Genetic Modulation of the GLUT1 Transporter Expression-Potential Relevance in Complex Diseases.
Anna KulinNóra KucsmaBalázs BohárBotond Literáti-NagyLászló KorányiJudit CserepesAnikó SomogyiBalazs SarkadiEdit SzabóGyörgy VáradyPublished in: Biology (2022)
The human GLUT1 (SLC2A1) membrane protein is the key glucose transporter in numerous cell types, including red cells, kidney, and blood-brain barrier cells. The expression level of this protein has a role in several diseases, including cancer and Alzheimer's disease. In this work, to investigate a potential genetic modulation of the GLUT1 expression level, the protein level was measured in red cell membranes by flow cytometry, and the genetic background was analyzed by qPCR and luciferase assays. We found significant associations between red cell GLUT1 levels and four single nucleotide polymorphisms (SNP) in the coding SLC2A1 gene, that in individuals with the minor alleles of rs841848, rs1385129, and rs11537641 had increased, while those having the variant rs841847 had decreased erythrocyte GLUT1 levels. In the luciferase reporter studies performed in HEK-293T and HepG2 cells, a similar SNP-dependent modulation was observed, and lower glucose, serum, and hypoxic condition had variable, cell- and SNP-specific effects on luciferase expression. These results should contribute to a more detailed understanding of the genetic background of membrane GLUT1 expression and its potential role in associated diseases.
Keyphrases
- genome wide
- poor prognosis
- blood brain barrier
- binding protein
- single cell
- cell therapy
- copy number
- induced apoptosis
- dna methylation
- flow cytometry
- endothelial cells
- gene expression
- stem cells
- adipose tissue
- type diabetes
- metabolic syndrome
- blood pressure
- protein protein
- papillary thyroid
- signaling pathway
- high density
- subarachnoid hemorrhage
- small molecule
- climate change
- cell death
- brain injury
- genetic diversity