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Data on the decreased expression of FOXO1 by miR-1271 in HepG2 hepatocytes
Won-Mo Yang1, Kyung-Ho Min1, Se-Whan Park1
1Department of Biochemistry, Dongguk University College of Medicine, Gyeongju-si, Gyeongsangbuk-do 38067, Republic of Korea.
Abstract:
Obesity and metabolic diseases are closely associated with insulin resistance. Obesity-induced miRNAs are also considered to be potential contributors to the development of insulin resistance and type 2 diabetes. Previously, the expression of miR-1271 was reported to be upregulated in the liver of diet-induced obese mice (Yang et al., 2016) [1]. In this data article, multiple in silico analysis predicted FOXO1 gene to be a direct target of miR-1271. Dual luciferase reporter gene analysis showed that miR-1271 suppressed FOXO1 expression by direct binding to 3'UTR. The overexpression of miR-1271 reduced the protein expression of FOXO1, thereby reducing the transcription of PEPCK, a downstream target of FOXO1. The data is related to a research article entitled "MiR-1271 upregulated by saturated fatty acid palmitate provokes impaired insulin signaling by repressing INSR and IRS-1 expression in HepG2 cells" (Yang et al., 2016) [1].
Insights
MicroRNA-1271 (miR-1271) upregulation in obesity impairs insulin signaling by targeting the FOXO1 gene. This leads to reduced PEPCK transcription, contributing to insulin resistance and type 2 diabetes.
Area of Science:
- Metabolic diseases
- Molecular biology
- Genetics
Background:
- Obesity and metabolic diseases are linked to insulin resistance.
- Obesity-induced microRNAs (miRNAs) may contribute to insulin resistance and type 2 diabetes.
- miR-1271 expression is upregulated in diet-induced obesity.
Purpose of the Study:
- To investigate the role of miR-1271 in insulin resistance.
- To identify the direct target of miR-1271.
- To elucidate the molecular mechanism by which miR-1271 affects insulin signaling.
Main Methods:
- In silico analysis to predict gene targets.
- Dual luciferase reporter gene assay to confirm direct binding.
- Western blot to assess protein expression.
- Quantitative real-time PCR to measure gene transcription.
Main Results:
- In silico analysis predicted FOXO1 as a direct target of miR-1271.
- Dual luciferase assay confirmed miR-1271 binds to the 3'UTR of FOXO1, suppressing its expression.
- Overexpression of miR-1271 reduced FOXO1 protein levels.
- Reduced FOXO1 expression led to decreased transcription of PEPCK, a downstream target.
Conclusions:
- miR-1271 directly targets and suppresses FOXO1 expression.
- This suppression of FOXO1 by miR-1271 impairs insulin signaling pathways.
- The findings suggest miR-1271 as a potential therapeutic target for insulin resistance and type 2 diabetes.
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