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Comprehensive map and functional annotation of the mouse white adipose tissue proteome

Authors :
Xiaoyue Tang
Juan Li
Wei-gang Zhao
Haidan Sun
Zhengguang Guo
Li Jing
Zhufang She
Tao Yuan
Shuai-nan Liu
Quan Liu
Yong Fu
Wei Sun
Source :
PeerJ, Vol 7, p e7352 (2019)
Publication Year :
2019
Publisher :
PeerJ Inc., 2019.

Abstract

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 106) 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.

Details

Language :
English
ISSN :
21678359
Volume :
7
Database :
Directory of Open Access Journals
Journal :
PeerJ
Publication Type :
Academic Journal
Accession number :
edsdoj.1acdc9e1da724fb5ad38dd030a8e02b0
Document Type :
article
Full Text :
https://doi.org/10.7717/peerj.7352