MicroRNA-212 targets SIRT2 to influence lipogenesis in bovine mammary epithelial cell line

被引:16
作者
Lu, Xubin [1 ]
Xia, Hailei [1 ]
Jiang, Jingyi [1 ]
Xu, Xin [1 ]
Li, Mingxun [1 ]
Chen, Zhi [1 ]
Sun, Yujia [2 ]
Zhang, Huimin [1 ]
Yang, Zhangping [1 ]
机构
[1] Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225002, Jiangsu, Peoples R China
[2] Yangzhou Univ, Joint Int Res Lab Agr & Agriprod Safety, Yangzhou 225009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Lipogenesis; miR-212; miR-375; miR-655; SIRT2; ADIPOCYTE DIFFERENTIATION; FOXO1; MIR-212/132; EXPRESSION; PATHWAY; CANCER; GAMMA; FAT;
D O I
10.1017/S0022029920000229
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
In this research paper we filter and verify miRNAs which may target silent information regulator homolog 2 (SIRT2) gene and then describe the mechanism whereby miRNA-212 might regulate lipogenic genes in mammary epithelial cell lines via targeting SIRT2. Bioinformatics analysis revealed that the bovine SIRT2 gene is regulated by three miRNAs: miR-212, miR-375 and miR-655. The three miRNAs were verified and screened by qRT-PCR, western blot, and luciferase multiplex verification techniques and only miR-212 was shown to have a targeting relationship with SIRT2. The results of co-transfecting miR-212 and silencing RNA (siRNA) showed that by targeting SIRT2, miR-212 can regulate the expression of fatty acid synthetase (FASN) and sterol regulatory element binding factor 1 (SREBP1) but not peroxisome proliferator-activated receptor gamma (PPAR gamma). Measurement of triglyceride (TAG) content showed that miR-212 increased the fat content of mammary epithelial cell lines. The study indicates that miR-212 could target and inhibit the expression of the SIRT2 gene to promote lipogenesis in mammary epithelial cell lines.
引用
收藏
页码:232 / 238
页数:7
相关论文
共 38 条
[1]   MicroRNA-146b promotes adipogenesis by suppressing the SIRT1-FOXO1 cascade [J].
Ahn, Jiyun ;
Lee, Hyunjung ;
Jung, Chang Hwa ;
Jeon, Tae Il ;
Ha, Tae Youl .
EMBO MOLECULAR MEDICINE, 2013, 5 (10) :1602-1612
[2]   FOXO1 represses peroxisome proliferator-activated receptor-γ1 and -γ2 gene promoters in primary adipocytes -: A novel paradigm to increase insulin sensitivity [J].
Armoni, Michal ;
Harel, Chava ;
Karni, Shiri ;
Chen, Hui ;
Bar-Yoseph, Fabiana ;
Ver, Marel R. ;
Quon, Michael J. ;
Karnieli, Eddy .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (29) :19881-19891
[3]   miR-132/212 is induced by stress and its dysregulation triggers anxiety-related behavior [J].
Aten, Sydney ;
Page, Chloe E. ;
Kalidindi, Anisha ;
Wheaton, Kelin ;
Niraula, Anzela ;
Godbout, Jon P. ;
Hoyt, Kari R. ;
Obrietan, Karl .
NEUROPHARMACOLOGY, 2019, 144 :256-270
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[5]   Comprehensive Luciferase-Based Reporter Gene Assay Reveals Previously Masked Up-Regulatory Effects of miRNAs [J].
Campos-Melo, Danae ;
Droppelmann, Cristian A. ;
Volkening, Kathryn ;
Strong, Michael J. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (09) :15592-15602
[6]   MicroRNAs as regulators of metabolic disease: pathophysiologic significance and emerging role as biomarkers and therapeutics [J].
Deiuliis, J. A. .
INTERNATIONAL JOURNAL OF OBESITY, 2016, 40 (01) :88-101
[7]   Development and Validation of a Novel Dual Luciferase Reporter Gene Assay to Quantify Ebola Virus VP24 Inhibition of IFN Signaling [J].
Fanunza, Elisa ;
Frau, Aldo ;
Sgarbanti, Marco ;
Orsatti, Roberto ;
Corona, Angela ;
Tramontano, Enzo .
VIRUSES-BASEL, 2018, 10 (02)
[8]   Transcriptional control of adipocyte formation [J].
Farmer, Stephen R. .
CELL METABOLISM, 2006, 4 (04) :263-273
[9]   A Circadian Rhythm Orchestrated by Histone Deacetylase 3 Controls Hepatic Lipid Metabolism [J].
Feng, Dan ;
Liu, Tao ;
Sun, Zheng ;
Bugge, Anne ;
Mullican, Shannon E. ;
Alenghat, Theresa ;
Liu, X. Shirley ;
Lazar, Mitchell A. .
SCIENCE, 2011, 331 (6022) :1315-1319
[10]   Exercise training prevents obesity-associated disorders: Role of miRNA-208a and MED13 [J].
Fernandes, Tiago ;
Barretti, Diego Lopes ;
Phillips, M. Ian ;
Oliveira, Edilamar Menezes .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2018, 476 :148-154