GLUT1

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SLC2A1
4pyp glut1.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases SLC2A1, CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN, solute carrier family 2 member 1
External IDs OMIM: 138140 MGI: 95755 HomoloGene: 68520 GeneCards: 6513
RNA expression pattern
PBB GE SLC2A1 201249 at tn.png

PBB GE SLC2A1 201250 s at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006516

NM_011400

RefSeq (protein)

NP_006507.2

NP_035530.2

Location (UCSC) Chr 1: 42.93 – 42.96 Mb Chr 4: 119.11 – 119.14 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Glucose transporter 1 (or GLUT1), also known as solute carrier family 2, facilitated glucose transporter member 1 (SLC2A1), is a uniporter protein that in humans is encoded by the SLC2A1 gene.[3] GLUT1 facilitates the transport of glucose across the plasma membranes of mammalian cells.[4]

Discovery[edit]

GLUT1 was the first glucose transporter to be characterized. GLUT 1 is highly conserved.[3] GLUT 1 of humans and mice have 98% homology. GLUT 1 has 40% homology with other GLUTs.

Function[edit]

Energy-yielding metabolism in erythrocytes depends on a constant supply of glucose from the blood plasma, where the glucose concentration is maintained at about 5mM. Glucose enters the erythrocyte by facilitated diffusion via a specific glucose transporter, at a rate about 50,000 times greater than uncatalyzed transmembrane diffusion. The glucose transporter of erythrocytes (called GLUT1 to distinguish it from related glucose transporters in other tissues) is a type III integral protein with 12 hydrophobic segments, each of which is believed to form a membrane-spanning helix. The detailed structure of GLUT1 is not known yet, but one plausible model suggests that the side-by-side assembly of several helices produces a transmembrane channel lined with hydrophilic residues that can hydrogen-bond with glucose as it moves through the channel.[5]

GLUT1 is responsible for the low level of basal glucose uptake required to sustain respiration in all cells. Expression levels of GLUT1 in cell membranes are increased by reduced glucose levels and decreased by increased glucose levels.[citation needed]

GLUT1 is also a major receptor for uptake of Vitamin C as well as glucose, especially in non vitamin C producing mammals as part of an adaptation to compensate by participating in a Vitamin C recycling process. In mammals that do produce Vitamin C, GLUT4 is often expressed instead of GLUT1.[6]

Tissue distribution[edit]

It is widely distributed in fetal tissues. In the adult it is expressed at highest levels in erythrocytes and also in the endothelial cells of barrier tissues such as the blood–brain barrier.[citation needed]

Structure[edit]

GLUT1 behaves as a Michaelis-Menten enzyme and contains 12 membrane-spanning alpha helices, each containing 20 amino acid residues. A helical wheel analysis shows that the membrane spanning alpha helices are amphipathic, with one side being polar and the other side hydrophobic. Six of these membrane spanning helices are believed to bind together in the membrane to create a polar channel in the center through which glucose can traverse, with the hydrophobic regions on the outside of the channel adjacent to the fatty acid tails of the membrane.[citation needed]

Clinical significance[edit]

Mutations in the GLUT1 gene are responsible for GLUT1 deficiency or De Vivo disease, which is a rare autosomal dominant disorder.[7] This disease is characterized by a low cerebrospinal fluid glucose concentration (hypoglycorrhachia), a type of neuroglycopenia, which results from impaired glucose transport across the blood–brain barrier.

GLUT1 is also a receptor used by the HTLV virus to gain entry into target cells.[8]

Glut1 has also been demonstrated as a powerful histochemical marker for haemangioma of infancy[9]

Interactions[edit]

GLUT1 has been shown to interact with GIPC1.[10]

GLUT1 has two significant types in brain 45k and 55k. GLUT1 45k is present on astroglia of neurons and GLUT1 55k is present on capillaries in brain and is responsible for glucose transport across blood brain barrier and its deficiency causes low level of glucose in CSF(less than 60 mg/dl) which may manifest as convulsion in deficient individuals.[citation needed]

Recently it has been described a GLUT1 inhibitor, DERL3, that is often methylated in colorectal cancer. In this cancer, DERL3 methylations seems to mediate the Warburg Effect.[11]

Inhibitors[edit]

Fasentin is a small molecule inhibitor of the intracellular domain of GLUT1 preventing glucose uptake.[12]

Interactive pathway map[edit]

Click on genes, proteins and metabolites below to link to respective articles. [§ 1]

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GlycolysisGluconeogenesis_WP534 go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to article go to Entrez go to article go to article go to article go to article go to article go to WikiPathways go to article go to Entrez go to article
|{{{bSize}}}px|alt=Glycolysis and Gluconeogenesis edit]]
Glycolysis and Gluconeogenesis edit
  1. ^ The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534". 

