DEDUCED AMINO-ACID-SEQUENCE, GENE STRUCTURE AND CHROMOSOMAL LOCATION OF A NOVEL HUMAN CLASS MU GLUTATHIONE-S-TRANSFERASE, GSTM4

被引:44
|
作者
ZHONG, S
SPURR, NK
HAYES, JD
WOLF, CR
机构
[1] ICRF, MOLEC PHARMACOL GRP, HUGH ROBSON BLDG, GEORGE SQ, EDINBURGH EH8 9XD, SCOTLAND
[2] ICRF, HUMAN GENET RESOURCES LAB, CLARE HALL LABS, POTTERS BAR EN6 3LD, HERTS, ENGLAND
[3] UNIV EDINBURGH, ROYAL INFIRM, DEPT CLIN BIOCHEM, EDINBURGH EH3 9YW, MIDLOTHIAN, SCOTLAND
关键词
D O I
10.1042/bj2910041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Mu-Class glutathione S-transferases (GSTs) are subject to marked inter-individual variation in man, owing to the fact that 40-50% of the population fail to express M1 subunits. Mu-Class GST from two lymphoblastoid cell lines (expressing M1 subunits and the other 'nulled' for M1) have been studied. Both cell lines were found to express a Mu-Class GST that has. not been described previously. The cDNA encoding this novel transferase, designated 'GSTM4', has been isolated and the enzyme shown to be comprised of 218 amino acids (including the initiator methionine residue) with an M(r) of approx. 25.5 kDa. Molecular cloning demonstrated that the lymphoblastoid cell line which expressed GSTM1 possessed the b allelic variant (i.e. that with an asparagine residue at position 173). The genes for GSTM4 and GSTM1b have been cloned and found to contain seven introns and eight exons. The coding region of the GSTM4 gene, including the seven introns, encompasses 5.0 kb, whereas the same region of GSTM1b is 5.5 kb; the difference in the size of the two genes is due to the length of intron 7. DNA sequencing allowed a GSTM4-gene-specific oligo-primer to be designed which has been utilized in a PCR-based assay to determine that the GSTM4 gene is located on chromosome 1.
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页码:41 / 50
页数:10
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