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Effect of ELOVL6 on the lipid metabolism of bovine adipocytes.

Authors :
Junjvlieke, Zainaguli
Khan, Rajwali
Mei, Chugang
Cheng, Gong
Wang, Sihu
Raza, Sayed Haidar Abbas
Hong, Jieyun
Wang, Xiaoyu
Yang, Wucai
Zan, Linsen
Source :
Genomics. May2020, Vol. 112 Issue 3, p2282-2290. 9p.
Publication Year :
2020

Abstract

This study investigated the effect of ELOVL6 (elongation of very long chain fatty acids protein 6) and its underlying mechanism on lipid metabolism in bovine adipocytes. The ELOVL6 gene was overexpressed in bovine adipocytes by adenoviruses, and RNA sequencing was performed. Overexpression of ELOVL6 showed reduced proportions of C14:0 (Myristic) and C16:0 (palmitate) fatty acids and increased proportions of C18.0 (stearate) and C20:4n6 (arachidonic) fatty acids in adipocytes. In addition, a total of 2170 differentially expressed genes (DEGs) were found, containing 1802 up-regulated and 368 down-regulated genes. KEGG pathway analysis revealed that the down-regulated genes were linked with the regulation of lipolysis and the Wnt signaling pathway. The up-regulated genes were mainly involved in the FoxO signaling pathway; the PI3K-Akt signaling pathway; and the cAMP signaling pathway. In conclusion, our results suggest that ELOVL6 could affect the fatty acid composition in bovine adipocytes. We identified numerous related DEGs and pathways, which may provide a basis for studying the function and molecular mechanism of the ELOVL6 gene in regulating lipid metabolism. • ELOVL6 regulate lipid metabolism in bovine adipocytes. • ELOVL6 is a positive regulator of C18.0 and C20:4n6 and negative regulator of C14:0 and C16:0 fatty acids. • ELOVL6 regulate lipogenesis and lipolysis through Wnt, cAMP, FoxO, and PI3K-Akt signaling pathways in bovine adipocytes. • ELOVL6 gene could be used as a candidate gene for the improvement of meat quality in cattle breed improvement program. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08887543
Volume :
112
Issue :
3
Database :
Academic Search Index
Journal :
Genomics
Publication Type :
Academic Journal
Accession number :
142275397
Full Text :
https://doi.org/10.1016/j.ygeno.2019.12.024