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Comprehensive map and functional annotation of the mouse white adipose tissue proteome
White adipose tissue (WAT) plays a significant role in energy metabolism and the obesity epidemic. In this study, we sought to (1) profile the mouse WAT proteome with advanced 2DLC/MS/MS approach, (2) provide insight into WAT function based on protein functional annotation, and (3) predict potential...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661141/ https://www.ncbi.nlm.nih.gov/pubmed/31380149 http://dx.doi.org/10.7717/peerj.7352 |
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author | Tang, Xiaoyue Li, Juan Zhao, Wei-gang Sun, Haidan Guo, Zhengguang Jing, Li She, Zhufang Yuan, Tao Liu, Shuai-nan Liu, Quan Fu, Yong Sun, Wei |
author_facet | Tang, Xiaoyue Li, Juan Zhao, Wei-gang Sun, Haidan Guo, Zhengguang Jing, Li She, Zhufang Yuan, Tao Liu, Shuai-nan Liu, Quan Fu, Yong Sun, Wei |
author_sort | Tang, Xiaoyue |
collection | PubMed |
description | White adipose tissue (WAT) plays a significant role in energy metabolism and the obesity epidemic. In this study, we sought to (1) profile the mouse WAT proteome with advanced 2DLC/MS/MS approach, (2) provide insight into WAT function based on protein functional annotation, and (3) predict potentially secreted proteins. A label-free 2DLC/MS/MS proteomic approach was used to identify the WAT proteome from female mouse WAT. A total of 6,039 proteins in WAT were identified, among which 5,160 were quantified (spanning a magnitude of 10(6)) using an intensity-based absolute quantification algorithm, and 3,117 proteins were reported by proteomics technology for the first time in WAT. To comprehensively analyze the function of WAT, the proteins were divided into three quantiles based on abundance and we found that proteins of different abundance performed different functions. High-abundance proteins (the top 90%, 1,219 proteins) were involved in energy metabolism; middle-abundance proteins (90–99%, 2,273 proteins) were involved in the regulation of protein synthesis; and low-abundance proteins (99–100%, 1,668 proteins) were associated with lipid metabolism and WAT beiging. Furthermore, 800 proteins were predicted by SignalP4.0 to have signal peptides, 265 proteins had never been reported, and five have been reported as adipokines. The above results provide a large dataset of the normal mouse WAT proteome, which might be useful for WAT function research. |
format | Online Article Text |
id | pubmed-6661141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66611412019-08-02 Comprehensive map and functional annotation of the mouse white adipose tissue proteome Tang, Xiaoyue Li, Juan Zhao, Wei-gang Sun, Haidan Guo, Zhengguang Jing, Li She, Zhufang Yuan, Tao Liu, Shuai-nan Liu, Quan Fu, Yong Sun, Wei PeerJ Bioinformatics White adipose tissue (WAT) plays a significant role in energy metabolism and the obesity epidemic. In this study, we sought to (1) profile the mouse WAT proteome with advanced 2DLC/MS/MS approach, (2) provide insight into WAT function based on protein functional annotation, and (3) predict potentially secreted proteins. A label-free 2DLC/MS/MS proteomic approach was used to identify the WAT proteome from female mouse WAT. A total of 6,039 proteins in WAT were identified, among which 5,160 were quantified (spanning a magnitude of 10(6)) using an intensity-based absolute quantification algorithm, and 3,117 proteins were reported by proteomics technology for the first time in WAT. To comprehensively analyze the function of WAT, the proteins were divided into three quantiles based on abundance and we found that proteins of different abundance performed different functions. High-abundance proteins (the top 90%, 1,219 proteins) were involved in energy metabolism; middle-abundance proteins (90–99%, 2,273 proteins) were involved in the regulation of protein synthesis; and low-abundance proteins (99–100%, 1,668 proteins) were associated with lipid metabolism and WAT beiging. Furthermore, 800 proteins were predicted by SignalP4.0 to have signal peptides, 265 proteins had never been reported, and five have been reported as adipokines. The above results provide a large dataset of the normal mouse WAT proteome, which might be useful for WAT function research. PeerJ Inc. 2019-07-25 /pmc/articles/PMC6661141/ /pubmed/31380149 http://dx.doi.org/10.7717/peerj.7352 Text en © 2019 Tang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Tang, Xiaoyue Li, Juan Zhao, Wei-gang Sun, Haidan Guo, Zhengguang Jing, Li She, Zhufang Yuan, Tao Liu, Shuai-nan Liu, Quan Fu, Yong Sun, Wei Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title | Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title_full | Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title_fullStr | Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title_full_unstemmed | Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title_short | Comprehensive map and functional annotation of the mouse white adipose tissue proteome |
title_sort | comprehensive map and functional annotation of the mouse white adipose tissue proteome |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661141/ https://www.ncbi.nlm.nih.gov/pubmed/31380149 http://dx.doi.org/10.7717/peerj.7352 |
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