Polymorphism of human Alpha class glutathione transferases

dc.contributor.authorTetlow, Natasha
dc.contributor.authorLiu, Dan
dc.contributor.authorBoard, Philip
dc.date.accessioned2015-12-13T23:41:37Z
dc.date.available2015-12-13T23:41:37Z
dc.date.issued2001
dc.date.updated2015-12-12T09:33:11Z
dc.description.abstractThe recognition of the importance and utility of single nucleotide polymorphisms has generated an interest in the development of new strategies for their identification. Analysis of the Expressed Sequence Tag (EST) database can provide a rapid and efficient means of identifying polymorphisms. Screening of the Alpha class glutathione transferases (GSTs) in the EST database identified 10 putative polymorphisms in the coding region of the GSTA1 and GSTA2 genes, six of which were subsequently verified by sequence analysis. Polymerase chain reaction/restriction fragment length polymorphism analysis revealed the existence of three variants, a silent base substitution, K125K (G365A) in GSTA1, and T112S and E210A in GSTA2, in European Australian, African and Chinese populations. The variant isoforms of GSTA2 were expressed in Escherichia coli, purified, and enzymatically characterized. Modelling of the two GSTA2 polymorphisms into a three-dimensional structure of GSTA2, and characterization of their enzymatic properties, has shown that the structure and function of the wild-type GSTA2-2 isoenzyme is not significantly altered by these polymorphisms. This report demonstrates that analysis of the EST database provides a rapid and efficient means of identifying variant proteins.
dc.identifier.issn1744-6872
dc.identifier.urihttp://hdl.handle.net/1885/94982
dc.publisherLippincott Williams & Wilkins
dc.sourcePharmacogenetics and Genomics
dc.subjectKeywords: enzyme variant; glutathione transferase; isoenzyme; article; data analysis; data base; enzyme activity; enzyme analysis; expressed sequence tag; human; nucleic acid base substitution; nucleotide sequence; polymerase chain reaction; priority journal; restr EST; Glutathione; Polymorphism; Transferases
dc.titlePolymorphism of human Alpha class glutathione transferases
dc.typeJournal article
local.bibliographicCitation.issue7
local.bibliographicCitation.lastpage617
local.bibliographicCitation.startpage609
local.contributor.affiliationTetlow, Natasha, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationLiu, Dan, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBoard, Philip, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidTetlow, Natasha, u9718329
local.contributor.authoruidLiu, Dan, u4245938
local.contributor.authoruidBoard, Philip, u7701651
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor060107 - Enzymes
local.identifier.ariespublicationMigratedxPub24704
local.identifier.citationvolume11
local.identifier.doi10.1097/00008571-200110000-00007
local.identifier.scopusID2-s2.0-0034790912
local.type.statusPublished Version

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