RGD Reference Report - Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain. - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain.

Authors: Uldry, M  Ibberson, M  Horisberger, JD  Chatton, JY  Riederer, BM  Thorens, B 
Citation: Uldry M, etal., EMBO J 2001 Aug 15;20(16):4467-77.
RGD ID: 634137
Pubmed: (View Article at PubMed) PMID:11500374
DOI: Full-text: DOI:10.1093/emboj/20.16.4467

Inositol and its phosphorylated derivatives play a major role in brain function, either as osmolytes, second messengers or regulators of vesicle endo- and exocytosis. Here we describe the identification and functional characterization of a novel H(+)-myo- inositol co-transporter, HMIT, expressed predominantly in the brain. HMIT cDNA encodes a 618 amino acid polypeptide with 12 predicted transmembrane domains. Functional expression of HMIT in Xenopus oocytes showed that transport activity was specific for myo-inositol and related stereoisomers with a Michaelis-Menten constant of approximately 100 microM, and that transport activity was strongly stimulated by decreasing pH. Electrophysiological measurements revealed that transport was electrogenic with a maximal transport activity reached at pH 5.0. In rat brain membrane preparations, HMIT appeared as a 75-90 kDa protein that could be converted to a 67 kDa band upon enzymatic deglycosylation. Immunofluorescence microscopy analysis showed HMIT expression in glial cells and some neurons. These data provide the first characterization of a mammalian H(+)-coupled myo- inositol transporter. Predominant central expression of HMIT suggests that it has a key role in the control of myo-inositol brain metabolism.



Gene Ontology Annotations    

Cellular Component

Objects Annotated

Genes (Rattus norvegicus)
Slc2a13  (solute carrier family 2 member 13)

Objects referenced in this article
Gene SLC2A13 solute carrier family 2 member 13 Homo sapiens

Additional Information