Identification of a novel glucose transporter-like protein—GLUT-12

Author:

Rogers Suzanne1,Macheda Maria L.1,Docherty Susan E.1,Carty Maynard D.2,Henderson Michael A.3,Soeller Walter C.2,Gibbs E. Michael2,James David E.4,Best James D.1

Affiliation:

1. Departments of Medicine and

2. Department of Cardiovascular Metabolic Diseases, Pfizer Global Research and Development, Pfizer Incorporated, Groton, Connecticut 06340

3. Surgery, The University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria 3065;

4. Institute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland, Australia 4072; and

Abstract

Facilitative glucose transporters exhibit variable hexose affinity and tissue-specific expression. These characteristics contribute to specialized metabolic properties of cells. Here we describe the characterization of a novel glucose transporter-like molecule, GLUT-12. GLUT-12 was identified in MCF-7 breast cancer cells by homology to the insulin-regulatable glucose transporter GLUT-4. The GLUT-12 cDNA encodes 617 amino acids, which possess features essential for sugar transport. Di-leucine motifs are present in NH2 and COOH termini at positions similar to the GLUT-4 FQQI and LL targeting motifs. GLUT-12 exhibits 29% amino acid identity with GLUT-4 and 40% to the recently described GLUT-10. Like GLUT-10, a large extracellular domain is predicted between transmembrane domains 9 and 10. Genomic organization of GLUT-12 is highly conserved with GLUT-10 but distinct from GLUTs 1–5. Immunofluorescence showed that, in the absence of insulin, GLUT-12 is localized to the perinuclear region in MCF-7 cells. Immunoblotting demonstrated GLUT-12 expression in skeletal muscle, adipose tissue, and small intestine. Thus GLUT-12 is potentially part of a second insulin-responsive glucose transport system.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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