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ a b Mueckler M, Caruso C, Baldwin SA, Panico M, Blench I, Morris HR, Allard WJ, Lienhard GE, Lodish HF (1985). "Sequence and structure of a human glucose transporter". Science. 229 (4717): 941–5. doi:10.1126/science.3839598. PMID 3839598. 
  4. ^ Olson AL, Pessin JE (1996). "Structure, function, and regulation of the mammalian facilitative glucose transporter gene family". Annual Review of Nutrition. 16: 235–56. doi:10.1146/annurev.nu.16.070196.001315. PMID 8839927. 
  5. ^ Nelson DL, Cox MM (2008). Lehninger, Principles of Biochemistry. W. H. Freeman and Company. ISBN 978-0-7167-7108-1. [page needed]
  6. ^ Montel-Hagen A, Kinet S, Manel N, Mongellaz C, Prohaska R, Battini JL, Delaunay J, Sitbon M, Taylor N (2008). "Erythrocyte Glut1 triggers dehydroascorbic acid uptake in mammals unable to synthesize vitamin C". Cell. 132 (6): 1039–48. doi:10.1016/j.cell.2008.01.042. PMID 18358815. Lay summaryScienceDaily (March 21, 2008). 
  7. ^ Seidner G, Alvarez MG, Yeh JI, et al. (1998). "GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood–brain barrier hexose carrier". Nat. Genet. 18 (2): 188–91. doi:10.1038/ng0298-188. PMID 9462754. 
  8. ^ Manel N, Kim FJ, Kinet S, Taylor N, Sitbon M, Battini JL (November 2003). "The ubiquitous glucose transporter GLUT-1 is a receptor for HTLV". Cell. 115 (4): 449–59. doi:10.1016/S0092-8674(03)00881-X. PMID 14622599. 
  9. ^ North PE, Waner M, Mizeracki A, Mihm MC (January 2000). "GLUT1: a newly discovered immunohistochemical marker for juvenile hemangiomas". Hum. Pathol. 31 (1): 11–22. doi:10.1016/S0046-8177(00)80192-6. PMID 10665907. 
  10. ^ Bunn RC, Jensen MA, Reed BC (1999). "Protein interactions with the glucose transporter binding protein GLUT1CBP that provide a link between GLUT1 and the cytoskeleton". Molecular Biology of the Cell. 10 (4): 819–32. doi:10.1091/mbc.10.4.819. PMC 25204free to read. PMID 10198040. 
  11. ^ Lopez-Serra P, Marcilla M, Villanueva A, Ramos-Fernandez A, Palau A, Leal L, Wahi JE, Setien-Baranda F, Szczesna K, Moutinho C, Martinez-Cardus A, Heyn H, Sandoval J, Puertas S, Vidal A, Sanjuan X, Martinez-Balibrea E, Viñals F, Perales JC, Bramsem JB, Ørntoft TF, Andersen CL, Tabernero J, McDermott U, Boxer MB, Vander Heiden MG, Albar JP, Esteller M (2014). "A DERL3-associated defect in the degradation of SLC2A1 mediates the Warburg effect". Nature Communications. 5: 3608. doi:10.1038/ncomms4608. PMC 3988805free to read. PMID 24699711. 
  12. ^ Wood TE, Dalili S, Simpson CD, Hurren R, Mao X, Saiz FS, Gronda M, Eberhard Y, Minden MD, Bilan PJ, Klip A, Batey RA, Schimmer AD (2008). "A novel inhibitor of glucose uptake sensitizes cells to FAS-induced cell death". Mol. Cancer Ther. 7 (11): 3546–55. doi:10.1158/1535-7163.MCT-08-0569. PMID 19001437. Retrieved 2015-04-25. 

Further reading[edit]

External links[edit]