Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/8302
Title: Expression cloning of a rat hepatic reduced glutathione transporter with canalicular characteristics
Author: Yi, Jian-Ri
Lu, Shilun
Fernández-Checa Torres, José Carlos
Kaplowitz, Neil
Keywords: Glutatió
Fetge
Metabolisme
Proteïnes de membrana
Transport biològic
Clonatge
Glutathione
Liver
Membrane proteins
Metabolism
Cloning
Issue Date: 1994
Publisher: American Society for Clinical Investigation
Abstract: Using the Xenopus oocyte expression system, we have previously identified an approximately 4-kb fraction of mRNA from rat liver that expresses sulfobromophthalein-glutathione (BSP-GSH)-insensitive reduced glutathione (GSH) transport (Fernandez-Checa, J., J. R. Yi, C. Garcia-Ruiz, Z. Knezic, S. Tahara, and N. Kaplowitz. 1993. J. Biol. Chem. 268:2324-2328). Starting with a cDNA library constructed from this fraction, we have now isolated a single clone that expresses GSH transporter activity. The cDNA for the rat canalicular GSH transporter (RcGshT) is 4.05 kb with an open reading frame of 2,505 nucleotides encoding for a polypeptide of 835 amino acids (95,785 daltons). No identifiable homologies were found in searching various databases. An approximately 96-kD protein is generated in in vitro translation of cRNA for RcGshT. Northern blot analysis reveals a single 4-kb transcript in liver, kidney, intestine, lung, and brain. The abundance of mRNA for RcGshT in rat liver increased 3, 6, and 12 h after a single dose of phenobarbital. Insensitivity to BSP-GSH and induction by phenobarbital, unique characteristics of canalicular GSH secretion, suggest that RcGshT encodes for the canalicular GSH transporter.
Note: Reproducció del document publicat a http://dx.doi.org/10.1172/JCI117170
It is part of: Journal of Clinical Investigation, 1994, vol. 93, núm. 4, p. 1841-1845.
URI: http://hdl.handle.net/2445/8302
ISSN: 0021-9738
Appears in Collections:Articles publicats en revistes (Medicina)

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