Estrogen Abolishes the Repression Role of gga-miR-221-5p Targeting ELOVL6 and SQLE to Promote Lipid Synthesis in Chicken Liver

Int J Mol Sci. 2020 Feb 27;21(5):1624. doi: 10.3390/ijms21051624.

Abstract

Few studies have been conducted regarding the biological function and regulation role of gga-miR-221-5p in the liver. We compared the conservation of miR-221-5p among species and investigated the expression pattern of gga-miR-221-5p, validating the direct target genes of gga-miR-221-5p by dual luciferase reporter assay, the biological function of gga-miR-221-5p in the liver was studied by gga-miR-221-5p overexpression and inhibition. Furthermore, we explored the regulation of gga-miR-221-5p and its target genes by treatment with estrogen and estrogen antagonists in vivo and in vitro. The results showed that miR-221-5p was highly conserved among species, expressed in all tested tissues and significantly downregulated in peak-laying hen liver compared to pre-laying hen liver. Gga-miR-221-5p could directly target the expression of elongase of very long chain fatty acids 6 (ELOVL6) and squalene epoxidase (SQLE) genes to affect triglyceride and total cholesterol content in the liver. 17β-estradiol could significantly inhibit the expression of gga-miR-221-5p but promote the expression of ELOVL6 and SQLE genes. In conclusion, the highly conservative gga-miR-221-5p could directly target ELOVL6 and SQLE mRNAs to affect the level of intracellular triglyceride and total cholesterol. Meanwhile, 17β-estradiol could repress the expression of gga-miR-221-5p but increase the expression of ELOVL6 and SQLE, therefore promoting the synthesis of intracellular triglyceride and cholesterol levels in the liver of egg-laying chicken.

Keywords: ELOVL6; SQLE; chicken; estrogen; gga-miR-221-5p; lipid metabolism.

MeSH terms

  • Animals
  • Cell Line
  • Chickens / genetics
  • Chickens / metabolism*
  • Cholesterol / metabolism
  • Estradiol / administration & dosage
  • Estradiol / pharmacology
  • Estrogen Antagonists / pharmacology
  • Estrogens / administration & dosage
  • Estrogens / pharmacology*
  • Fatty Acid Elongases / genetics
  • Fatty Acid Elongases / metabolism*
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / genetics
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Liver / drug effects*
  • Liver / metabolism*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Squalene Monooxygenase / genetics
  • Squalene Monooxygenase / metabolism*
  • Triglycerides / metabolism
  • Up-Regulation

Substances

  • Estrogen Antagonists
  • Estrogens
  • MicroRNAs
  • Triglycerides
  • Estradiol
  • Cholesterol
  • Squalene Monooxygenase
  • Fatty Acid Elongases