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miR-2382-5p Regulates Lipid Metabolism by Targeting NDRG2 in Mammary Epithelial Cells of Dairy Cattle.

Authors :
Xia, Lixin
Zhao, Zhihui
Yang, Runjun
Jiang, Ping
Liu, Yinuo
Yu, Haibin
Bai, Zitong
Mi, Jiaqi
Yu, Xianzhong
Fang, Xibi
Source :
DNA & Cell Biology; Dec2020, Vol. 39 Issue 12, p2125-2133, 9p
Publication Year :
2020

Abstract

microRNA is a class of single-stranded RNA molecules of about 22–24 nucleotides in length, which regulate a variety of biological processes, including lipid metabolism and triglyceride synthesis at transcriptional and translational levels by degrading target mRNAs or interfering with the protein production. In this study, the effect of miR-2382-5p on triglyceride levels was examined in bovine mammary epithelial cells (BMECs), and the results showed that miR-2382-5p could decrease the content of triglyceride. Furthermore, miR-2382-5p regulated the expression of lipoprotein lipase (LPL), peroxisome proliferator-activated receptor gamma co-activator 1beta (PPARGC1B), hormone-sensitive lipase (HSL), and peroxisome proliferator-activated receptor gamma (PPARγ), which are known to increase triglyceride decomposition in lipid metabolism. Luciferase reporter assay and quantitative real-time PCR (qPCR) validated that miR-2382-5p downregulated the mRNA expression of target gene N-myc downstream-regulated gene 2 (NDRG2) by specifically recognizing and binding to its 3′-untranslated region (UTR). Meanwhile, overexpression of NDRG2 led to increased triglyceride and cholesterol production in BMECs. In summary, this study suggested that miR-2382-5p regulated lipid metabolism by targeting NDRG2, which might be a potential target for molecular manipulation of milk fat composition to produce healthy milk. This study also provided basic data for further understanding lipid metabolism in dairy cattle. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10445498
Volume :
39
Issue :
12
Database :
Complementary Index
Journal :
DNA & Cell Biology
Publication Type :
Academic Journal
Accession number :
147502277
Full Text :
https://doi.org/10.1089/dna.2020.5658