PMID: 11324718Apr 28, 2001Paper

cDNA cloning and expression of a bovine phenol UDP-glucuronosyltransferase, BovUGT1A6

Life Sciences
H IwanoA Yuasa

Abstract

A full-length cDNA encoding a phenol UDP-glucuronosyltransferase was isolated by plaque hybridization, RT-PCR and 5'-RACE from a cDNA library prepared from the bovine liver. The deduced amino acid sequence (529 amino acid residues) has A signal sequence (23 amino acid residues) at the amino terminus and a transmembrane-anchoring domain (17 amino acid residues) at the carboxyl terminus. The encoded protein has a potential asparagine-linked glycosylation site (Asn291). The cloned cDNA was named bovUGT1A6 on the basis of the amino acid similarity. BovUGT1A6 cloned in the pAAH5 expression vector was transformed into Saccharomyces cerevisiea AH22 cells to obtain an active 54-kDa bovUGT1A6 enzyme. The expressed enzyme represented UDP-glucuronosyltransferase activities toward 1-naphthol and 4-methylumbelliferone, confirming that the isolated cDNA is an isoform of bovine phenol UDP-glucuronosyltransferase. Microsomal UDP-glucuronosyltransferase activity toward 1-naphthol in the bovine kidney cortex was found to be higher than that in the liver and other organs, and mRNA of bovUGT1A6 was more strongly detected in the kidney on Northern blotting analysis. These results suggest that the bovine kidney, which strongly expresses bovUGT1A6, i...Continue Reading

Citations

Mar 1, 2011·Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology·Manoja PretheebanDan Rurak
Jun 19, 2010·Journal of Veterinary Pharmacology and Therapeutics·G VirkelC Nebbia
Nov 11, 2010·Journal of Veterinary Pharmacology and Therapeutics·L MatéC Lanusse
Jun 15, 2012·Xenobiotica; the Fate of Foreign Compounds in Biological Systems·Vanessa ZancanellaMauro Dacasto
Feb 21, 2002·World Journal of Gastroenterology : WJG·X LiY L Qian

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