Single nucleotide polymorphisms in 5'-UTR of the SLC2A4 gene regulate solute carrier family 2 member 4 gene expression in visceral adipose tissue

Gene. 2016 Jan 15;576(1 Pt 3):499-504. doi: 10.1016/j.gene.2015.10.067. Epub 2015 Oct 31.

Abstract

Background: The glucose uptake by numerous cells like adipocytes or skeletal muscle cells requires activation of specific proteins called glucose transporters. GLUT4 content and its activation as well as SLC2A4 gene expression level are decreased in patients with type 2 diabetes. The SLC2A4 gene expression rate might be modulated by genetic variances in UTRs. The relationship between two SNPs in 5'UTR and one SNP in 3'UTR and SLC2A4 gene expression rate in adipose tissue and lymphocytes has been evaluated.

Methods: The study was performed on lymphocytes collected from 34 type 2 diabetic patients and equal number of controls. Visceral adipose tissue biopsies were collected from 15 patients with T2DM and from 24 controls.

Results: SLC2A4 gene expression level was slightly lower within type 2 diabetic patients in both type of tissues. Furthermore, the negative correlation between SLC2A4 gene expression level in visceral adipose tissue and BMI has been noticed. The genotypes of two SNPs in 5'UTRs (rs5417 and rs5418) were correlated with lower mRNA amount of GLUT4 within recessive homozygotes belonging to control group.

Conclusions: Present results suggest the relationship between genetic variances within UTRs of SLC2A4 gene and gene expression rate. However, the relationship is tissue specific and is noticeable in adipose tissue of lean and healthy subjects.

Keywords: Lymphocytes; SLC2A4 gene; SNP; Type 2 diabetes; UTR; Visceral adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5' Untranslated Regions*
  • Diabetes Mellitus, Type 2 / genetics
  • Glucose Transporter Type 4 / genetics*
  • Humans
  • Intra-Abdominal Fat / metabolism*
  • Polymorphism, Single Nucleotide*

Substances

  • 5' Untranslated Regions
  • Glucose Transporter Type 4
  • SLC2A4 protein, human