regulated and 50 down-regulated in the high-FE pigs. Ten randomly selected differentially expressed proteins (DEPs) were validated by Western blotting and quantitative PCR (qPCR). Gene ontology (GO) analysis showed that all the 25 DEPs located in mitochondria were down-regulated in the high-FE pigs. Furthermore, the glucose-pyruvate-tricarboxylic acid (TCA)-oxidative phosphorylation energy metabolism signaling pathway was found to differ between high- and low-FE pigs. The key enzymes involved in the conversion of glucose to pyruvate were up-regulated in the high-FE pigs. Thus, our results suggested mitochondrial energy metabolism in the skeletal muscle tissue was negatively correlated with FE in pigs, and glucose utilization to generate ATP was more efficient in the skeletal muscle tissue of high-FE pigs. This study offered new targets and pathways for improvement of FE in pigs. Nature Publishing Group 2017-03-27 /pmc/articles/PMC5366906/ /pubmed/28345649 http://dx.doi.org/10.1038/srep45291 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Fu, Liangliang
Xu, Yueyuan
Hou, Ye
Qi, Xiaolong
Zhou, Lian
Liu, Huiying
Luan, Yu
Jing, Lu
Miao, Yuanxin
Zhao, Shuhong
Liu, Huazhen
Li, Xinyun
Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title_full Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title_fullStr Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title_full_unstemmed Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title_short Proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
title_sort proteomic analysis indicates that mitochondrial energy metabolism in skeletal muscle tissue is negatively correlated with feed efficiency in pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366906/
https://www.ncbi.nlm.nih.gov/pubmed/28345649
http://dx.doi.org/10.1038/srep45291
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